Long-Term Outcomes of Patients Undergoing the Ross Procedure
Language English Country United States Media print
Document type Journal Article, Observational Study
PubMed
33736823
DOI
10.1016/j.jacc.2021.01.034
PII: S0735-1097(21)00203-5
Knihovny.cz E-resources
- Keywords
- Ross procedure, aortic valve replacement, long-term outcomes, pulmonary autograft, right-ventricular outflow tract,
- MeSH
- Survival Analysis MeSH
- Aortic Valve * pathology surgery MeSH
- Transplantation, Autologous * adverse effects methods MeSH
- Heart Valve Prosthesis Implantation * adverse effects instrumentation methods MeSH
- Long Term Adverse Effects * diagnosis epidemiology etiology MeSH
- Adult MeSH
- Echocardiography methods MeSH
- Risk Assessment methods MeSH
- Humans MeSH
- Aortic Valve Disease * diagnosis epidemiology surgery MeSH
- Postoperative Complications * diagnosis epidemiology etiology surgery MeSH
- Prognosis MeSH
- Registries statistics & numerical data MeSH
- Reoperation * classification methods statistics & numerical data MeSH
- Risk Factors MeSH
- Heart Valve Prosthesis adverse effects statistics & numerical data MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Geographicals
- Germany epidemiology MeSH
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).
Centre of Cardiovascular Surgery and Transplantation Brno Czech Republic
Department of Cardiac and Vascular Surgery Robert Bosch Hospital Stuttgart Germany
Department of Cardiac Surgery Medical University of Vienna Vienna Austria
Department of Cardiac Surgery University of Bonn Bonn Germany
Department of Cardiology University Hospital Schleswig Holstein Lübeck Campus Lübeck Germany
Department of Cardiovascular Surgery German Heart Center Munich Germany
Department of Cardiovascular Surgery University Heart Center Hamburg Hamburg Germany
Department of Cardiovascular Surgery University Hospital Würzburg Würzburg Germany
Department of Congenital Heart Disease and Paediatric Cardiology German Heart Center Berlin Germany
Department of Thoracic and Cardiovascular Surgery University Hospital Frankfurt Frankfurt Germany
References provided by Crossref.org
ClinicalTrials.gov
NCT00708409