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The Ross Procedure in Children and Infants: A Systematic Review With Pooled Analyses
Nabil Dib1,2, Walid Ben Ali1, Thierry Ducruet3
1Department of Medicine, Montreal Heart Institute, Université de Montréal, Montreal, Québec, Canada.
Insights
The Ross procedure offers modest survival rates in children with congenital aortic stenosis. However, infants undergoing this surgery face significantly higher mortality and reintervention risks, highlighting the need for careful consideration.
Area of Science:
- Pediatric Cardiac Surgery
- Congenital Heart Disease
- Aortic Valve Replacement
Background:
- The Ross procedure is a surgical option for congenital aortic stenosis, replacing the aortic valve with a pulmonary autograft.
- Outcomes in children, especially infants, following the Ross procedure are not well-established.
Purpose of the Study:
- To systematically review and analyze survival and reintervention rates after the Ross procedure in children.
- To specifically evaluate outcomes in infants (younger than 1 year) compared to older children.
Main Methods:
- Systematic review and pooled analysis of 25 studies including 2737 patients, adhering to PRISMA criteria.
- Extraction of inferred individual patient data from life tables to assess primary endpoints: early (≤30 days) and late (>30 days) mortality.
- Secondary endpoints included freedom from reintervention for the right ventricular outflow tract and pulmonary autograft, with sensitivity analyses for infants.
Main Results:
- Overall pooled early survival was 96.0%, but significantly lower at 86.8% for infants.
- Pooled 10-year survival was 91.1% overall and 79.3% for infants.
- Infants had substantially higher mortality (HR: 3.38) and reintervention rates (51.2% for RVOT) compared to non-infant children, with younger age strongly linked to poorer outcomes.
Conclusions:
- The Ross procedure demonstrates modest survival and autograft reoperation rates in the pediatric population.
- Infancy is a critical factor associated with significantly poorer survival and increased reintervention rates following the Ross procedure.
Background:
The Ross procedure is a surgical option for congenital aortic stenosis that involves replacing the diseased aortic valve with a pulmonary autograft. Little is known about outcomes in children, particularly those younger than 1 year.
Methods:
A systematic review with pooled analyses was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria. Inferred individual patient data were extracted from life tables. The primary end points were early (≤30 days) and late (>30 days) mortality rates following the Ross procedure in children. Secondary end points were freedom from reintervention for the right ventricular outflow tract and pulmonary autograft. These end points were assessed in the overall population of children. Sensitivity analyses were performed in subgroups younger than 1 year of age (infants) and in noninfant children.
Results:
A total of 25 studies on 2737 patients met inclusion criteria. The pooled early survival rate was 96.0% (95% confidence interval [CI]: 95.1%-96.8%) overall and 86.8% (95% CI: 82.1%-90.3%) among infants. Pooled overall 10-year survival, freedom from pulmonary autograft reintervention, and freedom from right ventricular outflow tract reintervention rates were 91.1%, 90.2%, and 79.7%, respectively. Corresponding pooled rates in infants were 79.3%, 87.1%, and 51.2%. Mortality was significantly higher among infants compared with noninfant children (hazard ratio: 3.38, 95% CI: 2.44-4.68; P < 0.001). In metaregression analyses, younger age was strongly associated with poorer survival and higher reintervention rates.
Conclusions:
Modest survival and autograft reoperation rates were observed following the Ross procedure in children. Surgery in infancy was strongly associated with poorer survival and higher reintervention rates.
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