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Updated: Aug 19, 2026

Echocardiographic Measurement of Right Ventricular Diastolic Parameters in Mouse
Published on: April 27, 2019
Double-chambered right ventricle
Insights
Approximately 10% of patients with ventricular septal defects (VSD) also have double-chambered right ventricles (DCRV). Early diagnosis and surgical correction of both VSD and DCRV lead to excellent long-term outcomes.
Area of Science:
- Cardiology
- Pediatric Cardiac Surgery
- Congenital Heart Disease
Background:
- Ventricular septal defect (VSD) is a common congenital heart anomaly.
- Double-chambered right ventricle (DCRV) is a rare condition that can be associated with VSD.
- Accurate diagnosis and surgical management are crucial for favorable outcomes.
Purpose of the Study:
- To determine the incidence of DCRV in patients undergoing VSD correction.
- To evaluate the diagnostic methods for DCRV.
- To assess the surgical outcomes for combined VSD and DCRV repair.
Main Methods:
- Retrospective review of 279 patients undergoing VSD correction between 1972 and 1986.
- Analysis of diagnostic data including two-dimensional echocardiography and cardiac catheterization.
- Surgical procedures involved VSD closure and resection of anomalous muscle bundles.
Main Results:
- Thirty patients (10.8%) had concomitant DCRV.
- Two-dimensional echocardiography, particularly with subcostal views, improved DCRV diagnosis.
- All patients survived surgery with excellent long-term results and significant reduction in right ventricular pressure.
Conclusions:
- DCRV is present in about 10% of VSD patients.
- Thorough preoperative evaluation using echocardiography and catheterization is essential for diagnosing DCRV.
- Intraoperative anatomical assessment is critical to avoid missing DCRV, especially with current surgical approaches.
Abstract:
Thirty (10.8%) of 279 patients undergoing correction of a ventricular septal defect (VSD) from January, 1972, to September, 1986, also had a double-chambered right ventricle (DCRV). Age at operation ranged from 1.3 to 18.8 years (mean, 6.7 +/- 4.5 years [+/- standard deviation]). Seventeen patients were male, and 13 were female. Two-dimensional echocardiography was used after 1978 in the initial evaluation of 20 patients; however, the diagnosis of DCRV was made with the use of subcostal views only since 1984 in 4 of 5 patients. Surgical correction consisted of closure of the VSD and resection of anomalous muscle bundles through a right ventriculotomy (28 patients), and right atriotomy (2 patients). All patients survived and are asymptomatic 4.2 +/- 3.4 years following operation. Six patients have undergone catheterization postoperatively and 8 patients had intraoperative pressure recordings. The mean preoperative ratio of right ventricular to left ventricular pressures was 0.67 +/- 0.22 compared with 0.34 +/- 0.15 postoperatively (p less than .001). In 2 patients, DCRV was not recognized preoperatively or at VSD closure through a right atriotomy, and reoperation was necessary after DCRV was demonstrated at postoperative catheterization. DCRV may occur in approximately 10% of patients undergoing correction of VSD. Careful evaluation of echocardiographic and catheterization data preoperatively and careful evaluation of the anatomy intraoperatively are necessary so that DCRV not be overlooked, especially because most VSDs are now closed through the right atrium. Successful correction of VSD and DCRV is associated with excellent long-term results.
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