抗利尿激素起始时间与脓毒性休克住院死亡率:大型公共数据库的观察性研究

IF 2.7 Q4 Medicine
Critical care explorations Pub Date : 2025-08-22 eCollection Date: 2025-09-01 DOI:10.1097/CCE.0000000000001284
Gretchen L Sacha, Abhijit Duggal, Anita J Reddy, Lu Wang, Seth R Bauer
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引用次数: 0

摘要

重要性:加压素用于三分之一的脓毒性休克患者,以增强血流动力学并减少儿茶酚胺的总体暴露。然而,启动抗利尿激素的最佳临床环境尚不清楚。目的:确定去甲肾上腺素当量剂量、乳酸浓度和抗利尿激素启动时休克发作时间与住院死亡率之间的关系。设计、设置和参与者:利用重症监护医学信息市场- iv和电子ICU合作研究数据库数据库对基于修改的败血症-3标准接受持续输注儿茶酚胺的成人脓毒性休克患者进行回顾性、观察性评估。主要结局和测量:用多变量回归模型评估抗利尿激素启动时去甲肾上腺素当量剂量、乳酸浓度和休克发作时间与住院死亡率的关系。结果:共纳入209家医院1409例患者。在抗利尿激素启动时,患者的去甲肾上腺素当量剂量中位数(四分位数范围)为28.4µg/min(16.4-42.6µg/min),乳酸浓度为3.7 mmol/L (2.5-6.2 mmol/L),休克发作后已经过5.6小时(2.0-13.5小时)。所有三个感兴趣的变量都与住院死亡率相关。三个限制三次样条结被确定,其中去甲肾上腺素当量剂量和住院死亡率之间的关系发生了实质性变化:9、28和72µg/min。当去甲肾上腺素当量剂量为28µg/min和72µg/min至9µg/min的抗利尿激素启动时,住院死亡率分别增加90%和3.9倍(校正优势比[OR], 1.90 [95% CI, 1.49-2.41]和3.93 [95% CI, 2.74-5.64])。抗利尿激素起始时乳酸浓度每升高1 mmol/L,住院死亡率增加16%(校正OR为1.16 [95% CI, 1.11-1.21])。最后,从休克发作到抗利尿激素启动的时间内,每小时住院死亡率增加3%(校正OR为1.03 [95% CI, 1.01-1.04])。结论及相关性:早期使用抗利尿激素可降低脓毒性休克患者的死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vasopressin Initiation Timing and In-Hospital Mortality in Septic Shock: An Observational Study of Large Public Databases.

Vasopressin Initiation Timing and In-Hospital Mortality in Septic Shock: An Observational Study of Large Public Databases.

Vasopressin Initiation Timing and In-Hospital Mortality in Septic Shock: An Observational Study of Large Public Databases.

Vasopressin Initiation Timing and In-Hospital Mortality in Septic Shock: An Observational Study of Large Public Databases.

Importance: Vasopressin is used in one-third of patients with septic shock to augment hemodynamics and reduce overall catecholamine exposure. However, the optimal clinical context in which to initiate vasopressin is unknown.

Objectives: To determine the association between norepinephrine-equivalent dose, lactate concentration, and time duration from shock onset at vasopressin initiation with in-hospital mortality.

Design, setting, and participants: Retrospective, observational evaluation utilizing Medical Information Mart for Intensive Care-IV and electronic ICU Collaborative Research Database databases of adult patients with septic shock based on modified Sepsis-3 criteria receiving continuous infusion catecholamines.

Main outcomes and measures: The associations of norepinephrine-equivalent dose, lactate concentration, and time duration from shock onset at vasopressin initiation with in-hospital mortality were evaluated with multivariable regression models.

Results: In total, 1409 patients from 209 hospitals were included. At vasopressin initiation patients had a median (interquartile range) norepinephrine-equivalent dose 28.4 µg/min (16.4-42.6 µg/min), lactate concentration 3.7 mmol/L (2.5-6.2 mmol/L), and 5.6 hours (2.0-13.5 hr) had elapsed since shock onset. All three variables of interest were associated with in-hospital mortality. Three restricted cubic spline knots were identified where the relationship between norepinephrine-equivalent dose and in-hospital mortality changed substantially: 9, 28, and 72 µg/min. The odds of in-hospital mortality increased by 90% and 3.9-fold when comparing vasopressin initiation at norepinephrine-equivalent doses of 28 µg/min and 72 µg/min to 9 µg/min, respectively (adjusted odds ratio [OR], 1.90 [95% CI, 1.49-2.41] and 3.93 [95% CI, 2.74-5.64]). The odds of in-hospital mortality increased by 16% for every mmol/L in the lactate concentration at vasopressin initiation (adjusted OR, 1.16 [95% CI, 1.11-1.21]). Finally, the odds of in-hospital mortality increased by 3% for every hour in the time duration from shock onset to vasopressin initiation (adjusted OR, 1.03 [95% CI, 1.01-1.04]).

Conclusions and relevance: Earlier adjunctive vasopressin initiation may decrease mortality in patients with septic shock.

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