Sudden cardiac death (SCD) is the most common mode of death in childhood hypertrophic cardiomyopathy (HCM). The newly developed HCM Risk-Kids model provides clinicians with individualized estimates of risk. The aim of this study was to externally validate the model in a large independent, multi-centre patient cohort.

External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy / Norrish, Gabrielle; Qu, Chen; Field, Ella; Cervi, Elena; Khraiche, Diala; Klaassen, Sabine; Ojala, Tiina H; Sinagra, Gianfranco; Yamazawa, Hirokuni; Marrone, Chiara; Popoiu, Anca; Centeno, Fernando; Schouvey, Sylvie; Olivotto, Iacopo; Day, Sharlene M; Colan, Steve; Rossano, Joseph; Wittekind, Samuel G; Saberi, Sara; Russell, Mark; Helms, Adam; Ingles, Jodie; Semsarian, Christopher; Elliott, Perry M; Ho, Carolyn Y; Omar, Rumana Z; Kaski, Juan P. - In: EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY. - ISSN 2047-4873. - 29:4(2022), pp. 678-686. [10.1093/eurjpc/zwab181]

External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy

Sinagra, Gianfranco;
2022-01-01

Abstract

Sudden cardiac death (SCD) is the most common mode of death in childhood hypertrophic cardiomyopathy (HCM). The newly developed HCM Risk-Kids model provides clinicians with individualized estimates of risk. The aim of this study was to externally validate the model in a large independent, multi-centre patient cohort.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2998401
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