Department of Clinical Laboratory, Taizhou Hospital, Wenzhou Medical University, Linhai, P.R. China.
Department of Clinical Laboratory, Taizhou Hospital, Wenzhou Medical University, Linhai 317000, P.R. China, Phone: +86 576 85120120.
Clin Chem Lab Med. 2020 Jun 25;58(7):1106-1115. doi: 10.1515/cclm-2020-0377.
Objectives In December 2019, there was an outbreak of coronavirus disease 2019 (COVID-19) in Wuhan, China, and since then, the disease has been increasingly spread throughout the world. Unfortunately, the information about early prediction factors for disease progression is relatively limited. Therefore, there is an urgent need to investigate the risk factors of developing severe disease. The objective of the study was to reveal the risk factors of developing severe disease by comparing the differences in the hemocyte count and dynamic profiles in patients with severe and non-severe COVID-19. Methods In this retrospectively analyzed cohort, 141 confirmed COVID-19 patients were enrolled in Taizhou Public Health Medical Center, Taizhou Hospital, Zhejiang Province, China, from January 17, 2020 to February 26, 2020. Clinical characteristics and hemocyte counts of severe and non-severe COVID patients were collected. The differences in the hemocyte counts and dynamic profiles in patients with severe and non-severe COVID-19 were compared. Multivariate Cox regression analysis was performed to identify potential biomarkers for predicting disease progression. A concordance index (C-index), calibration curve, decision curve and the clinical impact curve were calculated to assess the predictive accuracy. Results The data showed that the white blood cell count, neutrophil count and platelet count were normal on the day of hospital admission in most COVID-19 patients (87.9%, 85.1% and 88.7%, respectively). A total of 82.8% of severe patients had lymphopenia after the onset of symptoms, and as the disease progressed, there was marked lymphopenia. Multivariate Cox analysis showed that the neutrophil count (hazard ratio [HR] = 4.441, 95% CI = 1.954-10.090, p = 0.000), lymphocyte count (HR = 0.255, 95% CI = 0.097-0.669, p = 0.006) and platelet count (HR = 0.244, 95% CI = 0.111-0.537, p = 0.000) were independent risk factors for disease progression. The C-index (0.821 [95% CI, 0.746-0.896]), calibration curve, decision curve and the clinical impact curve showed that the nomogram can be used to predict the disease progression in COVID-19 patients accurately. In addition, the data involving the neutrophil count, lymphocyte count and platelet count (NLP score) have something to do with improving risk stratification and management of COVID-19 patients. Conclusions We designed a clinically predictive tool which is easy to use for assessing the progression risk of COVID-19, and the NLP score could be used to facilitate patient stratification management.
目的 2019 年 12 月,中国武汉爆发了 2019 年冠状病毒病(COVID-19),此后,该疾病在世界范围内的传播日益广泛。不幸的是,关于疾病进展早期预测因素的信息相对有限。因此,迫切需要调查发生严重疾病的危险因素。本研究的目的是通过比较严重和非严重 COVID-19 患者的血细胞计数和动态谱差异,揭示发生严重疾病的危险因素。
方法 本回顾性队列研究纳入了 2020 年 1 月 17 日至 2 月 26 日期间来自中国浙江省台州公共卫生医学中心台州医院的 141 例确诊的 COVID-19 患者。收集了严重和非严重 COVID 患者的临床特征和血细胞计数。比较了严重和非严重 COVID-19 患者的血细胞计数和动态谱差异。采用多变量 Cox 回归分析确定预测疾病进展的潜在生物标志物。计算一致性指数(C 指数)、校准曲线、决策曲线和临床影响曲线,以评估预测准确性。
结果 数据显示,大多数 COVID-19 患者(分别为 87.9%、85.1%和 88.7%)在入院当天的白细胞计数、中性粒细胞计数和血小板计数正常。82.8%的严重患者在症状发作后出现淋巴细胞减少,随着疾病的进展,淋巴细胞减少明显。多变量 Cox 分析显示,中性粒细胞计数(危险比[HR] = 4.441,95%CI = 1.954-10.090,p = 0.000)、淋巴细胞计数(HR = 0.255,95%CI = 0.097-0.669,p = 0.006)和血小板计数(HR = 0.244,95%CI = 0.111-0.537,p = 0.000)是疾病进展的独立危险因素。C 指数(0.821[95%CI,0.746-0.896])、校准曲线、决策曲线和临床影响曲线表明,该列线图可准确预测 COVID-19 患者的疾病进展。此外,涉及中性粒细胞计数、淋巴细胞计数和血小板计数(NLP 评分)的信息与改善 COVID-19 患者的风险分层和管理有关。
结论 我们设计了一种临床预测工具,用于评估 COVID-19 的进展风险,使用方便,NLP 评分可用于促进患者分层管理。