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Welcome to the QIP Consulting Policy and Procedure Manual (Version 1, 1 July 2011 –
aligned with the RACGP 4th edition Standards). This manual has been developed to assist
practices with the policies and procedures that are required for accreditation and the day-to-day
running of a general practice.
Please note:





this manual is a generic template, designed for general practices in Australia. It must be
adapted and changed to make it relevant to your individual practice situation and
state/country.
there are additional procedures included in this manual that are not directly required to
meeting the flagged RACGP standards for General Practice. These are included because
the authors believe practices should be aiming to exceed the minimum standards.
please delete or amend the procedures as required. However, deleting some parts may
jeopardise your opportunity to obtain reduced insurance subsidies, accreditation or
maintain compliance with legal obligations and standards.
please refer to the RACGP 4th edition Standards when amending policies.
always refer to local, State or Territory and/or Federal legislation to ensure that your
policies and procedures are aligned with these requirements.
Customising this manual
(Select Option X)
As this is a generic manual the best practice or current practice guidelines have been used
where possible to determine the procedures listed. However, in some cases the equipment
available can determine the way something is achieved.
The option choices (usually written in italic font) will guide you to select the correct procedure for
your situation. It is important to delete the other options according to the instructions, as they will
not be applicable to your practice.
(*Insert Name)
Sometimes the specific name of a person or the supplier of a service needs to be added. Delete
this symbol after adding the name or details required.
Quality in Practice Consulting would like to acknowledge and thank Dandenong Casey General
Practice Association (DCGPA) and the members of the Dandenong Accreditation Advisory
Group for developing this manual.
Whilst every effort is made to ensure accuracy, Quality in Practice Pty Ltd do not accept any
liability for any injury, loss or damage incurred by use of, or reliance on the information included
within this document. Users of this document are required to customise it according to local,
State or Territory and/or Federal legislative requirements as well as that which is listed in the
latest version of the RACGP Standards for General Practices.
Developed by Dandenong Casey General Practice Association and purchased under
licence by QIP Consulting as a resource for AGPAL accredited general practices.
Page i of 260
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(*Practice Name)
Policy & Procedure
Manual
(*Date of Creation)
(*Date of Revision)
Developed by Dandenong Casey General Practice Association and purchased under
licence by QIP Consulting as a resource for AGPAL accredited general practices.
Page ii of 260
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Table of Contents
1
Introduction
1.1
1.2
1.3
1.4
1.5
1.6
1.7
Mission Statement ........................................................................................................ 1
Practice background .................................................................................................... 1
Practice profile .............................................................................................................. 1
Practice team................................................................................................................. 2
Practice services........................................................................................................... 3
Practice hours ............................................................................................................... 3
Practice consultation fees ........................................................................................... 3
2
Human Resources
2.1
2.2
2.3
2.4
2.5
2.6
2.7
2.8
2.9
2.10
Awards & Entitlements................................................................................................. 4
Position Evaluation and Recruitment ......................................................................... 8
Staff Employment Records ........................................................................................ 14
Staff Induction ............................................................................................................. 18
Privacy ......................................................................................................................... 21
Performance Review .................................................................................................. 21
Disciplinary Process .................................................................................................. 26
Staff Code of Conduct ................................................................................................ 33
Staff Presentation ....................................................................................................... 35
Equal Opportunity, Bullying & Harassment............................................................. 36
3
Occupational Health & Safety
3.1
Manual Handling ......................................................................................................... 46
3.1.2 Incidents and Injury and Adverse Patient Events ....................................................... 48
3.1.3 Sharps Injury Management and Other Body Fluid Exposure..................................... 50
3.1.4 Staff Immunisation ...................................................................................................... 53
3.1.5 Smoking, Drugs & Alcohol .......................................................................................... 56
3.1.6 Staff Health and Wellbeing (including GPs) ............................................................... 57
3.2
Practice Facilities........................................................................................................ 59
3.2.1 Consulting Rooms ...................................................................................................... 60
3.2.2 Hand Washing Facilities ............................................................................................. 61
3.2.3 Waiting Area ............................................................................................................... 62
3.2.4 Toilets ......................................................................................................................... 62
3.2.5 Telecommunication System ....................................................................................... 63
3.2.6 Unauthorised Access Areas ....................................................................................... 64
3.3
Security ........................................................................................................................ 65
3.4
Non Medical Emergencies ......................................................................................... 67
4
Infection Control
4.1
4.2
4.3
4.4
4.5
4.6
Principles of infection control ................................................................................... 69
Blood and body fluid spills ........................................................................................ 71
Hand washing and hand hygiene .............................................................................. 74
Handling and use of chemicals ................................................................................. 77
Single Use Equipment ................................................................................................ 79
Instrument and equipment processing area............................................................ 80
Developed by Dandenong Casey General Practice Association and purchased under
licence by QIP Consulting as a resource for AGPAL accredited general practices.
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4.7
4.8
4.8.1
4.8.2
4.8.3
4.8.4
4.8.5
4.8.7
4.8.8
4.9
4.10
4.11
4.12
4.13
4.14
4.15
4.16
5
Cleaning reusable Instruments and equipment ...................................................... 83
Provision of sterile items ........................................................................................... 86
Loading the steriliser ................................................................................................... 93
Sterilisation cycle parameters ..................................................................................... 95
Unloading the steriliser ............................................................................................... 96
Documentation of the Cycle. ....................................................................................... 98
Maintenance of the steriliser ....................................................................................... 99
Monitoring the Sterilisation Process ......................................................................... 100
Validation of the sterilisation processes.................................................................... 101
Storage of sterile items ............................................................................................ 104
Management of waste .............................................................................................. 105
Sharps Management................................................................................................. 108
Standard Precautions............................................................................................... 110
Transmission Based Precautions ............................................................................ 111
Personal Protective Equipment (PPE) .................................................................... 112
Laundry ...................................................................................................................... 115
Safe handling of pathology specimens .................................................................. 116
Practice Management
5.1
Access & Parking...................................................................................................... 117
5.2
Appointments ............................................................................................................ 119
5.3
Home Visits ............................................................................................................... 122
5.4
Telephone .................................................................................................................. 124
5.4.1 Communication with patients via electronic means .................................................... 128
5.5
Visitors ....................................................................................................................... 131
5.6
Medical Emergencies & Urgent Queries ................................................................ 132
5.7
After Hours Service .................................................................................................. 134
5.8
Practice Meetings ..................................................................................................... 136
5.9
Patient Rights ............................................................................................................ 139
5.10
Complaints ................................................................................................................ 141
5.11
Non English Speaking Patients ............................................................................... 144
5.11.1 Culturally Appropriate Care........................................................................................ 146
5.12
Directory of Local Health and Community Services............................................. 148
5.13
Provision of Brochures, Leaflets and Pamphlets for Patients ............................ 149
5.13.1 Practice Information Sheet ........................................................................................ 151
5.14
Office Supplies .......................................................................................................... 153
5.15
Environmental Cleaning Service............................................................................. 154
6
Privacy and Personal Health Information
6.1
6.1.1
6.1.2
6.2
6.3
6.3.1
6.3.2
6.4
6.4.1
Privacy and Security of Personal Health Information .......................................... 158
Computer Information Security ................................................................................... 163
Practice Privacy Policy ................................................................................................ 165
3rd Party Requests for Access to Medical Records/Health Information ............. 167
Request for Access to Personal Health Information ............................................ 172
Privacy Officer........................................................................................................... 177
Privacy Audit ............................................................................................................. 178
Medical Records Administration Systems............................................................. 179
Creating a New Medical Record ............................................................................... 180
Developed by Dandenong Casey General Practice Association and purchased under
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6.4.2
6.4.3
6.4.4
6.4.5
6.4.6
6.4.7
6.4.8
7
Retrieving a Medical Record for a Current Patient................................................... 180
Filing Reports (Pathology, X-Ray, Consultant’s etc) ................................................ 180
Errors in Medical Record ......................................................................................... 181
Allergies & Alerts...................................................................................................... 181
Back Up of electronic medical records .................................................................... 181
Retention of Records and Archiving ........................................................................ 182
Transfer of Medical Records ................................................................................... 184
Clinical Management
7.1
Clinical Autonomy .................................................................................................... 186
7.2
Clinical Content of Medical Records ...................................................................... 187
7.3
Informed Consent ..................................................................................................... 193
7.4
Referral Protocols .................................................................................................... 196
7.5
Clinical Handover..................................................................................................... 199
7.6
Patient Identification ................................................................................................ 200
7.7
Follow up of Tests, Results and Referrals ............................................................. 202
7.8
Reminder Systems for Preventative Care .............................................................. 206
7.9
Notifiable Diseases ................................................................................................... 208
7.10
3rd Party Observing or Clinically involved in the Consultation .......................... 210
7.12
Management of a Patient Refusing Treatment or Advice .................................... 213
7.13
Refusal to Treat a Patient......................................................................................... 214
7.14
Practice Equipment .................................................................................................. 215
7.14.1 Medical Equipment and Resources ......................................................................... 216
7.14.2 Doctor’s Bag ............................................................................................................ 218
7.14.4 Vaccine Administration ............................................................................................ 221
7.14.5 Drug Storage, Supply and Administration ............................................................... 222
7.14.6 Clinical References and Resources......................................................................... 230
7.14.7 Checking and Rotating Medical Supplies ................................................................ 231
8
Continuous Improvement
8.1 Risk Assessment & Management .................................................................................. 232
8.1.1 Review of Policies & Procedures.............................................................................. 234
8.1.2 Continuing Staff Education ....................................................................................... 235
8.1.3 Accreditation & Continuous Improvement ................................................................ 239
8.1.4 Patient Feedback ...................................................................................................... 242
8.1.5 Management of Potential Medical Defence Claims .................................................. 244
8.1.6 Continuity of Care ..................................................................................................... 245
8.1.7 Clinical Governance.................................................................................................. 247
Developed by Dandenong Casey General Practice Association and purchased under
licence by QIP Consulting as a resource for AGPAL accredited general practices.
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Table of Contents
a)
b)
Reverse Index: 4th Edition RACGP Standards and relevant Protocols
Notes to Policy and Procedure Manual
Forward / Disclaimer
1. Introduction
1.1
1.2
1.3
1.4
1.5
1.6
Mission Statement
Practice Philosophy
Practice Background
Practice Structure
Organisational Chart
Services
2. Human Resource Management
2.1
2.2
2.3
2.4
2.5
2.6
2.7
2.8
2.9
2.10
2.11
Awards and Entitlements
Position Evaluation and Recruitment
Staff Employment Records
Staff Induction
Privacy
Performance Review
Disciplinary Process
Staff code of Conduct
Staff Presentation
Equal Opportunity Bullying and Harassment
Forms, Templates and Checklists
 4.1.1
 3.1.3 & 4.1.1
 3.2.1, 3.2.3, 3.2.2 & 4.1.1
 4.1.1 & 5.3.3
 4.2.1
 4.1.1
 4.1.1
 5.3.3, 3.1.2 & 4.1.1
 4.1.2 & 4.1.1
3. Workplace Health & Safety
3.1
3.1.1
3.1.2
3.1.3
3.1.4
3.1.5
3.1.6
3.2
3.2.1
3.2.2
3.2.3
3.2.4
3.2.5
3.2.6
Occupational Health and Safety
Manual Handling
Incidents and Injury and Adverse Patient Events
Sharps injury Management and other Body fluid
Exposure
Staff Immunisation
Smoking, Drugs and Alcohol
Staff & GP Wellbeing
Practice Facilities
Consulting Rooms
Hand washing Facilities
Waiting Area
Toilets
Telecommunication System
Unauthorised Access Areas
 4.1.2, 5.3.3 & 3.1.3
 5.1.1 & 4.1.2
 1.5.2, 3.1.4 & 3.1.2
 5.3.3
 5.3.3
 4.1.2
 5.1.1 & 5.1.2
 5.1.1 & 5.1.2
 5.3.3
 5.1.1 & 5.1.2
 5.1.1
 5.1.2
 5.1.1
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3.3
3.4
3.5
Security
Non Medical Emergencies
Forms, Templates and Checklists
 5.1.1 & 4.1.2
 4.1.2 & 3.1.2
4. Infection Control
4.1
4.2
4.3
4.4
4.5
4.6
4.7
4.8
4.9
4.10
4.11
4.12
4.13
4.14
4.15
4.16
4.17
Principles of Infection control
Blood and body fluid spills
Hand Washing and Hand Hygiene
Handling and use of Chemicals
Single use equipment
Instrument and Equipment processing area
Cleaning reusable Instruments and Equipment
Provision of Sterile items
Storage of Sterile items
Management of Waste
Sharps Management
Standard Precautions
Transmission Based Precautions
Personal Protective equipment PPE
Laundry
Safe Handling of Pathology specimens
Forms, Templates and checklists
 5.3.3
 5.3.3
 5.3.3
 5.3.3 & 4.1.2
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
 5.3.3
5. Practice Administration
5.1
5.2
Access and Parking
Appointments
5.3
5.4
5.4.1
5.5
5.6
5.7
5.8
5.9
5.10
5.11
5.11.1
5.12
5.13
Home Visits
Telephone
Communication with Patients via Electronic Means
Visitors
Medical Emergencies and Urgent Queries
After Hours Service
Practice Meetings
Patient Rights
Complaints
Non English Speaking Patients
Culturally Appropriate Care
Directory of Local Health and Community Services
Provision of Brochures, Leaflets and Pamphlets for
Patients
Practice Information Sheet
Office Supplies
Environmental Cleaning Service
5.13.1
5.14
5.15
 5.1.3 & 5.1.1
 1.1.1, 1.2.4, 3.1.4, 1.4.2 &
2.1.1
 1.1.3
 1.1.1, 1.1.2, 1.1.4 & 1.2.3
 1.1.2 & 1.2.1
 5.1.1
 1.1.1, 1.2.4 & 1.1.4
 1.1.1, 1.1.4, 1.2.4 & 1.5.2
 1.4.1, 3.1.2 & 4.1.1
 1.2.1, 1.2.2 & 2.1.1
 2.1.2
 2.1.2, 1.2.3 & 2.1.1
 1.4.1, 1.7.1 & 2.1.1
 1.6.1
 1.2.3 & 1.3.1
 1.2.1, 1.2.3 & 1.2.4
 5.3.3
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6. Privacy and Medical Records
6.1
6.1.1
6.1.2
6.2
6.3
6.3.1
6.3.2
6.4
6.4.1
6.4.2
6.4.3
6.4.4
6.4.5
6.4.6
6.4.7
6.4.8
Privacy and Security of Personal Health Information
Computer Information Security
Practice Privacy Policy
3rd Party Requests for Access to Medical Records /
Health Information
Patients Request for Access to Personal Health
Information Under the Privacy Legislation
Privacy Officer
Privacy Audit
Medical Records Administration
Creating a new Medical Record
Retrieving a Medical Record for a current Patient
Filing Reports (Pathology, X-Ray, Consultant’s etc)
Errors in Medical Record
Allergies & Alerts
Back Up of electronic medical records
Retention of Records and Archiving
Transfer of Medical Records
 4.2.1 & 3.1.4
 4.2.1 & 4.2.2
 4.2.1
 4.2.1, 3.1.4 & 4.2.2
 4.2.1
 4.2.1
 3.1.4
 4.2.1
 1.7.2
 4.2.2
 4.2.2, 4.2.1 & 1.7.1
 4.2.1 & 4.2.2
7. Clinical Management
7.1
7.2
Clinical Autonomy
Clinical content of Medical Records
7.3
7.3.1
Informed Consent
Referral Protocols
7.3.2
7.4
7.5
7.6
7.7
7.8
Clinical Handover
Patient Identification
Follow Up of Tests, results and referrals
Reminder Systems for preventative care
Notifiable Diseases
3rd Party Observing or Clinically involved in the
consultation
Research Projects
Management of a patient refusing treatment or
advice
Refusal to treat a patient
Practice Equipment
Medical equipment and Resources
Doctors bag
Vaccine Storage
Vaccine Administration
7.9
7.10
7.11
7.12
7.12.1
7.12.2
7.12.3
7.12.4
 1.4.2
 1.7.1, 1.7.2, 1.7.3, 1.1.3,
1.1.4, 5.3.1, 1.5.1 & 3.1.4
 1.2.2, 1.2.4 & 5.3.1
 1.2.4, 3.1.4, 1.5.2, 1.6.1,
5.3.1 & 1.6.2
 1.5.2 & 5.3.1
 3.1.4 & 5.3.1
 1.1.4, 3.1.4 & 1.5.3
 1.3.1
 4.2.1
 1.2.3 & 2.1.3
 4.2.1
 2.1.1
 2.1.1
 5.2.1
 1.4.2 & 5.2.1
 5.2.2
 5.3.1 & 5.3.2
 5.3.1 & 1.5.2
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7.12.5
7.12.6
7.12.7
7.13
Drug Storage Supply and administration
Clinical References and resources
Checking and Rotating Medical supplies
Forms, Templates and Checklists
 5.3.1
 1.3.1, 1.4.1 & 5.3.1
 5.3.1
8. Continuous Improvement and Education
8.1
8.1.1
8.1.2
8.1.3
8.1.4
8.1.5
8.1.6
8.1.7
Risk Assessment & Management
Review of Policies & Procedures
Continuing Staff Education
Accreditation & Continuous Improvement
Patient Feedback
Management of Potential Medical defence claims
Continuity of Care
Clinical Governance
 3.1.2 & 4.1.2
 3.1.1 & 5.3.3
 3.2.1, 3.2.2, 3.2.3 & 5.3.3
 4.2.1, 2.1.2, 3.1.1 & 3.1.3
 2.1.2
 3.1.2
 1.1.1, 1.4.1, 1.5.1 & 1.5.2
 3.1.3, 5.3.1, 5.3.2, 5.3.3,
4.1.1 & 4.2.2
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Reverse Index
RACGP 4th edition Standard
Location of written protocols
in AGPALs Policy and
Procedure manual
Section 1 - Practice services
Standard 1.1 Access to Care
1.1.1
Scheduling care in opening hours
1.1.2
Telephone & Electronic advice
1.1.3
Home & Other visits
1.1.4
Care Outside Normal opening hours
Standard 1.2 Information about the practice
1.2.1
Practice information
1.2.2
Informed Patient Decisions
1.2.3
Interpreter and other communication services
1.2.4
Costs associated with care initiated by the practice
 5.2, 5.4, 5.6, 5.7 & 8.1.6
 5.4 & 5.4.1
 5.3 & 7.2
 5.4, 5.6, 5.7,7.2 & 7.5
 5.4.1, 5.9 & 5.13.1
 5.9 & 7.3
 5.4, 5.13, 5.13.1, 7.8 & 5.11
 5.2, 5.6, 5.7, 5.13.1, 7.3 &
7.3.1
Standard 1.3 Health Promotion & Prevention of Disease
1.3.1
Health Promotion and Preventative care
 5.13, 7.6 & 7.12.6
Standard 1.4 Diagnosis & Management of Health Problems
1.4.1
Consistent Evidence Based Practice
 5.8, 5.11.1, 7.12.6 & 8.1.6
1.4.2
Clinical Autonomy for General Practitioners
 5.2, 7.1 & 7.12.1
Standard 1.5 Continuity of care
1.5.1
Continuity of Comprehensive care and the
 7.2 & 8.1.6
Therapeutic relationship
1.5.2
Clinical Handover
 3.1.2, 5.7, 7.3.1, 7.3.2,
7.12.4 & 8.1.6
1.5.3
System for follow up of tests and results
 7.5
Standard 1.6 Coordination of Care
1.6.1
Engaging with other services
 5.12 & 7.3.1
1.6.2
Referral Documents
 7.3.1
Standard 1.7 Content of Patient Health Records
1.7.1
Patient Health records
 5.11.1, 6.4.7 & 7.2
1.7.2
Health summaries
 7.2 & 6.4.5
1.7.3
Consultation notes
 7.2
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Section 2 - Rights and needs of patients
Standard 2.1 Collaborating with Patients
2.1.1
Respectful & Culturally appropriate care
2.1.2
2.1.3
Patient feedback
Presence of a third party
 5.2, 5.9, 5.11, 5.11.1, 7.10 &
7.11
 5.10, 5.11, 8.1.3 & 8.1.4
 7.8
Section 3 - Safety quality improvement and education
Standard 3.1 Safety and Quality
3.1.1
Quality Improvement activities
3.1.2
Clinical Risk Management system
3.1.3
Clinical Governance
3.1.4
Patient Identification
Standard 3.2 Education & Training
3.2.1
Qualifications of general practitioners
3.2.2
Qualifications of clinical staff other than medical
practitioners
3.2.3
Training of administrative staff
 8.1.1 & 8.1.3
 2.8, 3.1.2, 3.4, 5.8 & 8.1
 2.2, 3.1, 8.1.3 & 8.1.7
 3.1.2, 5.2, 6.1, 6.2, 6.4, 7.2,
7.3.1, 7.5 & 7.4
 2.3 & 8.1.2
 8.1.2 & 2.3
 2.3 & 8.1.2
Section 4 – Practice management
Standard 4.1 Practice Systems
4.1.1
Human Resource System
4.1.2
Occupational Health and Safety
Standard 4.2 Management of Health Information
4.2.1
Confidentiality & privacy of health information
4.2.2
Information security
 2.10, 2.1, 2.2, 2.3, 2.4, 2.6,
2.7, 2.8, 5.8 & 8.1.7
 3.1, 3.1.1, 3.1.6, 3.3, 3.4,
4.4, 8.1 & 2.10
 8.1.3, 2.5, 6.1, 6.1.1, 6.1.2,
6.2, 6.3, 6.3.1, 6.4.2, 6.4.7,
6.4.8, 7.7 & 7.9
 8.1.7, 6.1.1, 6.2, 6.4.6, 6.4.7
& 6.4.8
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Section 5 – Physical factors
Standard 5.1 Facilities and Access
5.1.1
Practice Facilities
5.1.2
Physical Conditions conductive to confidentiality &
privacy
5.1.3
Physical Access
Standard 5.2 Equipment for Comprehensive care
5.2.1
Practice Equipment
5.2.2
Doctors Bag
Standard 5.3 Clinical Support Processes
5.3.1
Safe and quality use of medicines
5.3.2
5.3.3
Vaccine Potency
Healthcare associated infections
 5.5, 3.3, 3.2.6, 5.1, 3.1.1,
3.2, 3.2.1, 3.2.2, 3.2.3 & 3.2.4
 3.2, 3.2.1, 3.2.3 & 3.2.5
 5.1
 7.12 & 7.12.1
 7.12.2
 7.2, 7.3, 7.3.1, 7.3.2, 7.4,
7.12.3, 7.12.4, 7.12.5, 7.12.6,
7.12.7 & 8.1.7
 7.12.3 & 8.1.7
 Section 4, 2.4, 2.8, 3.1,
3.1.3, 3.1.4, 3.2.2, 5.15, 8.1.1,
8.1.2 & 8.1.7
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1
Introduction
1.1 Mission Statement
Option 1: Use the sample practice mission statement below
Our mission is to provide the highest standard of patient care whilst incorporating a
holistic approach toward diagnosis and management of illness.
We are committed to promoting health, wellbeing and disease prevention to all patients.
We do not discriminate in the provision of excellent care and aim to treat all patients with
dignity and respect.
Option 2: Add your own practice mission statement here
1.2 Practice background
Write a short description of your practice here. Areas you may wish to include are the
history behind your practice, location, particular interest areas, communities the practice
services and other important information you would like to add.
1.3
Practice profile
Name of practice
* name of practice
Street address
* street address
Postal address
* postal address
In hours phone number
* in hours phone number
After hours phone number
* after hours phone number
Fax number
* fax number
Email address
* email address
Web address
* web address
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1.4
Practice team
Medical
* Medical position
* name of medical person
* Medical position
* name of medical person
* Medical position
* name of medical person
* Medical position
* name of medical person
* Medical position
* name of medical person
Allied health
* Allied health professional
* name of allied health professional
* Allied health professional
* name of allied health professional
Nursing
* Nursing position
* name of nurse
* Nursing position
* name of nurse
Administrative
* Administrative position
* name of administrative person
* Administrative position
* name of administrative person
* Administrative position
* name of administrative person
* Administrative position
* name of administrative person
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1.5
Practice services
In addition to general medical consultations, our practice offers the following services:
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
* insert practice services
(* customise this section as appropriate)
There is a range of posters, leaflets, and brochures about health issues relevant to the
community available for all of our patients in:

the waiting room

the consultation rooms.
1.6
Practice hours
Monday to Friday
* Monday to Friday hours
Saturday
* Saturday hours
Sunday
Home visits
* Sunday hours
* Regular hours that home visits are conducted
Home visit appointments can be made outside these times by
prior arrangement with the receptionist at the discretion of the
doctor.
1.7
Practice consultation fees
(* customise this section as appropriate)
An up-to-date copy of our schedule of fees is located:

at reception

in the practice information sheet.
Further information about informing patients of the cost of care can be found in Practice fees.
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2
Human Resources
Medical practices are advised to be continually informed and up to date in respect of workplace
relations legislation, regulations and decisions of Fair Work Australia. As the Fair Work Act 2009
is new, it is subject to amendment.
2.1 Awards & Entitlements
Policy
This practice complies with all its legal obligations towards its employees. These include:
 provision of rates of pay, leave and other entitlements as set out in the relevant Award
or workplace agreement;
 a safe and healthy workplace;
 equal opportunity and freedom from discrimination and harassment
 protection of employee and patient privacy; and
 maintenance of appropriate staff records.
Additionally, this practice follows established procedures and policies for employment and
management of staff, including:
 clear communication of expectations and standards, using position descriptions and
job specifications as well as staff codes for conduct and presentation.
 recruitment procedures which are fair, thorough and facilitate selection of the best
candidate.
 a formal induction procedure for all staff, to familiarise them with important practice
procedures relating to patient care, occupational health and safety, emergencies,
confidentiality and conduct.
 regular feedback and opportunities for development through performance review.
Research from both general practice and other industries supports the importance of
attention to human resources. For example, the alignment of role, competence and (where
required) licensing was identified by the authors of a study of high performing clinical teams
as a common element.
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Procedure
Under the Fair Work Act 2009, medical practices are bound by Workplace Agreements or
Federal Awards which set out minimum employee entitlements. If medical practices are not
bound by a workplace agreement, then they must abide by the relevant awards.
From 1 January 2010, the 10 National Employment standards (NES) became law and
replaced the Australian Fair Pay and Conditions Standards. All modern Awards, Enterprise
Agreements, contracts of employment, ITEA’s and old Workplace Agreements must provide
for these 10 NES as minimum conditions.
The NES applies to all employees covered by the national workplace relations system, however
only certain entitlements apply to casual employees.
Under the NES, employees have certain minimum conditions. Together with pay rates in modern
awards (which also generally take effect from 1 January 2010) and minimum wage orders, the
NES makes up the safety net that cannot be altered to the disadvantage of the employee.
In addition to the NES, generally an employee’s terms and conditions of employment come from
a modern award, agreement, award and agreement based transitional instruments, minimum
wage orders, transitional minimum wage instruments, state or federal laws.
The NES are set out in the Fair Work Act 2009 and comprise 10 minimum standards of
employment. In summary, the NES involve the following minimum entitlements:








Maximum weekly hours of work – 38 hours per week, plus reasonable additional hours.
Requests for flexible working arrangements – allows parents or carers of a child under
school age or of a child under 18 with a disability, to request a change in working
arrangements to assist with the child’s care.
Parental leave and related entitlements – up to 12 months unpaid leave for every
employee, plus a right to request an additional 12 months unpaid leave, plus other forms of
maternity, paternity and adoption related leave.
Annual leave – 4 weeks paid leave per year, plus an additional week for certain shift
workers. Nurses are classified as shift workers entitled to an additional week of annual
leave.
Personal / carer’s leave and compassionate leave – 10 days paid personal / carer’s
leave, two days unpaid carer’s leave as required, and two days compassionate leave
(unpaid for casuals) as required.
Community service leave – unpaid leave for voluntary emergency activities and leave for
jury service, with an entitlement to be paid for up to 10 days for jury service.
Long service leave – a transitional entitlement for certain employees who had certain LSL
entitlements before 1/1/10 pending the development of a uniform national long service
leave standard.
Public holidays – a paid day off on a public holiday, except where reasonably requested
to work.
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

Notice of termination and redundancy pay – up to 4 weeks notice of termination (5
weeks if the employee is over 45 and has at least 2 years of continuous service) and up to
16 weeks redundancy pay, both based on length of service.
Provision of a Fair Work Information Statement – From 1 January 2010, all employers
covered by the national workplace relations system have an obligation to give each new
employee a Fair Work Information Statement (the Statement) before, or as soon as
possible after, the employee starts employment. It contains information about the NES,
modern awards, agreement-making, the right to freedom of association, termination of
employment, individual flexibility arrangements, rights of entry, transfer of business, and
the respective roles of Fair Work Australia and the Fair Work Ombudsman
Option 1:
Employment under Awards (Select the appropriate option/s depending on what you use at
your practice and list staff groups employed under each option).
Awards provide for minimum rates of pay and a safety net of employment terms and
conditions. Often employers will negotiate additional over-award terms and conditions in
order to attract, retain and reward their staff.
Awards Applicable to Medical Practices
Health Professionals and Support Services Award 2010 (Award code MA000027) Reception staff, practice managers, bookkeepers, payroll people, and cleaners
Nurses Award 2010, (Award code MA000034).
(ii) Medical Practitioners Award 2010 (Award code MA000031).
Royal Australian College of General Practitioners & General Practice Training Employees Award
2003 (transitional) Award (MAA000027).
Copies of awards and lots of other information is available from the Fair Work Australia web
site: www.fairwork.gov.au or telephone 131394.
Option 2:
Workplace Agreements (Select the appropriate option/s depending on what you use at
your practice and list staff types employed under each option).
Employers and employees may enter an agreement to override or vary award provisions to
provide greater flexibility in respect of entitlements and conditions of employment, e.g.
working hours, salary packaging or work-life balance initiatives.
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The previous Work Choices legislation provided for two forms of Agreement.
1. Australian Workplace Agreement, (AWA’s). The making of new AWA’s is no
longer allowed under the Fair Work Act 2009. AWA’s made in accordance with the
old Work Choices Legislation will continue for their nominated life up to a maximum
period of 5 years. Upon the attainment of the nominal expiry date, the AWA’s cease
to operate and the employee and the employer are bound by the terms of the
respective Award.
2. Collective Agreements (CA). Collective Agreements made under the previous
work Choices legislation continue on until replaced by a new Agreement or are
cancelled by Fair work Australia.
The new Fair Work Act 2009 provides for three forms of agreements.
1. Individual Transitional Employment Agreements (ITEA’s).
The making of new ITEA’s was permitted under the Fair Work Act 2009 until 31
December 2009 ITEA’s made in accordance with the new Fair Work Act 2009 continue
until they are replaced by an Enterprise Agreement or are cancelled by Fair work
Australia. In the absence of an Enterprise Agreement, the ITEA having been cancelled,
the employee and the employer are bound by the terms of the respective Award.
2. Enterprise Agreements (EA).
Enterprise Agreements are made between the Employer and a group of employees, (i.e.
more than one employee), must satisfy the Better Off Overall Test, (the “BOOT”), and be
approved by Fair Work Australia.
3. Individual Flexibility Agreements
The Employer and the employee may enter into an Individual flexibility Agreement which
is based on the employee’s Award. The Award lists the conditions which may be varied
and any variation agreed must ensure that the minimum Award conditions are met and
for the employer is Better Off Overall; (the BOOT).
RACGP 4th edition Standards 4.1.1.
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2.2 Position Evaluation and Recruitment
Policy
Effective selection and management of staff is critical to the success of this practice. Our ability
to care for patients and operate a successful medical practice depends upon attracting,
developing and retaining the right people.
All new positions are evaluated in terms of the current needs and future goals of the practice.
Practice members need clarity regarding their role and responsibilities in the practice. A job
description is developed, to clearly communicate the responsibilities and expectations of the
position. A position description establishes the role of the employee within the organisation
documents the parameters of the responsibilities and duties associated with that position and
forms the basis for evaluation and lines of accountability. Recruitment, training and development,
performance evaluation, remuneration management and succession planning can all be based
on the parameters of a position description.
Selection criteria are developed based on the job description.
The selection procedure is non-discriminatory and all candidates treated with courtesy and
respect.
The successful candidate is provided with a Letter of Offer of Employment prior to
commencement, which is signed by both the candidate and the employer. This ensures both
parties have a clear understanding and a written record of the agreed terms and conditions of
employment.
Procedure
General practitioners and other staff need documented position descriptions that outline and
define their current roles, responsibilities and conditions of employment.
Position descriptions are signed by employees to indicate that roles and responsibilities are
acknowledged and understood.
Included within our position descriptions are any designated areas of responsibility and that all
members of our practice team take responsibility for a multidisciplinary culture of safety, quality
and open communication.
Practice team members need to know who is responsible for various aspects of the practices
operations, including who has primary responsibility and who has delegated responsibility. (Refer
Section 8 Clinical governance).
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Designated areas of responsibility and leadership include:
 RACGP STD 3.1.2 Clinical Risk management systems including receiving and
disseminating any important communication or updates (e.g. health alerts) and
contingency plans.
 RACGP STD 3.1.3 Clinical leadership.
 RACGP STD 4.1.1 Leader of quality improvement and risk management processes (non
clinical).
 RACGP STD 4.1.1 Clinical care.
 RACGP STD 4.1.1 Information management.
 RACGP STD 4.1.1 Human resources.
 RACGP STD 4.1.1 Coordinates the seeking of feedback and the investigation and
resolution of administrative and/or other complaints.
 RACGP STD 4.1.2 Occupational Health and Safety (Health and Safety representative).
 RACGP STD 4.2.1 Privacy Officer.
 RACGP STD 4.2.2 Electronic systems and computer security.
 RACGP STD 5.3.1 Proper storage and security of medicines
 RACGP STD 5.3.2 Cold chain management.
 RACGP STD 5.3.3 Infection control Infection control processes within our practice.
(e.g. sterilisation process, staff immunisation, staff education).
 RACGP STD 5.3.3 Environmental cleaning.
Recruitment process
Our recruitment process includes the following:
Step 1: Position evaluation
Look at the position in relation to other staff and the future needs of the practice. There may be
an opportunity for existing staff to develop new skills. Can some jobs be redistributed to increase
efficiency or even eliminate the need for this position? Are there additional skills which may be
incorporated into this position to assist the practice achieve its goals for the future? Is there
room for the new person to work at the practice, or can the position include some off-site work?
Speak to your division about options.
Consult with current staff and include them in the decision-making process.
Consider the long-term goals of the practice and use this as an opportunity to plan strategically
towards achieving them.
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Step 2: Job description
Determine the key requirements of the position, considering which ones are essential and which
are desirable and use this information to compile a job description with clear specifications for
the position. Include the following:






skills: what skills does the position require? Is training an option?
qualifications: what is the minimum required? Are there others which would be an
advantage?
personal attributes: what personal attributes are needed? Are there physical requirements
essential to the position such as the ability to lift and bend?
hours per week: full time or part time? Is there weekend or night work?
is the position permanent, casual or fixed-term contract? How long is the qualifying or
probationary period (usually 3-6 months)?
remuneration: what award is applicable? What award/agreement classification will the
position be (if applicable)? What is the salary range or hourly rate? Are there any other
benefits offered, such as flexible hours, family friendly options, training, salary packaging or
incentive payments.
Step 3: Advertising the vacancy
Write the advertisement, ensuring it complies with EEO legislation – see procedure 2.10. Include
information about duties, required skills, qualifications, hours and location. For practice nurses,
the award requires that the salary grade classification be included in all job advertisements
(Refer to the hints below for more information). Consider how candidates are to apply – by
email, mail, fax, or telephone? Is there a closing date for applications?
Vacancies can be advertised in a number of ways:
 advertisements can be placed in newspapers (local and/or state) on the internet or in
professional journals.
 professional associations and networks may also advertise vacancies in their newsletters
or web sites, such as the DCGPA web site.
 for non-clinical staff local Job Network organisations will find candidates at no charge.
 employment agencies and recruitment consultants will handle the entire recruitment
process.
 junior or graduate staff may be sourced from local schools and educational institutions.
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Step 4: Selection of applicants to interview
Selection criteria form: Compile a list of selection criteria based on the job description and other
factors (e.g. previous stability of employment), making sure of compliance with EEO - procedure
2.10.


selection: Compare all applications received against the selection criteria, and select
those who best fit the criteria.
arrange interviews: Contact the candidates selected to arrange an interview. Candidates
may be required to bring documents to the interview, such as proof of qualifications,
samples of previous work or evidence of their right to work in Australia (for nonresidents).
Step 5: Prepare for Interviews




forms & Information: Prepare application forms (see sample following) and documents to
be given to applicants – this should include the job description and may also include
information about the practice, code of conduct, dress code etc.
interview procedure and location.
decide who will conduct the interview – an individual or a panel?
what questions will be asked? (Remember EEO - procedure 2.10.)
Set aside a suitable place for the interviews, free from interruptions.
Step 6: Conduct the Interviews
When the candidate arrives, provide them with an application form to fill in and a copy of the job
description.
Make sure all interviews are conducted by the same people and similar questions are asked,
although it is acceptable to include additional questions related to the candidate’s resume or in
response to comments made in the interview.
Allow the candidate to ask questions.
View original copies of qualifications, proof of membership of professional organisations,
professional indemnity insurance or right to work in Australia if the candidate has been required
to bring these to the interview. Note down document numbers on the application form, or
photocopy and attach to the form.
Discuss the impressions of each candidate after each interview and make brief notes on their
application form to record any employment arrangements or salary agreed upon. Do not make
notes which are in breach of EEO guidelines or are not relevant to the position.
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Step 7: Reference checks
Contact the referees nominated by the best candidates to confirm information given in the
interview or resume and find out about previous job performance.
Step 8: Medical examination, police checks or other tests
If relevant to the position, candidates may be required to take a pre-employment medical
examination, police checks and personality or skills tests. For more information on preemployment testing contact your division, employer group or a specialist recruitment agency.
These tests must be conducted prior to the job offer, as they are used to confirm suitability to the
position.
These tests must only examine characteristics which are directly relevant to the job, or they
could be in breach of EEO legislation.
Step 9: Job Offer
Once the successful candidate has been chosen they may be contacted by telephone to confirm
their acceptance of the position but this must be confirmed by a written Letter of Offer of
Employment.
Getting the contract or letter of appointment right in the first place means both parties are much
less likely to have problems later on.
As a minimum it should state:








employees name/address
position title and reference to the job description.
pay rate including which specific Award/agreement employed under including
classification or relevant Qualifications/Allowances.
full time/part time or casual, details such as days, shifts & minimum hours per week to be
worked.
name of employer.
workplace location/campus/ other work sites.
date of commencement.
probationary period any other special terms or conditions which have been negotiated
outside the award e.g. acknowledgement of prior service/entitlements (sick leave, long
service).
The letter of offer is provided prior to commencement, allowing the candidate time to read
through the offer and sign it to indicate their acceptance. This letter of offer should be written
carefully – a poorly worded phrase, a typing mistake or the omission of an important item may
prove to be very costly to the practice. The official employment agreement should be provided
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upon commencement of employment. This should refer to the award which covers the employee
and also any other items which are not listed within the award.
Take a photocopy of the Letter of Offer of Employment and keep it on file at the practice as a
record of the contract until a signed Letter of Offer is received from the candidate.
It is recommended that the practice compile an employee handbook containing all terms and
conditions of employment and the major policies of the practice as well as introductory
information about the practice and this is sent with the Letter of Offer of Employment. If a
handbook is not used, the Letter of Offer must inform new employees of the hours of work and
practice policies in relation to staff conduct, staff induction, privacy, occupational health & safety
and termination of employment, as described in the sample letter of offer at the end of this
section. This means the new employee is aware of all their key legal obligations and entitlements
before commencement.
The Letter of Offer of Employment should include a section for the employee to sign and return
to the practice indicating that they have read the Letter and Handbook and they accept all the
terms and conditions contained in them.
Once the signed letter is returned it should be filed in the employee’s personnel file and the copy
may be destroyed, if desired
Step 10: Notification of unsuccessful applicants
Unsuccessful candidates should be notified as soon as possible after the position is filled. Care
must be taken when advising unsuccessful applicants, to ensure equal opportunity or
discrimination legislation is not breached.
In line with the Privacy Act 1998, applicant’s details are kept for a specified period of time and
then disposed of as confidential documents.
Step 11: Prepare for the new employee
Prior to commencement, ensure facilities and resources such as a computer, desk, chair and
stationery are prepared for the new employee.
Is the necessary software set up on their computer?
(Make sure passwords and software access for previous employees have been removed, if
applicable).
Will they need a uniform or name tag?
Set up a Staff employment record file for the person. Refer to procedure 2.3
Step 12: Induction of new staff member
Please refer to procedure 2.4.
RACGP 4th edition Standards 3.1.3 & 4.1.1.
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2.3 Staff Employment Records
Policy
A range of information must be made and kept for each employee as prescribed by the Fair
Work Act 2009 and Fair Work Regulations 2009. Our practice understands that penalties apply
to employers who fail to comply with the record-keeping requirements of the Fair Work Act 2009.
Therefore we maintain staff employment records which comply with all legal and statutory
obligations. These include:





employment Records: Personnel files are kept for each employee recording
employment arrangements, clinical qualifications & registrations, professional
development, performance reviews and any other agreements or documents which
are relevant to employment relationship and the functions of the practice.
payroll records and pay slips: Which comply with regulations under the Fair Work Act
2009.
currency of Records: Employment records are reviewed at least annually to ensure
currency of clinical qualifications & registrations, professional indemnity insurance,
training records, immunisations and personal contact details.
confidentiality: Employment records are kept confidential, as required by the Privacy
Act 1998.
retention: Employment records are kept for 7 years.
In addition other staff records relating to professional standards or to provide documentary
evidence of meeting the RACGP Accreditation requirements are also maintained and kept
(e.g. staff education and training plans or evidence of qualification and competence).
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Procedure
Employment records
Documentation which is relevant to the employment relationship and practice functions is
retained on each employee, including but not limited those itemised in the Employee Records
checklist provided at the end of this section.
Our employee records are:







in a form that is readily accessible to a Fair Work Inspector
legible and in English (preferably in plain, simple English)
kept for seven years
not altered unless for the purposes of correcting an error
not false or misleading to the employer’s knowledge.
private and confidential. Generally, no one can access them other than the employee, their
employer, and relevant payroll staff.
made available at the request of an employee or former employee (copy only).
Payroll Records and Pay slips
In addition to the information kept in each individual employee’s file the practice maintains
records on payroll, taxation and superannuation transactions, as required by the Fair work Act
2009. These include:
Time and Wages Records
1)
2)
3)
4)
5)
6)
The name of the employer and the name of the employee.
From 1 January 2010 - the Australian Business Number (ABN) (if any) of the employer.
Date the employee started employment.
If the employee is full-time, part-time.
If the employee is permanent, temporary or casual.
The employee's pay rate, including gross and net amounts paid and any deductions from
the gross amount.
7) Any loadings, monetary allowances, bonuses, incentive-based payments, penalty rates or
other entitlements paid that can be singled out.
8) If a penalty rate or loading must be paid for overtime hours actually worked, the number of
hours of overtime worked, or when the employee started and finished working overtime.
9) Hours worked if the employee works casual or irregular part-time hours and is guaranteed
a pay rate set by reference to a period of time worked.
10) A copy of the written agreement if you and your employee have agreed to average the
employee's work hours.
11) If you and your employee have agreed to an individual flexibility arrangement, a copy of
that agreement, and, if the agreement is terminated, a copy of the termination.
12) Leave information for all types of leave, including:
a. leave taken
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b. leave balance
c. a copy of any agreement to cash out accrued leave, the rate of payment for the leave
and when the payment was made.
13) Employees paid superannuation (excluding payments to a defined benefit fund):
a. amount paid
b. pay period
c. date(s) paid
d. name of super fund
e. reason you paid super into the fund (e.g. a record of the employee's super fund
choice and the date that choice was made).
14) If the employee or employer terminates their employment:
a. name of the person who terminated the employment
b. how the termination took place - by consent, by notice, summarily or in some other
way (need to include details).
15) If the employee has been provided with a written guarantee of annual earnings for an
amount over $108,300 a year (indexed annually):
a. a copy of the written agreement
Pay Slips
Pay slips are given to each employee and these include the following, as required by the Fair
Work Act 2009.

