Yakşi Osman, Kılıçgün Ali
Department of Thoracic Surgery, Bolu Abant Izzet Baysal University Faculty of Medicine, Bolu, Turkey.
Turk Gogus Kalp Damar Cerrahisi Derg. 2022 Jan 28;30(1):109-116. doi: 10.5606/tgkdc.dergisi.2022.22738. eCollection 2022 Jan.
The aim of this study was to investigate the factors affecting pneumothorax development, lung expansion difficulty, and the impact on mortality in novel coronavirus 2019 (COVID-19) patients.
Between March 2020 and January 2021, a total of 6,108 COVID-19 patients (3,050 males, 3,058 females; mean age: 49±17.6 years, range, 12 to 89 years) who presented to our hospital were retrospectively analyzed. The patients were divided into two groups. Group 1 (the COVID-19-pneumothorax group) consisted of patients developing pneumothorax while under treatment for COVID-19. Group 2 (COVID-19-without pneumothorax group) consisted of consecutive patients with pulmonary involvement during the same period, requiring intensive care, but not developing pneumothorax. Biochemical test results were examined for the day of hospitalization, day of transfer to intensive care unit, and Day 5 of intensive care unit stay. Lung parenchyma involvement rates on thoracic computed tomography, duration of drainage, duration of intensive care unit stay, and morbidity/mortality data were investigated.
Of all patients with COVID-19, 2,342 were admitted to our clinic and 460 needed intensive care. Pneumothorax developed in 21 patients (0.34% of all patients and 0.9% of hospitalized patients). Significant involvement diffusion on computed tomography, ferritin and D-dimer elevation, and low lymphocyte (%) values were observed in the COVID-19 patients with pneumothorax. Pneumothorax development, and ferritin and D-dimer elevation were most correlated with mortality at regression analysis. There was a significant difference in difficulty in lung expansion between COVID-19 patients who developed pneumothorax and who did not.
Pneumothorax may develop in COVID-19 patients whose biochemical parameters worsen, and expansion difficulty may be experienced, which is likely to be associated with mortality.
本研究旨在调查影响2019年新型冠状病毒(COVID-19)患者气胸发生、肺扩张困难以及对死亡率影响的因素。
回顾性分析2020年3月至2021年1月期间到我院就诊的6108例COVID-19患者(男性3050例,女性3058例;平均年龄:49±17.6岁,范围12至89岁)。患者分为两组。第1组(COVID-19气胸组)由在COVID-19治疗期间发生气胸的患者组成。第2组(COVID-19无气胸组)由同期有肺部受累、需要重症监护但未发生气胸的连续患者组成。检查住院当天、转入重症监护病房当天以及在重症监护病房停留第5天的生化检测结果。研究胸部计算机断层扫描上肺实质受累率、引流持续时间、重症监护病房停留时间以及发病率/死亡率数据。
在所有COVID-19患者中,2342例入院,460例需要重症监护。21例患者发生气胸(占所有患者的0.34%,占住院患者的0.9%)。在发生气胸的COVID-19患者中观察到计算机断层扫描上显著的受累扩散、铁蛋白和D-二聚体升高以及低淋巴细胞(%)值。回归分析显示,气胸发生、铁蛋白和D-二聚体升高与死亡率最相关。发生气胸的COVID-19患者与未发生气胸的患者在肺扩张困难方面存在显著差异。
生化参数恶化的COVID-19患者可能发生气胸,并可能出现扩张困难,这可能与死亡率相关。