Clinical characteristics and risk factors of fatal patients with COVID-19: a retrospective cohort study in Wuhan, China

Meng Jin(Wuhan University), Zequn Lu(Huazhong University of Science and Technology), Xu Zhang(Ministry of Ecology and Environment), Yanan Wang(Tongji Hospital), Jing Wang(Tongji Hospital), Yimin Cai(Huazhong University of Science and Technology), Kunming Tian(Huazhong University of Science and Technology), Zezhong Xiong(Tongji Hospital), Qiang Zhong(Tongji Hospital), Xiao Ran(Tongji Hospital), Chunguang Yang(Tongji Hospital), Xing Zeng(Tongji Hospital), Lu Wang(Huazhong University of Science and Technology), Yao Li(Huazhong University of Science and Technology), Shanshan Zhang(Huazhong University of Science and Technology), Tianyi Dong(Huazhong University of Science and Technology), Xinying Yue(Huazhong University of Science and Technology), Heng Li(Tongji Hospital), Bo Liu(Tongji Hospital), Xin Chen(Tongji Hospital), Hongyuan Cui(Chinese Academy of Medical Sciences & Peking Union Medical College), Jirong Qi(Nanjing Children's Hospital), Haining Fan(Qinghai University Affiliated Hospital), Haixia Li(Tongji Hospital), Xiang‐Ping Yang(Huazhong University of Science and Technology), Zhiquan Hu(Tongji Hospital), Shaogang Wang(Tongji Hospital), Jun Xiao(Tongji Hospital), Ying Wang(Tongji Hospital), Jianbo Tian(Wuhan University), Zhihua Wang(Tongji Hospital)
BMC Infectious Diseases
September 14, 2021
Cited by 43Open Access
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Abstract

BACKGROUND: The coronavirus disease 2019 (COVID-19) has caused a global pandemic, resulting in considerable mortality. The risk factors, clinical treatments, especially comprehensive risk models for COVID-19 death are urgently warranted. METHODS: In this retrospective study, 281 non-survivors and 712 survivors with propensity score matching by age, sex, and comorbidities were enrolled from January 13, 2020 to March 31, 2020. RESULTS: Higher SOFA, qSOFA, APACHE II and SIRS scores, hypoxia, elevated inflammatory cytokines, multi-organ dysfunction, decreased immune cell subsets, and complications were significantly associated with the higher COVID-19 death risk. In addition to traditional predictors for death risk, including APACHE II (AUC = 0.83), SIRS (AUC = 0.75), SOFA (AUC = 0.70) and qSOFA scores (AUC = 0.61), another four prediction models that included immune cells subsets (AUC = 0.90), multiple organ damage biomarkers (AUC = 0.89), complications (AUC = 0.88) and inflammatory-related indexes (AUC = 0.75) were established. Additionally, the predictive accuracy of combining these risk factors (AUC = 0.950) was also significantly higher than that of each risk group alone, which was significant for early clinical management for COVID-19. CONCLUSIONS: The potential risk factors could help to predict the clinical prognosis of COVID-19 patients at an early stage. The combined model might be more suitable for the death risk evaluation of COVID-19.


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