Clinical characteristics of COVID-19 infection in chronic obstructive pulmonary disease: a multicenter, retrospective, observational study

Coronavirus disease 2019 (COVID-19) has been a global pandemic disease, with more than 4 million cases and nearly 300,000 deaths. Little is known about COVID-19 in patients with chronic obstructive pulmonary disease (COPD). We aimed to evaluate the influence of preexisting COPD on the progress and o...

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Published inJournal of thoracic disease Vol. 12; no. 5; pp. 1811 - 1823
Main Authors Wu, Fan, Zhou, Yumin, Wang, Zhongfang, Xie, Min, Shi, Zhe, Tang, Zhiqiang, Li, Xiaohe, Li, Xiaochen, Lei, Chunliang, Li, Yimin, Ni, Zhengyi, Hu, Yu, Liu, Xiaoqing, Yin, Wenguang, Cheng, Linling, Ye, Feng, Peng, Jieqi, Huang, Lingmei, Tian, Jia, Zhang, Lingjuan, Mo, Xiaoneng, Zhang, Ying, Hu, Ke, Jiang, Yongliang, Guan, Weijie, Xiang, Jie, Liu, Yingxia, Peng, Yixiang, Wei, Li, Hu, Yahua, Peng, Peng, Wang, Jianming, Liu, Jiyang, Huang, Wei, Chen, Ruchong, Zhao, Jianping, Li, Shiyue, Zhang, Nuofu, Zhao, Jincun, Zhong, Nanshan, Ran, Pixin
Format Journal Article
LanguageEnglish
Published China AME Publishing Company 01.05.2020
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Online AccessGet full text
ISSN2072-1439
2077-6624
DOI10.21037/jtd-20-1914

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Abstract Coronavirus disease 2019 (COVID-19) has been a global pandemic disease, with more than 4 million cases and nearly 300,000 deaths. Little is known about COVID-19 in patients with chronic obstructive pulmonary disease (COPD). We aimed to evaluate the influence of preexisting COPD on the progress and outcomes of COVID-19. This was a multicenter, retrospective, observational study. We enrolled 1,048 patients aged 40 years and above, including 50 patients with COPD and 998 patients without COPD, and with COVID-19 confirmed via high-throughput sequencing or real-time reverse transcription-polymerase chain reaction, between December 11, 2019 and February 20, 2020. We collected data of demographics, pathologic test results, radiologic imaging, and treatments. The primary outcomes were composite endpoints determined by admission to an intensive care unit, the use of mechanical ventilation, or death. Compared with patients who had COVID-19 but not COPD, those with COPD had higher rates of fatigue (56.0% 40.2%), dyspnea (66.0% 26.3%), diarrhea (16.0% 3.6%), and unconsciousness (8.0% 1.7%) and a significantly higher proportion of increased activated partial thromboplastin time (23.5% 5.2%) and D-dimer (65.9% 29.3%), as well as ground-glass opacities (77.6% 60.3%), local patchy shadowing (61.2% 41.4%), and interstitial abnormalities (51.0% 19.8%) on chest computed tomography. Patients with COPD were more likely to develop bacterial or fungal coinfection (20.0% 5.9%), acute respiratory distress syndrome (ARDS) (20.0% 7.3%), septic shock (14.0% 2.3%), or acute renal failure (12.0% 1.3%). Patients with COPD and COVID-19 had a higher risk of reaching the composite endpoints [hazard ratio (HR): 2.17, 95% confidence interval (CI): 1.40-3.38; P=0.001] or death (HR: 2.28, 95% CI: 1.15-4.51; P=0.019), after adjustment. In this study, patients with COPD who developed COVID-19 showed a higher risk of admission to the intensive care unit, mechanical ventilation, or death.
