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氟哌啶醇在危重症患者谵妄治疗中的剂量策略。

Haloperidol dosing strategies in the treatment of delirium in the critically ill.

机构信息

Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.

出版信息

Neurocrit Care. 2012 Feb;16(1):170-83. doi: 10.1007/s12028-011-9643-3.

Abstract

Delirium is the most common mental disturbance in critically-ill patients and results in significant morbidity and mortality. Haloperidol is a preferred agent for the treatment of delirium in this population because of its rapid onset of action and lack of hemodynamic effects. Despite its widespread use in the critical care setting, most of the relevant data are obtained from case series or extrapolated from non-critically-ill populations. This review provides an overview of haloperidol pharmacokinetics and a comprehensive summary of the evidence for various haloperidol dosing regimens in the treatment of delirium in critically-ill patients. A comprehensive literature search was conducted in Medline, Embase, and International Pharmaceutical Abstracts with "haloperidol", "delirium", "agitation", "critically-ill", and "intensive care" as keywords. Studies involving haloperidol for delirium prophylaxis, non-critical care settings, and terminally-ill subjects were excluded. Eleven studies were identified: four with intermittent IV haloperidol, four with continuous IV infusion haloperidol, two with oral/enteral haloperidol, and one with IM haloperidol. All of the case reports, case series, and descriptive studies have shown a benefit with haloperidol, but publication bias is likely present. Only three studies were controlled studies, but all had small sample sizes and methodological flaws. Randomized, double-blind, active-comparator trials of haloperidol with allocation concealment are needed. Subsequent research should focus on using validated delirium screening and assessment scales for more objective identification and measurement of delirium outcomes.

摘要

谵妄是危重症患者最常见的精神障碍,可导致发病率和死亡率显著增加。氟哌啶醇由于其起效迅速且对血液动力学无影响,成为该人群治疗谵妄的首选药物。尽管在重症监护环境中广泛使用,但大多数相关数据来自病例系列或从非重症患者人群中推断得出。本综述提供了氟哌啶醇药代动力学概述,并全面总结了各种氟哌啶醇剂量方案治疗重症患者谵妄的证据。我们在 Medline、Embase 和 International Pharmaceutical Abstracts 中使用“氟哌啶醇”、“谵妄”、“激越”、“危重症”和“重症监护”作为关键词进行了全面的文献检索。排除了涉及氟哌啶醇用于预防谵妄、非重症监护环境和终末期患者的研究。确定了 11 项研究:4 项间歇性 IV 氟哌啶醇,4 项连续 IV 输注氟哌啶醇,2 项口服/肠内氟哌啶醇,1 项肌内氟哌啶醇。所有病例报告、病例系列和描述性研究都表明氟哌啶醇有效,但可能存在发表偏倚。只有 3 项研究是对照研究,但所有研究的样本量都很小且存在方法学缺陷。需要进行氟哌啶醇与安慰剂对照、随机、双盲、阳性对照试验。后续研究应侧重于使用经过验证的谵妄筛查和评估量表,以更客观地识别和衡量谵妄结局。

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