Pulmonary Artery Stenosis in Tetralogy of Fallot.

Journal

Cardiology in review

ISSN: 1538-4683

Titre abrégé: Cardiol Rev

Pays: United States

ID NLM: 9304686

Informations de publication

Date de publication:
15 Nov 2023

Historique:

medline: 15 11 2023

pubmed: 15 11 2023

entrez: 15 11 2023

Statut: aheadofprint

Résumé

Tetralogy of Fallot (TOF) is the most common cyanotic congenital cardiac defect. The survival rate after primary complete repair is high (98-100%); however, pulmonary artery stenosis (PAS) is not uncommon after TOF repair, and severe PAS aggravates pulmonary regurgitation, resulting in right ventricle dilation, ventricular arrhythmia, and possibly death. PAS in TOF can be congenital due to hypoplasia or coarctation or can be acquired secondary to a surgical procedure. The latter may be caused by an exogenous conduit implant, compression from the adjacent enlarged ascending aorta, or outflow tract dilation after transannular patch repair. PAS can also be caused by the pulmonary artery plasty strategy itself. Here, the intrinsic mechanisms underlying PAS and pulmonary artery plasty techniques and strategies are reviewed to provide guidance for surgeons.

Identifiants

DOI: 10.1097/CRD.0000000000000627 PMID: 37966279

pubmed: 37966279

doi: 10.1097/CRD.0000000000000627

pii: 00045415-990000000-00172

doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

Informations de copyright

Déclaration de conflit d'intérêts

Disclosure: The authors declare no conflict of interest.

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