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The Journal of Thoracic and Cardiovascular Surgery, Vol 89, 121-127, Copyright © 1985 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
A Pellegrino, PB Deverall, RH Anderson, A Smith, JL Wilkinson, P Russo, DA Girod and M Tynan
Operation for coarctation in infancy is a lifesaving procedure, but it
still carries a high mortality and is followed frequently by recurrence of
stenosis. This is especially true when the procedure is performed in the
first 3 months of life. To determine a correlation, if any, between anatomy
of coarctation and surgical procedures, we have studied a series of 42
autopsy specimens from patients younger than 3 months who had aortic
coarctation. We found that concepts of coarctation based solely on a
discrete lesion or isthmic hypoplasia were simplistic. The anatomy was much
more complex, the findings being relevant to surgical techniques currently
in use (resection and end-to-end anastomosis, subclavian flap aortoplasty).
Of equal significance in the cases we studied to the presence of a shelf of
ductal tissue within the aortic lumen or hypoplasia of a segment of the
arch was the finding of "waist" lesions. In these cases the wall of the
aorta was constricted to form the obstruction. Such "waists" coexisted with
discrete shelves or with shelves and isthmic narrowing. While we recognize
the danger of extrapolating from autopsy findings to predict clinical
results, our observations suggest that surgical procedures might best be
tailored to the precise anatomy present. It seemed that in may cases a
subclavian flap procedure offered the best chance of success. Cases with
anatomy suitable for resection and end-to-end anastomosis were less
frequent. Percutaneous angioplasty seemed at best to offer only palliative
options in limited cases.
ARTICLES
Aortic coarctation in the first three months of life. An anatomopathological study with respect to treatment
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