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INTRATHECAL CHEMOTHERAPY IN ADULTS POLICY - ONCOLOGY AND HAEMATOLOGY DEPARTMENTS Version 15 Name of responsible (ratifying) committee Formulary and Medicines Group Date ratified 17 March 2017 Document Manager (job title) Lead Pharmacist for Oncology/ Haematology Date issued 25 April 2017 Review date 24 April 2019 Electronic location Clinical Policies Related Procedural Documents Cytotoxic drug management for adults in oncology and haematology Trust policy for the safe labeling and dilution of vincristine and other vinca alkaloids -oncology, haematology and paediatric departments. Key Words (to aid with searching) Intrathecal; chemotherapy; intrathecal and intra-thecal chemotherapy; intrathecal register; drug therapy; intrathecal injections; cancer; patient safety; safety measures; drug administration; adults; nurses; medical staff; pharmacists; regulations Version Tracking Version Date Ratified 15 17/03/17 14 21/11/2014 Brief Summary of Changes Author Addition of vinflunine as a vinca alkaloid Rob Williams Numbers of procedures updated with latest information. Documented compliance with NHS/PSA/D/2014/002 Stage Three: Directive. Non – Luer spinal (intrathecal) devices for chemotherapy. 20 February 2014 Disposal of syringe if procedure fails / aborted. Change name of Pharmacist from Catrin Watkinson to Rob Williams. Numbers of procedures were updated with latest information. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Catrin Watkinson Page 1 of 20 CONTENTS QUICK REFERENCE GUIDE....................................................................................................... 3 1. INTRODUCTION.......................................................................................................................... 4 2. PURPOSE ................................................................................................................................... 4 3. SCOPE ........................................................................................................................................ 4 4. DEFINITIONS .............................................................................................................................. 5 5. DUTIES AND RESPONSIBILITIES .............................................................................................. 5 6. PROCESS ................................................................................................................................... 6 7. TRAINING REQUIREMENTS .................................................................................................... 14 8. REFERENCES AND ASSOCIATED DOCUMENTATION .......................................................... 15 9. EQUALITY IMPACT STATEMENT ............................................................................................ 15 APPENDIX A: ................................................................................................................................... 17 EQUALITY IMPACT SCREENING TOOL ......................................................................................... 19 Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 2 of 20 QUICK REFERENCE GUIDE This policy must be followed in full when developing or reviewing and amending Trust procedural documents. For quick reference the guide below is a summary of actions required. This does not negate the need for the document author and others involved in the process to be aware of and follow the detail of this policy. 1. Intrathecal chemotherapy remains an important patient safety issue. A major patient safety issue is the danger to patients if intravenous vinca alkaloids (vincristine, vinblastine, vindesine, vinflunine and vinorelbine) are injected intrathecally (via spinal or intraventricular injections) during the chemotherapy treatment of a cancer patient. Vinca alkaloids are intended for intravenous use only. If injected intrathecally they cause paralysis almost always followed by death. 2. NPSA/2008/RRR004 and supporting information on Using Vinca Alkaloid Minibags (Adult/Adolescent Units) should be read in conjunction with this guidance. 3. A register has been established and maintained which lists designated personnel who have been trained and authorised to prescribe, dispense, issue, check or administer intrathecal chemotherapy. Staff moving from one hospital to another should not be automatically included on the new hospital’s register. 4. The ‘designated lead’ has delegated responsibility for induction, training and continuing professional development related to intrathecal chemotherapy to a lead trainer. 5. Tasks on the register are competency based i.e. they can be carried out by any members of staff (except for training grades) who have been appropriately trained, deemed competent by the designated lead or lead trainer(s) and whose names appears on the register of designated personnel for that task. This is relevant to prescribing, dispensing, issuing, checking and administration. 6. A purpose designed intrathecal chemotherapy chart is used. 7. Intrathecal chemotherapy drugs are kept in a dedicated lockable container/refrigerator in the pharmacy between dispensing and issuing and are stored in a dedicated lockable container/refrigerator between issuing and administration when they cannot be administered immediately. 