Pediatric Cardiology

When a child has a heart condition, the Pediatric Cardiology program at Providence Heart Institute of Spokane provides the seamless, expert heart care they need – from infancy through adulthood. With the only congenital heart program in the region, we know what it takes to offer specialized diagnosis, treatment and long-term support for pediatric patients and families.

Pediatric Cardiology doctor with baby listening to heart

Our Approach to Pediatric Cardiology

Whether you’re a mom-to-be whose baby may have a heart defect, a child who develops a heart condition or an adult with congenital heart disease, your heart care team at Providence Heart Institute of Spokane is by your family’s side for every step of treatment and recovery.

We take a personalized approach to treating congenital heart disease and related conditions. Families from all over the Inland Northwest trust us with their care, as the only nationally accredited congenital heart program in the region and one of 50 accredited centers in the United States.

Our board-certified heart care specialists know how to treat complex heart conditions in children. We bring together pediatric specialists in cardiology, cardiac surgery and cardiac anesthesiology to deliver expert, personalized procedures – all in one location.

Additionally, the Providence Adult and Teen Congenital Heart (PATCH) program provides a seamless transition from pediatric to adult medical care.

Heart Care for Life

Some patients with congenital heart disease require care not only as infants or children but also later in life. We’re proud to offer everything needed to treat complex heart conditions at any age. Hear from one of our patients, Brian, who has adult congenital heart disease and received his second open-heart surgery to treat a faulty valve.

Patient Stories

Elliott Naftzger has needed heart monitoring since birth. Now, Rachel and Carter, can save the three-hour drive to Spokane because Providence is bringing the imaging unit to their and others’ communities.

“The most comforting part was they knew what it looked like,” Rachel says. “They told us about the surgeries she’d need and that they’d follow her for her whole life. They had a plan.” Read more.

Elliott Naftzger
The Naftzger Family

“The most comforting part was they knew what it looked like,” Rachel says. “They told us about the surgeries she’d need and that they’d follow her for her whole life. They had a plan.” Read more.

Melissa was born with congenital heart disease (CHD), a birth defect that affects how blood flows through the heart and the body. For years, Melissa didn’t believe that having children would be an option for her, but she never gave up hope.

“With every ultrasound it was always so reassuring that everything was ok. Seeing the babies on the little screen and bouncing around with their little hearts pounding away was the biggest joy,” Read more.

Melissa Faucher
Melissa Faucher

“With every ultrasound it was always so reassuring that everything was ok. Seeing the babies on the little screen and bouncing around with their little hearts pounding away was the biggest joy,” Read more.

During a routine prenatal anatomy scan, Joe and Cora learned that baby Abigail’s heart was not developing as expected, and a heart defect had been discovered. They were referred to Sacred Heart Children’s Hospital, where the preparations and guidance began.

“Knowing that Abigail's care team has the education, patience, compassion and skills to support us was what kept our spirits up. Finally, when she was 27 days old, we were able to take her home for the first time and snuggle her without tubes, wires and monitors in the way!" Read more.

Abigail Kelly
The Kelly Family

“Knowing that Abigail's care team has the education, patience, compassion and skills to support us was what kept our spirits up. Finally, when she was 27 days old, we were able to take her home for the first time and snuggle her without tubes, wires and monitors in the way!" Read more.