Fourth Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, ATTIKON University General Hospital, 1 Rimini Street, 124 62 Athens, Greece.
Hellenic Institute for the Study of Sepsis, Athens, Greece.
Cell Rep Med. 2022 Feb 25;3(3):100560. doi: 10.1016/j.xcrm.2022.100560. eCollection 2022 Mar 15.
Most patients infected with SARS-CoV-2 (COVID-19) experience mild, non-specific symptoms, but many develop severe symptoms associated with an excessive inflammatory response. Elevated plasma concentrations of soluble urokinase plasminogen activator receptor (suPAR) provide early warning of progression to severe respiratory failure (SRF) or death, but access to suPAR testing may be limited. The Severe COvid Prediction Estimate (SCOPE) score, derived from circulating concentrations of C-reactive protein, D- dimers, interleukin-6, and ferritin among patients not receiving non-invasive or invasive mechanical ventilation during the SAVE-MORE study, offers predictive accuracy for progression to SRF or death within 14 days comparable to that of a suPAR concentration of ≥6 ng/mL (area under receiver operator characteristic curve 0.81 for both). The SCOPE score is validated in two similar independent cohorts. A SCOPE score of 6 or more is an alternative to suPAR for predicting progression to SRF or death within 14 days of hospital admission for pneumonia, and it can be used to guide treatment decisions.
大多数感染 SARS-CoV-2(COVID-19)的患者出现轻度、非特异性症状,但许多患者出现严重症状,伴有过度炎症反应。血浆中可溶性尿激酶型纤溶酶原激活物受体(suPAR)浓度升高可早期预警向严重呼吸衰竭(SRF)或死亡进展,但 suPAR 检测的可及性可能有限。在 SAVE-MORE 研究中,未接受无创或有创机械通气的患者循环中 C 反应蛋白、D-二聚体、白细胞介素-6 和铁蛋白浓度推导的严重 COVID 预测估计(SCOPE)评分,对 14 天内进展为 SRF 或死亡的预测准确性与 suPAR 浓度≥6ng/mL 相当(两者的受试者工作特征曲线下面积均为 0.81)。SCOPE 评分在两个类似的独立队列中得到验证。SCOPE 评分≥6 分可替代 suPAR 预测肺炎住院后 14 天内向 SRF 或死亡进展,可用于指导治疗决策。