8. Intrathecal chemotherapy can only be administered in the designated areas on the combined haematology and oncology day unit and on F5 ward. 9. Under normal circumstances intrathecal chemotherapy is administered within normal working hours. (Monday to Friday 08.00 to 18.00) Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 3 of 20 1. INTRODUCTION This document is produced in response to the updated National Guidance on the safe administration of intrathecal chemotherapy, Dept of Health HSC 2008/001 issued 11 August 2008. This guidance was designed to achieve the Government target to reduce the number of patients dying or being paralyzed by mal-administered spinal injections to zero by the end of 2001. This updated guidance replaces HSC 2003/010. It sets out the minimum that should be expected of an NHS Trust providing an intrathecal chemotherapy service. The section (including the waiver) on dilutions of intravenous vinca alkaloids originally in HSC2003/010 has been removed. The guidance now cross-refers to a new national Patient Safety Agency (NPSA) rapid response report NPSA/2008/RRR004 entitled Using Vinca Alkaloid Minibags (Adult/Adolescent Units) which can be found at http://www.npsa.nhs.uk/patientsafety/alerts-and-directives/rapidrr and which should be read in conjunction with this document. 2. PURPOSE This policy is designed to ensure the safe prescribing, handling and administration of Intrathecal Chemotherapy for Portsmouth Hospitals NHS Trust patients. 3. SCOPE PHT has a unified intrathecal chemotherapy service which caters for adult patients with solid tumours and haematological malignancies. PHT does not provide intrathecal chemotherapy for children. This is a single divisional policy, which applies to all Portsmouth Hospitals’ clinical, nursing and pharmacy staff, particularly those working in Haematology, Oncology and Pharmacy . It applies to the induction, training, assessment and continuing professional development of staff on the intrathecal register, and also of those staff not on the register who are prohibited from involvement in any aspect of intrathecal activity. It applies to prescribing, managing intrathecal chemotherapy drugs, patient consent, reviews, location, checks and administration to patients and when the service will be available. It also describes where in the Trust to find copies of key documents such as national guidance, relevant local policies, procedures and the Intrathecal Chemotherapy Register. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 4 of 20 4. DEFINITIONS Portsmouth Hospitals Portsmouth Hospitals NHS Trust The Trust Portsmouth Hospitals NHS Trust ST3 Specialist Registrar LP Lumbar Puncture Junior ST Junior Doctor (ST1, ST2, FT1, FT2) CSF Cerebrospinal fluid Designated personnel Personnel whose names appear on the Intrathecal Chemotherapy Register who have been trained and certified competent in one or more of the following tasks: prescribing, dispensing, checking and administration of intrathecal chemotherapy Intrathecal Register . All references to “the register” in this policy refer to the Intrathecal Chemotherapy Register and not to any other register such as the medical register. This register will be located on the pharmacy web pages of the PHT intranet website and specified locations within the Trust (see Para 6.3 below). Chemotherapy Guidance in HSC 2008/001 Designated Lead Designated Lead Trainer National guidance provided in Health Service Circular HSC 2008/001 Updated National Guidance on the Safe Administration of Intrathecal Chemotherapy (August 2008). The single lead clinician appointed by the Chief Executive to oversee compliance with Guidance in HSC 2008/001, The Lead Pharmacist for Oncology and Haematology Services to be responsible for training and day-to-day maintenance of the Intrathecal Chemotherapy Register. 5. DUTIES AND RESPONSIBILITIES Portsmouth Hospitals NHS Trust provides an intrathecal chemotherapy service therefore the Chief Executive has overall responsibility for compliance with Guidance in HSC 2008/0001. The Chief Executive has appointed Dr A O’ Callaghan as the single lead clinician to oversee compliance with Guidance in HSC 2008/001. She will be accountable to the Chief Executive. This lead person is referred to as the Designated Lead. The Designated Lead has appointed a Designated Lead Trainer, the Senior Directorate Pharmacist for Oncology and Haematology Services, Rob Williams to oversee training within the Trust. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 5 of 20 Staff may only perform the specific task(s) for which they have been trained and certified competent unless performing a task under direct supervision, in the constant presence of an assessor, for the specific purpose of being assessed for inclusion on the intrathecal register. 6. PROCESS Overall Responsibility Portsmouth Hospitals NHS Trust provides an intrathecal chemotherapy service therefore the Chief Executive has overall responsibility for compliance with Guidance in HSC 2008/0001. The Chief Executive has appointed Dr A O’ Callaghan as the single lead clinician to oversee compliance with Guidance in HSC 2008/001. She will be accountable to the Chief Executive. This lead person is referred to as the Designated Lead. The Designated Lead has appointed a Designated Lead Trainer, the Lead Pharmacist for Oncology and Haematology Services, Rob Williams to oversee training within the Trust. Volume of Service In Portsmouth Hospitals Trust there were 43 intrathecal chemotherapy administrations between April 2014 - March 2015 and 41 administrations between April 2015 – March 2016. It therefore is neither a low volume provider nor a high volume provider. Document