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





the name of the employer and ABN (if any).
the name, position & classification of the employee.
the period to which the pay relates and the date it is paid.
the hourly rate (or annual rate, if applicable).
the hours worked, itemised as normal hours, overtime, penalty rates & loadings, leave
payments, etc, and the amount paid per hour for each income type.
details of any additional allowances or deductions.
the gross amount of the pay, taxation deducted and the net payment made.
superannuation contributions for the period with the fund name and employer & employee
contributions itemised separately.
Currency of Records
At least once per year the employment records for each staff member are reviewed. Each
employee is asked to provide:
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evidence of appropriate current national registration, if applicable.
for GPs evidence of satisfactory participation in the RACGP QI&CPD program or
equivalent.
for practice nurses evidence of sufficient hours of CPD to meet re-registration
requirements.
for all our staff, evidence that they have completed appropriate CPR training at least
once in the last 3 years.
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evidence of current professional indemnity insurance, if applicable.
evidence of currency of immunisations, or refusal.
evidence of competency in relevant infection control processes.
Training records and personal contact details are also reviewed annually to ensure the
employment records are current and correct.
Confidentiality
This practice complies with the requirements of the Privacy Act 1998, in keeping and maintaining
employment records:
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only information directly relevant to the activities of each employee or the functioning of the
practice is kept in employee files.
all information kept in employment records is obtained by lawful and fair means.
personal and sensitive information about employees is kept confidential and employment
records are stored in a secure place. Paper files are kept in a locked filing cabinet and
electronic records are password protected.
employees are entitled to view their personal files, with exceptions as allowable under the
Act
Retention
Under the Fair Work Act 2009 all employment records including payroll and personnel files
must be are kept for 7 years. These records must be kept in English and made available for
inspection by workplace inspectors if required.
RACGP 4th edition Standards 3.2.1, 3.2.2 & 3.2.3 & 4.1.1.
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2.4 Staff Induction
Policy
Practices need a system for assisting new members of the practice team to learn their role. This
includes new GPs (including registrars and locums) and other new staff.
This practice has an induction program for all new General Practitioners and practice staff which
includes ongoing monitoring of progress in their new role. To ensure staff and patient safety,
new members of the general practice team must be able to demonstrate knowledge of the key
procedures in the Policy and Procedure Manual and key operating systems relevant to their role
within the practice by the end of the induction period. In some cases it may be appropriate to
have a program where other contractors using rooms in the facility are also provided an overview
of relevant practice systems.
Staff are also expected to familiarise themselves with the Policy and Procedure Manual and use
it as a resource in the course of their employment.
All new staff must complete a full induction program including OH&S as detailed on the Staff
Induction Checklist as part of their orientation. A sample Staff Induction Checklist is included at
the end of this section.
In-house training is provided to staff members responsible for inducting new employees to
ensure they understand the requirements of the induction process and the importance of an
effective induction program in relation to job performance, legal liability and OHS. This is
recorded on their training records to show they are authorised to induct new employees.
It is essential that new staff understand the day-to-day operations of the practice including the
occupational health and safety issues relevant to their role, the practice code of conduct,
infection control policies and the processes by which the privacy of patient health information.
It is useful for new staff to have an understanding of the local health and cultural environment in
which the practice operates. For example, if the practice is located in an area with a high level of
problems caused by illicit drug use, it is useful for new staff to understand the practice’s policy
concerning management of Schedule 8 medicine prescribing. Furthermore, staff and GPs in
particular need to be aware of key public health regulations (such as reporting requirements for
communicable diseases or mandatory reporting of child abuse) that will affect how they work.
General practitioners need to be made aware of local health and community services including
pathology, hospital and other services they are likely to refer to in the course of normal
consulting.
The Staff Induction Checklist provides the general knowledge essential for any position within a
medical practice. Job specific orientation and induction will also need to be undertaken and
documented.
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As each stage of the induction program is completed the new staff member and their induction
supervisor sign the Staff Induction Checklist and the completed document is filed in the
employee’s Staff Record file. This written record of induction is important to protect the practice
against legal liability and injury claims in the future.
New staff members are not permitted to work independently until competency in specific areas of
induction such as infection control, confidentiality and OHS have been demonstrated and signedoff.
Procedure
The following overview and checklist can be customised to reflect the practice’s needs.
Process
Before the first
day.
First day
First week
First month

Description
Ensure all staff members responsible for induction are trained and have
sufficient time allocated.
Assign a staff member to be responsible for the induction of the new
employee.
Prepare Staff Induction Checklist and have copy of procedures manual
& job description available to refer to. A sample Induction Checklist is
provided at the end of this section.
Make the new staff member feel welcome.
Go through all items on the Staff Induction Checklist
Prepare Staff Induction Checklist - Induction &Training Plan
Sign the Staff Induction Checklist Part 1 - First Day to show all items
have been completed
File Staff Induction Checklist Part 1 - First Day and a copy of Part 2 Induction &Training Plan in the new employee’s staff records file.
Give a copy of all induction forms including Staff induction Checklist Key policies and procedures to the employee.
Make time each day to go through key policies, procedures and other
training needs identified on the Induction &Training Plan
Arrange induction and training with other staff members in areas such
as reception systems, record-keeping, sterilisation/infection control &
spills, doctor’s requirements, customer service and complaints, patient
privacy, triage.
Provide opportunities for the new staff member to ask questions, and
make sure they receive plenty of feedback and encouragement.
Tick off each item on the Induction &Training Plan as it is completed.
Continue to provide the new employee with opportunities to ask
questions as well as encouragement and support with regular informal
meetings.
Link the new staff member into local networks and professional
organisations, such as those at the division.
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After 3 months
Continue Induction &Training Plan until all items are completed.
Sign the Induction &Training Plan to show it has been completed. Give
a copy to the employee and file the original in the employee’s Staff
Records File.
Review the induction and training plan and their performance. Provide
recognition for the areas which they are performing well in and develop
a new plan to resolve any remaining training needs or provide skills
enhancement – Performance Review.
RACGP 4th edition Standards 4.1.1, 5.3.3.
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2.5 Privacy
Policy
All patient information is private and confidentiality of patient information must be maintained
at all times. The rights of every patient are to be respected. All information collected by this
practice in providing a health service is deemed to be private and confidential.
This practice complies with Federal and State privacy regulations including the Privacy Act
1998, the Privacy Amendment (Private Sector) Act 2000 and Victorian Health Records Act
2001 as well as the standards set out in the RACGP Handbook for the Management of
Health Information in Private Medical Practice 1st Edition (2002). (Refer Section 6 Privacy
and Security of Health Information).
Under no circumstances are employees of this practice to discuss or in any way reveal
patient conditions or documentation to unauthorised staff, colleagues, other patients, family
or friends, whether at the practice or outside it, such as in the home or at social occasions.
This includes patient’s accounts, referral letters or other clinical documentation.
General Practitioners and staff are aware of confidentiality requirements for all patient
encounters and recognise that significant breaches of confidentiality may provide grounds
for disciplinary action or dismissal.
Every employee of this practice is aware of the privacy policy and has signed a privacy
statement as part of their terms and conditions of employment. This privacy statement
continues to be binding on employees even after their employment has terminated.
Procedure
All employees of this practice are issued with the privacy policy and sign a privacy statement
as part of their terms and conditions of employment. The policies and procedures of the
practice are further explained during the induction of new staff members, and the induction
form is signed by the new employee as confirmation that they understand and accept their
obligations in relation to patient privacy and the confidentiality of medical information.
A sample Privacy Statement Form to sign can be found in the Job Package forms provided
at the end of this section.
RACGP 4th edition Standards 4.2.1.
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2.6 Performance Review
Policy
Annual staff reviews are conducted to ensure continuing high levels of work performance and to
assist in job enrichment. The review is part of a continuous process of feedback to individual
staff on their work performance. It is extended to include performance improvement and career
development.
Performance reviews benefit the practice and its employees by:
 ensuring all staff know what is expected of them and how their work is important to the
practice.
 providing staff with formal recognition and appreciation for their work.
 providing an opportunity to review goals, celebrate achievements and set objectives for the
future.
 helping staff to develop their skills and performance to achieve practice goals and further
their own career.
 dealing with problems and resolving grievances – see also Grievance Procedure in 2.10
Equal Opportunity, Bullying and Harassment.
A review involves identifying, evaluating and developing the work performance of staff so that
Practice goals are more effectively achieved. At the same time the process benefits staff in
terms of recognition, receiving feedback, catering for work needs and offering career guidance
and support.
The relevant position description forms the basis for evaluation and lines of accountability.
The performance review document, including comments concerning current progress and future
goals, is signed by both parties, with a copy retained by the staff member. The original is filed in
the Staff Record File.
Reviews are not directly linked to salary levels nor is it the forum for seeking a pay increase.
The performance review should not be the forum for sorting out issues which have occurred over
the previous year. Any issues which may arise should be addressed immediately.
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Procedure
A review is conducted 3 months after commencement of the position and at least annually
thereafter.
A performance review checklist to assist with planning and to ensure all steps are completed is
provided at the end of this section.
A detailed description of each step and hints follows.
Step 1: Plan & prepare
An effective performance review process can increase productivity, staff motivation and morale,
but a badly handled review can have a damaging effect on the employee and result in decreased
performance. Provide staff responsible for conducting performance reviews with basic training in
giving feedback, using specific examples and evidence rather than vague comments and the
legal restrictions on what can be said (see Procedure 2.7). Guidelines on giving feedback can be
downloaded from the DCGPA web site.
Notify the employee of the impending review at least 1 week in advance, at which time a
mutually convenient time can be arranged for the meeting. Allow at least one hour which should
be free from interruptions, if possible.
Provide the employee with a self-appraisal questionnaire and a copy of their current job
description to help them prepare for the review, and have an opportunity to reflect on examples
of their achievements, problems they have encountered and areas they would like to improve.
This encourages employee ownership and involvement in the process as well as changing the
review relationship towards counselling and coaching instead of judgement. A sample selfappraisal questionnaire is included at the end of this section.
Review the employee’s job description, their self-appraisal and records of previous performance
reviews. If appropriate, speak to co-workers and others the employee has contact with in the
course of their work to get feedback on their performance.
Plan what to say and how to say it during the appraisal. Focus on productivity, quality of work,
reliability and team work. Be objective and provide supporting evidence, examples and
documentation, especially in relation to poor performance. Use positive reinforcement to
encourage desired behaviours.
Step 2: Conduct the review
Reviews should be conducted in a quiet location away from distractions and interruptions.
Begin with a description of the aim and process of the review, to help the employee feel
comfortable and non-defensive, as described on the Self-appraisal questionnaire.
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Performance reviews give employees an opportunity to receive appreciation and recognition for
their achievements, raise problems and resolve grievances, set goals for the future and discuss
the training and development opportunities they need to do their job better and further their
career.
Performance reviews provide practice management with a chance to re-motivate employees, refocus attention on practice goals and strategies, acknowledge employee achievements, deal with
problems, align employee goals with those of the practice, assess staff development needs,
learn more about each employee and determine those who are ready for additional
responsibilities.
Set a positive tone for the discussion by starting the review with a brief account of the
employee’s strengths, recognition of their achievements and appreciation for their contribution to
the practice.
Discuss the employee’s self-appraisal, listening carefully to show genuine interest. Do not
disagree with their assessment, unless they have underestimated their performance. Ask them
for suggestions on how they could improve their performance or develop their skills – even when
they have performed well there may still be opportunities for improvement.
Deal with any issues arising sensitively and constructively, following the guidelines for giving
feedback which can be downloaded from the DCGPA web site. Remain calm at all times,
focusing on the facts and not personalities. If the discussion is getting out of control, suggest
taking a 10-minute break, bring in another member of staff who may be able to act as a mediator
or arrange another time to continue the review. (See also hints below on dealing with various
types of employee responses and the guidelines for dealing with poor performance which can be
downloaded from the DCGPA web site)
If communication is regular and open there should be no surprises for either party in
performance appraisals. However, if an issue is raised for which one party is not prepared, listen
carefully to the problem and ask for specific examples and evidence. Arrange to respond at a
later time, once there has been an opportunity to consider the problem and conduct further
investigations if required. Do not be tempted to make hasty decisions or ignore problems, hoping
they will go away.
Review the job description and the targets or goals set in previous reviews. Ask about the
employee’s plans and goals for the future, looking at their career development. Discuss the
future needs of the practice, seeking to find opportunities for the employee to achieve their goals
in ways which will also add value to the practice.
Work together to set new goals for the future, using the SMART principle for goals:
Specific, Measurable, Achievable, Relevant (to both the needs of the practice and the employee)
and Timely. Establishing mutually agreed goals will result in greater employee ownership and
commitment to achievement of the goals.
Identify areas where the employee’s performance or career development would benefit from
training, additional resources or equipment, a different allocation of responsibilities for better use
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of time etc. For both parties it is important to only make promises and commitments which can
be kept, or a loss of trust will result.
Adjust the job description to reflect any new responsibilities or role changes. Document any
agreed goals and targets as well as commitments to training or support made by the practice.
Agree on a time line for completion of agreed tasks and for the next review. Generally the time
frame for the next review will be 12 months but if an employee has been given new
responsibilities or an improvement in performance is required the next review may be in 1-3
months.
Record the details of discussions and any agreements made on the Performance Review Form.
Allow the employee to read the record of the review and suggest any changes or additions.
Once both parties are satisfied that the document is a correct record of the discussions, sign the
last page of the Performance Review Form and date it. Give a copy to the employee and file the
original on their Staff Records File.
Finish the review by thanking the employee for their participation in the review process,
concluding with a positive statement about what has been achieved and the benefits anticipated
in the future.
Step 3: Follow through
Ensure the practice keeps all commitments made in the review, ranging from promises for
additional training and career development or consequences for continued poor performance
(such as written warnings, as per Procedure 2.7).
After the review these commitments should be incorporated into the staff member’s planning
schedule.
Issue an updated job description, if required. Give a copy of the new job description to the
employee and let them check it before adding it to the employee’s Staff Records file and marking
the previous job description ‘superseded’.
If promises made by the practice are not kept the employee may lose trust in the practice
management, which will lead to a loss of motivation and commitment and any improvements in
performance will not be sustained.
If unsatisfactory behaviour continues after the practice has taken all reasonable steps to address
possible causes including provision of adequate instructions, training, resources and time,
disciplinary action may be required.
RACGP 4th edition Standards 4.1.1.
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2.7 Disciplinary Process
Whilst this procedure is advised, there is no longer the requirement of three warnings. However,
the employee must be given ‘a fair go’ and have an opportunity to improve within a reasonable
time frame. Always document these issues.
Policy
The Practice Manager has the day to day responsibility for ensuring that employees meet the
required standards for work performance and conduct. Generally the focus is on positive ways of
motivating staff, including:
 communicating clearly what has to be done.
 setting joint goals or targets.
 coaching staff.
 resolving problems as they occur.
 informal feedback and counselling about poor performance.
If this approach is not sufficient, or when a serious breach of policy occurs, the disciplinary
process will be followed. The purpose of the disciplinary process is to:
 avoid repetition of mistakes or unacceptable behaviour – it is corrective, not punitive.
 ensure fairness in the treatment of all employees.
 provide a clear, written statement about the expectations of the practice in relation to
conduct and behaviour at work.
 encourage an improvement in work performance and behaviour.
 provide support or training to assist in improvement.
 advise of the consequences of failure to comply with expectations, including written
warnings and termination of employment.
For the process to be effective the following points need to be considered:
 listen carefully.
 gather the facts.
 remain objective.
 don’t avoid the problem.
 document all discussions and evidence.
 be fair and reasonable, balancing the safety and privacy of patients and staff with the rights
of the employee.
Under the Fair Work Act 2009 there have been changes to unfair dismissal laws.
An employee is eligible to make an application for unfair dismissal if they have completed the
minimum employment period of:
 one year – where the employer employs less than 15 full-time equivalent employees (a
small business employer).
 six months – where the employer employs 15 or more full-time equivalent employees.
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
employees are still entitled to sue for unlawful dismissal, on the grounds of a breach of the
“general protections”, e.g. discrimination, bullying or harassment, employee making a claim
or joining a union etc.
dismissal provisions in Workplace agreements will continue to apply for the life of the
agreement.
treating staff fairly and having appropriate systems is important for workplace morale.
Research clearly shows that perceptions of management unfairness decrease employee
commitment, motivation & performance.

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More information about dismissals and the changes under the Fair Work Act 2010
http://www.fwa.gov.au/index.cfm?pagename=dismissalsabout.
Procedure
Counselling or disciplining problem employees is a difficult component of any Manager’s role.
This process is usually stressful and unpleasant for those involved, and can lead to anger and
resentment. This can be minimised by:
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treating the employee with respect and dignity, focussing on specific behaviours and not
the person.
preserving the employee’s self-esteem by acknowledging their good points such as
useful skills or pleasant personality but recognising that the current job may not be a
good match for their talents, interests and abilities. Try to avoid making the employee feel
‘not good enough’ – they simply may not be a good fit with this position. Success in any
job is reliant on the right combination of the attributes of the employee, the position and
the practice.
understanding that most employees desire the satisfaction of performing their job well
and will not be happy in a position which does not suit their skill-level or abilities. Helping
them through the disciplinary process in a respectful and affirming way will provide a
greater understanding of their strengths and limitations and assist them to find a more
satisfying position in the future.
providing all reasonable assistance to help employees improve their performance. See
‘Giving and receiving Feedback’ which also includes guidelines on dealing with poor
performance.
Avoiding the issue will not make the problem go away. Failure to deal with employee problems
can send ‘messages’ to the problem employee and other employees that poor performance or
behaviour is condoned.
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Counselling and Disciplinary Action
The disciplinary process involves four steps:
1) counselling (optional)
2) first written warning
3) second written warning
4) termination
These steps may not always be followed in full. For example, in some cases counselling will be
sufficient to resolve the problem. Although a minimum of two written warnings are usually
provided prior to termination, severe misconduct may warrant immediate dismissal.
At each step, the following procedure occurs:
 problem arises or incident occurs.
 investigation of facts, including collecting witness statements. In some circumstances the
employee may be stood down (asked not to remain at the workplace) with pay while the
investigation takes place.
 the allegations and supporting evidence are presented to the employee. The employee is
entitled to have a representative present, such as another staff member or union
representative. It is advisable for the manager to have a witness present in all interviews
related to disciplinary procedure. Preferably this should be a staff member with mediation
skills or who is trusted by both parties.
 the employee is given an opportunity to respond, including requesting any reasonable
assistance which would prevent a reoccurrence.
 a decision is made – this could range from deciding to take no action, to agreeing upon
clear guidelines about expected future behaviour or even termination of employment.
 the process is documented and the employee is given a copy with the original being placed
in the Staff Records File.
Step 1: Counselling
Counselling is usually the first formal step in the disciplinary process. It can be used to discuss
poor performance, grievances raised by other employees or to deal with a breach of policy.
Details of the problem, available evidence, the employee’s response and decisions taken are
documented on an Employee Counselling/Written Warning Form. A sample Employee
Counselling/Written Warning Form can be found at the end of this section. For more serious
incidents or breaches of policy a written warning may be issued at the same time as counselling.
The Grievance Procedure in 2.10 Equal Opportunity, Bullying and Harassment may also be used
to resolve grievances, especially those involving more than one employee.
Agree upon a timeframe for improvement and the next review date. Allow sufficient time for the
employee to improve - usually 2 weeks to one month.
If the behaviour continues it will be necessary to move on to a written warning.
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Step 2: First Written Warning should outline
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
the problem with the employee’s performance.
the evidence arising from investigation including statements from any witnesses (A sample
Witness Statement Form is included at the end of this section).
the employee’s response for the problem.
the agreed plan for improvement.
any assistance, support or training to be provided by the practice to facilitate improved
performance. This includes reasonable requests for reduced hours or changes to duties.
the timeframe for improvement and the next review date. Allow sufficient time for the
employee to improve - usually 2 weeks to one month.
the consequences of failure to improve (usually one more warning and then termination).
the process should be documented on the Employee Counselling / Written Warning
Record – tick the box to indicate that this is a first written warning (A sample form is
provided at the end of this section).
The content and outcome of the interview must be documented with a copy each for the
employee and employer. Ensure any resources or assistance agreed upon in the interview are
promptly provided.
Step 3: The Second and Final Written Warning
The second and final written warning is issued when there has been no improvement or change
following the first warning. The interview should follow the same format as the first warning,
including reference to the first warning and the previous plan for improvement. The employee
must be made aware of the likelihood of termination, and this should be documented, with a copy
each for the employee and the employer.
If the improvement in employee performance, attitude or behaviour is still not made then a Notice
of Termination of Employment (as per the Award or employment agreement- ensure the correct
wording is provided to avoid confusion) is given to the employee.
Step 4: Termination
Termination as a result of the disciplinary process. If the unsatisfactory behaviour continues after
two written warnings, termination may be necessary. The employee will be well aware of the
likelihood of this consequence.
Before terminating an employee, all employers must ensure that the termination meets the
minimum requirements as set out in the Small Business Fair Dismissal Code. Whilst this code is
applicable to employers who have less than 15 employees, it is recommended that all
employers use this code as a minimum set of procedural steps.
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A copy of the Small Business fair Dismissal Code is at
http://www.fwa.gov.au/documents/dismissals/Small_Business_Fair_Dismissal_Code.pdf.
For general information on dismissals from fair work Australia
http://www.fwa.gov.au/index.cfm?pagename=dismissalscoverage#harsh.
Termination of employment may also occur due to:
Summary Dismissal: Employees may be summarily dismissed without any warnings for serious
breaches of policies, misconduct or illegal activity. Employees must be informed of behaviours
which would justify summary dismissal as part of their terms and conditions of employment. In
this manual this information has been included in the staff handbook. Some examples include:
 negligence or carelessness which could affect patient safety.
 actual or threatened assault, serious abuse or harassment.
 fraud or theft, including falsification of records and unauthorised possession of property
belonging to the practice or another employee.
 breaches of the practice’s privacy policy.
 unauthorised use or possession of alcohol or drugs at work.
 attending work in a condition which is a risk to the health or safety of patients, colleagues
or the employee concerned.
 serious and willful disobedience (seek advice first).
In many cases an employee will be stood down on full pay while an investigation is undertaken
prior to summary dismissal, to ensure the dismissal is warranted.
Redundancy: This occurs when a particular job is no longer required at the practice or less
people are needed to perform the amount of work available.
It is a requirement of the Fair Work Act 2009 and the relevant Award for the Employer to consult
with the employee prior to the redundancy occurring.
Generally, an employee who is made redundant will not be replaced. Employees who are made
redundant are often entitled to several weeks’ severance pay, depending on their age and the
length of time they have been employed at the practice – check the relevant award or workplace
agreement. Seek advice from your division or employer group before proceeding with a
redundancy to ascertain whether the situation will qualify as a valid redundancy and the
severance pay applicable.
Abandonment of employment: Abandonment of employment occurs when an employee fails
to attend his/her place of employment for three days or more without having prior authorisation
for the absence and has not contacted the employer to explain the reason for the absence.
During the 3 days the practice should attempt to contact the employee by telephone and if this is
unsuccessful a letter should be sent by registered mail to the employee’s last known address
stating that the employee's unauthorised absence is unacceptable, seeking an explanation for
the absence and advising that if the employee fails to return by a set time and date it will be
determined that he/she has abandoned his/her employment. If there is no response after 3-4
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days send a second notice, and if there is still no response after a further 3-4 days a third letter
should be sent advising that as a result of his/her failure to return to his/her place of employment
the practice has determined that he/she has abandoned his/her employment. At this stage the
employment is terminated and all entitlements should be paid. Under some awards the
employee forfeits annual leave and notice entitlements if they abandon their employment. Any
personal effects left at the practice can be sent with the final letter. For more information and
sample letters contact DDGP.
Employee initiated termination, such as resignation: All employees are required to notify the
practice in writing of their intention to resign from their employment, giving at least the amount of
notice required under the relevant award or workplace agreement. Employees who fail to give
the required notice may forfeit some of their entitlements.
Note: Despite changes to the law on unfair dismissal, the legislation relating to unlawful
termination remains in place. This means employees cannot be terminated because of:
 temporary absence from work because of illness or injury,
 trade union membership/non-membership or participation in trade union activities,
 the filing of a complaint, or the participation in proceedings, against an employer,
 race, colour, sex, sexual preference, age, physical or mental disability, marital status,
family responsibilities, pregnancy, religion, political opinion, national extraction or social
origin,
 refusing to negotiate, sign, extend, vary or terminate an AWA,
 absence from work during maternity leave or other parental leave, and
 temporary absence from work because of the carrying out of a voluntary emergency
management activity.
Procedure for termination:
The following will need to be considered as part of the termination of any employee:
Notice period: The practice can require an employee to work out their notice or it can be paid in
advance, so they leave immediately. If an employee refuses to work out their notice they may
lose some of their entitlements. The required notice period and entitlements upon termination
will be determined by the relevant award or workplace agreement.
Termination pay: Amounts payable on termination include accrued pay in lieu of notice (if
applicable), redundancy pay, annual leave, outstanding wages and long service leave
entitlements. In some cases, such as summary dismissal, failure to give notice on resignation or
abandonment of employment, employees may forgo some of their entitlements. Check the
relevant award or workplace agreement to ensure all relevant entitlements are included in the
employee’s termination pay.
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Administrative matters: A number of administrative matters should be attended to at the time of
termination:
 the arrangements for termination, including reason for the termination and notice.
arrangements should be documented – a sample Termination form is included at the end
of this section.
 all keys and other practice property should be returned.
 the components of the employee’s termination pay should be explained.
 it is advisable to obtain the employee’s permission for the practice to provide written or
verbal references on the employee’s performance.
 the employee should be reminded about their continuing obligations under the practice’s
privacy policy.
 centrelink may need to be notified if the person wishes to register for unemployment.
benefits or there have been payroll garnishee arrangements in place, such as child support
payments.
RACGP 4th edition Standards 4.1.1.
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2.8 Staff Code of Conduct
Policy
We encourage an environment that fosters robust general practice teams.
Our staff conducts themselves in a manner that promotes the attributes we believe are desirable
characteristics of general practice team:
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a just, supportive, transparent, cohesive and collaborative culture, which is associated
with improved patient outcomes and enhanced patient safety.
defined goals, including an identifiable overall practice ‘mission’ and specific, measurable
operational objectives that are shared by all team members.
a ‘systems’ approach that includes the development of both clinical systems and
administrative systems.
division of labour, including the delegation of tasks and assignment of tasks among team
members, based on the principles outlined earlier in these Standards.
effective training, both for the functions that people routinely perform and cross training to
substitute for other roles in cases of absences or changed/increased work demands.
excellent communication, including supportive interpersonal communication through well
designed communication structures and processes.
Procedure
It is expected that all employees will behave in a courteous manner, which portrays the
image of the practice in a positive and professional way, while maintaining the levels of
service and care which our patients expect.
Any staff member who interacts with patients, other visitors or employees is expected to
behave according to acceptable professional and social standards at all times.
Clinical and non-clinical staff perform duties within their legal scope of responsibilities and
maintain their knowledge, skills and attitudes through their professional specialty
organisations such as the AMA, ANF or AAPM.
Staff do not discuss patients outside the practice and are mindful of the sensitive nature of
patient’s private medical information while at work.
Staff avoid making judgemental comments about patient’s treatment by other staff or
medical practitioners inside and outside work.
It is expected that all employees act in accordance with specific practice policies and
procedures and/or the specific details contained in the job description or employment
contract.
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The entire practice team is committed to encouraging quality improvement and identifying
opportunities to make changes that will increase the quality and safety for patients.
All staff have an individual responsibility to identify any potential infection risks within the
practice and to be familiar with and implement the relevant infection control procedures of
our practice.
All staff are required to be punctual when starting and finishing work each day.
The consumption of food or drink is not permitted at reception.
Employees failing to meet acceptable codes of conduct will be counselled or disciplined in
accordance with the Disciplinary Procedures outlined in Section 2.7
RACGP 4th edition Standards 5.3.3, 3.1.2, 4.1.1.
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2.9 Staff Presentation
Policy
It is expected that all staff maintain a clean, neat and tidy appearance and dress in a
manner which is not likely to be offensive to the patients attending this practice. Jewellery
and makeup should not be excessive.
Procedure
Staff are required to wear the prescribed uniform whilst on duty. In cases where a uniform is
not able to be worn, staff should wear neat clothing similar to the prescribed uniform or
clothing which conforms to acceptable standards of professional dress. Clothing should be
ironed, clean and kept in good condition.
Staff should maintain high levels of personal hygiene paying particular attention to excessive
body odours and general cleanliness.
All staff with long hair should have it tied back neatly. Make up and jewellery should be kept
to a minimum.
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2.10 Equal Opportunity, Bullying & Harassment
Policy
Our practice is committed to the principles of merit, fairness and respect for all people. This
practice seeks to provide a working environment in which all employees are able to perform their
duties without being subject to discrimination or inappropriate behaviour. Our practice complies
with our legal obligations and has a range of policies and procedures to encourage Equal
Opportunity and prevent discrimination, bullying and harassment. These include:
 a policy preventing bullying and harassment of any kind, including sexual harassment,
in this workplace.
 a procedure to deal with the personal threat of violence. (This is available in the Non
medical emergency procedure manual that is recommended to download form the
DCGPA web site as part of the OH&S requirements).
 an Anti-discrimination policy which is complemented by a Family-friendly Workplace
policy.
 a grievance procedure for complaints arising from breaches of these policies. For
serious breaches the practice’s disciplinary procedures may be used, including
termination of employment.
Workplace discrimination, bullying and harassment can occur:
 during employment procedures such as recruitment, performance review and
termination of employment.
 in the way people are treated at work and the allocation of resources such as training,
privileges and responsibilities.
 at work-related functions.
 when calling a work colleague at home.
 between people working in the same building, even if they have different employers
 in the provision of goods and services – for example it is illegal to discriminate against
a patient or a supplier on the basis of an irrelevant characteristic.
All staff working at this practice have the responsibility to:
 treat all people in this workplace fairly and with respect.
 refrain from behaviour which could constitute harassment, bullying or discrimination
 report any incidents of harassment, bullying or discrimination to the Practice Principal
or Practice Manager.
 maintain confidentiality if they are involved in complaints.
Additionally, the Practice Principal and Practice Manager are expected to:
 follow appropriate procedures when a complaint is reported to them, making sure they are
taken seriously, properly investigated, treated confidentially and resolved in a timely
manner.
 ensure staff are aware of their obligations and the practice’s policies and procedures
relating to harassment, bullying or discrimination.
 promote a work environment free from harassment, bullying or discrimination.
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Bullying and Harassment Policy
There are a number of laws in Australia dealing with issues related to bullying and harassment
including EEO legislation, OHS requirements, criminal law, defamation and common law
provisions such as negligence. These laws all require the employer to take all reasonable steps
to stop bullying and harassment in the workplace, including:
1) Policies and procedures to prevent bullying and harassment
2) Dealing with grievances in a fair, appropriate and timely manner.
Bullying and harassment is defined as any unwelcome behaviour or communication which has
no legitimate function in the workplace and intimidates, humiliates or offends another person.
Any form of bullying or harassment is totally unacceptable in this practice.
Bullying and harassment includes, but is not limited to:
 name-calling and insults directed at another employee.
 writing of notes which are personally offensive to another.
 practical jokes (this may also be a safety issue).
 unwanted physical contact of any kind.
 interfering with the personal property of any other employee.
 remarks or written comments which are personally insulting or offensive to other
employees based on their race, background, gender, religion, sexual preference,
appearance or any other personal attribute.
 unwelcome sexual advances, requests for sexual favours and other verbal or physical
conduct of a sexual nature.
 interfering with the equipment, property or work of another employee in a way which is
outside the normal course of your duties. (Also a safety issue).
 bullying can include isolating or excluding a person, psychological abuse, setting
impossible deadlines, being overly critical and using aggressive language.
Behaviour is inappropriate and may constitute harassment if it is offensive to another person,
even if this was not the intention of the one initiating the behaviour. Bullying and harassment may
be a once-off incident or a pattern of behaviour.
(*Insert Practice Name) regards these actions and any similar behaviour as serious misconduct
and any person who is found to be behaving in this manner may have their employment
terminated.
Any employee who is subjected to bullying, harassment or intimidation by a fellow employee,
manager or supervisor should notify the Practice Principal or the Practice Manager. All
complaints of harassment will be promptly and confidentially investigated using the practice’s
grievance procedure. Any employee or manager who violates this policy will be subjected to
disciplinary action, as described above.
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Anti-discrimination policy
This practice does not discriminate on the basis of:
 race (including colour, nationality and ethnic origin).
 family status including marital status and responsibilities as a carer.
 sexual orientation and lawful sexual activity.
 age.
 gender and gender identity.
 physical Features.
 political beliefs or activity.
 religious beliefs or activity.
 breastfeeding.
 impairment including physical, intellectual or psychiatric.
 pregnancy or potential pregnancy.
 political opinion or activity.
 criminal record.
 union membership or industrial activity.
 personal association with a person with any of the above characteristics.
As with the practice’s harassment policy, any behaviour which is discriminatory is unacceptable
in this practice. This includes racist, sexist or ageist remarks and making fun of people’s
differences. Discriminatory behaviour will lead to disciplinary action and may result in
termination of employment.
This practice will take all reasonable steps to ensure all policies, procedures and practices
comply with EEO principles.
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Family Friendly Workplace Policy
Policy
This practice values its employees and aims to provide a family friendly culture that promotes life
work balance with a management philosophy that fosters a sense of fun and camaraderie &
promotes self care for all staff.
This policy recognises that all employees have varying family responsibilities. It recognises a
broad definition of family including family as defined by various legislative & industrial
instruments, people in same sex relationships and other close personal relationships.
We are committed to ensuring that family-friendly policies are developed, endorsed,
implemented and monitored.
We endeavor to work in partnership with its staff to identify work practices that support
arrangements to find the best possible match between the interests of the organization and those
of individual employees. These practices can include: flexi time; leave such as carers’ and
parental leave. Workplaces can also be made more family friendly through the way jobs are
designed, in how work is organized and having supportive and understanding staff & managers.
Good communication and co-operation are essential for the achievement of a successful family
friendly organisation.
Key Principles
The following key principles underpin this policy:
 this practice operates using the minimum standards as outlined in our
(insert whichever applicable e.g. Workplace agreement/ enterprise bargain/contracts).
 provision of entitlements will be made equally available to men & women
 provision of entitlements will be made available to all employees in a fair manner.
 this practice has a social responsibility to organise work in a manner that assists
employees to meet family responsibilities
Procedure
Family friendly practice will be considered in all policies and procedures.
Points to guide the development of family friendly policies include:
 benefit the organisation and its employees
 acknowledge that the needs of both the organisation and employees are not static but
change over time
 encourage a partnership approach to meeting the needs of both the organisation and
employees
 highlight the need for management, employees and where applicable employee
representatives to discuss workable solutions
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be fair and consistent
be economically feasible
takes into account the equality implications of any policies introduced
Developments and changes to policies will be communicated to all staff at regular intervals.
Grievance Procedure
If you or any employee of this practice is exposed to any form of behaviour which constitutes
discrimination, bullying or harassment, the following procedure must be adopted. Do not ignore
harassment – ignoring the behaviour could be interpreted as consent.
This procedure may also be used for handling of other workplace grievances such as complaints
about working conditions, wages or work colleagues. Grievances undermine morale and affect
teamwork and need to be dealt with promptly.
1) Inform the offender that the behaviour is offensive and unacceptable.
2) Seek assistance in having the behaviour stopped by reporting the incident to your Practice
Principal or Practice Manager.
3) The Practice Principal or Practice Manager will conduct a detailed investigation of the
incident(s) to assist in the resolution of the grievance. Witness statements and evidence
may be collected. For the investigation to be properly conducted confidentiality must be
maintained, it must be impartial, the person reporting the incident must not be victimised or
experience adverse repercussions and the complaint must be dealt with as quickly as
possible.
4) Actions taken to resolve the grievance will depend on the circumstances and the results of
the investigation. Generally the main aim will be to ensure the incident does not occur
again. Possible solutions may include:
 an apology.
 an undertaking that the behaviour will cease.
 formal counselling of the alleged harasser, using the disciplinary procedure (2.7)
 disciplinary action, including termination for serious misconduct.
 training for groups of staff or the whole staff to raise awareness of EEO obligations.
 covering costs associated with the harassment, such as medical or psychology
expenses.
 notifying the police.
 if the complaint cannot be substantiated when it is investigated it must still be taken
seriously, including attempting to find a resolution of the mater with the employees
involved.
 it may be appropriate to take action against a complainant who makes a serious
allegation against a work colleague which is found to be false or frivolous after
investigation. This could include termination of employment.
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5) A record is kept of the complaint, its investigation and actions taken. A sample Staff
Grievance Record is included at the end of this section.
6) After action has been taken and the problem appears to have been resolved there is a
need for occasional monitoring and follow-up to ensure that those involved are satisfied
with the outcome, and the problem has not reoccurred or surfaced in a different form.
7) If the matter remains unresolved, the grievance provisions in the relevant awards or
workplace agreements require that it be referred to an external party. This party may be
specified in the award or agreement. Seek advice from your division or employer group.
Instructions for the Practice Principal or Practice Manager in handling of grievances:
The following four steps will assist with handling grievances.
1) Listen with an open mind
 listen, no matter how trivial the grievance may seem to you.
 be patient and show a sincere interest in the employee’s grievance.
 do not argue.
2) Get all of the facts
 encourage the person to repeat the substance of the grievance to ensure the facts
are understood.
 discuss any solution the employee may have to solve the problem.
 question any discrepancies.
 discuss with others if necessary.
 do not jump to conclusions.
 consult senior management if necessary.
3) Take action promptly
 do not delay taking action.
 do not make any rash decisions.
 advise all relevant employees of the action.
 do not use your authority to force a decision unless there is no alternative.
4) Follow up
 check that those involved are satisfied with the outcome.
 consider whether preventative action can be taken to avoid a reoccurrence. This may
include training, awareness raising or changes to systems and procedures.
 refer to an external party if the matter remains unresolved.
RACGP 4th edition Standards 4.1.1, 4.1.2.
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3
Occupational Health & Safety
Policy
This practice is committed to preventing workplace injury and illness and ensuring a safe
and secure working environment for doctors, staff, patients and all other visitors.
We recognise that health and safety is an integral part of every activity we perform and as such
we maintain current knowledge of our obligations under State/Territory and Federal OH&S
legislation and we understand that non compliance with these legal requirements can result in
being prosecuted and fined.
It is a legal duty of every workplace to maintain standards to protect the health, safety and
welfare of every person within the workplace This includes staff, patients, visitors and
anyone else who may enter the premises.
As an employer we must provide a safe and healthy workplace for our workers and
contractors.
All our workers have a duty of care to ensure that they work in a manner that is not harmful
to their own health and safety and the health and safety of others.
The Occupational Health and Safety Act 2004 is the cornerstone of legislative and administrative
measures to improve occupational health and safety in Victoria. The Act sets out the key
principles, duties and rights in relation to occupational health and safety.
The Occupational Health and Safety Regulations 2007 are made under the Act. They specify
the ways duties imposed by the Act must be performed, or prescribe procedural or administrative
matters to support the Act, such as requiring licenses for specific activities, keeping records, or
notifying certain matters.
Effective OHS regulation requires that WorkSafe provides clear, accessible advice and guidance
about what constitutes compliance with the Act and Regulations.
To find out your obligations for your state go to:
http://www.business.gov.au/BusinessTopics/Occupationalhealthandsafety/pages/Employero
bligationsinyourstateorterritory.aspx.
For detailed examples relating to the Health and aged care sector go to:
http://www.worksafe.vic.gov.au/wps/wcm/connect/wsinternet/worksafe/home/safety+and+pr
evention/your+industry/health+and+aged+care+sector/d_health+and+aged+care+sector.
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Procedure
This practice has a designated elected health and safety representative (HSR). The name and
telephone extension of our HSR is kept on the staff notice board. Information relating to OH&S
issues are posted on the notice board/conveyed to all members of staff and updated regularly
by the HSR. We consult with employees on matters that may directly affect their health, safety
or welfare and the HSR, is also involved in the consultation
We have current workplace Injury Insurance. We keep a Register of Injuries to keep track of
work-related injuries and illnesses and for workplace incidents that cause or could have
caused serious injury or death we understand that we must notify WorkSafe on 13 23 60.
When an injured worker records an injury or illness in the Register of Injuries, we acknowledge
this registration in writing to the worker.
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the Practice Manager informs new staff, in writing of the nature of their work and asks if
they have any pre-existing injury that may be affected by the new job. New staff are also
notified, in writing that failure to inform or hiding a pre-existing injury which might be
affected by the nature of the proposed new job, could result in that injury not being
eligible for future compensation claims.
we ensure workers have adequate information, instruction, training and supervision to
work in a safe and healthy manner.
we maintain the workplace in a safe condition (such as ensuring fire exits are not
blocked, emergency equipment is serviceable, and the worksite is generally tidy) and
provide staff with adequate facilities (such as clean toilets and hygienic eating areas).
To support the safety health and wellbeing of our practice team we have policies and
procedures in the following areas:

tasks involving manual handling are identified and measures are taken to reduce or
eliminate the risk of injury to doctors and staff as far as reasonably practical.

incidents and all injuries involving all staff and patients and others that occur in the
workplace are documented and managed professionally and ethically, according to
relevant medical standards and guidelines.

at induction and periodically all staff are instructed in safety and infection control
protocols ensuring risks are known and precautions taken, including staff
immunisation.

we strive to work together to maintain a safe physical work environment and that
supports the health and wellbeing of Doctors, staff, patients and visitors. Including
ensuring regular breaks, adequate staffing levels and a smoke free environment.

we have a duty of care to safeguard the health of employees which also covers
psychological as well as physical health.
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
we strive to encourage consultation between management and staff on all matters
pertaining to OH&S matters as obligated under the legislation.

we endeavour to provide a working environment in which all Doctors, staff, patients
and visitors are not subject to unlawful discrimination, sexual harassment, violence or
bullying.

audits are undertaken to ascertain that all practice and office equipment is appropriate
for its purpose. Records of maintenance, including electrical safety checks and
calibration schedules are maintained.

records of updates and training provided to all staff in relevant equipment operation
and maintenance, manual handling skills, and compliance with OH&S requirements
are maintained.

we strive to ensure the practice environment and facilities are adequate, and provide
for the comfort, safety and security of Doctors, staff, patients and visitors.

we will not tolerate violence of any nature.

non medical emergency procedures and fire safety precautions are clearly
documented and designated members of the emergency team have a reference and a
basis for their decisions and actions within that role.

we have appointed one member of staff with primary responsibility for the
development and consistent implementation of our infection control systems and
procedures which includes environmental cleaning. (Refer Section 4 Principles of
Infection control) Specific areas of responsibility may be delegated to nominated
members of the practice team and these particular responsibilities should be
documented in the relevant position descriptions.

to minimise harm to our patients we have clear lines of accountability and
responsibility for the delivery of safe and effective quality care.

we have a requirement for two members of the staff to be present during the normal
opening hours of the practice.
Visit Work safe website for up to date information on your obligations:
www.workcover.vic.gov.au.
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Hazardous Substances
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we implement arrangements for the safe use, handling, storage and transport of
chemicals and hazardous substances. (Refer Section 4 Handling and Use of
Chemicals).
regular audits of products used by the practice are undertaken and hazardous
substances are stored, handled and documented according to assessed risk.
material safety data sheets (MSDS) and Product Data sheets (PDS) are maintained
and visibly placed on equipment and hazardous substances, to describe them and
give clear instructions for their use.
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a Material Safety Data Sheet (MSDS), also referred to as a Safety Data Sheet (SDS), is a
document that describes the chemical and physical properties of a material and provides
advice on its safe storage, handling and use. It includes details of health and
physicochemical hazards, exposure controls, personal protective equipment, safe handling
and storage instructions, emergency procedures and disposal advice. It is a requirement
under the legislation to have MSDS available. MSDS sheets can be obtained by the
supplier’s website or by phoning the supplier. Free MSDS search http://www.msds.com/.
Remember chemicals and hazardous materials are not only in cleaning products for
example - consider toners in printers/photocopiers, liquid nitrogen, oxygen etc.

