A nomogram prediction of outcome in patients with COVID‐19 based on individual characteristics incorporating immune response‐related indicators. Issue 1 (27th August 2021)

• Record Type: Journal Article
• Authors: Tang, Fang; Zhang, Xiaoshuai; Zhang, Bicheng; Zhu, Bo; Wang, Jun
• Other Names: Luo Guangxiang (George) guestEditor.; Ly Hinh guestEditor.; Gao Shou‐Jiang guestEditor.
• Is Part Of: Journal of medical virology. Volume 94:Issue 1(2022)
• Page Start: 131
• Page End: 140
• Publication Date: 2021-08-27
• Subjects: COVID‐19 -- IgG -- neutrophil‐to‐lymphocyte ratio -- nomogram -- prediction; Virology -- Periodicals; 616
• DOI: 10.1002/jmv.27275
• Languages: English
• ISSNs: 0146-6615

Abstract

Abstract: Introduction: The coronavirus disease 2019 (COVID‐19) has quickly become a global threat to public health, and it is difficult to predict severe patients and their prognosis. Here, we intended developing effective models for the late identification of patients at disease progression and outcome. Methods: A total of 197 patients were included with a 20‐day median follow‐up time. We first developed a nomogram for disease severity discrimination, then created a prognostic nomogram for severe patients. Results: In total, 40.6% of patients were severe and 59.4% were non‐severe. The multivariate logistic analysis indicated that IgG, neutrophil‐to‐lymphocyte ratio (NLR), lactate dehydrogenase, platelet, albumin, and blood urea nitrogen were significant factors associated with the severity of COVID‐19. Using immune response phenotyping based on NLR and IgG level, the logistic model showed patients with the NLR hi IgG hi phenotype are most likely to have severe disease, especially compared to those with the NLR lo IgG lo phenotype. The C‐indices of the two discriminative nomograms were 0.86 and 0.87, respectively, which indicated sufficient discriminative power. As for predicting clinical outcomes for severe patients, IgG, NLR, age, lactate dehydrogenase, platelet, monocytes, and procalcitonin were significant predictors. The prognosis of severe patients with the NLR hi IgG hi phenotype was significantly worse than the NLR lo IgG hi group. The two prognostic nomograms also showed good performance in estimating the risk of progression. Conclusions: The present nomogram models are useful to identify COVID‐19 patients with disease progression based on individual characteristics and immune response‐related indicators. Patients at high risk for severe illness and poor outcomes from COVID‐19 should be managed with intensive supportive care and appropriate therapeutic strategies.