高流量鼻插管供氧与无创通气治疗急性心源性肺水肿:随机对照试验研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-02-16 DOI:10.1097/MEJ.0000000000001128
Nicolas Marjanovic, Melyne Piton, Jennifer Lamarre, Camille Alleyrat, Raphael Couvreur, Jérémy Guenezan, Olivier Mimoz, Jean-Pierre Frat
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引用次数: 0

摘要

背景:高流量鼻氧能否改善急性心力衰竭(AHF)患者急性呼吸衰竭的临床症状尚不确定:比较高流量吸氧与无创通气(NIV)对急诊科(ED)收治的急性心力衰竭相关急性呼吸衰竭患者呼吸频率的影响:法国三家急诊室的多中心随机试验研究。研究对象包括疑因 AHF 导致急性呼吸衰竭的成人患者。主要排除标准为急需插管、格拉斯哥昏迷量表干预:结果测量:主要结果是治疗后一小时内呼吸频率的变化,并采用线性混合模型进行分析。次要结果包括脉搏血氧饱和度、心率、血压、血气样本、舒适度、治疗失败和死亡率的变化:在三个参与中心的 145 名符合条件的患者中,有 60 名患者被纳入分析[中位年龄为 86(四分位数间距(IQR),90;92)岁]。60 分钟时,高流量鼻氧组和 NIV 组的中位呼吸频率分别为 30.5(IQR,28;33)次/分钟和 29.5(IQR,27;35)次/分钟,中位变化分别为:高流量鼻氧-10(IQR,-12;-8)次/分钟,NIV-7(IQR,-11;-5)次/分钟[估计差异为-2.6 次/分钟(95% 置信区间 (CI),-0.5-5.7),P = 0.052]。高流量吸氧组和 NIV 组的 SpO2 中位数分别为 95(IQR,92;97)和 96(IQR,93;97),60 分钟时的中位数变化为:高流量鼻氧为 2(IQR,0;5)%,NIV 为 2(IQR,-1;5)%[估计差异为 0.8%(95% CI,-1.1-2.8),P = 0.60]。1小时后各组的PaO2、PaCO2和pH值没有差异,治疗失败率、插管率和死亡率也没有差异:在这项试验性研究中,我们没有观察到因 AHF 导致急性呼吸衰竭并接受高流量供氧或 NIV 治疗的患者的呼吸频率变化有显著的统计学差异。然而,点估计值及其较大的置信区间可能表明高流量供氧有一定的益处:NCT04971213 (https://clinicaltrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-flow nasal cannula oxygen versus noninvasive ventilation for the management of acute cardiogenic pulmonary edema: a randomized controlled pilot study.

Background: Whether high-flow nasal oxygen can improve clinical signs of acute respiratory failure in acute heart failure (AHF) is uncertain.

Objective: To compare the effect of high-flow oxygen with noninvasive ventilation (NIV) on respiratory rate in patients admitted to an emergency department (ED) for AHF-related acute respiratory failure.

Design, settings and participants: Multicenter, randomized pilot study in three French EDs. Adult patients with acute respiratory failure due to suspected AHF were included. Key exclusion criteria were urgent need for intubation, Glasgow Coma Scale <13 points or hemodynamic instability.

Intervention: Patients were randomly assigned to receive high-flow oxygen (minimum 50 l/min) or noninvasive bilevel positive pressure ventilation.

Outcomes measure: The primary outcome was change in respiratory rate within the first hour of treatment and was analyzed with a linear mixed model. Secondary outcomes included changes in pulse oximetry, heart rate, blood pressure, blood gas samples, comfort, treatment failure and mortality.

Main results: Among the 145 eligible patients in the three participating centers, 60 patients were included in the analysis [median age 86 (interquartile range (IQR), 90; 92) years]. There was a median respiratory rate of 30.5 (IQR, 28; 33) and 29.5 (IQR, 27; 35) breaths/min in the high-flow oxygen and NIV groups respectively, with a median change of -10 (IQR, -12; -8) with high-flow nasal oxygen and -7 (IQR, -11; -5) breaths/min with NIV [estimated difference -2.6 breaths/min (95% confidence interval (CI), -0.5-5.7), P  = 0.052] at 60 min. There was a median SpO 2 of 95 (IQR, 92; 97) and 96 (IQR, 93; 97) in the high-flow oxygen and NIV groups respectively, with a median change at 60 min of 2 (IQR, 0; 5) with high-flow nasal oxygen and 2 (IQR, -1; 5) % with NIV [estimated difference 0.8% (95% CI, -1.1-2.8), P  = 0.60]. PaO 2 , PaCO 2 and pH did not differ at 1 h between groups, nor did treatment failure, intubation and mortality rates.

Conclusion: In this pilot study, we did not observe a statistically significant difference in changes in respiratory rate among patients with acute respiratory failure due to AHF and managed with high-flow oxygen or NIV. However, the point estimate and its large confidence interval may suggest a benefit of high-flow oxygen.

Trial registration: NCT04971213 ( https://clinicaltrials.gov ).

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