| Literature DB >> 24180540 |
Steven E Lipshultz1, Thomas R Cochran, David A Briston, Stefanie R Brown, Peter J Sambatakos, Tracie L Miller, Adriana A Carrillo, Liat Corcia, Janine E Sanchez, Melissa B Diamond, Michael Freundlich, Danielle Harake, Tamara Gayle, William G Harmon, Paolo G Rusconi, Satinder K Sandhu, James D Wilkinson.
Abstract
Pediatric cardiomyopathies, which are rare but serious disorders of the muscles of the heart, affect at least one in every 100,000 children in the USA. Approximately 40% of children with symptomatic cardiomyopathy undergo heart transplantation or die from cardiac complications within 2 years. However, a significant number of children suffering from cardiomyopathy are surviving into adulthood, making it an important chronic illness for both pediatric and adult clinicians to understand. The natural history, risk factors, prevalence and incidence of this pediatric condition were not fully understood before the 1990s. Questions regarding optimal diagnostic, prognostic and treatment methods remain. Children require long-term follow-up into adulthood in order to identify the factors associated with best clinical practice including diagnostic approaches, as well as optimal treatment approaches. In this article, we comprehensively review current research on various presentations of this disease, along with current knowledge about their causes, treatments and clinical outcomes.Entities:
Mesh:
Year: 2013 PMID: 24180540 PMCID: PMC3903430 DOI: 10.2217/fca.13.66
Source DB: PubMed Journal: Future Cardiol ISSN: 1479-6678