Research Group "Cancer, Haemostasis and Angiogenesis," INSERM U938, Centre de Recherche Saint-Antoine, Institut Universitaire de Cancérologie, Faculty of Medicine, Sorbonne University, Paris, France.
Service d'Hématologie Biologique Hôpital Tenon, Hôpitaux Universitaires de l'Est Parisien, Assistance Publique Hôpitaux de Paris, Faculté de Médecine Sorbonne Université, Paris, France.
Thromb Haemost. 2020 Dec;120(12):1680-1690. doi: 10.1055/s-0040-1716544. Epub 2020 Sep 22.
The prospective observational cohort study COMPASS-COVID-19 aimed to develop a risk assessment model for early identification of hospitalized COVID-19 patients at risk for worsening disease. Patients with confirmed COVID-19 ( = 430) hospitalized between March 18 and April 21, 2020 were divided in derivation ( = 310) and validation ( = 120) cohorts. Two groups became evident: (1) (G-group) with patients hospitalized at the conventional COVID-19 ward and (2) (W-group) with patients admitted to the intensive care unit (ICU) from the emergency departments. The study end point was disease worsening (acute respiratory failure, shock, myocardial dysfunction, bacterial or viral coinfections, and acute kidney injury) requiring ICU admission. All patients were routinely evaluated for full blood count, prothrombin time, fibrinogen, D-dimers, antithrombin (AT), and protein C activity. Data from the first hospitalization day at the conventional ward or the ICU were analyzed. Cardiovascular risk factors and comorbidities were routinely registered. Obesity, hypertension, diabetes and male gender, increased fibrinogen and D-dimers, thrombocytopenia, AT deficiency, lymphopenia, and an International Society on Thrombosis and Haemostasis (ISTH) score for compensated disseminated intravascular coagulation score (cDIC-ISTH) 5 were significant risk factors for worsening disease. The COMPASS-COVID-19 score was derived from multivariate analyses and includes obesity, gender, hemoglobin, lymphocyte, and the cDIC-ISTH score (including platelet count, prothrombin time, D-dimers, AT, and protein C levels). The score has a very good discriminating capacity to stratify patients at high and low risk for worsening disease, with an area under the receiver operating characteristic curve value of 0.77, a sensitivity of 81%, and a specificity of 60%. Application of the COMPASS-COVID-19 score at the validation cohort showed 96% sensitivity. The COMPASS-COVID-19 score is an accurate clinical decision-making tool for an easy identification of COVID-19 patients being at high risk for disease worsening.
前瞻性观察队列研究 COMPASS-COVID-19 旨在开发一种风险评估模型,以早期识别 COVID-19 住院患者病情恶化的风险。2020 年 3 月 18 日至 4 月 21 日期间住院的确诊 COVID-19 患者( = 430)分为推导队列( = 310)和验证队列( = 120)。两组患者明显不同:(1)(G 组)患者在常规 COVID-19 病房住院,(2)(W 组)患者从急诊病房转入重症监护病房(ICU)。研究终点是疾病恶化(急性呼吸衰竭、休克、心肌功能障碍、细菌或病毒合并感染和急性肾损伤)需要 ICU 住院治疗。所有患者均常规评估全血细胞计数、凝血酶原时间、纤维蛋白原、D-二聚体、抗凝血酶(AT)和蛋白 C 活性。分析常规病房或 ICU 住院的第 1 天的数据。常规登记心血管危险因素和合并症。肥胖、高血压、糖尿病和男性、纤维蛋白原和 D-二聚体增加、血小板减少、AT 缺乏、淋巴细胞减少以及国际血栓和止血学会(ISTH)用于代偿性弥散性血管内凝血评分(cDIC-ISTH)的评分 5 是疾病恶化的显著危险因素。COMPASS-COVID-19 评分源自多变量分析,包括肥胖、性别、血红蛋白、淋巴细胞和 cDIC-ISTH 评分(包括血小板计数、凝血酶原时间、D-二聚体、AT 和蛋白 C 水平)。该评分具有很好的区分能力,可以对高风险和低风险的患者进行分层,其受试者工作特征曲线下面积值为 0.77,灵敏度为 81%,特异性为 60%。在验证队列中应用 COMPASS-COVID-19 评分,敏感性为 96%。COMPASS-COVID-19 评分是一种准确的临床决策工具,可用于简单识别 COVID-19 患者病情恶化的高风险患者。