Kai Swenson, Juan P Uribe, Alvaro Ayala, Mihir Parikh, Chenchen Zhang, Alichia Paton, Molly Trachtenberg, Adnan Majid
{"title":"急性新冠肺炎肺炎的胸膜疾病:单中心回顾性队列研究。","authors":"Kai Swenson, Juan P Uribe, Alvaro Ayala, Mihir Parikh, Chenchen Zhang, Alichia Paton, Molly Trachtenberg, Adnan Majid","doi":"10.1097/LBR.0000000000000896","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Pleural diseases encompass pleural effusion and pneumothorax (PTX), both of which were uncommon in coronavirus disease of 2019 (COVID-19). We aimed to describe the frequency, characteristics, and main outcomes of these conditions in patients with COVID-19 pneumonia.</p><p><strong>Methods: </strong>We performed a retrospective cohort analysis of inpatients with COVID-19 pneumonia between January 1, 2020 and January 1, 2022, at Beth Israel Deaconess Medical Center in Boston, Massachusetts.</p><p><strong>Results: </strong>Among 4419 inpatients with COVID-19 pneumonia, 109 (2.5%) had concurrent pleural disease. Ninety-four (2.1%) had pleural effusion (50% seen on admission) and 15 (0.3%) had PTX, both with higher rates of underlying conditions such as heart failure, liver disease, kidney disease, and malignancy. A total of 28 (30%) pleural effusions were drained resulting in 32% being exudative, 43% pseudoexudative, and 25% transudative. Regarding PTX, 5 (33%) were spontaneous and 10 (67%) were due to barotrauma while on mechanical ventilation. We found that the presence of underlying lung disease was not associated with an increased risk of developing PTX. In addition, patients with pleural disease had a higher incidence of severe or critical illness as represented by intensive care unit admission and intubation, longer hospital and intensive care unit stay, and a higher mortality rate as compared with patients without the pleural disease.</p><p><strong>Conclusion: </strong>Pleural effusions and pneumothoraces are infrequent findings in patients admitted due to COVID-19 pneumonia, worsened outcomes in these patients likely reflect an interplay between the severity of inflammation and parenchymal injury due to COVID-19 disease and underlying comorbidities.</p>","PeriodicalId":15268,"journal":{"name":"Journal of Bronchology & Interventional Pulmonology","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pleural Disease in Acute COVID-19 Pneumonia: A Single Center Retrospective Cohort Study.\",\"authors\":\"Kai Swenson, Juan P Uribe, Alvaro Ayala, Mihir Parikh, Chenchen Zhang, Alichia Paton, Molly Trachtenberg, Adnan Majid\",\"doi\":\"10.1097/LBR.0000000000000896\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Pleural diseases encompass pleural effusion and pneumothorax (PTX), both of which were uncommon in coronavirus disease of 2019 (COVID-19). We aimed to describe the frequency, characteristics, and main outcomes of these conditions in patients with COVID-19 pneumonia.</p><p><strong>Methods: </strong>We performed a retrospective cohort analysis of inpatients with COVID-19 pneumonia between January 1, 2020 and January 1, 2022, at Beth Israel Deaconess Medical Center in Boston, Massachusetts.</p><p><strong>Results: </strong>Among 4419 inpatients with COVID-19 pneumonia, 109 (2.5%) had concurrent pleural disease. Ninety-four (2.1%) had pleural effusion (50% seen on admission) and 15 (0.3%) had PTX, both with higher rates of underlying conditions such as heart failure, liver disease, kidney disease, and malignancy. A total of 28 (30%) pleural effusions were drained resulting in 32% being exudative, 43% pseudoexudative, and 25% transudative. Regarding PTX, 5 (33%) were spontaneous and 10 (67%) were due to barotrauma while on mechanical ventilation. We found that the presence of underlying lung disease was not associated with an increased risk of developing PTX. 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引用次数: 0
摘要
背景:胸腔疾病包括胸腔积液和肺气肿(PTX),这两种疾病在2019年冠状病毒病(新冠肺炎)中都不常见。我们旨在描述新冠肺炎肺炎患者出现这些情况的频率、特征和主要结果。方法:我们对2020年1月1日至2022年1月31日期间在马萨诸塞州波士顿Beth Israel Deaconess医疗中心住院的新冠肺炎患者进行了回顾性队列分析。结果:在4419名新冠肺炎住院患者中,109人(2.5%)并发胸膜疾病。94例(2.1%)有胸腔积液(入院时有50%),15例(0.3%)有PTX,这两种疾病的潜在疾病发生率都较高,如心力衰竭、肝病、肾病和恶性肿瘤。共排出28(30%)个胸腔积液,其中32%为渗出性,43%为假渗出性,25%为渗出性。关于PTX,5例(33%)是自发的,10例(67%)是由于机械通气时的气压损伤。我们发现,潜在肺部疾病的存在与PTX发病风险的增加无关。此外,与无胸膜疾病的患者相比,胸膜疾病患者的重症或危重症发生率更高,表现为重症监护室入院和插管、住院时间和重症监护室住院时间更长,死亡率更高。结论:在因新冠肺炎肺炎入院的患者中,胸腔积液和肺胸是罕见的,这些患者的恶化结果可能反映了新冠肺炎疾病引起的炎症和实质损伤的严重程度与潜在合并症之间的相互作用。
Pleural Disease in Acute COVID-19 Pneumonia: A Single Center Retrospective Cohort Study.
Background: Pleural diseases encompass pleural effusion and pneumothorax (PTX), both of which were uncommon in coronavirus disease of 2019 (COVID-19). We aimed to describe the frequency, characteristics, and main outcomes of these conditions in patients with COVID-19 pneumonia.
Methods: We performed a retrospective cohort analysis of inpatients with COVID-19 pneumonia between January 1, 2020 and January 1, 2022, at Beth Israel Deaconess Medical Center in Boston, Massachusetts.
Results: Among 4419 inpatients with COVID-19 pneumonia, 109 (2.5%) had concurrent pleural disease. Ninety-four (2.1%) had pleural effusion (50% seen on admission) and 15 (0.3%) had PTX, both with higher rates of underlying conditions such as heart failure, liver disease, kidney disease, and malignancy. A total of 28 (30%) pleural effusions were drained resulting in 32% being exudative, 43% pseudoexudative, and 25% transudative. Regarding PTX, 5 (33%) were spontaneous and 10 (67%) were due to barotrauma while on mechanical ventilation. We found that the presence of underlying lung disease was not associated with an increased risk of developing PTX. In addition, patients with pleural disease had a higher incidence of severe or critical illness as represented by intensive care unit admission and intubation, longer hospital and intensive care unit stay, and a higher mortality rate as compared with patients without the pleural disease.
Conclusion: Pleural effusions and pneumothoraces are infrequent findings in patients admitted due to COVID-19 pneumonia, worsened outcomes in these patients likely reflect an interplay between the severity of inflammation and parenchymal injury due to COVID-19 disease and underlying comorbidities.