Association between benzodiazepine coprescription and mortality in people on opioid replacement therapy: a population-based cohort study

被引:2
作者
Best, Catherine Susan [1 ]
Matheson, Catriona [2 ]
Robertson, James [3 ,4 ]
Ritchie, Trina [5 ]
Cowden, Fiona [6 ]
Dumbrell, Josh [2 ]
Duncan, Clare [7 ]
Kessavalou, Karthigayan [7 ]
Woolston, Caroline [7 ]
Schofield, Joe [8 ]
机构
[1] Univ Stirling, Fac Hlth Sci & Sport, Stirling, Scotland
[2] Univ Stirling, Stirling, Scotland
[3] Muirhouse Med Grp, Edinburgh, Scotland
[4] Univ Edinburgh, Usher Inst, Edinburgh, Scotland
[5] NHS Greater Glasgow & Clyde, Glasgow, Scotland
[6] NHS Tayside, Dundee, Scotland
[7] NHS Ayrshire & Arran, Ayr, Scotland
[8] Univ Edinburgh, Coll Humanities & Social Sci, Sch Hlth & Social Sci, Edinburgh, Scotland
来源
BMJ OPEN | 2024年 / 14卷 / 03期
关键词
Substance misuse; EPIDEMIOLOGY; CLINICAL PHARMACOLOGY; METHADONE-MAINTENANCE; BUPRENORPHINE; OVERDOSE; IMPACT; DRUG;
D O I
10.1136/bmjopen-2023-074668
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:9
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