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褪黑素及褪黑素激动剂预防和治疗危重症患者谵妄:一项系统评价方案

Melatonin and melatonin agonists to prevent and treat delirium in critical illness: a systematic review protocol.

作者信息

Foster Jennifer, Burry Lisa D, Thabane Lehana, Choong Karen, Menon Kusum, Duffett Mark, Cheung Alexandra, Guenette Melanie, Chimunda Timothy, Rose Louise

机构信息

Department of Paediatrics, Schulich School of Medicine & Dentistry, Western University, London, Canada.

IWK Health Centre, Dalhousie University, 5850/5980 University Avenue, Halifax, NS, B3K 6R8, Canada.

出版信息

Syst Rev. 2016 Nov 24;5(1):199. doi: 10.1186/s13643-016-0378-2.

Abstract

BACKGROUND

Delirium is a syndrome characterized by acute fluctuations and alterations in attention and arousal. Critically ill patients are at particularly high risk, and those that develop delirium are more likely to experience poor clinical outcomes such as prolonged duration of ICU and hospital length of stay, and increased mortality. Melatonin and melatonin agonists (MMA) have the potential to decrease the incidence and severity of delirium through their hypnotic and sedative-sparing effects, thus improving health-related outcomes. The objective of this review is to synthesize the available evidence pertaining to the efficacy and safety of MMA for the prevention and treatment of ICU delirium.

METHODS

We will search Ovid MEDLINE, Web of Science, EMBASE, PsycINFO, the Cochrane Central Register of Controlled Trials (CENTRAL), and CINAHL to identify studies evaluating MMA in critically ill populations. We will also search http://apps.who.int/trialsearch for ongoing and unpublished studies and PROSPERO for registered reviews. We will not impose restrictions on language, date, or journal of publication. Authors will independently screen for eligible studies using pre-defined criteria; data extraction from eligible studies will be performed in duplicate. The Cochrane Risk of Bias Scale and the Newcastle-Ottawa Scale will be used to assess the risk of bias and quality of randomized and non-randomized studies, respectively. Our primary outcome of interest is delirium incidence, and secondary outcomes include duration of delirium, number of delirium- and coma-free days, use of physical and chemical (e.g., antipsychotics or benzodiazepines) restraints, duration of mechanical ventilation, ICU and hospital length of stay, mortality, long-term neurocognitive outcomes, hospital discharge disposition, and adverse events. We will use Review Manager (RevMan) to pool effect estimates from included studies. We will present results as relative risks with 95% confidence intervals for dichotomous outcomes and as mean differences, or standardized mean differences, for continuous outcomes.

DISCUSSION

Current guidelines make no pharmacological recommendations for either the prevention or treatment of ICU delirium. This systematic review will synthesize the available evidence on the efficacy and safety of MMA for this purpose, thus potentially informing clinical decision-making and improving patient outcomes.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO CRD42015024713.

摘要

背景

谵妄是一种以注意力和觉醒的急性波动及改变为特征的综合征。危重症患者尤其高危,而发生谵妄的患者更有可能经历不良临床结局,如重症监护病房(ICU)住院时间和住院总时长延长以及死亡率增加。褪黑素及褪黑素激动剂(MMA)有可能通过其催眠和减少镇静作用降低谵妄的发生率和严重程度,从而改善与健康相关的结局。本综述的目的是综合有关MMA预防和治疗ICU谵妄的有效性和安全性的现有证据。

方法

我们将检索Ovid MEDLINE、科学引文索引(Web of Science)、EMBASE、心理学文摘数据库(PsycINFO)、Cochrane对照试验中心注册库(CENTRAL)和护理学与健康领域数据库(CINAHL),以识别评估MMA在危重症人群中的研究。我们还将检索世界卫生组织国际临床试验注册平台(http://apps.who.int/trialsearch)以查找正在进行和未发表的研究,并检索国际系统评价注册库(PROSPERO)以查找注册的综述。我们不会对语言、日期或发表期刊施加限制。作者将使用预定义标准独立筛选符合条件的研究;将对符合条件的研究进行重复数据提取。Cochrane偏倚风险量表和纽卡斯尔 - 渥太华量表将分别用于评估随机和非随机研究的偏倚风险和质量。我们感兴趣的主要结局是谵妄发生率,次要结局包括谵妄持续时间、无谵妄和无昏迷天数、使用身体和化学(如抗精神病药物或苯二氮䓬类药物)约束措施、机械通气持续时间、ICU和住院时长、死亡率、长期神经认知结局、出院处置情况以及不良事件。我们将使用Review Manager(RevMan)汇总纳入研究的效应估计值。对于二分结局,我们将结果表示为具有95%置信区间的相对风险;对于连续结局,我们将结果表示为均值差或标准化均值差。

讨论

当前指南对于ICU谵妄的预防或治疗未给出药理学建议。本系统综述将综合关于MMA用于此目的的有效性和安全性的现有证据,从而可能为临床决策提供参考并改善患者结局。

系统综述注册

国际系统评价注册库(PROSPERO)CRD42015024713

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