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The Journal of Thoracic and Cardiovascular Surgery, Vol 104, 945-953, Copyright © 1992 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
G Rizzoli, A Mazzucco, F Maizza, L Daliento, M Rubino, V Tursi and D Scalia
The appropriateness of surgical correction of complete atrioventricular
canal defect in patients with Down syndrome has been questioned on a
cost-benefit basis. Our experience with nonselective correction of all
patients with atrioventricular canal defects gave us the opportunity to
evaluate the impact of Down syndrome on postoperative survival. Between
January 1, 1975, and December 31, 1989, we operated on 94 patients with
Down syndrome and on 127 genetically normal patients. One hundred
thirty-four patients had partial or intermediate atrioventricular canal
defect (28% Down patients) and 87 had complete atrioventricular canal
defect (74% Down patients). Thirty-two patients died perioperatively and 10
patients died during the 15-year follow-up. The actuarial survival was 90%
in the genetically normal patients and 57% in patients with Down syndrome
(p < 0.0001). Nonetheless, when the confounding effects of pulmonary
vascular resistance and the prevalence of more severe anatomic forms in
patients with Down syndrome were eliminated with a multivariable analysis
in the hazard domain, Down syndrome was not a significant independent
incremental risk factor. This was verified by fitting parametric survival
to actuarial survival graphically and by a testing of fit. Patients with
Down syndrome underwent fewer reoperations and fared as well as or even
better, on clinical and echocardiographic investigation, than their
genetically normal counterparts.
ARTICLES
Does Down syndrome affect prognosis of surgically managed atrioventricular canal defects?
Istituto di Chirurgia Cardiovascolare, Universita di Padova, Italy.
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