非癌症患者术后止痛的阿片类药物退出计划:系统综述。

IF 2.6 Q1 SURGERY Patient Safety in Surgery Pub Date : 2024-07-30 DOI:10.1186/s13037-024-00408-w
Marcel Rainer, Sarah Maleika Ommerli, Andrea Michelle Burden, Leo Betschart, Dominik Stämpfli
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引用次数: 0

摘要

背景:越来越多的国家报告阿片类镇痛药的使用和危害急剧增加。据观察,术后患者开始使用阿片类药物的比例很高。为此,多家三级医疗机构制定了阿片类药物退出计划(OEP),以遏制阿片类药物相关的潜在危害:方法:对 PubMed 和 Embase 进行了系统检索,以识别、总结和比较 2000 年 1 月 1 日至 2024 年 6 月 4 日期间发表的针对术后患者群体的 OEPs 干预要素。两名研究人员按照 PRISMA 2020 指南独立筛选文章,提取数据,评估研究质量和偏倚风险。对研究特点、干预细节、疗效和发展进行了数据综合:共筛选出 2,585 篇文章,其中 8 篇符合资格标准。所有研究均在北美进行,主要针对接受全髋关节或膝关节置换术(5 项)或神经外科手术(3 项)的骨科手术患者。大多数研究(7 项)采用了前后对比(4 项)或随机临床设计(3 项)。三项研究的质量良好,无一存在低偏倚风险。干预措施各不相同,从教育课程(1 项)到个性化减药方案(4 项)或两者结合(2 项)。主要内容包括指导如何预测患者术后对阿片类镇痛药的需求,以及根据患者出院前24小时的阿片类药物消耗量制定减量策略。六项研究在分析中将疗效作为终点,其中四项研究评估了统计显著性,所有四项研究都认为OEPs成功地减少了术后阿片类药物的使用:结论:尽管在设计和实施方面存在差异,但已确定的OEPs表明,它们在减少门诊阿片类药物的使用方面是有效的。它们提供了对术后镇痛剂需求量的可靠估算,并为缩减持续时间和速度提供了依据。不过,还需要更严格的研究来评估其实际效果。
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Opioid exit plans for tapering postoperative pain control in noncancer patients: a systematic review.

Background: A growing number of countries have reported sharp increases in the use and harm of opioid analgesics. High rates of new opioid initiation are observed in postoperative patients. In response, various tertiary care institutions have developed opioid exit plans (OEPs) to curb potential opioid-related harm.

Methods: PubMed and Embase were systematically searched to identify, summarize, and compare the interventional elements of OEPs for postoperative patient populations published from January 1, 2000, to June 4, 2024. Two researchers independently screened the articles for eligibility following the PRISMA 2020 guidelines, extracted the data, and assessed the study quality and risk of bias. Data synthesis was performed for study characteristics, intervention details, efficacy, and development.

Results: A total of 2,585 articles were screened, eight of which met the eligibility criteria. All studies were conducted in North America and focused on orthopedic surgery patients following total hip or knee arthroplasty (n = 5) or neurosurgery (n = 3). Most studies (n = 7) included a pre-post (n = 4) or randomized clinical design (n = 3). Three studies were of good quality, and none had a low risk of bias. The interventions varied and ranged from educational sessions (n = 1) to individualized tapering protocols (n = 4) or a combination of the two (n = 2). Key elements were instructions on how to anticipate patients' postoperative need for opioid analgesics and tapering strategies based on 24-h predischarge opioid consumption. Six studies included efficacy as an endpoint in their analysis, of which four assessed statistical significance, with all four identifying that the OEPs were successful in reducing postoperative opioid use.

Conclusion: Despite differences in design and implementation, the identified OEPs suggest that they are efficacious in reducing outpatient opioid consumption. They provide a robust estimate of postoperative analgesic requirements and a rationale for tapering duration and rate. However, more rigorous studies are needed to evaluate their real-world effectiveness.

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来源期刊
CiteScore
6.80
自引率
8.10%
发文量
37
审稿时长
9 weeks
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