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The Annals of Thoracic Surgery, Vol 52, 621-631, Copyright © 1991 by The Society of Thoracic Surgeons
PS Rao and PS Chopra
Since the initial report of coarctation balloon angioplasty in 1982,
several groups have used this technique for native coarctations in
neonates, infants, and children and for postoperative recoarctations.
However, recommendations for use of balloon angioplasty as a treatment
procedure of choice are clouded by reports of aneurysm development at the
site of coarctation. Here we review our experience as well as that
published in the literature, including Valvuloplasty and Angioplasty of
Congenital Anomalies Registry data, and present evidence in support of
balloon angioplasty as a therapeutic procedure of choice for treating
native and recurrent postoperative aortic coarctations. Balloon angioplasty
of native aortic coarctations in 20 neonates and infants 1 year old or less
reduced peak systolic pressure gradient across the coarctation from 40 +/-
12 mm Hg (mean +/- standard deviation) to 11 +/- 8 mm Hg (p less than
0.001); no patient required immediate surgical intervention. The residual
gradient at follow-up (mean follow-up, 12 months) in 16 infants was 18 +/-
16 mm Hg, a significant improvement (p less than 0.01) compared with
preangioplasty values. In none of the patients did an aneurysm develop.
Recoarctation developed in 5 (31%) of the 16 infants and was successfully
treated either by surgical resection (in 2) or by repeat balloon
angioplasty (in 3). A comparison of mortality and recurrence rates between
the balloon angioplasty and surgical groups was made with the help of data
pooled from the literature published since 1980. The initial (7% versus
23%) and late (2% versus 25%) mortality and recoarctation (11% versus 18%)
rates were higher (p less than 0.025) after surgical intervention than
after balloon therapy. When only reports in which patients were operated on
after 1979 were included in this type of analysis, the initial and late
mortality rates remained higher (p less than 0.01) after operation than
after angioplasty, and the recoarctation rates became similar (p greater
than 0.1). Thirty-two children (greater than 1 year old) underwent balloon
angioplasty of native coarctation with a resultant reduction in peak
systolic pressure gradient from 48 +/- 19 mm Hg to 10 +/- 9 mm Hg (p less
than 0.001), which continued to remain low (14 +/- 11 mm Hg; p less than
0.001) at follow-up catheterization in 24 children 13 months (mean) later.
There were no immediate or late deaths. A small aneurysm developed in 1
patient (4%) but did not require intervention. Recoarctation developed in 2
patients (8%), and in both, repeat balloon angioplasty was performed with
good results.(ABSTRACT TRUNCATED AT 400 WORDS)
ARTICLES
Role of balloon angioplasty in the treatment of aortic coarctation
Department of Pediatrics, University of Wisconsin Medical School, Madison.
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