Journal article
Long-term outcomes of dilated cardiomyopathy diagnosed during childhood: Results from a national population-based study of childhood cardiomyopathy
PMA Alexander, PEF Daubeney, AW Nugent, KJ Lee, C Turner, SD Colan, T Robertson, AM Davis, J Ramsay, R Justo, GF Sholler, I King, RG Weintraub
Circulation | LIPPINCOTT WILLIAMS & WILKINS | Published : 2013
Abstract
BACKGROUND - : Existing studies of childhood dilated cardiomyopathy deal mainly with early survival. This population-based study examines long-term outcomes for children with dilated cardiomyopathy. METHODS AND RESULTS - : The diagnosis of dilated cardiomyopathy was based on clinical, echocardiographic, and pathological findings. The primary study end point included time to the combined outcome of death or cardiac transplantation. There were 175 patients 0 to <10 years of age at the time of diagnosis. Survival free from death or transplantation was 74% (95% confidence interval, 67-80) 1 year after diagnosis, 62% (95% confidence interval, 55-69) at 10 years, and 56% (95% confidence interval, ..
View full abstractGrants
Awarded by Royal Children's Hospital Research Foundation
Awarded by National Heart Foundation of Australia
Funding Acknowledgements
This study was supported by grant 98001 from the Royal Children's Hospital Research Foundation; grants G 98M 0159, G 04M 1586, G 05M 2151, and G 07M 3180 from the National Heart Foundation of Australia; an NACCS grant from the Australia and New Zealand Children's Heart Research Centre; and an NACCS grant from Heartkids Australia. Dr Daubeney is supported by the Biomedical Research Unit at the Royal Brompton Hospital.