Availability and Control A system is in place to ensure that only the latest edition of the national guidance, this policy and the intrathecal chemotherapy register is available to Trust staff. Master copies of each of the above are held on the pharmacy intranet website. In addition papers copies are kept at the following locations: Copy Number Location 1 2 3 4 5 6 Oncology Pharmacy QAH Pharmacy Manufacturing Unit – Railway Triangle F5 QAH Procedure Rm F1321 HODU – Haematology / Oncology Day unit Designated Lead Designated Trainer Pharmacy Work Instruction PHPSWI.22.003 describes how up-to-date hard copies are maintained in the above locations. The maintenance of up-to-date documentation is the subject of annual audit as part of the pharmacy medicines management audit process. This policy complements the Portsmouth Hospitals Policy for administration of chemotherapy and is subject to separate document control work instructions. Intrathecal Chemotherapy Register Portsmouth Hospitals NHS Trust has a single intrathecal chemotherapy register of people who have been trained and certified competent in one or more of the following tasks: Prescribing intrathecal chemotherapy; Clinical screening (verification) of intrathecal chemotherapy; Dispensing intrathecal chemotherapy (i.e. preparing the dose, filling the syringe, production pharmacist release and placing it in packaging for transport); Checking and Issuing intrathecal chemotherapy from the pharmacy; Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 6 of 20 Checking intrathecal chemotherapy drugs prior to administration; Administering intrathecal chemotherapy. Assessors for intrathecal chemotherapy training. Staff may only perform the specific task(s) for which they have been trained and certified competent unless performing a task under direct supervision, in the constant presence of an assessor, for the specific purpose of being assessed for inclusion on the intrathecal register. Following the successful completion of induction, formal training, and performance of the intrathecal task under supervision by an assessor, only the Designated Lead or the Lead Trainer can authorise the inclusion of that person onto the relevant section of the intrathecal register. Registration only lasts a year, an individual will therefore be deleted from the register unless the individual can satisfactorily demonstrate continued competence. The Designated Lead has overall responsibility for holding the register and ensuring that it is maintained and kept up-to-date. Day-to-day responsibility for holding the register and ensuring that it is maintained and kept up-to-date is delegated to the Designated Lead Trainer (Para 22 ). Pharmacy Work Instruction PHPSWI.22.003 describes the system to ensure that only the latest edition of the intrathecal chemotherapy register is available to Trust staff. Master copies of each of the above are held on the pharmacy intranet website. In addition paper copies are kept at the locations listed in Document and Availability Control above. The Designated Lead is responsible for monitoring how often staff on the register carry out procedures related to intrathecal chemotherapy and assessing whether they remain on the register. She will be assisted in this process by the Senior Directorate Pharmacist, who will monitor prescriptions and report individual activity annually. The Designated Lead will hold a regular review of staff participation, continued competence, confirmation of rereading national and local guidance. The Designated Lead has the authority to delete individuals from the register if they fail to demonstrate satisfactory competence in intrathecal tasks. Individuals performing a low number of procedures may require refresher training under supervision before re-certification and re-inclusion on the register. Staff transferring from other trusts Automatic inclusion in Portsmouth Hospitals’ intrathecal chemotherapy register will not occur. Staff who were on the intrathecal register at their previous hospital at the time of transfer will need to provide written confirmation of their certification, undergo the Portsmouth Hospitals Trust induction, perform one supervised procedure, and demonstrate their competence. No form of “provisional” entry to the register is allowed for any staff. Induction, training and continuing professional development The designated lead for intrathecal chemotherapy for the Trust has overall responsibility for induction, training, assessment, annual recertification and Continuing professional development related to intrathecal chemotherapy. The responsibility for training for all professionals is delegated to the lead trainer. For medical staff training is delivered by clinical lead overseen by training lead. For nursing staff the clinical educator assists in this training role. The lead trainer will ensure that the Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 7 of 20 following are in place: Induction for all staff in departments involved in intrathecal chemotherapy. All staff including consultants who are new to the ward or department involved with intrathecal chemotherapy are provided with a formal induction covering all potential clinical hazards associated with intrathecal chemotherapy and the danger posed to patients if intravenous vinca alkaloids are accidentally administered intrathecally. Staff working in areas where chemotherapy is prescribed and administered or in the pharmacy service, but who are not involved in providing an intrathecal