We provide advanced treatment, compassionate care and hope to families with babies diagnosed with CDH.
In the Johns Hopkins All Children’s Center for Congenital Diaphragmatic Hernia (CDH), families find hope during a time that may otherwise feel hopeless. Led by CDH expert David Kays, M.D., our team combines compassionate care, innovative techniques, and cutting-edge technology and equipment to treat babies with CDH.
In CDH, the diaphragm—the muscle that separates the abdomen from the chest—does not develop completely, causing a hole where abdominal organs can migrate into the chest. When that happens, it doesn’t leave enough space for the lungs to develop normally, making it hard for the baby to breath.
Johns Hopkins All Children’s founded the first inpatient center in the country dedicated solely to the treatment of CDH. Infants treated at Johns Hopkins All Children’s experience a survival rate greater than 90%*, which exceeds national benchmarks. Every case of CDH is different—whatever you may have been told about your child’s chances with CDH, we urge you to speak with our team and learn about options for your baby.
We also provide specialized care for infants and children who have been treated for CDH and are later readmitted due to illness.
Why choose the CDH Center at Johns Hopkins All Children’s
Our dedicated team provides your child and your family with personalized, advanced care. Our approach has led to excellent outcomes in CDH care, even in severe cases. Our team includes surgeons, neonatologists, cardiologists, neuropsychologists, nutritionists and other specialists who work in tandem to provide expert care for your child. We provide:
Expert ventilator care: Babies with CDH are born with critically small and fragile lungs. Any lung injury, including from the use of life-saving equipment, can affect a baby’s outcome. Dr. Kays and his team recognize this delicate balance and practice “kinder, gentler ventilation” for CDH infants.
Inclusive and expert use of ECMO when needed: Extracorporeal membrane oxygenation (ECMO) is a form of heart-lung bypass sometimes used in the treatment of more severe CDH patients.
Appropriate care for every baby: Repairing CDH does not automatically make small lungs become big lungs, but it allows the lungs to grow to the fullest extent possible. It can be frightening for parents because babies with severe CDH often get worse for a period of time before they get better after CDH repair.
Dr. Kays has spent decades studying the optimal time to perform CDH repair, and how the severity of the CDH affects the outcome of those decisions. We assess the severity of CDH through multidisciplinary prenatal testing, including ultrasound, fetal echocardiography, fetal MRI and consultation with our surgical team.
Consistency of care: Parents know their child better than anyone, and parents are integral members of the care team at Johns Hopkins All Children's. Our team communicates the plan for your child’s care, and because our team is dedicated to CDH care, we provide consistent oversight that makes a difference in the experience for you and your baby.
We help our patients lead productive, healthy lives. We know that the number of babies who survive is about how well we take care of both their lungs and their brains. That link is our No. 1 priority every day.
Families that have received a CDH diagnosis for their baby should know they are not alone. Our team is here to answer your questions. In addition, there are a number of resources that can assist you during this challenging time.
The Tiny Hero Foundation and the Fore Hadley Foundation provide support to families affected by CDH. Learn more about them, and other available resources, on the Patient Information & Resources page.
*Infants with severe CDH plus a highly severe second anomaly, such as uni-ventricular heart defect, severe chromosomal defects, or severe bilateral CDH, face complex physiologic challenges we have generally not been able to overcome. This statement relates to the spectrum of CDH excluding those with a highly severe or fatal second anomaly.