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Updated: Jan 25, 2026

A Rodent Model of The Ross Operation: Syngeneic Pulmonary Artery Graft Implantation in A Systemic Position
Published on: April 1, 2022
Long-Term Fate of the Neoaortic Root After Neonatal Ross Operation: A Case Series
Nicola Pradegan1, Biagio Castaldi2, Danila Azzolina3
11 Pediatric and Congenital Cardiac Surgery Unit, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Padua, Italy.
Insights
The pulmonary autograft shows excellent long-term adaptation in children after the Ross procedure. This study confirms the viability of using infant pulmonary tissue for aortic valve replacement during growth.
Area of Science:
- Cardiovascular Surgery
- Pediatric Cardiology
- Thoracic Surgery
Background:
- The Ross operation is a surgical procedure for aortic valve disease.
- Pulmonary autografts are used as a substitute for the aortic valve.
- Long-term adaptation of infant pulmonary autografts during somatic growth requires further investigation.
Purpose of the Study:
- To analyze the adaptation properties of the pulmonary autograft in infants undergoing the Ross operation.
- To assess the long-term outcomes of pulmonary autografts in pediatric patients.
Main Methods:
- Serial echocardiographic assessments of autograft diameters were performed.
- Autograft diameters were reported as Z scores relative to normal aortic and pulmonary diameters.
- Follow-up data was collected for a median of 18.5 years.
Main Results:
- All patients survived the follow-up period.
- No autograft reinterventions were required.
- The pulmonary autograft demonstrated excellent adaptation and growth potential.
Conclusions:
- The infant pulmonary autograft exhibits excellent long-term adaptation potential.
- The Ross operation using a pulmonary autograft is a viable option for pediatric aortic valve replacement.
- Pulmonary autografts can accommodate somatic growth in pediatric patients effectively.
Abstract:
The aim of this study is to analyze the adaptation properties of the pulmonary autograft in four infants who underwent the Ross operation before one year of life. The patients underwent serial echocardiographic assessments of the autograft diameters at short- and long-term follow-up and values were reported as the Z scores for normal aortic and pulmonary diameters. At a median follow-up time of 18.5 years (range: 18.2-19.4 years), all the patients are alive, none requiring autograft reinterventions. This series shows excellent adaptation potential of the "infant pulmonary autograph" in the long-term, during somatic growth of the patient.
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