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Medication for Opioid Use Disorder After Nonfatal Opioid Overdose and Association With Mortality: A Cohort Study.非致死性阿片类药物过量后治疗阿片类药物使用障碍的药物与死亡率的关系:一项队列研究。
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Increases in Acute Hepatitis C Virus Infection Related to a Growing Opioid Epidemic and Associated Injection Drug Use, United States, 2004 to 2014.2004 年至 2014 年美国与阿片类药物流行及相关注射吸毒相关的急性丙型肝炎病毒感染增加。
Am J Public Health. 2018 Feb;108(2):175-181. doi: 10.2105/AJPH.2017.304132. Epub 2017 Dec 21.
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Injectable naltrexone, oral naltrexone, and buprenorphine utilization and discontinuation among individuals treated for opioid use disorder in a United States commercially insured population.在美国商业保险人群中,接受阿片类药物使用障碍治疗的个体中,可注射纳曲酮、口服纳曲酮和丁丙诺啡的使用和停药情况。
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Drug Alcohol Depend. 2017 Mar 1;172:34-42. doi: 10.1016/j.drugalcdep.2016.11.037. Epub 2017 Jan 11.
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Cognitive Behavioral Therapy Improves Treatment Outcomes for Prescription Opioid Users in Primary Care Buprenorphine Treatment.认知行为疗法改善了初级保健丁丙诺啡治疗中处方阿片类药物使用者的治疗效果。
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Hospitalizations Related To Opioid Abuse/Dependence And Associated Serious Infections Increased Sharply, 2002-12.2002年至2012年期间,与阿片类药物滥用/依赖相关的住院治疗及相关严重感染大幅增加。
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与丁丙诺啡类物质成瘾治疗项目长期保留相关的因素:系统评价。

Factors Associated with Long-Term Retention in Buprenorphine-Based Addiction Treatment Programs: a Systematic Review.

机构信息

Ambulatory Care Network, Department of Health Services, Los Angeles County, Los Angeles, CA, USA.

Health Sciences Library Systems, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

J Gen Intern Med. 2022 Feb;37(2):332-340. doi: 10.1007/s11606-020-06448-z. Epub 2021 Jan 19.

DOI:10.1007/s11606-020-06448-z
PMID:33469778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8810983/
Abstract

BACKGROUND

The average length of buprenorphine treatment for opioid use disorder is less than 6 months.

OBJECTIVE

We conducted a systematic review to determine what factors were associated with longer retention in buprenorphine treatment.

DESIGN

We searched Medline, Embase, and Cochrane Database of Systematic Reviews in February 2018. Articles were restricted to randomized controlled trials on human subjects, written in English, which contained ≥ 24 weeks of objective data on retention in buprenorphine treatment.

MAIN MEASURES

We assessed whether dose of buprenorphine, treatment setting, or co-administration of behavioral therapy was associated with retention rates.

KEY RESULTS

Over 14,000 articles were identified. Thirteen articles (describing 9 studies) met inclusion criteria. Measures of retention varied widely. Three studies compared doses of buprenorphine between 1 and 8 mg and showed significantly higher rates of retention with higher doses (p values < 0.01). All other studies utilized buprenorphine doses between 8 and 24 mg daily, without comparison. No study found a significant difference in retention between buprenorphine alone and buprenorphine plus behavioral therapy (p values > 0.05). Initiating buprenorphine while hospitalized or within criminal justice settings prior to outpatient treatment programs was significantly associated with retention in buprenorphine treatment (p values < 0.01 respectively).

CONCLUSIONS

Setting of treatment initiation and a higher buprenorphine dose are associated with improved long-term treatment retention. More objective data on buprenorphine treatment programs are needed, including a standardized approach to defining retention in buprenorphine treatment programs.

REGISTRATION

This review was registered with PROSPERO (#CRD42019120336) in March 2019.

摘要

背景

阿片类药物使用障碍的丁丙诺啡治疗平均持续时间不足 6 个月。

目的

我们进行了一项系统评价,以确定哪些因素与丁丙诺啡治疗的长期保留有关。

设计

我们于 2018 年 2 月在 Medline、Embase 和 Cochrane 系统评价数据库中进行了检索。文章仅限于针对人类受试者的随机对照试验,用英文书写,包含丁丙诺啡治疗保留期的客观数据至少 24 周。

主要措施

我们评估了丁丙诺啡剂量、治疗环境或行为治疗联合应用是否与保留率相关。

主要结果

共检索到 14000 多篇文章。符合纳入标准的有 13 篇文章(描述了 9 项研究)。保留率的衡量标准差异很大。有 3 项研究比较了 1 至 8 毫克之间的丁丙诺啡剂量,结果显示高剂量的保留率显著更高(p 值均<0.01)。所有其他研究均使用每日 8 至 24 毫克的丁丙诺啡剂量,没有进行比较。没有研究发现丁丙诺啡单独治疗与丁丙诺啡联合行为治疗之间保留率存在显著差异(p 值均>0.05)。与门诊治疗方案相比,在住院期间或在刑事司法系统中启动丁丙诺啡治疗与丁丙诺啡治疗的保留显著相关(p 值分别<0.01)。

结论

治疗开始时的环境和较高的丁丙诺啡剂量与长期治疗保留率的提高有关。需要更多关于丁丙诺啡治疗方案的客观数据,包括丁丙诺啡治疗方案保留率的标准化方法。

注册

本研究于 2019 年 3 月在 PROSPERO(#CRD42019120336)进行了注册。