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The Journal of Thoracic and Cardiovascular Surgery, Vol 90, 490-501, Copyright © 1985 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
JL Cox, JJ Gallagher and ME Cain
Between July 1, 1980, and April 1, 1985, 118 patients underwent operation
for correction of the Wolff-Parkinson-White syndrome. There were 72 male
and 46 female patients with ages ranging from 9 months to 70 years (mean 28
+/- 6 years). The major indications for operation were medical
refractoriness or drug intolerance (60%) and previous cardiac arrest (14%).
Associated abnormalities included Ebstein's anomaly (12%), other
arrhythmias (34%), coronary artery disease (6%), cardiomyopathy (6%), and
congenital heart disease other than Ebstein's anomaly (22%). Two patients
had undergone operations for Wolff- Parkinson-White syndrome previously at
other institutions. Twenty percent of patients had multiple (two to four)
accessory pathways, a total of 149 pathways being present in the 118
patients. Distribution of the accessory pathways was as follows: 58% left
free wall, 24% posterior septal, 13% right free wall, and 5% anterior
septal. The surgical technique employed previously for the
Wolff-Parkinson-White syndrome and for the first 10 patients in the present
series was modified in August, 1981, to include 2.5 power optical
magnification, exclusive use of the endocardial approach under cardioplegic
arrest, wider margins of surgical dissection, sharp dissection of the
involved valve anulus, division of only the ventricular insertion of the
accessory pathway, and internal identification of the ventricular
epicardial peel in all regions of dissection. Of the 149 accessory pathways
present, 148 were successfully divided in the 118 patients and, by means of
the above modifications, 137 of 137 accessory pathways have been divided
successfully in the last 108 patients in the series. The surgical results
in these patients document an increase in the success rate for division of
accessory pathways from 86% to 99.3%, a decrease in the reoperation rate
from approximately 15% to 0%, and a decrease in the incidence of permanent
complete heart block from 10.5% to 0.8%. The mortality was 5.0% in the
entire series, but only one death occurred following elective operation in
the absence of associated cardiac abnormalities (0.8%). Using the present
surgical technique, these results suggest that surgical therapy is a
conservative alternative to a lifetime of medical therapy in young,
otherwise healthy patients with the Wolff-Parkinson-White syndrome.
ARTICLES
Experience with 118 consecutive patients undergoing operation for the Wolff-Parkinson-White syndrome
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