chemotherapy service, must be made aware that there is strict national guidance and this local policy, which prohibits their involvement in any aspect of the service. All staff are required to read the local training documentation. All staff are required to sign a written confirmation that they have read this documentation before being allowed to practice their respective roles. As part of the induction training it is made clear to all staff involved with the treatment and care of patients receiving intrathecal chemotherapy that they should challenge colleagues if, in their judgement, either protocols are not being adhered to or the actions of an individual may cause potential risk to a patient. Challenging should not be seen as adversarial but as an additional check to improve patient safety and reduce risk. It is the responsibility of staff who are on the Intrathecal Register to ensure that all other colleagues that are participating in the process are also on the Intrathecal Register. Training of Staff for intrathecal chemotherapy There is a common formal induction course for nursing, pharmaceutical and medical staff including consultants new to the hospital. This covers all potential clinical hazards associated with intrathecal chemotherapy and the danger posed to patients if intravenous vinca alkaloids are accidentally administered intrathecally. It includes information appropriate to their proposed role in the intrathecal chemotherapy service i.e. prescribing, dispensing, issuing, checking and administration of intrathecal chemotherapy. All staff participating in the intrathecal service must read the national guidance on intrathecal chemotherapy and this local policy. Assessment Assessment will be performed by personnel designated as assessors on the register. Staff will be required to demonstrate satisfactory completion of the training course, written confirmation that they have read both the national guidance and local protocol and satisfactorily perform the relevant task under the supervision of an assessor. Staff will receive a certificate to confirm that they have completed their training and are competent and become eligible to be included on the register for their designated task(s) The Designated Lead will agree with the Lead Trainer those staff who are competent to assess the competence of others to perform the tasks listed in the Intrathecal Chemotherapy Register above and authorise entry of the names of those who have been trained and certified competent in one or more of the tasks listed. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 8 of 20 Annual Confirmation of Competence All staff on the register must provide annual written confirmation that they have reread the national guidance and local policy. They must be able to demonstrate they are competent in the roles they undertake and that this competence is reviewed annually. The practical administration of intrathecal chemotherapy is regarded as part of continuing professional education and training for all professional staff who remain on the register. The Designated Lead and Lead Trainer will hold a regular intrathecal meeting to review the competence of all staff on the register Training is in the form of an “in house” training package titled “Intrathecal Chemotherapy – Training package for designated staff to allow entry onto the intrathecal register” and includes reference to the national training toolkit issued by the Department of Health. Prescribing Only Consultant Medical Staff, Associate Specialists or ST3 grade or above, whose names appear on the current intrathecal chemotherapy register as prescribers shall prescribe intrathecal chemotherapy. No other persons may prescribe intrathecal chemotherapy under any circumstances. Newly appointed medical staff, including consultants, will be informed at induction that they cannot prescribe intrathecal chemotherapy until they have received the appropriate induction/training and, their name added to the Intrathecal chemotherapy register as competent to prescribe intrathecal chemotherapy. Junior medical grades below ST3 are not, in any circumstances, permitted to prescribe intrathecal chemotherapy. Drugs prescribed intrathecally: Adult Oncology: Methotrexate Cytarabine Depocyte (Liposomal Cytarabine) Adult Haematology: Methotrexate Cytarabine Depocyte (Liposomal Cytarabine) Hydrocortisone The use of an intrathecal drug not on the above list must be discussed with the Designated Lead and the Senior Directorate Pharmacist Oncology/Haematology. Its use must be recorded in compliance with the agreed local and network policy Prescription Chart (See Appendix 1) A purpose designed intrathecal chemotherapy prescribing and administration record chart will be used for recording the prescribing, issue, collection/delivery, nurse checking and administration of intrathecal chemotherapy. It will not be part of any other chemotherapy chart. The drug and route of administration will be clearly written on the chart and it will have space for the full signatures of all those undertaking prescribing, issue, Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 9 of 20 collection/delivery, nurse checking and administration of intrathecal chemotherapy to ensure a clear audit trail There is continuous audit of intrathecal chemotherapy administration and audit sheet must be completed with details of each procedure Intrathecal chemotherapy is documented in patients clinical notes Following administration the prescription chart will be filed in the Intrathecal