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Updated: Dec 9, 2025

Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Right ventricle in heart failure with preserved ejection fraction
Felix Berglund1, Pamela Piña2, César J Herrera3,4
1Cardiology, Södersjukhuset Anestesi Intensivvårdsverksamheten, Stockholm, Sweden.
Right ventricular dysfunction (RVD) is common in heart failure with preserved ejection fraction (HFpEF). Current treatments show limited efficacy, highlighting the need for novel therapeutic strategies and improved diagnostic methods for RVD in HFpEF patients.
Area of Science:
- Cardiology
- Pulmonology
- Medical Imaging
Background:
- Heart failure with preserved ejection fraction (HFpEF) impacts numerous patients, with the right ventricle (RV) emerging as a key area of research.
- Right ventricular dysfunction (RVD) affects a significant portion of HFpEF patients, often linked to pulmonary hypertension and comorbidities.
- Assessing RVD is complex due to the RV's unique anatomy, physiology, and load conditions.
Purpose of the Study:
- To review the current understanding of right ventricular dysfunction (RVD) in heart failure with preserved ejection fraction (HFpEF).
- To discuss the diagnostic challenges and emerging imaging techniques for RVD assessment.
- To highlight the limitations of current pharmacotherapies and the need for novel interventions.
Main Methods:
- Review of existing literature on RVD in HFpEF.
- Discussion of echocardiographic parameters (e.g., FAC, TAPSE, S') for RV function assessment.
- Exploration of advanced imaging modalities like speckle tracking echocardiography and cardiac magnetic resonance (CMR).
- Consideration of RV [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging.
Main Results:
- RVD prevalence in HFpEF ranges from 4% to 50%.
- Pulmonary hypertension and comorbidities like COPD, obesity, sleep apnea, and atrial fibrillation contribute to RVD.
- Standard RV function measurements have limitations; advanced imaging like CMR shows promise.
- RV [18F]FDG PET imaging requires further validation for prognostic significance.
- Current pharmacotherapies (PDE inhibitors, GC stimulators, nitrates) have not improved RVD in HFpEF.
Conclusions:
- RVD is a critical factor in HFpEF pathophysiology and patient outcomes.
- Novel diagnostic tools and imaging techniques are essential for accurate RVD assessment.
- There is an urgent need to develop and evaluate new pharmacological treatments targeting RVD in HFpEF.
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