Evidence map›Paper›PMID 28334661›Full record

Trial reportDrug and alcohol dependence2017

Extended-release naltrexone reduces alcohol consumption among released prisoners with HIV disease as they transition to the community.

Sandra A Springer, Angela Di Paola, Marwan M Azar, Russell Barbour, Archana Krishnan, Frederick L Altice

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Drug and alcohol dependence, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  3. Trial
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  8. Article
  9. HIV and Substance Use Disorders.Infectious disease clinics of North America · 2024
    Review
  10. Article
  11. Integrated Care Models: HIV and Substance Use.Current HIV/AIDS reports · 2023
    Review
  12. Article
  13. Article
  14. Article
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  17. Review
  18. Article
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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

6 authors at 2 institutions in 2 countries.

Sandra A SpringerDepartment of Internal Medicine, Section of Infectious Diseases, AIDS Program, Yale School of Medicine, 135 College Street, Suite 323, New Haven, CT 06510-2283, United States; Yale University School of Public Health, Center for Interdisciplinary Research on AIDS, New Haven, CT 06510-2283, United States. Electronic address: Sandra.springer@yale.edu.
Angela Di PaolaDepartment of Internal Medicine, Section of Infectious Diseases, AIDS Program, Yale School of Medicine, 135 College Street, Suite 323, New Haven, CT 06510-2283, United States.
Marwan M AzarDepartment of Internal Medicine, Section of Infectious Diseases, AIDS Program, Yale School of Medicine, 135 College Street, Suite 323, New Haven, CT 06510-2283, United States.
Russell BarbourYale University School of Public Health, Center for Interdisciplinary Research on AIDS, New Haven, CT 06510-2283, United States.
Archana KrishnanState University of New York at Albany, Department of Communication, Albany, NY, United States.
Frederick L AlticeDepartment of Internal Medicine, Section of Infectious Diseases, AIDS Program, Yale School of Medicine, 135 College Street, Suite 323, New Haven, CT 06510-2283, United States; Yale University School of Public Health, Center for Interdisciplinary Research on AIDS, New Haven, CT 06510-2283, United States; Yale University School of Public Health, Division of Epidemiology of Microbial Diseases, New Haven, CT, United States; Centre of Excellence in Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia.
Yale University · USUniversity at Albany, State University of New York · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
TRAINING IN THE PATHOGENESIS OF INFECTIOUS DISEASEST32AI007517 · NIAID · YALE UNIVERSITY · PI Jaimie Meyer, Albert C Shaw · 1997 to 2026
$6.1M
Alcohol Pharmacotherapies Among Released PrisonersR01AA018944 · NIAAA · YALE UNIVERSITY · PI ALTICE, FREDERICK LEWIS, SPRINGER, SANDRA ANN · 2009 to 2013
$3.8M
Enhancing Health Outcomes Among HIV+ Substance AbusersK24DA017072 · NIDA · YALE UNIVERSITY · PI ALTICE, FREDERICK LEWIS · 2003 to 2012
$1.5M
Medication Assisted Therapy as a Conduit to Care for HIV+ CJS Populations TransitK02DA032322 · NIDA · YALE UNIVERSITY · PI SPRINGER, SANDRA ANN · 2011 to 2022
$1.3M
NCATS NIH HHS UL1 TR001863NIAAA NIH HHS R01 AA018944NIAID NIH HHS T32 AI007517NIDA NIH HHS K02 DA032322NIDA NIH HHS K24 DA017072
6 · The paper itself

Abstract

backgroundAlcohol use disorders (AUDs) are highly prevalent among persons living with HIV (PLH) within the criminal justice system (CJS). Extended-release naltrexone (XR-NTX) has not been previously evaluated among CJS-involved PLH with AUDs.

methodsA randomized, double-blind, placebo-controlled trial was conducted among 100 HIV+ prisoners with AUDs. Participants were randomized 2:1 to receive 6 monthly injections of XR-NTX or placebo starting one week prior to release. Using multiple imputation strategies for data missing completely at random, data were analyzed for the 6-month post-incarceration period. Main outcomes included: time to first heavy drinking day; number of standardized drinks/drinking day; percent of heavy drinking days; pre- to post-incarceration change in average drinks/day; total number of drinking days; and a composite alcohol improvement score comprised of all 5 parameters.

resultsThere was no statistically significant difference overall between treatment arms for time-to-heavy-drinking day. However, participants aged 20-29 years who received XR-NTX had a longer time to first heavy drinking day compared to the placebo group (24.1 vs. 9.5days; p<0.001). There were no statistically significant differences between groups for other individual drinking outcomes. A sub-analysis, however, found participants who received ≥4 XR-NTX were more likely (p<0.005) to have improved composite alcohol scores than the placebo group. Post-hoc power analysis revealed that despite the study being powered for HIV outcomes, sufficient power (0.94) was available to distinguish the observed differences.

conclusionsAmong CJS-involved PLH with AUDs transitioning to the community, XR-NTX lengthens the time to heavy drinking day for younger persons; reduces alcohol consumption when using a composite alcohol consumption score; and is not associated with any serious adverse events.

Indexed as

PrisonersAdultAlcohol DrinkingDelayed-Action PreparationsDouble-Blind MethodFemaleHIV InfectionsHumansMaleMiddle AgedNaltrexoneNarcotic AntagonistsTreatment OutcomeYoung AdultDelayed-Action PreparationsNaltrexoneNarcotic AntagonistsAlcohol Use DisorderExtended-release naltrexoneHazardous drinkingHIVPrisonersRandomized controlled trial

Identifiers

PMID28334661
PMCPMC5407009
OpenAlexW2593980501

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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 Socratic graph.