the current manufacturer’s, importer’s or supplier’s copy of the MSDS is used by the
practice and this information is never altered.
the practice endeavours to control risk associated with the use of hazardous
substances which are stored in labelled containers.
a register of hazardous substances is kept and maintained by the practice. (see hint
above about this).
staff members are instructed on how to handle hazardous substances appropriately
and documentation and ongoing training is provided regarding this.
regular risk assessment is undertaken by this practice in order to control risk
associated with the use of hazardous substances.
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RACGP 4th edition Standards 4.1.2 & 5.3.3 & 3.1.3.
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3.1 Manual Handling
Policy
Manual handling is any activity requiring the use of force exerted by a person to lift, push,
pull, carry, or otherwise move or restrain any animate or inanimate object. It includes
activities involving awkward posture and repetitive actions. Manual handling injuries account
for nearly 50% of all Workcover claims. The objectives of the Occupational Health and
Safety Manual Handling Regulations 1999, are to reduce the number and severity of
musculoskeletal disorders associated with tasks involving manual handling.
Under these regulations, this Practice aims to identify tasks involving hazardous manual
handling and to undertake risk assessments. Risks to staff are thus reduced or eliminated
as far as practicable.
Risk factors likely to cause manual handling injuries and therefore include in Practice Risk
Assessments include:
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force applied.
actions & movements used.
range of weights.
how often & for how long, manual handling is done.
where the load is positioned & how far it has to be moved.
availability of mechanical aids.
layout & condition of the work environment.
work organisation.
position of the body whilst working.
analysis of injury statistics.
age, skill & experience of workers.
nature of the object handled.
any other risk factor considered relevant.
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Procedure
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avoid tasks that involve:
o twisting, bending or extensive reaching
o repeated or prolonged stooped posture
o lifting requiring extended reach
o repetitive lifts from below mid thigh or using forceful movements
o prolonged bent neck posture when working on low flat bench
o repetitive tasks for a prolonged time
o using excessive force to push, pull or hold object
reduce the size or weight of objects to be lifted or carried.
prevent slips or falls by wearing appropriate footwear.
ensure adequate lighting.
clean area regularly; spills should be wiped up immediately.
check equipment is in good working order and there is adequate space in which to
work.
weight limits: Seated – 4.5 kg. Standing – 16 to 20 kg. (For ideal conditions and with a
compact load held close to the body and with a short carrying distance).
Before doing any type of manual handling assess the situation ask the following questions:
 should two people be lifting this or am I able to lift this safely and without risk or injury?
 is my pathway clear of all objects?
 what distance am I going to be going?
 can I see clearly?
 can I split the load to make it lighter?
 size up the load – if in doubt seek assistance.
Our practice has one or more height adjustable examination couch/s to assist in the care of
patients with a disability, and to reduce the risk of staff injuring themselves when assisting
patients on or off the examination couch. Where our practice facilities are inadequate for
staff and visitors to safely assist patients with a disability we make alternative arrangements.
e.g. Home visits.
Staff Responsibility
If you identify a task, piece of equipment, or work area that may be a risk, report it to the
Practice Manager or the OH&S representative. A further detailed risk assessment will be
conducted and if necessary, changes will be made to reduce the risk of injury with training
for staff as needed.
RACGP 4th edition Standards 5.1.1 & 4.1.2.
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3.1.2 Incidents and Injury and Adverse Patient Events
Policy
This practice has designated (*insert staff members name) with primary responsibility for clinical
risk management including following up on incidents, injuries and adverse patient events and
near misses.
It is a legal requirement under the Occupational Health & Safety legislation and for
insurance purposes, to report any injury sustained or thought to be sustained in the
workplace, recognizing that good reporting also leads to effective prevention.
Our practice encourages the identification, analysis and prevention of errors, failure or
inadequate systems that can potentially be a risk to patient safety to assist with risk management
strategies not to apportion blame.
Incidents that should be reported (regardless of whether harm has occurred) to assist with
making improvements to minimise the risk of recurrence, include:
 needle stick injury or mucous membrane exposure to blood or bodily fluids.
 slip or fall.
 drug or vaccine incident (loss, misplacement or other).
 adverse patient outcome.
 failure or inadequate patient handover or identification of a patient at the point of
transfer of care.
 delayed treatment or delayed follow up or unnecessary repeat of tests.
 medication errors.
 any deviations from standard clinical practice.
Accidents or incidents may involve the following:
 staff (employed directly by this practice).
 non-staff (patients, visitors, contractors).
 events (e.g. theft, non-patient assault, gas leak, bomb hoax, security breach,
medication error or patient complication following medical intervention, breakdown in
clinical handover).
Actual and potential risks are identified and actions are taken to increase the safety and
improve quality care. The privacy of individuals involved is maintained.
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Procedure
Reporting
Staff use the “Adverse Outcome Report” to report any slips, lapses or near misses in clinical care
or deviations in patient care that might result in harm. The medical defence organisation is
contacted for events that might give rise to a claim.
Completed “Adverse Outcome Reports” are:
 completed as soon as possible after incident occurs, preferably within 24 hours.
 filed in the “significant event register” folder.
Any additional medical or other certificates, reports or pathology related to the
accident/incident are dealt with as soon as possible original documents are submitted.
For injury occurring in the practice or course of work, WorkCover reporting protocols must
also be followed. It is a legal requirement to report all injuries sustained in the workplace
The Doctor should refer patients to another practitioner if there is a possible conflict of
interest, for example a staff WorkCover claim being managed by the employing practitioner.
Risk assessment
The designated staff member conducts a thorough review of all the hazards relevant to the
cause(s) of any injury that has occurred with a view to identifying appropriate controls.
(Refer Section 8 Risk Assessment and Management).
Risk control
Involves identifying and implementing all the practicable strategies to minimise subsequent
similar events or eliminate/ reduce the causes(s) of the injury or incident.
Informing relevant staff are about changes and why they have been implemented (usually at
the staff meeting) to reduce the likelihood of recurrences.
Retaining any documentation or evidence of the implementation of any improvements.
Conducting subsequent review/s to ascertain whether the implementation of the improvements
was successful.
Documentation
Retain documentation of the investigation process and any agreed actions implemented to
minimise the re-occurrence of the incident and to log trends.
RACGP 4th edition Standards 1.5.2 & 3.1.4 & 3.1.2.
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3.1.3 Sharps Injury Management and Other Body Fluid
Exposure
Policy
The employer is responsible to ensure that all staff:
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are familiar with the practice policy regarding management of blood and body fluid
exposure.
consider the blood and body substances of all patients as potential sources of infection.
understand how to prevent exposure to blood and body fluids.
have access to education and regular in service training in infection control matters.
have documented their immunisation status and have been offered NHMRC recommended
immunisations appropriate to their role.
analyse any incidents and modify procedures as required to reduce the risk of recurrence.
In our practice, we understanding that the management of occupational exposure to blood or
body fluids includes:
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rapid assessment of the staff member and the source patient.
documentation of the incident.
counselling for the staff member.
timely administration of medications where appropriate.
investigation of the incident to enable modification of procedures if required.
Occupational exposure to needle stick injuries and body substances can be prevented by using
standard precautions, wearing personal protective equipment (PPE) and implementing safe work
processes.
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Procedure
Preventing blood and body fluid exposure
Use standard Precautions where there is a risk or blood or body fluid exposure.
Implement Safe work practices around the handling of sharps, specimens, and waste, cleaning
of environment and reusable items.
Assess and manage any blood and body fluid exposure immediately.
Following Occupational Exposure
In our practice, we follow this procedure after occupational exposure:
1. Clean/decontaminate
 skin: wash with soap and water
 mouth/nose/eyes: rinse well with water or saline.
2. Notify the practice principal or GP on duty immediately
The source:
 explain and reassure the source and offer pre test counselling.
 obtain consent to have the source patient’s blood tested for Hepatitis B, Hepatitis C
and HIV
 the results should be available in 1-2 hrs if marked “urgent – needle stick” and
received at an appropriate testing laboratory.
 take a history from the source – maintain the source patient’s confidentiality and do not
interview them in front of relatives
o unprotected sexual intercourse
o sharing needles, tattoos, body piercing
o sharing razor blades or toothbrushes
o blood or body fluid exposure of mucous membranes or non intact skin.
o blood transfusion before Feb 1990 (for HCV)
o infection with HIV, HBV, HCV
o if the source patient has a history of at - risk activities inform them about the
window period in diagnosis.
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if any of the staff member’s blood went into the patient or onto instruments that were
then used, the staff member also needs to be listed as a source.
The Exposed person
 if the source is unknown the person needs to be tested and post exposure prophylaxis
(PEP) needs to be considered
 obtain consent from the exposed person for urgent baseline testing for Hepatitis B,
Hepatitis C and HIV to establish if the staff member has previously acquired an
infection from other exposures.
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the exposed person’s confidentiality must be maintained especially if a staff member.
the exposed person may elect to have these tests performed at a different facility or
their own GP
advise them to practice safe sex until their results and the source’s results and history
have been reviewed
give the exposed person the telephone number for the state/territory Health department
communicable disease contact and other advisory services.
3. Treatment
 needs to be commenced if it is anticipated that the sources blood test results will not be
available within 24hrs and the source patient could be HIV positive or in the window
period.
 if the HBV status of the exposed person is not known, and the sources HBV status will
not be available within 24-48 hrs then give:
o Hepatitis B immunoglobulin
o Hepatitis B Vaccination 1st Dose
o ADT (Adult Diphtheria and Tetanus)
 the exposed health care worker should be referred for immediate consultation with an
infectious diseases specialist for consideration of PEP for HIV :
o if the injury is classified as high risk, or
o if the source patient has participated in at risk activities, or
o If the source patient is positive for HIV or other significant blood borne
infections.
o If the source patient is unknown
4. Document Exposure:
We have appointed one member of staff with primary responsibility for the development
and consistent implementation of our infection control systems and procedures. (Refer
Section 4 Principles of Infection control). Report any exposure to this person or delegated
authority in addition to normal incident reporting protocols.
 what procedure was being undertaken
 how the injury happened and the name of anyone that witnessed it
 the nature and extent of the injury
 exactly what you were injured with (specify gauge of the needle)
 the body substance involved
 how much blood or body fluid was the health professional exposed to.
 what personal protective equipment was being used?
 the full name and address of the source. If the source cannot be identified document
“source patient not known”.
RACGP 4th edition Standards 5.3.3.
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3.1.4 Staff Immunisation
Policy
We have appointed one member of staff with primary responsibility for the development and
consistent implementation of our infection control systems and procedures which includes staff
immunisation. (Refer Section 4 Principles of Infection control).
Specific areas of responsibility may be delegated to nominated members of the practice
team and these particular responsibilities should be documented in the relevant position
descriptions
All practice staff should be advised of the risks of infection and be encouraged to be
immunised against vaccine-preventable diseases to prevent transmission of disease to and
from practice staff and patients. Staff should be offered additional vaccinations where
appropriate depending upon the likelihood of their contact with patients and/or blood supply
substances. These vaccinations may include Hepatitis A and other disease vaccinations.
The practice will keep an extensive and up-to-date record of the immunisation history of
each staff member. This will assist in identifying non immune staff to ensure they are
excluded from contact with patients during disease outbreaks.
Subject to informed consent, the immunisation status of staff is known and recorded
including the documentation of any refusal.
Procedure
1. A vaccination history is sought from all new staff at orientation.
2. Staff should receive the vaccines they require within the first few weeks of
employment with the exception of influenza which should be administered annually
between March and May.
3. Each staff should be individually assessed for specific vaccines, taking possible
contraindications into account.
4. Staff immunisation history will be recorded on the “Staff Immunisation
consent/refusal and record form” located at the end of this procedure.
Hint - this form is also located in Section 2 in the “Job Package”.
5. Informed consent should be obtained before screening and vaccination.
6. Staff will be given a personal immunisation record that documents vaccinations
given and test results.
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Guidelines for immunisation
Staff members are offered NHMRC recommended immunisations as appropriate to their
duties. The following vaccines should be considered for practice staff:
Diphtheria, Tetanus
If not immunised, give three doses of ADT at one monthly intervals followed by booster
doses at 10 and 20 years after primary course. It is recommended to give Boostrix as the
first dose to provide immunisation against Pertussis. Give a further dose at age 50 if no
booster dose in past 10 years. Boostrix is also recommended although not funded, to be
used when giving a booster against Tetanus as it will give the added protection of Pertussis
immunity.
Pertussis
Single dose of dTpa given for practice staff/healthcare workers in paediatric settings
especially maternity and neonatal.
Poliomyelitis
Offer single dose to staff that may be exposed to polio and have not received a booster
vaccination within the past 10 years. (Page 255 The Australian Immunisation Handbook 9th
Edition.)
Measles Mumps & Rubella
Staff, with no known history of Measles, Mumps or Rubella, or vaccination should receive 2
doses of MMR one month apart. Antibody testing to ensure immunity should follow a few
months after. Generally, those born prior to 1966 are considered immune.
Women, however, should not be vaccinated whilst pregnant or if there is a chance that they
may be pregnant. Pregnancy should be avoid for 28 days after vaccination. (pg 279 The
Australian Immunisation Handbook 9th Edition)
Meningococcal Type C
Meningococcal infections are transmitted via respiratory droplets and have the capacity to
have a rapidly fatal course in previously healthy individuals. Staff members not immunised
should be offered immunisation.
Influenza
Due to the highly transmissible nature of the influenza virus and possible serious
consequences for the young and elderly, offer all practice staff an annual influenza vaccine
for their own and their patient’s protection.
Hepatitis B
All staff should be vaccinated. This is a course of 3 injections at 0, 1 & 6 months. Female
staff that are or may be pregnant should not be vaccinated.
For staff who may deal with contaminated medical equipment and blood or body fluid spills,
Hepatitis B vaccination is essential. All staff should have their Hepatitis B antibody status
documented.
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Chicken Pox
Varicella history or serology to confirm immunity is recommended for all staff. If seronegative,
vaccination should be offered in a 2 dose schedule. (pg 315. The Australian Immunisation
Handbook 9th Edition)
Staff Records
 records are initiated for all staff employed detailing their immunisation status. These
will be maintained and include details of:
o disease history.
o vaccination.
o antibody results.
o test (e.g. Serology results) results.
o a record of vaccines consented/refused.
 these records remain confidential, secure and accessible by authorised practice staff
24 hours a day, 7 days a week.
 records are maintained by a designated staff member and are routinely updated
whenever new vaccinations, tests or disease occur.
 for all work related immunisations, staff should be given a verbal explanation about
each disease (and its effects), from the General Practitioner.
 to further enhance informed consent, It is strongly recommended that staff are given a
‘Fact Sheet’ for all work related immunisations, similar to those which are available on
the Immunise Australia Program website (Refer to Hints at end of this section)
 staff are required to sign the forms attached, providing written consent for either:
o Vaccination.
o Serology.
o Supply of record.
o Refusal of vaccination.
 if vaccination is given the following details must be recorded:
o informed written consent.
o date vaccine administered.
o brand name.
o batch number.
o expiry date.
RACGP 4th edition Standards 5.3.3.
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3.1.5
Smoking, Drugs & Alcohol
Policy
As a prominent health care provider our aim is to promote the health and well being of all
staff, patients and others whilst they are on our premises.
Smoking is therefore not permitted in this practice and is discouraged on the premises or the
surrounding environs. The use of illegal drugs and alcohol is prohibited on and around the
site.
Staff should not present for work if under the adverse effects of alcohol or illegal drugs.
Procedure
Staff members who are smokers should make an effort to remove any nicotine odour on or
about clothing and self prior to returning to duty.
No smoking signs are visible in the waiting and reception area. Signs are not to be
removed, except to replace worn or frayed items.
Brochures and posters for ‘QUIT’ and related no smoking, drug free strategies are to be
placed in waiting room and visibly displayed to ensure our valued patients are aware of our
commitment to better health strategies.
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3.1.6
Staff Health and Wellbeing (including GPs)
Policy
This practice is committed to providing and maintaining a safe and healthy workplace for
doctors, staff, patients and all other visitors. This includes psychological as well as physical
health.
Health and safety is an integral part of every activity we perform, and as such, the
occupational health and safety of General Practitioners and practice staff is a priority of this
practice, and is governed by Occupational Health & Safety State/Territory and Federal
legislation and regulations.
The practice has implemented strategies to ensure the occupational health and safety of the
General Practitioners and staff, and in addition, there should be current information on
programs that support the health and wellbeing of General Practitioners.
This practice recognises that that breaks may reduce fatigue and support the health and
wellbeing of both the General Practitioner and practice staff, as well as enhancing the
quality of patient care.
Our Doctors and practice team can discuss concerns about violence in the practice and we
have to right to discontinue care. (Refer to Section 7 Refusal to treat a patient)
Procedure
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when staff of this practice require a break or are unexpectedly absent, the practice
should have strategies in place for managing work flow, that are known to all staff.
Cover should be organised by the Practice Manager or another senior member of the
team.
regular breaks should be scheduled for all staff members, dependent upon the hours
or shifts worked, and during consulting sessions for General Practitioners. The
practice should schedule appropriate breaks for all staff both during and/or between
the sessions undertaken by the same General Practitioner.
when a work break has been organised, where possible, a relieving staff member will
complete the workload of an absent staff member, in addition to their own workload.
strategies should be been implemented to manage workflow whenever a General
Practitioner or practice staff member is unexpectedly absent, or scheduled for leave.
Unplanned leave will be covered by existing practice staff or by agency or locum staff
as required.
the practice should ensure that staff take regular leave and that leave is not permitted
to accrue to an excessive amount.
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the practice should have current information on programs that support the health and
wellbeing of staff, including General Practitioners.
occasionally staff may be confronted by physically or verbally aggressive patients or
other stressful incidents or situations, including assisting with emergencies. The
practice should provide emotional debriefing or counselling in these situations within a
reasonable period of time after the incident.
during normal practice hours at least one staff member, who is trained to take
telephone calls and make appointments, assess the urgency of requests for
appointments and assist with medical emergencies and CPR, must be present in
addition to the GP(s).
outside normal practice opening hours, for emergency surgeries, appropriate staffing
is encouraged to assist in providing security and safety for patients and doctors.
RACGP 4th edition Standards 4.1.2.
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3.2 Practice Facilities
Policy
The practice premises, including the facilities and equipment are safe and adequate to meet
the needs of the staff and patients.
The facilities at our practice make adequate provision for, and encourage patient auditory
and visual privacy.
Facilities are well maintained and visibly clean with surfaces accessible for cleaning.
Every reasonable effort is made to make the environment safe and comfortable for staff and
people who use the practice.
Where possible the practice has heating and/or air conditioning to assist in the comfort of
staff, patients and visitors.
Our waiting area/s are sufficient to accommodate the usual numbers of patients who would
usually be waiting at any given time.
Our practice has one or more height adjustable beds. The physical conditions in our practice
support patient privacy and confidentiality.
RACGP 4th edition Standards.5.1.1 & 5.1.2.
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3.2.1 Consulting Rooms
Policy
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practice facilities should be safe for General Practitioners, staff and patients.
the practice has at least one dedicated consulting or examination room for every
doctor working at any one time. Areas where consultations or treatment occur are
appropriate for the health and safety of General Practitioners, staff and patients.
the consulting rooms should have sufficient space, and are free from excessive
extraneous noise and have adequate lighting for observation.
the temperature in the consulting rooms should be maintained at a comfortable range
to allow for the patient to undress if necessary for an examination.
there must be an examination couch in each consulting room or an attached
examination room (at a minimum one examination couch in the practice must be
height adjustable).
consultations with patients must be confidential and private. The practice ensures that
both visual and auditory privacy is afforded to all patients in all examination areas,
treatment rooms and consulting rooms.
provision must be made in the examination areas and treatment rooms for maintaining
patient privacy when undressing or receiving treatment. Where required a gown or
sheet is made available to patient to the privacy during an examination or procedure.
visual privacy will be afforded to patients during clinical examinations and when
patients are required to undress/dress in the presence of the General Practitioner or
the general practice nurse. In situations where there is a door opening to an area
where the public may have access a curtain or screen is used.
the practice should provide appropriate care and privacy for patients and others in
distress during the consultation, examination or treatment of a patient.
privacy and confidentiality of patient information should be considered at all times,
including during telephone conversations between staff and patients.
computer screens are not readily visible to patients and visitors and screen savers are
activated.
patient health information is treated with respect and letters, forms or notes
concerning patients are not readily visible to other patients.
examination couches should be able to be cleaned and are cleaned regularly.
linen (including gowns and sheets), curtains and screens should be laundered or
cleaned regularly by the practice.
the consulting room should be well maintained and visibly clean with surfaces
accessible for cleaning.
storage areas for sterile/non sterile items should be dust proof and dry and be able to
maintain their sterility and prevent exposure to blood and body substances.
the security of the practice (and the staff) is an important issue and strategies should
be in place in the event of a breach of security.
RACGP 4th edition Standards.5.1.1& 5.1.2.
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3.2.2 Hand Washing Facilities
Dedicated hand washing facilities with hot and cold water, liquid soap and single use paper
towel should be readily available in every clinical management or treatment area.
Ideally every consulting room should also have a basin dedicated for the purpose of
washing hands. Where this is not possible, washbasins are situated within close proximity.
Appropriate facilities for drying hands are provided. Hot air dryers are not used in clinical areas.
Single use towels (paper or cloth) are provided in shared locations and clinical areas.
Disposable paper towel is used prior to aseptic procedures.
Hand disinfectants designed for use without water, such as alcohol based hand gel are available
in:
The Doctors Bags to use when hand washing facilities are inadequate, e.g. home visits
 in all treatment and examination areas to encourage hand hygiene in addition to hand
washing facilities.
 in patient and staff areas during flu season to encourage hand hygiene.
All new staff are informed about our Hand washing procedures (Refer Section 4) and we
provide regular updates and training in infection prevention.
RACGP 4th edition Standards 5.3.3.
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3.2.3 Waiting Area
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the practice waiting room area is sufficient to accommodate the usual number of
patients and others who would be waiting at any one time.
the health and safety of GPs, staff, patients and visitors is considered when selecting
seating, furniture and toys for the waiting room, and the area is kept tidy and clean to
maintain a safe environment.
the practice is able to provide appropriate and respectful care for patients and others
in distress. Strategies should be in place to deal with distressed patients. i.e.
vomiting, upset or in severe pain. Privacy for such patients could be provided by
allowing them to sit in an unused room, staff room or other designated area, rather
than waiting in the general waiting area.
auditory privacy within the waiting area can be enhanced by staff discretion and the
use of background music or a television to mask conversations.
conversations with a member of the clinical team cannot be overheard by patients in
the waiting room.
privacy and confidentiality of patient health information is considered when staff are
discussing patients health information at the reception area.
computer screens are not readily visible and screen savers are used.
where appropriate our waiting area caters for the specific needs of children with play
equipment or toys that can be washed regularly.
the waiting room furniture and toys are in good condition, without sharp edges, and
the room is maintained in a clean and tidy state with surfaces easily accessible for
cleaning.
a range of posters, leaflets or brochures about health issues relevant is available or on
display in the waiting room for patients to self select.
RACGP 4th edition Standards 5.1.1 & 5.1.2.
3.2.4 Toilets
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toilets should be located within the practice. Where this is not possible they need to
be adjacent or within very close proximity.
the toilets need to be easily accessible and well signposted.
hand washing facilities, including liquid soap and single use paper towel or hand air
dryers need to be readily available for use by patients and others and situated in close
proximity to the toilets.
there should be separate toilets for staff and patients if possible.
the toilets should be well maintained and visibly clean with surfaces accessible for
cleaning and if a baby change room is provided then that also must be kept
adequately maintained and located close to hand washing facilities.
RACGP 4th edition Standards 5.1.1.
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3.2.5 Telecommunication System
Our practice’s telecommunication system facilitates patient access to the practice services
and aims to adequately meet the needs of patients and staff.
It is recognised that the telecommunications needs of the practice may change over time, in
line with staffing changes and growth of the practice. Strategies should be in place,
designed to monitor, review and make the appropriate changes to the telecommunications
system as required. This may include patient and staff feedback.
The auditory privacy and confidentiality needs of patients have been considered when
locating our telephones and facilities for electronic communication.
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a telephone line must be available for staff to summon assistance in an emergency. A
dedicated line is provided for this purpose. (*insert details of how to access this line).
the telephone system must provide sufficient inward and outward call capacity and
needs to have the capacity for electronic communication (either email or Facsimile).
the practice has (*insert number) of lines dedicated for telephone calls and (*insert
number) of lines for electronic communication.
patient feedback is sought on a regular basis to ensure that ‘access’ to the practice
facilities and services is easily available by telephone.
RACGP 4th edition Standards 5.1.2.
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3.2.6 Unauthorised Access Areas
General Practitioners and staff need to ensure the confidentiality and security of patient
health information and other sensitive practice materials.
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signage is present to prevent unauthorised public access to specified areas in the
practice where patient health information and other sensitive practice materials are
stored.
the presence of an additional person in the practice (besides the GP(s) on duty) will
increase security and safety for patients, GPs & staff and reduces the risk of
unauthorised access to patient health information or sensitive practice materials.
the confidentiality and security of medical records, prescription pads/paper, letterhead,
administrative records and other official documents must be maintained by all staff
and storage in a restricted access area is recommended.
patient personal health information is stored in an area or manner that is not
accessible to unauthorised persons.
facsimile machines, printers and other communication devices are not readily
accessible to people other than the General Practitioner(s) and authorised staff.
all sensible security measures are taken to prevent unauthorised access to
medications and the Doctor’s bag.
RACGP 4th edition Standards 5.1.1.
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3.3 Security
Policy
Our practice ensures as much as possible that our facilities provide appropriate security for
patients, staff and visitors. All practice staff are aware of, and are able to, implement
protocols to ensure the safety and security of all persons within the practice.
Procedure
The premises are protected by a computerised alarm system that has motion detection
sensors located at various points on the site. Refer to plan in the office for further details.
A ‘Panic’ button, linked to the security system, is located under the reception desk. Our
security firm also patrols the site after hours.
During routine practice hours at least one other practice staff member, in addition to the
General Practitioner(s), is present in the practice.
Another staff member, in addition to the General Practitioners can provide practical help in
an emergency situation, reduce the risk of unauthorised access to patient health
information, ensure the security of sensitive practice resources, and provide security and
safety for patients, General Practitioners and staff.
Staff rosters are checked daily and staffing is then planned for the next workday. Where
possible, this same strategy is strongly encouraged to be implemented outside of normal
working hours (e.g. at weekends and on public holidays or when non-routine ‘emergency
surgeries’ are conducted for patients needing urgent care).
Equipment on site is engraved with practice name and item number. The Practice Manager
maintains the number register.
Contracts and warranties for medical, office and other site equipment are securely locked,
maintained and updated by the Practice Manager.
Security codes are routinely changed for computers and the security system.
Patients, visitors and trades people are to report to the reception desk. Where appropriate
visitor’s and trades people should wear an identification name badge on site. The Reception
staff and Practice Manager are informed of the presence of all visitors (except patients and
relatives who report to reception only).
Confidential waste is placed in a locked storage box prior to shredding or secure destruction
by our security documentation storage and destruction firm.
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All drugs of dependency and Schedule 8 medications are locked in the safe. See Section 7:
Clinical Management – Drug Storage.
Staff members are encouraged to be vigilant whilst on duty and act to ensure the continuing
safety of all GPs, patients, visitors and other staff.
Open and Lock up protocol
At start of day:
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after unlocking premises, deactivate security alarm system, using security code
check all exits for unimpeded access and unlock/open windows as required for routine
practice operation
turn on lights, heating/cooling system, computers, photocopier, unlock medical record
filing cabinets, checking for items out of place or for any unusual objects not in correct
placement
turn off answering machine and retrieve messages left after hours
check fax machine for any incoming messages and action as required
report unusual issues or missing items to Practice Manager or Principal, documenting
same
At end of day:
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lock all windows and doors
ensure computer back up is complete or scheduled after hours as required
switch off designated computers, photocopier, heating/cooling system
check drug cabinet & safe is locked
check that bins are empty
check that no-one is in toilets and windows are locked
check offices for unsecured confidential documents including medical and finance
records. Lock medical record filing cabinets
ensure prescription pads, prescription computer generated paper, letterhead,
medications, health records, and other administrative records or official documents are
out of view.
secure the cash box
check that answering machine is on
turn off all lights, keeping the security lights on
Activate security system
RACGP 4th edition Standards 5.1.1 & 4.1.2.
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3.4 Non Medical Emergencies
Policy
Non medical emergencies may occur that will require a quick, informed and effective staff
response.
Types of non-medical emergencies include: failure of electricity supply, telephone or water,
fire or false fire alarm, property damage, break-in, abusive or threatening telephone calls or
persons at the practice, leakage of toxic chemicals, bomb threats and letter bombs.
We also have a contingency plan for unexpected events such as natural disasters, national or
local infection outbreaks or the sudden, unexpected absence of clinical staff or computer system
failures. (Refer to 8.1 Risk Assessment and Management and 6.1.1 Computer Information
security)
We have mechanisms in place to ensure the timely acquisition and dissemination of information
(including regular updates) about alerts, emerging diseases, local disasters or emergencies.
The practice has appointed a designated member of staff to have primary responsibility for our
risk management systems. These may include clinical and non clinical risks and events. Specific
areas of responsibility can be delegated to other nominated members of the practice team and
these particular responsibilities should be documented in the relevant position descriptions.
Procedure
Our practice has a “Non medical Emergency Manual’ which reflects the relevant Australian
Standards, as per occupational health and safety regulations e.g. Fire protocols.
(*insert where to find your practices Non medical Manual)
The purpose of this manual is to formalise emergency procedures, and fire safety
precautions within the practice, so that those who are required to take actions related to the
protection of life and property have a reference and a basis for their decisions and actions.
Designated members of the Emergency team are familiar with procedures in the manual
and all staff knows the correct emergency procedures and are able to carry them out in
times of emergency.
We also have a business continuity plan for unexpected events that may disrupt care or stretch
practice resources to the limit, including disasters (e.g. bushfires, prolonged power failure) or
Infectious disease outbreak (e.g. pandemic), or unexpected staff absenteeism. e.g. illness. This
includes how we notify our staff and patients of such events or local disasters or emergencies.
(*insert where to find your practices business continuity plan).
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We have a system for monitoring and obtaining information and alerts about national and local
infection outbreaks, disasters, emergencies and other relevant matters. We are registered on
local networks to receive alerts and we check on a daily basis for any new or updated alerts and
disseminate these to all staff.
(*insert your procedure for the timely receiving and dissemination of any important
communication or updates. Include the name of the designated staff member who has this
responsibility)
RACGP 4th edition Standards 4.1.2, 3.1.2.
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4
Articl e II.
Infection Control
4.1 Principles of infection control
Policy
Because many infectious agents are present in health care settings, patients may be infected
while receiving care, health care workers and others such as receptionists and cleaners may be
infected during the course of their duties or when working or interacting with patients and other
people. Potential infection risks to the practice team and our patients need to be reduced.
Our practice has implemented systems that minimise the risk of health care associated
infections.
We have appointed one member of staff with primary responsibility for the development and
consistent implementation of our infection control systems and procedures. (Refer to Section 8 Clinical Governance).
Specific areas of responsibility may be delegated to nominated members of the practice team
and these particular responsibilities should be documented in the relevant position descriptions
(e.g.. infection control processes, sterilisation process, environmental cleaning, staff
immunisation, staff education). (Refer Section 2 - Position Evaluation and Recruitment).
Our practice has written polices relating to key infection control processes which are reviewed
and updated regularly. (Refer section 8 - Review of policies and procedures).
All staff has an individual responsibility to identify any potential infection risks within the practice
and to be familiar with and implement the relevant infection control procedures of our practice.
(Refer Section 2 - staff code of conduct).
New staff, including contracted staff and casuals, are familarised with our infection control
policies that are appropriate to their duties as part of their induction to our workplace. Where
appropriate their competency is assessed and this assessment recorded or evidence of previous
competency is obtained and recorded. Mechanisms are in place to ensure ongoing education
and competency on a regular basis and when changes occur to our procedures. (Refer to
Section 8 - Continuing Staff Education).
Subject to informed consent, the immunisation status of staff is known and recorded including
the documentation of any refusal. Staff members are offered NHMRC recommended
immunisations as appropriate to their duties. (Refer Section 3 - Staff Immunisation).
Our practice remains alert to changes to guidelines for infection control, and can implement
them accordingly in a timely manner. We have a system for monitoring and obtaining information
about national and local infection outbreaks, as well as about emerging new risks of cross
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infection and we have an effective mechanism for timely receiving and dissemination of any
important communication or updates about emerging diseases or infection control measures to
all relevant staff. (Refer Section 8 - Risk Assessment and Management).
Procedure
We have a designated staff member (*insert staff member/s name) who has responsibility for co
coordinating and sustaining our infection control processes. This includes:
 continually modifying and improving our procedures and written policies in accordance with
the most recent evidence and guidelines and adopting a risk management approach when
implementing infection control measures.
 ensuring the timely dissemination of information concerning changes to infection control
procedures or information about national and local infection control outbreaks.
 maintaining staff knowledge, education and competency in infection control activities and
ensuring the consistent implementation of our infection control policies and procedures.
 ensuring the practice remains visible clean and environmental cleaning processes are
documented.
 appropriate delegation of infection control responsibilities and documentation of such
delegation
To ensure consistency of workplace practices our policy and procedure manual contains the
following written infection control protocols:
 prevention of disease in the workplace by serology and immunisation. (Refer to Section
3).
 blood and body fluid spills management.
 blood and body fluid exposure & sharps injury management (Refer to Section 3)
 hand hygiene.
 a cleaning schedule for clinical and non clinical areas of the practice which describes the
 frequency of cleaning, products to use and person responsible. Where appropriate we
have documented evidence of cleaning activity.(Refer to section 5).
 procedures for the all aspects of the provision of sterile instruments whether by the use
of disposables, or by onsite or offsite sterilisation.
 safe storage and stock rotation of sterile products.
 procedures for waste management including the safe storage and disposal of clinical
waste and general waste.
 the appropriate use and application of standard and transmission based precautions.
 access for patients and staff to PPE including evidence of education on the appropriate
 application, removal and disposal of PPE.
 triage of patients with potential communicable diseases.
 pathology testing done within the practice.
 ongoing education and training provided to each staff member and the mechanism for
 assessing staff competency in infection control procedures.
RACGP 4th edition Standards 5.3.3.
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4.2 Blood and body fluid spills
Policy
Our practice has management systems for dealing with blood and body substance spills.
 blood and body fluids, include blood, vomit, urine, faeces, sputum and body tissue are
treated a potentially infectious substances that can transmit disease should contact occur.
 doctors, Nurses, other health professionals, practice staff and external contractors (e.g.
cleaners) consistently use standard precautions to achieve a basic level of infection control
regardless of the known or perceived infection status of the patient.
 any spillage needs to be treated promptly to reduce the potential for contact with other
patients, staff or visitors.
 the employer is responsible to ensure all staff are familiar with the practice’s policy and
procedure for the management of blood and body fluid spills and staff receive adequate
training on how to appropriately clean blood and body substance spills which is appropriate
for the tasks they are expected to perform.
 staff are also familiar with the actions to take in the event of exposure to blood or body
fluids while cleaning a spill. (Refer to Section 3 - Sharps injury Management and other
Body fluid Exposure.)
Our practice has a spills kit readily available consisting of a rigid walled container with a lid
containing:
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1 small bucket (with water level marked) and pre-measured amount of detergent * (in a
labelled container) to be made up when necessary.
utility rubber gloves.
face and eye protection: Goggles/safety glasses/face shield/mask.
disposable or reusable impermeable/plastic apron/gown.
roll of paper towelling (that retains strength when wet).
scrapers (2 pieces of firm cardboard or plastic).
hazard/cleaning sign.
biohazard bag.
polymerising beads or other absorbent material.
list of contents to assist restocking after use.
copy of the instructions for cleaning spills.
*The detergent used for general cleaning is satisfactory for treating most spills (Source: Infection
control standards for office based practices, 4th Edition)
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Procedure
As part of the induction process all staff are provided with information about our practice’s
protocol for managing spills of blood and body fluids and what to do in the event of a needle stick
injury or exposure to blood or body fluid (Refer section 3 Sharps Injury Management and other
body fluid exposure).
In our practice, the Spills Kit is located (*insert the location of the Spills Kit here).
It is the responsibility of (*insert staff member here e.g. the practice nurse) to maintain the Spills
Kit and to ensure all items are replaced after each use and the items are not expired.
The management of spills should be flexible enough to cope with different types of spills, taking
into account the following factors:
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the nature of the spill, for example sputum, vomit, faeces, urine or blood.
the pathogens most likely to be involved in these different types of spills, for example stool.
samples may contain viruses or bacteria, whereas sputum may contain Mycobacterium
tuberculosis.
the size of the spill, such as a spot, small or large spill.
the type of surface, for example carpet or vinyl flooring.
the area involved, such as whether the spill occurs in a contained area such as a
consultation room or in a public area such as the waiting area.
the possibility of some material remaining on a surface where cleaning is difficult (e.g.
between tiles) and of bare skin contact with that surface.
The affected area must be left clean and dry. Disposable items in the Spills Kit must be replaced
after each use and reusable items cleaned according to protocol.
Only staff with confirmed vaccination status and training are permitted to clean spills of blood or
body fluid and perform other high risk activities such as instrument reprocessing. (Refer to
Section 3 Staff Immunisation)
Method for cleaning spills
 standard precautions apply. Use Personal Protective equipment.
 get the practice spills kit.
 prepare detergent and water.
 tear off enough paper towel.
 prepare rubbish bag.
If the spill is on a hard surface
 wipe up any solid matter and excess material.
 clean with detergent and water using a clean piece of paper towel each time.
 dry the surface.
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If the spill is on a soft fabric or carpet
 use polymerising beads or other absorbent material.
 scrape up residue.
 dispose of contaminated material.
 clean with detergent and water using a fresh piece of paper towel each time.
 quarantine the area until dry.
 consider arranging for the carpet to be ‘steam’ cleaned.
 a disinfectant may be used after cleaning.
RACGP 4th edition Standards 5.3.3.
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4.3 Hand washing and hand hygiene
Policy
Effective Hand hygiene has been proven to reduce the spread of infection. This minimises the
risk of cross-contamination through physical contact with patients and co-workers, and touching
inanimate objects which include door handles and telephones.
Gloves are not a substitute for hand cleaning. Fingernails are kept short and clean and Jewellery
to a minimum as these may harbour bacteria. Cuts and abrasions are covered with water
resistant dressings. Nailbrushes are not used.
The employer is responsible to ensure all staff members have been educated on effective hand
hygiene and hand care.
Staff must wash their hands:
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before and after examining and treating
patients
before and after and between performing
any procedure
before and after taking blood,
before and after giving an injection
after handling pathology specimens
after handling any equipment that might
have been soiled with blood or other body
substance
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after routine use of gloves
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before and after eating
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before and after smoking
after blowing your nose
after going to the toilet
when visibly soiled or perceived
to be soiled
Easy access to hand hygiene facilities is promoted with dedicated hand washing facilities (with
hot and cold water, liquid soap and single use paper towel) readily available in every clinical
management or treatment area.
Hand disinfectants designed for use without water, such as alcohol based hand gel can be used
in the following situations:
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emergency situations where there may be insufficient time and/or facilities e.g. in the
doctors bags.
when hand washing facilities are inadequate, e.g. reception areas, home visits.
in all treatment and examination areas to encourage hand hygiene in addition to hand
washing facilities.
In patient and staff areas during flu season to encourage hand hygiene.
Visible soil must be removed with detergent based wipes first. If significant direct physical
contact with a patient or patient’s blood or body fluids is likely to occur this should ideally take
place in an area where access to hand washing facilities is available.
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Hand Hygiene products need to be selected with consideration of the following factors:
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type of hand hygiene requires i.e. routine, aseptic (clinical), or surgical.
the location of the product.
compatibility of agents if multiple agents are used e.g. hand creams, ointments.
care and protection of staff hands and sensitivities.
There are no soap bars utilised in our practice. Where possible liquid hands wash dispensers
with disposable cartridges, including a disposable dispensing nozzle, are used; where these are
not available a pump pack is used. These are never topped up and are ideally discarded when
empty. Should they need to be refilled, the container is washed and dried thoroughly prior. The
nozzle is kept clean and free of dried soap.
Appropriate facilities for drying hands are provided. Hot air dryers are not used in clinical areas.
Single use towels (paper or cloth) are provided in shared locations and clinical areas.
Disposable paper towel is used prior to aseptic procedures. Hand moisturiser is made available
for staff use.
Procedure
Routine hand cleaning for soiled hands
The following procedure is followed for a routine hand wash:
1. wet hands thoroughly and lather vigorously using liquid soap.
2. wash for 10-15 seconds.
3. rinse thoroughly.
4. dry with paper towel or single use cloth towel.
5. use paper towel to turn taps off if not ‘hands free’.
Hand Washing for aseptic (non-surgical or clinical) procedures
The following procedure is followed for a non-surgical hand wash:
1. wash hands thoroughly using neutral liquid soap or an anti-microbial cleaner (e.g. 2%
Chlorohexidine).
2. wash for 1 minute.
3. rinse thoroughly.
4. dry thoroughly with paper towel or single use cloth towel.
5. use paper towel to turn taps off if not ‘hands free’.
Hand washing prior to surgical (invasive) procedures
The following procedure is followed for a surgical hand wash:
1. Remove Jewellery
2. Wet hands and forearms
3. Wash hands, nails and forearms thoroughly with an antimicrobial cleaner
i. (e.g. 4% chlorohexidine, 0.75% detergent based povidine or 1% aqueous povidine)
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4.
5.
6.
7.
First wash 5 minutes and each subsequent wash 3 minutes
Rinse carefully keeping hands above the elbows
Do not touch taps (ask another staff member to do this if not ‘hands free’.
Dry thoroughly with sterile paper or cloth towels.
Location
hand washing
facilities
Patient toilets
Liquid soap
Paper towel/air dryer
Liquid Soap
Antimicrobial cleaner
(2% Chlorhexidine)
Paper towel
Liquid Soap
Antimicrobial cleaner
(4% Chlorhexidine)
Paper towel
Sterile towel
Consulting rooms
Treatment room
Equipped for
routine hand
washing
yes
Equipped for
aseptic hand
washing
no
Equipped for
Surgical hand
washing
no
yes
yes
no
yes
yes
yes
RACGP 4th edition Standards 5.3.3.
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4.4 Handling and use of chemicals
Policy
Our practice does not use cleaning agents or other chemicals, which are known to be toxic to the
user, such as glutaraldehyde and chlorine based products. Chemicals and cleaning agents used
in our practice are used according to the manufacturer’s instructions.
Cleaning solution (detergents) that is mixed with other liquids by our practice is made at the
beginning of each working day and discarded at the end of each working day with the container
rinsed and left upside down to dry overnight. This is to avoid the spread of micro-organisms,
which may have contaminated the solution. To avoid wastage, only enough solution is made up
for the day.
All containers of chemical agents are appropriately labelled. This is to ensure that the contents of
containers can be readily identified and used correctly. For this reason, labels must be kept fixed
to the container at all times and clearly understood.
Specifically, it is recommended that a container with diluted cleaning agent state:
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name, type and purpose of chemical agent
instructions on preparing and discarding the solution
warnings and/or health and safety instructions.
Material Safety Data Sheets (MSDS) are made available for all substances used in our practice
as required by State or Territory legislation. The use and handling of chemicals, including
cleaning agents, must comply with the manufacturer’s instructions, and these can be found on
the label or MSDS.
It is also important that chemicals are stored in a safe area, to prevent unauthorised access.
Check local, state or territory legislation for specific handling and storage requirements.
Containers of chemicals are stored in a cupboard out of the reach of children. If the cupboard is
below the waist, a childproof lock should be fitted.
Staff members who are required to handle chemicals are trained in their correct and safe use,
and this includes the correct use of personal protective equipment (PPE).
All chemicals and cleaning equipment is used for the purpose intended and in accordance with
the manufacturers instructions and dilution ratios are strictly adhered to.
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Procedure
Our practice has the listed chemical and cleaning products for the following uses:
Product
Use
Storage location
MSDS
available
Material safety data sheets are located (*Insert where your practice stores Material Safety Data
Sheets).
RACGP 4th edition Standards 5.3.3, 4.1.2.
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4.5 Single Use Equipment
Policy
Equipment and medications labelled by the manufacturer as disposable or single patient use are
not reprocessed (cleaned) or re-used in this Practice.
This includes, but is not limited to: Oxygen masks and tubing, nebulizer sets, spacers, razors,
spatulas, auriscope tips, liquid nitrogen applicators, pins for sensory testing and medications
such as eye drops and ointment, lancets for blood testing, Spirometer and peak flow
mouthpieces and disposable instruments.
Single use packaging is the only acceptable presentation for dressings, suture materials, suture
needles, hypodermic needles, syringes and scalpels.
Single use vials should be used in preference to multi dose vials of injectable substances as
multi dose vials present an infection hazard if incorrectly used.
If multi dose vials are used, education and ongoing compliance with prescribed protocols are
required to prevent the potential transmission of infectious diseases, to minimise the potential
risk of vial contamination, to minimise the potential risk of medical errors, to reduce potential
wastage associated with the use of multi-dose vials, and in the case of vaccines to ensure the
delivery of a potent vaccine to the patient.
Items marked by the manufacturer as “single use” must never be reused under any
circumstances. Some items may be reprocessed for use by the same patient if labelled “single
patient use” and in this case the manufacturer’s instructions for reuse must be followed. These
may include cleaning requirements and limitations to the number of times the item can be
reprocessed.
Single use items or equipment contaminated with blood or body fluid are clinical waste and are
disposed of accordingly.
Where possible saline solution and skin preps are purchased in single use sachets or
containers; larger containers, if used, are dated when opened and changed regularly.
RACGP 4th edition Standards 5.3.3.
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4.6 Instrument and equipment processing area
Policy
The RACGP Standards recommend a designated area should be used for processing all
instruments and equipment for reuse to prevent possible contamination of processed items.
A workflow pattern, systematically moving from dirty to clean, must be established within the
designated area. All staff must understand and adhere to the designated work flow pattern. The
workflow pattern must enable items to progress from the cleaning area to the steriliser
packaging/unloading and sterile stock storage area without re-contamination.
The equipment processing area needs to include:

adequate bench space with surfaces made of a smooth, non-porus material without cracks
or crevices to allow for cleaning
good lighting
bins for specific waste
adequate storage space for materials and equipment.
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Specified cleaning equipment such as:
1. heavy duty utility gloves, plastic apron to protect clothing, protective eyewear and if items
are grossly soiled, a mask or visor.
2. a non-corrosive, non-abrasive, free rinsing and mildly alkaline detergent in the original
container or a clean, well labelled bottle.
3. cleaning brushes of a suitable size to effectively reach all parts of the item being cleaned.
4. low-linting towelling for drying the cleaned items.
This area, including sinks and containers need to be cleaned daily.
Procedure
In our practice, our equipment processing area is located (*insert location here) and our facilities
include:
(Select from option 1, 2 or 3 depending on which best describes your practice equipment
cleaning facilities. Delete other options and return italic text to normal)
(Option 1). Dedicated double sink with adequate bench space either side for work to flow from
dirty to clean area. A separate hand washing area is also available elsewhere in the room.

use the sink on the dirtiest side (according to the workflow pattern) to wash the dirty
instruments with the plug inserted. This is the dirty sink.
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

use the other sink to initially rinse the instruments and then for the final rinse. Do not
insert the plug but rinse under running water.
use the separate hand washing area for hand cleansing
(Option 2). A double sink with adequate bench space either side for work to flow from dirty to
clean area. This sink is also the only area available for hand washing.
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obtain and label a large plastic container to act as the dirty sink and place this on the
dirtiest side (according to the workflow pattern) of the existing sink. Use this container to
wash the dirty instruments in.
use the sink directly adjacent to initially rinse the instruments and then for the final rinse.
Do not insert the plug.
use the second adjacent sink as a dedicated hand washing area.
OR
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use sink can also be used for washing hands. However, it must be cleaned after washing
the sink on the dirtiest side (according to the workflow pattern) to wash the dirty
instruments with the plug inserted. This is the dirty sink.
use the other sink to initially rinse the instruments and then for the final rinse. Do not
insert the plug but rinse under running water. This is the clean sink.
the clean instruments to render it suitable for hand washing.
(Option 3). A single sink available to use for cleaning items, Separate hand washing facilities are
available.

