Comparative effectiveness of extended‐release naltrexone versus buprenorphine‐naloxone on treatment interruption: Comparing findings from a reanalysis of the X:BOT RCT and harmonized target trial emulation using population‐based observational data

Buprenorphine-naloxone might be superior to extended-release naltrexone in real-world settings where the majority of people struggle to remain on medications for opioid use disorder. Buprenorphine-naloxone initiators had a lower risk of treatment interruption than extended-release naltrexone initiators in an observational emulation, but similar risks in a randomized controlled trial, although confidence intervals were wide. Trial participation, study size and residual confounding may explain these differences.

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Publication Details

Journal
Addiction
Published
2025-03-19
DOI
https://doi.org/10.1111/add.70040
Primary Topic
Opioid Use Disorder Treatment
Type
article
Field-Weighted Citation Impact
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article

Comparative effectiveness of extended‐release naltrexone versus buprenorphine‐naloxone on treatment interruption: Comparing findings from a reanalysis of the X:BOT RCT and harmonized target trial emulation using population‐based observational data

Benjamin J. Bovell-Ammon, Patricia Novo, Sara Lodi, Marc R. Larochelle et al.
2 links
Addiction
Opioid Use Disorder Treatment
article

Comparative effectiveness of extended‐release naltrexone versus buprenorphine‐naloxone on treatment interruption: Comparing findings from a reanalysis of the X:BOT RCT and harmonized target trial emulation using population‐based observational data

Benjamin J. Bovell-Ammon, Patricia Novo, Sara Lodi, Marc R. Larochelle, Joshua D. Lee, Alexander Yale Walley, Dana Bernson, Jane M. Liebschutz, Heather Hsu, John Rotrosen, Paul J. Christine, Shapei Yan
article en

Abstract

Buprenorphine-naloxone might be superior to extended-release naltrexone in real-world settings where the majority of people struggle to remain on medications for opioid use disorder. Buprenorphine-naloxone initiators had a lower risk of treatment interruption than extended-release naltrexone initiators in an observational emulation, but similar risks in a randomized controlled trial, although confidence intervals were wide. Trial participation, study size and residual confounding may explain these differences.

AddictionVol. 120(8)
Boston University (US), Boston Medical Center (US), Massachusetts Department of Public Health (US), University of Pittsburgh (US), New York University (US)
National Institute on Drug Abuse
Good health and well-being
Openalex Percentile: Top 93%
Opioid Use Disorder Treatment
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