Affiliation:
1. Centre de recherche du Centre hospitalier de l'Université de Montréal Montreal Canada
2. Department of Family Medicine and Emergency Medicine University of Montreal Montreal Canada
3. National Drug and Alcohol Research Centre UNSW Sydney Sydney Australia
4. Bristol Medical School Bristol University Bristol UK
5. Monash Addiction Research Centre, Eastern Health Clinical School Monash University Clayton Australia
6. Faculty of Health and Medical Sciences University of Adelaide Adelaide Australia
Abstract
AbstractAimsTo quantify the association between opioid agonist treatment (OAT) and overdose death by age group; test the hypothesis that across different age groups, opioid overdose mortality is lowest during OAT with buprenorphine compared with time out of treatment or OAT with methadone; and test associations between OAT and opioid overdose mortality in the presence of chronic circulatory, respiratory, liver and kidney diseases.DesignRetrospective observational cohort study using linked administrative data.SettingNew South Wales, Australia.ParticipantsA total of 37 764 people prescribed OAT, 1 August 2002 and 31 December 2017.MeasurementsOAT exposure, opioid overdose mortality and key confounders were measured using linked population data sets on OAT entry and exit, hospitalization, mental health care, incarceration and mortality. ICD‐10 codes were used to define opioid overdose mortality and chronic disease groups of interest.FindingsRelative to time out of treatment, time in OAT was associated with a lower risk of opioid overdose death across all age groups and chronic diseases. Among people aged 50 years and older, there was weak evidence that buprenorphine may be associated with greater protection against opioid overdose death than methadone [generalized estimating equation (GEE) adjusted incident rate ratio (aIRR) = 0.47; 95% confidence interval (CI) = 0.21, 1.02; marginal structural models (MSM) aIRR = 0.49; 95% CI = 0.17, 1.41]. Buprenorphine was associated with greater protection against overdose death than methadone for clients with circulatory (MSM aIRR = 0.27; 95% CI = 0.11, 0.67) or respiratory (MSM aIRR = 0.26; 95% CI = 0.07, 0.94) diseases, but not liver (MSM aIRR = 0.59; 95% CI = 0.14, 2.43) or kidney (MSM aIRR = 1.16; 95% CI = 0.31, 4.36) diseases.ConclusionsOpioid agonist treatment (OAT) appears to reduce mortality risk in people with opioid use disorder who are older or who have physical comorbidities. Opioid overdose mortality during OAT with buprenorphine appears to be lower and reduced in clients with circulatory and respiratory diseases compared with OAT with methadone.
Funder
National Institutes of Health
NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research
NSW Health
Centre for Health Record Linkage
Subject
Psychiatry and Mental health,Medicine (miscellaneous)
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献