Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia

被引:43
作者
Sogaard, Kirstine K. [1 ,2 ]
Baettig, Veronika [3 ,4 ,5 ]
Osthoff, Michael [6 ,7 ]
Marsch, Stephan [8 ]
Leuzinger, Karoline [9 ]
Schweitzer, Michael [1 ,2 ]
Meier, Julian [2 ,10 ]
Bassetti, Stefano [6 ,7 ]
Bingisser, Roland [11 ]
Nickel, Christian H. [11 ]
Khanna, Nina [3 ,4 ,5 ]
Tschudin-Sutter, Sarah [3 ,4 ,5 ,7 ]
Weisser, Maja [3 ,4 ,5 ]
Battegay, Manuel [3 ,4 ,5 ]
Hirsch, Hans H. [3 ,4 ,5 ,9 ,12 ]
Pargger, Hans [8 ]
Siegemund, Martin [7 ,8 ]
Egli, Adrian [1 ,2 ]
机构
[1] Univ Hosp Basel, Clin Bacteriol & Mycol, Petersgraben 4, CH-4031 Basel, Switzerland
[2] Univ Basel, Dept Biomed, Appl Microbiol Res, Basel, Switzerland
[3] Univ Hosp Basel, Div Infect Dis, Basel, Switzerland
[4] Univ Hosp Basel, Hosp Epidemiol, Basel, Switzerland
[5] Univ Basel, Basel, Switzerland
[6] Univ Hosp Basel, Div Internal Med, Basel, Switzerland
[7] Univ Hosp Basel, Dept Clin Res, Basel, Switzerland
[8] Univ Hosp Basel, Dept Intens Care Med, Basel, Switzerland
[9] Univ Hosp Basel, Clin Virol, Lab Med, Basel, Switzerland
[10] Univ Hosp Basel, Hosp Pharm, Basel, Switzerland
[11] Univ Hosp Basel, Dept Emergency Med, Basel, Switzerland
[12] Univ Basel, Dept Biomed, Transplantat & Clin Virol, Basel, Switzerland
关键词
COVID-19; SARS-CoV-2; Bacterial secondary infections; Pneumonia; Sepsis;
D O I
10.1186/s40560-021-00526-y
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives SARS-CoV-2 may cause acute lung injury, and secondary infections are thus relevant complications in patients with COVID-19 pneumonia. However, detailed information on community- and hospital-acquired infections among patients with COVID-19 pneumonia is scarce. Methods We identified 220 SARS-CoV-2-positive patients hospitalized at the University Hospital Basel, Switzerland (between 25 February and 31 May 2020). We excluded patients who declined the general consent (n = 12), patients without clinical evidence of pneumonia (n = 29), and patients hospitalized for < 24 h (n = 17). We evaluated the frequency of community- and hospital-acquired infections using respiratory and blood culture materials with antigen, culture-based, and molecular diagnostics. For ICU patients, all clinical and microbial findings were re-evaluated interdisciplinary (intensive care, infectious disease, and clinical microbiology), and agreement reached to classify patients with infections. Results In the final cohort of 162 hospitalized patients (median age 64.4 years (IQR, 50.4-74.2); 61.1% male), 41 (25.3%) patients were admitted to the intensive care unit, 34/41 (82.9%) required mechanical ventilation, and 17 (10.5%) of all hospitalized patients died. In total, 31 infections were diagnosed including five viral co-infections, 24 bacterial infections, and three fungal infections (ventilator-associated pneumonia, n = 5; tracheobronchitis, n = 13; pneumonia, n = 1; and bloodstream infection, n = 6). Median time to respiratory tract infection was 12.5 days (IQR, 8-18) and time to bloodstream infection 14 days (IQR, 6-30). Hospital-acquired bacterial and fungal infections were more frequent among ICU patients than other patients (36.6% vs. 1.7%). Antibiotic or antifungal treatment was administered in 71 (43.8%) patients. Conclusions Community-acquired viral and bacterial infections were rare among COVID-19 pneumonia patients. By contrast, hospital-acquired bacterial or fungal infections were frequently complicating the course among ICU patients.
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页数:10
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