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American Heart Association reports an increasing number of U.S. Adults living with Congenital Heart Defects

 

American Heart Association Journal Report

American Heart AssociationDallas, TX – More adults are living with congenital heart defects in the United States, creating the need for more health services and tracking systems to collect data across all ages, not just at birth, according to new research in the American Heart Association’s journal Circulation.

Congenital heart defects are structural problems with the heart present at birth. They are diagnosed in eight to 10 per 1,000 live births in the United States and are the most common type of birth defect, according to researchers.

More adults are living with congenital heart defects in the United States, creating the need for specialized health services and systems that track this medical condition across all ages. (American Heart Association)

More adults are living with congenital heart defects in the United States, creating the need for specialized health services and systems that track this medical condition across all ages. (American Heart Association)

Medical and surgical advances in the last 30 years have decreased death rates and a growing number of babies are surviving to reach their adult years. Yet most patients will need lifelong cardiac care and many don’t receive care as they transition to adulthood.

A new study estimates that about 2.4 million people – 1.4 million adults and 1 million children – were living with these medical conditions in the United States in the year 2010. Nearly 300,000 of them had severe heart defects.

Compared with the estimates for the year 2000, these figures represent a 40 percent increase in the total number of people living with congenital heart defects in the United States and a 63 percent increase among adults.

More adults survivors now live with congenital heart defects than children so it is no longer solely a pediatric condition, researchers say.
“This is a substantial population of adults in the United States who have survived infancy and childhood are living with congenital heart defects,” said Suzanne Gilboa, Ph.D., first author of the study and an epidemiologist with the Centers for Disease Control and Prevention. “They need the appropriate care in order to have full and productive lives.”

Although state surveillance systems in the U.S. track how many babies are born with congenital heart defects, Gilboa noted, they do not continue to track long term.

The study confirms that congenital heart disease is a public health issue with more adults affected than children, and that’s important from a health care delivery and a policy standpoint, said senior study author Ariane Marelli, M.D. MPH and professor of medicine at McGill University in Montreal.

“People used to think of congenital heart disease as a pediatric condition. There’s really no question now that congenital heart disease falls squarely in the realm of adult medicine,” she said. “We need to have more congenital heart disease programs and more manpower to meet the needs of this population.”

Researchers extrapolated data from published estimates in Quebec, Canada. They assumed Quebec prevalence data on congenital heart defects was equal to similar sex and age data for the U.S. non-Hispanic whites, then adjusted to those estimates to derive rates for blacks and Hispanics. The majority of people living with congenital heart defects in the United States are non-Hispanic white, about 1.7 million, compared with non-Hispanic black or Hispanic, about 700,000.

This current report is the first contemporary assessment of the number of people living with congenital heart defects in the United States based on factors such as age, sex and ethnicity.

Other co-authors are Owen Devine, Ph.D.; James Kucik, Ph.D., M.P.H.; Matthew Oster, M.D., M.P.H.; Tiffany Riehle-Colarusso, M.D., M.P.H.; Wendy Nembhard, Ph.D., M.P.H.; Ping Xu, Ph.D., M.P.H.; Adolfo Correa, M.D., M.P.H., Ph.D.; and Kathy Jenkins, M.D., M.P.H. Author disclosures are on the manuscript.

Study funding was provided by the Canadian Institute of Health Research, Heart and Stroke Foundation of Canada, Fonds de la recherché en santé du Québec, National Heart, Lung, and Blood Institute, National Institute on Minority Health and Health Disparities, National Center for Complementary and Alternative Medicine, and the Arkansas Biosciences Institute.

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