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Transcript
Risk of Transmission of
Different Viruses Following Accidental
Needle Injury

Hepatitis B virus
6-30%

Hepatitis C virus
0-7% (1.8%)

Human
Immunodeficiency Virus
0.3%
Transmission of HIV Infection to HCPS

Who is at risk?

What is the risk?

What are the factors which influence the risk?

How can the risk be reduced?

What is the role of antiretrovirals in reducing
the risk?
Who Is at Risk?

All HCPs who come in contact with blood
or bloody fluids in hospitals or laboratories

Nurses, laboratory workers, doctors,
residents, paramedics, emergency
doctors, medical students
Professionals with Frequent
Blood Exposures

Dentists

Surgeons

Emergency care providers

Phlebotomists

Nurses

Labour and delivery personnel

(Laboratory workers)
What Is The Risk?
Occupational
Percutaneous
0.3%
Mucous membrane
0.09%
Sexual transmission
0.018% to 3%
Mother to child
25%
Infected blood products
95%
Antiviral therapy 1998; 3 (Suppl 4): 45-47
Types of occupational injuries

Needle sticks, scalpels, broken glass

Contact with skin which is abraded, chapped,
inflamed or an open wound

Direct contact with concentrated HIV in a
laboratory

Isolated skin exposure
Consultant Jan 1999; 230-6
Factors Influencing Risk









Depth of injury
Device visibly contaminated with blood
Procedure involving a needle placed in artery or vein
Type of needle (hollow bore or solid)
Size of needle
Source patient’s viral load
Amount of blood
Duration of exposure
Immune status of HCP
Natural history of HIV infection
Body Fluids Which Can Transmit HIV

Blood, bloody fluids

Potentially infectious: semen, vaginal
secretions, CSF, pleural, peritoneal,
pericardial, amniotic fluids or tissue

No risk: saliva, tears, sweat, non-bloody
urine or faeces
Areas Of Contact

Hands

Body contact in cases of increased
blood loss

Face contact, common in
orthopaedics and obstetrics

Eye/mucous membrane contact
How Can Risks Be Reduced?

Universal precautions

Protocols for evaluation, counselling and
treatment of occupational exposures

Access to clinicians during all working hours

Availability of antiretroviral agents for PEP
on-site or easily

Availability of trained personnel for
counselling
How To Reduce Risk?





Number of procedures
Double gloves
Gowns, facemasks, goggles. Care during
procedures such as endoscopy, ENT surgery,
others where splattering of blood is
anticipated
Use of impervious needle-disposal containers
Transport of samples in sealed containers
Evaluation Of Exposure



What is the source material?
What is the kind of exposure?
What is the status of source
person/specimen?
(HIV positive, end-stage disease,
primary HIV infection, unknown)

Is the HCP pregnant?
Treatment Of Exposure
Immediate Measures







Use of soap and water to wash any wound or skin
Flush exposed mucous membrane with water
Open wounds - irrigate with sterile saline or
disinfectant solution
Eyes should be irrigated with clean water, saline or
sterile eye irrigants
Report to the concerned authority
Counselling
Antiretroviral therapy
General Guidelines For PEP

Therapy should be recommended after exposure

Therapy should be initiated within 1-2 hours

2- and 3-drug regimens, based on level of risk

Source patient’s HIV status unknown, decide on a
case-to-case basis

Follow up counselling and HIV testing using ELISA
periodically for at least 6 months (baseline, 6
weeks, 12 weeks and 6 months)

Potential benefits should be weighed against
potential risks
Regimens For PEP
Type
Drugs
Basic
(28 days)
Zidovudine 300 mg tid + Lamivudine 150 mg bid
(Duovir) OR
Stavudine 30-40 mg bid + Lamivudine 150 mg bid
(Lamivir-S)
As above, plus
Indinavir (Indivan) 800 mg 8 hourly
OR
Efavirenz (Efavir) 600 mg od at bedtime
OR
Nelfinavir (Nelvir) 750 mg tid
Expanded
(28 days)
POST EXPOSURE PROPHYLAXIS FOR HCP
Source material: blood, bloody fluid, other potentially infectious fluid
Type of exposure
Intact Skin
Mucous membrane or
non-intact skin
Percutaneous exposure
(no PEP needed)
Volume
Small
(ie few drops)
Severity
Large
(ie major blood
splash)
Consider or recommend Basic
regimen if source is HIV positive; consider Basic
regimen if source HIV status
unknown
Less severe
(eg solid
needle)
Recommend Basic or Expanded
regimen if source is HIV-positive;
consider Basic regimen if source
HIV status unknown
More severe
(eg large bore
hollow needle)
Recommend Expanded
regimen; consider Basic
regimen if source HIV
status unknown
Common Adverse Effects of PEP

Nausea

Diarrhoea

Malaise/fatigue

Myalgia/arthralgia

Headache

Abdominal pain

Vomiting

Rash
Counselling the exposed HCP

Monitor for drug toxicity (minimally, CBC
and LFT at baseline and at 2 wks)

Evaluation of symptoms such as rash,
fever, hyperglycemia, back or abdominal
pain or pain on urination should not be
delayed

Potential drug interactions

Failures can still occur

Behavioural modifications