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简短通讯:丁丙诺啡起始微诱导方法有效性的系统评价

Short communication: Systematic review on effectiveness of micro-induction approaches to buprenorphine initiation.

作者信息

Moe Jessica, O'Sullivan Fiona, Hohl Corinne M, Doyle-Waters Mary M, Ronsley Claire, Cho Raymond, Liu Qixin, Azar Pouya

机构信息

Department of Emergency Medicine, University of British Columbia, 2775 Laurel Street, Vancouver, British Columbia V5Z IM9, Canada; Department of Emergency Medicine, Vancouver General Hospital, 920 West 10(th) Avenue, Vancouver, British Columbia V5Z 1M9, Canada; BC Centre for Disease Control, 655 West 12(th) Avenue, Vancouver, British Columbia V5Z 4R4, Canada.

Department of Emergency Medicine, University of British Columbia, 2775 Laurel Street, Vancouver, British Columbia V5Z IM9, Canada.

出版信息

Addict Behav. 2021 Mar;114:106740. doi: 10.1016/j.addbeh.2020.106740. Epub 2020 Nov 25.

Abstract

BACKGROUND/OBJECTIVES: Micro-induction is a novel buprenorphine induction approach that seeks to avoid withdrawal and minimize precipitated withdrawal, both barriers to standard inductions. We aimed to synthesize evidence on micro-induction effectiveness, and regimens described.

METHODS

We searched scientific databases and grey literature for studies including adolescents or adults with opioid use disorder who received buprenorphine micro-induction. Study selection, data extraction and quality assessments occurred in duplicate. We narratively synthesized results.

RESULTS

We screened 4,752 citations and included 19 case studies/series and one feasibility study (n = 57 patients; mean age 38 years [SD 12.0]; 57.9% male [33/57]). Studies described 26 regimens; starting and maintenance doses ranged from 0.03 to 1.0 mg, and 8 to 32 mg, respectively. We calculated rate of increase to 8 mg. All patients achieved the desired maintenance dose. Among 54 patients in whom precipitated withdrawal was not reported, mean increases were 1.36 mg/day (SD 0.41). For three patients in whom precipitated withdrawal was specifically reported, mean increase was 1.17 mg/day (SD 0.11). All studies were low quality.

DISCUSSION

Described regimens are highly variable. Inconsistent reporting, selection bias, and poor quality evidence limit conclusions regarding optimal dosing, and patient characteristics and clinical settings in which micro-induction is likely beneficial.

CONCLUSIONS

This systematic review provides the most up-to-date synthesis on buprenorphine micro-induction regimens. Rigorous studies evaluating effectiveness and safety of micro-induction, and patient and clinical factors influencing its success, are needed.

摘要

背景/目的:微诱导是一种新型丁丙诺啡诱导方法,旨在避免戒断反应并将急性戒断反应降至最低,这两者都是标准诱导方法的障碍。我们旨在综合关于微诱导有效性及所描述方案的证据。

方法

我们检索了科学数据库和灰色文献,查找纳入接受丁丙诺啡微诱导的阿片类物质使用障碍青少年或成人的研究。研究筛选、数据提取和质量评估均重复进行。我们对结果进行了叙述性综合分析。

结果

我们筛选了4752篇文献,纳入了19项病例研究/系列研究和1项可行性研究(n = 57例患者;平均年龄38岁[标准差12.0];57.9%为男性[33/57])。研究描述了26种方案;起始剂量和维持剂量分别为0.03至1.0毫克和8至32毫克。我们计算了增加至8毫克的速率。所有患者均达到了期望的维持剂量。在未报告急性戒断反应的54例患者中,平均每日增加量为1.36毫克(标准差0.41)。对于专门报告有急性戒断反应的3例患者,平均每日增加量为1.17毫克(标准差0.11)。所有研究质量均较低。

讨论

所描述的方案差异很大。报告不一致、选择偏倚和证据质量差限制了关于最佳剂量以及微诱导可能有益的患者特征和临床环境的结论。

结论

本系统评价提供了关于丁丙诺啡微诱导方案的最新综合分析。需要进行严格研究以评估微诱导的有效性和安全性,以及影响其成功的患者和临床因素。

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