Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/128823
Título: Predicting sudden cardiac death in adults with congenital heart disease
Autores/as: Oliver, JM
Gallego, P
Gonzalez, AE
Avila, P
Castro Alonso, Ayoze 
Garcia-Hamilton, D
Peinado, R
Dos-Subirà, L
Pijuan-Domenech, A
Rueda, J
Rodriguez-Puras, MJ
Garcia-Orta, R
Martínez Quintana, Efrén 
Datino, T
Fernandez-Aviles, F
Bermejo, J
Clasificación UNESCO: 32 Ciencias médicas
320501 Cardiología
Palabras clave: Cardiac arrest
Congenital heart disease
Study design
Sudden cardiac death
Ventricular tachycardia
Fecha de publicación: 2021
Publicación seriada: Heart 
Resumen: Objectives To develop, calibrate, test and validate a logistic regression model for accurate risk prediction of sudden cardiac death (SCD) and non-fatal sudden cardiac arrest (SCA) in adults with congenital heart disease (ACHD), based on baseline lesion-specific risk stratification and individual's characteristics, to guide primary prevention strategies. Methods We combined data from a single-centre cohort of 3311 consecutive ACHD patients (50% male) at 25-year follow-up with 71 events (53 SCD and 18 non-fatal SCA) and a multicentre case-control group with 207 cases (110 SCD and 97 non-fatal SCA) and 2287 consecutive controls (50% males). Cumulative incidences of events up to 20 years for specific lesions were determined in the prospective cohort. Risk model and its 5-year risk predictions were derived by logistic regression modelling, using separate development (18 centres: 144 cases and 1501 controls) and validation (two centres: 63 cases and 786 controls) datasets. Results According to the combined SCD/SCA cumulative 20 years incidence, a lesion-specific stratification into four clusters - very-low (<1%), low (1%-4%), moderate (4%-12%) and high (>12%) - was built. Multivariable predictors were lesion-specific cluster, young age, male sex, unexplained syncope, ischaemic heart disease, non-life threatening ventricular arrhythmias, QRS duration and ventricular systolic dysfunction or hypertrophy. The model very accurately discriminated (C-index 0.91; 95% CI 0.88 to 0.94) and calibrated (p=0.3 for observed vs expected proportions) in the validation dataset. Compared with current guidelines approach, sensitivity increases 29% with less than 1% change in specificity. Conclusions Predicting the risk of SCD/SCA in ACHD can be significantly improved using a baseline lesion-specific stratification and simple clinical variables.
URI: http://hdl.handle.net/10553/128823
ISSN: 1355-6037
DOI: 10.1136/heartjnl-2020-316791
Fuente: Heart [1355-6037], v. 107(1), p. 67-75 (Enero 2021)
Colección:Artículos
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