An unusual application of percutaneous pulmonary valve implantation in congenitally corrected transposition of the great arteries
Percutaneous pulmonary valve implantation has emerged as a non-surgical intervention for patients with right ventricular outflow tract dysfunction. Congenitally corrected transposition of the great arteries is a rare congenital heart disease characterized by atrioventricular and ventriculoarterial discordance. The long-term follow-up and management of patients with this condition can be challenging. In this case report, we present a successful percutaneous pulmonary valve implantation in a 19-year-old male patient with physiologically repaired congenitally corrected transposition of the great arteries.
Authors
- Ugan Atik S
- Alper GÜZELTAŞ
- Hicran Gül Emral (ORCID: https://orcid.org/0000-0002-6904-535X)
- İbrahim Cansaran Tanıdır
- Selman Gökalp
Institutions
- University of Health Science (KH)
- Sağlık Bilimleri Üniversitesi (TR)
- Burdur Mehmet Akif Ersoy Üniversitesi (TR)
- University of Health Sciences Antigua (AG)
Publication Details
- Journal
- Turkish Journal of Thoracic and Cardiovascular Surgery
- Published
- 2026-01-09
- DOI
- https://doi.org/10.4274/tjtcs.2025.27478
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00