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评估手术患者服用美沙酮后的呼吸抑制:系统评价与荟萃分析方案

Evaluating respiratory depression after methadone administration in surgical patients: protocol for a systematic review and meta-analysis.

作者信息

Nunez-Rodriguez Eduardo, Mazzinari Guido, Lumsden Sarah, Krause Kate J, Cortes Nicolas, Kharasch Evan D, Cata Juan P

机构信息

Department of Anesthesiology and Perioperative Medicine, MD Anderson Cancer Center, Houston, Texas, USA.

Anesthesiology and Surgical Oncology Research Group, Houston, Texas, USA.

出版信息

BMJ Open. 2025 May 30;15(5):e099463. doi: 10.1136/bmjopen-2025-099463.

Abstract

INTRODUCTION

Methadone has emerged as a promising option for perioperative pain management, primarily due to its rapid onset of action and prolonged duration of effect, which provides sustained analgesic benefits. Despite its clinical advantages and minimal reported risks for postoperative respiratory depression, concerns about its potential respiratory complications persist. This protocol outlines a meta-analysis aimed at evaluating the risk of respiratory depression associated with methadone administration in the perioperative setting compared with other opioids or placebo.

METHODS AND ANALYSIS

We will perform a systematic review of literature published in English from 1 January 1970 to the present using Ovid MEDLINE, Ovid Embase and Cochrane CENTRAL. Eligible studies will consist of randomised controlled trials, cohort studies and case-control studies reporting respiratory depression in surgical patients receiving intravenous methadone. Case reports, reviews and non-English studies will be excluded. The primary outcome is respiratory depression, defined as naloxone administration, a respiratory rate of fewer than 8 breaths per minute, or an arterial oxygen saturation below 90%. Secondary outcomes include the timing and dose-response effect of methadone on respiratory depression. Bias will be evaluated using the Cochrane Risk of Bias Assessment 2 and ROBINS-I tools. Meta-analyses will be performed, and effect estimates will be presented as relative risks or ORs with 95% CIs. The certainty of the evidence will be assessed using Grading of Recommendations Assessment, Development and Evaluation methodology.

ETHICS AND DISSEMINATION

Ethics approval is not necessary for this systematic review and meta-analysis. The results will be published in a peer-reviewed journal and presented at national and international conferences focused on perioperative medicine and pain management.

PROSPERO REGISTRATION NUMBER

CRD42025630383.

摘要

引言

美沙酮已成为围手术期疼痛管理的一个有前景的选择,主要是因为其起效迅速且作用持续时间长,能提供持续的镇痛效果。尽管其具有临床优势且术后呼吸抑制的报告风险极小,但对其潜在呼吸并发症的担忧依然存在。本方案概述了一项荟萃分析,旨在评估围手术期使用美沙酮与其他阿片类药物或安慰剂相比,与呼吸抑制相关的风险。

方法与分析

我们将使用Ovid MEDLINE、Ovid Embase和Cochrane CENTRAL对1970年1月1日至今以英文发表的文献进行系统综述。符合条件的研究将包括随机对照试验、队列研究和病例对照研究,这些研究报告了接受静脉注射美沙酮的手术患者的呼吸抑制情况。病例报告、综述和非英文研究将被排除。主要结局是呼吸抑制,定义为使用纳洛酮、呼吸频率低于每分钟8次或动脉血氧饱和度低于90%。次要结局包括美沙酮对呼吸抑制的时间和剂量反应效应。将使用Cochrane偏倚风险评估2和ROBINS-I工具评估偏倚。将进行荟萃分析,效应估计值将以相对风险或比值比及95%置信区间表示。将使用推荐分级评估、制定和评价方法评估证据的确定性。

伦理与传播

本系统综述和荟萃分析无需伦理批准。研究结果将发表在同行评审期刊上,并在专注于围手术期医学和疼痛管理的国内和国际会议上展示。

PROSPERO注册号:CRD42025630383。

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