新型冠状病毒肺炎所致急性呼吸窘迫综合征中无创通气与死亡率的关联
The Association of Non-invasive Ventilation and Mortality in COVID-19 Induced Acute Respiratory Distress Syndrome.
作者信息
Puri Chahat, Duddu Akshay, Patel Gina, Singh Sahib, Negrin Juan, Greenburg Lauren, Vitberg David, Carr Elisabeth M
机构信息
Department of Pulmonary and Critical Care, University of Arizona, Phoenix, AZ, USA.
Department of Internal Medicine, Greater Baltimore Medical Center, Towson, MD, USA.
出版信息
J Community Hosp Intern Med Perspect. 2025 Jul 3;15(4):14-20. doi: 10.55729/2000-9666.1499. eCollection 2025.
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.
背景
新冠疫情给医疗系统带来了巨大负担。自疫情开始以来,新冠病毒诱导的急性呼吸窘迫综合征(ARDS)患者的插管时机一直存在争议。
研究问题
对新冠患者进行无创通气(NIV)试验是否会增加因ARDS插管患者的死亡率?
研究设计与方法
对2020年3月至2022年9月期间入住重症监护病房(ICU)的所有成年新冠患者(n = 161)进行单中心回顾性队列研究,这些患者均患有急性低氧性呼吸衰竭。将患者分为接受NIV试验后插管的患者(N = 100)和未接受NIV试验直接插管的患者(N = 61)。主要结果是比较两组的死亡率。
测量指标与主要结果
与未接受NIV试验的患者相比,接受NIV试验后插管的患者ICU死亡率(定义为ICU住院期间死亡)更高(69% 对52%,p = 0.044)。与未接受NIV试验直接插管的患者相比,最初接受NIV试验治疗的患者死亡比值比(OR)为2.17(95% CI 1.04 - 4.54)。接受NIV试验后插管组的ICU住院时间更长,分别为11.9天和7.7天(p = 0.001)。接受NIV试验后插管的患者住院时间更长(住院时间比值比1.39,95% CI 1.05 - 1.85,p = 0.022)。然而,两组的机械通气时间相似(住院时间比值比1.23,95% CI 1.93 - 4.68,p = 0.35)。两组气胸、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,低潮气量的肺保护策略已被证明可改善患者预后。插管前进行NIV试验与死亡率增加有关。
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