PrEP uptake and HIV viral suppression when PrEP is integrated into Ugandan ART clinics for HIV-negative members of HIV-serodifferent couples: A stepped wedge cluster randomized trial.

ART PrEP Serodifferent couples Stepped-wedge trial Viral suppression

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 27 05 2022
revised: 15 07 2022
accepted: 22 07 2022
entrez: 22 8 2022
pubmed: 23 8 2022
medline: 23 8 2022
Statut: epublish

Résumé

Global scale-up of HIV pre-exposure prophylaxis (PrEP) includes services to HIV-negative people in partnerships with people living with HIV (serodifferent couples). Data are needed on HIV outcomes, including uptake and adherence to PrEP and antiretroviral treatment (ART), to describe the impact of integrating PrEP into an existing HIV program. Using a stepped-wedge cluster randomized trial design, we launched PrEP delivery for HIV-negative members of serodifferent couples in Uganda by integrating PrEP into existing ART programs for people living with HIV. The program provided PrEP training for ART providers, ongoing technical assistance, and a provisional supply chain mechanism for PrEP medication. Primary data on PrEP initiation, PrEP refills, ART initiation, and HIV viremia at 6 months (measured at 42-270 days) were collected through data abstraction of medical records from HIV-serodifferent couples sequentially enrolling at the ART clinics. Modified Poisson regression models, controlling for time and cluster, compared viral suppression (<1000 copies/ml) before and after launch of the PrEP program. This trial was registered at ClinicalTrials.gov, NCT03586128. From June 1, 2018-December 15, 2020, 1,381 HIV-serodifferent couples were enrolled across 12 ART clinics in Kampala and Wakiso, Uganda, including 730 enrolled before and 651 after the launch of PrEP delivery. During the baseline period, 99.4% of partners living with HIV initiated ART and 85.0% were virally suppressed at 6 months. Among HIV-negative partners enrolled after PrEP launched, 81.0% (527/651) initiated PrEP within 90 days of enrolling; among these 527, 11.2% sought a refill 6 months later. In our powered intent-to-treat analysis, 82.1% and 76.7% of partners living with HIV were virally suppressed, respectively, which was not a statistically significant difference (RR=0.94, 95% CI: 0.82-1.07) and was stable across sensitivity analyses. Integration of PrEP into ART clinics reached a high proportion of people in HIV-serodifferent relationships and did not improve the already high frequency of HIV viral suppression among partners living with HIV. National Institute of Mental Health (R01MH110296).

Sections du résumé

Background UNASSIGNED
Global scale-up of HIV pre-exposure prophylaxis (PrEP) includes services to HIV-negative people in partnerships with people living with HIV (serodifferent couples). Data are needed on HIV outcomes, including uptake and adherence to PrEP and antiretroviral treatment (ART), to describe the impact of integrating PrEP into an existing HIV program.
Methods UNASSIGNED
Using a stepped-wedge cluster randomized trial design, we launched PrEP delivery for HIV-negative members of serodifferent couples in Uganda by integrating PrEP into existing ART programs for people living with HIV. The program provided PrEP training for ART providers, ongoing technical assistance, and a provisional supply chain mechanism for PrEP medication. Primary data on PrEP initiation, PrEP refills, ART initiation, and HIV viremia at 6 months (measured at 42-270 days) were collected through data abstraction of medical records from HIV-serodifferent couples sequentially enrolling at the ART clinics. Modified Poisson regression models, controlling for time and cluster, compared viral suppression (<1000 copies/ml) before and after launch of the PrEP program. This trial was registered at ClinicalTrials.gov, NCT03586128.
Findings UNASSIGNED
From June 1, 2018-December 15, 2020, 1,381 HIV-serodifferent couples were enrolled across 12 ART clinics in Kampala and Wakiso, Uganda, including 730 enrolled before and 651 after the launch of PrEP delivery. During the baseline period, 99.4% of partners living with HIV initiated ART and 85.0% were virally suppressed at 6 months. Among HIV-negative partners enrolled after PrEP launched, 81.0% (527/651) initiated PrEP within 90 days of enrolling; among these 527, 11.2% sought a refill 6 months later. In our powered intent-to-treat analysis, 82.1% and 76.7% of partners living with HIV were virally suppressed, respectively, which was not a statistically significant difference (RR=0.94, 95% CI: 0.82-1.07) and was stable across sensitivity analyses.
Interpretation UNASSIGNED
Integration of PrEP into ART clinics reached a high proportion of people in HIV-serodifferent relationships and did not improve the already high frequency of HIV viral suppression among partners living with HIV.
Funding UNASSIGNED
National Institute of Mental Health (R01MH110296).

