Key Findings: Trends in Survival Among Infants with Critical Congenital Heart Defects
The journal Pediatrics has published a new study: “Temporal Trends in Survival Among Infants with Critical Congenital Heart Defects.” You can read the article’s abstract here. See below for a summary of the findings from this article.
Main Finding from this Study
For infants with critical congenital heart defects, survival up to one year of life has improved over time. However, the chance of these infants dying is still high.
About this study
- Why is this study important?
Some babies born with a CCHD look healthy at first. They can be sent home with their families before their heart defect is found. In the first days or weeks of life, these babies can have serious problems and will often need emergency care. Screening for CCHDs soon after birth can identify some infants with these defects before they show any signs or problems. After they have been identified, these infants can be seen by heart doctors and receive the treatment they need.
In 2011, the United States Secretary of Health and Human Services approved adding screening for critical congenital heart disease to the recommended list of health conditions that babies are checked for soon after birth (also known as newborn screening). To measure the effects of this screening, we will need to be able to compare survival rates of infants with CCHDs before and after screening becomes common. This study provides important information about survival of infants with CCHDs from 1979-2005, before screening started. This study also helps us to identify what factors affect survival.
- What were the study results?
For this study, researchers used data from the Metropolitan Atlanta Congenital Defects Program (MACDP), which is a population-based tracking system for birth defects among babies born to residents of metropolitan Atlanta. This study looked at infants with heart defects born in Atlanta, Georgia from 1979-2005.
- Over 1 million babies were born during that time period, of which about 7,000 were born with a congenital heart defect. Nearly 2,000 (about one-quarter) of these had a CCHD.
- Among those without chromosomal anomalies or other birth defects, about 75% of those with a CCHD survived to one year of age. About 69% survived to 18 years of age.
- Survival for infants with a CCHD improved over time. From 1979-1993, about 67% of infants survived to one year of life. Because medical care and treatment have gotten better over time, from 1994-2005, about 83% of infants survived to one year of life.
- For babies with a CCHD, certain factors were related to a higher chance of death before one year of age:
- if they were born earlier in the time period,
- if they were diagnosed sooner after birth (which might be because they had a more severe defect),
- if they had a younger mother, and
- if they were born at a low birth weight.
Heart Defects: CDC’s Activities
Centers for Disease Control and Prevention (CDC) works to identify causes of CHDs and ways to prevent them. We do this through:
- Surveillance or disease tracking:
- State programs: CDC funds and coordinates the Metropolitan Atlanta Congenital Defects Program (MACDP). CDC also funds 14 population-based state tracking programs. Birth defects tracking systems are vital to help us find out where and when birth defects occur and whom they affect.
- Adolescents and adults: CDC recently started 3 projects to track congenital heart defects among adolescents and adults in order to learn about their health issues and needs across the lifespan.
- Research: CDC funds a large study of birth defects called the National Birth Defects Prevention Study. This study is working to identify risk factors for birth defects, including heart defects.
- CDC is assessing states’ needs for help with CCHD screening and reporting of screening results. CDC worked with New Jersey and Georgia to assess their ability to track CCHD screening. CDC is also helping states and hospitals to better understand how much hospitals spend for each baby screened.
- CDC promotes collaboration between birth defects tracking programs and newborn screening programs for CCHD screening activities. State birth defects programs collect data on CHDs and could help evaluate the effectiveness of screening by looking at false positives (babies who failed the CCHD screening but do not actually have a CCHD after further evaluation) and false negatives (babies who passed the screen suggesting there was no CCHD but actually did have a CCHD).
- CDC provides technical assistance to the Congenital Heart Public Health Consortium and to states receiving funding from the Health Resources and Services Administration (HRSA) for CCHD screening activities.
1. Oster M, Lee K, Honein M, Colarusso T, Shin M, Correa A. Temporal Trends in Survival for Infants with Critical Congenital Heart Defects. Pediatrics. 2013. (In Press).
Reference for Key Findings Feature:
Oster ME, Lee KA, Honein MA, Colarusso T, Shin M, Correa A. Temporal Trends in Survival Among Infants with Critical Congenital Heart Defects. Pediatrics. 2013 [epub ahead of print].