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Updated: Jul 14, 2026

Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Evolving role of multidetector computed tomography in evaluation of arrhythmogenic right ventricular
Chandra Bomma1, Darshan Dalal, Harikrishna Tandri
1Division of Cardiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Insights
Multidetector computed tomography (MDCT) shows promise in diagnosing arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) by identifying key right ventricular abnormalities. This imaging technique offers an alternative for patients with implantable cardioverter-defibrillators who cannot undergo cardiac MRI.
Area of Science:
- Cardiology
- Radiology
- Medical Imaging
Background:
- Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) diagnosis relies on identifying right ventricular (RV) dilatation and dysfunction.
- Cardiac magnetic resonance imaging (MRI) is the preferred diagnostic tool for ARVD/C.
- Implantable cardioverter-defibrillators (ICDs) in patients with suspected ARVD/C preclude the use of MRI.
Purpose of the Study:
- To evaluate the utility of multidetector computed tomography (MDCT) in diagnosing ARVD/C.
- To assess MDCT's ability to detect qualitative and quantitative abnormalities of the right ventricle in ARVD/C patients.
Main Methods:
- Retrospective analysis of contrast-enhanced cardiac MDCT in 31 patients with suspected ARVD/C.
- Evaluation of qualitative findings (trabeculation, intramyocardial fat, scalloping) and quantitative measurements (RV volumes, dimensions, surface area).
- Comparison of MDCT findings with Task Force criteria for ARVD/C diagnosis.
Main Results:
- Seventeen of 31 patients were confirmed to have ARVD/C.
- Increased RV trabeculation, RV intramyocardial fat, and scalloping were significantly associated with ARVD/C (p <0.001).
- Patients with ARVD/C showed increased RV volumes, inlet dimensions, and outflow tract surface area compared to controls.
Conclusions:
- Cardiac MDCT effectively detects qualitative and quantitative RV abnormalities in ARVD/C.
- MDCT serves as a viable alternative imaging modality for ARVD/C evaluation in patients with ICDs.
- Limitations include ICD interference, motion artifacts, radiation exposure, and contrast reactions.
Abstract:
The purpose of this study was to report 1 center's experience with multidetector computed tomography (MDCT) in the evaluation of patients suspected to have arrhythmogenic right ventricular (RV) dysplasia/cardiomyopathy (ARVD/C). RV dilatation/dysfunction is 1 of the most important criteria for establishing the diagnosis of ARVD/C. Cardiac magnetic resonance imaging (MRI) is the most preferred imaging modality for the diagnosis of ARVD/C. However, many patients with suspected ARVD/C have implantable cardioverter-defibrillators, prohibiting the use of MRI. Thirty-one patients (19 men; mean age 41 +/- 12 years) referred for evaluation of known or suspected ARVD/C had a complete reevaluation including contrast-enhanced cardiac MDCT at the center. Two patients underwent both cardiac MRI and MDCT. Seventeen of 31 patients met Task Force criteria for ARVD/C and were confirmed to have ARVD/C. Multidetector computed tomographic images were analyzed for qualitative and quantitative characteristic findings of ARVD/C. Increased RV trabeculation (p <0.001), RV intramyocardial fat (p <0.001), and scalloping (p <0.001) were significantly associated with the final diagnosis of ARVD/C. RV volumes, RV inlet dimensions, and RV outflow tract surface area were increased in patients with ARVD/C compared with patients who did not meet the criteria. RV and left ventricular functional analysis was performed in 2 patients. In conclusion, cardiac MDCT has a strong potential to detect many qualitative and quantitative abnormalities of the right ventricle in patients with ARVD/C. Limitations include implantable cardioverter-defibrillators and motion artifacts, along with well-known radiation and contrast-induced reaction.
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