Naturalistic follow-up after a trial of medications for opioid use disorder: Medication status, opioid use, and relapse.


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:
12 2021
Historique:
received: 05 10 2020
revised: 23 04 2021
accepted: 26 04 2021
pubmed: 8 6 2021
medline: 22 3 2022
entrez: 7 6 2021
Statut: ppublish

Résumé

This report examined naturalistic opioid use outcomes and utilization of medications for opioid use disorder (MOUD) 36 weeks post-randomization in the National Drug Abuse Treatment Clinical Trials Network (CTN) Extended-Release Naltrexone (XR-NTX) versus Buprenorphine-Naloxone (BUP-NX) for Opioid Treatment trial (CTN-0051, X:BOT). X:BOT was a multisite, randomized, 24-week comparative effectiveness trial of BUP-NX (N = 287) and XR-NTX (N = 283). Study medications were discontinued following treatment completion, relapse, or dropout. Participants were encouraged to continue MOUD. This report examined opioid use outcomes in 428 (75%) of the 570 participants who attended the 36-week follow-up visit. Adults with opioid use disorder recruited from 8 community treatment programs across the United States. Outcomes included medication status (on/off MOUD), type of MOUD (BUP-NX, XR-NTX, or methadone), abstinence from non-prescribed opioids, opioid use days, relapse, and other substance use 30 days prior to the 36-week visit. Relapse was defined as opioid use for 4 consecutive weeks or 7 consecutive days in the past month. Baseline and clinical variables included opioid use severity, intravenous drug use, study medication assignment, and induction status. Of the 428 participants who completed the 36-week visit, 225 (53%) of participants were receiving MOUD and 203 (47%) were not. Compared to those off medication, participants on medication had fewer opioid use days (4.4 days (SD 9.0) versus 9.8 days (SD 12.1)), fewer met relapse criteria (37 (16.4%) versus 79 (38.9%)), and reported less stimulant use (34 (15.2%) versus 56 (27.7%)) and sedative use (14 (6.3%) versus 31 (15.3%)). There was no difference in abstinence rates between those on or off MOUD. A greater proportion of participants on XR-NTX (47 (53.4%) of 88 participants) were abstinent from non-prescribed opioids compared to those on buprenorphine (28 (23.3%) of 120 participants). Naturalistic outcomes data showed that despite potential barriers to continuing treatment in the community, about half of individuals were on opioid use disorder pharmacotherapy at follow-up and those on medication generally had better outcomes. Future research should explore barriers and facilitators to treatment retention in community settings; and developing interventions tailored to improve treatment engagement and adherence.

Identifiants

pubmed: 34098301
pii: S0740-5472(21)00173-2
doi: 10.1016/j.jsat.2021.108447
pmc: PMC8556394
mid: NIHMS1701783
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Delayed-Action Preparations 0
Narcotic Antagonists 0
Naltrexone 5S6W795CQM

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

108447

Subventions

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

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

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Auteurs

Miranda G Greiner (MG)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: miranda.greiner@nyspi.columbia.edu.

Matisyahu Shulman (M)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: matisyahu.shulman@nyspi.columbia.edu.

Tse-Hwei Choo (TH)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: tse.hwei@nyspi.columbia.edu.

Jennifer Scodes (J)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: jennifer.scodes@nyspi.columbia.edu.

Martina Pavlicova (M)

Columbia University Mailman School of Public Health, 722 West 168th Street, New York, NY 10032, United States of America. Electronic address: mp2370@columbia.edu.

Aimee N C Campbell (ANC)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: anc2002@cumc.columbia.edu.

Patricia Novo (P)

New York University Grossman School of Medicine, 550 First Avenue, New York, NY 10016, United States of America. Electronic address: patricia.novo@nyulangone.org.

Marc Fishman (M)

Johns Hopkins University School of Medicine and Maryland Treatment Centers, 3800 Frederick Ave, Baltimore, MD 21229, United States of America.

Joshua D Lee (JD)

New York University Grossman School of Medicine, 550 First Avenue, New York, NY 10016, United States of America. Electronic address: joshua.lee@nyulangone.org.

John Rotrosen (J)

New York University Grossman School of Medicine, 550 First Avenue, New York, NY 10016, United States of America. Electronic address: john.rotrosen@nyulangone.org.

Edward V Nunes (EV)

New York State Psychiatric Institute and Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States of America. Electronic address: edward.nunes@nyspi.columbia.edu.

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