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
obtain and label a large plastic container to act as the dirty sink and place this on the
dirtiest side (according to the workflow pattern) of the existing sink .Use this container to
wash the dirty instruments in.
use the sink to initially rinse the instruments and then for the final rinse. Do not insert the
plug.
use the separate hand washing area for hand cleansing
(Option 4). A single sink is available to use for cleaning items and washing hands.



obtain and label a large plastic container to act as the dirty sink and place this on the
dirtiest side (according to the workflow pattern)of the existing sink .Use this container to
wash the dirty instruments in.
use the sink to initially rinse the instruments and then for the final rinse. Do not insert the
plug
the sink can also be used for washing hands. However, it must be cleaned after washing
instruments to render it suitable for hand washing.
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Environmental Issues
The area and equipment associated with instrument and equipment processing:
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is only cleaned or managed by appropriately trained Practice Staff.
must remain in a clean and tidy manner throughout the day.
is thoroughly cleaned at the end of the day.
Section 2.01
If a plastic utility container is used as the Dirty sink for washing the instruments this container
must be treated with due care. The container is not touched with ungloved hands and it is
thoroughly washed at the end of the day as part of the practice’s routine cleaning. This container
is not to be used for any purpose other than instrument pre-cleaning
RACGP 4th edition Standards 5.3.3.
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4.7 Cleaning reusable Instruments and equipment
Policy
A basic risk assessment is required to determine the appropriate level of processing required for
specific instruments. The site/manner where an instrument will be used can assist in determining
the risk of infection. This analysis determines the level of processing required to minimise the
probability of infection to the patient.
More information to assist with this risk assessment can be obtained from RACGP Infection
Control Standards for Office Based Practices, 4th Edition (page 51).
Staff whose duties require them to process equipment for reuse must have received adequate
training and competency assessment in this area.
More information about aspects that require training and competency can be obtained from
RACGP Infection Control Standards for Office Based Practices, 4th Edition (page 52).
Thorough physical cleaning of items to remove blood and other debris is needed if effective
disinfection or sterilisation is to be achieved. Preliminary cleaning must be done as soon as
possible during or after use to prevent coagulation of blood and other proteins.
Any delay will increase the bio-burden (through bacterial multiplication) and also increases the
difficulty of removing adherent soil. The effectiveness of sterilisation is dependent on the bioburden being as low as possible.
Procedure
All staff cleaning reusable items:




wear appropriate PPE.
use equipment as specified.
have received appropriate formal or in house training.
are appropriately immunised.
Our practice follows this procedure for all instruments and equipment that is going to be reused
for patient care. This includes items that need to be:
 clean but are not required to be sterile for re-use e.g. kidney dishes, ear syringes.
 sterilised after use, but not used as sterile e.g. vaginal speculums.
 sterile for re-use e.g. surgical instruments.
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Step 1
Wash hands with liquid soap and dry thoroughly with paper or single use
towel.
Step 2
Put on personal protective equipment including goggles, plastic apron and
heavy duty kitchen gloves.
Step 3
During or immediately after use open instruments and, dry- or damp-wipe off
gross soil. Rinse the item under gently running tepid water over the clean
sink.
Step 4
If unable to clean instruments immediately, open instruments and soak in a
container with a lid in tepid water and detergent until they can be cleaned.
Clean instruments as soon as possible as prolonged soaking damages
instruments. Use fresh water and detergent
Step 5
Prepare dirty sink/basin by filling with sufficient tepid water and the correct
amount of detergent to cover the items being washed.
Step 6
Thoroughly wash each instrument in the dirty sink/basin to remove all
organic matter. Open and disassemble items to be cleaned. Keeping items
under the waterline to minimise splashing and droplets, scrub items with a
clean, firm-bristled nylon brush. Use a thin brush to push through lumens,
holes or valves.
Step 7
Rinse the washed instruments in gently running hot water over the clean
sink/basin.
Step 8
Inspect instruments to ensure they are clean. Look at hinges, handles and
working surfaces.
Step 9
Place each washed instrument on a clean lint free cloth or surface and
repeat the above process until all instruments have been cleaned and rinsed.
Step 10
Carefully discard dirty water down the sink. If using a container, aim to pour
the dirty water directly into the plughole rinsing the sink afterwards with
running water.
Step 11
Wash cleaning brushes/cloths with detergent and tepid water after every use.
Hang to dry. Can consider sterilising these in the last load of the day.
Step 12
Wash the dirty and clean sink/basin by rinsing it with tepid water and
detergent. Wipe down the sink/basin with a disposable towel.
Step 13
Remove kitchen gloves and replace with non sterile disposable
gloves...Carefully dry each instrument with a clean, lint free cloth. Do not
allow to air dry.
Step 14
Remove and Clean personal protective equipment by washing or wiping
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down and drying.
Step 15
Wash hands with liquid soap and dry thoroughly with paper or single use
towel.
RACGP 4th edition Standards 5.3.3.
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4.8 Provision of sterile items
There are 3 options for the provision of sterile items.
1. Single use disposable items are purchased
2. Items are transported to an off site facility for sterilisation
3. Items are sterilised on site.
Please select the appropriate option (and delete the others) to personalise this section according
to how your practice provides sterile items.
Option 1. Select if “single use disposable” instruments are used. Delete options 2 & 3 and
proceed to “4.10 Storage of Sterile Equipment".
Policy
This practice is able to provide assurance that any items provided for procedures into normally
sterile tissue, sterile cavities or the bloodstream are sterile.
This practice understands that the process of sterility assurance includes all aspects of
equipment procurement storage and use, and staff education.
Procedure
This practice purchases single use sterile disposable instruments to use where appropriate.
It is the responsibility of all staff to ensure that disposable instruments are placed in the correct
waste bins (yellow topped contaminated waste bins) following use. This waste must be removed
from our practice in such manner to prevent patient-to-patient or patient-to-staff cross
contamination.
Appropriate PPE is worn when handling waste.
The batch number of all instruments used is recorded to enable tracking of the instruments if
necessary.
The Class 1 Chemical Indicator and packaging integrity is checked prior to opening an
instrument pack for use.
After using an instrument, replacement stock is ordered to maintain an adequate stock of
instruments for our requirements.
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Option 2. Select if an “off site facility is used to provide sterilisation services. Delete Options 1 &
3 and proceed to “4.10 Storage of Sterile Items" procedure.
Policy
This practice is able to provide assurance that any items provided for procedures into normally
sterile tissue, sterile cavities or the bloodstream are sterile.
This practice understands that sterilisation is more than simply putting loads through a steriliser
and the process of sterility assurance includes all aspects of equipment reprocessing, and staff
education.
Our practice has a supply of reusable instruments that are maintained in good working order and
are free of rust and surface damage. The correct procedures must be followed to ensure that
these instruments are cleaned and sterilised after each use. We do not have a Steriliser on our
premises therefore we have arranged for the instruments to be autoclaved offsite. Our practice
has contracted (*Insert name of the off site sterilisation providers) to provide this service.
The following documentation is maintained:
 a copy of the offsite facilities current accreditation certificate (e.g. accredited general
practice or ACHS accredited hospital).
 our procedures for safe transport of instruments and equipment to and from the offsite
facility.
 an agreement between our practice and off site sterilisation facility stating who is
responsible for, washing packaging items, transport, turnaround time, quoted prices and
names of contact people for both organisations.
 evidence that the offsite facility correctly performs the sterilisation and validates it
processes. e.g. validation documentation or certification provided annually.
 our practice has appropriate policies and procedures to ensure preliminary cleaning of
items, packaging and transportation arrangements including evidence of staff training and
competency.
Procedure
It is the responsibility of (*Insert staff member’s name) to co-ordinate the off site sterilisation
arrangements.




ensure that all instruments that require sterilisation are cleaned in accordance with the
steps outlined in the Cleaning of reusable items” procedure.
items are packaged and labelled prior to despatch to the facility in accordance with the
“Packaging of Instruments” procedure below.
place all instruments in a plastic container labelled “contaminated” with a firmly fitting lid. If
items are not cleaned prior, standard precautions must be adhered to when handling this
container and contents.
document all instruments leaving the practice.
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


telephone to inform the offsite sterilisation service provider that a cycle of instrument
sterilisation needs to be undertaken for our practice and to arrange a delivery and pick-up
time
use a different plastic container “labelled sterilised items” to collect the items from the
sterilisation facility
on return of the instruments following sterilisation, check the packages for damage
thoroughly before signing off.
Packaging of Items for offsite sterilisation.
Policy
Our practice ensures the packaging of items for sterilisation provides an effective barrier
against sources of potential contamination in order to maintain sterility and to permit aseptic
removal of the contents at point of use.
A copy of the procedure for packaging items is located with the packaging materials so all
staff can readily refer to these instructions. All staff follow this procedure when packaging
instruments.
The designated area for packaging items is (*Insert description in accordance with your work
flow e.g. the bench on the Left side of the instrument washing area)
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Procedure
Step 1
Visually check items have been cleaned and dried, and are in good working
condition and free of rust or surface damage
Step 2
If your workplace uses specific sets then group items according to your protocols.
Step 3
Insert the items into the package considering the following principles
Step 4

Ensure package is the appropriate size for required items.

Open and unlock items with hinges or ratchets.

Package in a manner that prevents damage to items or injury to end user and
facilitates steam movement across the surface of items.

Use tip protectors if necessary to prevent sharp instruments from perforating
the packaging.
Check each package has a class 1 indicator integrated on the packaging.
(Steriliser indicator tape or a separate class 1 indicator must be used if absent on
the packaging material.)
Step 5
Select Option 1 Remove peel-off strip from pouch, and fold precisely along the
marked line to seal the pouch
Or Option 2:
Cut packaging from roll and fold each end over twice. Apply sterilisation tape
(usually has a class 1 indicator stripe) to seal over the fold extending it around the
edge of the package.
Step 6
Use a felt-tip, non-toxic, solvent-based marker pen to label the pack with

Initials of the person packaging the item

Date of sterilisation & load number (this may be added prior to loading the
steriliser if not known).

Contents of the package (if opaque packaging).
Step 6
Inspect pack to ensure packaging material is intact.
Step 7
Store item/s in a container with lid, cupboard or drawer, clearly marked as
“unsterile items” until ready to load into the steriliser.
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Option 3. Select if the practice’s own steriliser is used to provide sterile items. Delete Option 1 &
2.
Policy
This practice is able to provide assurance that any items provided for procedures into normally
sterile tissue, sterile cavities or the bloodstream are sterile.
This practice understands that sterilisation is more than simply putting loads through a steriliser
and the process of sterility assurance includes all aspects of equipment reprocessing, and staff
education.
Our practice has a supply of reusable instruments that are maintained in good working order and
are free of rust and surface damage. The correct procedures must be followed to ensure that
these instruments are cleaned and sterilised after each use. Our practice uses steam at high
temperature under pressure for sterilising cleaned instruments. This is the most reliable and cost
effective method of sterilisation and is recommended for use in general practice.
Specific instructions on the packaging and use of the autoclave must be displayed next to the
machine. These instructions must include a comprehensive workflow schedule to ensure that
there is no possible contamination of the clean areas where the sterile instruments are unloaded
and stored.
All items to be sterilised must be thoroughly cleaned first. Our practice documents each cycle in
a sterilisation log.
Our portable steam steriliser has a closed door drying cycle that must be used when processing
wrapped articles so as to ensure that instrument packs are dry before unloading.
Our practice validates our sterilisation process annually at the servicing of the steriliser. Refer to
“Validation of the sterilisation process”.
(*Insert name of staff member) is responsible for correct operation and training staff on how to
process instruments.
All staff are aware of the processing time required and the maximum load limits as determined by
the validation process
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Holding times for steam sterilisation
All times are based on the assumption that the items to be sterilised are thoroughly clean.
Temperatur
e @ C
Pressure
Holding time for
steam
sterilisation (this
includes safety
factor)
KPa
psi
121C
103
15
15 minutes
126C
138
20
10 minutes
134C
(wrapped
items)
203
30
3 minutes
Penetration
time if
applicable (as
determined by
technician)
Total
Sterilisation
Time
The “holding time” does not include:
 the time taken for heating the load to the desired temperature
 any large volumes of material or heavily wrapped/packaged items included in a given
load, and
 time taken to allow the inside of the packs to achieve the desired temperature.
This is the “Penetration time” and must be added to the holding time.
STERILISATION TIME = PENETRATION TIME + HOLDING TIME.
Packaging of items for sterilisation
Policy
Our practice ensures the packaging of items for sterilisation provides an effective barrier against
sources of potential contamination in order to maintain sterility and to permit aseptic removal of
the contents at point of use.
A copy of the procedure for packaging items is located with the packaging materials so all staff
can readily refer to these instructions. All staff follow this procedure when packaging instruments.
The designated area for packaging items is (*Insert description in accordance with your work
flow e.g. the bench on the Left side of the steriliser).
Items that are being sterilised for disinfection but do not need to be kept sterile for reuse can be
processed unwrapped e.g. vaginal speculums
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Procedure
Step 1
Step 2
Step 3
Step 4
Step 5
Step 6
Step 6
Step 7
Visually check items have been cleaned and dried, and are in good working
condition and free of rust or surface damage
If your workplace uses specific sets then group items according to your protocols.
Insert the items into the package considering the following principles
 Ensure package is the appropriate size for required items
 open and unlock items with hinges or ratchets
 Package in a manner that prevents damage to items or injury to end user and
facilitates steam movement across the surface of items
 use tip protectors if necessary to prevent sharp instruments from perforating
the packaging
Check each package has a class 1 indicator integrated on the packaging.
(Steriliser indicator tape or a separate class 1 indicator must be used if absent on
the packaging material.)
Select
Option 1. Remove peel-off strip from pouch, and fold precisely along the marked
line to seal the pouch
Or Option 2.
Cut packaging from roll and fold each end over twice. Apply sterilisation tape
(usually has a class 1 indicator stripe) to seal over the fold extending it around the
edge of the package.
Use a felt-tip, non-toxic, solvent-based marker pen to label the pack with
 initials of the person packaging the item
 date of sterilisation & load number
 (this may be added prior to loading the steriliser if not known)
 contents of the package (if opaque packaging).
Inspect pack to ensure packaging material is intact.
Store item/s in a container with lid, cupboard or drawer, clearly marked as
“unsterile items” until ready to load into the steriliser.
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4. 8.1 Loading the steriliser
Policy
Correct loading of sterilisers is needed for successful sterilising to:

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

allow efficient air removal
permit total steam penetration of the load
allow proper drainage of condensation and to prevent wet loads
prevent damage to items in the load
maximise efficient utilisation of steriliser
when loading the steriliser, care needs to be taken that the steam can circulate effectively
and that all surfaces are accessible and exposed to steam.
never exceed the validated load (*insert location where details of the validated load can be
found e.g. on the wall near the steriliser)
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Procedure
Our practice follows this process when loading the steriliser:
Step 1
Load items into the steriliser following these points:
allow enough space between each item to allow air removal, steam
penetration and drying to occur
do not crush items together
do not allow items to touch the floor, top or walls of the
chamber
Follow the pattern of loading described in the practice validation protocol
when doing a full load.
Step 2
Fill the chamber with or ensure reservoir has sufficient
deionised/demineralised water as per the manufacturer’s instructions.
Step 3
If the steriliser allows you to select different loads check that the
appropriate load parameters are selected.
Step 4
Monitor the sterilisation process by one of the following:

automatic printout or computerised data logger download
(records at a minimum of 60 second intervals).

use of a class 4, 5 or 6 chemical indicator with every cycle.

Manually record time and temperature throughout the cycle at least
every 30 seconds.
Step 5
Close and secure chamber door as per manufacturer’s instructions.
Step 6
Press “Start” button or relevant button to commence the cycle as per
manufacturer’s instructions.
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4.8.2 Sterilisation cycle parameters
The steriliser settings used at our practice are based on the manufacturer recommendations and
Instructions for use, and the results of the validation of the sterilisation process.
All staff operating the steriliser are conversant with the sterilisation cycle parameters required to
yield sterile items at our practice and the settings/ operation of our steriliser required to achieve
this.
*Insert the parameter settings used at your practice (refer to the validation documentation) and
any instructions if these need to be manually set by the operator.
Parameter
Confirmed parameter setting for
routine wrapped load
134oC
Temperature
Total Processing Time:
(TPT=PT+H)
Pressure
Drying Cycle
activated
Article III.
Staff members are able to interpret printouts or loggers and other monitoring requirements to
ensure these required parameters have been met for every cycle.
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4.8.3 Unloading the steriliser
Policy
For packaged items, the period of time between their removal from a steriliser (any type) and
their return to room temperature is recognised as being the most critical time with respect to
assurance of sterility.
Cooling generates a tiny flow of room air into the pack at flow rates demonstrated to breach
porous packaging materials leading to their failure to provide a microbiological barrier.
Correct cooling practice is needed to maintain sterility. When a sterile item is not cooled in the
correct manner the article can have moisture build up, which can contaminate stock. The item
must be reprocessed if the packaging is torn, punctured or wet.
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Procedure
Our practice follows this process when unloading the steriliser:
Step 1
When cycle is complete, check printout, data logger, or Class 4, 5 or 6
chemical indicator to ensure the temperature has reached the parameters
of at least 3 minutes at 134c and stayed above 134c for the specified
period determined during penetration study.
Note a minimum of 3 minutes at 134c is required for unwrapped goods.
For wrapped, packed or pouched items, these measurements need to be
confirmed by a technician, known as penetration time and time at
temperature testing at validation.
Step 2
Circle and sign these parameters on the printout and attach to the
sterilisation log.
Step 3
Open the steriliser door to its maximum to allow contents to cool.
Step 4
Turn off electricity or as per manufacturer’s instructions.
Step 5
Wash hands with liquid soap and dry thoroughly with paper or single use
towel or put on clean, dry gloves. Use gloves specifically designed for
removing hot sterilising racks from the chamber to prevent staff receiving
burns.
Step 6
Visually examine packages to ensure that:

the load is dry

the packages are intact

The indicators have changed colour.
Any items that are dropped on the floor, torn, wet or have broken or
incomplete seals are contaminated and must be repackaged and
reprocessed.
Step 7
Take items from the sterilising chamber and place on a cooling rack on a
clean field until cool (or allow items to cool inside the chamber once
packages have been checked).
Step 8
Record details in the sterilisation log.
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4.8.4 Documentation of the Cycle.
Policy
A sterilisation log is maintained which contains details of:










date of cycle.
steriliser Identification (only if more than 1 steriliser in the practice).
load Number.
contents of the load.
identification of the person who prepared the load.
class 1 Chemical indicator change.
condition of the packs. (dry with seals and package integrity intact).
evidence of the process such as a print out or class 4,5 or 6 Chemical Indicator or if
a data download logger is used, sign off that it was viewed and is correct.
signature of the person releasing the load.
any comments or problems such as failed cycles and actions taken.
Procedure



the Loading section of the sterilisation log is completed and signed when the steriliser is
loaded.
the unloading section of the sterilisation log is completed and signed when the steriliser
is unloaded.
sterilisation log sheets are retained and filed according to the procedures for medical
records.
Failed cycle
In the event of a failed cycle:
 document failed cycle with a brief summary of the problem in the Steriliser General
Logbook.
 notify appropriate staff members.
 do not use items from the steriliser until the error is rectified.
 refer to the troubleshooting guide on the operating instructions.
 replace the packaging and re-process the instruments.
 if fault occurs again contact the service technician for advice and record any actions
in the Steriliser Maintenance Log Sheet.
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4.8.5 Maintenance of the steriliser
Policy
It is critical that the steriliser is maintained by practice staff and service personnel, in accordance
with the steriliser manufacturer’s instructions and that routine servicing by suitably qualified
person occurs at least annually.
The maintenance procedures must be clearly documented, performed and recorded on an
ongoing basis (daily, weekly and monthly) by practice staff and service technicians. The
operating instructions are located next to the steriliser. (*insert location).
Procedure
Changing the water
Deionised or distilled water is used and the water reservoir is checked prior to use and
drained and refilled weekly
Cleaning the steriliser
Scale build up and corrosion in the chamber is regularly cleaned using a phosphoric acid or
citric acid solution or paste. Outlet drains are visually checked to ensure they are free of
debris and seals are visually checked for signs of wear and tear.
4.8.6 Servicing the steriliser
A maintenance contract for servicing of the steriliser is established with (*insert name of
organisation) the steriliser is serviced at least 12 monthly or more frequently if required and
is next due (*insert month and year).
The servicing companies contact number is (*Insert number and contact person's name if
known).
Validation of the sterilisation process
Performed at least annually or more frequently if required. Usually this is following the service.
Validation is undertaken, according to the validation protocol.
Documentation
All maintenance and servicing is documented in the maintenance log. This includes maintenance
performed by staff such as changing the water, cleaning and checking the door seal and outlet
drain. Evidence of validation is documented and retained. The 3 validation cycles are recorded in
the sterilisation log.
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4.8.7 Monitoring the Sterilisation Process
Policy
Monitoring is a programmed series of checks and challenges, repeated periodically, and carried
out according to a documented protocol, which demonstrates that the process being studied is
both reliable and repeatable.
If the temperature or pressure of the steam inside the autoclave is above or below what it should
be, the steam will not be able to condense and sterilisation will be unreliable. The efficiency of
the sterilisation process should therefore be checked on a regular basis according to the
manufacturer’s specifications or those documented in the current edition of AS/NZS 4815.
Procedure
Our practice follows these methods of monitoring:
Test – Processed
Method
Class 1 chemical indicator
Frequency
A class 1 chemical indicator must be used for:
every wrapped item (external), or
every load, if unwrapped.
Test – Time, temperature and pressure
Method
Frequency
Time, temperature and pressure can be measured by using:
a steriliser with a print out facility, or
data logger/computer download, or
manually recording of temperature and pressure throughout the
cycle, or
Class 4, 5 or 6 chemical indicator (time and temperature only).
Every load
Test – Calibration
Method
By a qualified service technician
Frequency
6 – 12 monthly (or more frequently as per manufacturer’s
instructions)
Test – Validation
Method
See definition and process below
Frequency
12 monthly and as required
RACGP 4th edition Standards 5.3.3.
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4.8.8 Validation of the sterilisation processes
Policy
“Validation” is a documented procedure for obtaining, recording and interpreting results required
to establish that the sterilisation protocols/procedures followed by our practice will consistently
yield sterile instruments and equipment, as exactly the same procedure is followed for every part
of each sterilisation process.
“Sterilisation” is more than simply putting loads through a steriliser. Successful sterilisation to
achieve and maintain sterility of equipment and instruments reliably and repeatedly is a process
which begins with pre-cleaning of equipment after use, cleaning of the instruments, drying,
packaging, loading the chamber, the sterilisation cycle, unloading the chamber, monitoring of
each cycle, recording cycle details and monitoring in the log book, storage and traceability of the
sterilised equipment, detection of abnormalities in the process and corrective appropriate action,
and daily, weekly and annual steriliser maintenance.
Validation covers three activities, which are:
 installation qualification (‘commissioning’)
 operational qualification (‘commissioning’)
 performance qualification.
The validation process must be carried out by our practice on installation and annually in
conjunction with a maintenance contractor. A qualified service technician must ensure that all
gauges and process recording equipment fitted to the steriliser are calibrated using independent
test equipment. The contractor must also document results of heat distribution studies on an
empty chamber and conduct a penetration test using our practice’s challenge pack.
Validation of the sterilisation processes must be completed as soon as possible after the
routine annual calibration and service and immediately after any of the events listed below:



commissioning a new steriliser (a service technician should install the steriliser according
to manufacturer’s instructions and should then check the operation of the machine)
significant changes are made to the existing steriliser, such as major repairs or recalibration, which could adversely affect the result of the sterilisation process
changes to any part of the sterilisation process, such as changes to the contents, packing
or packaging of the “challenge pack” or to loading details of the “challenge load”.
If validation of the sterilisation process is successful then any load subsequently processed over
the next twelve months can be treated as sterile. This is provided that:


all the validated documented sterilisation procedures continue to be followed exactly
the pack contents, packing, and packaging and chamber loading do not exceed the
parameters of the validated packs/loading
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
each cycle is monitored correctly and no changes are made to any part of the sterilisation
process, which could adversely affect it.
Procedure
Our practice follows this procedure when conducting validation:
Step 1
Step 2
Step 3
Step 4
Step 5
Step 6
Review and perform your infection control policies and procedures including:
 workflow issues
 cleaning of instruments
 pack contents, packing and packaging
 loading of the steriliser
 sterilisation cycle
 unloading the steriliser
 storage of sterile items
 maintenance of the steriliser.
Check that the procedures were successful in terms of performance and
reliability and sign-off each one using the validation methodology checklist.
Attach the validation methodology checklist to the validation record.
Select the hardest to sterilise items (challenge pack) in terms of product or
pack density to create your challenge pack and record details on the
validation record.
At time of routine service, request the service person to:
 calibrate the machine
 conduct a heat distribution or “cold spots” study in an empty chamber
(usually performed only on installation, or available from the
manufacturer or otherwise determined by the sterilisation technician)
 obtain the penetration time using a thermocouple or data logger by
choosing the hardest to sterilise items in terms of product or pack density
to create your challenge pack
 undertake a time at temperature analysis to ensure the temperature is
maintained throughout the entire sterilisation phase.
 provide servicing/testing documentation detailing the outcome.
Where onsite technical support is not immediately available, please refer to
the current edition of the AS/NZS 4815.
Using the validation record template, record the following details:
 date of annual validation
 batch number and biological indicators
 cycle that is being used for validation
 temperature and time at which validation is being done
 attach your servicing/testing documentation to the validation record.
Select the items that you will include in the load and record details on the
validation record including the “challenge pack”.
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Step 7
Step 8
Step 9
Step 10
Step 11
Step 12
Step 13
Step 14
Label the biological indicators to reflect cycle as follows:
1st Cycle label one Indicator 1M (for the 1st Indicator placed in the 1st cycle
challenge pack in the middle of the pack) and the other 1C (for the non
packed Indicator placed on the tray nearest the coldest part of the
steriliser chamber)
nd
2 Cycle label one Indicator 2M (for the 2nd Indicator placed in the 2nd cycle
challenge pack in the middle of the pack) and the other 2C (for the non
packed Indicator placed on the tray nearest the coldest part of the
steriliser chamber)
3rd Cycle label one Indicator 3M (for the 3rd Indicator placed in the 3rd cycle
challenge pack in the middle of the pack) and the other 3C (for the non
packed Indicator placed on the tray nearest the coldest part of the
steriliser chamber)
the 7th Indicator can be labelled Z. This indicator is never sterilised and is
usually placed beside the steriliser whilst the three (3) consecutive
cycles are being run. This 7th indicator will prove that the batch of
indicators was active.
Place the biological indicators inside the challenge pack and in the coldest
spot of the chamber and outside of the steriliser. Record the location in the
test indicator diagram on your validation record.
Load the steriliser as documented above and draw or photograph details in
the loading diagram on your validation record.
Perform three consecutive, identical loads and cycles including the test
indicators as marked. With each load, unpack and repack the challenge
pack. All items for each load must be at room temperature.
Send the biological indicators for testing/incubation to the pathology
company or use an in-house incubator set at correct temperature for
incubation.
Document the findings and investigate any failures (a pass result is 100%).
Any load run subsequently and which does not exceed the parameters of the
validated load can be treated as a load not requiring biological test
indicators.
Attach this checklist to the validation record.
RACGP 4th edition Standards 5.3.3.
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4.9 Storage of sterile items
Policy
All sterile items, including those processed in the practice facility and those procured from
commercial supplies, shall be stored and handled in a manner that maintains the sterility of the
packs and prevents contamination from any source.
Factors that influence shelf life are event-related (not time-related) and are dependent on storage
and handling conditions.
Procedure
Instruments in our practice are stored:
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in a clean, dry and well ventilated area
in an area free from draughts
in an area where there is reduced chance of contamination from dust and water
with dust covers should items be stored for a long period of time
in a manner which allows stock rotation, e.g. place recently used items at the back and
take from the front
with the contents of the package clearly visible to reduce handling of instruments.
Instruments and items used for procedures in other locations such as aged care facilities and
home visits are transported to the facility in a separate rigid walled container with a lid labelled
sterile items. Care is taken to maintain the sterility of these while transporting to the facility.
Waste and sharps or disposable single use instruments are disposed of into the appropriate
waste stream according to the waste protocols.
Instruments and items requiring cleaning for reuse are wiped of gross soil at the time of use and
placed in a separate rigid walled container with a lid labelled “dirty items”. These are cleaned as
soon as possible in accordance with the cleaning of reusable items protocol. This dirty container
and items within are managed using standard precautions.
RACGP 4th edition Standards 5.3.3.
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4.10 Management of waste
Policy
Since the introduction of the RACGP Standards for General practices (3rd Edition) The National
Health and Medical Research Council (NHMRC) National Guidelines for Waste Management in
the Health Care Industry published in 1999 have been rescinded.
The RACGP Infection Control Standards for Office Based Practices outline policies and
procedures to assist our practice to safely manage waste. We are also aware of any relevant
local, State or Territory and/or Federal regulations that impact on our waste management.
Our waste policies include:
 use of Standard precautions when handling waste
 correct segregation of waste into three streams: “Clinical”, “Related” and “General”
waste.
 storage of waste
 disposal of waste
Effective and safe waste management is important for infection control and also to reduce the
impact on the environment and reduce costs.
All staff receives education regarding the management and handling of waste, appropriate to
their role, including the safe use and disposal of sharps.
These categories are defined as:
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clinical waste has the potential to cause sharps injury, infection or public offence and
includes: discarded sharps, human tissues (but excluding hair, teeth, urine and faeces)
and materials or solutions containing free flowing or expressible blood. It also includes
related waste such as cytotoxic waste, pharmaceutical waste, chemical waste and
radioactive waste
general Waste is any waste that does not fall into the clinical or related category. And
may include office waste, Kitchen waste, urine, faeces, teeth, hair, nails, sanitary
napkins, tampons, disposable nappies, used tongue depressors, disposable vaginal
specula, cervical cytology spatulas and plastic cytology brushes, nonhazardous
pharmaceutical waste (e.g. out of date saline). NB: General waste contaminated with
blood or body substances (though not to such an extent that it would be considered
clinical waste, i.e. not contaminated with ‘expressible blood’) must be stored in out of
reach or access to children.
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Procedure
All staff use appropriate personal protective equipment which always includes gloves as a
minimum when handling waste. Clinical waste is removed by trained staff. Waste, either general
or clinical is not compressed by hand.
Clinical waste includes sharps disposal containers and designated biohazard bins. These are
located in each area where clinical waste is generated. They are emptied at the end of each day
or when full.
Containers used for “non sharp” Clinical Waste in our practice:
 have a good sealing lid.
 hand free operation (e.g. wide open mouth, foot pedal or sensor operated)
 rigid walls
 should be lined with a plastic bag (preferably a yellow biohazard identified bag)
 have a biohazard sign affixed to the outside.
 are located away from the reach of children.
While awaiting collection non sharp clinical waste is double bagged using a biohazard identified
yellow bag and stored securely inside a locked yellow biohazard identified bin in an area that is
separate from clean stores and with restricted access.
Sharps are defined as anything that can penetrate the skin and some examples include: needles,
scalpels, stitch cutters, glass ampoules, sharp plastic items, punch biopsy equipment, lancets,
wire cytology brushes, razors, scissors and disposable surgical instruments.
Containers used for disposal of “sharp” clinical waste:
 comply with Australian standards
 are placed out of reach of children
 cannot be knocked over
 are located so that the neck is clearly visible to health professionals when disposing on
items
 have scalpel blade removers securely mounted to the walls
 are closed and replaced when the full indicator is reached.
While awaiting collection sharps containers are never reopened and are stored with the other
clinical waste for collection.
Related waste
 cytotoxic products are disposed of into the sharps containers.
 pharmaceutical waste is disposed of in accordance with the state/ regulations. Refer to
Drugs and Poisons Unit website for more information. Usually it is taken to the pharmacy
for appropriate disposal.
 chemical waste such as formalin need to be disposed of according to state/territory and
local government regulations and OH&S requirements.
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This practice has a service agreement, with (*insert name of company), who are contractors
specifically licensed to dispose clinical waste through special burial and high temperature
incineration. The bins are collected every (*Insert frequency of clinical waste collection). (*Insert
name or title, e.g. principle Doctor, nurse, practice manager) is delegated responsibility to ensure
adequate stock levels of clinical waste containers are maintained and collection schedules are
timely.
General Waste
General waste is segregated at the point of use into recyclable, non recyclable and shred only
waste at the point of use according to the local regulations and being mindful of privacy.
 waste contaminated with blood or body fluids, that are not considered clinical waste,
cannot be recycled and is placed into a bin lined with a bag which kept out of reach of
children. This is disposed of into the normal garbage collection.
 waste containing sensitive information is shredded in accordance with privacy
requirements.
 all other eligible recyclable waste is disposed of into the recycle bin.
Contaminated general waste and clinical waste is not accessible to children.
(Reference: RACGP, 4th edition Standards, p. 76)
RACGP 4th edition Standards 5.3.3.
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4.11
Sharps Management
Policy
Our practice makes every attempt to minimise the risk of injury to both staff and patients, and
prevent the possible transmission of disease by discarded sharps.
Sharps represent the major cause of accidents involving potential exposure to blood-borne
diseases. All sharp items contaminated with blood and body fluids are regarded as a source of
potential infection. Safe handling and disposal of sharps is essential to protect the operator and
staff from injury and possible transmission of disease. Sharps may be defined as any object or
device that could cause a penetrative injury.
Consideration is given to the purchase and use of devices that significantly reduce the risk of
sharps injury.
The staff member who generates or uses a sharp is responsible for the safe use and disposal of
that sharp. This responsibility cannot be delegated.
The employer is responsible to ensure all staff are familiar with the practice’s policy and
procedure for the safe handling and disposal of sharps and staff are also familiar with the actions
to take in the event of a sharps injury. (Refer to Section 3 Sharps injury Management and other
Body fluid Exposure)
Procedure
Sharps disposal containers are placed in all areas where sharps are generated. Where possible
they are located between hip and shoulder height. Sharps are placed into rigid-walled, punctureresistant yellow containers that meet the relevant Australian Standard. Containers are not in a
location accessible to children either when in use or when awaiting collection.
The following procedures are undertaken when disposing of sharps:
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the person using the sharp is legally responsible for its safe disposal.
sharps must be disposed of immediately or at the end of the procedure whichever is
most appropriate.
sharps must be placed in a yellow puncture-resistant container bearing the black
biohazard symbol (AS 4031).
used sharps must not be carried about unnecessarily.
injection trays must be used to transport the needle and syringe to and from the patient.
needles and syringes must be disposed of as one unit.
needles must not be recapped.
needles must not be bent or broken prior to disposal.
containers must not be overfilled as injuries can occur whilst trying to force the sharp into
an overfilled container – close container securely when at the fill line.
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the lid must be sealed once the container is full. For push-on lids, use both hands and
apply pressure only to the edges of the lid.
sharps disposal units must be conveniently placed in all areas where sharps are
generated and should be mounted on a wall or on a bench to prevent spillage.
sharps containers must not be placed on the floor or in areas where unauthorised access
or injury to children can occur.
sharps containers must not be placed directly over other waste or linen receptacles
assistance must be obtained when taking blood or giving injections to an uncooperative
patient or to a child.
For removal and disposal of the sharps container, refer to the instructions detailed under ‘Waste
Disposal’ above.
This practice assumes an active role in reducing the opportunities for sharps injury by purchasing
safe equipment whenever such an option is available without compromising the quality and
safety of patient care. Examples include:
 self retracting single use lancets for blood glucose testing
 self retracting canula insertion devices and needleless. IV administration systems.
 vacuum blood collection tubes
 scalpel blade removal devices
 plastic ampoules
Our induction process includes information about the safe disposal of sharps and actions to take
in the event of a sharps injury. (Refer to Section 3 Sharps injury Management and other Body
fluid Exposure)
RACGP 3rd edition Standards 5.3.4.
RACGP 4th edition Standards 5.3.3.
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4.12 Standard Precautions
Policy
Standard precautions apply to work practices that assume that all blood and body substances,
including respiratory droplet contamination, are potentially infectious.
The NHMRC recommends the use of personal protective equipment including heavy duty
protective gloves, gowns, plastic aprons, masks, eye protection or other protective barriers when
cleaning, performing procedures, dealing with spills or handling waste
Standard precautions are standard operating procedures that apply to the care and treatment of
all patients, regardless of their perceived or confirmed infectious status. Standard precautions
also apply to the handling of blood and other body fluids.
Standard precautions are work practices that are used consistently to achieve a basic level of
infection control in all health care settings and all situations.
Standard precautions are designed to protect both patients and staff, and comprise the following
measures:
 hand washing
 use of appropriate personal protective equipment (PPE) for example gloves, plastic
aprons and eyewear
 use of aseptic technique to reduce patient exposure to microorganisms
 safe management of sharps, blood and body fluid spills, linen and clinical waste
 appropriate immunisation of GPs, clinical and administrative staff
 routine environmental cleaning
 effective reprocessing of reusable equipment and instruments
 evironmental controls such as design and maintenance
Procedure
All staff involved in Patient care or who may have contact with blood or body fluids are required
to understand and use standard precautions when they are likely to be in contact with:
 blood
 other body fluids, secretions or excretions, except sweat (e.g. urine, faeces)
 non intact skin
 mucous membranes
RACGP 4th edition Standards 5.3.3.
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4.13
Transmission Based Precautions
Policy
Transmission based precautions are used for patients known or suspected to be infected with
highly transmissible pathogens. Transmission based precautions are measures used in addition
to standard precautions when extra barriers are required to prevent transmission of specific
infectious diseases.
Our staff are educated in how to triage and apply transmission based precautions for patients
known or suspected or with a potential communicable disease.
Transmission based precautions require:
 ‘isolation’ of the infectious source to prevent transmission of the infectious agent to
susceptible people in the health care setting
 a means for alerting people entering an isolation area of the need to wear particular
items to prevent disease transmission.
There are three Transmission based precautions categories based on routes of infection
transmission in a health care environment. These are:
 contact precautions
 droplet precautions
 airborne precautions.
Procedure
Transmission based precautions are used for patients known or suspected to be infected with
highly transmissible pathogens (e.g. influenza).
In general practice the main goal is minimising exposure to other patients and staff. This may be
achieved through:
 the use of PPE
 distancing techniques (one metre between patients in the waiting room, isolating the
patient in a separate room or their car)
 effective triage and appointment scheduling including putting these patients ahead of
others
 hand hygiene
 encouraging cough etiquette and respiratory hygiene
 surface cleaning
 avoid touching your nose & mouth
To help prevent the transmission of communicable diseases our patients are educated in
respiratory etiquette, hand hygiene, our practice precautionary techniques (e.g. phoning
reception first if they suspect they may have flu) and our distancing techniques by posters and
information leaflets in the waiting room and via our recorded “on hold” message.
RACGP 4th edition Standards 5.3.3.
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4.14 Personal Protective Equipment (PPE)
Policy
Our practice has available Personal Protective Equipment (PPE) which includes heavy duty
protective gloves, gowns, plastic aprons, masks (surgical & P2), eye protection; or other
protective barriers in all cases where there is potential for contact with blood or body fluids such
as when cleaning, performing procedures, dealing with spills or handling waste and when dealing
with infectious diseases.
Procedure
All staff and patients have easy access to appropriate PPE. In areas where PPE is used there
are posters providing education on the appropriate application, removal and disposal of PPE
PPE is also used when handling chemicals such as cleaning products or Liquid Nitrogen.
Our practice ensures and documents that all staff receive education, at induction and on an
ongoing basis, as to the appropriate use of various types of PPE, and where to access PPE.
PPE includes:
 gloves (sterile, non sterile and standard rubber type).
 face masks including standard surgical and P2 masks.
 face and eye shields.
 gowns (long and short sleeved).
 plastic aprons.
All staff understands and are competent in:
 determining the appropriate use and selecting the correct type of PPE for the
presenting situation.
 explaining the purpose of different PPE equipment.
 demonstrating the correct fitting and removal of PPE and the safe disposal of these
items.
PPE is located (*Insert the location of Personal Protective equipment) maintenance and
reordering of PPE is the responsibility of (*insert staff member name).
Type of personal protective equipment and its appropriate use
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PPE
Appropriate use
Disposable
gloves
Disposable gloves should be used:
Sterile gloves
Heavy duty
gloves
Surgical Masks
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when handling blood and body substances or when contact with
such is likely
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when handling equipment or surfaces contaminated with such
substances
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during contact with non-intact skin
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during venipuncture – although needlestick injury may still occur,
the presence of the glove layer could reduce the volume of any
inoculum.
Sterile gloves should be used:
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during any surgical procedure involving penetration of the skin or
mucous membrane and/or other tissue
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when venipuncture is performed for the purpose of collecting
blood for culture.
Heavy duty gloves should be used:
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during general cleaning and disinfection
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during instrument processing
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during cleaning blood or body fluid and other substance spills.
Surgical Masks can be used:
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during procedures or activities that might result in splashing and
the generation of droplets of blood, body substances or bone
fragments
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When there is a risk of droplet transmission of disease.

