Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep, Wayne State University School of Medicine and Detroit Medical Center, Detroit, Michigan, United States of America.
Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
PLoS One. 2022 Aug 5;17(8):e0271964. doi: 10.1371/journal.pone.0271964. eCollection 2022.
Pneumothorax has been increasingly observed among patients with coronavirus disease-2019 (COVID-19) pneumonia, specifically in those patients who develop acute respiratory distress syndrome (ARDS). In this study, we sought to determine the incidence and potential risk factors of pneumothorax in critically ill adults with COVID-19.
This retrospective cohort study included adult patients with laboratory-confirmed SARS-CoV-2 infection admitted to one of the adult intensive care units of a tertiary, academic teaching hospital from May 2020 through May 2021.
Among 334 COVID-19 cases requiring ICU admission, the incidence of pneumothorax was 10% (33 patients). Patients who experienced pneumothorax more frequently required vasopressor support (28/33 [84%] vs. 191/301 [63%] P = 0.04), were more likely to be proned (25/33 [75%] vs. 111/301 [36%], P<0.001), and the presence of pneumothorax was associated with prolonged duration of mechanical ventilation; 21 (1-97) versus 7 (1-79) days, p<0.001 as well as prolonged hospital length of stay (29 [9-133] vs. 15 [1-90] days, P<0.001), but mortality was not significantly different between groups. Importantly, when we performed a Cox proportional hazard ratio (HR) model of multivariate parameters, we found that administration of tocilizumab significantly increased the risk of developing pneumothorax (HR = 10.7; CI [3.6-32], P<0.001).
Among 334 critically ill patients with COVID-19, the incidence of pneumothorax was 10%. Presence of pneumothorax was associated with prolonged duration of mechanical ventilation and length of hospital stay. Strikingly, receipt of tocilizumab was associated with an increased risk of developing pneumothorax.
新冠肺炎(COVID-19)患者中气胸的发生率越来越高,特别是在发生急性呼吸窘迫综合征(ARDS)的患者中。在本研究中,我们旨在确定危重症 COVID-19 成人患者气胸的发生率和潜在危险因素。
这是一项回顾性队列研究,纳入了 2020 年 5 月至 2021 年 5 月期间入住一家三级学术教学医院成人重症监护病房的实验室确诊 SARS-CoV-2 感染的成年患者。
在需要入住 ICU 的 334 例 COVID-19 病例中,气胸的发生率为 10%(33 例)。发生气胸的患者更频繁地需要血管加压支持(28/33 [84%] 比 191/301 [63%],P=0.04),更有可能被俯卧位(25/33 [75%] 比 111/301 [36%],P<0.001),且气胸的存在与机械通气时间延长相关;21(1-97)天比 7(1-79)天,P<0.001,以及住院时间延长;29(9-133)天比 15(1-90)天,P<0.001,但两组间死亡率无显著差异。重要的是,当我们对多变量参数进行 Cox 比例风险比(HR)模型分析时,我们发现托珠单抗的使用显著增加了发生气胸的风险(HR=10.7;95%CI [3.6-32],P<0.001)。
在 334 例危重症 COVID-19 患者中,气胸的发生率为 10%。气胸的存在与机械通气时间和住院时间延长相关。令人惊讶的是,托珠单抗的使用与气胸发生风险增加相关。