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Estimates of Per-Exposure Infection Risk | ||
% Probability | 95% Cl | |
Percutaneous occupational exposure
Gerberding 96 (pooled data) |
0.32 |
0.18-0.46 |
Sharing needles
Kaplan & Heiner 92 |
0.67 |
(not provided) |
Receptive anal intercourse
DeGrutolla 89DeGrutolla 89 |
0.80 |
0.5-1.1 |
Receptive vaginal intercourse
Peterman 96/Wiley 89 |
0.14 0.07-0.100.05-0.15 |
0.05-0.23 0.03-0.170.03-0.07 |
PEP Treatment Regimens |
Basic Regimen
Zidovudine (ZDV): 200mgtid (300 mg PO bid)Lamivudine (3TC): 150mg bid (125 mg bid If <60kg) |
Protease Inhibitor
Indinavir (IND): 800 mg q8hor Nelfinavir (NEL): 750 mg tid(if needed to ensure 2 new antiviral drugs or for very risky exposure) |
Alternate PEP Treatment Regimens |
Alternate Regimen I
Didanosine (DDI): 200 mg bid (125mg bid if <60 kg)Stavudine (D41): 40 mg bid (30 mg bid if <60 kg) |
Alternate Regimen II
Stavudine (D4T): 40 mg bid (30 mg bid lf <60 kg)Lamivudine (3TC): 150 mg bid (125 mg bid if <60 kg |
Current Post-Exposure Prophylaxis (PEP) |
Initiation: ASAP after potential exposure still treat serious exposures even after 72 hours
Duration: 4 weeksMonitor Labs: baseline, q 2 wks on treatment (or until all labs normalize)HIV antibody: baseline, 6 wks, 3 mo, 6 mo, (12 mo)HIV PCR: only with acute HIV symptoms |