Author:
Zhou Fei,Wang Yimin,Liu Yingmei,Liu Xuedong,Gu Li,Zhang Xiaoju,Pu Zenghui,Yang Guoru,Liu Bo,Nie Qingrong,Xue Bing,Feng Jing,Guo Qiang,Liu Jianhua,Fan Hong,Chen Jin,Zhang Yongxiang,Xu Zhenyang,Pang Min,Chen Yu,Nie Xiuhong,Cai Zhigang,Xu Jinfu,Peng Kun,Li Xiangxin,Xiang Pingchao,Zhang Zuoqing,Jiang Shujuan,Su Xin,Zhang Jie,Li Yanming,Jin Xiuhong,Jiang Rongmeng,Dong Jianping,Song Yuanlin,Zhou Hong,Wang Chen,Cao Bin
Abstract
Although broad knowledge of influenza viral pneumonia has been established, the significance of non-influenza respiratory viruses in community-acquired pneumonia (CAP) and their impact on clinical outcomes remains unclear, especially in the non-immunocompromised adult population.Hospitalised immunocompetent patients with CAP were prospectively recruited from 34 hospitals in mainland China. Respiratory viruses were detected by molecular methods. Comparisons were conducted between influenza and non-influenza viral infection groups.In total, 915 out of 2336 adult patients with viral infection were enrolled in the analysis, with influenza virus (28.4%) the most frequently detected virus, followed by respiratory syncytial virus (3.6%), adenovirus (3.3%), human coronavirus (3.0%), parainfluenza virus (2.2%), human rhinovirus (1.8%) and human metapneumovirus (1.5%). Non-influenza viral infections accounted for 27.4% of viral pneumonia. Consolidation was more frequently observed in patients with adenovirus infection. The occurrence of complications such as sepsis (40.1% versus 39.6%; p=0.890) and hypoxaemia (40.1% versus 37.2%; p=0.449) during hospitalisation in the influenza viral infection group did not differ from that of the non-influenza viral infection group. Compared with influenza virus infection, the multivariable adjusted odds ratios of CURB-65 (confusion, urea >7 mmol·L−1, respiratory rate ≥30 breaths·min−1, blood pressure <90 mmHg (systolic) or ≤60 mmHg (diastolic), age ≥65 years) ≥3, arterial oxygen tension/inspiratory oxygen fraction <200 mmHg, and occurrence of sepsis and hypoxaemia for non-influenza respiratory virus infection were 0.87 (95% CI 0.26–2.84), 0.72 (95% CI 0.26–1.98), 1.00 (95% CI 0.63–1.58) and 1.05 (95% CI 0.66–1.65), respectively. The hazard ratio of 90-day mortality was 0.51 (95% CI 0.13–1.91).The high incidence of complications in non-influenza viral pneumonia and similar impact of non-influenza respiratory viruses relative to influenza virus on disease severity and outcomes suggest more attention should be given to CAP caused by non-influenza respiratory viruses.
Funder
Beijing Science and Technology Project
Innovation Fund for Medical Sciences
National Key Technology Support Program
National Science Fund for Distinguished Young Scholars
Publisher
European Respiratory Society (ERS)
Subject
Pulmonary and Respiratory Medicine