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比较急性呼吸衰竭患者使用神经调节辅助通气或压力支持通气的无创通气。

Comparing Noninvasive Ventilation Delivered Using Neurally-Adjusted Ventilatory Assist or Pressure Support in Acute Respiratory Failure.

机构信息

Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

出版信息

Respir Care. 2021 Feb;66(2):213-220. doi: 10.4187/respcare.07952. Epub 2020 Sep 1.

Abstract

BACKGROUND

The use of neurally-adjusted ventilatory assist (NAVA) during noninvasive ventilation (NIV) results in better patient-ventilator interaction. Whether this improves clinical outcomes lacks dedicated study.

METHODS

In this randomized controlled trial, we compared NAVA with PSV for delivering NIV in consecutive subjects with de novo acute respiratory failure. The primary outcomes were NIV failure rates and 28-d mortality. The secondary outcomes were asynchrony index, NIV-related complications, and others.

RESULTS

We enrolled 100 subjects (50 subjects each for NAVA and PSV, 60% male) with a mean ± SD age of 56.7 ± 12 y. There was no difference in NIV failure rates (30% vs 32%, = .83) and 28-d mortality rates (18% vs 34%, = .07) between the NAVA and PSV arms, respectively. The median asynchrony index was significantly lower with NAVA (6.7 vs 44.8, < .001). The use of NAVA significantly reduced NIV-related complications (32% vs 58%, = .01). In a post hoc analysis, the use of NAVA significantly reduced the 28-d mortality in subjects with COPD exacerbation.

CONCLUSIONS

The use of NAVA during NIV did not improve NIV failure rate or 28-d mortality in subjects with acute respiratory failure. However, patient-ventilator asynchrony and NIV-related complications were reduced with NAVA.

TRIAL REGISTRY

www.clinicaltrials.gov (NCT03271671).

摘要

背景

在无创通气(NIV)中使用神经调节通气辅助(NAVA)可改善患者-呼吸机交互作用。但这种方法是否能改善临床结局尚无专门研究。

方法

本随机对照试验比较了 NAVA 和 PSV 在新发急性呼吸衰竭连续患者中应用 NIV 的效果。主要结局为 NIV 失败率和 28 天死亡率。次要结局为人机不同步指数、与 NIV 相关的并发症等。

结果

共纳入 100 例患者(NAVA 和 PSV 组各 50 例,60%为男性),平均年龄±标准差为 56.7±12 岁。NAVA 组和 PSV 组的 NIV 失败率(30%比 32%, =.83)和 28 天死亡率(18%比 34%, =.07)无差异。NAVA 组的中位人机不同步指数显著较低(6.7 比 44.8, <.001)。NAVA 组的 NIV 相关并发症发生率显著较低(32%比 58%, =.01)。在事后分析中,NAVA 可降低 COPD 加重患者的 28 天死亡率。

结论

在急性呼吸衰竭患者中,NIV 期间使用 NAVA 并未降低 NIV 失败率或 28 天死亡率。但 NAVA 可减少人机不同步和与 NIV 相关的并发症。

试验注册

www.clinicaltrials.gov(NCT03271671)。

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