Author: Linssen, Joachim; Ermens, Anthony; Berrevoets, Marvin; Seghezzi, Michela; Previtali, Giulia; van der Sar-van der Brugge, Simone; Russcher, Henk; Verbon, Annelies; Gillis, Judith; Riedl, Jürgen; de Jongh, Eva; Saker, Jarob; Münster, Marion; Munnix, Imke CA; Dofferhof, Anthonius; Scharnhorst, Volkher; Ammerlaan, Heidi; Deiteren, Kathleen; Bakker, Stephan JL; Van Pelt, Lucas Joost; Kluiters-de Hingh, Yvette; Leers, Mathie PG; van der Ven, Andre J
Title: A novel haemocytometric COVID-19 prognostic score developed and validated in an observational multicentre European hospital-based study Cord-id: o90xvg4n Document date: 2020_11_26
ID: o90xvg4n
Snippet: COVID-19 induces haemocytometric changes. Complete blood count changes, including new cell activation parameters, from 982 confirmed COVID-19 adult patients from 11 European hospitals were retrospectively analysed for distinctive patterns based on age, gender, clinical severity, symptom duration, and hospital days. The observed haemocytometric patterns formed the basis to develop a multi-haemocytometric-parameter prognostic score to predict, during the first three days after presentation, which
Document: COVID-19 induces haemocytometric changes. Complete blood count changes, including new cell activation parameters, from 982 confirmed COVID-19 adult patients from 11 European hospitals were retrospectively analysed for distinctive patterns based on age, gender, clinical severity, symptom duration, and hospital days. The observed haemocytometric patterns formed the basis to develop a multi-haemocytometric-parameter prognostic score to predict, during the first three days after presentation, which patients will recover without ventilation or deteriorate within a two-week timeframe, needing intensive care or with fatal outcome. The prognostic score, with ROC curve AUC at baseline of 0.753 (95% CI 0.723–0.781) increasing to 0.875 (95% CI 0.806–0.926) on day 3, was superior to any individual parameter at distinguishing between clinical severity. Findings were confirmed in a validation cohort. Aim is that the score and haemocytometry results are simultaneously provided by analyser software, enabling wide applicability of the score as haemocytometry is commonly requested in COVID-19 patients.
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