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药物辅助治疗对阿片类药物使用者死亡率的影响:系统评价和荟萃分析。

Effects of medication-assisted treatment on mortality among opioids users: a systematic review and meta-analysis.

机构信息

National Institute on Drug Dependence and Beijing Key Laboratory of Drug Dependence, Peking University, 100191, Beijing, China.

School of Public Health, Peking University, 100191, Beijing, China.

出版信息

Mol Psychiatry. 2019 Dec;24(12):1868-1883. doi: 10.1038/s41380-018-0094-5. Epub 2018 Jun 22.

Abstract

Opioid use disorder (OUD) is associated with a high risk of premature death. Medication-assisted treatment (MAT) is the primary treatment for opioid dependence. We comprehensively assessed the effects of different MAT-related characteristics on mortality among those with OUD by a systematic review and meta-analysis. The all-cause and overdose crude mortality rates (CMRs) and relative risks (RRs) by treatment status, different type, period, and dose of medication, and retention time were pooled using random effects, subgroup analysis, and meta-regression. Thirty cohort studies involving 370,611 participants (1,378,815 person-years) were eligible in the meta-analysis. From 21 studies, the pooled all-cause CMRs were 0.92 per 100 person-years (95% CI: 0.79-1.04) while receiving MAT, 1.69 (1.47-1.91) after cessation, and 4.89 (3.54-6.23) for untreated period. Based on 16 studies, the pooled overdose CMRs were 0.24 (0.20-0.28) while receiving MAT, 0.68 (0.55-0.80) after cessation of MAT, and 2.43 (1.72-3.15) for untreated period. Compared with patients receiving MAT, untreated participants had higher risk of all-cause mortality (RR 2.56 [95% CI: 1.72-3.80]) and overdose mortality (8.10 [4.48-14.66]), and discharged participants had higher risk of all-cause death (2.33 [2.02-2.67]) and overdose death (3.09 [2.37-4.01]). The all-cause CMRs during and after opioid substitution treatment with methadone or buprenorphine were 0.93 (0.76-1.10) and 1.79 (1.47-2.10), and corresponding estimate for antagonist naltrexone treatment were 0.26 (0-0.59) and 1.97 (0-5.18), respectively. Retention in MAT of over 1-year was associated with a lower mortality rate than that with retention ≤1 year (1.62, 1.31-1.93 vs. 5.31, -0.09-10.71). Improved coverage and adherence to MAT and post-treatment follow-up are crucial to reduce the mortality. Long-acting naltrexone showed positive advantage on prevention of premature death among persons with OUD.

摘要

阿片类使用障碍(OUD)与过早死亡风险增加有关。药物辅助治疗(MAT)是治疗阿片类药物依赖的主要方法。我们通过系统评价和荟萃分析全面评估了不同 MAT 相关特征对 OUD 患者死亡率的影响。使用随机效应、亚组分析和荟萃回归,汇总了治疗状态、不同类型、时期和剂量的药物以及保留时间对全因和过量死亡率(CMR)和相对风险(RR)的影响。荟萃分析纳入了 30 项队列研究,涉及 370611 名参与者(1378815人年)。21 项研究中,全因 CMR 在接受 MAT 治疗时为 0.92/100 人年(95%CI:0.79-1.04),MAT 治疗停止后为 1.69(1.47-1.91),未治疗期间为 4.89(3.54-6.23)。基于 16 项研究,CMR 为 0.24(0.20-0.28),MAT 治疗停止后为 0.68(0.55-0.80),未治疗期间为 2.43(1.72-3.15)。与接受 MAT 治疗的患者相比,未治疗的患者全因死亡率(RR 2.56 [95%CI:1.72-3.80])和过量死亡率(8.10 [4.48-14.66])风险更高,出院患者全因死亡(RR 2.33 [2.02-2.67])和过量死亡(3.09 [2.37-4.01])风险更高。接受美沙酮或丁丙诺啡替代治疗期间和之后的全因死亡率分别为 0.93(0.76-1.10)和 1.79(1.47-2.10),而拮抗剂纳曲酮治疗的相应估计值分别为 0.26(0-0.59)和 1.97(0-5.18)。MAT 保留时间超过 1 年与保留时间≤1 年相比,死亡率较低(1.62,1.31-1.93 vs. 5.31,-0.09-10.71)。提高 MAT 的覆盖率和依从性,并在治疗后进行随访,对于降低死亡率至关重要。长效纳曲酮在预防 OUD 患者过早死亡方面具有积极优势。

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