Results 21 to 30 of about 200,194 (156)

Intraoperative Hemodynamic Instability in a Patient With Ebstein’s Anomaly Complicated With Eisenmenger Syndrome

open access: yesCase Reports in Cardiology
Ebstein’s anomaly is a rare congenital displacement of the tricuspid valve resulting in atrialization of the right ventricle. About half of the patients with Ebstein’s anomaly also have atrial septal defects, which may lead to chronic shunting and ...
Leonardo A. Marquez Roa   +4 more
doaj   +2 more sources

Ebstein Anomaly in Pregnancy [PDF]

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   +3 more sources

Ebstein\'s anomaly and a rare coagulation disorder – Case report and review of literature [PDF]

open access: yesZdravniški Vestnik, 2009
Backgrounds: Ebstein’s anomaly of tricuspid valve is a rare congenital heart anomaly. Surgical implantation of artefi cial tricuspid valve is a standard treatment modality.
Jure Dolenc   +4 more
doaj   +1 more source

Perioperative Management for Surgical Repair of Ebstein's Anomaly.

open access: yesAlbanian Journal of Trauma and Emergency Surgery, 2021
Background: Ebstein's anomaly is a rare and complex heart defect that affects the tricuspid valve and is accountable for around 1% of congenital cardiac abnormalities.
Marsela Goga   +6 more
doaj   +1 more source

Agonal Rhythm: Not Always a Herald of Death! A Rare Presentation of Ebstein’s Anomaly

open access: yesIndian Journal of Clinical Cardiology, 2023
An agonal rhythm is a variant of idioventricular rhythm often preceding asystole. It reflects significant myocardial or metabolic derangement and has a grave prognosis.
Syed Imamuddin   +4 more
doaj   +1 more source

Atrial septal defect device closure and concurrent atrio‐fascicular Mahaim ablation in adult patient with Ebstein's anomaly

open access: yesClinical Case Reports, 2022
Ebstein's anomaly is an uncommon congenital malformation which might be associated with atrial septal defect and atrio‐fascicular Mahaim. Here, we report a known case of Ebstein's anomaly with atrial septal defect and concomitant atrio‐fascicular Mahaim ...
Zahra Khajali   +4 more
doaj   +1 more source

Anesthetic management for patient with severe cyanosis following bioprosthetic valve stenosis [PDF]

open access: yesRevista Brasileira de Anestesiologia, 2019
We presented a 39-year-old female patient with life-threatening hypoxemia after tricuspid valve replacement because of Ebstein's anomaly. And the severe cyanosis is due to bioprosthetic valve stenosis and atrial septal defect.
Jun Zeng, Wei Wei
doaj   +5 more sources

Successful pregnancy in a patient with Ebstein’s anomaly: a case report and review of literature [PDF]

open access: yes, 2017
Ebstein’s anomaly, a rare congenital heart disease, has an extremely variable natural history, depending on variety of pathological features. We here describe a case of a patient with Ebstein’s anomaly who had an uneventful vaginal delivery of a healthy ...
Pegu, Bhabani   +3 more
core   +1 more source

Postpartum Deterioration of Hemodynamics in a Case of Uncorrected Ebstein's Anomaly

open access: yesCase Reports in Cardiology, 2012
Ebstein's anomaly is a rare congenital cardiac malformation that is characterized by abnormalities of the tricuspid valve and right ventricle. Pregnancy is usually well tolerated unless cyanosis or arrhythmia develops.
Masato Kimura   +5 more
doaj   +1 more source

Congenital tricuspid valve malformation with Ebstein’s anomaly in a Golden Retriever

open access: yes, 2006
A case of Ebstein’s anomaly leading to right-sided heart failure in a one-year-old female Golden Retriever is reported. Clinical examination and investigations such as blood analysis, ECG, X-Ray, echocardiography and conservative therapy are described ...
Chiers, K., Deprest, C., French, A.
core   +4 more sources

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