Risk factors for invasive pulmonary aspergillosis in patients with severe fever with thrombocytopenia syndrome: A multicenter retrospective study

Author:

Yao Lu1,Shi Yuan1,Fu Jiaji1,Fang Xiaowei2,Zhang Hongling3,Luo Dengli4,Zhou Yi5,Pan Aijun2,Yu Yuan1,Yang Xiaobo1,Shu Huaqing1,Zou Xiaojing1,Xu Jiqian1,Shang You1

Affiliation:

1. Department of Critical Care Medicine, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

2. The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine University of Science and Technology of China Hefei China

3. Department of Critical Care Medicine, Lu'an People's Hospital Anhui Medical University Lu'an China

4. Department of Critical Care Medicine Macheng People's Hospital Macheng China

5. Department of Infectious Diseases Macheng People's Hospital Macheng China

Abstract

AbstractInvasive pulmonary aspergillosis (IPA) is a life‐threatening complication in patients with severe fever with thrombocytopenia syndrome (SFTS), yet SFTS‐associated IPA (SAPA)'s risk factors remain undefined. A multicenter retrospective cohort study across Hubei and Anhui provinces (May 2013–September 2022) utilized least absolute shrinkage and selection operator (LASSO) regression for variable selection. Multivariable logistic regression identified independent predictors of SAPA, Cox regression highlighted mortality‐related risk factors. Of the 1775 screened SFTS patients, 1650 were included, with 169 developing IPA, leading to a 42‐day mortality rate of 26.6% among SAPA patients. Multivariable logistic regression revealed SAPA risk factors including advanced age, petechia, hemoptysis, tremor, low albumin levels, elongated activated partial thromboplastin time (APTT), intensive care unit (ICU) admission, glucocorticoid usage, intravenous immunoglobulin (IVIG) and prolonged hospital stays. Cox regression identified predictors of 42‐day mortality, including ecchymosis at venipuncture sites, absence of ICU admission, elongated prothrombin time (PT), vasopressor and glucocorticoid use, non‐antifungals. Nomograms constructed on these predictors registered concordance indexes of 0.855 (95% CI: 0.826–0.884) and 0.778 (95% CI: 0.702–0.854) for SAPA onset and 42‐day mortality, respectively. Lower survival rates for SAPA patients treated with glucocorticoids (p < 0.001) and improved 14‐day survival with antifungal therapy (p = 0.036). Improving IPA management in SFTS‐endemic areas is crucial, with effective predictive tool.

Publisher

Wiley

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