Transcatheter Pulmonary Valve Replacement With the Melody Valve in Small Diameter Expandable Right Ventricular Outflow Tract Conduits
Autor: | Jamil Aboulhosn, Britton C. Keeshan, Younes Boudjemline, Daniel S. Levi, Hoang H. Nguyen, Doff B. McElhinney, Lynn F. Peng, Robert G. Gray, Athar M. Qureshi, Thomas K. Jones, Henri Justino, David T. Balzer, Jeremy D. Asnes, Mary Hunt Martin, Holly Bauser-Heaton, Shabana Shahanavaz |
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Rok vydání: | 2017 |
Předmět: |
Adult
Male medicine.medical_specialty Cardiac Catheterization Small diameter Time Factors Adolescent medicine.medical_treatment 030204 cardiovascular system & hematology Prosthesis Design Ventricular Outflow Obstruction 03 medical and health sciences Blood Vessel Prosthesis Implantation Young Adult 0302 clinical medicine Pulmonary Valve Replacement Internal medicine medicine.artery medicine Ventricular outflow tract Humans 030212 general & internal medicine Child Tetralogy of Fallot Retrospective Studies Heart Valve Prosthesis Implantation Pulmonary Valve business.industry Angiography Graft Occlusion Vascular Hemodynamics Stent medicine.disease United States Blood Vessel Prosthesis Treatment Outcome Child Preschool Heart Valve Prosthesis Pulmonary artery Cardiology Feasibility Studies Female Cardiology and Cardiovascular Medicine business Preliminary Data |
Zdroj: | JACC. Cardiovascular interventions. 11(6) |
ISSN: | 1876-7605 |
Popis: | This study sought to evaluate the safety, feasibility, and outcomes of transcatheter pulmonary valve replacement (TPVR) in conduits ≤16 mm in diameter.The Melody valve (Medtronic, Minneapolis, Minnesota) is approved for the treatment of dysfunctional right ventricular outflow tract (RVOT) conduits ≥16 mm in diameter at the time of implant. Limited data are available regarding the use of this device in smaller conduits.The study retrospectively evaluated patients from 9 centers who underwent percutaneous TPVR into a conduit that was ≤16 mm in diameter at the time of implant, and reported procedural characteristics and outcomes.A total of 140 patients were included and 117 patients (78%; median age and weight 11 years of age and 35 kg, respectively) underwent successful TPVR. The median original conduit diameter was 15 (range: 9 to 16) mm, and the median narrowest conduit diameter was 11 (range: 4 to 23) mm. Conduits were enlarged to a median diameter of 19 mm (29% larger than the implanted diameter), with no difference between conduits. There was significant hemodynamic improvement post-implant, with a residual peak RVOT pressure gradient of 7 mm Hg (p 0.001) and no significant pulmonary regurgitation. During a median follow-up of 2.0 years, freedom from RVOT reintervention was 97% and 89% at 2 and 4 years, respectively, and there were no deaths and 5 cases of endocarditis (incidence rate 2.0% per patient-year).In this preliminary experience, TPVR with the Melody valve into expandable small diameter conduits was feasible and safe, with favorable early and long-term procedural and hemodynamic outcomes. |
Databáze: | OpenAIRE |
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