Correction of Type C complete atrioventricular canal

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Complete atrioventricular canal

Complete atrioventricular canal (CAVC), also referred to as complete atrioventricular septal defect, is characterised by an ostium primum atrial septal defect, a common atrioventricular valve and a variable deficiency of the ventricular septum inflow. CAVC is an uncommon congenital heart disease, accounting for about 3% of cardiac malformations. Atrioventricular canal occurs in two out of every...

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Correction of tye C atrioventricular canal associated with tetralogy of Fallot.

Type C complete atrioventricular canal associated with tetralogy of Fallot in a 5-year old child was successfully corrected. Repair of the atrioventricular canal was combined with infundibular resection and the insertion of an outflow tract patch across the pulmonary valve ring. The postoperative course was uneventful, and the child is well one year after operation.

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Echocardiographic differentiation of partial and complete atrioventricular canal.

Retrospective examination of echocardiograms was performed in 34 patients with persistent atrioventricular (A-V) canal who had undergone cardiac catheterization. Characteristic findings in 16 patients with partial A-V canal were lack of continuity of mitral and tricuspid valves, paradoxical interventricular septal motion, definite E and A waves of the mitral valve anterior leaflet (MVAL) echoes...

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Echocardiographic estimation of ventricular hypoplasia in complete atrioventricular canal.

Echocardiograms from 10 patients with complete atrioventricular canal (CAVC) were compared with autopsy specimens to determine the capabilities of echocardiography in identifying patients with ventricular hypoplasia. On the basis of echographic ventricular size, patients could be divided into three groups: 1) "balanced" CAVC patients had both increased right and left ventricular end-diastolic d...

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Complete atrioventricular canal with survival to the eighth decade.

Survival to the eighth decade of patients with atrioventricular canal is extremely rare. A patient is presented with such survival of the complete form of the defect. This possibly represents the first such report in the medical literature. The value of 2-dimensional echocardiography, particularly with venous contrast studies, in establishing the diagnosis, is shown.

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ژورنال

عنوان ژورنال: The Journal of Thoracic and Cardiovascular Surgery

سال: 1976

ISSN: 0022-5223

DOI: 10.1016/s0022-5223(19)40256-0