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The Journal of Thoracic and Cardiovascular Surgery, Vol 91, 738-746, Copyright © 1986 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
GR Sanchez, RK Balsara, JM Dunn, AV Mehta and AC O'Riordan
Recoarctation is a problem in some patients after subclavian flap
aortoplasty. To investigate the reason for recoarctation, we reviewed the
records of 26 infants who underwent subclavian flap repair for symptomatic
coarctation of the aorta at less than 3 months of age between June, 1979,
and December, 1983. Age at repair ranged from 2 to 65 days (median 16 days)
and weight from 2.1 to 4.9 kg (median 3.4 kg). In 14 patients the
coarctation was associated with significant intracardiac defects (complex
in six). There were two intraoperative deaths and one early death (surgical
mortality 12%). The survivors were followed from 6 weeks to 66 months
(median 12 months). Five survivors (22%), all operated on at less than 14
days of age, developed severe recoarctation 6 weeks to 6 months (median 5
months) after repair. The obstruction appeared to be due to lumen
obliteration by shelf-life posterior wall tissue. Morphometric analysis of
preoperative angiograms showed no correlation between recoarctation and
distance between the left subclavian artery and the site of coarctation,
length of the isthmus, diameter of the isthmus, combined cross-sectional
area of the left subclavian artery and isthmus, or the ratio of the
combined cross- sectional area of the left subclavian artery and isthmus to
the cross- sectional area of the descending thoracic aorta. Recoarctation
did not correlate with weight at operation, but it correlated significantly
with age at aortoplasty (p = 0.02). The results suggest that intrinsic
abnormalities of the periductal aortic wall are responsible for
recoarctation after subclavian flap aortoplasty. Particular attention to
this abnormal tissue at repair may prevent early recurrence in young
infants.
ARTICLES
Recurrent obstruction after subclavian flap repair of coarctation of the aorta in infants. Can it be predicted or prevented?
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