AbstractList Coronavirus disease 2019 (COVID-19) has been a global pandemic disease, with more than 4 million cases and nearly 300,000 deaths. Little is known about COVID-19 in patients with chronic obstructive pulmonary disease (COPD). We aimed to evaluate the influence of preexisting COPD on the progress and outcomes of COVID-19.BACKGROUNDCoronavirus disease 2019 (COVID-19) has been a global pandemic disease, with more than 4 million cases and nearly 300,000 deaths. Little is known about COVID-19 in patients with chronic obstructive pulmonary disease (COPD). We aimed to evaluate the influence of preexisting COPD on the progress and outcomes of COVID-19.This was a multicenter, retrospective, observational study. We enrolled 1,048 patients aged 40 years and above, including 50 patients with COPD and 998 patients without COPD, and with COVID-19 confirmed via high-throughput sequencing or real-time reverse transcription-polymerase chain reaction, between December 11, 2019 and February 20, 2020. We collected data of demographics, pathologic test results, radiologic imaging, and treatments. The primary outcomes were composite endpoints determined by admission to an intensive care unit, the use of mechanical ventilation, or death.METHODSThis was a multicenter, retrospective, observational study. We enrolled 1,048 patients aged 40 years and above, including 50 patients with COPD and 998 patients without COPD, and with COVID-19 confirmed via high-throughput sequencing or real-time reverse transcription-polymerase chain reaction, between December 11, 2019 and February 20, 2020. We collected data of demographics, pathologic test results, radiologic imaging, and treatments. The primary outcomes were composite endpoints determined by admission to an intensive care unit, the use of mechanical ventilation, or death.Compared with patients who had COVID-19 but not COPD, those with COPD had higher rates of fatigue (56.0% vs. 40.2%), dyspnea (66.0% vs. 26.3%), diarrhea (16.0% vs. 3.6%), and unconsciousness (8.0% vs. 1.7%) and a significantly higher proportion of increased activated partial thromboplastin time (23.5% vs. 5.2%) and D-dimer (65.9% vs. 29.3%), as well as ground-glass opacities (77.6% vs. 60.3%), local patchy shadowing (61.2% vs. 41.4%), and interstitial abnormalities (51.0% vs. 19.8%) on chest computed tomography. Patients with COPD were more likely to develop bacterial or fungal coinfection (20.0% vs. 5.9%), acute respiratory distress syndrome (ARDS) (20.0% vs. 7.3%), septic shock (14.0% vs. 2.3%), or acute renal failure (12.0% vs. 1.3%). Patients with COPD and COVID-19 had a higher risk of reaching the composite endpoints [hazard ratio (HR): 2.17, 95% confidence interval (CI): 1.40-3.38; P=0.001] or death (HR: 2.28, 95% CI: 1.15-4.51; P=0.019), after adjustment.RESULTSCompared with patients who had COVID-19 but not COPD, those with COPD had higher rates of fatigue (56.0% vs. 40.2%), dyspnea (66.0% vs. 26.3%), diarrhea (16.0% vs. 3.6%), and unconsciousness (8.0% vs. 1.7%) and a significantly higher proportion of increased activated partial thromboplastin time (23.5% vs. 5.2%) and D-dimer (65.9% vs. 29.3%), as well as ground-glass opacities (77.6% vs. 60.3%), local patchy shadowing (61.2% vs. 41.4%), and interstitial abnormalities (51.0% vs. 19.8%) on chest computed tomography. Patients with COPD were more likely to develop bacterial or fungal coinfection (20.0% vs. 5.9%), acute respiratory distress syndrome (ARDS) (20.0% vs. 7.3%), septic shock (14.0% vs. 2.3%), or acute renal failure (12.0% vs. 1.3%). Patients with COPD and COVID-19 had a higher risk of reaching the composite endpoints [hazard ratio (HR): 2.17, 95% confidence interval (CI): 1.40-3.38; P=0.001] or death (HR: 2.28, 95% CI: 1.15-4.51; P=0.019), after adjustment.In this study, patients with COPD who developed COVID-19 showed a higher risk of admission to the intensive care unit, mechanical ventilation, or death.CONCLUSIONSIn this study, patients with COPD who developed COVID-19 showed a higher risk of admission to the intensive care unit, mechanical ventilation, or death.
