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 in | Journal of thoracic disease Vol. 12; no. 5; pp. 1811 - 1823 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
China
AME Publishing Company
01.05.2020
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Online Access | Get full text |
ISSN | 2072-1439 2077-6624 |
DOI | 10.21037/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. |
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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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Copyright | 2020 Journal of Thoracic Disease. All rights reserved. 2020 Journal of Thoracic Disease. All rights reserved. 2020 Journal of Thoracic Disease. |
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Keywords | Clinical characteristics chronic obstructive pulmonary disease (COPD) coronavirus disease 2019 (COVID-19) |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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Title | Clinical characteristics of COVID-19 infection in chronic obstructive pulmonary disease: a multicenter, retrospective, observational study |
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