First Nations Health Authority, #540-757 West Hastings St., Vancouver, British Columbia V6C 1A1, Canada; Faculty of Health Sciences, Simon Fraser University, Blusson Hall, Room 11300 8888 University Drive, Burnaby, British Columbia V5A 1S6, Canada.
Centre for Health Evaluation and Outcome Sciences (CHÉOS), St. Paul's Hospital, #588-1081 Burrard St., British Columbia V6Z 1Y6, Canada.
Drug Alcohol Depend. 2023 Sep 1;250:110908. doi: 10.1016/j.drugalcdep.2023.110908. Epub 2023 Jul 23.
Despite the prevalence of alcohol use among people with opioid use disorder (PWOUD) engaged in opioid agonist therapy (OAT), clinical care guidance for concurrent alcohol use disorder (AUD) and OUD is scarce. We assessed the prevalence and risk of mortality for concurrent AUD among PWOUD who accessed OAT in British Columbia (BC).
Data were obtained from six linked population-level health administrative datasets to identify PWOUD from January 1996 to March 2020. All-cause age and sex standardized mortality ratios (SMR) were calculated to determine the mortality risk by OAT status (on vs. discontinued), stratified by First Nations and other residents with concurrent AUD and OUD. Adjusted risk ratios compared the relative risk of mortality by AUD status (AUD detected vs. not) among First Nations and other residents.
We identified 62,110 PWOUD who received OAT, including 6305 (10.2%) First Nations. OAT substantially lowered the SMR among First Nations (SMR=6.6, 95% CI: 5.4-8.1) and other residents (SMR=6.6; 95% CI: 6.2-7.0) with concurrent AUD and OUD, compared to those who discontinued (SMR=22.7, 95% CI: 20.4-25.1, SMR=17.5, 95% CI: 16.8-18.2 respectively). The risk of mortality was 1.9 (95% CI: 1.6-2.2) times higher for First Nations and 2.0 (95% CI: 1.8-2.2) times higher for other residents with concurrent OUD and AUD compared to those without an indication of AUD.
The protective effect of OAT remained despite the presence of a concurrent AUD among both First Nations and other residents with OUD. Findings have implications for clinical care management of concurrent disorders.
尽管在接受阿片类激动剂治疗(OAT)的阿片类药物使用障碍(PWOUD)人群中普遍存在酒精使用问题,但针对同时存在的酒精使用障碍(AUD)和 OUD 的临床护理指导却很少。我们评估了在不列颠哥伦比亚省(BC)接受 OAT 的 PWOUD 中并发 AUD 的流行率和死亡率风险。
从六个链接的人群健康管理数据集获取数据,以确定从 1996 年 1 月至 2020 年 3 月期间的 PWOUD。计算全因年龄和性别标准化死亡率比(SMR),以确定 OAT 状态(持续与停止)分层时并发 AUD 和 OUD 的 PWOUD 的死亡率风险。调整后的风险比比较了 AUD 状态(检测到 AUD 与未检测到 AUD)在原住民和其他居民中的死亡率相对风险。
我们确定了 62,110 名接受 OAT 的 PWOUD,其中包括 6305 名原住民。OAT 显著降低了同时患有 AUD 和 OUD 的原住民(SMR=6.6,95%CI:5.4-8.1)和其他居民(SMR=6.6;95%CI:6.2-7.0)的 SMR,与停止治疗的患者相比(SMR=22.7,95%CI:20.4-25.1,SMR=17.5,95%CI:16.8-18.2)。与没有 AUD 迹象的患者相比,同时患有 OUD 和 AUD 的原住民的死亡率风险高 1.9 倍(95%CI:1.6-2.2),其他居民的死亡率风险高 2.0 倍(95%CI:1.8-2.2)。
OAT 的保护作用仍然存在,尽管同时存在 AUD,但原住民和其他患有 OUD 的居民仍然如此。这些发现对同时存在的疾病的临床护理管理具有重要意义。