Pediatric cardiomyopathies: causes, epidemiology, clinical course, preventive strategies and therapies

Author:

Lipshultz Steven E1,Cochran Thomas R2,Briston David A2,Brown Stefanie R2,Sambatakos Peter J2,Miller Tracie L23,Carrillo Adriana A2,Corcia Liat2,Sanchez Janine E2,Diamond Melissa B2,Freundlich Michael2,Harake Danielle2,Gayle Tamara2,Harmon William G2,Rusconi Paolo G2,Sandhu Satinder K2,Wilkinson James D23

Affiliation:

1. Department of Pediatrics, University of Miami Miller School of Medicine, 1601 NW 12th Avenue, 9th Floor, Miami, FL 33136, USA.

2. Department of Pediatrics, University of Miami Miller School of Medicine, 1601 NW 12th Avenue, 9th Floor, Miami, FL 33136, USA

3. Holtz Children’s Hospital of the University of Miami/Jackson Memorial Medical Center & Sylvester Comprehensive Cancer Center, Miami, FL, USA

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.

Publisher

Future Medicine Ltd

Subject

Cardiology and Cardiovascular Medicine,Molecular Medicine

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