Identifiants

pubmed: 35990584
doi: 10.1016/j.eclinm.2022.101611
pii: S2589-5370(22)00341-8
pmc: PMC9386395
doi:

Banques de données

ClinicalTrials.gov
['NCT03586128']

Types de publication

Journal Article

Langues

eng

Pagination

101611

Subventions

Organisme : NIMH NIH HHS
ID : P30 MH123248
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH110296
Pays : United States

Investigateurs

Renee Heffron (R)
Jared M Baeten (JM)
Jane Simoni (J)
Deborah Donnell (D)
Ruanne Barnabas (R)
Katherine K Thomas (KK)
Dorothy Thomas (D)
Erika Feutz (E)
Cole Grabow (C)
Allison Meisner (A)
Kristin Ciccarelli (K)
Caitlin Scoville (C)
Katrina Ortblad (K)
Andrew Mujugira (A)
Timothy R Muwonge (TR)
Joseph Kibuuka (J)
Lylianne Nakabugo (L)
Florence Nambi (F)
Mai Nakitende (M)
Diego Izizinga (D)
Vicent Kasita (V)
Brenda Kamusiime (B)
Alisaati Nalumansi (A)
Collins Twesige (C)
Grace Kakoola (G)
Charles Brown (C)
Sylvia Namanda (S)
Herbert Kadama (H)
Norma C Ware (NC)
Monique A Wyatt (MA)
Emily Pisarski (E)
Ingrid T Katz (IT)

Informations de copyright

© 2022 The Authors.

Déclaration de conflit d'intérêts

JMB reports being an employee of Gilead Sciences, with salary and stock/options, outside the submitted work. All other authors declare no competing interests.

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Auteurs

Renee Heffron (R)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.
University of Alabama Birmingham, Birmingham, Alabama, USA.

Timothy R Muwonge (TR)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Katherine K Thomas (KK)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.

Florence Nambi (F)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Lylianne Nakabugo (L)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Joseph Kibuuka (J)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Dorothy Thomas (D)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.

Erika Feutz (E)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.

Allison Meisner (A)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.
Fred Hutch, Vaccine and Infectious Disease Division, 1100 Fairview Ave N, Seattle, Washington, USA.

Norma C Ware (NC)

Harvard Medical School, 25 Shattuck St., Boston, Massachusetts, USA.
Brigham and Women's Hospital, Harvard Medical School, 75 Francis St, Boston, Massachusetts, USA.

Monique A Wyatt (MA)

Harvard Medical School, 25 Shattuck St., Boston, Massachusetts, USA.
Harvard Global, Cambridge, Massachusetts, USA.

Jane M Simoni (JM)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.

Ingrid T Katz (IT)

Brigham and Women's Hospital, Harvard Medical School, 75 Francis St, Boston, Massachusetts, USA.
Brigham and Women's Hospital, Harvard Medical School, 75 Francis St, Boston, Massachusetts, USA.

Herbert Kadama (H)

Ministry of Health, Box 7272, Kampala, Uganda.

Jared M Baeten (JM)

University of Washington, 325 Ninth Avenue, Box 359927 Seattle, Washington, USA.
Gilead Sciences LLC, Foster City, California, USA.

Andrew Mujugira (A)

Infectious Diseases Institute, Makerere University, Kampala, Uganda.

Classifications MeSH