Accurate risk stratification in COVID-19 patients consists a major clinical need to guide therapeutic strategies. We sought to evaluate the prognostic role of estimated pulse wave velocity (ePWV), a marker of arterial stiffness which reflects overall arterial integrity and aging, in risk stratification of hospitalized patients with COVID-19. This retrospective, longitudinal cohort study, analyzed a total population of 1671 subjects consisting of 737 hospitalized COVID-19 patients consecutively recruited from two tertiary centers (Newcastle cohort: n = 471 and Pisa cohort: n = 266) and a non-COVID control cohort (n = 934). Arterial stiffness was calculated using validated formulae for ePWV. ePWV progressively increased across the control group, COVID-19 survivors and deceased patients (adjusted mean increase per group 1.89 m/s, P < 0.001). Using a machine learning approach, ePWV provided incremental prognostic value and improved reclassification for mortality over the core model including age, sex and comorbidities [AUC (core model + ePWV vs. core model) = 0.864 vs. 0.755]. ePWV provided similar prognostic value when pulse pressure or hs-Troponin were added to the core model or over its components including age and mean blood pressure (p < 0.05 for all). The optimal prognostic ePWV value was 13.0 m/s. ePWV conferred additive discrimination (AUC: 0.817 versus 0.779, P < 0.001) and reclassification value (NRI = 0.381, P < 0.001) over the 4C Mortality score, a validated score for predicting mortality in COVID-19 and the Charlson comorbidity index. We suggest that calculation of ePWV, a readily applicable estimation of arterial stiffness, may serve as an additional clinical tool to refine risk stratification of hospitalized patients with COVID-19 beyond established risk factors and scores.

Estimated pulse wave velocity improves risk stratification for all-cause mortality in patients with COVID-19

Tiseo G.;Barbieri G.;Masi S.;Mengozzi A.;Ghiadoni L.;Falcone M.;Tiseo G.;Mengozzi A.;Ghiadoni L.;Monzani F.;Menichetti F.;Virdis A.;Forfori F.;Paolo M.;Alessandro C.;Carrozzi L.;Santini M.;Alessandro C.;Martina B.;Antognoli R.;Calsolaro V.;Simone P.;
2021-01-01

Abstract

Accurate risk stratification in COVID-19 patients consists a major clinical need to guide therapeutic strategies. We sought to evaluate the prognostic role of estimated pulse wave velocity (ePWV), a marker of arterial stiffness which reflects overall arterial integrity and aging, in risk stratification of hospitalized patients with COVID-19. This retrospective, longitudinal cohort study, analyzed a total population of 1671 subjects consisting of 737 hospitalized COVID-19 patients consecutively recruited from two tertiary centers (Newcastle cohort: n = 471 and Pisa cohort: n = 266) and a non-COVID control cohort (n = 934). Arterial stiffness was calculated using validated formulae for ePWV. ePWV progressively increased across the control group, COVID-19 survivors and deceased patients (adjusted mean increase per group 1.89 m/s, P < 0.001). Using a machine learning approach, ePWV provided incremental prognostic value and improved reclassification for mortality over the core model including age, sex and comorbidities [AUC (core model + ePWV vs. core model) = 0.864 vs. 0.755]. ePWV provided similar prognostic value when pulse pressure or hs-Troponin were added to the core model or over its components including age and mean blood pressure (p < 0.05 for all). The optimal prognostic ePWV value was 13.0 m/s. ePWV conferred additive discrimination (AUC: 0.817 versus 0.779, P < 0.001) and reclassification value (NRI = 0.381, P < 0.001) over the 4C Mortality score, a validated score for predicting mortality in COVID-19 and the Charlson comorbidity index. We suggest that calculation of ePWV, a readily applicable estimation of arterial stiffness, may serve as an additional clinical tool to refine risk stratification of hospitalized patients with COVID-19 beyond established risk factors and scores.
2021
Stamatelopoulos, K.; Georgiopoulos, G.; Baker, K. F.; Tiseo, G.; Delialis, D.; Lazaridis, C.; Barbieri, G.; Masi, S.; Vlachogiannis, N. I.; Sopova, K.; Mengozzi, A.; Ghiadoni, L.; van der Loeff, I. S.; Hanrath, A. T.; Ajdini, B.; Vlachopoulos, C.; Dimopoulos, M. A.; Duncan, C. J. A.; Falcone, M.; Stellos, K.; Tiseo, G.; Barbieri, G.; Masi, S.; Mengozzi, A.; Ghiadoni, L.; Falcone, M.; Monzani, F.; Menichetti, F.; Virdis, A.; Forfori, F.; Rubia, B.; Pietro, B.; Giulia, B.; Francesco, C.; Alessandra, D. R.; Fabio, G.; Paolo, M.; Marco, M.; Chiara, P.; Naria, P.; Alessandro, C.; Carrozzi, L.; Francesco, C.; Santini, M.; Alessandro, C.; Martina, B.; Matteo, B.; Elia, N.; Stefano, S.; Francesca, R.; Giovanna, F.; Maria, S.; De Marco, S.; Antognoli, R.; Calsolaro, V.; Simone, P.; Luciano, C.; Chiara, S.; Valentina, G.; Uliana, M.; Baker, K. F.; van der Loeff, I. S.; Hanrath, A. T.; Duncan, C. J. A.; Tee, S. A.; Capstick, R.; Marchitelli, G.; Li, A.; Barr, A.; Eid, A.; Ahmed, S.; Bajwa, D.; Mohammed, O.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1121224
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