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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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