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Cell reports. Medicine · 2022

Development and validation of SCOPE score: A clinical score to predict COVID-19 pneumonia progression to severe respiratory failure.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
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Giamarellos-Bourboulis Evangelos J, Poulakou Garyfallia, de Nooijer Aline, Milionis Haralampos, Metallidis Simeon, Ploumidis Michalis, Grigoropoulou Pinelopi, Rapti Aggeliki, Segala Francesco Vladimiro, Balis Evangelos, Giannitsioti Efthymia, Rodari Paola, Kainis Ilias, Alexiou Zoi, Focà Emanuele, Lucio Brollo, Rovina Nikoletta, Scorzolini Laura, Dafni Maria, Ioannou Sofia, Tomelleri Alessandro, Dimakou Katerina, Tzatzagou Glykeria, Chini Maria, Bassetti Matteo, Trakatelli Christina, Tsoukalas George, Selmi Carlo, Samaras Charilaos, Saridaki Maria, Pyrpasopoulou Athina, Kaldara Elisabeth, Papanikolaou Ilias, Argyraki Aikaterini, Akinosoglou Karolina, Koupetori Marina, Panagopoulos Periklis, Dalekos George N, Netea Mihai G

Аннотация

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.

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