Associations of methadone and buprenorphine‐naloxone doses with unregulated opioid use, treatment retention, and adverse events in prescription‐type opioid use disorders: Exploratory analyses of the OPTIMA study

Author:

Bakouni Hamzah1,McAnulty Christina12,Tatar Ovidiu12ORCID,Socias M. Eugenia34,Le Foll Bernard56789,Lim Ron10,Ahamad Keith311,Jutras‐Aswad Didier12ORCID,

Affiliation:

1. Research Centre Centre Hospitalier de l'Université de Montréal (CRCHUM) Quebec Montréal Canada

2. Department of Psychiatry and Addictology Université de Montréal Québec Montréal Canada

3. British Columbia Centre on Substance Use Vancouver British Columbia Canada

4. Department of Medicine University of British Columbia, St. Paul's Hospital Vancouver British Columbia Canada

5. Department of Pharmacology and Toxicology, Faculty of Medicine, Medical Sciences Building University of Toronto Ontario Toronto Canada

6. Department of Family and Community Medicine, Faculty of Medicine University of Toronto Ontario Toronto Canada

7. Department of Psychiatry University of Toronto Ontario Toronto Canada

8. Dalla Lana School of Public Health University of Toronto Ontario Toronto Canada

9. Translational Addiction Research Laboratory, Campbell Family Mental Health Research Institute Center for Addiction and Mental Health (CAMH) Ontario Toronto Canada

10. Department of Family Medicine and Psychiatry, Cumming School of Medicine University of Calgary Calgary Alberta Canada

11. Department of Family Medicine, Faculty of Medicine University of British Columbia Vancouver British Columbia Canada

Abstract

AbstractBackground and ObjectivesBuprenorphine/naloxone (BUP‐NX) and methadone are used to treat opioid use disorder (OUD), yet there is insufficient evidence on the impact of doses on interventions' effectiveness and safety when treating OUD attributable to other opioids than heroin.MethodsWe explored associations between methadone and BUP‐NX doses and treatment outcomes using data from OPTIMA, a 24‐week, pragmatic, open‐label, multicenter, pan‐Canadian, randomized controlled, two‐arm parallel trial with participants (N = 272) with OUD who primarily use opioids other than heroin. Participants were randomized to receive flexible take‐home BUP‐NX (n = 138) or standard supervised methadone treatment (n = 134). We examined associations between highest BUP‐NX and methadone doses, and (1) percentage of opioid‐positive urine drug screens (UDS); (2) retention in the assigned treatment; and (3) adverse events (AEs).ResultsThe mean (SD) highest BUP‐NX and methadone dose were 17.31 mg/day (8.59) and 67.70 mg/day (34.70). BUP‐NX and methadone doses were not associated with opioid‐positive UDS percentages or AEs. Methadone dose was associated with higher retention in treatment (odds ratio [OR]: 1.025; 95% confidence interval [CI]: 1.010; 1.041), while BUP‐NX dose was not (OR: 1.055; 95% CI: 0.990; 1.124). Higher methadone doses (70–110 mg/day) offered higher odds of treatment retention.Discussion and ConclusionMethadone dose was associated with higher retention, which may be related to its full µ‐opioid receptor agonism. Future research should notably ascertain the effect of pace of titration on a wide range of outcomes.Scientific SignificanceOur results extend previous findings of high doses of methadone increasing retention to be applied in our population using opioids other than heroin, including highly potent opioids.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Psychology,Medicine (miscellaneous)

Reference35 articles.

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4. CCSA.Prescription Opioids (Canadian Drug Summary). CCSA. Accessed January 1 2023.https://www.ccsa.ca/prescription-opioids-canadian-drug-summary

5. Statistics Canada.Pain Relief Medication Containing Opioids 2018. Statistics Canada. Accessed January 1 2023.https://www150.statcan.gc.ca/n1/pub/82-625-x/2019001/article/00008-eng.htm

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