Folder for the unit where the procedure has been performed, prior to filing in the patient’s notes. Managing intrathecal chemotherapy drugs Dispensing Only pharmacy staff, who appear on the intrathecal chemotherapy register will dispense intrathecal chemotherapy drugs. For the purposes of this policy, dispensing is the activity of preparing the dose, filling the syringe and placing the syringe in packaging for transport. Dispensing will take place only in the Pharmacy Manufacturing Unit based at Railway Triangle, Farlington. Batches of intrathecal chemotherapy may be prepared but they will always be issued as individual patient doses and signed for as such before they are released from the pharmacy. To ensure compliance with NHS/PSA/D/2014/002 Stage Three directive. Non – Luer spinal (intrathecal) devices for chemotherapy 20 February 2014 intrathecal injections are manufactured using Surety syringes, needles and hubs. These have been independently evaluated for physical, microbiological and clinical efficacy by an independent laboratory on behalf of NHS England. At the point of administration a Surety spinal needle is used. Storage in the pharmacy Intrathecal chemotherapy drugs (except Depocyte®) will only be stored in dedicated, lockable refrigerators at QAH pharmacy, reserved solely for the purpose of storing intrathecal chemotherapy drugs. The refrigerators will be clearly labeled and they will never be used to store any other products including intravenous chemotherapy. Intrathecal chemotherapy drugs (except Depocyte) will not be stored in any other location. Depocyte® is stored at room temperature in a dedicated lockable box, reserved solely for the storage of depot cytarabine, in QAH pharmacy, positioned adjacent to the intrathecal refrigerator. Issuing of Intrathecal chemotherapy drugs Only pharmacy staff on the intrathecal register for issuing can issue intrathecal chemotherapy drugs. Intrathecal chemotherapy drugs will only be issued from either QAH pharmacy, immediately prior to administration, to the registered doctor who will be administering the drug (the collector) or taken to the ward by a designated member of pharmacy staff whose name appears on the intrathecal chemotherapy register. If the drugs are taken to the ward they must be handed to the doctor who will be administering the intrathecal chemotherapy. Once received by the administering doctor, individual patient dose(s) of intrathecal chemotherapy drug(s) will be placed on the lower shelf of the lumbar puncture trolley, in the intrathecal area, ready for administration. If treatment is delayed for any purpose the intrathecal chemotherapy will be returned to the pharmacy for secure storage. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 10 of 20 Administration to patients Patient consent Full written, informed patient consent is required for the course of intrathecal chemotherapy rather than each dose within the course. However, when attending for each dose, patients will be explicitly told the nature of the procedure, the route of administration and the drug to be administered and ongoing consent confirmed verbally In clinical circumstances where consent is not possible due to nature of condition being treated effecting capacity appropriate procedure for obtaining consent will be followed. Once patient has regained capacity they will provide informed consent for ongoing treatment course Patient reviews A consultant or appropriately trained and nominated deputy from the Intrathecal chemotherapy register who can administer intrathecal chemotherapy will review each patient before intrathecal chemotherapy is administered. This is to ensure that the patient is fit for treatment, the correct tests have been conducted, the correct chemotherapy has been prescribed and that arrangements have clearly been made for the intrathecal chemotherapy to be administered by the appropriate medical staff. The completion of this review process will be signed for on each occasion by the administering Doctor, on the Intrathecal Chemotherapy Chart Location Intrathecal chemotherapy will be administered in an area or room where no other chemotherapy drugs are stored or administered. For Portsmouth Hospitals these areas are as follows: HODU – Procedure Rm 4 – B1512 F5 – Procedure Rm – F1321 - This is the designated area for any in-patients regardless on whether they are on F5, F6 or F7. The bed/area designated for the administration of intrathecal chemotherapy will be reserved for that purpose for the duration of that session. When intrathecal chemotherapy is being administered in that area it will not be used for any other purpose. Under no circumstances will any other form of chemotherapy take place in this area during that session. Chemotherapy drugs for intravenous infusion must never been stored in these areas, even when the area is not in use. In exceptional circumstances it may be necessary to administer intrathecal chemotherapy in a non-designated place. This should only be considered after careful consultation with the Trust Lead for Intrathecal Chemotherapy. The reason should be documented in the patient’s notes, and noted in annual report and reviewed at annual Intrathecal review meeting. These circumstances could include a patient too ill to move, infection control hazard, or requirement for placement of the lumbar puncture needle in theatre with anesthetic assistance. In these exceptional circumstances, the intrathecal administration of chemotherapy must be performed by a consultant on the