无创通气与COVID-19急性呼吸窘迫综合征死亡率的关系

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Chahat Puri, Akshay Duddu, Gina Patel, Sahib Singh, Juan Negrin, Lauren Greenburg, David Vitberg, Elisabeth M Carr
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引用次数: 0

摘要

背景:2019冠状病毒病大流行给卫生保健系统造成了重大负担。自大流行开始以来,COVID-19诱导的急性呼吸窘迫综合征(ARDS)患者的插管时机仍然是一个有争议的领域。研究问题:在COVID-19患者中进行无创通气(NIV)的试验是否会加重因ARDS插管患者的死亡率?研究设计和方法:一项单中心、回顾性队列研究纳入了2020年3月至2022年9月期间因急性缺氧性呼吸衰竭入住ICU的所有成年COVID-19患者(n = 161)。分组分为经无创通气试验后插管患者(N = 100)和未经无创通气试验插管患者(N = 61)。主要结果是比较两组之间的死亡率。测量结果和主要结果:与未进行无创通气试验的患者相比,接受无创通气试验后插管患者的ICU死亡率(定义为ICU入院期间死亡)更高(69% vs 52%, p = 0.044)。与未接受无创通气试验的插管患者相比,最初接受无创通气试验的患者死亡率的优势比(OR)为2.17 (95% CI 1.04-4.54)。NIV组插管后的ICU住院时间更长,分别为11.9天和7.7天(p = 0.001)。在NIV试验后插管的患者住院时间(LOS)较长(IRR 1.39, 95% CI 1.05-1.85, p = 0.022)。然而,两组机械通气持续时间相似(IRR 1.23, 95% CI 1.93-4.68, p = 0.35)。两组患者气胸、呼吸机相关性肺炎(VAP)和静脉血栓栓塞(VTE)的发生率相似。结论:在ARDS中,低TV的肺保护策略已被证明可以改善患者的预后。在插管前使用无创通气试验与死亡率增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Association of Non-invasive Ventilation and Mortality in COVID-19 Induced Acute Respiratory Distress Syndrome.

The Association of Non-invasive Ventilation and Mortality in COVID-19 Induced Acute Respiratory Distress Syndrome.

Background: The COVID-19 pandemic caused a major burden on the healthcare system. Since the beginning of the pandemic, the timing of intubation in patients with COVID-19 induced acute respiratory distress syndrome (ARDS) remained an area of debate.

Research question: Does a trial of non-invasive ventilation (NIV) in COVID-19 patients worsen mortality in patients intubated due to ARDS?

Study design and methods: A single-center, retrospective cohort study of all adult patients (n = 161) with COVID-19 admitted to the ICU between March 2020 through September 2022 with acute hypoxic respiratory failure were included. The group was divided into patients intubated after a trial of NIV (N = 100) and patients intubated without a trial of NIV (N = 61). The primary outcome was to compare the mortality rates between the two groups.

Measurements and main results: ICU mortality (defined as death during ICU admission) was higher in patients intubated after a trial of the NIV group compared to those without a trial of NIV (69% vs 52%, p = 0.044). Patients initially treated with a trial of NIV had an odds ratio (OR) of 2.17 for mortality compared to those intubated without a trial of NIV (95% CI 1.04-4.54). ICU length of stay was higher in the intubation after a trial of the NIV group, 11.9 vs 7.7 days (p = 0.001). Patients intubated after a trial of NIV had a longer hospital Length of stay (LOS) (IRR 1.39, 95% CI 1.05-1.85, p = 0.022). However, the duration of mechanical ventilation was similar in the two groups (IRR 1.23, 95% CI 1.93-4.68, p = 0.35). The incidence of pneumothorax, ventilator associated pneumonia (VAP), and venous thromboembolism (VTE) were similar in the two groups.

Conclusion: In ARDS, a lung protective strategy with low TV has been proven to improve patient outcomes. The use of a trial of NIV prior to intubation is associated with an increase in mortality.

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来源期刊
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发文量
106
审稿时长
17 weeks
期刊介绍: JCHIMP provides: up-to-date information in the field of Internal Medicine to community hospital medical professionals a platform for clinical faculty, residents, and medical students to publish research relevant to community hospital programs. Manuscripts that explore aspects of medicine at community hospitals welcome, including but not limited to: the best practices of community academic programs community hospital-based research opinion and insight from community hospital leadership and faculty the scholarly work of residents and medical students affiliated with community hospitals.
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