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Resuscitation Quick Actions • First 2 Minutes

High-Acuity

Immediate Wound Care

Wash needle-stick or puncture site with soap and water for 5 minutes; flush mucous membranes with copious sterile saline; DO NOT milk or squeeze wound (does not decrease transmission and increases micro-trauma).

Transmission Probability 'Rule of 3s'

Hepatitis B (HBeAg+ source) ~ 30%; Hepatitis C ~ 3%; HIV ~ 0.3% (3 in 1,000 percutaneous) and 0.09% (mucous membrane).

HIV PEP Timing

Must start within 72 hours of exposure; 28-day course of 3-drug antiretroviral therapy; dispense a 3-7 day starter pack directly in the ED.

Preferred HIV PEP Regimen

Biktarvy (Bictegravir/Emtricitabine/Tenofovir alafenamide) 1 tablet PO daily x 28 days OR Dolutegravir 50 mg PO daily PLUS Truvada (Tenofovir DF/Emtricitabine) 1 tablet PO daily.

Hepatitis B PEP

If exposed worker is unvaccinated or known non-responder -> Administer Hepatitis B Immune Globulin (HBIG 0.06 mL/kg IM) + first dose of Hep B vaccine series within 24 hours.

Hepatitis C

NO effective post-exposure prophylaxis exists; obtain baseline HCV Ab and RNA PCR; if seroconversion occurs at 4-6 weeks, refer for curative Direct-Acting Antivirals (DAAs).

Bottom-Line Clinical Pearl

Occupational HIV Post-Exposure Prophylaxis (PEP) must be initiated as soon as possible after exposure, ideally within 2 hours, and no later than 72 hours. Administer the first dose immediately in the emergency department using modern single-tablet 3-drug regimens (Biktarvy or Dolutegravir + Truvada) for 28 days. Never squeeze or milk a puncture wound.

1. Bloodborne Pathogen Transmission Risks & The 'Rule of 3s'

The risk of bloodborne viral transmission following a percutaneous hollow-bore needle injury from a known infected source patient follows the classic 'Rule of 3s':

PathogenPercutaneous Transmission Risk (Hollow-Bore Needle)Mucous Membrane Transmission RiskPost-Exposure Prophylaxis (PEP) Availability
Hepatitis B Virus (HBV)~ 30% (if source is HBeAg positive); ~ 1-6% if HBeAg negativeClinically significantHIGHLY EFFECTIVE: Hepatitis B Immune Globulin (HBIG) + Hepatitis B Vaccine series initiated within 24 hours (reduces transmission by > 90%).
Hepatitis C Virus (HCV)~ 1.8% to 3.0%Extremely rare (< 0.1%)NO POST-EXPOSURE PROPHYLAXIS AVAILABLE. Immunoglobulin and antivirals are NOT recommended for prophylaxis. Perform baseline HCV Ab and HCV RNA; repeat RNA at 4-6 weeks; curative direct-acting antivirals (DAAs) achieve > 98% cure if transmission occurs.
Human Immunodeficiency Virus (HIV)~ 0.3% (approximately 1 in 330 percutaneous exposures)~ 0.09% (approximately 1 in 1,000 splash exposures)HIGHLY EFFECTIVE: 3-drug antiretroviral PEP regimen started within 72 hours and continued for 28 days reduces transmission by > 81-90%.

Immediate First-Aid Rule: Never Squeeze or Milk the Wound

Immediately wash contaminated puncture wounds with gentle soap and water for 5 minutes. Flush eyes or mucous membranes with copious saline or tap water. DO NOT squeeze, milk, or apply tourniquets to the puncture site, and DO NOT instill caustic antiseptics (bleach, alcohol, iodine). Squeezing induces local tissue hyperemia and micro-tears that actually increase viral uptake into regional capillary beds.

2. Preferred 28-Day HIV Post-Exposure Prophylaxis Regimens

CDC guidelines mandate initiating PEP as rapidly as possible—ideally within 2 hours, and strictly within a 72-hour window. Provide a 3-to-7 day starter pack directly from the emergency department to ensure no doses are missed while awaiting outpatient pharmacy fulfillment:

Regimen CategoryMedications & Exact Adult DosingClinical Advantages & Pregnancy Considerations
Preferred Single-Tablet Regimen (First-Line)Biktarvy: Bictegravir 50 mg/Emtricitabine 200 mg/Tenofovir alafenamide (TAF) 25 mg — 1 tablet PO once daily with or without food for 28 days.Single daily tablet; superior patient compliance; lowest rates of nausea and GI side effects; minimal renal/bone toxicity due to TAF backbone.
Preferred Multi-Tablet RegimenDolutegravir (Tivicay) 50 mg PO once daily PLUS Truvada (Tenofovir DF 300 mg/Emtricitabine 200 mg) 1 tablet PO once daily for 28 days.Potent integrase strand transfer inhibitor (INSTI) with high barrier to resistance; standard global reference regimen.
Alternative/Pregnancy RegimenDolutegravir 50 mg PO daily PLUS Truvada 1 tablet PO daily OR Raltegravir (Isentress) 400 mg PO BID PLUS Truvada 1 tablet PO daily.Safe and approved across all trimesters of pregnancy. Tenofovir disoproxil fumarate (TDF) and emtricitabine have extensive safety data in pregnancy.

3. Hepatitis B Virus (HBV) Post-Exposure Prophylaxis Algorithm

Exposed Healthcare Worker HBV StatusSource Patient HBsAg PositiveSource Patient HBsAg NegativeSource Patient Unknown/Untestable
Documented Vaccinated RESPONDER (anti-HBs >= 10 mIU/mL)NO TREATMENT REQUIRED (complete immune protection)NO TREATMENT REQUIREDNO TREATMENT REQUIRED
Documented Vaccinated NON-RESPONDER (anti-HBs < 10 mIU/mL after 2 complete series)Administer HBIG (0.06 mL/kg IM) x 2 doses (1st dose immediately, 2nd dose 1 month later) OR HBIG x 1 + start new vaccine seriesNO TREATMENT REQUIREDTreat as if source is HBsAg positive: Administer HBIG (0.06 mL/kg IM) x 2 doses
UNVACCINATED or Incompletely VaccinatedAdminister HBIG (0.06 mL/kg IM) ONCE immediately within 24 hours + INITIATE 3-DOSE HEP B VACCINE SERIES (Days 0, 1 month, 6 months) at separate anatomic siteInitiate and complete the 3-dose Hepatitis B vaccine seriesInitiate and complete the 3-dose Hepatitis B vaccine series
Vaccinated with UNKNOWN Response/TiterTest exposed worker for anti-HBs STAT: If >= 10 mIU/mL -> no treatment. If < 10 mIU/mL -> administer HBIG x 1 dose + vaccine boosterNO TREATMENT REQUIREDTest exposed worker for anti-HBs: If < 10 mIU/mL, administer 1 vaccine booster dose and recheck in 1-2 months
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