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Left ventricular outflow tract obstruction in patients with Ebstein anomalyCentral MessagePerspective [PDF]

open access: yesJTCVS Open, 2023
Objective: In this study, we investigated the clinical characteristics of patients with Ebstein anomaly and left ventricular outflow tract (LVOT) obstruction as well as possible mechanisms of obstruction as assessed by 2-dimensional echocardiography ...
Defne Gunes Ergi, MD   +5 more
doaj   +2 more sources

Catheter ablation of macro-reentrant atrial tachycardia in adults with Ebstein anomaly: A narrative review [PDF]

open access: yesHeart Rhythm O2
Improving survival rates of patients with Ebstein anomaly have increased the relevance of catheter ablation of macro-reentrant atrial tachycardia (MRAT). Our objectives were, first, to present a case report and, second, to provide a comprehensive review.
Norman C. Wang, MD, MS, FHRS   +8 more
doaj   +2 more sources

Late‐Onset Third Degree Atrioventricular Block in Adult With Surgically Corrected Ebstein Anomaly: A Case Report [PDF]

open access: yesClinical Case Reports
Late‐onset third‐degree atrioventricular (AV) block is a rare life‐threatening complication that may develop years after surgical correction of Ebstein anomaly.
Bishal Kumar Yadav   +6 more
doaj   +2 more sources

Management of Ebstein Anomaly in the Current Era: The Story of One Fetus and the Collaboration of Many—A Case Report [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Collaborative multicenter research has significantly increased our understanding of fetal Ebstein anomaly, delineating risk factors for adverse outcomes as well as predictors of postnatal management.
Ann Kavanaugh-McHugh   +8 more
doaj   +2 more sources

Tricuspid valve septal displacement cutoff value for mortality risk following biventricular repair in Ebstein anomaly [PDF]

open access: yesAnnals of Pediatric Cardiology
Background: Surgical intervention is the definitive treatment for Ebstein anomaly, offering both biventricular and nonbiventricular repair options.
Dicky Fakhri   +6 more
doaj   +2 more sources

Open window mapping for redo accessory pathway ablation in Ebstein anomaly [PDF]

open access: yesIndian Pacing and Electrophysiology Journal
Accessory pathway ablation in Ebstein anomaly can be significantly more challenging than in structurally normal hearts. An alternative to the conventional approach to mapping APs is to detect points with a high-density mapping catheter based on an ...
Anindya Ghosh   +3 more
doaj   +2 more sources

Ebstein Anomaly in Pregnancy

open access: yesActa Medica Indonesiana, 2017
A 27-year-old primiparous woman with 28 weeks gestational age was admitted to our hospital with worsening shortness of breath. She was diagnosed with Ebstein’s anomaly three years ago, but preferred to be left untreated. The patient was not cyanotic and
Lusiani Rusdi   +4 more
doaj   +4 more sources

Successful ablation of concealed accessory pathway mediated supraventricular tachycardia in a 5-year-old child with Ebstein anomaly [PDF]

open access: yesActa Clinica Croatica
Here we report a case of a 5-year-old boy with Ebstein anomaly and supraventricular tachycardia. He was diagnosed with Ebstein anomaly at the age of 3 months during the workup for afebrile convulsions, and has been followed by a pediatric cardiologist ...
Nikola Krmek   +2 more
doaj   +2 more sources

Ebstein’s Anomaly [PDF]

open access: yesNeonatal Network, 2007
EBSTEIN’S ANOMALY IS A RARE congenital heart defect characterized by displacement of the tricuspid valve leaflets into the right ventricle.1The defect was first described by Wilhelm Ebstein in 1866.2This anomaly of the tricuspid valve causes the right atrium to thin and become enlarged, resulting in a wide range of clinical presentations.3Clinical ...
Christine H, Attenhofer Jost   +4 more
openaire   +4 more sources

Ebstein Anomaly and Right Aortic Arch in Patient with Charge Syndrome

open access: yesMedicina, 2021
Ebstein anomaly is a rare congenital heart disease characterized by a varying degree of anatomical and functional abnormalities of tricuspid valve and right ventricle. It often coexists with other congenital cardiac malformations.
Inguna Lubaua, Madara Teraudkalna
doaj   +1 more source

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