Coronavirus disease 2019 (COVID-19) has been a global pandemic disease, with more than 4 million cases and nearly 300,000 deaths. Little is known about COVID-19 in patients with chronic obstructive pulmonary disease (COPD). We aimed to evaluate the influence of preexisting COPD on the progress and outcomes of COVID-19. This was a multicenter, retrospective, observational study. We enrolled 1,048 patients aged 40 years and above, including 50 patients with COPD and 998 patients without COPD, and with COVID-19 confirmed via high-throughput sequencing or real-time reverse transcription-polymerase chain reaction, between December 11, 2019 and February 20, 2020. We collected data of demographics, pathologic test results, radiologic imaging, and treatments. The primary outcomes were composite endpoints determined by admission to an intensive care unit, the use of mechanical ventilation, or death. Compared with patients who had COVID-19 but not COPD, those with COPD had higher rates of fatigue (56.0% 40.2%), dyspnea (66.0% 26.3%), diarrhea (16.0% 3.6%), and unconsciousness (8.0% 1.7%) and a significantly higher proportion of increased activated partial thromboplastin time (23.5% 5.2%) and D-dimer (65.9% 29.3%), as well as ground-glass opacities (77.6% 60.3%), local patchy shadowing (61.2% 41.4%), and interstitial abnormalities (51.0% 19.8%) on chest computed tomography. Patients with COPD were more likely to develop bacterial or fungal coinfection (20.0% 5.9%), acute respiratory distress syndrome (ARDS) (20.0% 7.3%), septic shock (14.0% 2.3%), or acute renal failure (12.0% 1.3%). Patients with COPD and COVID-19 had a higher risk of reaching the composite endpoints [hazard ratio (HR): 2.17, 95% confidence interval (CI): 1.40-3.38; P=0.001] or death (HR: 2.28, 95% CI: 1.15-4.51; P=0.019), after adjustment. In this study, patients with COPD who developed COVID-19 showed a higher risk of admission to the intensive care unit, mechanical ventilation, or death.
Author Li, Xiaochen
Li, Yimin
Liu, Jiyang
Peng, Peng
Zhao, Jincun
Cheng, Linling
Jiang, Yongliang
Zhao, Jianping
Huang, Lingmei
Zhong, Nanshan
Zhang, Lingjuan
Chen, Ruchong
Yin, Wenguang
Tian, Jia
Peng, Yixiang
Ni, Zhengyi
Mo, Xiaoneng
Zhang, Nuofu
Wang, Zhongfang
Liu, Xiaoqing
Peng, Jieqi
Xie, Min
Wu, Fan
Li, Shiyue
Liu, Yingxia
Hu, Yahua
Xiang, Jie
Ran, Pixin
Lei, Chunliang
Guan, Weijie
Ye, Feng
Wang, Jianming
Zhou, Yumin
Li, Xiaohe
Huang, Wei
Zhang, Ying
Hu, Ke
Tang, Zhiqiang
Shi, Zhe
Hu, Yu
Wei, Li
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/32642086$$D View this record in MEDLINE/PubMed
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2020 Journal of Thoracic Disease. All rights reserved. 2020 Journal of Thoracic Disease.
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Medical Treatment Expert Group for COPD and COVID-19
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Keywords Clinical characteristics
chronic obstructive pulmonary disease (COPD)
coronavirus disease 2019 (COVID-19)
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Contributions: (I) Conception and design: P Ran, N Zhong, Y Zhou; (II) Administrative support: None; (III) Provision of study materials or patients: M Xie, Z Shi, Z Tang, X Li, K Hu, C Lei, Y Li, Z Ni, Y Hu, X Liu, L Cheng, F Ye, L Huang, J Tian, L Zhang, X Mo, Y Zhang, X Li, Y Jiang, W Guan, J Xiang, Y Liu, Y Peng, L Wei, Y Hu, P Peng, J Wang, J Liu, W Huang, R Chen, J Zhao, S Li, N Zhang, J Zhao; (IV) Collection and assembly of data: F Wu, Y Zhou, J Peng, W Guan; (V) Data analysis and interpretation: F Wu, Y Zhou, Z Wang, W Yin, P Ran; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.
These authors contributed equally to this work.
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References 32677478 - J Am Heart Assoc. 2020 Aug 18;9(16):e017756
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