Cardiac Developmental Follow-up Program

The Cardiac Developmental Follow-up Program at the Herma Heart Institute helps babies who have undergone specialized heart care overcome the potential developmental challenges to which they are prone. We’re recognized across the country for establishing the first Developmental Follow-up Program for infants with congenital heart disease in the nation. Our team of specialists will monitor and foster your child's healthy development so he or she can live life to the fullest.

The critical first three years

For many reasons, skills like talking, crawling, and playing can develop more slowly in children who have had heart surgery or care for complex congenital (present at birth) heart defects early in life. They can also be more susceptible to other medical conditions. Our team collaborates with the Healthy Outcomes Post-ICU Engagement (HOPE) Developmental Follow-up Clinic during the important first three years of life. They will work with you to monitor for developmental delays and encourage your child’s abilities in many areas of life. We recommend that all children with complex heart disease or who undergo surgery as infants participate in follow-up even if doing well. Our team is skilled in detecting subtle signs of a problem that may respond well to early therapy. 

Resources as your child matures

For children ages 3 and older, the Herma Heart Institute’s psychologists and neuropsychologists can help parents with their child's transition into school and their progression from elementary school to middle school to high school and beyond. Our psychologists can work closely with school officials to educate them about your child's special care needs. We also partner with the Educational Achievement Partnership Program to help advocate for any special services a child may need at school to help them reach their full potential.

We recommend that children have an updated assessment at least once during the preschool, school-age and adolescent years. This is important because new issues may develop as the expectations in school increase over time. Short-term psychotherapy services are also available for children with behavioral or emotional difficulties related to their congenital heart disease.

Continued cardiac support into adulthood

For the Herma Heart Institute, our work does not end when your child turns 18. Adults with congenital heart disease may develop new or unique problems later in life and may require specialized care. The Adult Congenital Heart Disease (ACHD) Program at Children’s Wisconsin is one of the leading ACHD programs in the nation, and the largest in the state of Wisconsin. Our five board-certified ACHD specialists are equipped to provide complete care as patients transition from adolescence to adulthood.

Learn more about our ACHD program.

Cardiac Neurodevelopmental Outcome Collaborative

Children's Wisconsin is proud to be part of the Cardiac Neurodevelopmental Outcome Collaborative (CNOC), an organization with over 25 pediatric hospitals that are dedicated to advancing outcomes for individuals with pediatric and congenital heart disease. Learn more about CNOC here.

Contact us

To make an appointment or talk to a developmental expert:

(414) 266-6898

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Why choose us

We believe patient families have a right to know what level of care we provide. Review our quality and outcomes reports.

Developmental follow-up recommended

For kids born with heart defects, neurodevelopmental follow-up is essential, per recommendation from  the American Heart Association and the American Academy of Pediatrics. Our clinical researchers Dr. Kathleen Mussatto and Dr. Cheryl Brosig are pioneers in these and other studies helping kids born with heart problems grow up as healthy as possible.