Imaging and guiding intervention for tricuspid valve disorders using 3-dimensional transesophageal echocardiography in pediatric and congenital heart disease.

3-dimensional transesophageal echocardiography Congenital heart disease Tricuspid regurgitation Tricuspid valve disorder Tricuspid valve intervention Tricuspid valve-in-valve procedure

Journal

The international journal of cardiovascular imaging
ISSN: 1875-8312
Titre abrégé: Int J Cardiovasc Imaging
Pays: United States
ID NLM: 100969716

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 24 02 2023
accepted: 09 06 2023
pubmed: 21 6 2023
medline: 21 6 2023
entrez: 21 6 2023
Statut: ppublish

Résumé

In the pediatric and congenital heart disease (CHD) population, tricuspid valve (TV) disorders are complex due to the variable TV morphology, its sophisticated interaction with the right ventricle as well as associated congenital and acquired lesions. While surgery is the standard of care for TV dysfunction in this patient population, transcatheter treatment for bioprosthetic TV dysfunction has been performed successfully. Detailed and accurate anatomic assessment of the abnormal TV is essential in the preoperative/preprocedural planning. Three-dimensional transthoracic and 3D transesophageal echocardiography (3DTEE) provides added value to 2-dimensional imaging in the characterization of the TV to guide therapy and 3DTEE serves as an excellent tool for intraoperative assessment and procedural guidance of transcatheter treatment. Notwithstanding advances in imaging and therapy, the timing and indication for intervention for TV disorders in this population are not well defined. In this manuscript, we aim to review the available literature, provide our institutional experience with 3DTEE, and briefly discuss the perceived challenges and future directions in the assessment, surgical planning, and procedural guidance of (1) congenital TV malformations, (2) acquired TV dysfunction from transvenous pacing leads, or following cardiac surgeries, and (3) bioprosthetic TV dysfunction.

Identifiants

pubmed: 37341949
doi: 10.1007/s10554-023-02898-8
pii: 10.1007/s10554-023-02898-8
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1855-1864

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature B.V.

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Auteurs

Tam T Doan (TT)

Echocardiography Laboratory, The Lillie Frank Abercrombie Section of Pediatric Cardiology, Texas Children's Hospital, 6651 Main Street, MC E1920, Houston, TX, 77030, USA. tam.doan@bcm.edu.
Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA. tam.doan@bcm.edu.

Ricardo H Pignatelli (RH)

Echocardiography Laboratory, The Lillie Frank Abercrombie Section of Pediatric Cardiology, Texas Children's Hospital, 6651 Main Street, MC E1920, Houston, TX, 77030, USA.
Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.

Dhaval R Parekh (DR)

Texas Adult Congenital Heart Center, The Lillie Frank Abercrombie Section of Pediatric Cardiology, Texas Children's Hospital, Houston, TX, 77030, USA.
Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.
Department of Medicine, Baylor College of Medicine, Houston, TX, 77030, USA.

Anitha Parthiban (A)

Echocardiography Laboratory, The Lillie Frank Abercrombie Section of Pediatric Cardiology, Texas Children's Hospital, 6651 Main Street, MC E1920, Houston, TX, 77030, USA.
Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.

Classifications MeSH