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Sudden Cardiac Death in Dilated Cardiomyopathies
Author(s) -
HAMILTON ROBERT M.,
AZEVEDO EDUARDO R.
Publication year - 2009
Publication title -
pacing and clinical electrophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.686
H-Index - 101
eISSN - 1540-8159
pISSN - 0147-8389
DOI - 10.1111/j.1540-8159.2009.02382.x
Subject(s) - medicine , dilated cardiomyopathy , sudden cardiac death , cardiology , etiology , cardiomyopathy , implantable cardioverter defibrillator , bridge to transplantation , sudden death , heart transplantation , heart failure , transplantation
Dilated cardiomyopathy (DCM) is the most prevalent form of cardiomyopathy, and sudden cardiac death (SCD) remains a common event in young patients. The disorder is highly heterogeneous and pediatric DCM often differs from adult DCM in etiologies, risk factors, and prognosis. Prognosis may be improving, likely secondary to specialized management. Both traditional and novel markers of risk have been studied in adults and are beginning to be applied to children with DCM. The major therapy for patients considered at risk remains implantable cardioverter‐defibrillator ( ICD) placement, although frequently this functions as a bridge to eventual transplantation.