Background and aims of the study: The potential advantages of the Ross proc
edure in children under 10 years of age have yet to be validated. Concerns
remain regarding progressive dilatation of the pulmonary autograft and pote
ntial homograft stenosis. We present our experience in this age population.
Methods: A retrospective analysis of aortic root replacement using the Ross
procedure in 11 young children (nine males, two females; median age 84 mon
ths; range 3 months to 10 years) between January 1996 and January 1999 was
performed jointly in two pediatric surgical centers.
Results: There were no operative deaths. Mean hospital stay was 12 +/- 4 da
ys, and mean follow up 14.5 +/- 8 months. The event-free survival (death, r
eoperation, endocarditis, arrhythmia) was 100%. Currently, nine children ar
e in NYHA functional class I, and two in class II. The autograft and homogr
aft were evaluated by serial echocardiography. There was no sign of progres
sive dilatation of the autograft. Aortic regurgitation was trivial in four
children and mild in seven. No growth of the autograft was noted; this was
consistent with minimal somatic growth. Homograft peak gradients remained l
ow during the follow up.
Conclusions: Although the pulmonary autograft procedure is more complex tha
n other types of aortic valve replacement, it can be safely applied in chil
dren. Early follow up indicates satisfactory performance of the autograft.
If dilatation will not occur, pulmonary root autograft may be an attractive
substitute for diseased aortic valves in children.