Evidence map›Paper›PMID 25564105›Full record

Trial reportJournal of acquired immune deficiency syndromes (1999)2015

Expanding substance use treatment options for HIV prevention with buprenorphine-naloxone: HIV Prevention Trials Network 058.

David S Metzger, Deborah Donnell, David D Celentano, J Brooks Jackson, Yiming Shao, Apinun Aramrattana, Liu Wei, Liping Fu, Jun Ma, Gregory M Lucas and 11 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of acquired immune deficiency syndromes (1999), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 11 institutions in 4 countries.

David S Metzger*Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and Treatment Research Institute, Philadelphia, PA; †Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA; ‡Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD; §Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD and Department of Pathology, University of Minnesota, Minneapolis, MN; ‖State Key Laboratory for Infectious Disease Prevention and Control, National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Beijing, China; ¶Department of Family Medicine, Faculty of Medicine, Chiang Mai University; #Guangxi Centers for Disease Control and Prevention, Guangxi Center for HIV/AIDS Prevention and Control, Nanning, China; **Xinjiang Autonomous Region Center for Disease Control and Prevention, Xinjiang, China; ††Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD; ‡‡Department of Psychiatry, Yale School of Medicine, New Haven, CT; §§Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD; ‖‖Division of AIDS, Pharmaceutical Affairs Branch, National Institute of Allergy and Infectious Diseases; ¶¶Division of Intramural Research, National Institute of Allergy and Infectious Diseases; ##Berman Institute of Bioethics, Johns Hopkins University, Baltimore, MD; ***FHI 360; †††Fred Hutchinson Cancer Research Center, Vaccine and Infectious Disease Division; and ‡‡‡Division of AIDS, Prevention Sciences Branch, National Institute of Allergy and Infectious Diseases.
Deborah Donnell
David D Celentano
J Brooks Jackson
Yiming Shao
Apinun Aramrattana
Liu Wei
Liping Fu
Jun Ma
Gregory M Lucas
Marek Chawarski
Yuhua Ruan
Paul Richardson
Katherine Shin
Ray Y Chen
Jeremy Sugarman
Bonnie J Dye
Scott M Rose
Geetha Beauchamp
David N Burns
HPTN 058 Protocol Team
Johns Hopkins University · USFamily Health International 360 · USNational Institute of Allergy and Infectious Diseases · USXinjiang Uygur Autonomous Region Disease Prevention and Control Center · CNCancer Research Center · USChiang Mai University · THFred Hutch Cancer Center · USGuangxi Center for Disease Prevention and Control · CNJohns Hopkins Berman Institute of Bioethics · USJohns Hopkins Medicine · USYale University · US

Funding

LOC: HIV Prevention Trials NetworkUM1AI068619 · NIAID · FAMILY HEALTH INTERNATIONAL · PI Sinead Delany-Moretlwe, RAPHAEL J LANDOVITZ · 2011 to 2026
$779.5M
SDMC: HPTN 084 Pregnancy SupplementUM1AI068617 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Elizabeth Renata Brown, Deborah J Donnell · 2011 to 2026
$204.9M
LC: HIV Prevention Trials Network - Laboratory Support for the SARS-CoV-2 Seroprevalence Study (CoVPN 5002)UM1AI068613 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SUSAN H ESHLEMAN, Mark A Marzinke · 2011 to 2026
$100.2M
Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVID S METZGER · 1999 to 2026
$78.6M
HIV Prevention trials Network (HPTN) Coordinating and Operations CenterU01AI068619 · NIAID · FAMILY HEALTH INTERNATIONAL · PI VERMUND, STEN H. · 2006 to 2010
$72.7M
Penn Mental Health AIDS Research CenterP30MH097488 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Karine Dube · 2013 to 2026
$23.5M
HIV Prevention Trials Network: Network LaboratoryU01AI068613 · NIAID · JOHNS HOPKINS UNIVERSITY · PI ESHLEMAN, SUSAN H · 2006 to 2010
$16.5M
International Tuberculosis Research in ChinaZIAAI001081 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BARRY, CLIFTON · 2010 to 2025
$12.2M
Johns Hopkins University-Guangxi, China Clinical Trials UnitUM1AI069482 · NIAID · JOHNS HOPKINS UNIVERSITY · PI JACKSON, JAY B · 2012 to 2014
$1.7M
Treatment outcomes and comorbidity in HIV-infected IDUK24DA035684 · NIDA · JOHNS HOPKINS UNIVERSITY · PI LUCAS, GREGORY M · 2014 to 2024
$1.5M
HIV/AIDS Clinical Trial Unit in NCAIDS, China CDCUM1AI069411 · NIAID · NATIONAL CENTER FOR AIDS/STD CONTROL AND PREVENTION · PI SHAO, YIMING · 2012 to 2020
$376k
NIAID NIH HHS P30 AI045008NIAID NIH HHS U01 AI068613NIAID NIH HHS U01 AI068619NIAID NIH HHS UM1 AI068613NIAID NIH HHS UM1 AI068617NIAID NIH HHS UM1 AI068619NIAID NIH HHS UM1 AI069411NIAID NIH HHS UM1 AI069482NIDA NIH HHS K24 DA035684NIMH NIH HHS P30 MH097488
6 · The paper itself

Abstract

backgroundInjection opioid use plays a significant role in the transmission of HIV infection in many communities and several regions of the world. Access to evidence-based treatments for opioid use disorders is extremely limited.

methodsHIV Prevention Trials Network 058 (HPTN 058) was a randomized controlled trial designed to compare the impact of 2 medication-assisted treatment (MAT) strategies on HIV incidence or death among opioid-dependent people who inject drugs (PWID). HIV-negative opioid-dependent PWID were recruited from 4 communities in Thailand and China with historically high prevalence of HIV among PWID. A total of 1251 participants were randomly assigned to either (1) a 1-year intervention consisting of 2 opportunities for a 15-day detoxification with buprenorphine/naloxone (BUP/NX) combined with up to 21 sessions of behavioral drug and risk counseling [short-term medication-assisted treatment (ST-MAT)] or (2) thrice-weekly dosing for 48 weeks with BUP/NX and up to 21 counseling sessions [long-term medication-assisted treatment (LT-MAT)] followed by dose tapering. All participants were followed for 52 weeks after treatment completion to assess durability of impact.

resultsAlthough the study was stopped early due to lower than expected occurrence of the primary end points, sufficient data were available to assess the impact of the interventions on drug use and injection-related risk behavior. At week 26, 22% of ST-MAT participants had negative urinalyses for opioids compared with 57% in the LT-MAT (P < 0.001). Differences disappeared in the year after treatment: at week 78, 35% in ST-MAT and 32% in the LT-MAT had negative urinalyses. Injection-related risk behaviors were significantly reduced in both groups after randomization.

conclusionsParticipants receiving BUP/NX 3 times weekly were more likely to reduce opioid injection while on active treatment. Both treatment strategies were considered safe and associated with reductions in injection-related risk behavior. These data support the use of thrice-weekly BUP/NX as a way to reduce exposure to HIV risk. Continued access to BUP/NX may be required to sustain reductions in opioid use.

Indexed as

AdultBuprenorphineChinaFemaleHIV InfectionsHumansIncidenceMaleNaloxoneOpiate Substitution TreatmentSubstance Abuse, IntravenousThailandTreatment OutcomeBuprenorphineNaloxone

Identifiers

PMID25564105
PMCPMC4382671
OpenAlexW2093699898

What OpenQuestion holds

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Registered trials

None linked

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.