Zhou Jiandong, Lee Sharen, Wang Xiansong, Li Yi, Wu William Ka Kei, Liu Tong, Cao Zhidong, Zeng Daniel Dajun, Leung Keith Sai Kit, Wai Abraham Ka Chung, Wong Ian Chi Kei, Cheung Bernard Man Yung, Zhang Qingpeng, Tse Gary
School of Data Science, City University of Hong Kong, Hong Kong, China.
Cardiovascular Analytics Group, Laboratory of Cardiovascular Physiology, Hong Kong, China.
NPJ Digit Med. 2021 Apr 8;4(1):66. doi: 10.1038/s41746-021-00433-4.
Recent studies have reported numerous predictors for adverse outcomes in COVID-19 disease. However, there have been few simple clinical risk scores available for prompt risk stratification. The objective is to develop a simple risk score for predicting severe COVID-19 disease using territory-wide data based on simple clinical and laboratory variables. Consecutive patients admitted to Hong Kong's public hospitals between 1 January and 22 August 2020 and diagnosed with COVID-19, as confirmed by RT-PCR, were included. The primary outcome was composite intensive care unit admission, need for intubation or death with follow-up until 8 September 2020. An external independent cohort from Wuhan was used for model validation. COVID-19 testing was performed in 237,493 patients and 4442 patients (median age 44.8 years old, 95% confidence interval (CI): [28.9, 60.8]); 50% males) were tested positive. Of these, 209 patients (4.8%) met the primary outcome. A risk score including the following components was derived from Cox regression: gender, age, diabetes mellitus, hypertension, atrial fibrillation, heart failure, ischemic heart disease, peripheral vascular disease, stroke, dementia, liver diseases, gastrointestinal bleeding, cancer, increases in neutrophil count, potassium, urea, creatinine, aspartate transaminase, alanine transaminase, bilirubin, D-dimer, high sensitive troponin-I, lactate dehydrogenase, activated partial thromboplastin time, prothrombin time, and C-reactive protein, as well as decreases in lymphocyte count, platelet, hematocrit, albumin, sodium, low-density lipoprotein, high-density lipoprotein, cholesterol, glucose, and base excess. The model based on test results taken on the day of admission demonstrated an excellent predictive value. Incorporation of test results on successive time points did not further improve risk prediction. The derived score system was evaluated with out-of-sample five-cross-validation (AUC: 0.86, 95% CI: 0.82-0.91) and external validation (N = 202, AUC: 0.89, 95% CI: 0.85-0.93). A simple clinical score accurately predicted severe COVID-19 disease, even without including symptoms, blood pressure or oxygen status on presentation, or chest radiograph results.
近期研究报告了众多可预测新冠病毒疾病不良结局的因素。然而,几乎没有可用于快速进行风险分层的简单临床风险评分。目的是基于简单的临床和实验室变量,利用全港数据开发一个用于预测重症新冠病毒疾病的简单风险评分。纳入了2020年1月1日至8月22日期间入住香港公立医院且经逆转录聚合酶链反应(RT-PCR)确诊为新冠病毒疾病的连续患者。主要结局是综合重症监护病房入住、插管需求或死亡,随访至2020年9月8日。使用来自武汉的外部独立队列进行模型验证。对237493名患者进行了新冠病毒检测,其中4442名患者(中位年龄44.8岁,95%置信区间(CI):[28.9, 60.8];50%为男性)检测呈阳性。其中,209名患者(4.8%)达到主要结局。通过Cox回归得出了一个包含以下因素的风险评分:性别、年龄、糖尿病、高血压、心房颤动、心力衰竭、缺血性心脏病、外周血管疾病、中风、痴呆、肝脏疾病、胃肠道出血、癌症、中性粒细胞计数、钾、尿素、肌酐、天冬氨酸转氨酶、丙氨酸转氨酶、胆红素、D-二聚体、高敏肌钙蛋白I、乳酸脱氢酶、活化部分凝血活酶时间、凝血酶原时间和C反应蛋白的升高,以及淋巴细胞计数、血小板、血细胞比容、白蛋白、钠、低密度脂蛋白、高密度脂蛋白、胆固醇、葡萄糖和碱剩余的降低。基于入院当天检测结果的模型显示出优异的预测价值。纳入连续时间点的检测结果并未进一步改善风险预测。通过样本外五重交叉验证(曲线下面积(AUC):0.86,95%CI:0.82 - 0.91)和外部验证(N = 202,AUC:0.89,95%CI:0.85 - 0.93)对得出的评分系统进行了评估。一个简单的临床评分能够准确预测重症新冠病毒疾病,即使不包括就诊时的症状、血压或氧状态,或胸部X光片结果。