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针对阿片类药物减用的以患者为中心的干预措施:系统评价概述。

Patient-targeted interventions for opioid deprescribing: An overview of systematic reviews.

机构信息

Centre for Medicine Use and Safety, Monash University, Parkville, Victoria, Australia.

Faculty of Medicine and Health, School of Pharmacy, The University of Sydney, Sydney, New South Wales, Australia.

出版信息

Basic Clin Pharmacol Toxicol. 2023 Dec;133(6):623-639. doi: 10.1111/bcpt.13844. Epub 2023 Feb 27.

Abstract

BACKGROUND

Deprescribing (reduction or cessation) of prescribed opioids can be challenging for both patients and healthcare professionals.

OBJECTIVE

To synthesize and evaluate evidence from systematic reviews examining the effectiveness and outcomes of patient-targeted opioid deprescribing interventions for all types of pain.

METHODS

Systematic searches were conducted in five databases with results screened against predetermined inclusion/exclusion criteria. Primary outcomes were (i) reduction in opioid dose, reported as change in oral Morphine Equivalent Daily Dose (oMEDD) and (ii) success of opioid deprescribing, reported as the proportion of the sample for which opioid use declined. Secondary outcomes included pain severity, physical function, quality of life and adverse events. The certainty of evidence was assessed using Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology.

FINDINGS

Twelve reviews were eligible for inclusion. Interventions were heterogeneous in nature and included pharmacological (n = 4), physical (n = 3), procedural (n = 3), psychological or behavioural (n = 3) and mixed (n = 5) interventions. Multidisciplinary care programmes appeared to be the most effective intervention for opioid deprescribing; however, the certainty of evidence was low, with significant variability in opioid reduction across interventions.

CONCLUSIONS

Evidence is too uncertain to draw firm conclusions about specific populations who may derive the greatest benefit from opioid deprescribing, warranting further investigation.

摘要

背景

减少或停止处方阿片类药物对患者和医疗保健专业人员来说都是具有挑战性的。

目的

综合评估针对各种类型疼痛的以患者为目标的阿片类药物减用干预措施的有效性和结果的系统评价证据。

方法

在五个数据库中进行了系统搜索,结果根据预定的纳入/排除标准进行了筛选。主要结果是(i)阿片类药物剂量的减少,以口服吗啡等效日剂量(oMEDD)的变化来报告;(ii)阿片类药物减用的成功,以样本中阿片类药物使用减少的比例来报告。次要结果包括疼痛严重程度、身体功能、生活质量和不良事件。证据的确定性使用推荐评估、制定与评价(GRADE)方法进行评估。

发现

有 12 篇综述符合纳入标准。干预措施在性质上存在差异,包括药理学(n=4)、物理(n=3)、程序(n=3)、心理或行为(n=3)和混合(n=5)干预措施。多学科护理方案似乎是阿片类药物减用最有效的干预措施;然而,证据的确定性较低,不同干预措施之间的阿片类药物减少存在显著差异。

结论

由于证据不确定性太大,无法就可能从阿片类药物减用中获益最大的特定人群得出明确结论,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eea/10953356/f753acdfa1aa/BCPT-133-623-g001.jpg

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