Long-Term Outcomes of Patients Undergoing the Ross Procedure.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
23 03 2021
Historique:
received: 19 08 2020
revised: 18 01 2021
accepted: 19 01 2021
entrez: 19 3 2021
pubmed: 20 3 2021
medline: 7 10 2021
Statut: ppublish

Résumé

Treatment of aortic-valve disease in young patients still poses challenges. The Ross procedure offers several potential advantages that may translate to improved long-term outcomes. This study reports long-term outcomes after the Ross procedure. Adult patients who were included in the Ross Registry between 1988 and 2018 were analyzed. Endpoints were overall survival, reintervention, and major adverse events at maximum follow-up. Multivariable regression analyses were performed to identify risk factors for survival and the need of Ross-related reintervention. There were 2,444 adult patients with a mean age of 44.1 ± 11.7 years identified. Early mortality was 1.0%. Estimated survival after 25 years was 75.8% and did not statistically differ from the general population (p = 0.189). The risk for autograft reintervention was 0.69% per patient-year and 0.62% per patient-year for right-ventricular outflow tract (RVOT) reintervention. Larger aortic annulus diameter (hazard ratio [HR]: 1.12/mm; 95% confidence interval [CI]: 1.05 to 1.19/mm; p < 0.001) and pre-operative presence of pure aortic insufficiency (HR: 1.74; 95% CI: 1.13 to 2.68; p = 0.01) were independent predictors for autograft reintervention, whereas the use of a biological valve (HR: 8.09; 95% CI: 5.01 to 13.08; p < 0.001) and patient age (HR: 0.97 per year; 95% CI: 0.96 to 0.99; p = 0.001) were independent predictors for RVOT reintervention. Major bleeding, valve thrombosis, permanent stroke, and endocarditis occurred with an incidence of 0.15% per patient-year, 0.07% per patient-year, 0.13%, and 0.36% per patient-year, respectively. The Ross procedure provides excellent survival over a follow-up period of up to 25 years. The rates of reintervention, anticoagulation-related morbidity, and endocarditis were very low. This procedure should therefore be considered as a very suitable treatment option in young patients suffering from aortic-valve disease. (Long-Term Follow-up After the Autograft Aortic Valve Procedure [Ross Operation]; NCT00708409).

Sections du résumé

BACKGROUND
Treatment of aortic-valve disease in young patients still poses challenges. The Ross procedure offers several potential advantages that may translate to improved long-term outcomes.
OBJECTIVES
This study reports long-term outcomes after the Ross procedure.
METHODS
Adult patients who were included in the Ross Registry between 1988 and 2018 were analyzed. Endpoints were overall survival, reintervention, and major adverse events at maximum follow-up. Multivariable regression analyses were performed to identify risk factors for survival and the need of Ross-related reintervention.
RESULTS
There were 2,444 adult patients with a mean age of 44.1 ± 11.7 years identified. Early mortality was 1.0%. Estimated survival after 25 years was 75.8% and did not statistically differ from the general population (p = 0.189). The risk for autograft reintervention was 0.69% per patient-year and 0.62% per patient-year for right-ventricular outflow tract (RVOT) reintervention. Larger aortic annulus diameter (hazard ratio [HR]: 1.12/mm; 95% confidence interval [CI]: 1.05 to 1.19/mm; p < 0.001) and pre-operative presence of pure aortic insufficiency (HR: 1.74; 95% CI: 1.13 to 2.68; p = 0.01) were independent predictors for autograft reintervention, whereas the use of a biological valve (HR: 8.09; 95% CI: 5.01 to 13.08; p < 0.001) and patient age (HR: 0.97 per year; 95% CI: 0.96 to 0.99; p = 0.001) were independent predictors for RVOT reintervention. Major bleeding, valve thrombosis, permanent stroke, and endocarditis occurred with an incidence of 0.15% per patient-year, 0.07% per patient-year, 0.13%, and 0.36% per patient-year, respectively.
CONCLUSIONS
The Ross procedure provides excellent survival over a follow-up period of up to 25 years. The rates of reintervention, anticoagulation-related morbidity, and endocarditis were very low. This procedure should therefore be considered as a very suitable treatment option in young patients suffering from aortic-valve disease. (Long-Term Follow-up After the Autograft Aortic Valve Procedure [Ross Operation]; NCT00708409).

Identifiants

pubmed: 33736823
pii: S0735-1097(21)00203-5
doi: 10.1016/j.jacc.2021.01.034
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00708409']

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1412-1422

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures The authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Anas Aboud (A)

Department of Cardiac and Thoracic Vascular Surgery, University Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Lübeck, Lübeck, Germany. Electronic address: Anas.Aboud@uksh.de.

Efstratios I Charitos (EI)

Department of Cardiac Surgery, University of Bonn, Bonn, Germany.

Buntaro Fujita (B)

Department of Cardiac and Thoracic Vascular Surgery, University Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Lübeck, Lübeck, Germany.

Ulrich Stierle (U)

Department of Cardiac and Thoracic Vascular Surgery, University Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany.

Jan-Christian Reil (JC)

Department of Cardiology, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany.

Vladimir Voth (V)

Sana Cardiac Surgery Stuttgart, Stuttgart, Germany.

Markus Liebrich (M)

Sana Cardiac Surgery Stuttgart, Stuttgart, Germany.

Martin Andreas (M)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Tomas Holubec (T)

Department of Thoracic and Cardiovascular Surgery, University Hospital Frankfurt, Frankfurt, Germany.

Constanze Bening (C)

Department of Cardiovascular Surgery, University Hospital Würzburg, Würzburg, Germany.

Marc Albert (M)

Department of Cardiac and Vascular Surgery, Robert-Bosch-Hospital, Stuttgart, Germany.

Petr Fila (P)

Centre of Cardiovascular Surgery and Transplantation, Brno, Czech Republic.

Jiri Ondrasek (J)

Centre of Cardiovascular Surgery and Transplantation, Brno, Czech Republic.

Peter Murin (P)

Department of Congenital Heart Disease and Paediatric Cardiology, German Heart Center, Berlin, Germany.

Rüdiger Lange (R)

Department of Cardiovascular Surgery, German Heart Center, Munich, Germany.

Hermann Reichenspurner (H)

Department of Cardiovascular Surgery, University Heart Center Hamburg, Hamburg, Germany.

Ulrich Franke (U)

Department of Cardiac and Vascular Surgery, Robert-Bosch-Hospital, Stuttgart, Germany.

Armin Gorski (A)

Department of Cardiovascular Surgery, University Hospital Würzburg, Würzburg, Germany.

Anton Moritz (A)

Department of Thoracic and Cardiovascular Surgery, University Hospital Frankfurt, Frankfurt, Germany.

Günther Laufer (G)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Wolfgang Hemmer (W)

Sana Cardiac Surgery Stuttgart, Stuttgart, Germany.

Hans-Hinrich Sievers (HH)

Department of Cardiac and Thoracic Vascular Surgery, University Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany.

Stephan Ensminger (S)

Department of Cardiac and Thoracic Vascular Surgery, University Heart Center Lübeck, University Hospital Schleswig-Holstein, Lübeck Campus, Lübeck, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Lübeck, Lübeck, Germany.

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