Author: Tang, Fang; Zhang, Xiaoshuai; Zhang, Bicheng; Zhu, Bo; Wang, Jun
Title: A nomogram prediction of outcome in patients with COVIDâ€19 based on individual characteristics incorporating immune responseâ€related indicators Cord-id: wwdc8d3g Document date: 2021_8_27
ID: wwdc8d3g
Snippet: INTRODUCTION: The coronavirus disease 2019 (COVIDâ€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 20â€day median followâ€up time. We first developed a nomogram for disease severity discrimination, then created a prognostic nomogram for severe
Document: INTRODUCTION: The coronavirus disease 2019 (COVIDâ€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 20â€day median followâ€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 nonâ€severe. The multivariate logistic analysis indicated that IgG, neutrophilâ€toâ€lymphocyte ratio (NLR), lactate dehydrogenase, platelet, albumin, and blood urea nitrogen were significant factors associated with the severity of COVIDâ€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 Câ€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 COVIDâ€19 patients with disease progression based on individual characteristics and immune responseâ€related indicators. Patients at high risk for severe illness and poor outcomes from COVIDâ€19 should be managed with intensive supportive care and appropriate therapeutic strategies.
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