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喹硫平作为机械通气成人非意识障碍镇静辅助治疗的有效性。

Effectiveness of Quetiapine as a Sedative Adjunct in Mechanically Ventilated Adults Without Delirium.

机构信息

Duke University Hospital, Durham, NC, USA.

出版信息

Ann Pharmacother. 2021 Feb;55(2):149-156. doi: 10.1177/1060028020944409. Epub 2020 Jul 22.

Abstract

BACKGROUND

Quetiapine is an atypical antipsychotic that is commonly used in the Intensive Care Unit (ICU). The utility of quetiapine as a sedative adjunct has not yet been evaluated, but has been described previously in studies evaluating quetiapine for delirium or delirium prophylaxis.

OBJECTIVE

To determine if adjunctive use of quetiapine reduces sedative dosage requirements among mechanically ventilated adults without delirium.

METHODS

This retrospective intrapatient comparator study included all mechanically ventilated adults admitted to a medical ICU who received quetiapine between July 1, 2013, and July 1, 2018. The primary outcome was the change in sedative dosage requirements over 24 hours following quetiapine initiation. Secondary outcomes included change in sedative dosage requirements 48 hours postquetiapine initiation, opioid dosage requirements 24 hours postquetiapine initiation, percent time at goal for both pain and sedation scores, depth of sedation, and QTc.

RESULTS

A total of 57 patients were included in the study cohort. There was no significant difference in 24-hour cumulative doses of propofol ( = 0.10), dexmedetomidine ( = 0.14), or benzodiazepines ( = 0.14). During the 48-hour treatment period, there was a significant increase in dexmedetomidine requirements ( = 0.03). There were no differences in 24-hour opioid dosage requirements, percent time at goal pain or sedation scores, depth of sedation, or QTc following quetiapine initiation.

CONCLUSION AND RELEVANCE

Adjunctive use of quetiapine was not associated with a significant reduction in sedative dosage requirements 24 or 48 hours following initiation among mechanically ventilated adults without delirium.

摘要

背景

喹硫平是一种常用于重症监护病房(ICU)的非典型抗精神病药。喹硫平作为镇静辅助药物的效用尚未得到评估,但在评估喹硫平治疗谵妄或谵妄预防的研究中已有描述。

目的

确定在没有谵妄的机械通气成人中,辅助使用喹硫平是否可以降低镇静剂剂量需求。

方法

这项回顾性患者内比较研究纳入了 2013 年 7 月 1 日至 2018 年 7 月 1 日期间在接受机械通气的成人 ICU 中接受喹硫平治疗的所有机械通气成人患者。主要结局是喹硫平起始后 24 小时内镇静剂剂量需求的变化。次要结局包括喹硫平起始后 48 小时内镇静剂剂量需求的变化、喹硫平起始后 24 小时内阿片类药物剂量需求、疼痛和镇静评分目标时间百分比、镇静深度和 QTc。

结果

研究队列共纳入 57 例患者。在丙泊酚( = 0.10)、右美托咪定( = 0.14)或苯二氮䓬类药物( = 0.14)的 24 小时累积剂量方面,无显著差异。在 48 小时治疗期间,右美托咪定的需求显著增加( = 0.03)。喹硫平起始后,24 小时阿片类药物剂量需求、目标时间疼痛或镇静评分百分比、镇静深度或 QTc 无差异。

结论和相关性

在没有谵妄的机械通气成人中,辅助使用喹硫平与起始后 24 或 48 小时内镇静剂剂量需求的显著降低无关。

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