To protect unimmunised staff and patients

Worn by the patient to prevent the spread of disease (suspected
or known)
P2 or N95 Masks
(Particulate filter
masks)
Worn by staff when there is a risk of airborne transmission of disease
(suspected or known) Tuberculosis and pandemic influenza.
Protective
eyewear
Protective eyewear should be used to prevent splashing or spraying of
blood and body fluids into the wearers eyes such as during surgical
procedures, venipuncture, or cleaning of spills, contaminated areas or
instruments.
Worn by staff when there is a risk of airborne/droplet transmission of
disease (suspected or known).
Gowns and
plastic aprons
Gowns and plastic aprons should be used when there is a risk of
contamination of wearer’s clothing or skin with blood and body
substances such as during surgical procedures, venipuncture, or
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cleaning of spills, contaminated areas or instrument processing.
Worn by staff when there is a risk of airborne/droplet transmission of
disease (suspected or known).
Sterile gowns
Sterile gowns should be used during procedures that require a sterile
field.
All staff use appropriate PPE when undertaking any of the following procedures:
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any examinations requiring contact with mucous membranes.
cleaning or dressing wounds, taking down bandages.
cleaning up after procedures.
preparing instruments and equipment for sterilisation.
assisting with or performing procedures.
cleaning of contaminated surfaces.
cleaning spills of blood & body fluids.
using chemicals.
taking blood.
handling all pathology specimens before they are bagged.
controlling bleeding.
RACGP 4th edition Standards 5.3.3.
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4.15 Laundry
Policy
All staff members at our practice have received education regarding the management of soiled
linen, including when to change linen, the use of appropriate precautions during handling, the
washing, drying and storage of linen.
Procedure
Linen needs to be changed if:
 a patient requires the use of contact precautions, (e.g. known or suspected of having
CAMRSA, scabies or lice)
 blood or body fluid has been spilt on the linen
 it is visibly soiled.
 before an operative procedure.
When changing linen:
 staff use PPE and standard precautions as required
 care is taken to ensure sharps are not caught up in the linen
Clean linen is located in a clean, dry dust free location away from dirty linen and items. (*insert
location)
Option 1: (select if you purchase all disposable linen for your practice)
This practice uses only disposable linen on all examination couches and patient treatment areas.
Linen is changed regularly and, provided it does not contain expressible blood or body fluid, it is
disposed of into the normal domestic rubbish.
Any linen that is contaminated with expressible blood or body fluid is disposed of immediately
into the clinical infectious waste bin.
(Please delete the rest of this procedure)
Option 2: Select you wash launder and reuse your linen (delete Option 1)
Used linen is stored in a covered, lined container which is located away from clean items in the
(*insert location) before laundering.
Any linen that is contaminated with blood or body fluids is collected in a plastic bag before being
(*insert option), (A) placed in the used linen receptacle and rinsed in cold water with oxygenated
stain removal at the earliest opportunity or (B) disposed of according to the management of
waste procedure.
All linen is transported in a leak proof container and a separate clean, container or basket is
used to return laundered linen to the practice.
Linen is washed in a washing machine on a hot or cold cycle using activated oxygen based
laundry detergent and dried in the dryer.
OR
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The laundering is contracted out to a commercial laundry service. A copy of our agreement
is available.
RACGP 4th edition Standards 5.3.3.
4.16 Safe handling of pathology specimens
Procedure
The following process is followed when handling pathology specimens:
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label and name containers before use to avoid the need for extensive handling after the
specimen has been collected.
after collection of blood and body substances these should be placed in the appropriate
specimen container, as specified by the testing laboratory.
wipe the container clean to remove any visible soiling and check specimen is correctly
identified.
securely seal to prevent any leakage during transport.
place the container upright in a waterproof bag or container.
take care to avoid contamination of pathology slips by keeping them separate from the
clinical specimens.
for transport between institutions and interstate, pack the primary specimen, surrounded
by sufficient material to absorb its contents, in a sealable inner container and provide a
sealable outer container of waterproof, robust material. Label in accord with postal and
other transport regulations. Keep cool if necessary.
RACGP 4th edition Standards 5.3.3.
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5
Practice Management
5.1 Access & Parking
Policy
The General Practitioners and staff
 recognise that access to the General Practice facilities is important to our patients.
 make all reasonable efforts to facilitate physical access to the premises and services
offered.
 are committed to considering how best to meet the needs of our patients that have
with physical disabilities or other special needs.
Where possible wheelchair access, suitable parking and pictorial signage is provided to
assist patients with a physical or intellectual disability.
Where physical access is limited to the practice and its facilities or where physically
attending the practice could result in an adverse outcome for the patient the practice
provides off site or home visits. (Refer to Section 5 Home Visits).
Car parking facilities are available within a reasonable distance from the practice for staff,
visitors and patients and where possible there are designated spots for disabled drivers.
External and internal lighting is sufficient to facilitate safe access for staff, visitors and
patients at night.
Sufficient signs are provided externally and internally to assist Staff, visitors and patients in
accessing the practice facilities.
Procedure
Designated staff parking is provided. Please ensure other areas are kept clear for patients.
This practice provides physical access to patients, visitors and staff via the main entrance.
(*insert additional).
Ambulance trolley access is also provided to the practice reception, toilets and
consulting/treatment rooms via (*insert location).
Our practice has a height adjustable examination couch located in (*insert location) to assist
in the care of patients with a disability, and to reduce the risk of patients injuring themselves
when getting on or off the examination couch or staff when assisting patients.
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Doorways and walkways are to be kept free of clutter, boxes etc. to ensure a clear pathway
for all persons and in an emergency
Prominent signs at the front of the site:
 allow the public to easily locate the Practice and the parking facilities from the street.
 display the Practice name, address, hours open, telephone numbers (work & after
hours).
If external lights are not operating please notify the Practice Manager immediately.
Option 1 (Please select correct option)
Access for patients with disabilities.
 wheelchair access is provided to reception, toilets and consulting rooms.
 the practice has installed ramps and railings as required to assist patients with
disabilities
 designated disabled parking is provided in close proximity to the entrance
Option 2
As our practice has limited access to all facilities and services, home or other visits are
available for patients with disabilities or that may be otherwise unable to access a practice
service or facility.
RACGP 4th edition Standards 5.1.3, 5.1.1.
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5.2 Appointments
Policy
Our patient scheduling system is flexible enough to accommodate patients with urgent,
non-urgent, complex and planned chronic care, and preventative needs.
The individual preference, of our General Practitioners or other health care providers such
as our nurses, is accommodated and members of the clinical team are consulted about the
length and scheduling of appointments.
Patients can request to see their preferred doctor or member of the health team.
The length of clinical consultations will vary according to individual patients needs. Our aim
is to provide enough time for adequate communication between patients and their doctors to
facilitate preventative care, effective record keeping and patient satisfaction. Patients are
encouraged to ask for a longer appointment if they think it is necessary.
Our practice endeavours to accommodate patients with urgent medical matters even when
fully booked.
Staff members are trained to have the skills and knowledge to assist patients in determining
the most appropriate length and timing of consultations and to recognise and act accordingly
for patients with urgent medical matters.
Where possible information is provided in advance about the cost of healthcare and the
potential for out of pocket expenses.
We endeavour to respect patients cultural background and where possible meet their needs
including providing privacy for patients and others in distress.
Procedure
Each doctor or other health care providers such as nurses and allied health has specific
times allocated to his/her consulting sessions with documented needs for interval times,
short & long consultations, diagnostic tests, procedures etc.
Generally not more than 6 appointments are made for any 1 hour period and normally there
will not be any appointments scheduled for less than 10 minutes.
Each doctor has a designated time allocated for home visits to see patients that are unable
to attend the Practice.
One appointment is required for each family member requesting to be seen.
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If a third party is to be present during an examination, whether requested by the doctor or
accompanying the patient, consent from the patient will be obtained prior to the consultation.
Patients are able to request their preferred doctor when making an appointment, and staff
will endeavour to ensure that patients generally see the same doctor. If patients are unable
to obtain an appointment with the doctor of their choice they are advised of the availability of
other doctors at this time. A patient can expect to see their doctor, or an alternative as
approved, within 2 working days.
Our Practice Information Brochure outlines the types of consultations that may require a
longer consultation and the costs. Patients can readily request a longer time when making
an appointment.
Our staff have the skills and knowledge to assist in determining the most appropriate length
and timing of appointments. Should a longer consultation be requested or determined by
information received from the patient, then our staff will endeavour to allocate the
appropriate time for a longer consultation.
Patients generally wait less than 30 minutes and patients are advised of any delays when a
doctor is running late. Wherever possible scheduled patients are called at home to advise
delay.
As a priority staff members are vigilant of the need to detect and place urgent callers or walk
in patients for immediate or earlier attention by a doctor. Patients are routinely asked if the
matter is urgent before being put on hold. Our practice accommodates urgent patients even
if we are fully booked. Should the matter be urgent please refer to Section 5 – “Medical
Emergencies & Urgent Queries”
Cancellations and ‘no-shows’ are monitored and marked accordingly in the Appointments
Book/Diary and these patients are followed up as appropriate. Attempts to contact patients
that fail to attend appointments are documented in the patient file.
Appointments made for patients required to attend a recall or periodic medical review
appointments are flagged and it is imperative the no shows are contacted and another
appointment re-scheduled.
Procedure (making an appointment)
Obtain patient’s name and correctly identify the patient using 3 approved identifiers
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determine the urgency of the appointment and if the patient requests an urgent
appointment refer.
determine the length of the appointment required. Does the patient have complex
medical or communication needs or multiple health matters they want to discuss?
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advise of any potential for additional or out of pocket costs associated with longer,
urgent or missed consultations.
patient new? Inform of Practice location, parking, costs & payment methods. Obtain
contact phone number, address and other demographics. Ask to bring list of current
medications and child health record (blue book) if applicable.
is doctor requested available at time requested? Give nearest available time; is this
to be a long consult?
if doctor not available, ask if another doctor would be suitable or another time slot or
date?
give suggested time and alternatives if needed.
write patient surname, given name in agreed timeslot for chosen doctor.
reconfirm patient name, time and doctor.
Note: appointments made for a periodic review (e.g. blood pressure check) or medical recall
(e.g. abnormal pathology result) are denoted as such so follow up procedures can be
instigated if the patient does not attend.
Cancellations & Missed appointments
Option 1 – Manual appointment book
Patients that miss appointments are phoned to remind them, if the patient cannot attend the
same day, cross through patients name, write your initials and record the patient as a
cancellation or no show.
Option 2 – Computerised appointment book
Patients that miss appointments are phoned to remind them. If the patient cannot attend the
same day use computer program instructions to delete appointments to track cancellations
for medico legal purposes.
Patients that fail to attend a recall or periodic medical review appointment
For significant appointments a follow up letter is sent if the patient could not be contacted by
the phone call. If the appointment is flagged as ‘recall’ it is imperative every attempt is made
to contact these patients and such attempts are documented in the medical record and also
in the recall book if applicable.
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persist in telephoning the patient over a few days at different times and, should the
patient not respond then send a letter asking that the patient ring the Practice. If no
response from the patient to the first letter, then send it again using registered mail.
Patients in distress
We respectfully manage patients and others in distress by providing privacy. (*Insert your
procedure for managing patients and others in distress).
RACGP 4th edition Standards 1.1.1, 1.2.4, 3.1.4, 1.4.2, 2.1.1.
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5.3 Home Visits
Policy
Doctors and other practice staff make visits to regular patients of our practice where it is safe and
reasonable. These visits may be to patients in their homes, residential aged care facility,
residential care facility, or hospital both within and outside normal opening hours where such
visits are deemed safe, and where the patients are acutely ill, immobile and elderly or have no
means of transport to the practice.
All patients are made aware that home visits or a suitable care alternative, are available both
within and outside normal opening hours.
Regular patients who meet the eligibility criteria are offered home visits.
For regular patients whose circumstances are deemed not safe and reasonable, e.g. the patient
is located too far away for a home or other visit, the practice ensures that there is an alternate
system of care that these patients can access.
There are arrangements to exchange clinical details about patient care for doctors who perform
home and other visits on behalf of the patient’s regular doctor and the care provided is
documented in the patient’s medical records.
Home and other visits are provided by appropriately qualified health professionals who have
received information and advice about safety and security when conducting home visits.
Any anticipated costs associated with home visits or alternative care systems are discussed with
the patient.
Procedure
A patient can arrange for a home visit or the doctor may request home visits if the criteria below
are met.
 regular patients of this practice
 live within a (*Insert km radius of the practice).
 where it is safe and reasonable
 has provided a phone number that you have called them back on
 patient has the type of problem that necessitates a home visit such as:
 acutely ill
 immobile
 elderly
 have no means of transport
 unable to access the practice facilities due to disability
 (*Insert your practice requirements here)
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refer to triage protocols and list of urgent conditions when determining if a caller needs a
visit urgently. When in doubt (to make a home visit booking) ask to put caller on hold
and refer to patient’s doctor for advice. Refer to Section 5 – “Medical Emergencies &
Urgent Queries
Our doctors home visit schedules, are recorded in the appointment record at reception.
Appointments for home visits can be made by either the patient or doctor. A doctor may ask
reception staff to note daily, weekly, fortnightly visits. Any requests for home visits outside these
scheduled times are referred to the doctor.
If another doctor or agent is conducting the visit ensure make arrangements to ensure they are
able to obtain and access to the patient health record for the timely exchange of clinical
information.
All visits provided within or outside normal opening hours are documented in the patient’s
medical records. If information is held about the patient in different records (electronic & paper
based or at a residential aged care facility) there must be a record made for every consultation in
each system indicating where the clinical notes for the consultation are recorded to ensure
patient health information is available when required.
All staff undertaking home visits are given information and advice about protecting their safety.
There may be occasions where it is unsafe or unreasonable to provide a patient requesting care
at home with a home visit. There may also be regular patients who can no longer attend the
practice due to disability. This may apply after hours or within opening hours. Our practice
advises the following options (*insert the alternate system of care that these patients can access
in your area.e.g. name, telephone number and location of the nearest emergency department of
the local hospital and ambulance) This advice is documented in the patient records, along with
evidence of the subsequent care provided.
RACGP 4th edition Standards 1.1.3.
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5.4 Telephone
Policy
An incoming telephone call is the principle method for initial and subsequent communication
by a patient and most other persons to this Practice. As such the telephone is recognised
as a vital vehicle for creating a positive first impression, displaying a caring, confident
attitude and acting as a reassuring resource for our patients and all others.
Our aim is to facilitate optimal communication opportunities with our patients. General
Practitioners and staff members are aware of alternative modes of communication used by
patients with a disability or a language barrier.
Some patients may be anxious, in pain or distracted by their own or a family member’s or
friends medical condition and our staff act to provide a professional and empathetic service
whilst attempting to obtain adequate information from the patient or caller.
Staff should not argue with, interrupt or patronise callers. Courtesy should be shown to all
callers and allow them to be heard. Every call should be considered important.
Staff members are mindful of confidentiality and respect the patient’s right to privacy. Patient
names are not openly stated over the telephone within earshot of other patients or visitors.
This Practice prides itself on the high calibre of customer service we provide, especially in
the area of patient security, confidentiality, and right to privacy, dignity and respect.
It is important for patients telephoning our practice to have the urgency of their needs
determined promptly. Staff should try to obtain adequate information from the patient to
assess whether the call is an emergency before placing the call on hold. Staff members
have been trained initially, and on an ongoing basis, to recognise urgent medical matters
and the procedures for obtaining urgent medical attention. Reception staff members have
been informed of when to put telephone calls through to the nursing and medical staff for
clarification.
Patients of our practice are able to access a doctor by telephone (*insert other if applicable
e.g. electronic) to discuss their clinical care. When telephone (or electronic) communication
is received, it is important to determine the urgency and nature of the information. Staff
members are aware of each doctor’s policy on accepting or returning calls. In non urgent
situations patient calls need not interrupt consultations with other patients but it is necessary
to ensure the information is given to the person in a timely manner.
Patient messages taken for subsequent follow-up by a doctor or other staff member are
documented for their attention and action, or in their absence to the designated person who
is responsible for that absent team members workload. Staff inserts the details of all calls
and telephone conversations assessed to be significant in a telephone call log.
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The doctor needs to determine if advice can be given on the phone or if a face to face
consultation is necessary, being mindful of clinical safety and patient confidentiality. Patients
are advised if a fee will be incurred for phone advice. Non medical Staff does not give
treatment or advice over the telephone. Results of tests are not given out, unless cleared
with the Doctor.
Staff do not give out details of patients who have consultations here nor any other identifying
or accounts information, except as deemed necessary by government legislation or for
health insurance funds.
Staff should be familiar with each doctor's policy of returning or accepting calls. Our doctors
preferences are available (*Insert location e.g. reception desk).
Personal calls should be kept brief, mindful of engaging telephone lines.
A comprehensive phone answering message is maintained and activated to advise patients
of how to access medical care outside normal opening hours. This includes advising
patients to call 000 if it is an emergency.
Staff are aware of alternative modes of communication that may be used by patients with a
disability or special needs.
Important or clinically significant communications with or about patients are noted in the
patients health record. We have provisions for Doctors to be contacted after hours for life
threatening or urgent matters or results.
All electronic communication or telephone messages are returned confirming receipt of the
message and if possible any actions taken to convey or respond to the message.
Incoming Call
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pick up receiver within 3 rings and state, (*Insert Practice Name), this is (*say your
name), How can I help you?
if caller has not identified themselves – ask their name.
if call is for an appointment then refer to Section 5. “Appointments” procedure
if the call is assessed as an emergency or urgent query staff should refer to the
steps outlined in Section 5- “Medical Emergencies and urgent queries”
if the caller is inquiring about pathology or imaging results do not disclose any
results and refer to the Section 7 “Review and Management of Pathology Results”
if the caller requests to speak with a specific Doctor refer to the Doctors policy on
receiving and returning phone calls. (*insert the practice policy for doctors receiving
and returning phone calls and also outline this in the practice information sheet or
on individual doctors business cards)
if taking a message or when assessing what the caller wants, do not hurry the caller,
nor speak with an urgent, loud voice. If necessary repeat your questions or
message clearly.
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(*Insert your practice policy for ensuring that telephone and electronic messages
from patients and others are given to the person for whom they are intended on the
day of receipt or in that persons absence, to the person who is caring for that absent
team members patients. e.g. place a note on the patient’s medical record, or in
doctor’s in tray or send an email or after hours numbers for Doctors).
never attempt to diagnose or recommend treatment over the phone.
when relaying a message from the doctor, stress his/her involvement in that patient's
care, even though he/she isn’t speaking directly to the patient.
encourage the caller to write down any instructions and advice given.
have the caller repeat any instructions given back to you to assess their
understanding of what you have said.
ensure you obtain the callers consent prior to placing them on hold in case the call is
an emergency.
Documentation of telephone calls
A log book or computer entry is used to record all significant and important telephone
conversations or electronic communications including after hours contacts and medical
emergencies and urgent queries. All the information can later be written into the patient's
chart if required.
The log records:
 the name and contact phone number of the patient/caller.
 the date and time of the call.
 the urgent or non urgent nature of the call.
 important facts concerning the patient’s condition.
 the advice or information received from the doctor.
 details of any follow up appointments.
Call on Hold
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it is important to try to obtain adequate information from the patient to assess
whether the call is an emergency before placing the call on hold.
if another incoming call registers and no other staff members are available to take it,
ask to put caller on hold or seek to terminate the call and ring caller back after first
taking their number.
do not leave the caller on hold for long periods. Return to reassure caller that we
haven’t forgotten them and thank them for waiting.
whilst on hold ensure music or Practice information tapes are working and can be
clearly heard.
where possible our practice “on hold” message provides advice to call 000 in case of
an emergency.
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Alternative modes of communication
Alternative modes of communication may be used, including;
 electronic (email or SMS)
 national Relay Service (NRS) for hearing impaired
 translation and Interpreter Service (TIS) for non English speaking background
Ensure their use is conducted with appropriate regard for the privacy and confidentiality of
health information and that patients are made aware of any risks these modes may pose to
the privacy and confidentiality of their health information or any additional out of pocket
costs e.g. the requirement for a longer appointment.
After Hours
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at the end of the day/session if a weekend, turn on the answer machine to take calls
and switch telephone service to night service.
telephone messages on the machine are to be updated as needed for changes to
consultation hours and locum service numbers.
test the message to ensure it is clear and easily understood.
RACGP 4th edition Standards 1.1.1, 1.1.2, 1.1.4, 1.2.3.
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5.4.1 Communication with patients via electronic means
Policy
Staff are mindful that even if patients have provided electronic contact details they may not
be proficient in communicating via electronic means and patient choice should be obtained
before using electronic communication.
Patients are able to obtain advice or information related to their care or appointment
reminders by electronic means, where the doctor determines that a face-to-face consultation
is unnecessary. Electronic communication includes: email, fax, and SMS.
Practice staff and doctors determine how they communicate electronically with patients,
both receiving and sending messages. All significant electronic contact with patients is
recorded in the patient health records.
Patients are informed of any costs incurred prior to electronic consultations.
Practice staff and doctors should be aware of alternative modes of communication used by
the disabled.
Patients are advised in the Practice Information sheet that they can request our written
policy on receiving and returning electronic communication.
Communication with patients via electronic means (e.g. email and Fax) is conducted with
appropriate regard to the privacy Laws relating to health information and confidentiality of
the patients health information. (Refer section 6)
Staff and Patients using email/SMS or other forms of electronic messaging should be aware that
it is not possible to guarantee that electronic communications will be private. All personal health
information or sensitive information sent by email must be securely encrypted. (Refer to section
6).
When an email message is sent or received in the course of a person's duties, that message is a
business communication and therefore constitutes an official record.
Internal or external parties, including patients may send electronic messages. Messages from
patients or those of clinical significance require a response to confirm receipt and should be
documented in the patient medial record if appropriate.
Employees should be aware that electronic communications could, depending on the technology,
be forwarded, intercepted, printed and stored by others. Electronic mail is the equivalent of a
post card.
Staff members have full accountability for emails sent in their name or held in their mailbox, and
are expected to utilise this communication tool in an acceptable manner.
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This includes (but is not limited to):
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limiting the exchange of personal emails
refraining from responding to unsolicited or unwanted emails
deleting hoaxes or chain emails
email attachments from unknown senders should not be opened
virus checking all email attachments
maintaining appropriate language within e-communications
ensuring any personal opinions are clearly indicated as such
confidential information (e.g. patient information) must be encrypted.
The Practice reserves the right to check individual email as a precaution to fraud, viruses,
workplace harassment or breaches of confidence by employees. Inappropriate use of the Email
facility will be fully investigated and may be grounds for dismissal.
The practice uses an email disclaimer notice on outgoing emails that are affiliated with the
practice. (*Insert message here).
Accessing the Internet
The Internet is a vast computer network, comprised of individual networks and computers all
around the world that communicate with each other to allow information sharing between users.
It is important to adopt secure practices when accessing and using the Internet.
The Internet can be accessed by all members of staff; however, excessive use of the Internet is
not acceptable.
Staff members are encouraged to use the Internet for research activities pertaining to their role,
however, should be aware that usage statistics are recorded and submitted to Management as
required.
Staff members have full accountability for Internet sites accessed on their workstations, and are
expected to utilise this tool in an acceptable manner.
This includes (but is not limited to):
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limiting personal use of the Internet
accessing ONLY reputable sites and subject matter
verifying any information taken off the Internet for business purposes prior to use
not downloading any unnecessary or suspect information
being aware of any potential security risks - i.e. access / viruses
not disclosing any confidential information via the Internet without prior permission from
the practice manager - i.e. Credit Card number
maintaining the Practices confidentiality and business ethics in any dealings across the
Internet
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observing copyright restrictions relating to material accessed/downloaded.
The Practice reserves the right to check individuals Internet history as a precaution to fraud,
viruses, workplace harassment or breaches of confidence by employees. Inappropriate use of
the Internet facility will be fully investigated and may be grounds for dismissal.
The Practice Website
In complying with the Privacy Amendment (Private Sector) Act 2000, our practice provides the
following advice to users of our website about the collection, use and disclosure of personal
information.
The aim of this advice is to inform users of this site about:
What personal information is being collected
Who is collecting personal information
How personal information is being used
Access to personal information collected on this site
Security of personal information collected on this site.
The practice privacy policy is posted on the website and available for download.
The website is continually monitored to ensure it is kept current and up to date. It contains the
minimum information required on the practice information sheet. Refer Section 5 Practice
information sheet. Any changes to the practice information sheet are also reflected on the
website.
If it contains any advertising the practice should include a disclaimer that the practice does
not endorse any advertised services or products. Advertising must comply with the MBA
Code of Conduct on advertising available at: http://goodmedicalpractice.org.au/.
RACGP 4th edition Standards 1.1.2 & 1.2.1.
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5.5 Visitors
Policy
Patients and other visitors are welcome to the Practice. Doctors and staff value the
principles of good relations whether it is in person, via written or electronic form, or on the
telephone. Persons including all types of visitors e.g. patients, relatives, friends, health care
providers, students, pharmaceutical and other business service representatives, food
service suppliers and tradesmen are shown friendly, courteous recognition and assistance.
Procedure
When a person presents at reception or lingers in the main entrance or other areas of the
Practice and remain unidentified, ask if you may help and elicit the reason for their presence
on the site.
Ask the person to wait in the waiting room.
If the visitor looks suspicious, call a Doctor or other staff member to assist.
If the person is booked to see a Doctor or staff member, check with them and their
appointment diary to ensure the visitor can be seen at that time.
If the visitor is an unsolicited representative with no appointment pre arranged, then check
the policy for each Doctor/staff member and request the visitor to come back at another pre
booked time.
Visitors who will require moving throughout the building are to sign the Visitors Book and
enter times of arrival and departure. A visitors badge is supplied whilst on the premises.
The Practice Manager is to be advised when these visitors are in the Practice.
RACGP 3rd edition Standards 4.1.2.
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5.6 Medical Emergencies & Urgent Queries
Policy
This Practice classifies patients seeking medical consultations, according to priority of need.
Our triage system ensures that clinical care is provided to patients with urgent medical
problems as a priority.
Patients telephoning the practice have the urgency of their needs determined promptly.
Where possible our phone messages include a recommendation to call 000 if the matter is
an emergency. Staff members know and use the triage process, a copy of which is
accessible at reception.
Administrative staff and members of the clinical team have the skills and knowledge to
assess the urgency of the need for care and can describe our procedures for dealing with
urgent medical matters including when the practice is fully booked.
Our induction process includes an orientation to our triage system and staff members are
given training to its effective use and are encouraged to regularly update CPR and other first
aid skills.
Our practice has a pandemic plan which outlines our response to and management of
patients with possible infectious diseases such as influenza.
The doctors and staff provide appropriate care and privacy for patients and others in
distress.
We have provisions for Doctors to be contacted after hours for life threatening or urgent
matters or results.
Procedure
Staff members receive regular training and update’s in CPR which is appropriate for their
duties at least every 3 years.
All Staff members receive information at induction and on an ongoing basis about our
triage guidelines and protocols for medical emergencies and possible communicable
diseases e.g. Pandemic Influenza.
Documentation of training is retained in the individual staff training record.
In accordance with these guidelines reception staff try to obtain adequate information from
the patient to assess the nature and urgency of their problem.
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This occurs:
 when making an appointment (for phone calls or walk ins)
 before placing the call on hold
 while observing the patient in the waiting room
Patients are informed that they will be asked about the nature of urgent problems to assist
with prioritising the scheduling of their appointment. Should the matter be urgent patients
are advised of any potential for out of pocket costs e.g. use of equipment or longer
consultation.
A log book or computer entry is used to record all significant telephone conversations or
actions including medical emergencies and urgent queries.
The log records:
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the name and contact phone number of the patient/caller
the date and time of the call
the urgent or non urgent nature of the call
important facts concerning the patient’s condition
the advice or information received from the doctor
details of any follow up appointments
RACGP 4th edition Standards 1.1.1, 1.2.4, 1.1.4.
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5.7 After Hours Service
Policy
This practice ensures reasonable arrangements for medical care, including the follow up of
seriously abnormal and life threatening pathology results for our patients are in place
outside our normal opening hours.
The arrangements for medical care outside normal opening hours, how to access this care
and the possibility of out of pocket costs, is communicated clearly to patients of this practice.
Feedback about the quality and timeliness of after hours care provided to our patients by a
deputising service is obtained. Patient satisfaction with our after hours service is regularly
evaluated and improvements implemented if necessary.
When the practice doctors are unable to deliver care outside normal opening hours, timely,
safe and reliable care is provided that is in line with after hours care provided by other
practices in our local area. The practice coverage is provided by Doctors of a similar
speciality and if a Locum service is used, it is well known to the practice and an accredited
service.
The practice has a formal written arrangement with this provider of after hour’s care that
outlines how it receives information about any care provided to their patients, and how the
GP providing the care can contact the practice for clarification or help regarding background
information relating to that patient, especially in an emergency.
Our patient health records contain reports or notes pertaining to consultations occurring
outside the normal opening hours for care provided on behalf or by our practice.
Our practice has provisions enabling designated providers of after hours care or pathology
providers to contact a patients Doctor, or in that persons absence, the person who is caring
for that absent team members patients.
Procedure
Our normal opening hours are (*insert your opening hours here).
Advice to our patients on how to access after hours care, including the potential for out of
pocket expenses is available:
 on the telephone (*insert appropriate option; answering machine, call diversion
system or paging system) message
 in the practice information brochure
 on a sign visible from outside the practice
 practice website
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Outside of normal hours the practice has a comprehensive message on the answering
machine, call diversion or paging system via our main telephone number. This message
includes recommending patients call 000 if the matter is an emergency. This is maintained
for all incoming calls when this Practice is closed.
The Patient feedback tool contains questions concerning adequate information being given
to patients about after hour’s services. The results of patient feedback are evaluated and
improvements implemented if indicated.
When the practice Doctors cannot deliver care outside normal opening hours formal written
arrangements exist with: (*select option/s)
 an accredited medical deputising service
 arrangements through a cooperative of one or more local practices
 an appropriately accredited local hospital or after hours facility.
Sometimes our doctors may need to be contacted outside normal working hours by the after
hours care provider or the pathology service about a serious or life threatening matter or
pathology result. These organisations include: (* insert list applicable for your practice). We
have provided the above organisations with a list of the after hours contact numbers of our
doctors, and in the event they cannot be contacted an alternative person to contact in their
absence. We have clearly explained that these numbers are for “exceptional circumstances”
and are not the “on call” contact for the practice should they need to use them. This list is
reviewed and updated on a regular basis to ensure the numbers and contacts remain
current. A date of last update is inserted in the footer to designate the most recent version.
Any correspondence or notification received about after hours care provided to a patient is
documented in their medical record.
Details of our written policy for after hour’s care arrangements are attached to ensure the
information is easily accessible to staff if required.
(*Insert a summary of how you provide after hours service and include any copies of
after hours agreements with external providers or detail your specific arrangements.)
Include the following:
 adequate information to ensure the provider is familiar with the practices
requirements especially in regard to receiving urgent and life threatening results for
a patient or managing an emergency or complex problem
 a defined means of access for the after hours service provider to the patient’s
medical records and in “exceptional circumstances” to the patients GP (or
designated GP in their absence).
 reference to the timely reporting of the care provided or handover of the patient back
to the patients nominated practice
 evidence that the care will be provided by appropriately qualified health
professionals
 evidence of the accreditation status of the after hours service provider.
RACGP 4th edition Standards 1.1.1& 1.1.4 & 1.2.4 & 1.5.2.
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5.8 Practice Meetings
Policy
Regular discussions where all staff are encouraged to have input are important in building a high
performing team. We aim to cultivate a just, open and supportive culture where individual
accountability and integrity is preserved, but there is a whole-of- team approach to the quality of
patient care.
Practice meetings are conducted on a regular basis or more frequently as required to
facilitate the exchange of practice news, other general administration and protocol issues,
complaints and to discuss risk management issues arising out of the practice. Matters
pertaining to clinical care may be discussed at these meeting if appropriate, or at the
practices clinical meetings.
Urgent daily notices and other general items for immediate attention are written in the
communication book which is kept at reception. All staff should read and initial for each work
session.
Procedure
Staff meetings
It is important that all members of the practice team have the opportunity to discuss
administrative issues with the practice directors and/or owners when necessary therefore staff
are supported and encouraged to attend staff meetings.
Staff meetings are held every two to three months and minutes are recorded. Items for the
agenda may be submitted to the Practice Manager up to one week prior to the scheduled
meeting. All staff are expected to attend unless on annual or sick leave.
Administrative and Occupational Health and Safety practices are regularly reviewed at these
meetings. Staff members are given the opportunity to discuss administrative matters with
the doctor(s), Practice Manager when necessary.
Discussion and suggestions for improvement to quality, patient safety or policies and
procedures associated with risk management is a standing item on our practice meeting
agenda.
Practice discussions about near misses or slips or lapses, with the intention of identifying
what went wrong and how to reduce the likelihood of it happening again are also included in
practice and clinical meetings where appropriate.
The decisions made at staff meetings should be documented along with the person responsible
for implementing the related action.
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Clinical Meetings
Good communication between members of the clinical team is important for ensuring a
consistent approach to clinical care. Doctors and clinical staff, such as nurses and in house
allied health meet face to face at least quarterly, to discuss clinical matters. In between
meetings a communication book and emails are used to consider and communicate clinical
issues.
The Practice Principal, Practice Nurse or Doctor responsible for leading the clinical improvement
chairs the meetings. Guest speakers are invited from time to time to speak on latest
developments or products. Practice protocols, near misses or latest literature may be discussed.
The meetings are recorded on the practice meeting schedule to ensure staff can arrange to
attend.
A clinical component is included to ensure consistency by doctors, practice nurses, allied
health workers and all clinical staff within the practice, in the diagnosis and management of
our patients. There is also a standing discussion item about clinical issues, support systems,
new guidelines and evidence. This includes a review of patient information brochures used
for preventative activities and to support management or treatment choices to ensure they
are an appropriate quality and all members of the team are giving consistent information.
Clinical issues, updates, case studies and reports of Continuous Quality Improvement (CQI)
activities, complaints and incident reviews are presented, discussed and action taken as required
helping improve processes and patient outcomes.
Drug representatives may from time to time arrange a lunch or breakfast meeting, providing a
specialist to speak on a particular topic. Practice Manager is required to authorise availability of
times for these meetings
RACGP 4th edition Standards 1.4.1, 3.1.2, 4.1.1.
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5.9 Patient Rights
Policy
The practice staff members respect the rights and needs of all patients.
No patient is refused access clinical assessment or medical treatment on the basis of
gender, race, disability, Aboriginality, age, religion, ethnicity, beliefs, sexual preference or
medical condition. Provisions are implemented to ensure patients with a disability can
access our services.
The practice identifies important/significant cultural groups within our practice including non
English speaking background patients, religious groups and those of Aboriginal and Torres
Strait Islander background. We endeavour to continue to develop any strategies required to
meet their needs.
The practice provides respectful care at all times and is mindful of patient's personal dignity.
We have a plan in place to respectfully manage patients in distress
Visual and auditory privacy for patients is provided in the waiting room and during the
consultation. The waiting room provides soft music or TV to assist patient auditory privacy.
Each doctor’s consulting room and the treatment room has a curtain around the examination
couch for patient privacy and the door is closed for each consultation.
Patient privacy and confidentiality is assured for consultations and in medical and accounts
records, appointments, telephone calls and electronic media including computer information.
Doctors and staff do not leave patient information in any format in areas of the Practice or
surrounds for unauthorised access by the public. Staff members sign a privacy agreement
upon acceptance of employment and risk immediate dismissal should a breach of this
agreement occur. Information no longer required that contains any reference to patients,
including diagnosis reports, specialist’s letters, accounts etc. is securely disposed of via
shredding.
Patients have a right to access their personal health information and may request to view
their record or obtain a copy.
Our privacy policy for the management of health information is displayed in the waiting room
and also on the practice information sheet. It should be made available to anyone who
asks. This policy includes information about the type of information this practice collects,
how we collect it, use and protect it and to whom we disclose it.
Patients have the right to refuse any treatment, advice or procedure. Our doctors discuss all
aspects of treatment and will offer alternatives should a patient seek another medical
opinion. (Refer section 7 - Clinical Management of a patient refusing advice and informed
consent).
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For ongoing management of patients, should they leave the area, our doctors will ask for the
forwarding doctor’s or Practice address.
A copy of the patient’s medical record or the health summary (if the record is bulky) will be
sent directly to the new location via secure priority post.
This Practice acknowledges a patient’s right to complain. We provide mechanisms to
ensure that this feedback in addition to positive comments and suggestions are freely
received and implemented where possible.
Patients are provided with sufficient information about the purpose, importance, benefits,
risks and possible costs associated with proposed investigations, referrals or treatments to
enable patients to make informed decisions about their health.
Patients are provided with adequate information about our practice to facilitate access to
care including our arrangements for care outside the normal opening hours .
This Practice participates in the RACGP Training Program and regularly has registrars on
site. Patients are advised of this with a notice in the waiting room. If undergraduate students
are on practice placement here and observe doctors’ consultations, then the patient is asked
for his/her consent. Each patient is given a written note describing our involvement in this
medical training program with details of the process we follow.
The patients consent is sought for participation in health reminder systems and research
projects. Consent can be withdrawn at any time by the patient.
RACGP 4th edition Standards 1.2.1 & 1.2.2 & 2.1.1.
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5.10 Complaints
Policy
Opportunities are available for patients and other visitors to tell us, ‘How we are doing” and we
collect systematic patient experience feedback at least every 3 years.
The practice information brochure provides patients with information on how to provide
feedback, including how to make a complaint.
We have a complaints resolution process which all staff can describe, and we also make the
contact details for the state or territory health complaints agencies readily available to
patients if we are unable to resolve their concerns ourselves.
Patients have a ‘right to complain’ and where possible patients and others are encouraged
to raise any concerns directly with the practice team who are trained to make sure patients
of the practice feel confident that any feedback or complaints made at the practice will be
handled appropriately.
We believe most complaints can be responded to and resolved at the time the patient or
other people such as carers (relative, friend other consumer) makes them known to us.
Under the Health Services (Conciliation & Review) Act 1987 people with complaints should
try to resolve them directly with the health service provider. If a satisfactory outcome is not
achieved then the complaint can go directly to the Health Services Commissioner for action.
The public may also call the Office of the Health Services Commissioner at any time
concerning a query or to report a complaint.
Under national and state privacy laws: Commonwealth Privacy Act - Privacy Amendment
(Private Sector) Act 2000 and Victorian Health Records Act 2001, this practice must provide
and adhere to a complaints process for privacy issues and those related to the National
Privacy Principles (NPPs)/Health Privacy Principles (HPPs).
All staff should be prepared to address complaints as they arise. Depending on the nature
of the complaint and advice received from medical indemnity company, complaints are
recorded and actioned, with a copy placed in the patient’s medical record if related to patient
care.
All clinical staff and the practice manger are aware of their professional and legal obligations
regarding the mandatory reporting of unprofessional conduct.
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Procedure
Patients and others have opportunities to register their complaints either verbally to staff, in
writing (letter) or via our suggestion box. Patients should feel free to complain anonymously
if desired.
All staff should be prepared to address complaints as they arise.
When receiving complaints staff should keep in mind the following in order to minimise
further patient anxiety and hostility, possible leading to litigation:
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handle all complaints seriously, no matter how trivial they may seem.
verbal complaints made in person should be addressed in a private area of the
practice where possible.
use tactful language when responding to complaints.
don’t blame other staff. Patients may not have all the facts or may distort them.
address the patient’s expectations regarding how they want the matter resolved.
assure the patient that their complaint will be investigated and the matter not
overlooked.
offer the patients the opportunity to complete a formal complaint form. (They may
accept or decline).
document or Log all complaints and other relevant information and place this in the
complaint folder so the designated complaints staff member is informed of the
complaint. (even if you believe the matter has been resolved).
alert the doctor or relevant clinical staff about disgruntled or hostile patients so
he/she can diffuse the situation immediately.
always inform the designated complaints officer if you become aware of any
significant statements made by the patient or significant change in patient attitude.
Often patients will tell staff when they are reluctant to tell the doctor.
The practice has identified a staff member to be the team leader responsible for feedback
collection and analysis and handling complaints. (*insert the person’s name here). This
person coordinates the investigation and resolution of complaints.
 acknowledge the patients right to complain
 use the Acknowledgment of Complaint letter provided and respond to complaints in
writing within 2 working days
 telephone the patient to let him/her know that you are working on the problem
 respond to all complaints promptly in an open and constructive manner including an
explanation and if appropriate an apology.
 work with the patient to resolve the complaint and communicate the outcome with
the patient including any changes made as a result of the complaint.
 if the complaint is of a medical nature always refer it to a doctor. Refer procedure
section 8 -”Management of potential medical defence claims”.
 where a complaint is made against a staff member provide them with an opportunity
to discuss the details in a private setting.
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as a routine contact the practices insurer when there is a complaint about a member
of the clinical team in order to seek advice on resolving the complaint before any
action is taken.
ensure the complaint does not adversely affect the patents care.
record the complaint, investigation, and actions, with a copy placed in the patient’s
medical record if related to patient care and the details also retained in the
complaints file.
ensure where appropriate complaints are reviewed at staff meetings. Analyse
trends and discuss the methods of resolution. Other types of patient feedback - i.e.
surveys, suggestion box are also reviewed at staff meetings
a record of improvement made in response to patient feedback or complaints is
maintained as evidence of quality assurance activity.
where appropriate inform the patient/s about practice improvements made as a
result of their input.
If the matter cannot be resolved advise the patient about how to contact the Health
Complaints commissioner.
The National Privacy Commissioner is able to receive complaints concerning privacy issues.
Complaints here will have a response within 28 days.
National Privacy Commissioner
Privacy hotline 1300 363 992.
GPO Box 5218
Sydney NSW 2001
http://www.privacy.gov.au/complaints
Members of the public may make a notification to Australian Health practitioner regulation
agency (AHPRA) http://www.ahpra.gov.au/ (AHPRA) about the conduct, health or
performance of a practitioner or the health of a student. Practitioners, employers and education
providers are all mandated by law to report notifiable conduct relating to a registered practitioner
or student to AHPRA.
RACGP 4th edition Standards 2.1.2.
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5.11 Non English Speaking Patients
Policy
Our Doctors and staff have a professional obligation to ensure they understand our patients
and that the patients understand any verbal instructions or written information.
Patients who do not speak or read English or who are more proficient in another language,
or who have special communication needs are offered the choice of using the assistance of
a language service to communicate with the Doctor or clinical team members.
We are also aware that alternative modes of communication may be used by our patients
with a disability and we endeavour to inform ourselves of how to access and use these
services or technology to achieve effective communication with these patients.
A contact list of translator and interpreter services and services for patients with a disability
is maintained, updated regularly and readily available to all staff. For example the National
Relay Service (NRS) for patients that are deaf or the translation and Interpreter service
(TIS) Doctors Priority Line (1300 131 450) for patients from a not English speaking
background.
Procedure
Once you have determined that the patient may have special communication needs ask the
patient consent to use assistance.
Check the patient’s medical record to see what if any services have been used before.
The patient may consider that a family member or friend could interpret at the consultation.
A member of the patient’s family may not be a suitable translator especially for sensitive
clinical situations or where serious decisions have to be made. The use of children as
interpreters is not encouraged. An appropriate staff member can act as interpreter if the
patient consents. Some of our staff members are bilingual, but not all are accredited
interpreters and should not be used as such. Qualified medical interpreters are our
preferred option and their use should be encouraged especially for sensitive clinical
situations.
Note this on the medical records the patient’s nominated interpreter or any professional
services that have been used and arrange these prior to the consultation.
A list of translator and interpreter services and other communication services used by this
practice is available (*Insert how to access this list).
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Each doctor is registered with the interpreter service and allocated a code number.
Registrations are renewed annually to ensure quick access when an interpreter is required.
Other clinical staff should access the service via the treating doctor.
If TIS National is the chosen option book an interpreter by ringing the Doctor Priority Line
Tel: 1300 131 450 (free service) or booking on line or by fax. This 24 hour service is
available via telephone at the time of consultation, or if appropriate advance notice is given
(usually 48 hours), the interpreter can be on site at the practice during a consultation
(subject to availability) or at the patients home. If an interpreter is attending the practice or
home it is important to ensure the appointment starts on time.
RACGP 4th edition Standards 2.1.1 & 2.1.2 & 1.2.3.
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5.11.1 Culturally Appropriate Care
Policy
We aim to identify important and significant cultural groups within our practice and have
implemented strategies to meet their needs.
We also aim to accommodate the specific needs of patients who experience disadvantage
and increased disease risk whether due to socioeconomic factors, educational or literacy
issues, cultural background, or disability. (Refer section 5 Patient Rights).
In order to improve health outcomes we:
 encourage our patients to self-identify their Aboriginal or Torres Strait Islander origin or
cultural background to practice staff.
 encourage our practice staff to ask the Aboriginal or Torres Strait Islander or other
cultural background of our patients.
We are sensitive and aware that there may be many reasons why patients are reluctant to
identify their Aboriginal or Torres Strait Islander or other cultural background and equally there
are reasons why practice staff are reluctant to ask about the cultural background of our patients.
When patients are distressed we provide appropriate care and privacy which also respects
their cultural practices. (Refer section 5 Appointments).
We know how to communicate with patients who do not speak the primary language of our
staff or who have communication impairment, and our practice has a list of contact details
for interpreter and other communication services including the Translating and Interpreter
Services (Refer Section 5 Non English Speaking Patients).
The entry of information about the Aboriginal or Torres Strait Islander or other cultural
background of patients into health records is undertaken in a standardised manner that enables
the extraction of data.
Procedure
Our practice is working towards identifying and recording the cultural background of our
new and existing patients. Cultural background and ethnicity e.g. Aboriginal and Torres
Strait Islander background, can be an important indication of clinical risk factors and can
assist GPs and clinical staff in providing disease prevention and delivering culturally
appropriate care.
We have identified the main cultural groups in our practice and endeavour to provide
culturally appropriate written health information.
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We collect information about the country of birth and languages spoken. We have a system
to regularly update our patient information using a standard ‘update your details form’ to
help collect additional cultural information from our patients. (*Insert or describe where a
copy of your form/s to obtain patient information are located-Refer to Section 7 Clinical
Content of the medical records).
The standard indigenous status question asked is ‘Are you of Aboriginal or Torres Strait
Islander origin?’ This question should be asked of all patients, irrespective of appearance,
country of birth or whether the staff know of the client or their family background. Our
practice collects this information as part of our ‘new patient’ questionnaire. (Refer to Section
7 Clinical content of the medical records).
Where our software has the option to input Aboriginal and/or Torres Strait Islander status or
cultural background/s we use the drop down options rather than free text to assist with extracting
the information for accreditation purposes or preventative activities. (*Insert any protocols or
rules you have developed around the documentation Aboriginal and/or Torres Strait Islander
status or cultural background/s in patients medical records.)
To encourage Aboriginal or Torres Strait Islander origin patients to self identify we have (*insert
any measures you have taken e.g. Self identification posters in the waiting room, Displaying the
Aboriginal and Torres Strait Islander flags on brochures, or having the Koori Mail in your waiting
room http://www.koorimail.com).
RACGP 4th edition Standards 1.4.1, 1.7.1, 2.1.1.
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5.12 Directory of Local Health and Community Services
Policy
Our practice engages with a range of health, community and disability services to plan and
facilitate optimal patient care to patients whose health needs require integration with other
services.
A readily accessible written or computerised directory of health and community services,
utilised by patients within our area, including how to refer or contact these agencies, is
maintained and updated regularly.
Clinical staff are encouraged to co ordinate patient care across the general practice setting
with other health services and to build good working relationships with these providers to
facilitate collaborative care
Procedure
This directory is located (*Insert how to access your directory of services).
The contact numbers in this list are checked and updated annually or more often if required
by the practice manager. The practice manager is notified of new providers to include on the
list. All new staff are made aware of how to access this list.
The directory of local health and community services lists:
 local medical/diagnostic services.
 local hospitals and specialist consulting services.
 primary healthcare nurses.
 pharmacists.
 disability and community services.
 health Promotion and public health services and programs.
 relevant Government departments in the Region.
 local allied health services.
 community, social or self help groups in the area.
 culturally appropriate services for non English speaking background and Aboriginal
and Torres Strait Islander patients.
A brief explanation about any fees applicable, contact numbers or names and procedures
for interacting with these services is included on this list.
Referral information may differ for public and private providers. See Section “Referral
Protocols”. Practice staff and doctors need to ensure requirements outlined in the Chronic
Disease initiatives are met if these item numbers are to be claimed.
RACGP 4th Edition Standards 1.6.1.
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5.13 Provision of Brochures, Leaflets and Pamphlets for
Patients
Policy
There is a range of posters, leaflets or brochures available or on display in the waiting room,
reception and or consulting rooms. Where appropriate these are available in more than one
language or in formats to assist patients with physical or intellectual disabilities. (Refer to
Section 5 Non English speaking Patients)
Leaflets, brochures and pamphlets can vary considerably in quality. The brochures used by
this practice are carefully selected and screened to ensure they are culturally appropriate
and contain current, evidence based information.
The quality and accuracy of any Audio visual resources or internet sites recommended to
patients or used to provide printed information to patients is also considered.
The brochures, posters, leaflets and pamphlets available include information about health
promotion, and illness prevention, specific diseases and medical procedures and privacy
and rights.
The doctors and clinical staff use written information during a consultation to:
 support diagnosis and management of conditions.
 for health promotion and illness prevention
Brochures and educational materials are also available for patients to self select.
Procedure
We are selective about the leaflets and brochures we provide both in the waiting room for
patients to self select and for clinical staff to use to support information provided during a
consultation. To ensure they contain current and evidence based information, items are
obtained from reputable sources. Where possible items should be dated, contain the name
of the source and referenced to supportive evidence.
At least annually we try to conduct an audit of our brochures, leaflets and patient information
sheets to ascertain if they are current and if better options are available.
Brochures and leaflets are displayed in the waiting room in brochure holders and are
checked monthly (more frequent if new or altered information becomes available) that
stocks are sufficient and up to date.
New brochures (e.g. seasonal, flu injections etc) are to be incorporated into collection.
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Information that is no longer current or damaged brochures is promptly discarded.
Low stocks to be reordered and note made in order book. Also check for brochures in other
languages if required.
The provision of specific written material to support advice given in consultations is
encouraged to help patients remember the key messages from the consultation and address
individual patients’ needs. (Refer to Section 7 Clinical references and resources.)
Verbal and written information is provided to patients about
 health promotion and specific disease prevention.
 to support a diagnosis and choice of treatment
RACGP 4th Edition Standards 1.2.3 & 1.3.1.
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5.13.1
Practice Information Sheet
Policy
The Practice Information Sheet provides our patients with information about our practice
facilities and how to access care. It is also a useful way to inform patients of current practice
information or changes to our services. We endeavour to ensure all patients, new and
existing, are provided with the most up to date version to ensure the information they have
is accurate.
If a patient is unable to read or understand our practice information sheet an alternative
method is used to supply this information. These may include:
 verbally.
 larger font versions.
 through the National Relay Service or AUSLAN for patients who are deaf.
 through the translation and Interpreter service (TIS) for patients who speak
languages other than English.
 getting our sheets translated into languages commonly used at our practice. (Refer
to section 5 Non English speaking patients).
Telephone messages, the on hold recording and our website is also used, where possible,
to reinforce some of the information about our practice and our services
Procedure
The practice information sheet is kept at reception; it is available to all patients and handed
to each new patient on their first visit.
Staff ensure essential information contained in the sheet is made available to all patients
whether new to our practice or existing patients.
Where patients are unable to read or understand our written sheet we use other means to
communicate the essential information. (Refer to Section 5 Non English speaking patients.)
To maintain the accuracy of our information sheet it is reviewed regularly and updated as
required. When this sheet is updated the date is inserted in the footer to denote the latest
version. Reception staff are advised there has been a change and are encouraged to bring
this new version to the attention of our patients
The Practice information sheet is must contain at a minimum:
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practice address and phone numbers
consulting hours and arrangements for care outside our normal opening hours,
including a contact telephone number.
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our practice’s billing principles such as bulk billing, accounts settlement,
opproximate cost for treatment, potential out of pocket expenses.
our practice’s communication policy including receiving and returning phone calls
and electronic communication (e.g. SMS & email).
our practices policies for the management of patient health information including that
patients can obtain a copy of their health information and where additional posters or
the full privacy policy can be obtained from the practice.
the process for the follow up of results e.g. who will contact whom and by when.
how to provide feedback or make a complaint to the practice (include the contact for
the local state health complaints conciliation body and the name of the person
responsible for feedback and complaints).
Other information it could contain includes:
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names and qualifications or special interests of doctors, nurses, allied health and
other practice team members (subject to their consent).
clinical and other services available.
that they can request a summary of the policy on home, hospital, and nursing home
visits.
inform patients that longer consultations are available on request.
encourage ways in which patients can give feedback (e.g. tell patients if you have a
suggestion box).
how patients are able to request their preferred doctor.
inform patients about your reminder systems and the option of opting out of
receiving reminders.
information about how patients can assist by telling the practice if their personal
information changes e.g. changed address or provide any court documentation to
advise any child custody arrangements.
where the practice has a website it should contain at a minimum, the information
required in the practice information sheet. The website information should be
accurate and updated regularly.
Information provided either on the practice information sheet, website or in general interest
health articles and posters may contain advertising. If this is the case the practice should
include a disclaimer that the practice does not endorse any advertised services or products.
Advertising must comply with the MBA Code of Conduct on advertising available at:
http://goodmedicalpractice.org.au/.
RACGP 4th edition Standards 1.2.1 & 1.2.3 & 1.2.4.
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5.14 Office Supplies
Policy
Supplies of stationery, other office and Practice stores including prescription pads,
letterhead, certificates etc. are accessible only to authorised persons.
The Practice Manager, or delegate, checks and maintains stock ensuring perishable
materials are rotated so oldest is used first.
Procedure
Stock is checked monthly and items are re-ordered when supplies are low. Incoming goods
are checked against orders and invoices.
When a staff member takes a supply of stationery e.g. pen, sticky notes etc. They are to
tick off the item as having been removed from the cupboard. See supply list on inside of
cupboard.
When extra supplies or new items are needed, direct the request to the Practice Manager or
delegate.
RACGP 3rd edition Standards 5.1.1.
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5.15 Environmental Cleaning Service
1) Policy
All areas of our practice environment are visibly clean.
Regular cleaning of work areas is necessary because dust, soil and microbes on surfaces can
transmit infection. Cleaning of our practice clinical and non clinical areas must be regular and
scrupulous.
We have a cleaning policy that sets out a schedule and responsibilities for cleaning all areas of
the practice in accordance with the requirements outlines in Chapters 2–5 of the RACGP
Infection control standards for office based practices (4th edition).
We have appointed one member of staff with primary responsibility for the development and
consistent implementation of our infection control systems and procedures which includes
environmental cleaning. (Refer Section 4 Principles of Infection control)
Specific areas of responsibility may be delegated to nominated members of the practice
team and these particular responsibilities should be documented in the relevant position
descriptions. The practice team member with delegated responsibility for environmental
cleaning can describe the process for the routine cleaning of all areas of the practice and
can provide documentation on the practice’s cleaning policy.
A good neutral detergent can be used for most of the cleaning requirements in a health care
setting, and this includes floors, walls, toilets and other surfaces. The use of disinfectants is
discouraged because they are expensive, often toxic and require contact times to be effective.
All work surfaces are made of smooth, non-porous material without cracks or crevices to allow
for efficient cleaning. Any gross soiling or body substance spills must be cleaned as soon as
possible.
Sinks and wash basins must be either sealed to the wall or sufficiently far from the wall to allow
cleaning of all surfaces.
Damp dusting and wet mopping is used in the cleaning of the environment. Dry dusting and
sweeping will disperse dust and bacteria into the air and then resettle. It is potentially hazardous
and inefficient, and must be avoided in patient treatment or food preparation areas.
All cleaning equipment is stored in a clean and dry condition, and in an area not accessible to the
public.
Our practice has a cleaning schedule with procedures for cleaning clinical and non-clinical areas
of our practice.
All cleaning staff must receive training in occupational health and safety issues appropriate to
general practice and the immunisation status of all cleaning staff is documented.
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All staff involved in cleaning receives ongoing education in our infection control policies
including Hand Hygiene and the correct use of Personal Protective Equipment (PPE) and
Waste management.
Procedure
(*Insert name) has the delegated responsibility for the development and consistent
implementation of our environmental cleaning processes. This includes education of staff
and following up any issues with the quality of environmental cleaning.
Our cleaning schedule below describes the frequency of cleaning, products to use and
person responsible for cleaning specific clinical and non clinical areas of the practice. Where
appropriate we have documented evidence of cleaning activity.
Additional and specific cleaning may be required in areas where patients known or
suspected to be infected with highly transmissible agents (e.g. influenza) have been.
Option 1: (Select if your practice is cleaned by staff and contract cleaners then delete all
other options)
Practice staff and contract cleaners are responsible for cleaning the premises as specified in
the attached cleaning guide.
Practice staff undertake daily cleaning and the contract cleaners provide general cleaning in
all areas of the Practice on a (*insert frequency) basis.
An annual contract with (*Insert contract cleaners name) is negotiated and reviewed every
June.
Option 2. (Select if all cleaning is performed by practice staff. Then delete all other
options)
Practice staff members are responsible for cleaning the premises as specified in the
attached cleaning guide.
Option 3 (select if cleaning is only performed by a contracted cleaning service. Then
delete all other options)
An external cleaning service (*Insert contract cleaners name) is responsible for cleaning the
premises as specified in the attached cleaning guide.
This service is contracted to provide general cleaning in all areas of the Practice on a daily
basis (Mon – Fri).
An annual contract is negotiated and reviewed every June.
The cleaning service operates after 5pm. Spills that occur during normal consulting hours
are the responsibility of the health practitioner (doctor, nurse) or if in non-clinical areas, the
practice nurse.
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Cleaning staff should adhere to the following principles when cleaning:
 don personal protective equipment (PPE) such as gloves and a waterproof apron
 make up water and detergent solution each day
 use clean dry cloths and mops
 wash and dry all surfaces
 promptly dispose of used cleaning solution in the dirty utility area, not in hand basins or
clinical sinks
 wash and dry buckets, cloths, mops and PPE after use
 wash hands when each task is completed.
Areas which are only cleaned/ managed by appropriately trained practice staff are:
 spillage of blood or body fluids
 medical instruments or items for re-use are cleaned according to the procedure for
cleaning instruments and re-usable items.
 treatment room benches and trolleys
 consulting room benches containing medical equipment
 infectious waste and sharps containers
All practice staff responsible for cleaning have been appropriately immunised as
documented in their staff records. Should cleaning not conform to the expectations of staff it
should be reported to the Practice Manager.
The Practice Manager, or delegate, conducts routine audits to ensure a high standard of
cleaning. Audits are done every two months or more frequently as required, using items as
defined in the cleaning contract.
Safety data sheets of cleaning solutions, disinfectants etc are kept on file in case of a
medical emergency i.e. swallowing, splashed in eyes.
The attached cleaning guide contains descriptions of all areas to be cleaned, frequency,
method and responsible person.
RACGP 4th edition Standards 5.3.3.
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Routine Cleaning Guide
Surface
Method and cleaning
agents to be used
Frequency
Cleaner
Responsible
Treatment room benches and
trolleys
Wash with hot water and
detergent. Dry thoroughly
Nightly and more
often if required
Authorised
practice staff
Benches/drawers containing
medical Items
Wash with hot water and
detergent. Dry thoroughly
Weekly and more
often if required
Authorised
practice staff
Re-usable medical items and
instruments
Refer to procedure in Section
4
As required
Authorised
practice staff
Benches and tables in kitchen
Wash with hot water and
detergent
Nightly
Sinks, hand basins and toilets
Hot water & detergent.
An abrasive cream cleanser
may be a useful stain
remover
Daily
Hard floors - Treatment Room
Vacuum and wet mop with
hot water and detergent
Daily
Hard floors - Other areas
Vacuum and wet mop with
hot water and detergent
Daily - weekly
depending on use
Carpeted areas
Vacuum
Daily – weekly
depending on use
6 –12 monthly
Steam Cleaned
Office desks, benches and
furniture
Damp mop with hot water
and detergent / Vacuum
Weekly
Examination couches
Hot water and detergent
Daily
Toys
Dishwasher / Hot water and
detergent
Daily - Weekly
depending on use
Waiting Room furniture
Hot water and detergent/
Vacuum
Daily
Curtains - Cubicle
Machine hot wash
3 monthly
Windows and window
furnishings
Dry clean / Vacuum
Annually
Walls and ceilings
Hot water and detergent
Annually
Storerooms
Hot water and detergent
3 monthly
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6
Privacy and Personal Health Information
6.1 Privacy and Security of Personal Health Information
Policy
This practice is bound by the Federal Privacy Act 1998 and National Privacy Principles, and
also complies with the Victorian Health Records Act 2001.
‘Personal health information’ a particular subset of personal information and can include any
information collected to provide a health service.
This information includes medical details, family information, name, address, employment and
other demographic data, past medical and social history, current health issues and future
medical care, Medicare number, accounts details and any health information such as a medical
or personal opinion about a person’s health, disability or health status.
It includes the formal medical record whether written or electronic and information held or
recorded on any other medium e.g. letter, fax, or electronically or information conveyed
verbally.
Our practice has a designated person (*Insert name) with primary responsibility for the practice’s
electronic systems, computer security and adherence to protocols as outlined in our Computer
Information Security policy (Refer 6.1.1). This responsibility is documented in the Position
Description. Tasks may be delegated to others and this person works in consultation with the
privacy officer.
Our Security policies and procedures regarding the confidentiality of patient health records and
information are documented and our practice team are informed about these at induction and
when updates or changes occur.
The practice team can describe how we correctly identify our patients using 3 patient
identifiers, name, and date of birth, address or gender to ascertain we have the correct
patient record before entering or actioning anything from that record.
For each patient we have an individual patient health record (paper, electronic or a combination
of both, “Hybrid”) containing all clinical information held by our practice relating to that patient.
The Practice ensures the protection of all information contained therein. Our patient health
records can be accessed by an appropriate team member when required. We also ensure
information held about the patient in different records (e.g. at a residential aged care facility) is
available when required.
Procedure
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Doctors, allied health practitioners and all other staff and contractors associated with this
Practice have a responsibility to maintain the privacy of personal health information and
related financial information. The privacy of this information is every patient’s right.
The maintenance of privacy requires that any information regarding individual patients,
including staff members who may be patients, may not be disclosed either verbally, in
writing, in electronic form, by copying either at the Practice or outside it, during or outside
work hours, except for strictly authorised use within the patient care context at the Practice
or as legally directed.
There are no degrees of privacy. All patient information must be considered private and
confidential, even that which is seen or heard and therefore is not to be disclosed to family,
friends, staff or others without the patient’s approval. Sometimes details about a person’s
medical history or other contextual information such as details of an appointment can identify
them, even if no name is attached to that information. This is still considered health information
and as such it must be protected under the Privacy Act 1998.
Any information given to unauthorised personnel will result in disciplinary action and
possible dismissal. Each staff member is bound by his/her privacy clause contained with the
employment agreement which is signed upon commencement of employment at this
Practice. (Refer Section 2).
Personal health information should be kept where staff supervision is easily provided and
kept out of view and access by the public e.g. not left exposed on the reception desk, in
waiting room or other public areas; or left unattended in consulting or treatment rooms.
Practice computers and servers comply with the RACGP computer security checklist and we
have a sound back up system and a contingency plan to protect the practice from loss of
data. (Refer 6.1.1 Computer information security)
Care should be taken that the general public cannot see or access computer screens that
display information about other individuals. To minimise this risk automated screen savers
should be engaged.
Members of the practice team have different levels of access to patient health information.
(Refer Section 6 Compute Information security) To protect the security of health information,
GPs and other practice staff do not give their computer passwords to others in the team.
Reception and other Practice staff should be aware that conversations in the main reception
area can often be overheard in the waiting room and as such staff should avoid discussing
confidential and sensitive patient information in this area.
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Whenever sensitive documentation is discarded the practice uses an appropriate method of
destruction (*Insert method e.g. shredding or security bin) or computer drive, memory sticks etc
are reformatted)
Correspondence
Electronic information is transmitted over the public network in an encrypted format using secure
messaging software. Where medical information is sent by post the use of secure postage or a
courier service is determined on a case by case basis.
Incoming patient correspondence and diagnostic results are opened by a designated staff
member.
Items for collection or postage are left in a secure area not in view of the public.
Facsimile
Facsimile, printers and other electronic communication devices in the practice are located in
areas that are only accessible to the general practitioners and other authorised staff. Faxing
is point to point and will therefore usually only be transmitted to one location
All faxes containing confidential information are sent to fax numbers after ensuring the
recipient is the designated receiver.
Confidential information sent by fax has Date, Patient Name, Description and Destination
recorded in a log book.
Write, “Confidential” on the fax coversheet
Check the number dialled before pressing ‘SEND’
Keep the transmission report produced by the fax as evidence that the fax was sent. Also
confirm the correct fax number on the report.
Faxes received are managed according to incoming correspondence protocols
The practice uses a fax disclaimer notice on outgoing faxes that affiliates with the practice.
(*Insert message here).
Emails
Emails are sent via various nodes and are at risk of being intercepted. Patient information
may only be sent via email if it is securely encrypted according to industry and best practice
standards.
Patient Consultations
Patient privacy and security of information is maximised during consultations by closing
consulting room doors. All Examination couches, including those in the treatment room,
have curtains or privacy screens.
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When, consulting, treatment room or administration office doors are closed prior to entering
staff should either knock and wait for a response or alternatively contact the relevant person
by internal phone or email.
Where locks are present on individual rooms these should not be engaged except when the
room is not in use
It is the doctor’s/health care professional’s responsibility to ensure that prescription paper,
sample medications, medical records and related personal patient information is kept
secure, if they leave the room during a consultation or whenever they are not in attendance
in their consulting/treatment room.
Medical Records
The physical medical records and related information created and maintained for the
continuing management of each patient are the property of this Practice. This information is
deemed a personal health record and while the patient does not have ownership of the
record he/she has the right to access under the provisions of the Commonwealth Privacy
and State Health Records Acts. Requests for access to the medical record will be acted
upon only if received in written format.
Our patient health records can be accessed by an appropriate team member when required.
(*Insert details or where they are located) about how you ensure the protection of all
information contained in medical records e.g. passwords, access details, storage and how you
ensure information held about the patient in different records (e.g. at a residential aged care
facility) is available when required.
Both active and inactive patient health records are kept and stored securely.
A patient health record may be solely electronic, solely paper based, or a combination (hybrid) of
paper and electronic records
Select the appropriate options, either paper based record security or electronic record
security or both depending on the systems used at your practice for the management of
personal health information and delete others.
Paper based Records
Security is maintained for paper based medical files at all times. During Practice hours the
reception and filing areas are supervised. These records are only retrieved by authorised
Practice staff and are secured when the practice is closed. Patient health records are easily
accessed by the authorised staff at time of consultation.
Paper based medical records are stored in the (*insert locations of Paper based medical
records in your practice). Folders are filed as follows: (*insert summary of Paper based
medical records filing system).
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Medical records are not placed on top of the reception counter. When doctors and other
Practice staff request a record or are to see a patient the medical record is placed in their intray, away from public view and access.
Records are not left in public or unauthorised areas of the Practice. If a doctor has borrowed
a record, it is to be kept locked inside the consulting room cupboard or returned to be filed if
no longer in use.
Computerised Records
Our practice is considered paperless and has systems in place to protect the privacy, security,
quality and integrity of the personal health information held electronically. Appropriate staff
members are trained in computer security policies and procedures.
Hybrid Records
Our practice utilises records comprised of a combination of physical paper, scanned
documentation and electronic digital records. We recognise that a hybrid approach creates
additional management and risk issues.
There must be a record made for every consultation in each system indicating where the clinical
notes for the consultation are recorded.
Security is maintained for paper based medical files at all times. During Practice hours the
reception and filing areas are supervised. These records are only retrieved by authorised
Practice staff and are secured when the practice is closed. Patient health records are easily
accessed by the authorised staff at time of consultation.
Paper based medical records are stored in the (*insert locations of Paper based medical
records in your practice). Folders are filed as follows: (*insert summary of Paper based
medical records filing system).
Medical records are not placed on top of the reception counter. When doctors and other
Practice staff request a record or are to see a patient the medical record is placed in their intray, away from public view and access.
Records are not left in public or unauthorised areas of the Practice. If a doctor has borrowed
a record, it is to be kept locked inside the consulting room cupboard or returned to be filed if
no longer in use.
RACGP 4th edition Standards 4.2.1 & 3.1.4.
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Section 3.02
6.1.1 Computer Information Security
Policy
Our practice has systems in place to protect the privacy, security, quality and integrity of the data
held electronically. Doctors and staff are trained in computer use and our security policies and
procedures and updated when changes occur.
A staff member (*insert name) has designated responsibility for overseeing the maintenance of
our computer security and our electronic systems.
All clinical staff have access to a computer to document clinical care. For medico legal reasons,
and to provide evidence of items billed in the event of a Medicare audit, staff, especially nurses
always log in under their own passwords to document care activities they have undertaken.
Our practice ensures that our practice computers and servers comply with the RACGP computer
security checklist and that:
 computers are only accessible via individual password access to those in the practice
team who have appropriate levels of authorisation.
 computers have screensavers or other automated privacy protection devices are enabled
to prevent unauthorised access to computers.
 servers are backed up and checked at frequent intervals, consistent with a documented
business continuity plan.
 back up information is stored in a secure off site environment.
 computers are protected by antivirus software that is installed and updated regularly
 computers connected to the internet are protected by appropriate hardware/software
firewalls.
 we have a business continuity plan that has been developed, tested and documented.
Electronic data transmission of patient health information from our practice is in a secure
format.
Our practice has the following information to support the computer security policy:
 current asset register documenting hardware and software including software licence
keys
 logbooks/print-outs of maintenance, backup including test restoration, faults, virus scans
 folder with warranties, invoices/receipts, maintenance agreements
This Practice reserves the right to check individual’s Computer System history as a precaution to
fraud, workplace harassment or breaches of confidence by employees. Inappropriate use of the
Practices Computer Systems or breaches of Practice Computer Security will be fully investigated
and may be grounds for dismissal.
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This practice has a sound backup system and a contingency plan to protect practice information
in the event of an adverse incident, such as a system crash or power failure. This plan
encompasses all critical areas of the practice’s operations such as making appointments, billing
patients and collecting patient health information. This plan is tested on a regular basis to ensure
backup protocols work properly and that the practice can continue to operate in the event of a
computer failure or power outage.
Procedure
The RACGP Computer security guidelines: A self assessment guide and checklist for
general practice (3rd edition) is available at www.racgp.org.au/ehealth/csg. The
accompanying template for developing a policy and procedure manual should be completed
by the designated staff member responsible for the practice’s computer security. (*Insert the
location of your practice computer security manual and protocols).
Our disaster Box stocked with items to enable the practice to operate in the event of a power
failure is located (*Insert location).
 torches.
 paper prescription pads/sick certificates etc.
 appointment schedule printout and manual book.
 letterhead.
 consultation notes.
 manual credit card/payment/Medicare processing equipment.
 emergency numbers.
RACGP 4th edition Standards 4.2.1 & 4.2.2.
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6.1.2 Practice Privacy Policy
Policy
National Privacy Principle 5 requires our practice to have a document that clearly sets out its
policies on handling personal information, including health information.
This document, commonly called a privacy policy, outlines how we handle personal information
collected (including health information) and how we protect the security of this information. It
must be made available to anyone who asks for it and patients are made aware of this.
The collection statement informs patients about how their health information will be used
including other organisations to which the practice usually discloses patient health information
and any law that requires the particular information to be collected. Patient consent to the
handling and sharing of patient health information should be provided at an early stage in the
process of clinical care and patients should be made aware of the collection statement when
giving consent to share health information.
In general, quality improvement or clinical audit activities for the purpose of seeking to improve
the delivery of a particular treatment or service would be considered a directly related secondary
purpose for information use or disclosure so we do not need to seek specific consent for this use
of patients’ health information, however we include information about quality improvement
activities and clinical audits in the practice policy on managing health information.(Refer Section
8 Accreditation and Continuous Improvement)
Procedure
We inform our patients about our practice’s policies regarding the collection and management of
their personal health information via:
 a sign at reception.
 brochure/s in the waiting area.
 our patient information sheet.
 new patient forms – ‘Consent to share information’.
 verbally if appropriate.
 the practice website.
(* Insert copies of your practices privacy policy and your collection statement. You may have
a combined statement. Use the points below as a guide or templates are available on the
web).
The privacy policy should outline:
 the practice’s contact details.
 what information is collected.
 why information is collected.
 how the practice maintains the security of information held at the practice.
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







