Kelty Erin, Joyce David, Hulse Gary
a Discipline of Psychiatry , University of Western Australia , Nedlands , Western Australian , Australia.
b School of Population and Global Health , University of Western Australia , Crawley , Western Australian , Australia.
Am J Drug Alcohol Abuse. 2019;45(3):285-291. doi: 10.1080/00952990.2018.1545131. Epub 2019 Mar 8.
Sustained release naltrexone has been shown to be a safer alternative to oral naltrexone in terms of mortality in patients with an opioid use disorder; however, a direct large-scale comparison has not been made between sustained release naltrexone and the more popular opioid pharmacotherapies: methadone and buprenorphine.
To examine and compare mortality rates in patients with an opioid use disorder treated with implant naltrexone, methadone, and buprenorphine.
Patients treated with implant naltrexone (n = 1461, 35.6% female), methadone (n = 3515, 33.3% female), or buprenorphine (n = 3250, 34.5% female) for the first time between 2001 and 2010 in Western Australia (WA) were cross-matched against the WA Death Registry.
Crude mortality rates in patients treated with methadone (8.1 per 1000 patient years (ptpy) (HR:1.13, CI:0.82-1.55, p = 0.447) or buprenorphine (7.2 ptpy) (HR:1.01, CI:0.72-1.42, p = 0.948) were not significantly different to those treated with implant naltrexone (7.1 ptpy). Similarly, no differences were observed between the three treatments in terms of cause-specific or age-specific mortality. However, high rates of mortality were observed in methadone-treated patients during the first 28 days of treatment (HR:8.19, CI:1.08-62.21, p = 0.042) compared to naltrexone-treated patients. Female patients treated with methadone (HR:2.96, CI:1.34-6.51, p = 0.007) also experienced a higher overall mortality rate compared to naltrexone-treated patients.
Crude mortality rates are comparable in patients with an opioid use disorder treated with implant naltrexone, methadone, and buprenorphine. However, implant naltrexone may be associated benefits during the first 28 days of treatment and in female patients compared to methadone.
在阿片类药物使用障碍患者的死亡率方面,缓释纳曲酮已被证明是口服纳曲酮的一种更安全的替代药物;然而,尚未对缓释纳曲酮与更常用的阿片类药物治疗方法:美沙酮和丁丙诺啡进行直接的大规模比较。
研究并比较接受植入式纳曲酮、美沙酮和丁丙诺啡治疗的阿片类药物使用障碍患者的死亡率。
将2001年至2010年期间在西澳大利亚州(WA)首次接受植入式纳曲酮治疗的患者(n = 1461,女性占35.6%)、美沙酮治疗的患者(n = 3515,女性占33.3%)或丁丙诺啡治疗的患者(n = 3250,女性占34.5%)与WA死亡登记处进行交叉匹配。
接受美沙酮治疗的患者的粗死亡率(每1000患者年(ptpy)8.1例)(HR:1.13,CI:0.82 - 1.55,p = 0.447)或丁丙诺啡治疗的患者(7.2 ptpy)(HR:1.01,CI:0.72 - 1.42,p = 0.948)与接受植入式纳曲酮治疗的患者(7.1 ptpy)无显著差异。同样,在特定病因或特定年龄死亡率方面,三种治疗方法之间未观察到差异。然而,与接受纳曲酮治疗的患者相比,接受美沙酮治疗的患者在治疗的前28天死亡率较高(HR:8.19,CI:1.08 - 62.21,p = 0.042)。与接受纳曲酮治疗的患者相比,接受美沙酮治疗的女性患者(HR:2.96,CI:1.34 - 6.51,p = 0.007)的总体死亡率也较高。
接受植入式纳曲酮、美沙酮和丁丙诺啡治疗的阿片类药物使用障碍患者的粗死亡率相当。然而,与美沙酮相比,植入式纳曲酮在治疗的前28天以及女性患者中可能具有相关益处。