Welcome to the world of NPC-QIC, where parents and clinicians dream together, create together, and transform the practice of medicine for HLHS infants-and-beyond together.

WELCOME TO NPC-QIC

 

Our mission is to decrease mortality and improve quality of life for all infants with single ventricle congenital heart disease and their families.

 
“By sharing their clinical stories, these 6,000 babies have taught us how to improve our practice and inspired us to continue our journey to transform the care of people with single ventricle congenital heart disease.”
— Dr. Alicia Chaves, NPC-QIC clinical data co-lead.

GET INVOLVED

ABOUT OUR NETWORK

PATIENTS & FAMILIES

PROSPECTIVE CENTERS & HEALTHCARE PROFESSIONALS

NEWS & HIGHLIGHTS

Featured
Save the Date: Fall 2024 Learning Session
Save the Date: Fall 2024 Learning Session
Milestone Achievement: NPC-QIC Enrolls 6,000 HLHS Babies into its Registry
Milestone Achievement: NPC-QIC Enrolls 6,000 HLHS Babies into its Registry

The National Pediatric Cardiology Quality Improvement Collaborative is excited to announce the enrollment of 6,000 participants into its registry of babies with hypoplastic left heart syndrome (HLHS), a single ventricle congenital heart defect.

UPCOMING EVENTS

Featured
FON Case Review Conference
May 21
FON Case Review Conference
FON Case Review Conference
Jul 16
FON Case Review Conference
FON Case Review Conference
Nov 21
FON Case Review Conference

SOCIAL MEDIA FEED

SPOTLIGHT


Clinicians and parents of HLHS babies share their perspective on the “Heart of the Matter.”