Results 31 to 40 of about 239,154 (181)
Anesthetic management for patient with severe cyanosis following bioprosthetic valve stenosis [PDF]
Revista 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
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Journal of Cardiovascular Magnetic Resonance, 2018 Background Myocardial fibrosis is a common pathophysiological process that is related to ventricular remodeling in congenital heart disease. However, the presence, characteristics, and clinical significance of myocardial fibrosis in Ebstein’s anomaly ...
Dan Yang +12 more
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Management of Ebstein’s anomaly [PDF]
Annals of Cardiothoracic Surgery, 2017 Ebstein malformation is a rare disease that presents with a spectrum of severity. We use a management paradigm that breaks the anomaly into two groups: neonates and children/adults. This leads to a discussion of management and operative techniques as well as pitfalls.
Irving L, Kron, Mark Elliot, Roeser
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, 2023 Ebstein's anomaly is a fairly rare congenital heart defect. The frequency is 1%. Patients with Ebstein's anomaly without heart failure and cyanosis are undergoing pregnancy well.
Kuvonchbek, Turkmanov +3 more
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Repair of Ebstein's Anomaly [PDF]
The Annals of Thoracic Surgery, 2004 Ebstein’s anomaly is a tricuspid valve anomaly associated with poor right ventricular contractility in severe cases. Surgery is indicated in all symptomatic patients. Tricuspid valve repair is possible in most of the cases with mobilization of the anterior leaflet and longitudinal plication of the atrialized chamber.
openaire +2 more sources
Mortality in Patients With Ebstein Anomaly
Journal of the American College of Cardiology, 2023 Low birth prevalence and referral bias constitute significant obstacles to elucidating the natural history of Ebstein anomaly (EA).An extensive 2-country register-based collaboration was performed to investigate the mortality in patients with EA.Patients born from 1970 to 2017 and diagnosed with EA were identified in Danish and Swedish nationwide ...
Filip Eckerström +4 more
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A Rare Manifestation of Asymptomatic Ebstein’s Anomaly with Tricuspid Valve Endocarditis
Case Reports in Cardiology, 2017 Ebstein’s anomaly is a rare congenital heart disease that presents with apical displacement of the septal and posterior leaflets of the tricuspid valve. It has a wide spectrum of clinical presentations and has been shown to manifest itself any time from ...
Carmel Moazez +3 more
doaj +1 more source
A case of severe Ebstein's anomaly with incompetent pulmonary valve
The Turkish Journal of Pediatrics, 2002 A case of Ebstein's anomaly with functional pulmonary atresia diagnosed in utero is presented. The diagnosis was confirmed by postnatal echocardiographic, angiographic, and postmortem pathologic findings.
Süheyla Ozkutlu +3 more
doaj +1 more source
BMJ Case Reports, 2012 A 36-year-old Gravida 2, Para 1 woman at 34 weeks’ menstrual age was referred for a fetal echocardiogram in view of fetal hydrops detected by obstetric sonography. She gave a history of consanguineous marriage and her first child was healthy. Fetal echocardiogram (four-chamber view) performed revealed findings consistent with Ebstein's anomaly; a ...
Ranjan K, Shetty +3 more
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Paradoxical embolism in Ebstein's anomaly [PDF]
, 2001 A 26-year-old man with Ebstein's anomaly had cerebellar infarction due to paradoxical embolism. Ebstein's anomaly is characterized by a downward displacement of the tricuspid valve into the right ventricle due to anomalous attachment of the tricuspid ...
Uyan, Ayten Pamukçu +3 more
core +2 more sources