[Double-chambered right ventricle: case series].

Area of Science:

• Cardiology
• Pediatric Cardiology
• Congenital Heart Disease

Background:

• Double-chambered right ventricle (DRV) is a rare congenital heart malformation.
• It results from anomalous muscle bands dividing the ventricle into high- and low-pressure chambers.
• DRV's progressive nature often leads to diagnosis in adolescence or adulthood.

Observation:

• Pediatric cardiologists now manage patients with congenital heart disease across all age groups, from fetal development to adulthood.
• This broad experience facilitates earlier and more comprehensive care for complex conditions like DRV.
• A new Congenital Heart Disease Section in Buenos Aires province is reporting on treated cases.

Findings:

• The study presents a series of cases of double-chambered right ventricle managed at a new public hospital.
• This highlights the increasing role of specialized pediatric cardiology centers in diagnosing and treating rare cardiac malformations.
• The cases underscore the importance of recognizing the evolving nature of DRV for timely intervention.

Implications:

• Early recognition and management by pediatric cardiologists are crucial for improving outcomes in patients with DRV.
• Establishing specialized congenital heart disease centers enhances the capacity to manage rare pediatric cardiac conditions.
• This case series contributes to the understanding of DRV management in a public healthcare setting.