HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Add to Personal Folders Download to citation manager Permission Requests Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Ceithaml, E. L. Articles by Ritter, D. G. Search for Related Content PubMed PubMed Citation Articles by Ceithaml, E. L. Articles by Ritter, D. G.

The Annals of Thoracic Surgery, Vol 38, 433-437, Copyright © 1984 by The Society of Thoracic Surgeons

ARTICLES

Results of the Damus-Stansel-Kaye procedure for transposition of the great arteries and for double-outlet right ventricle with subpulmonary ventricular septal defect

EL Ceithaml, FJ Puga, GK Danielson, DC McGoon and DG Ritter

From 1975 through 1982, the Damus-Stansel-Kaye procedure was performed on 20 patients with complete transposition of the great arteries (TGA) and on 4 with double-outlet right ventricle (DORV) and subpulmonary ventricular septal defect (VSD). The patients ranged from 6 days to 20 years old (median age, 13 months). Associated anomalies included atrial septal defect (24 patients), VSD (14), and others (25). Thirteen patients had had palliative operations previously. Of the 14 hospital deaths (58%), 13 occurred among the 17 patients with one or more risk factors: age less than 18 months, weight less than 10 kg, and left ventricular peak systolic pressure less than 75% of systemic pressure. Follow-up ranged from 12 to 87 months (mean, 51 months). One patient died of cardiac failure two years postoperatively, and 2 required conduit replacement at 40 and 50 months because of stenosis. All 9 survivors are free from major symptoms. The Damus-Stansel-Kaye repair is most suitable for patients with TGA or DORV with subpulmonary VSD who are older than 18 months, weight more than 10 kg, and have a "prepared left ventricle," and whose coronary artery anatomy precludes transplantation.

This article has been cited by other articles:

				H. L. Walters III, C. Mavroudis, C. I. Tchervenkov, J. P. Jacobs, F. Lacour-Gayet, and M. L. Jacobs Congenital Heart Surgery Nomenclature and Database Project: double outlet right ventricle Ann. Thorac. Surg., April 1, 2000; 69(4): S249 - 263. [Abstract] [Full Text] [PDF]

				Z. Amin, C. L. Backer, C. E. Duffy, and C. Mavroudis Does banding the pulmonary artery affect pulmonary valve function after the Damus-Kaye-Stansel operation? Ann. Thorac. Surg., September 1, 1998; 66(3): 836 - 841. [Abstract] [Full Text] [PDF]

				C. Mavroudis, C. L. Backer, A. J. Muster, A. P. Rocchini, A. H. Rees, and M. Gevitz Taussig-Bing Anomaly: Arterial Switch Versus Kawashima Intraventricular Repair Ann. Thorac. Surg., May 1, 1996; 61(5): 1330 - 1338. [Abstract] [Full Text]