Differential effect of cannabis use on opioid agonist treatment outcomes: Exploratory analyses from the OPTIMA study.
Humans
Analgesics, Opioid
/ therapeutic use
Cannabis
/ adverse effects
Narcotic Antagonists
Bayes Theorem
Opiate Substitution Treatment
/ methods
Buprenorphine
Buprenorphine, Naloxone Drug Combination
/ therapeutic use
Opioid-Related Disorders
/ drug therapy
Methadone
/ therapeutic use
Substance Withdrawal Syndrome
/ drug therapy
Cannabinoid
Cannabis
Craving
Opioid use disorder
Withdrawal
Journal
Journal of substance use and addiction treatment
ISSN: 2949-8759
Titre abrégé: J Subst Use Addict Treat
Pays: United States
ID NLM: 9918541186406676
Informations de publication
Date de publication:
06 2023
06 2023
Historique:
received:
24
08
2022
revised:
09
11
2022
accepted:
27
03
2023
medline:
22
5
2023
pubmed:
2
4
2023
entrez:
1
4
2023
Statut:
ppublish
Résumé
Conflictual evidence exists regarding the effects of cannabis use on the outcomes of opioid agonist therapy (OAT). In this exploratory analysis, we examined the effect of recent cannabis use on opioid use, craving, and withdrawal symptoms, in individuals participating in a trial comparing flexible buprenorphine/naloxone (BUP/NX) take-home dosing model to witnessed ingestion of methadone. We analyzed data from a multi-centric, pragmatic, 24-week, open label, randomized controlled trial in individuals with prescription-type opioid use disorder (n = 272), randomly assigned to BUP/NX (n = 138) or methadone (n = 134). The study measured last week cannabis and opioid use via timeline-follow back, recorded at baseline and every two weeks during the study. Craving symptoms were measured using the Brief Substance Craving Scale at baseline, and weeks 2, 6, 10, 14, 18 and 22. The study measured opioid withdrawal symptoms via Clinical Opiate Withdrawal Scale at treatment initiation and weeks 2, 4, and 6. The mean maximum dose taken during the study was 17.3 mg/day (range = 0.5-32 mg/day) for BUP/NX group and 67.7 mg/day (range = 10-170 mg/day) in the methadone group. Repeated measures generalized linear mixed models demonstrated that cannabis use in the last week (mean of 2.3 days) was not significantly associated with last week opioid use (aβ ± standard error (SE) = -0.06 ± 0.04; p = 0.15), craving (aβ ± SE = -0.05 ± 0.08, p = 0.49), or withdrawal symptoms (aβ ± SE = 0.09 ± 0.1, p = 0.36). Bayes factor (BF) for each of the tested models supported the null hypothesis (BF < 0.3). The current study did not demonstrate a statistically significant effect of cannabis use on outcomes of interest in the context of a pragmatic randomized-controlled trial. These findings replicated previous results reporting no effect of cannabis use on opioid-related outcomes.
Identifiants
pubmed: 37003540
pii: S2949-8759(23)00081-4
doi: 10.1016/j.josat.2023.209031
pii:
doi:
Substances chimiques
Analgesics, Opioid
0
Narcotic Antagonists
0
Buprenorphine
40D3SCR4GZ
Buprenorphine, Naloxone Drug Combination
0
Methadone
UC6VBE7V1Z
Banques de données
ClinicalTrials.gov
['NCT03033732']
Types de publication
Randomized Controlled Trial
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
209031Subventions
Organisme : CIHR
ID : CIS-144301
Pays : Canada
Organisme : CIHR
ID : CIS-144302
Pays : Canada
Organisme : CIHR
ID : CIS-144303
Pays : Canada
Organisme : CIHR
ID : CIS-144304
Pays : Canada
Organisme : CIHR
ID : SMN-139148
Pays : Canada
Organisme : CIHR
ID : SMN-139149
Pays : Canada
Organisme : CIHR
ID : SMN-139150
Pays : Canada
Organisme : CIHR
ID : SMN-139151
Pays : Canada
Investigateurs
Susan Bornemisza
(S)
Helen Bouman
(H)
Sarah Elliott
(S)
Laura Evans
(L)
Monty Ghosh
(M)
Lucas Gursky
(L)
Lydia Vezina
(L)
Cam Wild
(C)
Alvis Yu
(A)
Keith Ahamad
(K)
Paxton Bach
(P)
Rupinder Brar
(R)
Nadia Fairbairn
(N)
Christopher Fairgrieve
(C)
Sonia Habibian
(S)
Sukhpreet Klaire
(S)
Scott MacDonald
(S)
Mark McLean
(M)
Seonaid Christine Nolan
(SC)
Gerrit Prinsloo
(G)
Christy Sutherland
(C)
Evan Wood
(E)
Nikki Bozinoff
(N)
Benedikt Fischer
(B)
Mike Franklin
(M)
Ahmed Hassan
(A)
Dafna Kahana
(D)
Dina Lagzdins
(D)
David Marsh
(D)
Jürgen Rehm
(J)
David Barbeau
(D)
Julie Bruneau
(J)
Sidney Maynard
(S)
Annie Talbot
(A)
Louis-Christophe Juteau
(LC)
Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare the following financial interests/personal relationships, none of these organizations were involved in this study. Laurent Elkrief reports a relationship with Strem Biotechnologies Inc. that includes: equity or stocks. Laurent Elkrief reports a relationship with OneCare Inc. that includes: equity or stocks. M. Eugenia Socias reports a relationship with Indivior that includes: funding grants. Bernard Le Foll reports a relationship with Pfizer Global Research and Development that includes: funding grants. Bernard Le Foll reports a relationship with Brainsway that includes: funding grants. Bernard Le Foll reports a relationship with Bioprojet that includes: funding grants. Bernard Le Foll reports a relationship with Alkermes Inc. that includes: funding grants. Bernard Le Foll reports a relationship with Canopy Growth Corporation that includes: funding grants. Bernard Le Foll reports a relationship with American Chemical Society that includes: funding grants. Bernard Le Foll reports a relationship with Aurora that includes: non-financial support. Bernard Le Foll reports a relationship with Indivior that includes: consulting or advisory and funding grants. Stephanie Marsan reports a relationship with Indivior that includes: consulting or advisory. Didier Jutras-Aswad reports a relationship with Cardiol Therapeutics that includes: non-financial support.