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The Annals of Thoracic Surgery, Vol 50, 562-568, Copyright © 1990 by The Society of Thoracic Surgeons
MD Rodefeld, JW Brown, DA Heimansohn, H King, DA Girod, RA Hurwitz and RL Caldwell
Twelve patients with cor triatriatum have been seen at our institution
since 1979. The clinical presentation, diagnostic evaluation, and surgical
results are outlined in this retrospective review. Operation is the
treatment of choice for this rare congenital cardiac defect. One patient
died 1 day before scheduled operation, and 2 patients died postoperatively,
yielding a surgical mortality rate of 17% and an overall mortality rate of
25%. Resection of the obstructing atrial membrane was performed using
hypothermic cardiopulmonary bypass in all cases. Left atriotomy was
performed in 6 patients, and right atriotomy was performed in 7. The two
postoperative deaths occurred in patients who had serious associated
cardiac defects. Associated anomalies include atrial septal defect,
persistent left superior vena cava, and partial anomalous pulmonary venous
return. The postoperative course has been excellent in all 9 surviving
patients; all remain asymptomatic. Cor triatriatum is amenable to surgical
repair with excellent results when diagnosed early and when not complicated
by other severe cardiac anomalies.
ARTICLES
Cor triatriatum: clinical presentation and surgical results in 12 patients
Department of Surgery, Indiana University School of Medicine, Indianapolis.
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