Background Treatment of hypoplasia of the entire arch in coarctation is a s
urgical challenge. The current approaches have technical difficulties, high
recurrence rates, and increased morbidity and mortality.
Methods. Over a 14-month period, a combined extended end-to-end repair with
patch enlargement of the concavity of the entire arch was performed in 6 n
eonates and 1 infant; Through a midsternotomy and using cardiopulmonary byp
ass and hypothermia, extended end-to-end repair was performed initially lea
ving the proximal anastomosis open. The enlarging polytetrafluoroethylene p
atch was then sutured starting at the incised descending aorta distal to th
e extended end-to-end repair and continued retrogradely through the transve
rse arch to the ascending aorta proximal to the aortic cannulation site. On
e neonate had a patent ductus arteriosus and another had ventricular septal
defect closure. One neonate had arterial switch and 3 had Norwood-type pro
cedures performed with the enlarging patch extended to the pulmonary artery
anastomosis. The remaining infant had arch enlargement performed after an
arterial switch procedure and extended end-to-end repair.
Results. All patients did well and showed no residual gradient up to 1 year
follow-up. Two patients successfully had bidirectional Glenn shunt at 9 mo
nths of age, and one had closure of residual arterial septal defect at 8 mo
nths of age.
Conclusion. The combined extended end-to-end repair and arch enlargement pr
ocedure should minimize recurrence rates because of a tension-free enlargem
ent of the entire aortic arch and elimination of the coarctation ridge and
ductile tissues. Combined with the arterial switch and Norwood-type procedu
res, the approach results in a large neoaorta. (C) 1999 by The Society of T
horacic Surgeons.