Pulse Ox Congenital Heart Disease Screening

Pulse oximetry test

Congenital heart disease (CHD) is the most common birth defect. Approximately eight per every 1,000 babies are born with a form of CHD and about 280 outwardly healthy babies are discharged from hospitals every year with unrecognized CHD.

In the first 24 hours of life, a pulse oximetry (pulse ox) test can quickly and painlessly determine whether a baby has critical congenital heart disease and possibly save his or her life. Screening for more serious forms of CHD is now a part of the recommended uniform screening panel and supported by the Health and Human Services, American Heart Association, American College of Cardiology, American Academy of Pediatrics and March of Dimes.

Children’s National Health System created the Congenital Heart Disease Screening Program to help to detect critical CHD while newborns are in the nursery. It can easily be part of the standard of care at any hospital. However, not all hospitals use the pulse oximetry test, which results in hundreds of babies going home with unrecognized critical congenital heart disease every year.

The promotes early detection through the use of pulse oximetry following 24 hours of age and prior to discharge from the newborn nursery. The program values the importance of the screening of all healthy newborns for congenital heart disease.

All babies with critical congenital heart disease are detected before leaving the newborn nursery. Pulse oximetry is part of routine testing performed on all infants that are not already thought to have CHD. It is recommended that pulse oximetry screening be done in conjunction with other standard-of-care newborn screening that requires the baby be at least 24 hours of age, such as PKU screening.

All healthy babies that are not thought to have CHD should be screened. If the pulse oximetry reading  is greater than or equal to 95 percent the infant will pass screening. If the pulse oximetry reading is less than 95 percent the baby's doctor may order an echocardiogram (an ultrasound of the heart) to check for CHD.

Contact Us

If you are an expectant mom or a clinician interested in the CHDSP, please contact Lisa Hom at 202-476-5063, PulseOx@childrensnational.org and lhom@cnmc.org.

Our Story

Our Story

Some babies born with serious congenital heart disease can appear normal and healthy at birth. These babies may be sent home with their mother without showing any signs or symptoms of their condition.  However several days after birth serious complications may occur that require that the baby be taken to an emergency department for lifesaving care. At this point, pediatric cardiologists work to stabilize the baby before surgical interventions can be performed. The cost can be considerable, as well as the risk to the baby’s life, growth and development.

As part of his Richard C. Beyda endowed professorship in 2007, Gerard R. Martin, MD, senior vice president and co-director of the Children’s National Heart Institute, reviewed past evidence and developed a research study to evaluate pulse oximetry (pulse ox) screening for CHD in neonates. Pulse ox is a common medical procedure used to measure the amount of oxygen in a person’s blood. The procedure is non-invasive, painless, inexpensive, and takes only seconds to perform. It has been found that pulse ox can be used to help identify serious CHD in newborns. Dr. Martin was inspired by the idea of using pulse ox to improve the early detection and diagnosis of serious CHD. In addition, Dr. Martin became interested in taking the current research a step further and investigating the implementation of pulse ox testing as a standard of care for newborns.

At a dinner with state legislators held a few weeks later, Dr. Martin discussed pulse ox screening for serious congenital heart disease with representatives and staff from the Maryland State House. The idea was well received, and the seed of interest grew into a plan of action. The Congenital Heart Disease Screening Program was taking shape. Dr. Joseph Wright, former senior vice president of the Child Health Advocacy Institute at Children’s National, joined Dr. Martin to begin advocating for this important procedure as standard of care for newborns. A plan to test the program, develop a toolkit to train health professionals to perform the assessment, and a method of data collection to use in future advocacy efforts was developed.

As with many programs, the key to getting it off the ground is funding. Representatives from Children’s Foundation approached the Elsie and Marvin Dekelboum Family Foundation, who selected the Congenital Heart Disease Screening Program (CHDSP) as a project to fund.

Dr. Martin knew collaboration with a community hospital was important to begin the program. He approached Dr. Sandra Cuzzi, a Children’s National hospitalist who sees patients at Holy Cross Hospital. Holy Cross is one of the busiest birthing centers in metropolitan Washington, DC, and is in close proximity to Children’s National. Dr. Martin and Dr. Cuzzi introduced the idea to the leadership at Holy Cross. 

Soon the team began working with the staff in the newborn nursery at Holy Cross and the institutional review board (or IRB) at Holy Cross. Dr. Martin and Elizabeth Bradshaw, a nurse brought on board to oversee the CHDSP research and program development, shepherded the project through the development and approval process. In January 2009, the study began and newborns at Holy Cross received pulse ox test before they left the nursery. The research study identified several babies with CHD before they left the nursery and when it was complete Holy Cross decided to make pulse ox screening standard of care.

The Child Health Advocacy Institute and clinicians at Children’s National’s Heart Institute share the ultimate goal of  making screening for congenital heart disease a standard practice for all newborns. The team created a toolkit that nurseries may use to start a screening program in their nursery. This toolkit has been sent to over 1,400 hospitals, associations and advocates both nationally and internationally who have expressed interest in improving detection of serious CHD.

In October, 2010 the Health and Human Services’ Advisory Committee on Heritable Disorders in Newborns and Children recommended to Secretary Kathleen Sebelius that CCHD screening become a part of the recommended uniform screening panel. In fall 2011, the Secretary supported this recommendation. The American Heart Association, American College of Cardiology, American Academy of Pediatrics and March of Dimes all endorse CCHD screening. Dr. Martin and Elizabeth Bradshaw have participated in associated advocacy and scholarship activities.

Participating hospitals

Participating hospitals

Participating national and international hospitals

Related video

Related video

Videos to understand the importance of screening for critical congenital heart disease include.

View other videos related to cardiology and read more about the Heart Smart videos, which were created in five languages to help new and expectant parents learn the importance of screening newborns for potentially critical heart disease.

Resources for Families

Resources for Families

Support Groups and Online Resources

Books for Parents

  • Heart Defects in Children: What Every Parent Should Know,” by Cheryl J. Wild
  • Heart of a Child,” by Catherine A. Neill, Edward B. Clark and Carleen Clark
  • It’s My Heart,” by Children’s Heart Foundation
  • The Heart of a Mother,” by Anna Marie Jaworski and Judy Norwood

Books for Children with Heart Defects

  • Blue Lewis and Sasha the Great,” by Carol Donsky Newell
  • Matty’s Heart,” by C.J. Hribal
  • Nathan’s Special Heart,” by Jessica Ennis (available as a virtual book)
  • Pump the Bear,” by Gisella Olivo Whittington

Books for Siblings

  • Cardiac Kids,” by Vicci Elder
  • My Brother Needs an Operation,” by Anna Marie Jaworski & Sarah Lualdi Moran
  • When Molly was in the Hospital,” by Debbie Duncan

Jeanne Ricks' Story

Jeanne Ricks

Jeanne Ricks, BSN, MS, RN, NE-BC, Director of Outpatient Nursing and Ambulatory Services in Children's National's Heart Institute, said she was meant to be a nurse.

Read More of Jeanne Ricks' Story

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