PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 21, 2005Swiss Medical Weekly184 citationsOpen Access

Ebsteins anomaly - review of a multifaceted congenital cardiac condition

DHDavid L. Hayes

Key Result

Ebstein's anomaly is a rare and complex congenital heart defect with a broad clinical spectrum, for which tricuspid valve repair is generally preferred over replacement when surgery is indicated.

Structured PICO

P
Population
A comprehensive review of the diagnosis, clinical features, natural history, and management options for patients with Ebstein's anomaly.

Ebstein's anomaly is a highly variable and complex congenital heart defect that requires individualized management by specialists in congenital heart disease.

Abstract

Ebstein's anomaly (EA) is a rare but fascinating congenital heart disorder accounting for <1% of all congenital heart defects. Since its description in 1866, dramatic advances in diagnosis and therapy have been made. In this review, we describe current diagnostic criteria and classification, natural history, clinical features, and prognosis, typical echocardiographic features and pathologic findings, and the spectrum of associated cardiac malformations including left heart anomalies associated with EA. Differences between Ebstein-like changes associated with congenitally corrected transposition and EA are described. The spectrum of typical ECG and conduction system changes, arrhythmias including accessory pathways and ectopic atrial tachycardias related to EA are also reviewed. Differential diagnosis of EA is discussed including tricuspid valve dysplasia and prolapse as well as arrhythmogenic right ventricular cardiomyopathy. The review describes management options in EA including catheter interventions, indication for operation and surgical options including tricuspid valve repair and replacement. Overall, EA is a complex congenital anomaly with a broad pathologic-anatomical and clinical spectrum and no two patients are alike. Therefore, precise knowledge of the different anatomic and hemodynamic variables, associated malformations and management options are essential. Management of EA patients is complex. Thus it is important that these patients are regularly seen by a cardiologist with expertise in congenital heart disease.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

David L. Hayes (2005) conducted a review in Ebstein's anomaly. Ebstein's anomaly is a rare and complex congenital heart defect with a broad clinical spectrum, for which tricuspid valve repair is generally preferred over replacement when surgery is indicated.

synapsesocial.com/papers/6a9f87914bb82c3c71b2101ahttps://doi.org/10.4414/smw.2005.10985
Ask AI
Helpful
Bookmark
Share
View Full Paper