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International reference ⚡ Urgency

HIV PEP — three protocols side-by-side

GeSIDA (Spain), BHIVA (United Kingdom) and CDC + US Public Health Service (United States) — the three leading authoritative guidelines for HIV post-exposure prophylaxis, presented comparatively. All recommend a 28-day course initiated within 72 h of exposure; they differ in preferred antiretroviral combinations.

Useful when the locally preferred drug is unavailable / contraindicated, or when the clinician wants to cross-check evidence positions across jurisdictions before deciding.

🇪🇸 2024

GeSIDA

Spain

Preferred regimen

Tenofovir disoproxil 245 mg + Emtricitabine 200 mg + Dolutegravir 50 mg

1 tablet every 24 h × 28 days

Alternatives

  • Tenofovir alafenamide (TAF) 25 mg + Emtricitabine 200 mg + Dolutegravir 50 mg (if TDF contraindicated)
  • Bictegravir/Emtricitabine/Tenofovir alafenamide (single-tablet) — increasingly used in clinical practice
Duration
28 days
Window
≤72 h
Timing detail

Ideal: <2 h after exposure

Max: <72 h (do not start after 72 h)

Scope

Occupational + non-occupational exposure (sexual, IDU). HCW shared decision with Infectious Diseases.

HBV approach

Anti-HBs ≥10 mUI/mL: no action. Anti-HBs 1–9 or unknown in prior responder: HBV vaccine booster. Non-responder: HBIG 0.06 mL/kg IM <72 h + repeat vaccine. Unvaccinated: HBIG + accelerated vaccine schedule 0-1-2-12 months.

HCV follow-up

Anti-HCV + HCV RNA baseline, week 6, week 12 and month 6. No effective PEP exists for HCV; if seroconversion → direct-acting antivirals (DAAs) achieve >95% cure.

🇬🇧 2021

BHIVA

United Kingdom

Preferred regimen

Tenofovir disoproxil 245 mg / Emtricitabine 200 mg + Raltegravir 1200 mg

Once daily × minimum 28 days

Alternatives

  • Tenofovir disoproxil / Emtricitabine + Raltegravir 400 mg twice daily (legacy dosing)
  • Tenofovir disoproxil / Emtricitabine + Dolutegravir 50 mg once daily
Duration
28 days
Window
≤72 h
Timing detail

Ideal: As soon as possible after exposure

Max: Up to 72 h (longer for high-risk sources by case-by-case decision)

Scope

Occupational + sexual exposure (PEPSE). NHS PEP available via emergency departments and GUM clinics.

HBV approach

Risk-based per Green Book Chapter 18. Booster vaccine for adequate-responder HCW exposed; HBIG + accelerated vaccine for non-responders or unvaccinated exposed to known HBsAg-positive source.

HCV follow-up

HCV RNA + anti-HCV baseline, then HCV RNA at week 6 and 12. Anti-HCV at week 24. Refer to hepatology if positive.

🇺🇸 2025

CDC + US Public Health Service

United States

Preferred regimen

Option A: Bictegravir / Emtricitabine / Tenofovir alafenamide (single tablet) — OR — Option B: Dolutegravir 50 mg + (Tenofovir alafenamide or Tenofovir disoproxil) + (Emtricitabine or Lamivudine)

Once daily × 28 days

Alternatives

  • Darunavir + cobicistat OR Darunavir + ritonavir + (Tenofovir alafenamide or Tenofovir disoproxil) + (Emtricitabine or Lamivudine) — for INSTI contraindications
Duration
28 days
Window
≤72 h
Timing detail

Ideal: As soon as possible (shorter time → greater HIV prevention efficacy)

Max: ≤72 h (PEP NOT recommended >72 h after exposure)

Scope

Adults + adolescents — both occupational PEP (OPEP, 2025 US PHS Guidelines) and non-occupational PEP (nPEP, CDC MMWR 2025;74(RR-1)). Children ≥2 y per separate INSTI-based combinations.

HBV approach

Test HBsAg + anti-HBs + anti-HBc at baseline. Tenofovir and FTC/3TC are active against HBV — abrupt withdrawal after PEP may cause HBV flare in chronic HBV carriers. CDC ACIP guidance for vaccination + HBIG separately.

HCV follow-up

HIV Ag/Ab 4th-gen baseline; final week 12. Interim weeks 4–6 only if PEP started >24 h after exposure or doses missed. HCV monitoring per CDC HCV guidance (anti-HCV + RNA baseline, follow-up per source status).

Where the three protocols agree

  • Duration: 28-day antiretroviral course.
  • Window: initiate within 72 h; sooner is better.
  • Three-drug regimen with tenofovir backbone (TDF or TAF) + FTC/3TC + integrase inhibitor (DTG, RAL or BIC) or boosted PI as alternative.
  • No PEP if >72 h (CDC explicit) or only by case-by-case decision (BHIVA).

Where they differ

  • Preferred integrase inhibitor: GeSIDA → DTG · BHIVA → RAL 1200 mg OD · CDC → BIC (single-tablet) or DTG.
  • Tenofovir form: CDC accepts TAF or TDF; GeSIDA + BHIVA default to TDF; TAF as alternative if TDF contraindicated.
  • HBV approach: GeSIDA most explicit (anti-HBs thresholds + HBIG dosing); BHIVA references Green Book Ch 18; CDC focuses on warning against tenofovir withdrawal in chronic HBV carriers.
  • HCV follow-up cadence: GeSIDA → baseline + W6 + W12 + M6 · BHIVA → baseline + W6 + W12 + W24 · CDC → per HCV guidance based on source status.

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