intrathecal register, in the presence of a nurse registered to check intrathecal chemotherapy. Checks Medical staff, when preparing a patient for treatment with intrathecal chemotherapy, will use a formal checking procedure to ensure that the right drug and the right dose is given to the Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 11 of 20 right patient via the correct route. These checks will include a chemotherapy trained nurse / pharmacist whose name appears on the Intrathecal chemotherapy register, the patient and, if appropriate the relative or guardian As a minimum the doctor administering the intrathecal chemotherapy will confirm the identity of the patient, verbally and with wrist band identification explain the nature of the procedure, the drug that is to be administered and the route of administration The patient, and the name and dose of drug must be checked by a chemotherapy trained nurse or pharmacist who is on the register for checking intrathecal chemotherapy. A chemotherapy trained nurse is a nurse who has been assessed to be competent both to administer intravenous chemotherapy and check both intravenous and intrathecal chemotherapy. Named nurses other than those who are chemotherapy trained nurses may check intrathecal chemotherapy provided they have been trained, certified competent to check intrathecal chemotherapy and whose names appear of the Intrathecal chemotherapy register. At Portsmouth Hospitals NHS Trust two doctors checking is NOTan appropriate substitute for a chemotherapy trained nurse / pharmacist in any circumstances. Some patients may choose to check the name and dose of the drug(s) written up on the chart with those on the label of the syringe. They will be enabled to do this if they so wish. Patients will not be expected to take on a burden of responsibility greater than they would be comfortable with. The checks made must be recorded using the intrathecal chemotherapy prescribing and administration record Intrathecal chemotherapy is not administered under anaesthesia in Portsmouth Hospitals. except in exceptional circumstances which must be discussed on a case by case basis with the clinical lead for intrathecal chemotherapy and a clear plan ensuring safety must be in place Methotrexate, the most commonly used drug given intrathecally, is yellow. If may be helpful to remember this but this does not reduce the burden on the clinician nurse or pharmacist on the intrathecal chemotherapy register to check the label on the relevant container Administration of Drugs The following doctors can be included in the register as authorised to administer intrathecal chemotherapy provided that their names appear on the current Intrathecal chemotherapy register as authorised to administer intrathecal chemotherapy: Consultants; Specialist Registrars ( ST3 grade and above) Associate Specialist Staff grades It will be made clear to medical staff (including consultants) new to the hospital that they do not administer intrathecal chemotherapy until they have received appropriate training, their competency agreed and documented and their name included on the Intrathecal chemotherapy register, as for all other staff seeking inclusion on the register. A technically difficult lumbar puncture may need assistance from staff not on the Intrathecal chemotherapy register, for example, an anaesthetist or radiologist to position the needle under imaging control. This is acceptable, however, these staff will never be involved in Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 12 of 20 any other aspect of the process and they will never administer intrathecal chemotherapy The intrathecal administration must be performed by a consultant on the intrathecal register, in the presence of a nurse / pharmacist registered to check intrathecal chemotherapy. If the procedure fails or is aborted the intrathecal syringe will be disposed of by the administering doctor as cytotoxic waste on the ward or on the day unit. This will be documented on the intrathecal prescription. In Portsmouth Hospitals NHS Trust Junior medical grades below ST3 will never administer intrathecal chemotherapy. Neither may they perform a lumbar puncture for the purpose of intrathecal chemotherapy. Times for administration of intrathecal chemotherapy Under normal circumstances intrathecal chemotherapy will only be administered during normal working hours Monday to Friday 08.00 – 18.00, i.e. at times when a full range of specialist expertise is available. Out of hours Only in exceptional circumstances (e.g. CNS relapse of leukaemia, requiring emergency treatment) intrathecal chemotherapy may be administered out-of-hours, when there is a clear clinical need that cannot wait until the next working day. Only Methotrexate is to be used out of hours. Only a consultant whose name appears on the Intrathecal chemotherapy register can prescribe the intrathecal chemotherapy out-of-hours but thereafter all normal procedures will apply. The pharmacy will be contacted through the pharmacy on-call system and an oncology / haematology pharmacist on the intrathecal chemotherapy register will issue and deliver the intrathecal chemotherapy. The pharmacy will issue an intrathecal chemotherapy syringe of intrathecal Methotrexate 12.5 mg held in the designated locked intrathecal refrigerator at QAH specifically for this purpose. The prescribing consultant will inform the Designated Lead, on the next working day. The designated lead will document the out-of-hours administration, reason and outcome. All