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SUPPLEMENTAL MATERIALAppendix 1. Congenital heart defectrelated Centers for Disease Control and Prevention (CDC)modified version of the British Pediatric Association (BPA) codes included in the Congenital Heart Survey To Recognize Outcomes, Needs, and wellbeinG (CH STRONG)Severe Codes 745.000Common Truncus745.010Aortic septal defect (ASD) / Aortopulmonary window745.100 745.190Transposition (all types) 745.100 Transposition of great vessels, complete (no VSD) Transposition of great vessels,...
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Congenital heart defect-related centers are specialized healthcare facilities that focus on the diagnosis, treatment, and management of congenital heart defects in patients, particularly in infants, children, and adults.
Healthcare providers, including hospitals and specialized heart centers that treat patients with congenital heart defects, are typically required to file reports pertaining to these centers.
To fill out congenital heart defect-related centers, providers must gather relevant patient data, such as diagnostic findings, treatment plans, outcomes, and any pertinent demographic information, then enter this data into standardized reporting forms.
The purpose of congenital heart defect-related centers is to ensure comprehensive care for individuals with congenital heart defects, improve patient outcomes, facilitate research, and enhance understanding of these conditions.
Information that must be reported includes patient demographics, specifics about the congenital heart defect, treatment procedures, follow-up care, outcomes, complications, and any other relevant clinical data.
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