ReviewCardiovascular diagnosis and therapy2021
Narrative review of Ebstein's anomaly beyond childhood: Imaging, surgery, and future perspectives.
Review in Cardiovascular diagnosis and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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Who cites it
8 citing papers in PubMed, 10 citations in OpenAlex.
- Review
- CCTA of Pediatric Congenital Right Heart Obstructive Lesions: A Pictorial Review.Diagnostics (Basel, Switzerland) · 2026Review
- Totally thoracoscopic beating-heart tricuspid valve repair 30 years after Ebstein's anomaly surgery: a case report and literature review.Journal of cardiothoracic surgery · 2026Review
- Advanced Echocardiographic Characterization of Neonatal Ebstein's Anomaly Using Myocardial Deformation Imaging: A Single-Center Study.Life (Basel, Switzerland) · 2026Article
- A comparison of the severity of tricuspid valve regurgitation between echocardiographic and cardiac magnetic resonance criteria in adults with congenital heart disease.Frontiers in cardiovascular medicine · 2026Article
- Article
- Favourable outcome ofSouthern African journal of infectious diseases · 2025Article
- Complimentary Cardiac Computed Tomography Ventricular Volumetry-Derived Metrics of Severity in Patients with Ebstein Anomaly: Comparison with Echocardiography-Based Severity Indices.Pediatric cardiology · 2024Article
Corrections and comments
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Authors and funding
16 authors at 3 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ebstein's anomaly is a rare congenital heart disease with malformation of the tricuspid valve and myopathy of the right ventricle. The septal and inferior leaflets adhere to the endocardium due to failure of delamination. This leads to apical displacement of their hinge points with a shift of the functional tricuspid valve annulus towards the right ventricular outflow tract with a possibly restrictive orifice. Frequently, a coaptation gap yields tricuspid valve regurgitation and over time the "atrialized" portion of the right ventricle may dilate. The highly variable anatomy determines the clinical presentation ranging from asymptomatic to very severe with need for early operation. Echocardiography and magnetic resonance imaging are the most important diagnostic modalities to assess the tricuspid valve as well as ventricular morphology and function. While medical management of asymptomatic patients can be effective for many years, surgical intervention is indicated before development of significant right ventricular dilatation or dysfunction. Onset of symptoms and arrhythmias are further indications for surgery. Modified cone reconstruction of the tricuspid valve is the state-of-the-art approach yielding the best results for most patients. Alternative procedures for select cases include tricuspid valve replacement and bidirectional cavopulmonary shunt depending on patient age and other individual characteristics. Long-term survival after surgery is favorable but rehospitalization and reoperation remain significant issues. Further studies are warranted to identify the optimal surgical strategy and timing before adverse right ventricular remodeling occurs. It is this article's objective to provide a comprehensive review of current literature and an overview on the management of Ebstein's Anomaly. It focuses on imaging, cardiac surgery, and outcome. Additionally, a brief insight into arrhythmias and their management is given. The "future perspectives" summarize open questions and fields of future research.
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