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Self-start HIV postexposure prophylaxis (PEPSE), to reduce time to first dose and increase efficacy.
Fox, Julie M; Lee, Ming Jie; Fairhead, Cassandra Leach; Ledwaba-Chapman, Lesedi M; Nori, Achyuta V; McQuillan, Orla; Wang, Yanzhong; Clarke, Amanda; Menon-Johansson, Anatole.
Afiliação
  • Fox JM; Department of GUM and HIV, Guy's and St Thomas' NHS Foundation Trust, London, UK julie.fox@kcl.ac.uk.
  • Lee MJ; Department of Infectious Diseases, King's College London, London, UK.
  • Fairhead CL; Department of Infectious Disease, Imperial College London, London, UK.
  • Ledwaba-Chapman LM; Department of GUM and HIV, Brighton Hove and Sussex Sixth Form College, Brighton and Hove, UK.
  • Nori AV; Department of Infectious Diseases, King's College London, London, UK.
  • McQuillan O; Department of GUM and HIV, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Wang Y; The Northern Contraception Sexual Health Service & HIV Service, Manchester University NHS Foundation Trust, Manchester, UK.
  • Clarke A; Department of Infectious Diseases, King's College London, London, UK.
  • Menon-Johansson A; Department of GUM and HIV, University Hospitals Sussex NHS Foundation Trust, Worthing, UK.
Sex Transm Infect ; 2022 Dec 23.
Article em En | MEDLINE | ID: mdl-36564186
BACKGROUND: Effectiveness of HIV postexposure prophylaxis (PEPSE) correlates with speed of uptake following HIV exposure. Time to first dose has not improved in the UK for over 10 years. On-demand pre-exposure prophylaxis (PrEP) has shown that people can self-start medication for HIV prevention.We hypothesised that advanced provision of PEPSE (HOME PEPSE) for men who have sex with men (MSM) to self- initiate would reduce time to first dose following HIV exposure. METHODS: Phase IV, randomised, prospective, 48-week, open-label study was carried out. MSM at medium risk of acquiring HIV were randomised (1:1) to immediate or deferred standard of care (SOC) HOME PEPSE. Every 12 weeks, participants self-completed mental health/risk behaviour surveys and had HIV/sexually transmitted infection (STI) testing.HOME PEPSE comprised a 5-day pack of emtricitabine/tenofovir disoproxil fumarate/maraviroc 600 mg once daily initiated following potential exposure to HIV. If taken, participants completed a risk survey; PEPSE continuation was physician directed. Primary outcome was time from potential exposure to HIV to first PEPSE dose. FINDINGS: 139 participants randomised 1:1; 69 to immediate HOME PEPSE and 70 to deferred HOME PEPSE. Median age 30 years (IQR 26-39), 75% white, 55% UK born and 72% university educated. 31 in HOME PEPSE and 15 in SOC arm initiated PEPSE. Uptake of HOME PEPSE was appropriate in 27/31 cases (87%, 95% CI: 71% to 95%). Median time from exposure to first dose was 7.3 hours (3.0, 20.9) for HOME PEPSE and 28.5 hours (17.3, 34.0) for SOC (p<0.01). HOME PEPSE was well tolerated with no discontinuations.No significant differences in missed opportunities for PEPSE uptake, sexual behaviour or bacterial STI infections between treatment arms. INTERPRETATION: HOME PEPSE reduced the time from exposure to first-dose PEPSE by 21+ hours, with no impact on safety. This significantly improves the efficacy of PEPSE and provides an option for people declining PrEP.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Sex Transm Infect Assunto da revista: DOENCAS SEXUALMENTE TRANSMISSIVEIS Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Sex Transm Infect Assunto da revista: DOENCAS SEXUALMENTE TRANSMISSIVEIS Ano de publicação: 2022 Tipo de documento: Article