Drive quality improvement and advance the development and delivery standards of care through the American College of Cardiology's two programs dedicated to adult and pediatric congenital heart disease (CHD) patients. These two programs are leaders in giving you access to the data you need to ensure you are providing the best quality of care for your patients. |
IMPACT Registry®
The IMPACT Registry assesses the prevalence, demographics, management and outcomes of CHD patients undergoing diagnostic catheterizations and catheter-based interventions. The data from the registry identifies procedure variances and links them to outcomes, provides benchmarks to assess performance and supports the development of evidence-based guidelines for CHD treatment that will improve outcomes for CHD patients of all ages. Click here to learn more.
Adult Congenital & Pediatric Quality Network™
The Adult Congenital & Pediatric Cardiology Quality Network is a national network of CHD centers dedicated to collecting and sharing data covering BMI, imaging, chest pain, Kawasaki Disease, Tetralogy of Fallot and more. Your participation in the network is crucial to building an effective data set that will drive quality improvement and advance the development and delivery of adult CHD and pediatric cardiology standards of care. The Network supports quality improvement through activities approved to earn MOC Part IV credit. Click here to learn more.