such instances must be reported to the monthly Chemotherapy Users Group meeting and discussed at the annual Intrathecal review Meeting. Prescribing and administering intraventricular chemotherapy (via omaya reservoir ) All requirements of this policy apply equally to the control of intraventricular chemotherapy and will be followed in full. If the patient has an Ommaya reservoir in place an intrathecal needle is not required as the intrathecal syringe is compatible with the device as they are both manufactured by Surety. In the Event of an Error If a medication has been given intrathecally in error, assess the clinical risk to the patient and take appropriate action, as specified below. The Designated Lead and the Senior Clinical Nurse must be informed immediately and they are responsible for completing an adverse incident form. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 13 of 20 If a vinca alkaloid has been administered intrathecally, management must be to transfer the patient to the Neurosurgery Department at University Hospital Southampton NHS Foundation Trust as soon as practicable. The Nurse assisting must Call 999 for transfer to neurosurgery. Contact must be made with the on-call Neurosurgical registrar and they should be advised of type of error and imminent transfer. If the LP needle is still in place, 20mls of CSF must be aspirated as soon as possible. A further 20mls should be allowed to drain freely if possible. N.B. the needle must be removed prior to transfer. The patient should be transferred in the sitting position. The patient should be informed of events. A nurse must accompany the patient to University Hospital Southampton. If lignocaine has been administered, management must be to transfer the patient to the Intensive Care Unit and assess the need for ventilation 7. TRAINING REQUIREMENTS Training of Staff for intrathecal chemotherapy There is a common formal induction course entitled “Intrathecal Chemotherapy – Training package for designated staff to allow entry onto the intrathecal register” This covers all groups of staff - nursing, pharmaceutical and medical staff including consultants new to the Trust. This covers all potential clinical hazards associated with intrathecal chemotherapy and the danger posed to patients if intravenous vinca alkaloids are accidentally administered intrathecally. It includes information appropriate to their proposed role in the intrathecal chemotherapy service i.e. prescribing, dispensing, issuing, checking and administration of intrathecal chemotherapy. All staff participating in the intrathecal service must read the national guidance on intrathecal chemotherapy and this local policy. Assessment Assessment will be performed by personnel designated as assessors on the register. Staff will be required to demonstrate satisfactory completion of the training course, written confirmation that they have read both the national guidance and local protocol and satisfactorily perform the relevant task under the supervision of an assessor. Staff will receive a certificate to confirm that they have completed their training and are competent and become eligible to be included on the register for their designated task(s) The Designated Lead will agree with the Lead Trainer those staff who are competent to assess the competence of others to perform the tasks listed in 6.4.1 above and authorise entry of the names of those who have been trained and certified competent in one or more of the tasks listed in 6.4.1 above: Annual Confirmation of Competence All staff on the register must provide annual written confirmation that they have reread the national guidance and local policy. They must be able to demonstrate they are competent in the roles they undertake and that this competence is reviewed annually. The practical administration of intrathecal chemotherapy is regarded as part of continuing professional education and training for all professional staff that remain on the register. The Designated Lead and Lead Trainer will hold a regular intrathecal meeting to review Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 14 of 20 the competence of all staff on the register Training will be in the form of an “in house” training package and will include reference to the national training toolkit issued by the Department of Health. 8. REFERENCES AND ASSOCIATED DOCUMENTATION Updated National Guidance on the safe administration of Intrathecal Chemotherapy, Dept of Health HSC 2008/001 11th October 2008. NPSA/2008/RRR004 – National Patient Safety Agency (NPSA) rapid response report using Vinca Alkaloid Minibags (Adult/Adolescent Units) which can be found at http://www.npsa.nhs.uk/patientsafety/alerts-and-directives/rapidrr PHPSWIO14D Work Instruction – Pharmacy Dispensing PHPSWI016D Work Instruction – Dispensing Injectable Cytotoxic Medicines Could add the NPSA 2009/PSA 004A NPSA 2009/PSA 004A. Compliance with this guidance will occur when the devices become available. A Trust working group is leading this. http://www.nrls.npsa.nhs.uk/EasySiteWeb/getresource.axd?AssetID=65257&type=full&servicet ype=Attachment NPSA /2011/PSA is an update to NPSA 2009/PSA 004A and has been issued to allow more time to become compliant due to lack of availability of devices. http://www.nrls.npsa.nhs.uk/EasySiteWeb/getresource.axd?AssetID=94507&type=full&servicet ype=Attachment NHS/PSA/D/2014/002 Stage Three: Directive. Non – Luer spinal (intrathecal) devices for chemotherapy. 