the range of people within the practice team (e.g. GPs, general practice nurses, general
practice registrars and students and allied health professionals), who may have access
to patient health records and the scope of that access.
the procedures for patients to gain access to their own health information on request.
the way the practice gains patient consent before disclosing their personal health
information to third parties.
the process of providing health information to another medical practice should patients
request that.
the use of patient health information for quality assurance, research and professional
development.
the procedures for informing new patients about privacy arrangements.
the way the practice addresses complaints about privacy related matters.
the practice’s policy for retaining patient health records.
A ‘collection statement’ sets out the following information:
 the identity of the practice and how to contact it.
 the fact that patients can access their own heath information.
 the purpose for which the information is collected.
 other organisations to which the practice usually discloses patient health information.
 any law that requires the particular information to be collected (e.g. notifiable diseases).
 the main consequence for the individual if important health information is not provided.
Prior to a patient signing consent to the release of their health information patients are made
aware they can request a full copy of our privacy policy and collection statement.
Patient consent for the transfer of health information to other providers or agencies is
obtained on the first visit. A copy of our consent form is included below.
Once signed this form is scanned into the patient’s record and its completion noted. Note:
Consent for transfer of information differs from procedural consent.
RACGP 4th edition standards 4.2.1.
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6.2 3rd Party Requests for Access to Medical
Records/Health Information
Policy
Requests for 3rd Party access to the medical record should be initiated by either receipt of
correspondence from a solicitor or government agency or by the patient completing a
Patient Request for Personal Health Information Form. Where a patient request form or and
signed authorisation is not obtained the practice is not legally obliged to release.
Where requests for access are refused the patient or third party may seek access under
relevant privacy laws.
An organisation ‘holds’ health information if it is in their possession or control. If you have
received reports or other health information from another organisation such as a medical
specialist, you are required to provide access in the same manner as for the records you create.
If the specialist has written ‘not to be disclosed to a third party’ or ‘confidential’ on their report,
this has no legal effect in relation to requests for access under the Health Records Act 2001.
You are also required to provide access to records which have been transferred to you from
another health service provider.
Requests for access to the medical record and associated financial details may be received
from various 3rd Parties including:
1. Subpoena/court order/coroner/search warrant
2. Relatives/Friends/carers
3. External doctors & Health Care Institutions
4. Police /Solicitors
5. Health Insurance companies/Workers Compensation/Social Welfare agencies
6. Employers
7. Government Agencies
8. Accounts/Debt Collection
9. Students (Medical& Nursing)
10. Research /Quality Assurance Programs
11. Media
12. International
13. Disease registers
14. Telephone Calls
We only transfer or release patient information to a third party once the consent to share
information has been signed and in specific cases informed patient consent has may be
sought. Where possible de identified information is sent
Our practice team can describe the procedures for timely, authorised and secure transfer of
patient health information in relation to valid requests.
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Procedure
The practice team can describe how we correctly identify our patients using 3 patient
identifiers, name, date of birth, address or gender to ascertain we have the correct patient
record before entering, actioning or releasing anything from that record.
Patient consent for the transfer of health information to other providers or agencies is
obtained on the first visit and retained on file in anticipation of when this may be required.
As a rule no patient information is to be released to a 3rd Party unless the request is made in
writing and provides evidence of a signed authority to release the requested information, to
either the patient directly or a third party. Where possible de identified data is released.
Written requests should be noted in the patient's medical record and also documented in the
practice’s Request Register. Requests should be forwarded to the designated person within
the practice for follow-up.
Requested records are to be reviewed by the treating medical practitioner or principal doctor
prior to their release to a third party. Where a report or medical record is documented for release
to a third party, having satisfied criteria for release, (including the patients written consent and
where appropriate written authorisation from the treating doctor), then the practice may specify a
charge to be incurred by the patient or third party, to meet the cost of time spent preparing the
report or photocopying the record.
Section 3.03
The practice retains a record of all requests for access to medical information including transfers
to other medical practitioners.
Where hard copy medical records are sent to patients or 3rd Parties copies are forwarded not
original documentation wherever possible. If originals are required copies are made in case of
loss.
Security of any health information requested is maintained when transferring requested
records and electronic data transmission of patient health information from our practice is in
a secure format.
Subpoena, Court Order, Coroner Search Warrant
Note the date of court case and date request received in the medical record. Depending on
whether a physical or electronic copy of the record is required follow procedures as
described above. Refer also to section 8 “Management of potential Medical defence claims’
On occasions a member of staff is required to accompany the medical record to court or
alternatively a secure courier service may be adequate. If the original is to be transported,
ensure a copy is made in case of loss of the original during transport. Ensure that the record
is returned after review by the court.
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Relatives/Friends
A patient may authorise another person to be given access if they have the legal right and a
signed authority. See 6.3 Patient Requests for Personal Health Information. See also NPP2
Use & Disclosure.
In 2008 the Australian Law Reform Commission recognised that disclosure of information to
‘a person responsible for an individual’ can occur within current privacy law. If a situation
arises where a carer is seeking access to a patient’s health information, practices are
encouraged to contact their medical defence organisation for advice before such access is
granted.
Individual records are advised for all family members but especially for children whose
parents have separated where care must be taken that sensitive demographic information
relating to either partner is not recorded on the demographic sheet. Significant court orders
relating to custody and guardianship should be recorded as an alert on the children’s
records.
External Doctors and Health Care Institutions
Direct the query to the patient’s doctor and or the practice manager/principal doctor.
Police/ Solicitors
Police and solicitors must obtain a case specific signed patient consent (or subpoena, court
order or search warrant) for release of information. The request is directed to the doctor.
Health Insurance Companies /Workers Compensation/ Social Welfare Agencies
Depending on the specific circumstances information may be need to be provided. It is
recommended that these requests are referred to the Doctor.
It is important that organisations tell individuals what could be done with their personal health
information and if it is within the reasonable expectation of the patient then personal health
information may be disclosed. Doctors may need to discuss such requests with the patient and
perhaps their medical defence organisation.
Employers
If the patient has signed consent to release information for a pre-employment questionnaire
or similar report then direct the request to the treating doctor.
Government Agencies - Medicare/Dept. Veterans Affairs
Depending on the specific circumstances information may be need to be provided. It is
recommended that doctors discuss such issues with the medical defence organisations.
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State Registrar of Births, Deaths and Marriages
Death certificates are usually issued by the treating doctor.
Centrelink
There are a large number of Centrelink forms (treating doctor’s reports) which are usually
completed in conjunction with the patient consultation
Accounts/ Debt Collection
The practice must maintain privacy of patient's financial accounts. Accounts are not stored
or left visible in areas where members of the public have unrestricted access.
Accounts must not contain any clinical information. Invoices and statements should be
reviewed prior to forwarding to third parties such as insurance companies or debt collection
agencies.
Outstanding account queries or disputes should be directed to the practice
manager/bookkeeper or principal.
Hint: Practices may like define an adequate period of time between the initial account and
pursuing aggressive collection.
Students (Medical & Nursing)
This practice does/ does not participate in medical/nursing student education.
The practice acknowledges that some patients may not wish to have their personal health
information accessed for educational purposes. The practice always advises patients of
impending student involvement in practice activities and seeks to obtain patient consent
accordingly. The practice respects the patient’s right to privacy.
Researchers/Quality Assurance Programs
Where the practice seeks to participate in human research activities and/or continuous
quality improvement (CQI) activities, patient anonymity will be protected. The practice will
also seek and retain a copy of patient consent to any specific data collection for research
purposes.
Research requests are to be approved by the Practice Principal/ practice partners and must
have approval from a Human Research Ethics Committee (HREC) constituted under the
NH&MRC guidelines. A copy of this approval will be retained by the practice.
Practice accreditation is a recognised peer review process and the reviewing of medical records
for accreditation purposes has been deemed as a "secondary purpose" by the Office of the
Federal Privacy Commissioner. As a consequence patients are not required to provide consent.
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Patients should be advised of the ways in which their health information may be used (including
for accreditation purposes) via a sign in the waiting room and the practice information brochure.
Media
Please direct all enquiries to Practice Manger/ Principal. Staff must not release any
information unless it has been authorised by the Practice Manager/ Principal and patient
consent has been obtained.
International
Where patient consent is provided then information may be sent overseas however the
practice is under no obligation to supply any patient information upon receipt of an
international subpoena.
NPP9 Transborder Data Flows
Disease Registers
This practice submits patient data to various disease specific registers (cervical, breast
bowel screening etc) to assist with preventative health management.
Consent is required from the patient with the option of opting in or opting out. Patients are
advised of this via a sign in the waiting area and in the practice’s information leaflet.
Telephone Calls
Requests for patient information are to be treated with care and no information is to be given
out without adherence to the following procedure:
Take the telephone number, name (and address) of the person calling and forward this onto
the treating doctor/principal or Practice Manager where appropriate,
RACGP 3rd edition Standards 4.2.1.
RACGP 4th edition Standards 4.2.1 & 3.1.4 & 4.2.2.
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6.3 Request for Access to Personal Health Information
Policy
Patients at this practice have the right to access their personal health information (medical
record) under legislation. Commonwealth Privacy Amendment (Private Sector) Act 2000 and the
Health Records Act 2001 (Victoria.) The HRA gives individuals a right of access to their personal
health information held by any organisation in the private sector in Victoria in accordance with
Health Privacy Principle 6 (HPP 6). This principle obliges health service providers and other
organisations that hold health information about a person to give them access to their health
information on request, subject to certain exceptions and the payment of fees (if any).
Public sector organisations continue to be subject to the Freedom of Information Act 1982.
This practice complies with both laws and the National and Health Privacy Principles (NPPs &
HPPs) adopted therein. See summary headings of Principles in this section. Both Acts give
individuals the right to know what information a private sector organisation holds about them, the
right to access this information and to also make corrections if they consider data is incorrect.
National Privacy Principles
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NPP 1: Collection of personal information by an organisation.
NPP 2: How an organisation may use and disclose personal information in its
possession.
NPP 3: Relates to the quality of the data held by an organisation.
NPP 4: Organisation must take reasonable steps to make sure the personal information
it holds is secure.
NPP 5: Requires an organisation to be open about what personal information it holds
and its policy on the management of personal information.
NPP 6: Relates to access and correction of personal information held by an
organisation about an individual, by that individual.
NPP 7: The use of identifiers assigned by a Commonwealth Agency.
NPP 8: Individuals have the option of not identifying themselves when entering
transactions with organisations.
NPP 9: Regulates the transfer of personal information held by an organisation in
Australia.
NPP10: Limits on when an organisation is permitted to collect sensitive information.
As adopted within Commonwealth Privacy Amendment (Private Sector) Act (2000):
We have a privacy policy in place that sets out how to manage health information and the steps
an individual must take to obtain access to their health information. This includes the different
forms of access and the applicable time frames and fees.
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Reports by Specialists
This information forms part of the patient's medical record, hence access is permitted under
privacy law.
Diagnostic Results
This information forms part of the patient's medical record, hence access is permitted under
privacy law.
Note: Amendments to the Privacy Act 1998 apply to information collected after 21st
December 2001, however they also apply to data collected prior to this date provided it is
still in use and readily accessible.
We respect an individual's privacy and allow access to information via personal viewing in a
secure private area. The patient may take notes of the content of their record or may be
given a photocopy of the requested information. A GP may explain the contents of the
record to the patient if required. An administrative charge may be applied, at the GPs
discretion and in consultation with the Privacy Officer, e.g. for photocopying record, X-rays
and for staff time involved in processing request.
Procedure
A notice is displayed in our waiting room and on our web site advising patients and others of
their rights of access and of our commitment to privacy legislation compliance. An
information brochure is also available that provides further details if required.
Release of information is an issue between the patient and the doctor. Information will only
be released according to privacy laws and at doctor's discretion. Requested records are
reviewed by the medical practitioner prior to their release and written authorisation is
obtained.
Request Received
When our patients request access to their medical record and related personal information
held at this practice, we document each request and endeavour to assist patients in granting
access where possible and according to the privacy legislation. Exemptions to access will
be noted and each patient or legally nominated representative will have their identification
checked prior to access being granted.
A patient may make a request verbally at the practice, via telephone or in writing e.g. fax,
email or letter. No reason is required to be given. The request is referred to the patient's
doctor or delegated Privacy Officer.
A Request for Personal Health Information form is completed to ensure correct processing.
Once completed a record of the request is logged in the Access Register and the form
filed/scanned in the patient record.
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Request by another (not patient)
An individual may authorise another person to be given access, if they have the right e.g.
legal guardian, and if they have a signed authority. Under NPP 2 Use & Disclosure, a
'person responsible' for the patient (including a partner, family member, care, guardian or
close friend), if that patient is incapable of giving or communicating consent, may apply for
and be given access for appropriate care and treatment or for compassionate reasons.
Identity validation applies.
The Privacy Act 1998 defines a 'person responsible' as a parent of the individual, a child or
sibling of the individual, who is at least 18 years old, a spouse or de facto spouse, a relative
(at least 18 years old) and a member of the household, a guardian or a person exercising an
enduring power of attorney granted by the individual that can be exercised for that person's
health, a person who has an intimate relationship with the individual or a person nominated
by the individual in case of emergency
Children
Where a young person is capable of making their own decisions regarding their privacy,
they should be allowed to do so according to Federal Privacy Commissioner's Privacy
Guidelines. The doctor could discuss the child's record with their parent. Each case is dealt
with subject to the individual's circumstances. A parent will not necessarily have the right to
their child's information.
Deceased Persons
A request for access may be allowed for a deceased patient's legal representative if the
patient has been deceased for 30 years or less and all other privacy law requirements have
been met. Ref: Sec 28 Health Records Act. No mention is made of deceased patient’s
access in Commonwealth privacy legislation.
Acknowledge Request
Each request is acknowledged with a letter sent to the patient, confirming request has been
received. Send the letter within 14 days or sooner as recommended by the National Privacy
Commissioner. Acknowledgment will include a statement concerning charges involved in
processing the request.
Fees Charged
Discuss with the individual what information they want access to, and the likely fees, before
undertaking their request for access.
The fees which an organisation can charge for providing access must not be excessive and must
not apply to the mere lodgment of a request for access. National Privacy Principle (NPP) 6.4
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aims to prevent organisations from using excessive charges to discourage individuals from
making requests for access to their medical records.
If an organisation incurs substantial costs in meeting a request for access, then the organisation
could charge a reasonable fee to meet the administrative costs involved. For example, an
organisation could recover some of the costs of photocopying or of the staff time involved.
Collate & Assess Information
Retrieve patient's hardcopy medical record or arrange for the treating doctor or practice
principal to access the computer record. Refer to the patient request form to help identify
what information is to be given to the patient.
Data may be withheld under privacy legislation NPP6 Access & Correction for the following
reasons.
 where access would pose a serious threat to the life or health of any individual
 where the privacy of others may be affected
 if a request is frivolous or vexatious
 if information relates to existing or anticipated legal proceedings
 if access would prejudice negotiations with the individual
 if access would be unlawful
 where denying access is required or authorised by law
See National Privacy Principles in full for comprehensive list of exclusions.
Access Denied
Reasons for denied access must be given to the patient in writing. Note these on request
form. In some cases refusal of access may be in part or full.
Use of Intermediary When Access Denied
If request for access is denied an intermediary may operate as facilitator to provide sufficient
access to meet the needs of both the patient and the doctor.
Provide Access
Personal health information may be accessed in the following ways:
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view and inspect information
view, inspect and talk through contents with the doctor
take notes
obtain a copy (can be photocopy or electronic printout from computer)
listen to audio tape or view video
information may be faxed to patient
check Identity of Patient
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ensure a visible form of ID is presented by the person seeking access. E.g. driver's
lecence, passport, other photo identification. Note details on request form.
does the person have the authority to gain access? Check age, legal guardian
documents; is person authorised representative?
If the patient is viewing the data, supervise each viewing so that patient is not disturbed and
no data goes missing.
If a copy is to be given to the patient ensure all pages are checked and this is noted in the
request form.
If the doctor is to explain the contents to a patient then ensure an appointment time is made.
Requests to Correct Information
A patient may ask to have their personal health information amended if he/she considers
that is not up to date, accurate and complete. (NPP 6.5/6/6)
Our practice must try to correct this information. Corrections are attached to the original
health record.
Where there is a disagreement about whether the information is indeed correct, our practice
attaches a statement to the original record outlining the patients' claims.
Time Frames
Acknowledge request - within 14 days. Complete the request - within 30 days
RACGP 4th edition Standards 4.2.1.
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6.3.1 Privacy Officer
Policy
This practice has a designated Privacy Officer who implements and monitors adherence to
all privacy legislation in this practice.
The Privacy Officer acts as liaison for all privacy issues and patient requests for access to
their personal health information.
If staff members have any queries concerning privacy law i.e. Commonwealth Privacy Act Privacy Amendment (Private Sector) Act 2000 or Victorian Health Records Act 2001 then
refer to the Privacy Officer.
The privacy officer is responsible for ensuring compliance with relevant Privacy principles
and legislation and for developing and maintaining our written protocols. The privacy officer
liaises with the person responsible for Computer security and systems.
RACGP 4th edition Standards 4.2.1.
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6.3.2 Privacy Audit
Policy
From time to time or in the event of any issues or complaints relating to privacy matters, this
practice conducts a review of privacy policies and procedures.
Procedure
The Privacy Officer reviews the following items:
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what is the primary purpose of this practice?
what data do we collect and document? NPP1/HPP1
how do we store this information? NPP5
what data do we disclose and to whom? NPP2
when and how do we obtain patient's consent? NPP2/HPP2
Information is collected from hard copy and electronic storage devices and issues discussed
with GPs and staff to gain the most current information.
National and state privacy laws are referenced with any updates being noted and acted
upon.
Policy Manual, Patient Access Forms/Register, Brochures and Poster
At this time the Practice policy & procedure manual may be reviewed and updated for
privacy items, if not already done.
Forms related to 'Patient Access to Health Information," including request for access and
access register forms can also be reviewed at this time.
Detailed patient privacy brochures, stating our practice privacy policy in general as per
privacy legislation is reviewed and updated as necessary. Obtain additional copies (in
English or other languages) or re-print as needed.
A general patient privacy wall poster, advising patients of our privacy policy is reviewed and
updated as necessary.
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6.4 Medical Records Administration Systems
The practice team can describe how we correctly identify our patients using 3 patient
identifiers, name, date of birth, address or gender to ascertain we have the correct patient
record before entering or actioning anything from that record.
Select the appropriate option for the medical records at your practice, throughout this
section.
Our practice uses paper based medical records for the storage or management of patient
health information.
Our practice uses (*Insert name of software) for the storage or management of patient
health information.
Our practice uses a Hybrid system to manage Patient medical information. This system
comprises of paper based records and computer records. (*insert the name of you software
program and any cut off dates for paper based records)
RACGP 4th edition Standards 3.1.4.
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6.4.1 Creating a New Medical Record
Once patient name, address, date of birth and related demographic details are received by
reception, enter this information into the patient record.
It is practice policy where papers files are utilised records contain a patient index number.
6.4.2 Retrieving a Medical Record for a Current Patient
Authorised Practice staff retrieve paper records prior to each consulting session or as
required. (*Insert procedure utilised at your practice if different). Using the patient’s surname
as a key, find the patient number using the patient number index. Go to the medical record
filing area and pull out the correct patient record. Insert a trace card in its place; write the
patient number, surname, date retrieved and destination (doctor’s name).
Computerised patient records are only accessed by authorised doctors and staff via secure
login/password.
RACGP 4th edition Standards 4.2.1.
6.4.3 Filing Reports (Pathology, X-Ray, Consultant’s etc)
Paper based diagnostic test results and other incoming patient correspondence must be
dated and passed on to the patient’s treating doctor or Practice Principal, if the doctor is not
in on the day, for follow-up.
Once the doctor has actioned and initialled the document it should be followed up
accordingly.
This practice scans/ does not scan all patient paper based correspondence with copies of
this data securely stored.
Original copies are retained/ not retained
If results are received electronically, they are to be checked by the referring doctor or
Practice Principal daily, and the appropriate action box marked. The doctor will ensure that
the action is completed.
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6.4.4 Errors in Medical Record
If an error occurs in the paper medical record, then it is corrected by crossing through as a
single line for the course of the entry, initialled and dated by the author with an explanatory
note beside or below the original item. Thus the reason for the incorrect entry is clearly
documented with the new entry underneath or in the next available position. The new entry
is signed or initialled and dated. Liquid paper/whiteout is not used in the medical record.
Corrections in the electronic record should be recorded by referring to the date of the
original entry and the associated amendment.
Refer to NPP6/HPP6 Access & Correction, which refers to the patients right’s to have their
personal health information amended if he/she can establish that it is not accurate,
complete, misleading or up to date.
6.4.5 Allergies & Alerts
Alert notification may be required for allergic responses, drug reactions, and previous
aggressive behaviour or guardianship/custody arrangements.
It is practice policy to ensure that all patients have their allergic status recorded especially
any allergies to medications to facilitate safer prescribing. In computer based records “no
known allergies” is recorded in the absence of any allergies to note.
Alert notifications are documented in the electronic medical record Health Summary.
Alerts are also noted on the front cover of the paper based medical record.
RACGP 4th edition Standards 1.7.2.
6.4.6 Back Up of electronic medical records
In order to avoid lengthy down time, disruption, and medico-legal issues frequent backups
are essential and form a critical component of the practice disaster recovery plan. A formal
policy for the back up of the practice computer systems must be in place. (Refer 6.1.1
Computer Information security)
RACGP 4th edition Standards 4.2.2.
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6.4.7 Retention of Records and Archiving
Patient Health Records must be kept until the patient is 25 years of age, if a child, or a
minimum of 7 years following the last year of the patients attendance, whichever is greater.
This Practice retains paper medical records for a minimum of (*Insert) years. Inactive
electronic patient records are retained indefinitely or as stipulated by the relevant national,
state or territory legislation.
Patient accounts records are also retained for a minimum of 7 years.
Records of Drugs of Addiction stock and administration must be retained for a minimum of 3
years.
Sterilisation Cycle records and evidence of vaccine fridge temperature monitoring are
retained as per patient health records.
Where our patients have chronic conditions or genetic diseases, or at the doctors discretion
their records are kept for (*Insert) years.
Records of patients that have been sought for legal purposes are retained for (*Insert)
years.
Records of deceased patients are kept for (*Insert) years following the year of death.
Outdated paper based test results that no longer have clinical relevance are culled to assist
with storage. This is done in consultation with the medical defence organisations and in
compliance with state legislation.
The practice has a process in place to allow for the timely identification, of information to be
culled, stored or archived and to enable timely retrieval of paper based patient health
records.
Procedure
(*This is an example of one way to do this, please insert the protocol relevant to your
practice below.)
Prior to filing a medical record, reception staffs mark record cover with the current year of
attendance.
The doctor will advise staff via a note on the front cover of the medical record of the number
of years it is to be held if special criteria applies. Staff identify the record to ensure it is held
permanently.
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Deceased records are marked, “DECEASED” on the record and filed in the Deceased
section of the inactive file storage area.
Annually, a record cull is conducted for old records not accessed within the last two years.
These records are removed from active file and filed in the inactive file area. Patient’s
accounts records are culled after each End of Financial year.
Privacy will be maintained during the destruction process to ensure information contained in
the records is not divulged or seen by unauthorised persons. Records will be destroyed by
shredding or pulping, in a secure environment. Where an outside bureau undertakes this
task, the Practice manager retains a copy of the contract with the bureau and any
certificates of destruction.
We consult with our GPs’ medical defence organisations when deciding on the practice’s policy
with respect to the retention of records or when we are unsure about culling or archiving medical
information.
RACGP 4th edition Standards 1.7.1 & 4.2.1 & 4.2.2.
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6.4.8 Transfer of Medical Records
Policy
Transfer of medical records from this Practice can occur in the following instances:
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for medico-legal reasons e.g. record is subpoenaed to court.
when a patient asks for their medical record to be transferred to another Practice,
due to moving residence or for other reasons.
where an individual medical record report is requested from another source.
where the Doctor is retiring and the practice is closing.
Our practice team can describe the procedures for timely, authorised and secure transfer of
patient health information to other providers and in relation to valid requests.
Procedure
Requests for Transfer of medical records for medico legal reasons
Receiving a request to transfer medical records to a patient’s new clinic
In accordance with state and federal privacy regulations, a request to transfer medical
records must be signed by the patient giving us authority to transfer their records.
The request form should contain:
 the name of the receiving practitioner or practice.
 the name, address (both current and former if applicable) and date of birth the
patient whose record is required.
 the reason for the request.
When fulfilling a request, this practice may choose to either
 prepare a summary letter (manually or via clinical software) and include copies of
relevant correspondence and results pertinent to the ongoing management of the
patient.
 make a copy of the medical record and dispatch the copy to the new Practice,
retaining the original on site for a minimum of 7 years.
The requesting clinic is advised if we propose to transfer a summary or a copy of the full
medical record. If they have a preference the format can be negotiated or they can choose
not to proceed with the transfer and seek a copy through a separate access request.
If there is going to be any expenses related to the transfer the requesting clinic is advised
prior to sending the medical records and once the fee has been paid we process the
request as soon as possible.
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Any charges must not exceed the prescribed maximum fee.
The patients’ signed request letter/form and a notation that the patient has transferred is
made on the medical record. Include the name and address of the new Practice and the
dispatch details (e.g. via priority mail or confidential courier or in an electronic form)
Electronic data transmission of patient health information from our practice is in a secure
format.
Note: There are a number of ways the information can be transferred, depending on the
request from the patient and clinic: via secure post; encrypted email (if computerised
records), or, if the practice is releasing copies of the entire record and the patient requests
access (Health Records Act), the practice may wish to make an appointment time with the
patient to offer an appropriate explanation and counsel from the GP or as an alternative may
choose to supply a summary of the history.
All reasonable steps are taken to protect the health information from loss and unauthorised
disclosure during the transfer.
This practice does not allow individuals to collect the file and take it to their new provider.
Making a request for a patient medical record from another source.
Access to a new patient’s previous record can assist with maintaining the continuity of care of the
patent.
When requesting records from another clinic a standard request for transfer of medical
records template (see sample below) should be used.
This should contain:
 the patient’s details, the patient should be identified by name address (both current
and former if applicable) and date of birth.
 the reason for request including the name of the Doctor making the request.
 the request for transfer of patient files should be authorized by the patient.
If the files will be requested electronically, specific details of the format needs to be included
such as HTML or XML
If the clinic advises you that the patients are likely incur out of pocket expenses related to
transfer please advise the patient prior to accepting the transferred medical records
When a Doctor is retiring and the practice is closing.
RACGP 4th edition Standards 4.2.1 & 4.2.2 .
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7
Clinical Management
7.1 Clinical Autonomy
Policy
Doctors in this Practice are free to make decisions that affect the management of their
patients in accordance with accepted clinical judgement, best available evidence and
adherence to valid clinical care guidelines.
Doctors exercise full autonomy in determining:
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the appropriate clinical care of their patients.
the health professionals including specialists, other general practitioners and
para-medical practitioners to whom they refer.
the pathology, diagnostic imaging or other investigations they order and the provider
they use.
how and when to schedule follow up appointments with individual patients.
whether to accept new patients provided that this action is non-discriminatory and
does not apply to emergencies.
GPs and clinical staff of our practice are consulted prior to the scheduling of appointments
and the purchase of new equipment and supplies.
Feedback is sought from doctors and other staff concerning the use of practice equipment,
appointment scheduling and other matters relating to professional autonomy.
All members of the clinical team comply with their professional and ethical obligations and
practice within the boundaries of their knowledge, skills and competence and their role
within the practice team.
RACGP 3rd edition Standards 1.4.2.
RACGP 4th edition Standards 1.4.2.
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7.2 Clinical Content of Medical Records
Policy
Patients at our practice have their own individual patient health record containing all the
health information held by our practice about that patient.
All patients that have attended the practice/service in the last 2 years should have essential
information in their health summary and active patients i.e. those attending 3 or more times
in 2 years should have a comprehensive health summary.
All staff endeavour to keep the information in patients’ health records up to date and where
possible data is entered using accepted coding or drop down selections rather than free text
to assist with practice audits and chronic disease registers. Care is taken when entering
sound alike or look alike medicines, particularly when using the “drop down” boxes in
electronic prescribing programs.
Medical records are essential to provide evidence of all services billed under the Medical
Benefits Schedule (Medicare) and the continuing care of our patients. The contents are
confidential and covered by privacy legislation. Doctors and staff have a responsibility to
maintain the confidentiality of every medical record, which is each patient’s right.
Recording of patient health information should be to the standard that a locum or another
doctor could easily and efficiently take over the care of the patient. As a key component for
the continuing management of our patients, contemporaneous, legible, accurate and
complete records are kept.
To ensure optimum documentation of medical care and to meet our legal risk obligations all
staff involved in clinical care are able to document their care activities in the medical records
logging in using their own password. Training appropriate to their level of access should be
provided to all staff recording clinical management in the medical records or utilising the
records for clinical management activities e.g. reminder/recall.
Our staff are also well aware of the importance of recording the cultural background of
patients since this background can be an important indication of clinical risk factors and can
assist GPs and other staff in providing relevant and culturally appropriate care. (Refer
Section 5 Culturally Appropriate Care).
An active patient health record is defined as the record of a patient that has attended the
practice/service three or more times in the last two years. Our practice can demonstrate
that:
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at least 75% of our active patient records have a current health summary containing
all the required information outlined below.
at least 90% of our active patient health records contain a record of known allergies.
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To assist in the provision of optimum care to patients, our practice integrates with other
services. Information, including referral arrangements for these public and private providers,
and contact details are maintained on a central register which is accessible to all practice
staff. Details of referrals are documented in the patient medical record.
The patient health records contain evidence of a system to review and follow up test results.
We are working towards a systematic approach to the entry of patient data in the medical
records to facilitate the search, extraction and utilisation of patient information for our
prevention and screening activities. This includes comprehensive patient health summaries
and documentation of preventative activities in the patient’s medical records.
Procedure
Before accessing or entering information into a patient’s health record we check for three
approved patient identifiers (full name, DOB, address) to ensure we have the correct patient
matched with the correct health record. (Refer section 7 Patient Identification).
Each patient has a dedicated individual medical record containing all health information held
by us about that person.
The record incorporates:
 the patients full name, DOB, address and gender (or additional information to assist
with correct patient identification).
 where appropriate patient contact and demographic information.
 medical history.
 clearly visible documentation of any allergies.
 a health summary.
 an updated problem list.
 progress or consultation notes (including care outside normal opening hours and
home visits).
 clinical correspondence including referrals made and letters or other responses
received including pathology, X-ray.
 documentation of telephone calls, home and hospital visits and after hour’s
communication and visits.
 it may also contain other relevant information such as WorkCover or insurance
information or legal reports.
The active patient health records also demonstrate that the practice routinely records:
 aboriginal and Torres Strait Islander status.
 the person the patient wishes to be contacted in an emergency (Not necessarily the
next of kin).
 and that we are working towards recording the cultural backgrounds of all our
patients.
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(*Delete as appropriate)
Option 1
Our practice has an active hybrid medical record system, and there is a record made in
each system for each consultation or interaction indicating where the clinical notes are
recorded. (Retain option 2 & 3).
Option 2
Our practice medical Information is placed in an A4 record cover and filed in order. Written
medical records should not be altered by “whiting out” but corrections made by crossing out
and re-writing with time and date of alteration if not done contemporaneously. (Delete other
options).
Option 3
Information is stored electronically in the practice’s computer system
Computerised medical records should be alterable only if an audit trial is automatically kept
by the system otherwise once created a lock-out facility must apply and any corrections
made by recording additional information separately. (Delete other options).
Doctors, Practice Nurses, allied health practitioners and authorised students of this Practice
are responsible for documenting the care provided by them to their patients. Reception and
practice management staff are responsible for documenting significant phone contacts and
evidence of attempting to contact patients.
Plans for the management of patients with complex or chronic conditions, that are consistent
with best available evidence, are documented in the patient’s health record to ensure there
is a consistent and co-ordinated approach to care between the Doctor/s, Practice nurse/s
and other allied health care workers.
Patient health records also document the role the patient takes in their health care &
evidence that education and counselling on illness prevention is provided.
Where the person making the entry is not identified by an electronic log in, entries are
identified by initials or name and date e.g. scanned documents or notes. All entries must be
able to be read and understood by another practitioner should they need to review or take
on the patients care. This includes scanned documents.
Medical records should be in ink or on the computer and only standard common
abbreviations are used.
Information in the medical record is not prejudicial, derogatory nor irrelevant and is legible,
being able to be read by other health care practitioners for the ongoing management of the
patient.
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Consultation notes
Each of our patient health records contains sufficient legible and understandable information
about each consultation to allow another member of our clinical team to safely and
effectively carry on the management of the patient.
Reports or notes of consultations occurring off-site, such as to home visits or after-hours,
whether by or on behalf of our practice, are notated to enable identification of place and time
of consultation and the details of the care provided.
Important or significant telephone or electronic communication between practice and patient
is recorded in the patient health records.
At the time of each consultation or as soon as practical or when information becomes
available (e.g. test results) the doctor or clinical team member (e.g. nurse) providing the
care notes the following details either in the paper record or on the computer:
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date of consultation
who conducted the consultation (e.g. by initial in the notes, or audit trail in an electronic
record and qualification if relevant).
patient reason for consultation or the problem(s) managed.
relevant clinical and examination findings.
diagnosis and or differential diagnosis.
recommended management plan and, where appropriate, expected process of review.
any medicines prescribed for the patient (including name, strength, directions for
use/dose frequency, number of repeats and date medicine started/ceased/changed).
complementary or over-the-counter medicines used by the patient (to minimise drug
interactions).
any relevant preventive care undertaken.
any referral to other healthcare providers or health services.
any special advice or other instructions.
follow up of any problems raised in previous consultations.
that we are working toward recording preventive care status (e.g. currency of
immunisation, smoking, nutrition, alcohol, physical activity, blood pressure, height
and weight [body mass index]).
Referrals
The medical records contain evidence of patient referrals to other health care providers such
as diagnostic services, hospital and specialist consultation, allied health services, disability
and community services and health promotion and public health services and programs.
Health Summaries
A current up to date patient health summary assists in providing ongoing care, both within
the practice and when referring to other health care providers,
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Health summaries are developed progressively and need to be accessible during
consultations for doctors, nurses and other health care providers who all contribute to
keeping them up to date. Care is taken to enter data using accepted coding or drop down
selections rather than free text to assist with practice audits and chronic disease registers or
CQI activities that require identifying patients with risk factors or particular chronic diseases.
90% or more health records of patients who have attended our practice on a regular basis
(3 or more times in the last two years), have their known allergies recorded in the health
summary and 75% or more or more have a comprehensive health summary that has been
updated to reflect recent important events.
It is recommended that GPs clarify a patient’s current medicines list and known allergies art
every patient contact and patients on multiple medicines should be provided with the most
recent list of their medicines.
A Health Summary should contain documentation of:
 known drug allergies and sensitivities including any adverse medicines events.
 accurate and current medicines list (include prescription, non prescription and
complementary products if known).
 current health problems/ diagnoses.
 relevant past health history including immunisations and positive family history of
disease.
 any health risk factors (e.g. smoking, nutrition, alcohol, and physical activity).
 relevant social history including cultural background
 immunisation status.
Tests and results
Pathology results, imaging reports, investigations reports and clinical correspondence
received by the practice are reviewed by the GP before being retained in the patient’s
medical records.
Follow up of clinically significant results is documented in the patient’s medical records.
Collecting Information from patients
Practice staff provide all new patients with a “New Patient” form and a copy of our “consent
for the collection and use of information” for patients to complete and sign.
The signed consent forms are scanned into the notes
The completed new patient information forms are (*Insert how you transfer this information
into the patients Health summary and medical records).
Additional information is added to the patient’s medical record during the first and
subsequent consultations.
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The standard indigenous status question asked is ‘Are you of Aboriginal or Torres Strait
Islander origin?’ This question should be asked of all patients, irrespective of appearance,
country of birth or whether the staff know of the client or their family background. Our
practice collects this information as part of our “new patient’ questionnaire.
We are also working towards a system whereby patient information is updated regularly so
that it remains current and accurate using a standard “update your details form”. (*Insert or
describe where a copy of your form/s to obtain patient information are located).
RACGP 4th edition Standards 1.7.1, 1.7.2, 1.7.3, 1.1.3, 1.1.4; 1.5.1, 3.1.4 & 5.3.1.
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7.3 Informed Consent
Policy
Our doctors, nurses and other healthcare workers inform their patients of the purpose,
importance, benefits, risks and possible costs of proposed investigations referrals or
treatments, including medicines and medicine safety. We believe that patients need to
receive sufficient information to allow them to make informed decisions about their care.
Our Doctors and staff have a professional obligation to ensure they understand our patients
and that the patients understand any verbal or written information.
 patients who do not speak or read English or who are more proficient in another
language, or who have special communication needs are offered the choice of using
the assistance of a specialised service to communicate with the Doctor or clinical
team members. (Refer section 5 Non English speaking patients).
 the clinical team uses information that is clear and given in a format that is easy to
understand, with verbal information supported by a diagram with explanation,
brochure, leaflet or poster, electronic information or website referral. (Refer Section
5 Provision of Brochures, Leaflets and Pamphlets for Patients).
 the patient’s competence to give consent is ascertained by establishing whether the
patient is able to understand, retain and weight the information they have been given
to arrive at an informed choice. Such a process is applied to all adults, mature
minors (within the Gillick test), intellectually and mentally impaired patients or
guardian or power of attorney for the patient.
In situations where patients are dependent on a third party for their ongoing care we
endeavour to provide all appropriate information to the carer.
Issues of personality, personal fears and expectations, beliefs and values are also
considered.
There is no coercion by our doctors, nurses or other allied health care workers. Our patients
can choose to reject their advice or seek a second opinion. Patient’s refusal of treatment is
documented in the medical record. (Refer Section 7 Management of a Patient refusing
treatment).
The cost of treatment or investigations is an important component of informed decision
making. Patients are advised of possible costs involved, including additional out of pocket
costs, for procedures, investigations and treatments conducted on site prior to them being
conducted. For referred services where costs are not known the patients are advised of the
potential for out of pocket expenses and encouraged or assisted to make their own
enquiries. If the patient indicates that the costs pose a barrier to the suggested treatment or
investigation alternatives may need to be discussed (e.g. referral to public services).
Patients are asked to be open and are able to feel free to discuss all health issues and
proposed treatments, without fear.
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The Privacy Act 1998 states that consent may be 'express' or 'implied', i.e. Express
Consent - clear and unmistakably states, obtained in writing, orally or in any clear other form
where consent is clearly communicated.
Implied Consent - e.g. patient presents to doctor, discloses health information and this is
written down by the doctor/entered on computer during the consultation; e.g. doctor collects
specimen and sends it to pathology, reason to consider that the patient is giving implied
consent to passing necessary information to the laboratory. See also Sec 6.1 Patient
Privacy and Access to Information.
Ref: Guidelines on Privacy in Private Sector Oct 2000.
Procedure
To encourage patients to actively discuss their health care and to help create an
understanding of shared responsibility between the patient and our practice we use the
publication “10 tips for safer healthcare” to guide our discussion. This is available at
www.health.gov.au/internet/safety/publishing.nsf/content/10-tips.
Clear communication is provided about the potential for out of pocket costs including any
unexpected developments and the possible costs of additional treatments or procedures
before proceeding.
Consent Forms
“Consent for medical treatment, procedure or examination” form attached is used for patient
consent to on site health services. The doctor explains the form to the patient and completes
it with the patient signature.
Written consent does not take the place of the doctor’s personal communication when
dealing with the risks benefits and alternatives of the procedure with the patient. This task
should never be delegated to office staff and they should direct any questions regarding
procedures to the doctor.
Office staff may witness a patient’s written consent provided they believe that the patient is
competent (not confused or disorientated), acknowledges the conversation with the doctor
and that the signature is the patients
Where immediate treatment is necessary to preserve a life or prevent serious injury, all
attempts are made to provide information and gain the patient’s consent. This may not be
successful in all cases prior to administering emergency care.
Using a range of brochures, leaflets or written information that is tailored to suit individual
patients needs to support their explanation of the diagnosis and management of conditions,
including medication safety Doctors, practice nurses and allied health care workers inform
patients of the following issues concerning treatment and investigations:
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
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possible nature of illness/disease.
proposed approach to investigation, diagnosis and treatment including describing if it
is conventional or experimental, common side effects and the clinician undertaking
the procedure/treatment.
purpose, importance, expected benefits and risks.
other options for investigations, diagnosis and treatment.
length of procedure/treatment.
potential for out of pocket expenses.
degree of uncertainty of a) any diagnosis found and b) therapeutic outcome.
potential result of not undertaking the specified procedure/treatment or any other
treatments.
any significant long term physical, emotional, mental, social, sexual, or other
outcome which may be associated with a proposed intervention.
the costs involved, including out of pocket costs.
We recognise that patients need to understand the purpose and importance of medicines
and this assists them to comply with the recommended treatment plan.
To assist patients to make informed decisions about their medicines or understand any
medication safety requirements we support our verbal information with leaflets from the
consumer medicines information (CMI) website. These online versions of the information
produced by pharmaceutical companies, for consumers are available at
www.nps.org.au/consumers.
The informed consent process (including use of interpreter), consent form, and details of
any information or post procedure instructions provided to a patient are documented in the
medical record.
Patient consent regarding the expected benefits, possible risks and possible cost is obtained
for the following:
 all procedural interventions on site (written consent).
 patient’s participation in research projects (written consent).
 clinical Training Program (by waiting room sign and verbal consent prior to entering
the consulting room).
 third Party observation or participation in patient consultation (by waiting room sign
and verbal consent prior to entering the consulting room).
Medical treatment or preventative activities (e.g. Childhood Vaccinations or
prescribed medications).

