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右美托咪定对重症监护患者谵妄和躁动的影响:系统评价和试验序贯分析的荟萃分析。

The effect of dexmedetomidine on delirium and agitation in patients in intensive care: systematic review and meta-analysis with trial sequential analysis.

机构信息

Department of Anaesthesiology, Faculty of Medicine, University of Malaya, Jalan University, Kuala Lumpur, Malaysia.

International Medical University, Bukit Jalil, Kuala Lumpur, Malaysia.

出版信息

Anaesthesia. 2019 Mar;74(3):380-392. doi: 10.1111/anae.14472. Epub 2018 Oct 27.

Abstract

Delirium is common in intensive care patients. Dexmedetomidine is increasingly used for sedation in this setting, but its effect on delirium remains unclear. The primary aim of this review was to examine whether dexmedetomidine reduces the incidence of delirium and agitation in intensive care patients. We sought randomised clinical trials in MEDLINE, EMBASE, PubMed and CENTRAL from their inception until June 2018. Observational studies, case reports, case series and non-systematic reviews were excluded. Twenty-five trials including 3240 patients were eligible for inclusion in the data synthesis. In the patients who received dexmedetomidine (eight trials, 1425 patients), delirium was reduced, odds ratio (95%CI) 0.36 (0.26-0.51), p < 0.001 and high quality of evidence. The use of dexmedetomidine was associated with a reduced incidence of agitation, OR (95%CI) 0.34 (0.20-0.59), p < 0.001, moderate quality of evidence. Patients who were randomly assigned to dexmedetomidine had a significantly higher incidence of bradycardia, OR (95%CI) 2.18 (1.46-3.24), p < 0.001, moderate quality of evidence; and hypotension, OR (95%CI) 1.89 (1.48-2.41), p < 0.001, high quality of evidence. We found no evidence of an effect on mortality, OR (95%CI) 0.86 (0.66-1.10), p = 0.23, moderate quality of evidence. The trial sequential analyses for the incidence of delirium, bradycardia and hypotension was conclusive but not for the incidence of agitation and mortality. In summary, this meta-analysis suggests that dexmedetomidine reduces the incidence of delirium and agitation in intensive care patients. The general quality of evidence ranged from moderate to high.

摘要

谵妄在重症监护病房患者中很常见。右美托咪定在这种情况下越来越多地被用于镇静,但它对谵妄的影响仍不清楚。本综述的主要目的是检查右美托咪定是否能降低重症监护病房患者发生谵妄和躁动的发生率。我们在 MEDLINE、EMBASE、PubMed 和 CENTRAL 中检索了从成立到 2018 年 6 月的随机临床试验。排除观察性研究、病例报告、病例系列和非系统评价。25 项试验(包括 3240 名患者)符合纳入数据综合的条件。在接受右美托咪定治疗的患者(8 项试验,1425 名患者)中,谵妄发生率降低,优势比(95%可信区间)为 0.36(0.26-0.51),p<0.001,证据质量为高。使用右美托咪定与躁动发生率降低相关,比值比(95%可信区间)为 0.34(0.20-0.59),p<0.001,证据质量为中。随机分配到右美托咪定组的患者心动过缓发生率显著升高,比值比(95%可信区间)为 2.18(1.46-3.24),p<0.001,证据质量为中;低血压发生率升高,比值比(95%可信区间)为 1.89(1.48-2.41),p<0.001,证据质量为高。我们没有发现右美托咪定对死亡率有影响的证据,比值比(95%可信区间)为 0.86(0.66-1.10),p=0.23,证据质量为中。对谵妄、心动过缓和低血压发生率的试验序贯分析是结论性的,但对躁动和死亡率的分析则不是。总之,这项荟萃分析表明,右美托咪定可降低重症监护病房患者发生谵妄和躁动的发生率。总体证据质量从中等到高。

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