Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1974;49:1175-1184

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by FREED, M. D.
Right arrow Articles by NADAS, A. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by FREED, M. D.
Right arrow Articles by NADAS, A. S.

(Circulation. 1974;49:1175.)
© 1974 American Heart Association, Inc.


Coarctation of the Aorta with Congenital Mitral Regurgitation

MICHAEL D. FREED M.D.1; JOHN F. KEANE M.D.1; RICHARD VAN PRAAGH M.D.1; ALDO R. CASTAÑEDA M.D.1; WILLIAM F. BERNHARD M.D.1; ALEXANDER S. NADAS M.D.1

1 From the Departments of Cardiology, Cardiac Surgery and Pathology of the Children's Hospital Medical Center and the Departments of Pediatrics, Surgery and Pathology, Harvard Medical School, Boston, Massachusetts.

Among 861 infants and children with coarctation of the aorta examined between 1950 and 1973, inclusive, 18 (2.1%) also had congenital mitral regurgitation (MR).

Resection of the coarctation of the aorta was performed in 16 of these 18 patients (89%). There were three operative deaths early in the series, giving a total mortality rate of 18% since 1950. Over the past decade, mortality in this group has been reduced to zero. Mitral valve replacement was performed following resection of the coarctation in 2/13 patients (13%), both successfully. The follow-up of the 13 postoperative patients and the two who have not undergone surgery has ranged from 5 to 18 years, with a median of nine years. At the last examination, an appreciable pressure gradient persisted between the right arm and the legs in 4/15 patients (27%). Weight remained below the third percentile in none. The clinical picture of congestive heart failure was present in none, but significant cardiomegaly was found radiologically in 11/15 (73%) and the electrocardiogram remained abnormal in 8/15 (53%). Over the period of follow-up, the MR became clinically worse in 4/15 patients (27%), remained unchanged in 7/15 (47%), and improved following resection of the coarctation in 4/15 patients (27%).

The pathologic anatomy of congenital MR associated with coarctation of the aorta was reviewed and classified. Two unique cases were presented — rupture of chordae tendineae and perforation of the posterior leaflet, both apparently congenital. When mitral surgery becomes necessary, an understanding of the pathologic anatomy of congenital MR may well make it possible to avoid mitral valve replacement in selected cases.


Key Words: Aorta • Xenograft • Coarctation of the aorta • Mitral valve replacement • Congenital mitral regurgitation

Submitted on January 14, 1974
Accepted on February 11, 1974




This article has been cited by other articles:


Home page
J. Thorac. Cardiovasc. Surg.Home page
M. S. Uva, L. Galletti, F. L. Gayet, D. Piot, A. Serraf, J. Bruniaux, J. Comas, R. Roussin, A. Touchot, J. P. Binet, et al.
Surgery for congenital mitral valve disease in the first year of life
J. Thorac. Cardiovasc. Surg., January 1, 1995; 109(1): 164 - 176.
[Abstract] [Full Text]


Home page
VASC ENDOVASCULAR SURGHome page
L. H. Smith
Pathogenesis of Coarctation of the Aorta
Vascular and Endovascular Surgery, January 1, 1978; 12(1): 30 - 46.
[Abstract] [PDF]