National Drug and Alcohol Research Centre, University of NSW, Sydney, NSW 2052, Australia.
Population Health Sciences, Bristol Medical School, University of Bristol, Bristol BS2 8DZ, UK.
Drug Alcohol Depend. 2022 Jul 1;236:109464. doi: 10.1016/j.drugalcdep.2022.109464. Epub 2022 Apr 15.
There are critical periods of mortality risk at onset and cessation of opioid agonist treatment. We aim to determine whether non-fatal overdose followed the same pattern as fatal overdose, comparing the first 4 weeks of treatment and treatment cessation and the remainder time off treatment, with the remainder treatment time, to determine intervention markers.
Retrospective cohort study of people with a history of opioid agonist treatment using linked New South Wales data. The incidence of non-fatal overdose hospitalization; emergency department presentation; and fatal overdose from national death records were compared. Rates were calculated using generalized estimating equations adjusting for demographics, year, and recent health and incarceration events.
The remainder time in OAT had the lowest incidence of overdose for all outcomes and is the reference level for the adjusted incident rate ratios (aIRR). Fatal overdose was lowest in treatment and highest in the first four weeks out of treatment, aIRR of 12.83 (95% CI 10.0-16.4). Whereas the highest overdose rate for non-fatal opioid overdose was in the first four weeks in treatment, aIRR of 3.11 (95% CI 2.19-4.42).
Retention on opioid agonist treatment is protective against drug related overdose. There is elevated risk of non-fatal overdose at treatment initiation that is not evident for fatal overdose, but the first month of treatment cessation is a critical period for both non-fatal and fatal overdose. These findings emphasize the importance of treatment retention and interventions for polysubstance overdose at cessation.
阿片类激动剂治疗开始和停止时存在死亡风险的关键时期。我们旨在确定非致命性药物过量是否遵循与致命性药物过量相同的模式,比较治疗开始的前 4 周和治疗停止以及停药后的其余时间,并确定干预标志物。
使用新南威尔士州的相关数据对有阿片类激动剂治疗史的人群进行回顾性队列研究。比较了非致命性药物过量住院治疗、急诊就诊和国家死亡记录中的致命性药物过量的发生率。使用广义估计方程,根据人口统计学、年份和最近的健康和监禁事件进行调整,计算发生率。
所有结局中,OAT 的剩余时间药物过量发生率最低,是调整后发生率比值比(aIRR)的参考水平。治疗期间致命性药物过量发生率最低,治疗开始后前 4 周最高,aIRR 为 12.83(95%CI 10.0-16.4)。而非致命性阿片类药物过量的最高发生率发生在治疗的前 4 周,aIRR 为 3.11(95%CI 2.19-4.42)。
保留阿片类激动剂治疗可预防与药物相关的药物过量。在开始治疗时,非致命性药物过量的风险增加,但在治疗停止的第一个月,非致命性和致命性药物过量的风险都很高。这些发现强调了治疗保留和在停止治疗时针对多种物质药物过量进行干预的重要性。