Outcomes after the Ross procedure with pulmonary autograft reinforcement by reimplantation.

CT, computed tomography Ross procedure aortic valve repair congenital heart disease

Journal

JTCVS techniques
ISSN: 2666-2507
Titre abrégé: JTCVS Tech
Pays: United States
ID NLM: 101768546

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 14 06 2022
revised: 31 10 2022
accepted: 14 11 2022
entrez: 23 2 2023
pubmed: 24 2 2023
medline: 24 2 2023
Statut: epublish

Résumé

Pulmonary autograft reinforcement to prevent dilatation and subsequent neo-aortic valve regurgitation has been reported; however, data on long-term function of the neo-aortic valve after this modified Ross procedure are lacking. Our objective here was to assess long-term outcomes of the modified Ross procedure with autograft reinforcement using the reimplantation technique. The outcomes of 61 consecutive patients managed using the Dacron-conduit reinforced Ross procedure between 2009 and 2021 were reviewed. Most patients had a unicuspid or bicuspid aortic valve (n = 52; 85%), predominant aortic valve regurgitation (n = 42; 77%), and >30 mm dilatation of the ascending aorta (n = 33; 54%). A prior aortic valve procedure was noted in 47 patients (77%) patients, including 38 (62%) with surgical repair and 9 (15%) with balloon dilatation. The pulmonary autograft was reimplanted within a Dacron conduit with a median diameter of 25.6 mm (range, 20-30 mm) using the David valve-sparing aortic root replacement technique. All patients survived. The median age at surgery was 16.8 years (range, 6-38 years). Neo-aortic valve replacement was required in 3 patients (4.9%; 95% CI, 0.34%- 12.7%) because of infective endocarditis, left ventricular false aneurysm, and leaflet perforation, respectively; the repeat procedure was done early in 2 of these patients (2 of 61; 3%). Six patients required right ventricular outflow conduit replacement, 5 by surgery and 1 percutaneously. The median duration of follow-up was 90 months (range, 10-124 months). The 5- and 10-year rates of reintervention-free survival were 84.3% (95% CI, 74%-95%) and 81.6% (95% CI, 72%-93%), respectively, and 5-year survival without aortic reintervention was 94.5% (95% CI, 88%-100%), with little change at 10 years. No patients experienced deterioration of initial neo-aortic valve function (ie, regurgitation or stenosis). Autograft reinforcement using the reimplantation technique allowed expansion of Ross procedure indications to all patients requiring aortic valve replacement and prevented neo-aortic root dilatation. Failures were uncommon. Long-term follow-up data showed stable neo-aortic valve function.

Sections du résumé

Background UNASSIGNED
Pulmonary autograft reinforcement to prevent dilatation and subsequent neo-aortic valve regurgitation has been reported; however, data on long-term function of the neo-aortic valve after this modified Ross procedure are lacking. Our objective here was to assess long-term outcomes of the modified Ross procedure with autograft reinforcement using the reimplantation technique.
Patients UNASSIGNED
The outcomes of 61 consecutive patients managed using the Dacron-conduit reinforced Ross procedure between 2009 and 2021 were reviewed. Most patients had a unicuspid or bicuspid aortic valve (n = 52; 85%), predominant aortic valve regurgitation (n = 42; 77%), and >30 mm dilatation of the ascending aorta (n = 33; 54%). A prior aortic valve procedure was noted in 47 patients (77%) patients, including 38 (62%) with surgical repair and 9 (15%) with balloon dilatation. The pulmonary autograft was reimplanted within a Dacron conduit with a median diameter of 25.6 mm (range, 20-30 mm) using the David valve-sparing aortic root replacement technique.
Results UNASSIGNED
All patients survived. The median age at surgery was 16.8 years (range, 6-38 years). Neo-aortic valve replacement was required in 3 patients (4.9%; 95% CI, 0.34%- 12.7%) because of infective endocarditis, left ventricular false aneurysm, and leaflet perforation, respectively; the repeat procedure was done early in 2 of these patients (2 of 61; 3%). Six patients required right ventricular outflow conduit replacement, 5 by surgery and 1 percutaneously. The median duration of follow-up was 90 months (range, 10-124 months). The 5- and 10-year rates of reintervention-free survival were 84.3% (95% CI, 74%-95%) and 81.6% (95% CI, 72%-93%), respectively, and 5-year survival without aortic reintervention was 94.5% (95% CI, 88%-100%), with little change at 10 years. No patients experienced deterioration of initial neo-aortic valve function (ie, regurgitation or stenosis).
Conclusions UNASSIGNED
Autograft reinforcement using the reimplantation technique allowed expansion of Ross procedure indications to all patients requiring aortic valve replacement and prevented neo-aortic root dilatation. Failures were uncommon. Long-term follow-up data showed stable neo-aortic valve function.

Identifiants

pubmed: 36820346
doi: 10.1016/j.xjtc.2022.11.016
pii: S2666-2507(22)00596-X
pmc: PMC9938391
doi:

Types de publication

Journal Article

Langues

eng

Pagination

121-128

Informations de copyright

© 2023 The Authors.

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Auteurs

Lisa Guirgis (L)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Sébastien Hascoet (S)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Isabelle Van Aerschot (I)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Jelena Radojevic (J)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Mohamed Ly (M)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Sarah Cohen (S)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Emre Belli (E)

Department of Pediatric and Congenital Heart Disease, Marie Lannelongue Hospital, University Paris-Saclay, Le Plessis-Robinson, France.

Classifications MeSH