Prognostic value of bedside lung ultrasound score in patients with COVID-19

被引:74
|
作者
Ji, Li [1 ,2 ]
Cao, Chunyan [1 ,2 ]
Gao, Ying [1 ,2 ]
Zhang, Wen [1 ,2 ]
Xie, Yuji [1 ,2 ]
Duan, Yilian [1 ,2 ]
Kong, Shuangshuang [1 ,2 ]
You, Manjie [1 ,2 ]
Ma, Rong [1 ,2 ]
Jiang, Lili [1 ,2 ]
Liu, Jie [1 ,2 ]
Sun, Zhenxing [1 ,2 ]
Zhang, Ziming [1 ,2 ]
Wang, Jing [1 ,2 ]
Yang, Yali [1 ,2 ]
Lv, Qing [1 ,2 ]
Zhang, Li [1 ,2 ]
Li, Yuman [1 ,2 ]
Zhang, Jinxiang [3 ]
Xie, Mingxing [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Ultrasound, 1277 Jiefang Ave, Wuhan 430022, Peoples R China
[2] Hubei Prov Key Lab Mol Imaging, 1277 Jiefang Ave, Wuhan 430022, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Emergency Surg, 1277 Jiefang Ave, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
COVID-19; Lung ultrasound; LUS score; Acute respiratory distress syndrome (ARDS); Prognosis; PULMONARY CONGESTION; HEART-FAILURE; DISEASE;
D O I
10.1186/s13054-020-03416-1
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Bedside lung ultrasound (LUS) has emerged as a useful and non-invasive tool to detect lung involvement and monitor changes in patients with coronavirus disease 2019 (COVID-19). However, the clinical significance of the LUS score in patients with COVID-19 remains unknown. We aimed to investigate the prognostic value of the LUS score in patients with COVID-19. Method: The LUS protocol consisted of 12 scanning zones and was performed in 280 consecutive patients with COVID-19. The LUS score based on B-lines, lung consolidation and pleural line abnormalities was evaluated. Results: The median time from admission to LUS examinations was 7 days (interquartile range [IQR] 3-10). Patients in the highest LUS score group were more likely to have a lower lymphocyte percentage (LYM%); higher levels of D-dimer, C-reactive protein, hypersensitive troponin I and creatine kinase muscle-brain; more invasive mechanical ventilation therapy; higher incidence of ARDS; and higher mortality than patients in the lowest LUS score group. After a median follow-up of 14 days [IQR, 10-20 days], 37 patients developed ARDS, and 13 died. Patients with adverse outcomes presented a higher rate of bilateral involvement; more involved zones and B-lines, pleural line abnormalities and consolidation; and a higher LUS score than event-free survivors. The Cox models adding the LUS score as a continuous variable (hazard ratio [HR]: 1.05, 95% confidence intervals [CI] 1.02 similar to 1.08; P < 0.001; Akaike information criterion [AIC] = 272; C-index = 0.903) or as a categorical variable (HR 10.76, 95% CI 2.75 similar to 42.05; P = 0.001; AIC = 272; C-index = 0.902) were found to predict poor outcomes more accurately than the basic model (AIC = 286; C-index = 0.866). An LUS score cut-off > 12 predicted adverse outcomes with a specificity and sensitivity of 90.5% and 91.9%, respectively. Conclusions: The LUS score devised by our group performs well at predicting adverse outcomes in patients with COVID-19 and is important for risk stratification in COVID-19 patients.
引用
收藏
页数:12
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