At the time of childhood immunisations, careful documentation of parental consent needs to be
considered, including details of Australian Standard Vaccination Schedule (ASVS)
recommendations discussed and parent’s decisions regarding these recommendations. The
Practice offers the recommended vaccines for whom they are applicable to, regardless of cost to
the client. The decision to accept or reject the vaccine must be made by the parent, after
receiving full details of the risks, benefits and costs from the GP or nurse immuniser.
RACGP 4th edition Standards 1.2.2 & 1.2.4 & 5.3.1.
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7.4
Referral Protocols
Policy
Patients are referred for diagnostic testing or to another medical specialist, general
practitioner or allied health professional which may be better placed to deliver a service that
may benefit the patient.
The practice has an up to date written or computerised directory of local allied health
providers, community and social services and also local specialists to assist when choosing
practitioners to facilitate optimal patient care. This information includes different referral
arrangements and how to engage with these providers to plan and facilitate care.
Referral documents (i.e. letters and pre-printed forms) to other health care providers are
legible and contain relevant and sufficient information to facilitate optimal patient care. This
should include at least 3 approved patient identifiers. (Refer section 7 Patient identification)
and an accurate and current medication list (Refer section 7 Clinical content of the Medical
records).
Clinical handover needs to occur when all or some aspects of the patients care is
transferred to another provider such as when a patient is referred. Patients are made aware
that patient health information is being disclosed in the referral documents.
The medical records contain evidence of patient referrals to other health care providers such
as diagnostic services, hospital and specialist consultation, allied health services, disability
and community services and health promotion and public health services and programs.
Patients are made aware that their health information is being disclosed in referral letters
and documents.
Procedure
Suggesting a referral to a particular practitioner or allied health professional carries with it an
implicit endorsement that the receiving practitioner or service provider is appropriately
skilled and qualified to administer the treatment or service. Generally this is not an issue, but
if it is, the referral is qualified (e.g.: if a patient requests a referral to a fringe practitioner the
referral could read patient requests referral to you regarding xyz)
Our directory of local allied health providers, community and social services and also local
specialists is available (*insert how to access this).
The patient is given information about the purpose, importance, benefits and risks
associated with investigations, referrals or treatments proposed by their doctor to enable the
patient to make informed decisions. The doctor may use leaflets, brochures or written
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information to support their explanation where appropriate. Clear communications about
unexpected developments can assist the patient to understand the need for additional costs.
Patients are advised of possible costs involved, including additional out of pocket costs, for
procedures, investigations and treatments conducted on site prior to them being conducted.
For referred services where costs are not known the patients are advised of the potential for
out of pocket expenses and encouraged or assisted to make their own enquiries. If the
patient indicates that the costs pose a barrier to the suggested treatment or investigation
alternatives may need to be discussed (e.g. referral to public services).
Special care is taken to advise patients of the costs of consultations or procedures that do
not attract a government subsidy.
Letters of referral may be paper or computer based. Referrals sent electronically should be
encrypted. Plain paper or practice letterhead is considered appropriate stationery. Routine
use of drug company notepads or prescription pads is unacceptable. For medico legal and
clinical reasons practices need to keep copies of important (non-routine) referral letters in
the patient health record.
In the case of an emergency or other unusual circumstance a telephone referral may be
appropriate. A telephone referral needs to be documented in the patient’s health record.
Referral letters should:
 be legible (preferably typed) on appropriate practice stationary.
 contain relevant background social information and history.
 contain the present problem and reason for the referral and additional relevant or
sufficient information for continuing health management and to avoid duplication.
 include relevant health problems, key examination findings and current
management.
 include any allergies, adverse drug reactions and a current accurate medications
list.
 include the reason/purpose for the referral and expectation of the referral.
 identify the Doctor or clinical staff member making the referral.
 identify the setting from which the referral is being made and also the setting to
which the referral is being sent.
 if known, identify the healthcare provider to whom the referral is being made
 be dated.
 contain at least 3 of the approved patient identifiers e.g. name, date of birth and
address.
 be electronically transmitted in a secure manner if appropriate.
Requests for pathology, diagnostic or other investigations should:
 be legible.
 contain relevant clinical information.
 contains at least 3 of the approved patient identifiers e.g. name, date of birth and
address.
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For medico-legal and clinical reasons copies of any clinically significant referral letters,
pathology, diagnostic or other investigation requests and especially those which contain
significant clinical details, are retained by the practice and documented in the patients
medical record.
 a copy of all significant or non-routine referrals is kept in the medical record through
the use of NCR pads, photocopying or electronically on the computer.
 results of referrals and continuation notes or letters received from consultants and
hospitals are also retained in the patient health records.
Clinically significant referrals are followed up.
Patients seeking a further clinical opinion from another healthcare provider are encouraged
to notify their General practitioner to allow an opportunity to reinforce any potential risks of
the decision. Any advice or actions taken when a patient seeks a further clinical opinion, or
refuses recommended clinical management are documented in the patients’ health record..
RACGP 4th edition Standards 1.2.4 & 3.1.4 & 1.5.2 & 1.6.1 & 5.3.1 & 1.6.2.
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7.5 Clinical Handover
Policy
Clinical handover has been defined by the Australian Medical Association as ‘the transfer of
professional responsibility and accountability for some or all aspects of a patient’s or a group
of patients’ care to another person or professional group on a temporary or permanent
basis’.
Failure or inadequate handover of care is a major risk to patient safety and a common cause
of serious adverse patient outcomes. It can lead to delayed treatment, delayed follow up of
significant test results, unnecessary repeat of tests, medication errors and increased risk of
medico legal action.
Clinical handover communications can be face-to-face, written, via telephone and also by
electronic means.
All staff are informed about our policy on clinical handover to ensure standard processes are
followed.
Clinical handover of patient care occurs frequently in general practice both within the practice to
other members of the clinical team, and to external care providers.
We have standard and documented processes for timely clinical handover with services that
provide care outside normal opening hours.
Procedure
Clinical handover needs to occur whenever there is a change of care providers. Examples of
clinical handover include:
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a GP covering for a fellow GP who is on leave or is unexpectedly absent.
a GP covering for a part time colleague.
a GP handing over care to another health professional such as a practice nurse,
physiotherapist, podiatrist or psychologist.
a GP referring a patient to a service outside the practice.
a shared care arrangement (e.g. team care of a patient with mental health problems).
When appropriate, the clinical handover is documented in the consultation notes including
that the patient has shared in decision making and has been informed.
Written or verbal clinical handover between GPs occurs on a formal arranged basis when
doctors cover for those working on a sessional basis or when a GP or other clinical staff
member is away because of annual leave or illness. In addition to a formal handover,
adequate clinical records, including a health summary, enable the routine care of patients to
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continue. Practitioners relieving for another should read the patient’s preceding clinical
records.
Our practice recognises that an accurate and current medication list helps to minimize errors and
promote safety when clinical handover occurs. Patients with multiple medications may be
provided with a copy of their medication list and encouraged to show the list to other providers of
health care.
Clinical handover of a patient’s care outside the practice occurs in many ways. It includes but is
not limited to: referral for an investigation, referral to an ancillary healthcare provider, referral to a
specialist and referral to a hospital, as an outpatient or as an in-patient. Referral letters include
sufficient information to facilitate optimal patient care, including details of the purpose of the
referral and clarification of who will manage the follow up of investigations.
The practice should ensure that sufficient information is provided to the emergency
department about the clinical condition of an inbound patient, to facilitate prompt and
appropriate care. This may be directly to the ambulance service or to the hospital.
We have arrangements in place with our pathology service to ensure abnormal and life
threatening results identified by pathology outside normal opening hours can be conveyed to a
medical practitioner in a timely way.
Where complex or high risk patients, such as suicidal patients, or patients on complex
medication regimens are handed over to another provider for all or part of their care, it is
important for the handing over provider to request notification if the new provider ceases to
care for the patient. Equally, a provider treating a patient on a handover basis has an
obligation to notify others in the treating team if they stop seeing the patient. (This issue has
been the subject of several coroners’ recommendations).
Our doctors notify the deputising care provider of patients that they anticipate may need
care and ensure the deputising service has a defined means of timely contact with the GP or
another from the practice who is aware of the patient’s condition should they need to access
more detailed health information.
Deputising services are responsible for handing the care of a patient back to the patient’s
regular medical practitioner in a timely and appropriate manner.
When errors in clinical handover occur, every member of the practice team is encouraged to
report the incident, so the event can be analysed and processes introduced to reduce the
risk of a recurrence and harm occurring to other patients (Refer to section 3.1.2 Incidents
and Injuries and Adverse Patient events).
RACGP 4th edition Standards 1.5.2 & 5.3.1.
7.6 Patient Identification
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Policy
Correct patient identification is vital for patient safety and the maintenance of patient
confidentiality. Our patients are correctly identified at each encounter with our practice team
using 3 approved patient identifiers. All members of the practice team are trained in how to
correctly identify a patient using 3 identifiers.
Procedure
Approved Patient identifiers include:
 patient name (Family and given name)
 date of birth
 gender (as identified by the patient themselves)
 address
 patient record number (where it exists)
Patients identification using 3 approved identifiers should be established or confirmed:
 when making an appointment or checking off arrival at the practice
 when commencing the consultation or treatment or investigation
 when opening or entering data into the medical records
 when a clinical handover occurs at the interface of care by different providers.
 when confirming signed consent for medical treatment
 when following up test results or communicating with the patient, especially by
electronic means.
 when managing the patients treatment without the patient attending the practice e.g.
ordering repeat prescriptions
 on referral documentation
When asking for patient identification practice staff should ask the patient to state their
name, date of birth and address. Staff should not volunteer the information from the records
and ask the patient to confirm as nervous or hearing impaired patients may agree and verify
incorrect information. When patients are noticed to have similar names or other identifiers
(e.g. DOB), a notation is entered in the medical record to flag this.
It is important to ensure the correct patient gets the correct procedure. A useful resource for
GPs undertaking procedural work and minor surgery, is the Ensuring Correct Patient (3
identifiers) , Correct Site, Correct Procedure Protocol from the Australian Commission on
Safety and Quality in Health Care, or an equivalent protocol that incorporates these five
steps. www.safetyandquality.org/5stpcorectpatnt.pdf.
An Incident form is completed when any errors in patient identification are noted (Refer
Section 3 Incidents, injury and adverse patient events)
RACGP 4th edition Standards 3.1.4 & 5.3.1.
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7.7 Follow up of Tests, Results and Referrals
Policy
Our practice’s system for the follow up of tests, results and referrals has a strong focus on
risk management.
Our practice team can describe:
 how patients are advised of the process for follow up of results.
 the system by which pathology results, imaging reports, investigations reports and
clinical correspondence received by our practice is reviewed by a GP, signed, acted
upon in a timely manner and incorporated into the patient’s medical record.
 how we follow up and recall patients when we order important or clinically significant
tests, investigations or important referrals.
 how we follow up and recall patients with clinically significant tests, results or
correspondence.
All test results, including pathology results, diagnostic imaging and investigation reports, and
clinical correspondence received is reviewed, initialled (or electronic equivalent) and, where
appropriate acted upon in a timely manner. This is all incorporated into the patient health
record.
The nature and extent of the practices responsibility for following up test results, diagnostic
imaging and investigation reports, and clinical correspondence/referrals depends on what is
reasonable in the circumstance and the clinical significance of the test, referral or result.
Whether something requires follow up is determined by:
 the probability that the patient will be harmed if follow up does not occur.
 the likely seriousness of the harm.
 the burden of taking steps to avoid the risk of harm.
Important referrals for consultations or tests ordered are followed up, by the patient’s doctor
or delegated authority, in a timely manner. This may include checking the patient has
attended the referred consultation or the expected investigation. That correspondence or
test results have been received and reviewed. A record of any follow up and subsequent
actions or recall process is incorporated into the patient health record.
Results of tests and investigations requiring follow up can be “abnormal” or “normal”.
Correspondence from referred specialists and other health providers may also need to be
followed up. The clinical significance needs to be considered in the overall context of the
patients presenting problem and history. There is a system to enable the practice to
determine that:
 ordered tests and investigations were actually performed.
 results/reports have been received by the practice.
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results/reports or correspondence were seen by a General Practitioner, dated and
signed (or the equivalent if in an electronic patient health record).
results/reports/correspondence has been filed in the patient’s record.
results/reports/correspondence have been acted upon, in a timely manner where
appropriate.
results/reports have been reported to the patient (or where this did not occur, that
attempts were made to do so).
any follow up required has occurred.
this is documented in the patient records or similar.
Sometimes our doctors may need to be contacted outside normal working hours by the
pathology service about a serious or life threatening result. We have provisions for Doctors
to be contacted after hours for life threatening or urgent results. Refer to Section 5 After
Hours Service.
Our patients (or their carers) are made aware of their obligations and responsibilities for
their own healthcare. This includes being informed about how to obtain their results and the
seriousness of not attending for ordered appointments/investigations and any recall or
subsequent follow up. Where appropriate this advice may be documented in the patient’s
medical records.
Where a patient indicates they do not intend to comply with a recommended test or referral
the patient is deemed to have refused medical treatment or advice and is managed
according to the practice procedure for a patient refusing treatment or advice.
In addition to an appreciation of the need for timeliness when following up and actioning
referrals, tests and results our staff members are also aware of the need for confidentiality
and discretion, with regard to referrals, diagnostic tests and results or correspondence.
Procedure
(The procedures used by general practice to review, follow up and recall patients are
complex and varied. The system needs to be designed in a way that anticipates that
individual cases will require different levels of follow up depending on the clinical
significance or importance of the case. *Insert the Procedure or outline the process that
occurs in your individual practice.
Some prompts have been provided below to assist.
When ordering diagnostic tests:
 how do you ensure requests for tests, investigations or referral correspondence is
correctly identified to assist with ensuring the results from any test ordered are
matched up with the correct patient.
 how do you encourage patients to make an informed decision about the
investigation, referral or test. Refer to Section 7 Informed Consent & Section 7
Referral protocols.
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how do you advise patients about:
o the significance of the investigations, results or referral & any costs.
o how to obtain results and who is responsible for follow up.
Review of all results, reports and clinical correspondence received
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what is the role of staff receiving and filing these?
how do you demonstrate they have been reviewed by a doctor before filing/scanning or
saving these in the medical records. Consider actions for electronic, faxed, posted,
verbal results.
how do you ensure the results for Doctors not on duty are reviewed and followed up in a
timely manner e.g. allocate another Doctor to do this.
how do you ensure any urgent results are communicated to the practice or a Doctor in
and outside opening hours?
how do you follow up normal and/or abnormal results? Normal results may still require
further investigation or patient follow up.
how does the doctor reviewing the results, reports or correspondence know they are
important or clinically significance. Especially if these were ordered by another Doctor.
how does the Doctor clearly communicate in writing with reception/nursing staff any
action delegated and the urgency or expected timeframe?
Communicating with patients about tests, results and referrals
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how do patients get their results?
how do you inform patient about the expected timeframe for getting tests or
investigations or appointments with specialists or allied health providers.
do patients know about how and when to get their results. Do you make an
appointment for them?
how do you maintain privacy if a patient calls about a test, investigation, report or
result, e.g. Patient identification required, who speaks to the patient or decides when
this is appropriate.
how do you confirm they have been notified of their results?
consider documenting the content of discussions with the patient in the health
record.
Identification for follow up of clinically significant investigations and referrals that
have been ordered
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how do your doctors identify when referral, tests or investigations ordered are
clinically significant.
how are received clinically significant results, reports or correspondence identified?
how do you follow up tests, reports, results, correspondence that are expected, but
have not been received e.g. Recall system
how do you define or know what is a timely manner to expect a response or start to
follow these up
how do you differentiate the level of follow up required
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What is your system to recall patients with clinically significant results, reports and
clinical correspondence?
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how do you contact recall patients e.g. phone calls at different times/numbers.
Letter - registered mail or other electronic communication.
how do you determine urgency and timeliness?
how do you ensure the patient makes and attends any follow up medical
appointments?
how do you document your follow up and subsequent actions in the patients health
record for medico legal reasons.
RACGP 4th edition Standards 1.1.4, 3.1.4, 1.5.3.
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7.8 Reminder Systems for Preventative Care
Policy
For the continuing management of our patient’s health we utilise a systematic reminder
system to provide health promotion, preventative care and early detection of disease.
Our system is based on the best available evidence and where possible incorporates clinical
guidelines.
All members of the practice team participate in CQI and PDSA activities to improve our
systematic approaches to health promotion and prevention of disease.
Where opportunities exist we also coordinate with other health professionals and key
agencies to achieve health promotion and preventative care objectives.
Our reminder systems and notifications are mindful of protecting the privacy and
confidentiality of patient information and we consider the needs of patients with a physical or
intellectual disability.
We also consider our responsibility to patients if we cease or significantly change our
reminder systems.
We are working towards a systematic approach to the entry of patient data in the medical
records to facilitate the search, extraction and utilisation of patient information for our
prevention and screening activities. This includes comprehensive patient health summaries
and documentation of preventative activities in the patient’s medical records.
Consideration of patient’s individual circumstances is encouraged when providing
information about health promotion and illness prevention for patients (and carers). Verbal
and written information is provided to patients about health promotion and specific disease
prevention. This is distinct from the education and information that is provided to patients to
support a diagnosis and choice of treatment.
Procedure
Patient presentations at the practice are used as an opportunity to identify risk factors and
provide health promotion and illness prevention.
 pamphlets and brochures from a variety of sources are available for patients to self
select or to be provided by staff to reinforce health promotion messages from a
consultation.
 patients are encouraged to self identify information that is recorded on the health
summary to assist with early identification of the patients main health issues or risk
factors e.g. Aboriginal and Torres Strait Islander or family medical history.
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clinical data is routinely and opportunistically collected by members of the clinical
team and this is entered into the medical records in a manner that assist with data
extraction for preventative activities.
doctors seek the patient's consent before placing their details on a formal reminder
system for preventative care. This consent is documented in the patient’s medical
record.
patients are advised of the availability of reminder systems and how to opt out via
the practice information brochure or notice board
the patient’s privacy and confidentiality is protected and patients are notified in
writing when reminder systems which they participated in are discontinued.
(*insert the procedural details of how your practice identifies patients and
administers your reminder system.)
You may want to include the following:
 an outline of the roles of administrative and clinical staff,
 how you select patients,
 how you collect information e.g. health assessments, self identification of risk factors
 how you document and record information e.g. Software fields to use, specific
coding
 how you search clinical data e.g. any data extraction tool used,
 list any screening programs you participate in e.g. bowel cancer screening program,
 list any registers you provide data to e.g. ACIR for immunisations,
 how you ensure all staff are aware of preventative activities,
 samples of letters, and
 list specific risk factors or diseases you target
RACGP 4th edition Standards 1.3.1.
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7.9 Notifiable Diseases
Policy
National Privacy Principle 5 requires our practice to have a document that clearly sets out its
policies on handling personal information, including health information. This document,
commonly called a privacy policy, must be made available to anyone who asks for it and
patients must be informed about how their health information will be used including other
organisations to which the practice usually discloses patient health information and any law
that requires the particular information to be collected. Patient consent to the handling and
sharing of patient health information should be provided at an early stage in the process of
clinical care.
Under the Health (Infectious Diseases) Regulations 2001, Medical Practitioners are to report
specified infectious diseases to the Department of Human services. |
The diseases are classified into groups (A, B, C & D) and listed on what to notify and how to
notify information can be located at: www.health.vic.gov.au/ideas/notifying/whatto.htm
Procedure
Step 1 Immediate notification by phone. (Mandatory for Group A diseases)
Notify Group A diseases by phone immediately at the time of initial or presumptive
diagnosis. These are bolded on the form and marked with a symbol.
Priority number: ph 1300 651 160
Advice regarding appropriate additional precautions to implement, while waiting for patient
transfer to hospital, should be sought for each case
For urgent notifications outside office hours, please telephone the departments after hours
service on 1300 790 733 and advise the operator that you wish to make an 'urgent
infectious disease notification'.
Step 2 Written notification (Mandatory for all diseases)
Written notification of all diseases is required within 5 days of diagnosis.
Group D diseases, include HIV & AIDS, requires using a separate notification form, which is
forwarded to the diagnosing medical practitioner with the laboratory confirmation of
diagnosis.
Group C diseases include STI’s, and to preclude identification of the patient, only the first
two letters of the family and given name of the patient and the postcode of the residence are
required.
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Patient consent is not required but they should be informed that their condition is being
reported as required by legislation. (Note that the pathology service also has this
requirement). Patient privacy information forms, available from the department, should be
given to patients.
For certain diseases patients may need to be contacted by the department to obtain more
detailed information. Patients will not be contacted without seeking the consent of the
notifying doctor prior.
RACGP 4th edition Standards 4.2.1.
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7.10 3rd Party Observing or Clinically involved in the
Consultation
Policy
Consent must always be obtained from patients prior to a 3rd Party Observing or being clinically
involved in the consultation.
This includes medical or nursing students, a person included at the doctor’s request, an
interpreter or person to assist with communication, a chaperone, or someone accompanying the
patient to the consultation at the patient’s request such as a care rot relative.
In some circumstances the patient or the GP may feel more comfortable if there is a chaperone
present during the consultation. For medico legal reasons it is recommended to consider offering
a chaperone for unaccompanied children.
In some cases it may be necessary to provide the 3rd Party with access to the patient’s medical
records. Consent may be required.
Procedure
Ideally we ask the patient to consent to a 3rd Party being present during the consultation when
making the appointment and re check that this consent remains upon arrival for their
appointment.
Record their consent in the consultation notes.
A notice is displayed in the waiting room in the case of teaching programs and patients are
handed a slip describing the program on arrival then permission is sought and documented.
It is not acceptable to ask permission for a 3rd party to be present during the consultation in the
consulting room as some patients may feel unable to refuse.
For patients requiring the presence of a 3rd party to assist with communication during a
consultation, Refer to section 5- Non English Speaking Patients
Practice staff are mindful of the particular needs of people with intellectual disabilities who
may not be able to provide consent. In such cases a legal guardian or advocate may need
to be appointed to oversee the interests of the patient.
RACGP 4th edition Standards 1.2.3 & 2.1.3.
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Research Projects
National Privacy Principle 5 requires our practice to have a document that clearly sets out its
policies on handling personal information, including health information. This document,
commonly called a privacy policy, must be made available to anyone who asks for it and patients
must be informed about how their health information will be used including other organisations to
which the practice usually discloses patient health information and any law that requires the
particular information to be collected. Patient consent to the handling and sharing of patient
health information should be provided at an early stage in the process of clinical care.
Policy
Research activity, both within the practice and through reputable external bodies is
encouraged.
Patients consent is essential for involvement in research projects. Whenever any member of
our practice team is conducting research involving our patients, we can demonstrate that the
research has appropriate approval from an ethics committee. The research protocol,
consent procedures and process for resolving problems should be retained by the practice.
Research activities are distinct from audits undertaken by the practice as part of Quality
improvement activities. Research projects require approval from an Ethics committee but “in
house” practice audits do not.
When we collect patient health information for quality improvement audits or professional
development activities, we only transfer de-identified patient health information to a third party
once informed patient consent has been obtained.
Privacy and confidentiality is particularly important especially when considering involvement
in commercial market research activities.
Our practice considers how identifiable their patient information will be using the following:
 identifiable patient information - by which individual patients can be identified.
 de-identified patient information - which can not be traced back to the individual
 potentially identifiable information - could possibly be traced back to individuals or
groups of individuals
Procedure
Research projects involving patient care:
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must have the explicit and documented written consent of the patient
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the patient must receive a written and oral explanation about the research and be able to
withdraw consent at any time
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the project must be approved by a relevant human research ethics committee (HREC)
established under the NH&MRC guidelines.
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privacy laws must be adhered to
Research Projects involving research or clinical audits using de-identified data should ideally
have patients consent. This can be in more general terms such as by waiting room notice or
practice information sheet.
 extreme care must be taken not to allow patient identification from small and/or
unusual cohorts.
For QA&CPD activities that require the transfer of patient information outside the practice
(e.g. NPS activities) we need to:
 ensure the activity complies with relevant guidelines on QA&CPD (issued by an
appropriate specialist medical college)
 ensure the activity is approved by that college
 retain a copy of the QA&CPD approval for the activity
 obtain patient consent if transferring identifiable patient information.
 transfer data in accordance with the written procedure in Section 6 of this manual
ensuring electronic transmission over a public network is encrypted
The practice should retain a record of the request for participation in any research project,
including the research protocol, consent procedures and process for resolving problems
should be retained by the practice.
RACGP 4th edition Standards 4.2.1.
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7.12 Management of a Patient Refusing Treatment or
Advice
Policy
This practice takes an active approach to ensure the best outcomes for patients at all times even
if they choose to reject investigation and/or management advice.
Our practice endeavors to help our patients understand the importance of medicines and
treatment advice to help them make informed decisions about their health care.
Our clinical team can demonstrate how we provide care for patients who refuse a specific
treatment, advice or procedure.
Procedure
Staff and doctors are to respect the right of all patients to make investigation and treatment
choices or to seek a further clinical opinion.
Patients should be advised to notify the doctor or nurse if they want to refuse a specific advice or
procedure.
An appropriate risk management strategy to be followed includes ensuring that:
 the patient has been provided with the full range of options available, including the risks
and benefits of each to enable them to make an informed choice.
 the consequences of the choices made are explained including those of
non-investigation and treatment.
 the patient is offered continued monitoring, support or timely referral appropriate to their
choices. This may be to another GP within our practice or to another practice.
 full documentation of the actions taken above and any referrals (including dates) to other
care providers in the medical record is essential.
RACGP 4th edition Standards 2.1.1.
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7.13 Refusal to Treat a Patient
Policy
The practice or individual clinical team members have the right to refuse to treat patients in
defined circumstances and ensures arrangements are made for the timely transfer of the patients
care to another member of the clinical team in our practice or to another practice.
Procedure
Any refusal to treat a patient is done for substantial reasons not based on discrimination (gender,
sexual preference, religion, race, illness type)
Patients in emergency situations will always be treated to the best of our ability. Emergency
medical treatment is defined as treatment that is necessary to:
 save a patient’s life
 prevent serious damage to health
 prevent or alleviate significant pain or distress
Reasons that may give rise for a GP or other member of the clinical team to no longer consider it
appropriate to treat a particular patient include breakdown in the doctor patient relationship,
patient threats or aggressive behaviour, overloaded practice or patients with conditions outside
the range treated by the doctor
An appropriate risk management strategy to be followed includes ensuring that
 the patient has been provided reasons why they cannot have ongoing treatment at this
clinic.
 the patient has been provided with alternative possible treatment locations and written
referral if appropriate.
 any complaints that may arise are dealt with according to the complaints procedure.
 full documentation of the actions taken above in the medical record is essential.
Our practice will endeavor to assist such patients with ongoing care including referral to other
health care providers and transfer of any medical history.
RACGP 4th edition Standards 2.1.1.
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7.14 Practice Equipment
Policy
The medical equipment, furniture and resources of this practice are appropriate and
adequate to ensure:
 comprehensive primary care and resuscitation
 patient, staff and visitors safety.
Any legislative requirements are met and complied with.
We maintain a register of equipment which includes the scheduling requirements for service
or maintenance. Any maintenance and calibration requirements are undertaken on a regular
basis in accordance with the manufacturer’s instructions to ensure the equipment is
maintained in good working order.
Our staff are informed and educated about any relevant standards or guidelines relating to
the operation or use of specific practice equipment.
Procedure
Practice staff members are instructed in the use of the practice equipment to ensure
equipment is used and maintained in a competent manner.
Electrical safety checks and biomedical checks are performed annually or as required.
Maintenance, repairs, electrical and biomedical checks are documented in the equipment
register. This register is retained as proof of the practices quality control and preventative
maintenance program.
Furniture used by the staff and in the patient waiting areas is maintained in good condition,
is ergonomically effective and can be easily cleaned and wiped down.
RACGP 4th Edition Standards 5.2.1.
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7.14.1
Medical Equipment and Resources
Policy
The practice has all basic equipment and emergency drugs expected in a general practice. The
practice ensures that these are maintained, safe and in a serviceable condition at all times.
The available equipment is sufficient for the procedures commonly performed within our practice
and meets the needs of our patients.
Our practice maintains our key equipment according to a documented schedule
Members of the clinical team are consulted about the equipment and supplies the practice uses
or purchases.
Procedure
The practice has the necessary medical equipment to ensure comprehensive primary care and
resuscitation, including the following:
 auriscope
 blood Glucose monitoring equipment
 disposable syringes and needles
 equipment for resuscitation, equipment for maintaining an airway (including airways for
children and adults), equipment to assist ventilation (including bag & mask), IV access,
and emergency medicines
 examination Light
 eye examination equipment (e.g. fluorescein eye staining)
 gloves (sterile & non-sterile)
 height measurement device
 at least one height adjustable patient examination couch
 measuring tape
 monofilament for sensation testing (10g Nylon)
 ophthalmoscope
 oxygen
 patella hammer
 peak flow meter or Spirometer
 scales
 spacer for inhaler
 specimen collection equipment
 sphygmomanometer (small, med and large cuffs)
 stethoscope
 surgical Masks
 thermometer
 torch
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tourniquet
urine testing strips
vaginal Specula
visual acuity charts
x Ray viewing facilities
Our practice has timely access to a
 spirometer
 electrocardiograph
(*insert description of your arrangements for timely access to Spirometery & ECG if it is not
located in your practice).
(* Insert any additional equipment the practice may have depending on the type of practice and
the interests and requirements of the doctors & the maintenance of such equipment. E.g.
defibrillator).
Relevant staff are trained in the care, use and maintenance of equipment and where appropriate
to analyse and interpret any results.
Liquid Nitrogen and oxygen are hazardous materials and are therefore stored securely and staff
are trained in their safe use.
Maintenance schedule
Key clinical equipment is present and in working order and is appropriately maintained in
accordance with the maintenance schedule recommended by manufacturer and checked
regularly by suitably trained practice staff.
(*insert you practice equipment maintenance sheet)
RACGP 3rd Edition Standards 5.2.1.
RACGP 4th Edition Standards 1.4.2 & 5.2.1.
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7.14.2
Doctor’s Bag
Policy
All of our doctor’s have access to a fully equipped Doctor’s Bag for emergency care and
routine off site visits. When not in use the doctor’s bag is stored securely.
In some instances doctors may share a doctor’s bag or items may be kept in two smaller
bags. Required items may be added to the bag prior to use to avoid doubling up on
equipment.
The practice nurse, in conjunction with the Doctor regularly reviews the contents of doctors
the bags and in addition to checking the condition and expiry date of equipment,
consideration is given to the addition of any items depending on the practice location,
clinical conditions encountered, the shelf life and climatic vulnerability of various medications
and the size of the bag.
Where doctors’ bags are shared, the arrangements are reviewed on an ongoing basis to
ensure that doctors have access the bag when required. Additional bags are purchased if
required.
Sensible security measures are taken at all times and any relevant legislation or regulations
relating to S8, S4 and drugs of dependence are adhered to. (Refer section 7 Drug Storage,
supple and administration)
In addition to containing the required equipment the bag also contains the recommended
medications. Additional items and medications may also be added after consideration of the
clinical conditions likely to be encountered.
The contents of our Doctors Bag are checked regularly to ensure items remain in date and
are restocked and medication administration records are maintained. (Refer section 7
Checking and rotating medical supplies)
Procedure
When attending an off site consultation or emergency each doctor has a fully equipped
Doctor’s Bag containing:
 auriscope
 disposable gloves
 equipment for maintaining an airway in both adults and children
 in date medicines for medical emergencies
 opthalmoscope
 practice stationary (including prescription pads and letterhead)
 sharps container
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sphygmomanometer
stethescope
syringes and needles in a range of sizes
thermometer
tongue depressors
torch
Each doctor maintains the Bag by replacing used items and maintaining the dangerous drug
register including keeping the supplies of drugs at optimum levels.
Three monthly reviews of Bag’s contents are undertaken by the Practice Nurse in
conjunction with the doctor. The bag contents, including equipment and stock levels of
drugs, are systematically checked. All drugs must be “in date” and the dangerous drug
register accurate and completed. Any out of date items are discarded as per policy. The
contents and availability of Doctors bags are a standing item on the agenda of our clinical
meetings.
A list of mandatory items and others as per Practice policy are kept inside the Doctor’s bag
with a copy held in the Practice Nurse’s office. If the doctor’s bag does not contain all the
mandated items as dedicated equipment then the doctor must routinely add such items
before leaving the practice. Commonly this applies to the otoscope and opthalmoscope as
these items are expensive to duplicate.
Annually, the Practice Nurse works with each doctor to conduct a major review of the items
to determine if current equipment is adequate based on accepted good clinical practice.
When not in use the doctor’s bag is stored securely in the practice or remains in the boot of
the Doctors car. When the doctor is going on leave arrangements are made for the secure
storage of the bag.
When selecting emergency drugs in the doctors bag consider:
 the health needs of the community,
 the location of the practice,
 the types of emergencies likely to be encountered
 the shelf life and climatic vulnerability of medicines also needs to be considered.
 the availability of emergency drugs at the practice if the doctor’s bag has been taken
by another doctor.
RACGP 4th Edition Standards 5.2.2.
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Vaccine Storage
December 2012
The vaccine storage section of this policy and procedure manual has been superseded by
the Vaccine Management Policy and Procedure Template located in AGPAL’s resource
area QbAY under Standard 5.3Clinical support processes.
Please refer to the vaccine management policy and procedure template. The above
template can be combined with this policy and procedure manual if you wish to create one
manual.
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7.14.4 Vaccine Administration
Policy
Vaccines are administered and recorded according to the Australian Standard Vaccination
Schedule Guidelines to ensure individuals and the general public are protected from preventable
diseases.
To assist patients to make informed decisions about their medicines and to understand any
medication safety requirements we recognise that patients need to understand the purpose and
importance of medicines. We believe this also helps our patients to comply with the
recommended treatment plan. We support our verbal information with leaflets where possible.
The clinical team ensures that medicines (including vaccines) are acquired, stored,
administered, supplied and disposed of in accordance with manufacturers’ directions to
maintain the potency of our vaccines.
Vaccines are classified as Schedule 4 medications and we comply with drugs and poisons
regulations and legislation.
We observe the principles of correct patient identification and handover during the process
of vaccination.
Procedure


follow the Australian Standard Vaccination Schedule and the recommendations of the
NHMRC at all times for routine immunisations. Specific evidence, guidelines and the
manufacturer’s instructions should be followed for travel and other more specialised
immunisation.
prior to administering any vaccines ensure there are adequately trained staff, emergency
equipment and drugs available to deal with serious adverse post-vaccination
complications.
RACGP 4th edition Standards 5.3.1, 1.5.2.
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7.14.5 Drug Storage, Supply and Administration
Please note: RACGP 4th Edition Standards state “Practices must comply with jurisdictional
requirements on Schedule 4 and Schedule 8 medicines.” The requirements can vary in
different states and Territories of Australia. Failure to comply with the legislation renders
individuals and practice entities liable to prosecution. Compliance with legislation does not
ensure compliance with other professional standards and other accreditation requirements
which should also be observed.
Policy
The clinical team ensures that medicines (including samples, vaccines and medical
consumables) are acquired, stored, administered, supplied and disposed of in accordance
with manufacturers’ directions and Legislative requirements applicable to the state of (*insert
name of state), where our practice is located.
Our practice does not hold a Health Services Permit (HSP) therefore all Schedule 8, 4, 2 & 3
medications are stored, prescribed and administered in line with the requirements of the
Drugs, Poisons and Controlled Substances Act 1981 and the Drugs, Poisons and Controlled
Substances Regulations 2006.
In line with accreditation standards:

