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Many people with congenital heart disease living longer

Date:
February 26, 2015
Source:
Penn State Milton S. Hershey Medical Center
Summary:
At one time, many children born with congenital heart disease (CHD) suffered from issues that carried fatal prognoses. But that's changing, thanks to technological advancements.
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At one time, many children born with congenital heart disease (CHD) suffered from issues that carried fatal prognoses. Thanks to technological advancements in the past 30 to 40 years, Dr. Elizabeth Adams of Penn State Hershey Children's Heart Group can predict that a child born today has a 90 percent chance of living to adulthood, even with severe CHD.

"Most children with CHD are now living to adulthood and historically that has not been the case," she says.

The ACHA now reports that there are an estimated 2 million adults living with CHD in the United States, meaning that, for the first time ever, there are more adults than children with CHD.

Affecting about 1 percent of the population, CHD is a genetic condition and is present from birth.

"Most of what we're talking about are structural problems with the way the heart is formed -- hearts that are missing chambers, hearts that have narrow or leaky valves, or structures that are not in the right place," Adams says.

CHD is usually detected prenatally via ultrasound during pregnancy followed by a cardiac ultrasound to confirm and identify a problem.

Occasionally children are not diagnosed until after birth and most of those cases are identified within the first year of life.

In some less serious cases, patients are not diagnosed until much later in life.

"Some conditions will produce symptoms very early on while others may not produce symptoms until well into adulthood," she says.

If a baby is not diagnosed prenatally, there are a number of warning signs suggestive of congenital heart disease. He or she may not feed properly, may have poor weight gain, may be pale or blue, and in more severe cases, could suffer cardiac collapse.

"At about a week of life, infants with some of the most severe types of congenital heart disease may get very sick, very quickly," Adams says.

Early detection is possible today due to sophisticated ultrasound capabilities that are now commonly used and allow doctors to find the majority of the cases prenatally.

Less invasive procedures have also been developed that can spare patients open heart surgery.

"For example, if a baby is born today with a narrow pulmonary valve, that child will probably not need surgery," Adams said.

The child would undergo a cardiac catheter procedure where a balloon is inserted into the valve to open it without an operation. In some cases, adult valve replacement or repairing small holes can be done via catheter as well.

"Instead of a week in the hospital, it's one night plus a week of recovery time instead of a couple of months," Adams said.

The incidence of congenital heart disease is increasing slightly, probably related to better detection, and in some cases, genetic transmission of cases from parent to child.

She personally takes care of a half dozen parent-child combinations with heart defects.

Researchers are currently trying to understand the ways in which congenital heart defects are transmitted and why some are more likely to be passed on to offspring than others.


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Materials provided by Penn State Milton S. Hershey Medical Center. Note: Content may be edited for style and length.


Cite This Page:

Penn State Milton S. Hershey Medical Center. "Many people with congenital heart disease living longer." ScienceDaily. ScienceDaily, 26 February 2015. <www.sciencedaily.com/releases/2015/02/150226110340.htm>.
Penn State Milton S. Hershey Medical Center. (2015, February 26). Many people with congenital heart disease living longer. ScienceDaily. Retrieved May 25, 2017 from www.sciencedaily.com/releases/2015/02/150226110340.htm
Penn State Milton S. Hershey Medical Center. "Many people with congenital heart disease living longer." ScienceDaily. www.sciencedaily.com/releases/2015/02/150226110340.htm (accessed May 25, 2017).

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