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

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  • BMC Infect Dis . characteristics and risk factors of fatal patients with COVID-19: a retrospective cohort study in Wuhan, China


    BMC Infect Dis


    . 2021 Sep 14;21(1):951.
    doi: 10.1186/s12879-021-06585-8.
    Clinical characteristics and risk factors of fatal patients with COVID-19: a retrospective cohort study in Wuhan, China


    Meng Jin # 1 , Zequn Lu # 2 , Xu Zhang # 3 , Yanan Wang # 4 , Jing Wang # 4 , Yimin Cai # 2 , Kunming Tian 5 , Zezhong Xiong 4 , Qiang Zhong 6 , Xiao Ran 6 , Chunguang Yang 4 , Xing Zeng 4 , Lu Wang 2 , Yao Li 2 , Shanshan Zhang 2 , Tianyi Dong 2 , Xinying Yue 2 , Heng Li 4 , Bo Liu 7 , Xin Chen 7 , Hongyuan Cui 8 , Jirong Qi 9 , Haining Fan 10 , Haixia Li 11 , Xiang-Ping Yang 12 , Zhiquan Hu 4 , Shaogang Wang 4 , Jun Xiao # 13 , Ying Wang # 14 , Jianbo Tian # 15 , Zhihua Wang # 16



    Affiliations

    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.

    Keywords: COVID-19; Death risk; Immune cells subsets; Risk prediction models.

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