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our patients are informed about the purpose, importance, benefits and risks of their
medicines and are made aware of their own responsibility to comply with the
recommended treatment plan.
our clinical team can access current information on medicines and review our prescribing
patterns in accordance with best available evidence.
our clinical team works towards maintaining a current and accurate medication list for our
patients, especially those on multiple medications.
our clinical team can demonstrate how we ensure other health providers to whom we
refer or hand over our patients can access an accurate medicines list.
the use by date of all drugs is checked on a systemic basis.
we observe the principles of correct patient identification
Procedure
To reduce the risk of errors when prescribing or referring, general practitioners ensure the
patient’s medication list is up-to-date. Prior to prescribing or changing treatment our doctors and
other clinical staff clarify a patient’s current medicines list and known allergies. Single use
medications, including antibiotics, should be removed from patients’ records when they are no
longer required. Care is taken with sound-alike or look alike medicines, particularly when using
‘drop down’ boxes in electronic prescribing programs.
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We also encourage reviewing the medicines list with the patient to provide an opportunity to
assess the patient’s compliance with a medication regime and to identify the need for any further
education/support.
Where appropriate doctors provide patients with a copy of their medicines list which is updated
when their medicines are changed.
It is useful to include all medicines (prescription and non-prescription medicines and
complementary healthcare products, if known) on the medication list.
General practitioners need to be aware of the use of complementary medicines and the potential
for side effects and drug interactions with conventional medicines. This should be noted on
letters of referral including those for hospital admissions.
All clinical staff ensure correct patient and patient record using 3 accepted patient identifiers,
name, DOB, address & gender before administering any medications, or writing any
prescriptions. When patients ask for a repeat of their medications without attending the
practice we require the request in writing and it must contain the name, address and DOB.
We also correctly identify patients when they come to collect their prescriptions by asking
the person collecting to sign
We help our patients to understand the Medication purpose, options, benefits and risks.
Where possible we use written material to support this.
Where patients cannot understand written language or where information is not available in
the patient’s language, the use of pictorial media or translators may be appropriate. It is
particularly important that patients understand the difference between generic drugs and
trade named drugs so dosage problems are avoided.
Our clinical staff can access the Therapeutic Guidelines and other references to refer to
where appropriate. We also encourage the use of the Home medications reviews for eligible
patients.
Consumer information about the practice prescribing policy is available to patients and
displayed in the waiting room.
Definitions:
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
“Schedule 8 drugs” (Labelled controlled Drug) are drugs with more strict legislative
controls. A permit might be required before prescribing Schedule 8 poisons. E.g.
morphine(Kapanol, MS-Contin), pethidine, oxycodone(Oxycontin, Endone),
methadone(Physeptone), hydromorphone(Dilaudud), flunitrazepam(Hypnodorm),
fentanyl(Sublimaze),
“Schedule 4 drugs” (Labelled Prescription only medication) include all other
drugs for which prescriptions are required e.g. diuretics, oral Contraceptives,
antibiotics, some compound analgesics (Panadeine Forte), vaccines and many
others
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
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The term “Drugs of Dependence” is used to describe all Schedule 8 plus those
Schedule 4 poisons that are subject to misuse or trafficking e.g. benzodiazepines,
propoxyphene(Digesic, Doloxene), anorectic drugs (Tenuate Dospan, Duromine),
and anabolic. Steroids .Doctors should take additional precautions before
prescribing S4drugs of dependence.
Prostaglandins, Ovulatory Stimulants and Retinoids (e.g. isotretinoin, acitretin,
clomiphene, dinoprost) are Schedule 4 poisons that may only be prescribed by a
medical practitioner with the appropriate qualifications and expertise and who holds
a warrant to prescribe the drug or by a medical practitioner acting in accordance
with the direction of the warrant holder (prescription to be endorsed with the name
of the warrant holder).
“Schedule 2 & 3 drugs” are those labelled Pharmacy medication or pharmacist
only medicine. These can only be supplied in an open shop by pharmacists.
Doctors must use and supply these in a similar manner to S4 drugs.
Storage & Access Requirements
Schedule 4 and Schedule 8 poisons (inc. Doctor’s Bag Emergency Drugs, Professional Samples
and vaccines) are obtained on the authorisation of the medical practitioner(s). These drugs are
the responsibility of the medical practitioner(s) and subject to regulatory controls.


in relation to drugs in a general practice, a nurse is not authorised to possess Schedule 4
or Schedule 8 poisons except when required for administration to a specific patient,
under the care of that nurse. Unless it is an emergency written authorization by a medical
practitioner is required prior.
registered Nurses can only access locked drug storage facilities to assist the doctor with
necessary activities, such as medical treatment, stock checks and reordering, under the
direction/supervision of a doctor who is personally present.
Schedule 8 drugs
Storage:
 S8 poisons must be stored in a locked facility, fixed to the floor or wall and meeting
the minimum security requirements detailed in Regulation 35(1.) Storage facilities for
Schedule 8 poisons must remain locked at all times except when it is necessary to
open it to carry out an essential operation such as medical treatment, stock checks
and reordering. Keys & combinations must not be accessible to or known by
unauthorised persons.
 when required to be transported for use in other locations, S8 drugs must be stored
in a locked receptacle (e.g. doctors Bag), in the doctors possession. If the receptacle
is necessarily out of the doctor’s immediate possession it should be secured, out of
sight, in a lockable facility (e.g. locked cupboard or locked vehicle) to prevent
unauthorised access.
 up to 6 divided doses (e.g. amps) of a S8 poison, for emergency use, may be stored
in a locked facility that does not comply with Regulation 35(1).
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Schedule 4 drugs
Schedule 4 poisons including sample packs may be stored in a filing cabinet, cupboard or
drawer, usually in the treatment room, (or other area e.g. storeroom). If an authorized person
(usually a medical practitioner) is present the storage facility may remain unlocked at their
discretion. This option requires the storage facility to be locked when the authorized person/s are
not present.
S4 drugs of dependence are either stored in the same manner as other S4 poisons or in the
drug cabinet with S8 poisons again at the discretion of the authorised person.
Schedule 4 vaccines that require refrigeration must be stored in either:
 a lockable refrigerator that is locked when an authorized person (usually a medical
practitioner) is not present.
 or in a refrigerator secured within a lockable room that is locked when an authorized
person is not present.
 nurse Immunisers are authorised to have access to specific vaccines and
medications to manage anaphylaxis.
Schedule 2 & 3 drugs
It is recommended these are stored and handled in a similar manner to Schedule 4 drugs to
prevent unlawful supply.
Prescription pads and pages for computer generated prescriptions are stored in a similar
manner to S4 drugs.
Administration & Records
Nursing
Depending on professional scope and competencies, Division 1 registered nurses or Medication
endorsed Enrolled Nurses (formally Division 2) can only administer S4 or S8 medications when
 there is a recent written instruction from a medical practitioner identifying the patient,
medication, dose, time, date and route of administration and date the order was written.
 an oral instruction from a medical practitioner if an emergency exists with written
confirmation ASAP by the doctor and nurse.
 on the written transcription of the oral instruction (given by a doctor in an emergency) by
the nurse who received those instructions. Must be countersigned ASAP by the doctor
 to the designated patient in accordance with the directions on the label when the
medications have been dispensed to the patient by a pharmacist or medical practitioner.
Registered nurses must document any medications administered in the patient’s medical
records, and sign the entry or use their individual log in.
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Enrolled nurses may have limitations on the routes of drug administration or types of drugs they
can administer depending on the endorsements they have attained in their training. (may not be
able to administer via the IV route).
Nurse Immunisers, employed or contracted by medical practitioners, may have access to
vaccines that are specifically approved by the Secretary (Department of Health) for use in
vaccinations and to Schedule 4 poisons necessary for the treatment of anaphylactic reactions to
the vaccines. For further information and the list of vaccines, please refer to the DPRG website
(www.health.vic.gov.au/dpu/approve.htm).
Nurse Immunisers should familiarise themselves with legislative issues that are applicable to
their situation.
Records
Records of all transactions (administration and/or supply) in S4 and S8 poisons must be true and
accurate*, retained in a readily retrievable form for 3 years.
S4 records must contain the patients name and address, the date of the transaction, the identity
of the person administering the medication and information that unambiguously identifies the
medication (including dose and route of administration if applicable).
Additional records for S8 drugs are kept to personally account for every dose of a S8 drug.
Transaction records of all S8 drugs received, transferred to the Doctors Bag, administered or
disposed of must be maintained. A separate record (usually a drug register or administration
book) is required, in a form that shows the true and accurate balance remaining after each
transaction and that cannot be altered without detection. (Loose-leaf books are not acceptable).
Each medical practitioner should have their own record book. (these are available from the
RACGP). Appropriate documentation includes the date of transaction, the name of the doctor
authorizing the administration of the drug, the name and address of the patient to whom the drug
was administered, the quantity used a progressive balance of each drug on hand at the
conclusion of the transaction, and the initials of the authorized person who administered the
drug. It must also record additions to stock levels from the pharmacy and disposal of expired
items.
Vaccine Administration
Division 1 nurses that have completed the accredited nurse immuniser course can administer
vaccines (including off site) independently of the medical practitioner.
Division 1 nurses or medication endorsed Enrolled Nurses that are not accredited nurse
immunisers must have a written authorisation and the doctor must be physically available to
assist with anaphylaxis and/or adverse events (including off site).
Enrolled nurses that have not completed medication endorsement are not authorized to
administer vaccines in any circumstances.
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Disposal of expired medications
WhenS2, S3 & S4 drugs reach their “Use by Dates’ then disposal is into the sharps or infectious
waste containers or via the pharmacy.
If a medical practitioner wishes to destroy expired or unwanted S8 poisons, the destruction must
be witnessed by a pharmacist, dentist, veterinary practitioner, nurse or another medical
practitioner. Their destruction must be recorded in the S8 record book by the medical
practitioner and the witness.
Prescribing/supplying
When a doctor supplies S2, S3, S4 or S8 medications (including professional samples), the
medication is labeled and a record of the supply is made.
S4 and S8 labels will require:

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
the name of the patient,
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directions for the correct use of the medicine
the date of dispensing and if necessary an identifying code,
the name , address and telephone number of the medical clinic or doctor providing
supply including the name of the prescribing doctor
directions for storage and expiry date (may be those on the packet if left uncovered).
the brand and generic names of the drug including strength and form.
the words “KEEP OUT OF THE REACH OF CHILDREN”
ancillary labels as specified in the “Australian Pharmaceutical Formulary”.
S2 and S3 labels will require the name, address and telephone number of the medical clinic or
doctor providing supply.
When prescribing or supplying S4 and S8 medications the doctor takes all reasonable steps,
given the time and circumstances that exist at the consultation to ensure a therapeutic need
exists. Prescribing to maintain an addiction is not a therapeutic need and is illegal.
Doctors do not prescribe to support drug dependence or for the purpose of self administration.
(Regardless of whether the treatment was initiated by another medical practitioner).
Doctors check if the patient has any drug allergies or sensitivities prior to prescribing.
In addition, for drugs of dependence, the identity of the patient must be ascertained.
For patients that are not regular clinic patients the doctor may need to:
 consult a previous prescriber.
 contact DHS.
 or insist on a further means of identification.
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Doctors must notify DHS if they believe a patient is drug dependent. DHS treats such
notifications as confidential.
Doctors are reminded that they are not obliged to prescribe the maximum PBS quantity of a
drug. A smaller quantity can often address an immediate need whilst minimising the potential
risks associated with drug-seeking behaviour.
Doctors should refrain from prescribing medications for family members and drugs of
dependence must not be prescribed to family members except in an emergency.
Prescription pads and paper is stored securely in area where patients do not have unrestricted
access or in the same manner as S4 poisons.
Software for prescribing is secured by passwords that remain strictly confidential to individual
prescribers.
Prescriptions contain;
 the full details of the prescriber (including an address and phone number).
 the name and address of the patient.
 the medication (unambiguously).
 the quantity and maximum number of repeats(written in words and figures for S8).
 the prescribers signature (preferably in a manner that prevents a patient adding another
item above the signature).
 precise directions. (Scripts for S8 and S4 drugs are not legal without these).
Computer generated prescriptions for drugs of dependence must also contain key elements in
the prescribers’ handwriting and include dosage amounts in figures and words
Doctors are to obtain permits from the Department of Human Services (DHS) prior to:
 treating a drug dependent person with a Schedule 8 drug.
 prescribing dexamphetamine, methylphenidate or methadone (exemptions may apply,
e.g. pediatricians treating ADHD; patients in oncology or pain clinics at hospital).
 treating a person with any Schedule 8 poison for a period greater than 8 weeks (except
where specifically exempt).
These permits should be filed/ scanned into the patient’s medical record. The police and DHS
will be notified of:
 lost or stolen drugs.
 lost or stolen S8 records.
 when a doctor has reason to believe a person has obtained S8 or S4 poisons (or
prescription for same) by false pretences.
 if a doctor suspects a patient is attempting to procure a prescription under false
pretences.
 loss or theft of prescription pads or paper.
Patients going overseas or patients who find it difficult to access the pharmacy
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The PBS will allow the repeats to be dispensed with the original supply. The Doctor must make
endorse the prescription with the words “regulation 24” for this to occur.
Note: It is illegal to supply medications:
 to Australian citizens not within the country at the time the prescription is written.
 for use other than the designated purpose for which it was prescribed.
 for anyone other than the person named on the prescription.
RACGP 4th edition Standards 5.3.1.
For information on jurisdictional requirements refer to the drugs and poisons branch of the
relevant jurisdiction:
Australian Capital Territory
Pharmaceutical Services, ACT Health
Telephone: 02 6205 1700 Fax: 02 6205 0997
Northern Territory
Poisons Control, Department of Health & Families
Telephone: 08 8922 7341 Fax: 08 8922 7200
New South Wales
Pharmaceutical Services Branch NSW Health
Telephone: 02 9391 9944 Fax: 02 9424 5860
Queensland
Drugs and Poisons Policy and Regulation, Environmental Health Unit, Queensland Health
Telephone: 07 3328 9310 Fax: 07 3328 9354
South Australia
Pharmaceutical Services and Strategy, Department of Health
Telephone: 08 8204 1942 Fax: 08 8226 9837
Tasmania
Pharmaceutical Services Branch, Department of Health and Human Services, Tasmania
Telephone: 03 6233 2064 Fax: 03 6233 3904
Victoria
Drugs and Poisons Regulation Group, Department of Health
Telephone: 1300 364 545 Fax: 03 9096 9168
www.health.vic.gov.au/dpu
Western Australia
Pharmaceutical Services Branch, Disaster Managements, Regulation and Planning Directorate,
Department of Health, Western Australia
Telephone: 08 9222 6883 Fax: 08 9222 2463
The RACGP has produced summaries of the jurisdictional requirements in relation to Schedule 8
medicines, available at www.racgp.org.au/standards/factsheets.
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7.14.6 Clinical References and Resources
Policy
Consistency and quality of care can be assisted by the use of current resources, access to
clinical guidelines and communication between team members. This process is encouraged and
facilitated by the practice clinical leader. (Refer Section 8 Clinical governance).
This practice provides medical, nursing and allied Health workers access to a range of resources
and materials for reference on clinical matters and items of interest for professional development.
General practitioners can access current information on medicines to enable best practice
prescribing.
We are selective about the resources clinical staff to use to support information provided
during a consultation. We aim to ensure they contain culturally appropriate, current and
evidence based information and are obtained from reputable source. Where possible these
resources should be dated, contain the name of the source and referenced to supportive
evidence.
The references available contain information that is consistent with current practice guidelines or
based on best available evidence. In the absence of well conducted trials or other higher order
evidence the opinion of consensus panels of peers is acceptable. References and resources
including practice guidelines should be accessible at the point of care.
There is an organised system of access for all practice staff to journals, clinical guidelines and
other reference material.
The clinical references available and any new additions, deletions or updated versions is
communicated to all staff and clinical team members to assist with consistency in the approach
to diagnosis and management of patient care.
Procedure
(*Insert the guidelines and references available at your practice and how or where they can be
accessed).
At least annually we conduct an audit of our clinical resources and references to ascertain if
they comply with current practices and are providing consistent management and
information to patients across the practice team.
It is a standing item at our clinical meetings to discuss any new clinical issues, resources or
clinical practice guidelines.
Medical publications such as AFP, Modern Medicine and Current therapeutics are kept in the
common room for 1 year and then discarded.
RACGP 4th edition Standards 1.3.1 & 1.4.1, 5.3.1.
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7.14.7 Checking and Rotating Medical Supplies
Policy
Perishable medical supplies including vaccines, pharmaceutical and medical consumables
are correctly stored, stock rotated and discarded if past expiry dates.
Our practice had appointed a designated person to take primary responsibility for the proper
storage and security of medicines, vaccines and other healthcare products.
Procedure
(*insert name and position title of the designated person) maintains a log of areas to be
checked such as the drug cupboard, doctors’ bags, and fridge and other cupboards
containing perishable medical stock kept. The log documents the location, date and initials
of the staff member checking the stock and is kept in the Practice Nurse’s office.
New stock is marked with a coloured dot to indicate the year of expiry to make checking
quicker and encourage easy identification of the oldest stock so it can be used first. Stock is
also rotated in a uniform manner with oldest nearest to the front of the shelf, drawer etc.
All sites are checked 3 monthly with note made in the log to re-check if items will pass expiry
date before the next review. i.e. name of item, location and expiry date.
Items with expired ‘use by dates’ are to be withdrawn from active storage location and
disposed of immediately (according to manufacturer’s instructions or see 7.12.5 for drug
destruction/disposal).
Necessary and regularly used items should be re-ordered on our supply form.
RACGP 4th edition Standards 5.3.1.
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8 Continuous Improvement
8.1 Risk Assessment & Management
Policy
This practice has multiple systems to regularly monitor, identify and report near misses and
mistakes in clinical care and to identify deviations from standard clinical practice that may result
in patient harm.
The practice has appointed a designated member of staff (*insert name) to have primary
responsibility for our risk management systems. These may include clinical and non clinical risks
and events. Specific areas of responsibility can be delegated to other nominated members of the
practice team and these particular responsibilities should be documented in the relevant position
descriptions.
The aim of risk assessment and management is to:
 identify all strategic risks using a risk management process.
 ensure risk management becomes part of day to day management.
 co-ordinate the undertaking of regular formal risk assessments and reviews with staff
involved.
 provide staff with education and policies and procedures necessary to manage risk.
 ensure employees are aware of risks and how to manage them.
 assign responsibility for overseeing the practice risk management systems to designated
staff, and document this in their position description.
 document and regularly review our risk management systems.
 monitor risk profile and implement a continuous improvement approach to risk
management.
 ensure successful implementation of changes and improvements made to our risk
management systems.
Our practice has a documented system for dealing with near misses and mistakes and we
ensure that Doctors, Nurses and other staff involved in clinical care are educated in what to do
and whom to notify when a slip, lapse or mistake occurs, or when there is an unanticipated
adverse outcome. Any improvements that are implemented to prevent identified slips, lapses and
mistakes or potential risks are documented and the practice team is informed.
Our practice has protocols for Non Medical Emergencies such as failure of electricity supply,
telephone or water, fire or false fire alarm, property damage, break-in, abusive or threatening
telephone calls or persons at the practice, leakage of toxic chemicals, bomb threats and letter
bombs, natural disasters and the sudden unexpected absence of staff.
We also have a contingency plan for unexpected events such national or local infection
outbreaks or the sudden, unexpected absence of clinical staff.
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These include a mechanism to ensure the timely acquisition and dissemination of information
(including regular updates) about alerts, emerging diseases, local disasters or emergencies.
Procedure
Staff use the “Adverse Outcome Report” to report any slips, lapses or near misses in clinical care
or deviations in patient care that might result in harm. The medical defence organisation is
contacted for events that might give rise to a claim.
Some of the tools and strategies used in this practice to manage risk include:
 achievement of RACGP standards via the accreditation process
 regular staff and clinical meetings and effective communication with our staff.
 appropriate staff qualifications, induction and training.
 patient feedback obtained via surveys/Suggestion Box /logbook of complaints/
comments.
 documentation of sterilisation procedures including servicing, details of individual
loads/cycles and staff training
 comprehensive medical records and back up of electronic data.
 documentation/ tracking of abnormal results.
 regular reviews of systems and procedures especially as a result of any analysis of
reported near misses.
 logging/recording of telephone exchanges with patients
 ensuring correct identification of patients at each face to face, telephone and electronic
encounter and on correspondence by using “name”, “date of birth”, “gender” or “address”.
 documented contingency plans for events that may disrupt care or stretch practice
resources to the limit, including disasters (e.g. bushfires, prolonged power failure,
sudden staff absence) and disease outbreaks (e.g. pandemic flu).
(*insert where to find your practice contingency plan/s for adverse and unexpected events.)
RACGP 4th edition Standards 3.1.2, 4.1.2.
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8.1.1 Review of Policies & Procedures
Policy
Policies and procedures relating to the administration of this Practice are formally reviewed
on an annual basis or when changes occur requiring earlier review or revision (e.g.
equipment changes).
Our practice has written polices relating to key infection control processes which are
reviewed and updated regularly
Our practice encourages and promotes sharing information about quality improvement and
patient safety including protocol and policy/procedure review or suggestions.
Procedure
Discussion and suggestions for improvement to quality, patient safety or policies and
procedure is a standing item on our practice meeting agenda.
Staff may informally approach the Practice Principal or Manager with suggestions for new
policies and procedures or with revisions to existing policies and procedures.
We have a designated staff member who has responsibility for co coordinating and sustaining
our infection control processes. This includes continually modifying and improving our
procedures and written policies in accordance with the most recent evidence and guidelines and
ensuring the timely dissemination of information concerning changes to infection control
procedures or information about national and local infection control outbreaks.
The Practice Principal, in consultation with the Practice Manager and staff approve all
policies and procedures. Once approved, documentation is amended in this manual and
elsewhere as necessary. e.g. in patient information brochures, clinical manual, and patient
forms.
Analysis of practice data may also inform any changes to services or other practice activities
to improve the health outcomes of our patients. These quality improvement activities may
necessitate a new or revised written protocol.
Formal revision and final approval of all new and revised policies and procedures is
presented at a staff meeting.
To ensure all staff are aware of new policies and recent changes we have a distribution
plan.
RACGP 4th Edition Standards 3.1.1 & 5.3.3.
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8.1.2 Continuing Staff Education
Policy
Continuing Education
The practice GP’s, nurses and other health care providers or administrative staff employed
by this practice and involved in clinical care:
 are appropriately qualified, trained and competent.
 are able to provide evidence of training qualifications and of appropriate current
national medical or nursing registration.
 participate in continuing education relevant to their roles and can provide evidence
of this.
 have undertaken training in CPR within the last 3 years and in the case of GPs this
training must be in accordance with the RACGP QI&CPD recommendations.
Staff education is crucial to effective infection control within the practice. Education needs to be
relevant to the role of particular staff members and needs to start with the staff induction
program. (Refer Section 2 Staff Induction).
Staff education and the evaluation of staff competency needs to be recorded in line with chapter
1 RACGP Infection control standards for office based practices (4th edition).
The administrative staff such as receptionists and practice managers, who do not provide
clinical care:
 have undertaken training in CPR within the last 3 years.
 have undertaken training relevant to their role within the past 3 years.
 can describe or provide records of such training.
The practice employs doctors who are recognised GPs.
 Note: The only exception to this, are other specialists practicing within their
specialty, or trainees undertaking a placement to gain experience in general practice
as part of some other specialist training program. Where recruitment of recognised
General Practitioners has been unsuccessful, the practice ensures that doctors have
the qualifications and training necessary to meet the needs of the patients of the
practice.
This practice ensures that it’s General Practitioner(s) maintain and improve the quality of
care they provide to their patients by participating in the RACGP QA & CPD Program.
 where this is not the case, the practice is able to provide evidence that doctors
participate in quality improvement and continuing professional development to at
least the same standard as the RACGP QA & CPD Program. In addition, medical
staff should participate in Hospital and or Divisions of general practice affiliated
programs and other programs, as relevant. Refer to ‘Training Schedule’ in Section
8.1.2 for further details of training.
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Records of GP continuing professional development activities including CPD points and
activity details are retained by individual GP’s and a copy must be given to the Practice
Manager to retain for the practice records annually.
The practice supports continuing professional development for all of the staff it employs.
Details of activities & dates are recorded and should be retained by the Practice Manager.
Copies of these records or an annual summary should be given to staff for their own
personal records.
All Doctors, Nurses and staff involved in clinical care practice within their legal scope of
responsibilities. We encourage our staff to maintain their knowledge, skills and attitudes
through membership to their professional specialty organisations. e.g. RACGP, AMA,
APNA, AAPM.
Both in house and external training programs are utilised. Staff should obtain a certificate of
attendance or evidence of participation and completion for all training, even informal training
sessions (e.g. provided by the General Practitioners or other staff in the practice).
Certificates should include the main aims or expected learning outcomes of the training, the
number of hours and the qualifications of the person delivering the training.
It is acknowledged that some crucial areas for staff training exist, depending on the staff
member’s role and responsibilities. These training requirements are met according to the training
schedule and documented in each staff member’s employment record.
Education is not limited to professional technical skill updates but includes a variety of
training and educational activities in areas of need as they arise.
Staff are encouraged to identify any training needs they may have and seek to find training
to meet these needs. Usually this occurs in consultation with their supervisor and this
process should be documented.
Staff training may include:
 education at formal institutions.
 educational seminars attended.
 online training.
 in service education given by company sales representatives or other staff.
 reading Journals, evidence based guidelines or researching information for the practice.
New staff are supported with any training they may require to perform their role. This may be
identified prior to commencement or during the induction phase. (Initial 3 months)
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The practice GP’s, nurses and other health care providers involved in clinical care must
provide evidence of current registration each year. The practice manager then copies and
retains this on file.
If a staff member locates a course, education session, workshop, or a meeting that they
wish to attend, they should advise the Practice Manager who will consult with the Practice
Principle and, if approved, authorise attendance and payment. Time may be granted on full
pay for certain meetings, education sessions and courses.
The Practice Principal and / or Practice Manager formally approves the education session in
writing and places details on the Continuing Education file, held in the Administration office.
The Practice Manager liaises with the staff member for application, fees etc. In seeking time
off to attend external sessions, staff should consider other staff and workloads, to ensure
adequate Practice coverage.
An application for study/conference leave form should be lodged with as much advance
notice as possible.
Evidence of all staff training will be documented in the ‘Staff Training Plan’ and ‘Staff Education
Form’.
Training schedule
It is acknowledged that to maintain the staff competency required for the efficient and smooth
running of this practice, and for medico legal reasons, all staff are required to undertake ongoing
training and up skilling and where appropriate competency assessment. The type of training and
up skilling that occurs will be dependent on their position and role within the practice as detailed
in the form below.
Other identified training needs for individual staff members can occur in addition to this list. The
‘Staff Training Plan’ is adhered to and reviewed at the annual performance appraisal.
As other clinical staff may be present during a medical emergency, they need to be trained in
CPR to assist the medical team therefore, at least every 3 years, all members of the practice
team undertake CPR training appropriate to their level.
The CPR training provided to GPs must be:

consistent with the Australian Resuscitation Council (ARC) guidelines

a minimum of 1 hour duration.

delivered by a trainer that has a current CPR instructor’s certificate that complies with
the ARC guidelines.
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CPR training for other clinical staff may be conducted by:
 medical staff and preferably those who have a current CPR instructor’s certificate that
complies with ARC guidelines on instructor competencies, or,
 by an accredited training provider.
CPR training for administrative staff may be conducted by

medical staff or other clinical staff who feel competent to train colleagues and preferably
those who have a current CPR instructor’s certificate that complies with ARC guidelines
on instructor competencies.
OR

by an accredited training provider.
Administrative staff and other relevant non clinical staff should receive triage training in order to
recognise medical emergencies and prioritise appointments for patients with urgent clinical
needs. Triage training may be delivered by clinical staff within the practice or by appropriate
external providers.
The practice team member with delegated responsibility for staff education on infection control
documents in each individual staff training records how the induction program and additional
ongoing training provided (as identified through discussion and competency assessment) covers
infection control as relevant to each staff members role. Training and regular updates should
include:
 hand Hygiene.
 standard precautions & Transmission based precautions including PPE use and the
triage of patients with potential communicable diseases.
 dealing with blood and body fluid spills and managing exposure to blood or body fluids.
 principles of environmental cleaning and reprocessing of medical equipment.
 where to find information on other aspects of infection control in the practice.
 safe handling and disposal of clinical and general waste.
RACGP 4th edition Standards 3.2.1 & 3.2.2 & 3.2.3 & 5.3.3.
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8.1.3 Accreditation & Continuous Improvement
Policy
This Practice is committed to attaining and where possible exceeding the Standards for General
Practice 4th Edition as defined by RACGP and as such AGPAL is our chosen accreditation
organisation.
The practice team is committed to encouraging quality improvement and identifying opportunities
to make changes that will improve the clinical care of patients and activities to promote health in
the overall practice population.
The practice uses patient and practice data to identify opportunities for improvement and to
monitor evidence of improvement occurring.
Quality improvement or clinical audit activities for the purpose of seeking to improve the delivery
of a particular treatment or service is considered a directly related secondary purpose for
information use or disclosure. Therefore we do not need to seek specific consent for this use of
patients’ health information. However we include information about quality improvement activities
and clinical audits in our practice consent form for the collection and use of health information.
Our practice can demonstrate improvements we have made in response to the analysis of
patient and others feedback, including complaints, and where appropriate we provide information
to patients about improvements made as a result of their input or feedback.
Our practice undertakes quality review activities such as audits, routine data checks, accounts
reviews and medical record reviews.
Our Practice has a planned approach for improvements where possible using the Plan Do Study
Act (PDSA) Cycle to provide evidence that the practice has implemented a quality improvement
plan, and that the outcome has been reviewed
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Discussion and suggestions for improvement to quality and patient safety is a standing item
on our practice meeting agenda.
Patient feedback is an essential component of our quality improvement activities.
Accreditation via a peer assessment of our performance against the RACGP 4th Edition
standards is a driver of quality improvement.
(*Delete this section in italics if you are a non computerised practice)
Our practice utilises information management techniques that allow us to collect and analyse our
data. Consistent data coding systems are used to facilitate this process including using “drop
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down box” functionality where possible instead of “free text” entries. We also use the search
tools in our clinical software and the (*insert which tool/s you use here) data extraction tool.
We utilise national registers to assist with quality improvement activities including our quarterly
PIP statements, reports from the Australian Childhood Immunisation Register and PAP
screening data.
Quality improvement is a team activity and provides opportunities for all staff members to
contribute to achieving improvements. We can describe and have documented aspects of our
practice that we have improved in the past 3 years including examples of where we have used
relevant patient data to implement the Plan Do Study Act (PDSA) Cycle of quality improvement.
The Plan Do Study Act (PDSA) Cycle of Quality Improvement
The Plan Do Study Act cycle is a tool that provides a framework for developing, testing and
implementing changes.
The four steps in the PDSA cycle are as follows;
Step 1: Plan
Planning the improvement activity involves identifying:
 what the improvement activity is
 who needs to be involved, or made aware of the activity
 when will the activity take place
 where the activity will take place
 what outcomes are predicted
 what data will be collected to measure the outcomes of the activity.
Step 2: Do
Implementing the improvement activity includes:
 involving the appropriate staff
 documenting the steps taken
 seeking feedback from all involved.
Step 3: Study
Studying the improvement activity involves:
 analysing and reflecting on the results
 reviewing whether the activity was successful
 determining if the results meet expectations
 identifying whether further improvements need to be implemented.
Step 4: Act
Acting on the improvement involves:
 identifying what will be taken forward from this cycle
 will something else be tested using a new PDSA cycle.
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If the CQI activity has been successful the practice looks at:
 how new policies or procedures will be incorporated into the way the practice team
works.
 how staff will be made aware of the change.
 where the new activity will be documented.
 how the new activity will be monitored to ensure all staff are participating.
If the CQI activity has been unsuccessful the practice looks at:
 what the activity has shown.
 what different improvements might be able to be made.
RACGP 4th edition Standards 2.1.2, 3.1.1, 3.1.3, 4.2.1.
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8.1.4 Patient Feedback
Policy
Our practice encourages patients and other people to give feedback, both positive and negative,
as part of our partnership approach to healthcare, and we have processes in place for
responding to feedback
In order to respond to patient feedback and make improvements, practices need to identify the
person in the practice with primary responsibility for examining issues raised by patients and
facilitating improvements in the practice. (*insert the name of the staff member with this
responsibility in your practice).
Opportunities are available for patients and other visitors to tell us, ‘How we are doing.’ Our
Suggestion Box in the waiting room allows patients to give us personal feedback on a day to day
basis. We aim to follow-up ideas and acknowledge notes of appreciation where we can.
Where possible patients are encouraged to raise any concerns directly with the practice team
and attempts are made for a timely resolution of such concerns within the practice in accordance
with our complaints resolution process.
We seek structured /systematic patient experience feedback at least once every 3 years which
meet the requirements outlines in the RACGP publication “Learning from our patients”. Feedback
collected includes, but is not limited to, the following 6 categories that are considered critical to
patient’s experiences within healthcare facilities.
 access and availability
 information provision
 privacy and confidentiality
 continuity of care
 communication skills of the clinical staff
 interpersonal skills of clinical staff
The data collected is analysed and the findings, including any improvements made, are
communicated back to our patients.
As part of our Risk Management Activity, a log of incidents, including complaints, is maintained in
an event log and the incident is noted on the patient’s history.
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At any time patients may provide feedback or make a complaint.



a notice is displayed in the waiting room and in the practice information sheet advising
how to make a complaint to our practice. We also advise the contact information for the
State/Territory health complaints agency and the commonwealth agency.
the Suggestion Box is located at reception and reception staff ensure there is an
attached pen and paper available.
staff are trained to ensure patients of the practice feel confident that any feedback or
complaints made at the practice will be handled appropriately.
At least every 3 years we use a systematic method for collection patient experience
feedback.
We have purchased or downloaded a copy of the RACGP publication “Learning from our
patients” (*insert where this is located) and we meet the requirements outlined in this
publication.
We collect feedback using:
(Practices have four options for collecting patient experience feedback select option/s used
and delete others)
 an RACGP approved questionnaire
 an individual practice specific questionnaire we have developed*
 a series of focus groups with patients*
 a series of interviews with patients.*
*Note: Where practices choose to collect patient feedback using methods other than an
RACGP approved questionnaire, these methods need to meet the requirements outlined in
the RACGP Patient feedback guide- Learning from our patients.
Data collected is analysed to identify potential opportunities for quality improvement. (Refer
Section 8 Accreditation and Continuous Improvement)
We communicate the findings of our feedback and any improvements made back to our patients
using either a poster in the waiting room, newsletters, the website or individually as appropriate.
RACGP 4th edition Standards 2.1.2.
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8.1.5 Management of Potential Medical Defence Claims
Policy
In line with the Common Law system of damages and taking into account reforms which came
into effect in Victoria on October 1st 2003, this practice undertakes to notify their Medical Defence
Organisation (MDO) immediately if there is suspicion that a claim will be initiated by a party
against the practitioner or practice, or upon receipt of an Impairment Certificate served upon the
practice or practitioner by a party making a claim. This practice understands that, since the
reforms, the organisation or person against whom the claim is made has only 60 days from
receipt of the impairment certificate to accept or challenge the claim.
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All staff should forward any legal documents delivered to the practice, or any complaints that
could result in a claim, directly to the Practice Manager who will notify the parties concerned.
The case is not discussed with anyone other than the relevant medical defence organisation, and
personal notes and communication with the insurance organisation are not kept in the patient’s
practice record.
Subpoena to produce records:
 check the description of what is to be produced
 the original records must be provided, but keep a photocopy
 place the original records in an envelope with the patients name clearly marked, plus the
court number which will be shown on the subpoena). Mark the envelope “confidential
Medical records”. Seal the envelope and attach a copy of the subpoena to the envelope.
 arrange for a courier to deliver the records to the court. NOT TO THE REQUESTING
SOLICITOR. Discuss courier arrangements with the solicitor who has served the
subpoena. If they do not provide the courier you are entitled to charge for the courier
service. Make sure you use a reliable firm and that they sign for the records and the
records go directly to the court.
 the court will return the records in due course.
Should an Impairment Certificate be served, both the Victorian Managed Insurance Authority
(VMIA) and the practice’s MDO will be notified and forwarded a copy of the Impairment
Certificate.
Members of the public may make a notification to AHPRA about the conduct, health or
performance of a practitioner or the health of a student. Practitioners, employers and education
providers are all mandated by law to report notifiable conduct relating to a registered practitioner
or student to AHPRA.
RACGP 4th edition Standards 3.1.2.
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8.1.6
Continuity of Care
Policy
This practice aims to encourage patients to develop a positive relationship with their doctor and
practice staff over time to enhance the provision of high quality comprehensive patient care
including effective health promotion and strategies for the early detection of disease.
This practice has strategies and policies that encourage continuity of comprehensive care by
facilitating:
 relational continuity: the sense of affiliation between the patient and the doctor ‘my
doctor’.
 management continuity: consistency of care by various people involved in the patients
care.
 informational continuity: Maintenance of information across health care events through
documentation, handover and review.
Our medical notes demonstrate relational, management and informational continuity of
comprehensive care. In addition 50% of our active patient health records have entries extending
back over two years.
Our practice provides home visits for our patients and has an agreement with an after hours
provider who provides communication back to the practice about the nature of any after hours
care delivered.
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Relational continuity
All members of the practice team appreciate that it is important that our patients have an
opportunity to develop an ongoing relationship with the practice, Doctors, nurses, allied health
workers and staff members.
 our appointment schedule has a separate appointment list for each general practitioner,
nurse or allied health worker.
 patients are able to request their preferred General practitioner or other health care
provider when making an appointment and this request is accommodated if possible.
 where possible “walk ins” are also able to see the doctor of their choice, or the doctor
they saw on previous visit/s.
 should the GP be retiring or leaving or taking extended leave we endeavour to minimise
the disruption to care. Patients are given at least 4 weeks notice and are informed of who
will take over their care in the absence of their usual Doctor and a clinical handover
either written, face to face or via the telephone is provided.
 special consideration is given to patients with high needs and, in the event of practice
closure or should these patients be taking a vacation we endeavour to assist these
patients with finding alternative appropriate care and consideration is given to measures
to make their records available.
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Management continuity
General practitioners, nurses and allied health workers co ordinate the management of individual
patient care and endeavour to maintain a consistent and cohesive approach.
 plans for the management of patients with complex clinical conditions are documented in
the patient health record to ensure consistent clinical care and advice is provided to the
patient.
 clinical handover occurs when the patients care is handed over to another health
professional both within and external to the practice.
 patient resources to support preventative activities or to assist with providing information
about specific diseases or management choices are shared by all Doctors, nurses and
allied health professionals to ensure as much as possible patients receive consistent
information and advice from all involved in their care.
 to ensure clinical care is consistent with the best available evidence, culturally sensitive
and consistent throughout the practice, Doctors, nurses and allied health professionals
regularly attend clinical meetings or staff in-service together.
 health summaries are updated to reflect recent significant events as information is
gathered by staff providing clinical care, so that care remains responsive to individual
patient needs.
 issues raised in consultations are documented in the patient health record to enable
other doctors, nurses or allied health workers providing subsequent clinical care to follow
up previous problems.
 patients are enrolled in diseased prevention and health promotion activities where
eligible and receive reminders for health checks.
 children receiving immunizations are recorded on the practice immunization reminder
schedule and notified when future vaccinations are due.
 where preventative activities such as Pap screening or immunization are provided the
patient is bulk billed.
Informational continuity
Doctors, nurses and allied health workers involved in the care of patients within the practice
have access to the patient’s health record and a clinical handover occurs whenever there is
an interface of care by different providers.
 clinical care administered by members of the practice team is documented in the patient
health records by the health professional administering the care.
 letters and correspondence from other external care providers e.g. Allied health can be
read by all members of the practice team providing care.
 external care providers are notified should the planned management of a patient change
or be reviewed.
 clinical handover of patient occurs both within the practice, to other members of the team
and to external care providers whenever there is an interface of care by different
providers. This may be face to face, written, via telephone and by electronic means.
RACGP 4th edition Standards 1.1.1, 1.4.1, 1.5.1, 1.5.2.
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8.1.7
Clinical Governance
Policy
The RACGP 4th Edition Standards describe Clinical governance as a ‘system through which
organisations are responsible for continuously improving the quality of their services and
safeguarding high standards of care by creating an environment in which excellence in clinical
care will flourish’.
We recognise that good clinical leadership is required to engage the entire practice team in a
commitment to excellence by nurturing a culture of openness and mutual respect that allows just
and open discussions about areas for improvement.
We aim to develop an organisational culture where participation and leadership in safety and
quality improvement are resourced, supported, recognised and rewarded and all staff feel
accountable and involved in monitoring and improving care and services.
To promote clear lines of accountability and responsibility for encouraging improvement in safety
and quality of clinical care and the sharing of information about quality improvement and patient
safety within the practice team we have appointed leaders who have designated areas of
responsibility for safety and quality improvement systems within the practice.
Our leaders promote a multidisciplinary team approach to endorse a climate of safety and quality
that does not blame, but rather seeks to solve problems.
Our practice leaders oversee the delegation of tasks to others but retain accountability for quality
and safety.
Roles and responsibilities are specified in our position descriptions and all members of the
practice team are aware of the designated leadership responsibilities of key staff.
Our leaders promote compliance with the RACGP 4th Edition Standards for general practice and
relevant jurisdictional legislation or accepted industry requirements.
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We have nominated key staff with primary responsibility for the clinical governance of specific
areas. Our leaders are resourced and supported to make improvements in their specified areas
of responsibility through the coordination of practice activities such as:
 education and information sharing
 clinical audits/research/data analysis
 promoting evidence based practices
 risk management analysis-clinical and general
 openness to suggestions and feedback
 policy and Procedure development and review
Our leaders can delegate specific areas of responsibility to other nominated members of the
practice team and these particular responsibilities should be documented in position
descriptions.
All members of our practice team can identify the staff members with primary or delegated
responsibility for:
 RACGP STD 3.1.2 Clinical Risk management systems including receiving and
disseminating any important communication or updates (e.g. health alerts) and
contingency plans
 RACGP STD 3.1.3 Clinical leadership
 RACGP STD 4.1.1 Quality improvement and risk management (non clinical)
 RACGP STD 4.1.1 Clinical care
 RACGP STD 4.1.1 Information management
 RACGP STD 4.1.1 Human resources
 RACGP STD 4.1.1 Feedback and complaints
 RACGP STD 4.1.2 Occupational Health and Safety (Health and Safety representative)
 RACGP STD 4.2.1 Privacy Officer
 RACGP STD 4.2.2 Electronic systems and computer security
 RACGP STD 5.3.1 Proper storage and security of medicines
 RACGP STD 5.3.2 Cold chain management
 RACGP STD 5.3.3 Infection control within our practice. (e.g. sterilisation process, staff
immunisation, staff education).
 RACGP STD 5.3.3 Environmental cleaning,
These responsibilities are noted in position descriptions.
RACGP 4th edition Standards 3.1.3, 5.3.1, 5.3.2, 5.3.3, 4.1.1, 4.2.2.
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