Wirth Adriana, Goetschi Andrea, Held Ulrike, Sendoel Ataman, Stuessi-Helbling Melina, Huber Lars Christian
Clinic for Internal Medicine, Department of Internal Medicine, City Hospital Zurich, Triemli, 8063 Zurich, Switzerland.
Department of Biostatistics, Epidemiology, Biostatistics and Prevention Institute, University of Zurich, 8001 Zurich, Switzerland.
Diagnostics (Basel). 2022 May 3;12(5):1129. doi: 10.3390/diagnostics12051129.
Prognostic models to predict the deterioration and mortality risk in COVID-19 patients are utterly needed to assist in informed decision making. Most of these models, however, are at high risk of bias, model overfitting, and unclear reporting. Here, we aimed to externally validate the modified (urea was omitted) 4C Deterioration Model and 4C Mortality Score in a cohort of Swiss COVID-19 patients and, second, to evaluate whether the inclusion of the neutrophil-to-lymphocyte ratio (NLR) improves the predictive performance of the models. We conducted a retrospective single-centre study with adult patients hospitalized with COVID-19. Both prediction models were updated by including the NLR. Model performance was assessed via the models' discriminatory performance (area under the curve, AUC), calibration (intercept and slope), and their performance overall (Brier score). For the validation of the 4C Deterioration Model and Mortality Score, 546 and 527 patients were included, respectively. In total, 133 (24.4%) patients met the definition of in-hospital deterioration. Discrimination of the 4C Deterioration Model was AUC = 0.78 (95% CI 0.73-0.82). A total of 55 (10.44%) patients died in hospital. Discrimination of the 4C Mortality Score was AUC = 0.85 (95% CI 0.79-0.89). There was no evidence for an incremental value of the NLR. Our data confirm the role of the modified 4C Deterioration Model and Mortality Score as reliable prediction tools for the risk of deterioration and mortality. There was no evidence that the inclusion of NLR improved model performance.
迫切需要能够预测新冠病毒疾病(COVID-19)患者病情恶化和死亡风险的预后模型,以帮助做出明智的决策。然而,这些模型大多存在高偏倚风险、模型过度拟合以及报告不清晰的问题。在此,我们旨在对一组瑞士COVID-19患者进行外部验证改良版(省略尿素)4C病情恶化模型和4C死亡评分,其次,评估纳入中性粒细胞与淋巴细胞比值(NLR)是否能提高模型的预测性能。我们对因COVID-19住院的成年患者进行了一项回顾性单中心研究。通过纳入NLR对两个预测模型进行了更新。通过模型的区分性能(曲线下面积,AUC)、校准(截距和斜率)及其整体性能(Brier评分)来评估模型性能。为了验证4C病情恶化模型和死亡评分,分别纳入了546例和527例患者。总共133例(24.4%)患者符合院内病情恶化的定义。4C病情恶化模型的区分度为AUC = 0.78(95%可信区间0.73 - 0.82)。共有55例(10.44%)患者在医院死亡。4C死亡评分的区分度为AUC = 0.85(95%可信区间0.79 - 0.89)。没有证据表明NLR具有增量价值。我们的数据证实了改良版4C病情恶化模型和死亡评分作为病情恶化和死亡风险可靠预测工具的作用。没有证据表明纳入NLR能改善模型性能。