Management of Needlestick Injuries in Healthcare Workers
After a needlestick injury, immediately wash the wound with soap and water, test the source patient for HBsAg, anti-HCV, and HIV antibody using rapid testing when possible, assess the exposed worker's hepatitis B immunity status, and initiate HIV post-exposure prophylaxis with bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) within 1-2 hours if the source is HIV-positive or unknown. 1, 2, 3
Immediate Wound Care
- Wash the puncture site thoroughly with soap and water and encourage bleeding from the wound. 1, 4
- Flush mucous membranes with water if splash exposure occurred. 1
- Do not delay care to determine source status—begin immediate decontamination first. 1
Source Patient Testing (Perform Immediately)
- Test the source patient for HBsAg, anti-HCV, and HIV antibody using rapid testing when available to guide prophylaxis decisions. 1
- Use fourth-generation HIV antigen/antibody combination tests for the most sensitive detection. 3, 5
- Do not test discarded needles or syringes for virus contamination—this is unreliable and delays appropriate care. 1, 3
- If the source is unknown, assess the epidemiologic risk of HBV, HCV, or HIV exposure based on the clinical setting. 1
Exposed Worker Baseline Testing
Immediate Assessment
- Perform a rapid or laboratory-based fourth-generation HIV antigen/antibody combination test on the exposed worker before initiating PEP to rule out pre-existing infection. 2, 3, 5
- Add HIV nucleic acid test (NAT) if the worker received long-acting injectable PrEP within the past 12 months. 3, 5
- Assess hepatitis B immunity status by reviewing vaccination history and prior anti-HBs titers. 1
- Obtain baseline renal function (creatinine, eGFR) before starting any tenofovir-based HIV PEP regimen. 2, 3
- Screen for other sexually transmitted infections at baseline. 5
HIV Post-Exposure Prophylaxis
Medication Regimen
- Initiate bictegravir 50mg/emtricitabine 200mg/tenofovir alafenamide 25mg (BIC/FTC/TAF) as a single tablet once daily for 28 days—this is the CDC's preferred first-line regimen. 2, 3, 5
- Alternative regimen: dolutegravir 50mg once daily PLUS emtricitabine 200mg/tenofovir alafenamide 25mg once daily for 28 days. 2, 3, 5
- Use tenofovir alafenamide (TAF) rather than tenofovir disoproxil fumarate (TDF) due to superior renal and bone safety. 2, 3, 5
Critical Timing
- Start PEP within 1-2 hours if possible, but no later than 72 hours post-exposure—efficacy decreases dramatically with each passing hour. 2, 3, 5
- Do not delay PEP initiation for source testing, risk assessment, or expert consultation—start immediately and adjust later if needed. 2, 3, 5
Duration and Adherence
- Complete the full 28-day course regardless of subsequent information about the source patient, as incomplete adherence significantly reduces effectiveness. 2, 3, 5
- Provide anti-emetics proactively to manage nausea and improve adherence. 3, 5
- Schedule follow-up visits or phone check-ins during the 28-day course to reinforce adherence and address side effects. 3, 5
Special Populations
- For renal impairment: Use TAF-based regimens exclusively due to minimal renal toxicity. 2, 3, 5
- For pregnancy: Do not withhold optimal PEP regimens—pregnancy is not a contraindication, though expert consultation is advised. 2, 3, 5
- For breastfeeding: Do not withhold PEP; counsel about temporary cessation during the 28-day course with expert guidance. 3
Hepatitis B Post-Exposure Prophylaxis
- For unvaccinated workers exposed to HBsAg-positive sources: Administer hepatitis B immunoglobulin (HBIG) and initiate the hepatitis B vaccine series immediately. 1, 4
- For vaccinated workers with known adequate anti-HBs response (≥10 mIU/mL): No treatment is needed. 1
- For vaccinated workers with inadequate or unknown response: Administer HBIG and a hepatitis B vaccine booster. 1, 4
- Test for anti-HBs 1-2 months after the last vaccine dose to confirm response (cannot be assessed if HBIG was given in the previous 3-4 months). 1
Hepatitis C Post-Exposure Management
- No post-exposure prophylaxis is recommended for HCV—no effective preventive medication exists. 1
- Perform baseline and follow-up anti-HCV and ALT testing at 4-6 months post-exposure. 1
- Perform HCV RNA at 4-6 weeks if earlier diagnosis is desired. 1
- Confirm repeatedly reactive anti-HCV enzyme immunoassays (EIAs) with supplemental tests. 1
Follow-Up Testing Schedule
HIV Follow-Up
- Within 72 hours: Clinical evaluation for drug toxicity and adherence assessment. 1, 2, 3, 5
- At 4-6 weeks: Fourth-generation HIV antigen/antibody test PLUS HIV nucleic acid test (NAT). 2, 3, 5
- At 12 weeks: Fourth-generation HIV antigen/antibody test PLUS HIV NAT to confirm absence of infection. 2, 3, 5
- Immediate testing if acute retroviral syndrome develops (fever, rash, lymphadenopathy, pharyngitis). 1, 3, 5
Monitoring for Drug Toxicity
- Monitor for adverse effects of antiretroviral PEP every 2 weeks through clinical evaluation and laboratory testing. 1
- Baseline and periodic monitoring should include complete blood count, renal function, and hepatic transaminases. 1
Counseling and Prevention of Secondary Transmission
- Advise the exposed worker to use barrier protection for sexual activity during the follow-up period. 1, 3, 5
- Instruct the worker to avoid blood or tissue donation during follow-up. 3, 5
- Provide counseling for emotional support and medication adherence. 1
- Seek immediate medical evaluation for any acute illness during follow-up, as this may indicate acute retroviral syndrome. 1, 2, 3, 5
Common Pitfalls to Avoid
- Never delay PEP while awaiting source testing or detailed risk assessment—start immediately and adjust later if the source is confirmed negative. 2, 3, 5
- Do not use two-drug HIV PEP regimens unless three-drug options are absolutely unavailable. 3, 5, 6
- Do not discontinue PEP early based on later source information—complete the full 28-day course. 2, 3, 5
- Do not withhold PEP from pregnant or breastfeeding workers—provide expert consultation concurrently, not as a prerequisite. 2, 3, 5
Expert Consultation Resources
- Contact the National Clinicians' Post-Exposure Prophylaxis Hotline (PEPline) at 1-888-448-4911 for complex cases, but do not delay PEP initiation while awaiting consultation. 2, 3
- Consult experts for drug-resistant source virus, pregnancy, renal/hepatic impairment, or concurrent medications with significant drug interactions. 1, 2