20 February 2014 https://www.england.nhs.uk/wp-content/uploads/2014/02/non-Luer-spinal-supp.pdf 9. EQUALITY IMPACT STATEMENT Portsmouth Hospitals NHS Trust is committed to ensuring that, as far as is reasonably practicable, the way we provide services to the public and the way we treat our staff reflects their individual needs and does not discriminate against individuals or groups on any grounds. This policy has been assessed accordingly Our values are the core of what Portsmouth Hospitals NHS Trust is and what we cherish. They are beliefs that manifest in the behaviours our employees display in the workplace. Our Values were developed after listening to our staff. They bring the Trust closer to its vision to be the best hospital, providing the best care by the best people and ensure that our patients are at the centre of all we do. We are committed to promoting a culture founded on these values which form the ‘heart’ of our Trust: Respect and dignity Quality of care Working together Efficiency This policy should be read and implemented with the Trust Values in mind at all times. Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 15 of 20 10. MONITORING COMPLIANCE WITH PROCEDURAL DOCUMENTS This document will be monitored to ensure it is effective and to assurance compliance. Minimum requirement to be monitored Competency of all Individuals on Intrathecal Register Lead Designated Lead Tool Audit Frequency of Report of Compliance Annual Review Reporting arrangements Lead(s) for acting on Recommendations Policy audit report to: Annual Inthrathecal Review meeting Chemotherapy Governance Group for noting Competency / Frequency of Tasks of all Individuals on Intrathecal Register Senior Directorate Pharmacist Audit Annual Review Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Policy audit report to: Annual Intrathecal Review meeting Chemotherapy Governance Group for noting Designated Lead The Designated Lead has the Authority to delete individuals from the register if they fail to demonstrate satisfactory competence in inthrathecal tasks. Individuals performing a low number of procedures may require refresher training under supervision before re-certification and re-inclusion on the register. Designated Lead Page 16 of 20 APPENDIX A: INTRATHECAL CHEMOTHERAPY PRESCRIPTION CHART Complete or Attach Patient label Blood results Ward: Hospital Number: Patient Review completed by: Haem: (full signature) Consultant: Surname: Diagnosis: First Name: Indication: WBC: Prophylaxis / Treatment * Neut: (*delete as appropriate) Date of Birth: Prescription Date: Course: date taken: Drug: Dose:(mg) Route: (written in full) Plat: Prescribed by: Doctor: (please print) (full signature) INTRATHECAL Has intravenous chemotherapy been prescribed for this patient for this date YES NO Doctor: (full Signature) I confirm that all intravenous chemotherapy prescribed for this date has been administered Date: Time: Pharmacist OR Doctor: (full Signature) Screening Pharmacist: (full Dispensed by: signature) (full signature) Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Batch Number: Expiry date / Time: Page 17 of 20 Issuing Pharmacist: Accepted by: Administrating Doctor ONLY (full signature) (full signature) Nurse Checked by: (full signature) Patient Written Consent taken: Patient ID checks completed: Time of Administered by: (please print) Admin (Please tick and initial to confirm) (Please tick and initial to confirm) Nurse Doctor PHPS FORM Intrathecal Cyto Prescription May 2013 ALL SECTIONS OF THIS CHART MUST BE COMPLETED Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 18 of 20 Administered by: (full signature) EQUALITY IMPACT SCREENING TOOL To be completed and attached to any procedural document when submitted to the appropriate committee for consideration and approval for service and policy changes/amendments. Stage 1 - Screening Title of Procedural Document: Intrathecal Chemotherapy In Adults Policy - - Oncology And Haematology Departments Date of Assessment Name of completing assessment 09/03/17 person Robert Williams Responsible Department Job Title Haematology / oncology Haematology pharmacist /Oncology Does the policy/function affect one group less or more favourably than another on the basis of : Yes/No Age No Disability Learning disability; physical disability; sensory impairment and/or mental health problems e.g. dementia No Ethnic Origin (including gypsies and travellers) No Gender reassignment No Pregnancy or Maternity No Race No Sex No Religion and Belief No Sexual Orientation No Comments If the answer to all of the above questions is NO, the EIA is complete. If YES, a full impact assessment is required: go on to stage 2, page 2 More Information can be found be following the link below www.legislation.gov.uk/ukpga/2010/15/contents Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 19 of 20 Stage 2 – Full Impact Assessment What is the impact Level of Impact Responsible Officer Mitigating Actions (what needs to be done to minimise / remove the impact) Monitoring of Actions The monitoring of actions to mitigate any impact will be undertaken at the appropriate level Specialty Procedural Document: Specialty Governance Committee Clinical Service Centre Procedural Document: Clinical Service Centre Governance Committee Corporate Procedural Document: Relevant Corporate Committee All actions will be further monitored as part of reporting schedule to the Equality and Diversity Committee Intrathecal Chemotherapy in Adults Policy Version: 15 Issue Date: 25 April 2017 Review Date: 24 April 2019 (unless requirements change) Page 20 of 20