Postintubation hypotension following rapid sequence intubation with full- vs reduced-dose induction agent.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY American Journal of Health-System Pharmacy Pub Date : 2025-01-24 DOI:10.1093/ajhp/zxae217
Alicia E Mattson, Caitlin S Brown, Benjamin J Sandefur, Kristin Cole, Brandon Haefke, Daniel Cabrera
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Abstract

Purpose: Rapid sequence intubation (RSI) is a common emergency department (ED) procedure with an associated complication of postintubation hypotension (PIH). It has not been clearly established whether the selection and dose of induction agent affect risk of PIH. The objective of this study was to determine the incidence of PIH in patients receiving full-dose compared to reduced-dose induction agent for RSI in the ED.

Methods: This was a health system-wide, retrospective cohort study comparing incidence of PIH based on the induction medication and dose given for RSI in the ED. Patients were included if they underwent RSI from July 1, 2018, through December 31, 2020, were 18 years of age or older, and received etomidate or ketamine. A reduced dose was defined as a ketamine dose of 1.25 mg/kg or less and an etomidate dose of 0.2 mg/kg or less.

Results: A total of 909 patients were included in the final analysis, with most receiving etomidate (n = 764; 84%) and a smaller number receiving ketamine (n = 145; 16%). Patients who received ketamine had a higher mean pre-intubation shock index (full dose, 1.08; reduced dose, 1.04) than those who received etomidate (full dose, 0.89; reduced dose, 0.92) (P ≤ 0.001). Reduced doses of induction agent were observed for 107 patients receiving etomidate (14.0%) and 60 patients receiving ketamine (41.4%). Patients who received full-dose ketamine for induction had the highest rate of PIH (n = 31; 36.5%), and the difference was statistically significant compared to patients receiving reduced-dose ketamine (16.7%; P = 0.021) and full-dose etomidate (22.8%; P = 0.010).

Conclusion: We observed that full-dose ketamine was associated with the highest rate of PIH; however, this group had the poorest baseline hemodynamics, confounding interpretation. Our results do not support broad use of a reduced-dose induction agent.

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使用全剂量与减剂量诱导剂进行快速顺序插管后出现的插管后低血压。
免责声明:为了加快文章的出版速度,AJHP在接受稿件后会尽快在网上发布。被录用的稿件已经过同行评审和校对,但在进行技术格式化和作者校对之前会在网上发布。这些稿件并非最终记录版本,稍后将以最终文章(按 AJHP 风格格式化并由作者校对)取代:目的:快速顺序插管(RSI)是急诊科(ED)的常见手术,其相关并发症为插管后低血压(PIH)。诱导剂的选择和剂量是否会影响 PIH 的风险,目前尚未明确。本研究旨在确定在急诊室接受全剂量与减剂量 RSI 诱导剂的患者中 PIH 的发生率:这是一项医疗系统范围内的回顾性队列研究,根据急诊室 RSI 的诱导药物和剂量比较 PIH 的发生率。从 2018 年 7 月 1 日到 2020 年 12 月 31 日接受 RSI 治疗、年龄在 18 岁或以上、接受依托咪酯或氯胺酮治疗的患者均被纳入研究范围。减少剂量的定义是氯胺酮剂量为 1.25 毫克/千克或更少,依托咪酯剂量为 0.2 毫克/千克或更少:共有909名患者被纳入最终分析,其中大部分患者接受了依托咪酯(764人;84%),少部分患者接受了氯胺酮(145人;16%)。接受氯胺酮诱导的患者的平均插管前休克指数(全剂量,1.08;减量剂量,1.04)高于接受依托咪酯诱导的患者(全剂量,0.89;减量剂量,0.92)(P ≤ 0.001)。107名接受依托咪酯诱导的患者(14.0%)和60名接受氯胺酮诱导的患者(41.4%)观察到诱导剂剂量减少。接受全剂量氯胺酮诱导的患者发生 PIH 的比例最高(n = 31;36.5%),与接受减量氯胺酮(16.7%;P = 0.021)和全剂量依托咪酯(22.8%;P = 0.010)的患者相比,差异具有统计学意义:我们观察到,全剂量氯胺酮与最高的 PIH 发生率相关;然而,这组患者的基线血流动力学最差,从而影响了解释。我们的结果不支持广泛使用减量诱导剂。
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来源期刊
CiteScore
2.90
自引率
18.50%
发文量
341
审稿时长
3-8 weeks
期刊介绍: The American Journal of Health-System Pharmacy (AJHP) is the official publication of the American Society of Health-System Pharmacists (ASHP). It publishes peer-reviewed scientific papers on contemporary drug therapy and pharmacy practice innovations in hospitals and health systems. With a circulation of more than 43,000, AJHP is the most widely recognized and respected clinical pharmacy journal in the world.
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