Pulmonary Infection in Patients with Severe Fever with Thrombocytopenia Syndrome: A Multicentre Observational Study.
Yan ZuoHeming WangJiaxiang HuangFang ZhangDongmei LvTao MengAsma BibiJilong ShenLianzi WangZhongxin WangYuanhong XuPublished in: Journal of medical virology (2023)
Co-infection in patients with severe fever with thrombocytopenia syndrome (SFTS) has been reported, posing a serious threat to survival and treatment. We aimed to systematically investigate the SFTS associated pulmonary infection, particularly invasive pulmonary fungal infection (IPFI). During April 2019 to October 2021, we conducted a multicentre observational study on adult hospitalized patients confirmed with SFTS from 3 tertiary hospital in central China. Demographic, clinical and laboratory data of patients were collected and re-assessed. A total of 443 patients (51.7% were male sex) were included for analysis with median age of 65 years old. Among them, 190 (42.9%) patients met the criteria for pulmonary infection. Pulmonary infection was associated with shorter survival time (p < 0.0001 by log-rank test), and adjusted hazard ratio was 1.729 [95% confidence interval, 1.076-2.780] (p = 0.024). Age (odds ratio (OR) 1.040 [1.019-1.062], p < 0.001), time from onset to admission (OR 1.163 [1.070-1.264], p < 0.001), having severe status (OR 3.166 [2.020-4.962], p < 0.001) and symptoms of skin change (OR 2.361 [1.049-5.316], p < 0.001) at admission and receiving intravenous immunoglobin (OR 2.185 [1.337-3.569], p = 0.002) were independent risk factors for the occurrence of pulmonary infection. After excluded false-positive/clinically irrelevant colonization, 70 (15.8%) patients were defined as IPFI. Multivariate analysis showed that time from onset to admission (OR 1.117 [1.016-1.229], p = 0.022), severe status (OR 5.737 [3.054-10.779], p < 0.001), having smoking history (OR 3.178 [1.251-8.070], p = 0.015) and autoimmunity disease (OR 7.855 [1.632-37.796], p = 0.010), receiving intravenous immunoglobin (OR 3.270 [1.424-7.508], p = 0.005) were independent risk factors for the occurrence of IPFI. In SFTS patients with pulmonary infection, white blood count < 2.09×10 9 per L (OR 6.521 [2.615-16.265], p < 0.001) and CD3 + CD4 + T cell count < 104.0 per μL (OR 8.707 [3.453-21.955], p < 0.001) could independently predict IPFI. This study showed the high prevalence and poor outcomes of pulmonary infection and IPFI in patients with SFTS. These findings highlighted the need for active surveillance of fungal pathogens and early antifungal treatment in patients with SFTS. This article is protected by copyright. All rights reserved.
Keyphrases
- pulmonary hypertension
- end stage renal disease
- ejection fraction
- newly diagnosed
- prognostic factors
- chronic kidney disease
- early onset
- peritoneal dialysis
- young adults
- case report
- patient reported outcomes
- patient reported
- machine learning
- electronic health record
- low dose
- multidrug resistant
- insulin resistance
- artificial intelligence
- type diabetes
- free survival