Abstract:
:Ebstein anomaly is a congenital malformation involving primarily the tricuspid valve, with failure of delamination from the underlying myocardium and right ventricular myopathy. Echocardiography is diagnostic in most patients and demonstrates apical displacement of the septal leaflet and variable tethering of leaflet tissue to the right ventricular myocardium. Operative intervention is considered for exertional symptoms, progressive right ventricular enlargement, or right ventricular dysfunction. Tricuspid valve cone repair is the preferred surgical approach. Tricuspid valve replacement and bidirectional cavopulmonary shunt also are considered in patients with advanced disease. Pregnancy generally is well tolerated. Patients with Ebstein anomaly require lifelong follow-up.
journal_name
Cardiol Clinjournal_title
Cardiology clinicsauthors
Fuchs MM,Connolly HMdoi
10.1016/j.ccl.2020.04.004subject
Has Abstractpub_date
2020-08-01 00:00:00pages
353-363issue
3eissn
0733-8651issn
1558-2264pii
S0733-8651(20)30027-8journal_volume
38pub_type
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journal_title:Cardiology clinics
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journal_title:Cardiology clinics
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journal_title:Cardiology clinics
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