Supatanakij Praphaphorn, Mungjadetanadee Thitipat, Boonyok Nitchakarn, Suttapanit Karn
Department of Emergency Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Emergency Department, Maharaj Nakhon Si Thammarat Hospital, Nakhon Si Thammarat 80000, Thailand.
Am J Emerg Med. 2025 Sep;95:41-48. doi: 10.1016/j.ajem.2025.05.021. Epub 2025 May 16.
Peri-intubation hypotension (PIH) is associated with increased mortality. Etomidate and ketamine are commonly used as induction agents for tracheal intubation in the emergency department (ED) due to their favorable hemodynamic profiles. However, the effects of these agents on PIH remain controversial, and data on elderly patients are limited. This study aimed to compare the effects of etomidate and ketamine on PIH and 28-day mortality.
A prospective, observational, propensity-matched cohort study was performed across two ED centers between March 23, 2022, and September 30, 2023. Patients aged 65 years and older requiring tracheal intubation and receiving either etomidate or ketamine as a single induction agent were included. The primary outcome was the incidence of PIH within 30 min post-induction, comparing etomidate and ketamine. PIH was defined as a systolic blood pressure (SBP) decrease of more than 20 % from baseline, SBP <100 mmHg (with or without fluid resuscitation), or the initiation or increased dose of vasopressor therapy. Secondary outcomes included 28-day mortality and subgroup analysis evaluating the effect of induction dose on PIH in patients with a shock index (SI) ≥0.9. Statistical analyses included a chi-square test to compare PIH incidence and Cox regression analysis to assess the association between induction agents and 28-day mortality. Multivariable Cox regression was adjusted for mortality by vasopressor initiation or escalation. Fractional polynomial regression was used to evaluate the relationship between induction agent dose and PIH.
A total of 418 patients were included in the analysis, with 222 patients matched in a 1:1 propensity score analysis. The incidence of PIH was 44.1 % in the etomidate group and 53.2 % in the ketamine group (risk difference 9.1 %, 95 % confidence interval [CI] -4.1 to 22.1, p = 0.179). 28-day mortality was 36.0 % in the etomidate group and 25.2 % in the ketamine group (hazard ratio [HR] 0.66, 95 % CI 0.41-1.07, p = 0.095). However, in patients who developed PIH and required vasopressors, ketamine was associated with a lower risk of 28-day mortality (adjusted HR 0.59, 95 % CI 0.36-0.97, p = 0.034). Among patients with SI ≥0.9, a higher induction agent dose was associated with an increased probability of PIH for both etomidate and ketamine.
There was no statistically significant difference in PIH and 28-day mortality between etomidate and ketamine as a single induction agent in elderly patients in the ED.
插管期低血压(PIH)与死亡率增加相关。依托咪酯和氯胺酮因其良好的血流动力学特征,常用于急诊科(ED)气管插管的诱导药物。然而,这些药物对PIH的影响仍存在争议,且老年患者的数据有限。本研究旨在比较依托咪酯和氯胺酮对PIH及28天死亡率的影响。
于2022年3月23日至2023年9月30日在两个急诊科中心进行了一项前瞻性、观察性、倾向匹配队列研究。纳入年龄≥65岁、需要气管插管并接受依托咪酯或氯胺酮作为单一诱导药物的患者。主要结局是诱导后30分钟内PIH的发生率,比较依托咪酯和氯胺酮。PIH定义为收缩压(SBP)较基线下降超过20%、SBP<100 mmHg(无论是否进行液体复苏)或开始使用血管升压药治疗或增加血管升压药剂量。次要结局包括28天死亡率,以及对休克指数(SI)≥0.9的患者进行亚组分析,评估诱导剂量对PIH的影响。统计分析包括用于比较PIH发生率的卡方检验和用于评估诱导药物与28天死亡率之间关联的Cox回归分析。多变量Cox回归针对因开始或增加血管升压药使用导致的死亡率进行了调整。采用分数多项式回归评估诱导药物剂量与PIH之间的关系。
共有418例患者纳入分析,其中222例患者在1:1倾向评分分析中匹配。依托咪酯组PIH发生率为44.1%,氯胺酮组为53.2%(风险差异9.1%,95%置信区间[CI]-4.1至22.1,p=0.179)。依托咪酯组28天死亡率为36.0%,氯胺酮组为25.2%(风险比[HR]0.66,95%CI 0.41-1.07,p=0.095)。然而,在发生PIH且需要血管升压药的患者中,氯胺酮与28天死亡率较低相关(调整后HR 0.59,95%CI 0.36-0.97,p=0.034)。在SI≥0.9的患者中,依托咪酯和氯胺酮的诱导药物剂量越高,PIH发生的可能性越大。
在急诊科老年患者中,依托咪酯和氯胺酮作为单一诱导药物在PIH和28天死亡率方面无统计学显著差异。