Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction

Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, an...

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Veröffentlicht in:The American journal of cardiology 1969-06, Vol.23 (6), p.818-821
Hauptverfasser: Moss, Arthur J., Marcano, Bertrand, Ruttenberg, Herbert D., Desilets, Donald T., Shapiro, Bertrand
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container_issue 6
container_start_page 818
container_title The American journal of cardiology
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creator Moss, Arthur J.
Marcano, Bertrand
Ruttenberg, Herbert D.
Desilets, Donald T.
Shapiro, Bertrand
description Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, and intrapulmonary right to left shunts were demonstrated in 4 of the 6 cases. These shunts appear to reflect venous admixture rather than true anatomic connections between the bronchial and pulmonary circulations.
doi_str_mv 10.1016/0002-9149(69)90376-2
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subjects Angiocardiography
Arteriovenous Anastomosis
Bronchial Arteries - pathology
Child
Cyanosis - complications
Dilatation
Female
Heart Defects, Congenital - complications
Heart Defects, Congenital - surgery
Heart Septal Defects, Atrial - surgery
Humans
Male
Postoperative Complications
Pulmonary Circulation
Pulmonary Valve Stenosis - surgery
Tetralogy of Fallot - surgery
title Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction
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