Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/35880
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles
Peer Review Status: Refereed
Title: Association between benzodiazepine coprescription and mortality in people on opioid replacement therapy: a population-based cohort study
Author(s): Best, Catherine Susan
Matheson, Catriona
Robertson, James
Ritchie, Trina
Cowden, Fiona
Dumbrell, Josh
Duncan, Clare
Kessavalou, Karthigayan
Woolston, Caroline
Schofield, Joe
Contact Email: catherine.best2@stir.ac.uk
Issue Date: 14-Mar-2024
Date Deposited: 15-Mar-2024
Citation: Best CS, Matheson C, Robertson J, Ritchie T, Cowden F, Dumbrell J, Duncan C, Kessavalou K, Woolston C & Schofield J (2024) Association between benzodiazepine coprescription and mortality in people on opioid replacement therapy: a population-based cohort study. <i>BMJ Open</i>, 14. https://doi.org/10.1136/bmjopen-2023-074668
Abstract: Objective To investigate the association between opioid replacement therapy (ORT) and benzodiazepine (BZD) coprescription and all-cause mortality compared with the prescription of ORT alone. Design Population-based cohort study. Setting Scotland, UK. Participants Participants were people prescribed ORT between January 2010 and end of December 2020 aged 18 years or above. Main outcome measures All-cause mortality, drug-related deaths and non-drug related deaths. Secondary outcome ORT continuous treatment duration. Analysis Cox regression with time-varying covariates. Results During follow-up, 5776 of 46 899 participants died: 1398 while on coprescription and 4378 while on ORT only. The mortality per 100 person years was 3.11 during coprescription and 2.34 on ORT only. The adjusted HR for all-cause mortality was 1.17 (1.10 to 1.24). The adjusted HR for drug-related death was 1.14 (95% CI, 1.04 to 1.24) and the hazard for death not classified as drug-related was 1.19 (95% CI, 1.09 to 1.30). Conclusion Coprescription of BZDs in ORT was associated with an increased risk of all-cause mortality, although with a small effect size than the international literature. Coprescribing was also associated with longer retention in treatment. Risk from BZD coprescription needs to be balanced against the risk from illicit BZDs and unplanned treatment discontinuation. A randomised controlled trial is urgently needed to provide a clear clinical direction. Trial registration number NCT04622995
DOI Link: 10.1136/bmjopen-2023-074668
Rights: © Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Licence URL(s): http://creativecommons.org/licenses/by-nc/4.0/

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