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The Annals of Thoracic Surgery, Vol 53, 864-870, Copyright © 1992 by The Society of Thoracic Surgeons
MP Leung, RN Lo, H Cheung, J Lee and CK Mok
During a 2 1/2-year period, staged procedures of transventricular closed
pulmonary valvotomy followed by balloon valvuloplasty were attempted in 12
babies with pulmonary atresia and an intact ventricular septum. All babies
immediately underwent valvotomy when echocardiography revealed a tripartite
right ventricle with adequate inflow and outflow dimensions and without
sinusoidal-coronary arterial fistulas. After valvotomy, the overall
mortality rate was 25% (3/12), but the only surgical death (1/12, 8%) was
due to failure to establish continuity between the right ventricular cavity
and the pulmonary trunk. The other 2 babies died of neonatal complications
after successful valvotomy. Angiocardiography performed 5 to 18 months
after valvotomy documented substantial growth of the right ventricular
inflow and outflow dimensions in the 9 survivors. Twelve balloon dilation
procedures were then performed in 7 babies. All except 1 achieved a
significant drop in the right ventricular to left ventricular peak systolic
pressure ratio (0.96 +/- 0.40 to 0.56 +/- 0.28; p less than 0.01). Balloon
valvuloplasty was not required in 1 baby and failed in the other, who then
underwent successful right ventricular outflow tract reconstruction. After
these staged procedures, follow-up at 1 month to 20 months (mean follow-up,
14.8 months) revealed resting cyanosis in 3 babies, which was related to
severe residual infundibular stenosis (55 mm Hg) in 1 and a subnormal
tricuspid valve annulus in 2. The remaining 5 babies (including 1 who
required no valvuloplasty) were active and pink (saturation greater than
97%) and had a mean Doppler estimated gradient of 19 mm Hg (range, 8 to 36
mm Hg) across the pulmonary valve.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Balloon valvuloplasty after pulmonary valvotomy for babies with pulmonary atresia and intact ventricular septum
Department of Paediatrics, Grantham Hospital, University of Hong Kong, Aberdeen.
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