Association between methadone or buprenorphine use during medically supervised opioid withdrawal and extended-release injectable naltrexone induction failure.


Journal

Journal of substance abuse treatment
ISSN: 1873-6483
Titre abrégé: J Subst Abuse Treat
Pays: United States
ID NLM: 8500909

Informations de publication

Date de publication:
05 2021
Historique:
received: 08 05 2020
revised: 13 01 2021
accepted: 13 01 2021
entrez: 27 3 2021
pubmed: 28 3 2021
medline: 29 7 2021
Statut: ppublish

Résumé

Extended-release naltrexone (XR-NTX) is an effective maintenance treatment for opioid use disorder, but induction from active opioid use is a challenge as individuals must complete detoxification before induction. We aimed to determine whether use of methadone or buprenorphine, long acting agonist opioids commonly used for detoxification, were associated with decreased likelihood of induction onto XR-NTX. We performed a secondary analysis of a large open-label randomized trial of buprenorphine versus XR-NTX for treatment of individuals with opioid use disorder recruited from eight short term residential (detoxification) units. This analysis only included individuals randomized to the XR-NTX arm of the trial (N = 283). The method of detoxification varied according to usual practices at each inpatient program. Logistic regression models estimating the log-odds of induction onto XR-NTX were fit, with detoxification regimen received as the predictor. In the unadjusted logistic regression model, detoxification drug received (either methadone or buprenorphine) was significantly associated with decreased likelihood of induction onto XR-NTX compared to receiving non-opioid detoxification (Overall: P < 0.001); buprenorphine vs non-opioid detoxification: OR (95% CI) = 0.32 (0.15-0.67); methadone vs non-opioid detoxification: OR (95% CI) = 0.23 (0.11-0.46). After controlling for site as a random effect, the association of detoxification drug with induction success lost statistical significance. Use of agonist medication during detoxification was associated with XR-NTX induction failure. Medication choice was determined by each site's clinical practice and therefore this association could not be separated from other site level variables. NCT02032433.

Sections du résumé

BACKGROUND
Extended-release naltrexone (XR-NTX) is an effective maintenance treatment for opioid use disorder, but induction from active opioid use is a challenge as individuals must complete detoxification before induction. We aimed to determine whether use of methadone or buprenorphine, long acting agonist opioids commonly used for detoxification, were associated with decreased likelihood of induction onto XR-NTX.
METHODS
We performed a secondary analysis of a large open-label randomized trial of buprenorphine versus XR-NTX for treatment of individuals with opioid use disorder recruited from eight short term residential (detoxification) units. This analysis only included individuals randomized to the XR-NTX arm of the trial (N = 283). The method of detoxification varied according to usual practices at each inpatient program. Logistic regression models estimating the log-odds of induction onto XR-NTX were fit, with detoxification regimen received as the predictor.
RESULTS
In the unadjusted logistic regression model, detoxification drug received (either methadone or buprenorphine) was significantly associated with decreased likelihood of induction onto XR-NTX compared to receiving non-opioid detoxification (Overall: P < 0.001); buprenorphine vs non-opioid detoxification: OR (95% CI) = 0.32 (0.15-0.67); methadone vs non-opioid detoxification: OR (95% CI) = 0.23 (0.11-0.46). After controlling for site as a random effect, the association of detoxification drug with induction success lost statistical significance.
CONCLUSIONS
Use of agonist medication during detoxification was associated with XR-NTX induction failure. Medication choice was determined by each site's clinical practice and therefore this association could not be separated from other site level variables.
CLINICAL TRIAL REGISTRATION
NCT02032433.

Identifiants

pubmed: 33771287
pii: S0740-5472(21)00018-0
doi: 10.1016/j.jsat.2021.108292
pmc: PMC8004552
mid: NIHMS1663936
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Delayed-Action Preparations 0
Narcotic Antagonists 0
Buprenorphine 40D3SCR4GZ
Naltrexone 5S6W795CQM
Methadone UC6VBE7V1Z

Banques de données

ClinicalTrials.gov
['NCT02032433']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

108292

Subventions

Organisme : NIDA NIH HHS
ID : T32 DA007294
Pays : United States
Organisme : NIDA NIH HHS
ID : U10 DA013035
Pays : United States
Organisme : NIDA NIH HHS
ID : UG1 DA013035
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

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Auteurs

Matisyahu Shulman (M)

New York State Psychiatric Institute, United States of America; Department of Psychiatry, Columbia University Medical Center, United States of America. Electronic address: matisyahu.shulman@nyspi.columbia.edu.

Tse-Hwei Choo (TH)

New York State Psychiatric Institute, United States of America.

Jennifer Scodes (J)

New York State Psychiatric Institute, United States of America.

Martina Pavlicova (M)

Department of Biostatistics, Mailman School of Public Health, Columbia University, United States of America.

Jonathan Wai (J)

New York State Psychiatric Institute, United States of America; Department of Psychiatry, Columbia University Medical Center, United States of America.

Patrick Haenlein (P)

Department of Psychiatry, Columbia University Medical Center, United States of America.

Babak Tofighi (B)

Department of Population Health, New York University, United States of America.

Aimee N C Campbell (ANC)

New York State Psychiatric Institute, United States of America; Department of Psychiatry, Columbia University Medical Center, United States of America.

Joshua D Lee (JD)

Department of Population Health, New York University, United States of America.

John Rotrosen (J)

Department of Psychiatry, New York University School of Medicine, United States of America.

Edward V Nunes (EV)

New York State Psychiatric Institute, United States of America; Department of Psychiatry, Columbia University Medical Center, United States of America.

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Classifications MeSH