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澳大利亚和新西兰脓毒症复苏评估:急诊科脓毒症中液体还是血管加压素(ARISE FLUIDS),一项描述澳大利亚和新西兰当前实践的多中心观察性研究。

The Australasian Resuscitation In Sepsis Evaluation: Fluids or vasopressors in emergency department sepsis (ARISE FLUIDS), a multi-centre observational study describing current practice in Australia and New Zealand.

机构信息

Department of Emergency Medicine, Gold Coast University Hospital, Gold Coast, Queensland, Australia.

School of Medicine, Bond University, Gold Coast, Queensland, Australia.

出版信息

Emerg Med Australas. 2020 Aug;32(4):586-598. doi: 10.1111/1742-6723.13469. Epub 2020 Feb 10.

Abstract

OBJECTIVES

To describe haemodynamic resuscitation practices in ED patients with suspected sepsis and hypotension.

METHODS

This was a prospective, multicentre, observational study conducted in 70 hospitals in Australia and New Zealand between September 2018 and January 2019. Consecutive adults presenting to the ED during a 30-day period at each site, with suspected sepsis and hypotension (systolic blood pressure <100 mmHg) despite at least 1000 mL fluid resuscitation, were eligible. Data included baseline demographics, clinical and laboratory variables and intravenous fluid volume administered, vasopressor administration at baseline and 6- and 24-h post-enrolment, time to antimicrobial administration, intensive care admission, organ support and in-hospital mortality.

RESULTS

A total of 4477 patients were screened and 591 were included with a mean (standard deviation) age of 62 (19) years, Acute Physiology and Chronic Health Evaluation II score 15.2 (6.6) and a median (interquartile range) systolic blood pressure of 94 mmHg (87-100). Median time to first intravenous antimicrobials was 77 min (42-148). A vasopressor infusion was commenced within 24 h in 177 (30.2%) patients, with noradrenaline the most frequently used (n = 138, 78%). A median of 2000 mL (1500-3000) of intravenous fluids was administered prior to commencing vasopressors. The total volume of fluid administered from pre-enrolment to 24 h was 4200 mL (3000-5661), with a range from 1000 to 12 200 mL. Two hundred and eighteen patients (37.1%) were admitted to an intensive care unit. Overall in-hospital mortality was 6.2% (95% confidence interval 4.4-8.5%).

CONCLUSION

Current resuscitation practice in patients with sepsis and hypotension varies widely and occupies the spectrum between a restricted volume/earlier vasopressor and liberal fluid/later vasopressor strategy.

摘要

目的

描述急诊科疑似感染性休克合并低血压患者的血流动力学复苏实践。

方法

这是一项在澳大利亚和新西兰 70 家医院进行的前瞻性、多中心、观察性研究。在每个地点,连续入选在研究期间 30 天内进入急诊科、存在疑似感染性休克(收缩压<100mmHg)和低血压(尽管已给予至少 1000ml 液体复苏)的成年患者。纳入标准:患者的基线人口统计学、临床和实验室变量、静脉输液量、基线和入组后 6 小时及 24 小时的血管加压素应用、抗菌药物应用时间、重症监护病房收治、器官支持和院内死亡率。

结果

共筛选了 4477 例患者,纳入 591 例患者,平均(标准差)年龄为 62(19)岁,急性生理学与慢性健康状况评分系统Ⅱ(Acute Physiology and Chronic Health Evaluation II)评分为 15.2(6.6),收缩压中位数(四分位数间距)为 94mmHg(87-100)。首次静脉使用抗菌药物的中位时间为 77min(42-148)。在 177 例(30.2%)患者中,在 24 小时内开始应用血管加压素,其中最常使用的是去甲肾上腺素(n=138,78%)。在开始应用血管加压素前,中位静脉输液量为 2000ml(1500-3000)。从入组到 24 小时,共输注液体 4200ml(3000-5661),范围为 1000-12200ml。218 例(37.1%)患者被收入重症监护病房。总的院内死亡率为 6.2%(95%置信区间 4.4%-8.5%)。

结论

目前,感染性休克合并低血压患者的复苏实践差异很大,涵盖了限制性液体/早期血管加压素和自由性液体/晚期血管加压素策略之间的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd9/7496107/5026006ad3fd/EMM-32-586-g001.jpg

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