Evidence map›Paper›PMID 18586174›Full record

Trial reportLancet (London, England)2008

Maintenance treatment with buprenorphine and naltrexone for heroin dependence in Malaysia: a randomised, double-blind, placebo-controlled trial.

Richard S Schottenfeld, Marek C Chawarski, Mahmud Mazlan

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Lancet (London, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00383045 (HIV Risk Reduction and Drug Abuse Treatment in Malaysia), which is not on this map. Cited by 40 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 9 pooled it
11.1field-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.

NCT00383045 phase2completednot on this map

HIV Risk Reduction and Drug Abuse Treatment in Malaysia

TypeinterventionalSponsorYale UniversityRan2003 to 2007Enrolled180ConditionsOpiate DependenceArmsBuprenorphine/Subutex, Naltrexone, Drug counseling
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 9 syntheses or guidelines pooled it, 103 citations in OpenAlex.

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  9. Oral naltrexone maintenance treatment for opioid dependence.The Cochrane database of systematic reviews · 2011
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Richard S SchottenfeldDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Marek C Chawarski
Mahmud Mazlan
Yale University · US

Funding

HIV Risk Reduction and Drug Abuse Treatment in MalaysiaR01DA014718 · NIDA · YALE UNIVERSITY · PI SCHOTTENFELD, RICHARD S · 2001 to 2013
$3.6M
IMPROVING EFFICACY OF DRUG ABUSE TREATMENTK24DA000445 · NIDA · YALE UNIVERSITY · PI SCHOTTENFELD, RICHARD S · 2000 to 2009
$1.3M
NIDA NIH HHS K24 DA000445NIDA NIH HHS R01 DA014718NIDA NIH HHS R01 DA14718
6 · The paper itself

Abstract

backgroundExpansion of access to effective treatments for heroin dependence is a worldwide health priority that will also reduce HIV transmission. We compared the efficacy of naltrexone, buprenorphine, and no additional treatment, in patients receiving detoxification and subsequent drug counselling, for maintenance of heroin abstinence, prevention of relapse, and reduction of HIV risk behaviours.

methods126 detoxified heroin-dependent patients, from an outpatient research clinic and detoxification programme in Malaysia, were randomly assigned by a computer-generated randomisation sequence to 24 weeks of manual-guided drug counselling and maintenance with naltrexone (n=43), buprenorphine (n=44), or placebo (n=39). Medications were administered on a double-blind and double-dummy basis. Primary outcomes, assessed by urine testing three times per week, were days to first heroin use, days to heroin relapse (three consecutive opioid-positive urine tests), maximum consecutive days of heroin abstinence, and reductions in HIV risk behaviours over 6 months. The study was terminated after 22 months of enrolment because buprenorphine was shown to have greater efficacy in an interim safety analysis. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00383045.

findingsWe observed consistent, linear contrasts in days to first heroin use (p=0.0009), days to heroin relapse (p=0.009), and maximum consecutive days abstinent (p=0.0007), with all results best for buprenorphine and worst for placebo. Buprenorphine was associated with greater time to first heroin use than were naltrexone (hazard ratio 1.87 [95% CI 1.21-2.88]) or placebo (2.02 [1.29-3.16]). With buprenorphine, we also recorded significantly greater time to heroin relapse (2.17 [1.38-3.42]), and maximum consecutive days abstinent than with placebo (mean days 59 [95% CI 43-76] vs 24 [13-35]; p=0.003); however, for these outcomes, differences between buprenorphine and naltrexone were not significant. Differences between naltrexone and placebo were not significant for any outcomes. HIV risk behaviours were significantly reduced from baseline across all three treatments (p=0.003), but the reductions did not differ significantly between the three groups.

interpretationOur findings lend support to the widespread dissemination of maintenance treatment with buprenorphine as an effective public-health approach to reduce problems associated with heroin dependence.

Indexed as

AdultBuprenorphineCounselingDouble-Blind MethodHeroin DependenceHIV InfectionsHumansMalaysiaNaltrexoneNarcotic AntagonistsRecurrenceRisk-TakingTreatment OutcomeBuprenorphineNaltrexoneNarcotic Antagonists

Identifiers

PMID18586174
PMCPMC4041792
OpenAlexW2051884986

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.