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用于酒精戒断的镁。

Magnesium for alcohol withdrawal.

作者信息

Sarai Michael, Tejani Aaron M, Chan Alice Hill Wah, Kuo I Fan, Li Juliana

机构信息

Department of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.

出版信息

Cochrane Database Syst Rev. 2013 Jun 5;2013(6):CD008358. doi: 10.1002/14651858.CD008358.pub2.

Abstract

BACKGROUND

Patients have been given magnesium to treat or prevent alcohol withdrawal syndrome (AWS). Evidence to support this practice is limited, and is often based on the controversial link between hypomagnesaemia and AWS.

OBJECTIVES

To assess the effects of magnesium for the prevention or treatment of AWS in hospitalised adults.

SEARCH METHODS

We searched the Cochrane Drugs and Alcohol Group Register of Controlled Trials (August 2012), PubMed (from 1966 to August 2012 ), EMBASE (from 1988 to August 2012), CINAHL (from 1982 to March 2010), Web of Science (1965 to August 2012). We also carried out Internet searches.

SELECTION CRITERIA

Randomised or quasi-randomised trials of magnesium for hospitalised adults with, or at risk for, acute alcohol withdrawal.

DATA COLLECTION AND ANALYSIS

Two review authors independently extracted data with a standardised data extraction form, contacting the correspondence investigator if the necessary information was not available in the reports. Dichotomous outcomes were analysed by calculating the risk ratio (RR) for each trial, with the uncertainty in each result expressed with a 95% confidence interval (CI). Continuous outcomes were to be analysed by calculating the standardised mean difference (SMD) with 95% CI. For outcomes assessed by scales we compared and pooled the mean score differences from the end of treatment to baseline (post minus pre) in the experimental and control groups.

MAIN RESULTS

Four trials involving 317 people met the inclusion criteria. Three trials studied oral magnesium, with doses ranging from 12.5 mmol/day to 20 mmol/day. One trial studied parenteral magnesium (16.24 mEq q6h for 24 hours). Each trial demonstrated a high risk of bias in at least one domain. There was significant clinical and methodological variation between trials.We found no study that measured all of the identified primary outcomes and met the objectives of this review. Only one trial measured clinical symptoms of seizure, delirium tremens or components of the Clinical Institute Withdrawal Assessment for Alcohol (CIWA) score. A single outcome (handgrip strength) in three trials (113 people), was amenable to meta-analysis. There was no significant increase in handgrip strength in the magnesium group (SMD 0.04; 95% CI -0.22 to 0.30). No clinically important changes in adverse events were reported.

AUTHORS' CONCLUSIONS: There is insufficient evidence to determine whether magnesium is beneficial or harmful for the treatment or prevention of alcohol withdrawal syndrome.

摘要

背景

已给予患者镁剂来治疗或预防酒精戒断综合征(AWS)。支持这种做法的证据有限,且往往基于低镁血症与AWS之间存在争议的联系。

目的

评估镁剂对住院成年患者预防或治疗AWS的效果。

检索方法

我们检索了Cochrane药物与酒精对照试验注册库(2012年8月)、PubMed(1966年至2012年8月)、EMBASE(1988年至2012年8月)、CINAHL(1982年至2010年3月)、科学引文索引(1965年至2012年8月)。我们还进行了互联网检索。

入选标准

针对患有急性酒精戒断或有急性酒精戒断风险的住院成年患者使用镁剂的随机或半随机试验。

数据收集与分析

两名综述作者使用标准化数据提取表独立提取数据,如果报告中没有必要信息,则与通信作者联系。二分法结局通过计算每个试验的风险比(RR)进行分析,每个结果的不确定性用95%置信区间(CI)表示。连续结局通过计算标准化均数差(SMD)及95%CI进行分析。对于通过量表评估的结局,我们比较并汇总了实验组和对照组从治疗结束到基线(治疗后减去治疗前)的平均得分差异。

主要结果

四项涉及317人的试验符合纳入标准。三项试验研究口服镁剂,剂量范围为12.5 mmol/天至20 mmol/天。一项试验研究胃肠外镁剂(16.24 mEq每6小时一次,共24小时)。每项试验在至少一个领域显示出高偏倚风险。各试验之间存在显著的临床和方法学差异。我们未发现有研究测量了所有确定的主要结局并符合本综述的目标。只有一项试验测量了癫痫、震颤谵妄的临床症状或酒精临床研究所戒断评估(CIWA)评分的组成部分。三项试验(113人)中的一个单一结局(握力)适合进行荟萃分析。镁剂组的握力没有显著增加(SMD 0.04;95%CI -0.22至0.30)。未报告不良事件有任何具有临床意义的变化。

作者结论

没有足够的证据来确定镁剂对治疗或预防酒精戒断综合征是有益还是有害。

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