Evidence map›Paper›PMID 35364026›Full record

SynthesisThe lancet. HIV2022

Discontinuation, suboptimal adherence, and reinitiation of oral HIV pre-exposure prophylaxis: a global systematic review and meta-analysis.

Jing Zhang, Chunyan Li, Junjie Xu, Zhili Hu, Sarah E Rutstein, Joseph D Tucker, Jason J Ong, Yongjun Jiang, Wenqing Geng, Sarah T Wright and 3 more

Registry-linked trialOpen access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in The lancet. HIV, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06133686 (Implementing Oral), which is not on this map. Cited by 142 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed, 4 pooled it
37.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06133686 phase3not yet recruitingnot on this mapstarted 2024, after this paper: background citation

Implementing Oral (Event-driven and Daily) and Long-acting Pre-Exposure Prophylaxis in Mobile Men in Sub-Saharan Africa: a Phase 3b, Open-label, Hybrid Type 2 Implementation and Effectiveness Trial

TypeinterventionalSponsorMRC/UVRI and LSHTM Uganda Research UnitRan2024 to 2027Enrolled400ConditionsHIVArmsTenofovir disoproxil fumarate/emtricitabine (TDF-FTC), cabotegravir (CAB-LA), Cabotegravir (CAB-LA), Tenofovir disoproxil fumarate/emtricitabine (TDF-FTC)
3 · Its place in the literature

Who cites it

142 citing papers in PubMed, 4 syntheses or guidelines pooled it, 204 citations in OpenAlex.

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82 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 2 countries.

Jing ZhangNHC Key Laboratory of AIDS Immunology and National Clinical Research Center for Laboratory Medicine, First Affiliated Hospital of China Medical University, Shenyang, China; Key Laboratory of AIDS Immunology, Chinese Academy of Medical Sciences, Shenyang, China; Key Laboratory of AIDS Immunology of Liaoning Province, Shenyang, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Shenyang, China.
Chunyan LiDepartment of Health Behavior, University of North Carolina, Chapel Hill, NC, USA.
Junjie XuPeking University Shenzhen Hospital, Shenzhen, China.
Zhili HuNHC Key Laboratory of AIDS Immunology and National Clinical Research Center for Laboratory Medicine, First Affiliated Hospital of China Medical University, Shenyang, China; Key Laboratory of AIDS Immunology, Chinese Academy of Medical Sciences, Shenyang, China; Key Laboratory of AIDS Immunology of Liaoning Province, Shenyang, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Shenyang, China.
Sarah E RutsteinDepartment of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Joseph D TuckerDepartment of Medicine, University of North Carolina, Chapel Hill, NC, USA; University of North Carolina Project-China, Guangzhou, China; Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Jason J OngFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK; Monash University, Melbourne, VIC, Australia.
Yongjun JiangNHC Key Laboratory of AIDS Immunology and National Clinical Research Center for Laboratory Medicine, First Affiliated Hospital of China Medical University, Shenyang, China; Key Laboratory of AIDS Immunology, Chinese Academy of Medical Sciences, Shenyang, China; Key Laboratory of AIDS Immunology of Liaoning Province, Shenyang, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Shenyang, China.
Wenqing GengNHC Key Laboratory of AIDS Immunology and National Clinical Research Center for Laboratory Medicine, First Affiliated Hospital of China Medical University, Shenyang, China; Key Laboratory of AIDS Immunology, Chinese Academy of Medical Sciences, Shenyang, China; Key Laboratory of AIDS Immunology of Liaoning Province, Shenyang, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Shenyang, China.
Sarah T WrightHealth Sciences Library, University of North Carolina, Chapel Hill, NC, USA.
Myron S CohenDepartment of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Hong ShangNHC Key Laboratory of AIDS Immunology and National Clinical Research Center for Laboratory Medicine, First Affiliated Hospital of China Medical University, Shenyang, China; Key Laboratory of AIDS Immunology, Chinese Academy of Medical Sciences, Shenyang, China; Key Laboratory of AIDS Immunology of Liaoning Province, Shenyang, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Shenyang, China.
Weiming TangDepartment of Medicine, University of North Carolina, Chapel Hill, NC, USA; University of North Carolina Project-China, Guangzhou, China; Dermatology Hospital of Southern Medical University, Guangzhou, China. Electronic address: weiming_tang@med.unc.edu.
University of North Carolina at Chapel Hill · USPeking University Shenzhen Hospital · CN

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Training in Sexually Transmitted Infections and HIVT32AI007001 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SENA-SOBERANO, ARLENE C. · 1985 to 2025
$10.9M
Mentoring Multidisciplinary Global HIV Patient-Oriented ResearchK24AI143471 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph David Tucker · 2019 to 2026
$1.4M
Development of an HIV Self-testing Intervention to Reduce HIV risks among MSM: Taking the Guess Out of SeroguessingR34MH109359 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WEI, CHONGYI · 2016 to 2018
$726k
Enhancing Partner Services among Men Who Have Sex with Men Living With HIV: A Pilot Randomized Controlled TrialR34MH119963 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TANG, WEIMING, TUCKER, JOSEPH DAVID · 2019 to 2021
$568k
NIAID NIH HHS K24 AI143471NIAID NIH HHS P30 AI050410NIAID NIH HHS T32 AI007001NIMH NIH HHS R34 MH109359NIMH NIH HHS R34 MH119963
6 · The paper itself

Abstract

backgroundPoor adherence to oral HIV pre-exposure prophylaxis (PrEP) diminishes its clinical and public health benefits. This study synthesises evidence regarding discontinuation, adherence, and reinitiation of PrEP among geographically diverse PrEP users.

methodsWe did a systematic review and meta-analysis evaluating studies published in MEDLINE, Embase, and Cochrane Central Register of Controlled Trials from inception to Dec 18, 2020. We included longitudinal studies that presented data for PrEP discontinuation, defined as investigator-reported loss to follow-up or participant self-reported PrEP stoppage. Data were extracted from published reports and assessed for risk of bias. We used a random-effects meta-analysis to pool estimates of discontinuation and I

findingsWe identified 4129 records, of which 59 articles were included (n=43 917 participants). 41·0% (95% CI 18·8-63·5) of participants discontinued PrEP within 6 months, with the highest rates in observational studies. The discontinuation rate in sub-Saharan Africa (47·5%, 95% CI: 29·4-66·4%) was higher than in other regions (p<0·001). Discontinuation rates were lower in studies with adherence interventions than in those without (24·7% vs 36·7%, p=0·015). Gay or bisexual men who have sex with men and transgender women offered daily or non-daily dosing options had lower discontinuation rates than those offered daily dosing alone (21·6% vs 31·5%; p<0·001). The pooled suboptimal adherence within 6 months was 37·7% (95% CI 8·4-66·9). Among people who discontinued PrEP, 47·3% (95% CI 31·5-63·2) reinitiated PrEP within 1 year of PrEP initiation. The included studies had poor quality in terms of study design, with a moderate risk of bias.

interpretationStrategies to encourage reinitiating PrEP for new or persistent risk should be a focus of future PrEP implementation strategies.

fundingNational Institutes of Health and Nature Science Foundation of China.

Indexed as

Anti-HIV AgentsHIV InfectionsPre-Exposure ProphylaxisSexual and Gender MinoritiesFemaleHomosexuality, MaleHumansMaleAnti-HIV Agents

Identifiers

PMID35364026
PMCPMC9124596
OpenAlexW4220828731

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.