丁丙诺啡对比其他药物治疗阿片类药物使用障碍戒断症状的效果:一项随机对照试验的系统评价。
Effects of buprenorphine on opioid craving in comparison to other medications for opioid use disorder: A systematic review of randomized controlled trials.
机构信息
San Francisco Veterans Affairs Health Care System, 4150 Clement St, San Francisco, CA 94121, United States; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, 401 Parnassus Ave, San Francisco, CA 94143, United States.
San Francisco Veterans Affairs Health Care System, 4150 Clement St, San Francisco, CA 94121, United States; Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, 401 Parnassus Ave, San Francisco, CA 94143, United States.
出版信息
Addict Behav. 2023 Apr;139:107589. doi: 10.1016/j.addbeh.2022.107589. Epub 2022 Dec 17.
BACKGROUND
Craving is a distressing symptom of opioid use disorder (OUD) that can be alleviated with medications for OUD (MOUD). Buprenorphine is an effective MOUD that may suppress craving; however, treatment discontinuation and resumed opioid use is common during the early phases of treatment. More information on the craving response through the high-risk period of initiating buprenorphine may provide meaningful information on how to better target craving, which in turn may enhance outcomes. This systematic review investigated buprenorphine doses and formulations on craving during the induction and maintenance phases of treatment, and for context also compared the craving response to other MOUD (i.e., methadone, extended-release naltrexone [XR-NTX]).
METHODS
PubMed, PsycInfo, Embase, and Cochrane Central databases were searched for randomized trials of buprenorphine versus placebo, various buprenorphine formulations/doses, or other MOUD that included a measure of opioid craving.
RESULTS
A total of 10 studies were selected for inclusion. Buprenorphine and buprenorphine/naloxone (BUP/NAL) were each associated with lower craving than placebo over time. Craving was greater among those prescribed lower versus higher buprenorphine doses. In comparison to other MOUD, buprenorphine or BUP/NAL was linked to greater craving than methadone in 3 of the 6 studies. BUP/NAL was associated with greater reported craving than XR-NTX.
DISCUSSION
Craving is reduced over time with buprenorphine and BUP/NAL, although other MOUD may provide greater reductions in craving. Although there is currently considerable variability in the measurement of craving, it may be a valuable concept to address with individuals receiving MOUD, especially early in treatment.
背景
成瘾是阿片类药物使用障碍(OUD)的一种痛苦症状,可以用 OUD 药物(MOUD)来缓解。丁丙诺啡是一种有效的 MOUD,可能会抑制成瘾;然而,在治疗的早期阶段,经常会出现治疗中断和重新使用阿片类药物的情况。更多关于开始使用丁丙诺啡时高危期的成瘾反应的信息,可以提供有关如何更好地针对成瘾的有意义信息,从而可能改善结果。本系统评价研究了丁丙诺啡在治疗诱导和维持阶段的剂量和配方对成瘾的影响,并为背景比较了其他 MOUD(即美沙酮、纳曲酮延长释放剂[XR-NTX])对成瘾的反应。
方法
在 PubMed、PsycInfo、Embase 和 Cochrane 中心数据库中搜索了丁丙诺啡与安慰剂、各种丁丙诺啡配方/剂量或其他包含阿片类药物成瘾测量的 MOUD 的随机试验。
结果
共选择了 10 项研究进行纳入。丁丙诺啡和丁丙诺啡/纳洛酮(BUP/NAL)在一段时间内都比安慰剂的成瘾反应更低。与服用较高剂量的丁丙诺啡相比,服用较低剂量的丁丙诺啡的患者的成瘾反应更大。与其他 MOUD 相比,在 6 项研究中的 3 项中,丁丙诺啡或 BUP/NAL 与美沙酮相比,与更大的成瘾反应相关。BUP/NAL 与 XR-NTX 相比,报告的成瘾反应更大。
讨论
丁丙诺啡和 BUP/NAL 的成瘾反应随时间减少,尽管其他 MOUD 可能会更大程度地减少成瘾。尽管目前对成瘾的测量存在相当大的差异,但对于接受 MOUD 的个体,尤其是在治疗早期,这可能是一个有价值的概念。