Ebstein's Anomaly of the Tricuspid Valve: an Overview of Pathology and Management.
ACHD
Cone repair
Congenital heart disease
Ebstein’s anomaly
Tricuspid valve
Journal
Current cardiology reports
ISSN: 1534-3170
Titre abrégé: Curr Cardiol Rep
Pays: United States
ID NLM: 100888969
Informations de publication
Date de publication:
09 10 2020
09 10 2020
Historique:
accepted:
02
09
2020
entrez:
10
10
2020
pubmed:
11
10
2020
medline:
24
4
2021
Statut:
epublish
Résumé
Ebstein's anomaly (EA) is a rare, but complex form of congenital heart disease consisting of a right ventricular myopathy and morphologic tricuspid valve disease leading to a high incidence of right ventricular dysfunction and arrhythmias. This review offers an updated overview of the current understanding and management of patients with EA with a focus on the adult population. Increased understanding of anatomic accessory atrioventricular pathways in EA has resulted in an improvement in ablation techniques and long-term freedom of atrial arrhythmia recurrence. Despite an improvement in understanding and recognition of EA, significant disease heterogeneity and complex treatment options continue to challenge providers, with the best outcomes achieved at expert congenital heart disease centers.
Identifiants
pubmed: 33037480
doi: 10.1007/s11886-020-01412-z
pii: 10.1007/s11886-020-01412-z
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM