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An analysis of baseline data from the PROUD study: an open-label randomised trial of pre-exposure prophylaxis.
Dolling, David I; Desai, Monica; McOwan, Alan; Gilson, Richard; Clarke, Amanda; Fisher, Martin; Schembri, Gabriel; Sullivan, Ann K; Mackie, Nicola; Reeves, Iain; Portman, Mags; Saunders, John; Fox, Julie; Bayley, Jake; Brady, Michael; Bowman, Christine; Lacey, Charles J; Taylor, Stephen; White, David; Antonucci, Simone; Gafos, Mitzy; McCormack, Sheena; Gill, Owen N; Dunn, David T; Nardone, Anthony.
Afiliación
  • Dolling DI; MRC Clinical Trials Unit at UCL, Aviation House, 125 Kingsway, London, WC2B 6NH, UK.
  • Desai M; MRC Clinical Trials Unit at UCL, Aviation House, 125 Kingsway, London, WC2B 6NH, UK.
  • McOwan A; HIV/STI Department, Public Health England, London, UK.
  • Gilson R; Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
  • Clarke A; The Mortimer Market Centre, Central and Northwest London NHS Foundation Trust, London, UK.
  • Fisher M; Claude Nichol Centre, Royal Surrey Sussex County Hospital, Brighton, UK.
  • Schembri G; Claude Nichol Centre, Royal Surrey Sussex County Hospital, Brighton, UK.
  • Sullivan AK; Manchester Centre for Sexual Health, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Mackie N; Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
  • Reeves I; St Mary's Hospital, Imperial College NHS Foundation Trust, London, UK.
  • Portman M; Homerton University Hospital NHS Foundation Trust, London, UK.
  • Saunders J; Ambrose King Centre, Barts Health NHS Trust, London, UK.
  • Fox J; Ambrose King Centre, Barts Health NHS Trust, London, UK.
  • Bayley J; Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Brady M; King's College Hospital NHS Foundation Trust, London, UK.
  • Bowman C; King's College Hospital NHS Foundation Trust, London, UK.
  • Lacey CJ; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Taylor S; York Hospitals NHS Foundation Trust, York, UK.
  • White D; Heart of England NHS Foundation Trust, Birmingham, UK.
  • Antonucci S; Heart of England NHS Foundation Trust, Birmingham, UK.
  • Gafos M; Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.
  • McCormack S; MRC Clinical Trials Unit at UCL, Aviation House, 125 Kingsway, London, WC2B 6NH, UK.
  • Gill ON; MRC Clinical Trials Unit at UCL, Aviation House, 125 Kingsway, London, WC2B 6NH, UK. s.mccormack@ucl.ac.uk.
  • Dunn DT; HIV/STI Department, Public Health England, London, UK.
  • Nardone A; MRC Clinical Trials Unit at UCL, Aviation House, 125 Kingsway, London, WC2B 6NH, UK.
Trials ; 17: 163, 2016 Mar 24.
Article en En | MEDLINE | ID: mdl-27013513
ABSTRACT

BACKGROUND:

Pre-exposure prophylaxis (PrEP) has proven biological efficacy to reduce the sexual acquisition of the human immunodeficiency virus (HIV). The PROUD study found that PrEP conferred higher protection than in placebo-controlled trials, reducing HIV incidence by 86 % in a population with seven-fold higher HIV incidence than expected. We present the baseline characteristics of the PROUD study population and place the findings in the context of national sexual health clinic data.

METHODS:

The PROUD study was designed to explore the real-world effectiveness of PrEP (tenofovir-emtricitabine) by randomising HIV-negative gay and other men who have sex with men (GMSM) to receive open-label PrEP immediately or after a deferral period of 12 months. At enrolment, participants self-completed two baseline questionnaires collecting information on demographics, sexual behaviour and lifestyle in the last 30 and 90 days. These data were compared to data from HIV-negative GMSM attending sexual health clinics in 2013, collated by Public Health England using the genitourinary medicine clinic activity database (GUMCAD).

RESULTS:

The median age of participants was 35 (IQR 29-43). Typically participants were white (81 %), educated at a university level (61 %) and in full-time employment (72 %). Of all participants, 217 (40 %) were born outside the UK. A sexually transmitted infection (STI) was reported to have been diagnosed in the previous 12 months in 330/515 (64 %) and 473/544 (87 %) participants reported ever having being diagnosed with an STI. At enrolment, 47/280 (17 %) participants were diagnosed with an STI. Participants reported a median (IQR) of 10 (5-20) partners in the last 90 days, a median (IQR) of 2 (1-5) were condomless sex acts where the participant was receptive and 2 (1-6) were condomless where the participant was insertive. Post-exposure prophylaxis had been prescribed to 184 (34 %) participants in the past 12 months. The number of STI diagnoses was high compared to those reported in GUMCAD attendees.

CONCLUSIONS:

The PROUD study population are at substantially higher risk of acquiring HIV infection sexually than the overall population of GMSM attending sexual health clinics in England. These findings contribute to explaining the extraordinary HIV incidence rate during follow-up and demonstrate that, despite broad eligibility criteria, the population interested in PrEP was highly selective. TRIAL REGISTRATION Current Controlled Trials ISRCTN94465371 . Date of registration 28 February 2013.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prevención Primaria / Infecciones por VIH / Homosexualidad Masculina / Inhibidores de la Transcriptasa Inversa / Fármacos Anti-VIH / Sexo Inseguro / Combinación Emtricitabina y Fumarato de Tenofovir Disoproxil Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Prevención Primaria / Infecciones por VIH / Homosexualidad Masculina / Inhibidores de la Transcriptasa Inversa / Fármacos Anti-VIH / Sexo Inseguro / Combinación Emtricitabina y Fumarato de Tenofovir Disoproxil Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido