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Published on: May 11, 2015
Clinical classification in pediatric pulmonary arterial hypertension associated with congenital heart disease
Willemijn M H Zijlstra1, Johannes M Douwes1, Mark-Jan Ploegstra1
1Center for Congenital Heart Diseases, Department of Pediatric Cardiology, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Insights
Pediatric pulmonary arterial hypertension (PAH) linked to congenital heart disease (CHD) is diverse. The Nice CHD classification aids characterization but needs refinement, as many children remain unclassified.
Area of Science:
- Cardiology
- Pediatric Pulmonology
- Medical Genetics
Background:
- Congenital heart disease (CHD) is a significant cause of pediatric pulmonary arterial hypertension (PAH).
- Understanding the heterogeneity of PAH associated with CHD (PAH-CHD) is crucial for effective management.
- The existing Nice CHD classification aims to categorize PAH-CHD patients.
Purpose of the Study:
- To describe phenotypic heterogeneity in pediatric PAH-CHD.
- To assess the applicability of the Nice CHD classification in a contemporary cohort.
- To explore if the classification reflects patient/disease characteristics and survival.
Main Methods:
- A cohort of 134 pediatric PAH patients with CHD was analyzed across three referral centers.
- Patients were characterized and classified using the 2013 Nice CHD classification criteria.
- Hemodynamic profiles, associated conditions, treatment intensity, and survival data were collected.
Main Results:
- The Nice CHD classification assigned 24% to group 1, 14% to group 2, 19% to group 3, and 30% to group 4; 11% were unclassified.
- Significant differences in CHD types and hemodynamics were observed between groups.
- Group 3 showed distinct characteristics, including frequent (un)defined syndromes and intensive PAH therapy, but no survival differences were found across groups.
Conclusions:
- Pediatric PAH-CHD is heterogeneous, often involving extracardiac and developmental factors.
- The Nice CHD classification identifies distinct patient groups but requires refinement for universal applicability.
- Group 3 represents a unique entity, though its prognostic impact requires further investigation due to limited events.
Abstract:
Congenital heart disease (CHD) is a frequent cause of pediatric pulmonary arterial hypertension (PAH), with diverse etiology and outcome. We aimed to describe phenotypic heterogeneity in pediatric PAH associated with CHD (PAH-CHD), assess the applicability of the Nice CHD classification, and explore whether this classification accurately reflects patient/disease characteristics and survival. All children with CHD from a contemporary cohort of consecutive pediatric PAH patients followed in three major referral centers (Denver, New York, the Netherlands) were characterized and classified on the basis of the latest proposed clinical classification for PAH-CHD (World Symposium on Pulmonary Hypertension, Nice, 2013). According to this classification, 24% of 134 children were classified into group 1, 14% into group 2, 19% into group 3, and 30% into group 4; 11% could not be classified. Types of CHD and hemodynamic profile differed between groups, with the highest right atrial pressure in group 4 (P < 0.040). Group 3 children had Down syndrome less frequently (P = 0.011) but other (un)defined syndromes most frequently (P = 0.063) and received most intense PAH-targeted therapy (P = 0.003). With 15 deaths and one lung transplant (12%; median follow-up: 4.3 years), survival differences could not be demonstrated between the groups in the Nice CHD classification. Pediatric PAH-CHD is a heterogeneous condition frequently associated with extracardiac, developmental factors that are believed to affect disease development. The Nice CHD classification identifies groups with specific patient/disease characteristics. However, a substantial proportion of children could not be classified. Group 3 forms a distinct disease entity. Its prognostic value could not be determined because of the low number of events. The Nice CHD classification supports clinical characterization of PAH-CHD; however, further refinement is needed to classify all children with PAH-CHD.
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