Some Infants still not receiving the recommended screenings and interventions for hearing loss and critical congenital heart disease at birth
Progress made, more work needed to close the gaps and ensure all infants receive screening and prompt medical care if needed
For Immediate Release: Thursday, August 24, 2017
Contact: Media Relations
Today’s Morbidity & Mortality Weekly Report from the U.S. Centers for Disease Control and Prevention (CDC) highlights the benefits of and gaps in assessing point-of-care newborn screening for hearing loss (HL) and critical congenital heart disease (CCHD). These critical gaps need to be closed to help all children have a better chance to reach their full potential.
About 1 in 500 infants are born with CCHD, which includes the more severe forms of congenital heart disease (CHD). CHD is the most common type of birth defect and accounts for more than 30 percent of all infant deaths from birth defects. Point-of-care screening can help identify many infants with CCHD before they go home.
Newborn screening, a public health program that benefits 4 million U.S. infants every year, identifies conditions that can affect a child’s long-term health or even survival. Besides laboratory testing of dried bloodspots for dozens of conditions, which has been in place since the 1970s, national guidelines now call for newborns to be screened for hearing loss and CCHD while at the birth facility.
“Newborn screening at birth is crucial to quickly identify infants at risk of hearing loss and congenital heart disease so they can receive early intervention and follow-up care,” said CDC Director Brenda Fitzgerald, M.D. “Finding these conditions early can give infants the best chance to properly develop and lead healthy lives.”
CDC estimates that without newborn screening, each year about 875 U.S. newborns with a CCHD were not diagnosed before discharge from birth facilities. However, most of these babies can now be identified using a non-invasive and painless test referred to as “pulse oximetry testing.” For every 200 infants with a CCHD, at least one death due to an undiagnosed CCHD can be avoided if all birth facilities screen newborn babies using pulse oximetry testing.
Similarly, permanent hearing loss present at birth affects nearly 2 infants per 1,000 in the United States. Most children with hearing loss are considered to have or be at risk for a developmental delay. Infants who are diagnosed before age 3 months and receive intervention services before age 6 months have significantly better language development than children who are not.
Federally funded state-based Early Hearing Detection and Intervention (EHDI) programs help ensure infants receive recommended diagnostic and intervention services. In short, EHDI focuses on nationally recognized “1-3-6” guidelines: children are screened for hearing loss before 1 month of age, and, if needed, diagnosed for hearing loss before age 3 months and enrolled in early intervention programs before age 6 months.
In contrast to EHDI, there is no federal support for state-based CCHD screening programs. Not detecting heart-related birth defects early can pose a significant increase in risk for permanent disability and even death. “The collaboration between EHDI programs, health professionals, and parents has led to great progress on hearing loss screening and follow-up,” said Stuart K. Shapira, M.D., Ph.D., Chief Medical Officer and Associate Director for Science at CDC’s National Center on Birth Defects and Developmental Disabilities. “We must apply the same effort and resources to CCHD screening to help prevent infant deaths and offer children the greatest chance to thrive.”
This MMWR complements the September 2016 Public Health Grand Rounds forum Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease.
To read the article, visit MMWR homepage.
For a video summary of the MMWR findings:
Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease