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Updated: May 14, 2026

Murine Fetal Echocardiography
Published on: February 15, 2013
[Presentation form and evolution of double-chambered right ventricle]
Mirna Rocío Yabur-Espitia1, Emilia Patiño-Bahena, Berenice Cruz-Prieto
1Departamento de Ecocardiografía, Instituto Nacional de Cardiología Ignacio Chávez, México DF, México; Departamento de Pediatría, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Insights
Double-chambered right ventricle (DCRV) is rare, diagnosed via echocardiography. Surgical treatment yields excellent results, improving symptoms and function in most patients with this congenital heart defect.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Double-chambered right ventricle (DCRV) is a rare congenital heart anomaly, accounting for 0.5% of all congenital cardiopathies.
- Clinical presentation varies, with some patients asymptomatic and others experiencing symptoms from infancy to adulthood.
Purpose of the Study:
- To characterize the clinical and echocardiographic features of 11 patients diagnosed with DCRV.
- To evaluate the outcomes of surgical intervention for DCRV.
Main Methods:
- Retrospective review of 11 DCRV patients.
- Data collection included medical history, chest radiography, electrocardiography, and transthoracic echocardiography.
Main Results:
- Median age was 10 years; 36.45% were asymptomatic at diagnosis.
- Echocardiography confirmed DCRV due to a muscular band in all patients.
- Common associated anomalies included VSD, PFO, subaortic stenosis, and Tetralogy of Fallot.
- Seven patients underwent surgery, with 6 achieving NYHA Class I post-operatively.
Conclusions:
- DCRV diagnosis is best achieved through echocardiography.
- Worsening NYHA functional class is a predominant symptom, with potential for progressive obstruction.
- Surgical treatment in this series demonstrated excellent mid-term hemodynamic and functional outcomes for 91% of patients.
Introduction:
The double-chambered right ventricle (DCRV) is an uncommon congenital heart disease; it represents the 0,5% of these congenital cardiopathies.
Objective:
To describe the clinical and echocardiographic characteristics of a series of 11 patients.
Methods:
Eleven patients with DCRV were studied. A complete medical history, chest radiograph, electrocardiogram, and transthoracic echocardiography were performed.
Results:
The median age of studied patients was 10 years. The 36.45% of cases were asymptomatic and the diagnosis was made by echocardiography. Other cases had weakness during food in the lactancy stage and worsening of NYHA functional class in older children. The echocardiogram showed double-chambered right by a muscular band in all studied patients. The most frequent associated anomalies were: ventricular septal defect, patent foramen ovale, subvalvular aortic stenosis, and Fallot's Tetralogy. Seven patients went to surgical treatment and now 6 of them are in NYHA functional class i.
Conclusions:
This paper has a special importance, because is the biggest series of patients with double-chambered right ventricle in Mexico and the results are comparable to the studies reported in the literature. The worsening of the NYHA functional class was the predominate symptom. The clinical manifestations can be presented from the lactancy to adulthood and the degree of obstruction could have a progressive character. The echocardiography is the method of choice in the diagnosis of these patients. The 91% of patients with DCRV who went to surgical treatment had excellent hemodynamic and functional results in the mid-follow-up.
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