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

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 71...

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Detalles Bibliográficos
Autores principales: Jin, Meng, Lu, Zequn, Zhang, Xu, Wang, Yanan, Wang, Jing, Cai, Yimin, Tian, Kunming, Xiong, Zezhong, Zhong, Qiang, Ran, Xiao, Yang, Chunguang, Zeng, Xing, Wang, Lu, Li, Yao, Zhang, Shanshan, Dong, Tianyi, Yue, Xinying, Li, Heng, Liu, Bo, Chen, Xin, Cui, Hongyuan, Qi, Jirong, Fan, Haining, Li, Haixia, Yang, Xiang-Ping, Hu, Zhiquan, Wang, Shaogang, Xiao, Jun, Wang, Ying, Tian, Jianbo, Wang, Zhihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439538/
https://www.ncbi.nlm.nih.gov/pubmed/34521370
http://dx.doi.org/10.1186/s12879-021-06585-8
Descripción
Sumario: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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06585-8.