(Circulation. 1995;92:309-314.)
© 1995 American Heart Association, Inc.
Articles |
From the Department of Pediatrics, Division of Pediatric Cardiology, and the Cardiovascular Research Institute, University of California, San Francisco.
Correspondence to James Bristow, MD, Division of Pediatric Cardiology, Box 0544, University of California, San Francisco, San Francisco, CA 94143-0544.
Background The cavopulmonary shunt procedure is now used for palliation of complex congenital heart lesions in infants. While pulmonary arteriovenous fistulae (PAVF) are a well-known complication of this surgery in older patients, no study of the prevalence of this condition in children and young infants has been reported.
Methods and Results We compared 29 patients with cavopulmonary shunts or total caval exclusion with 53 control subjects evaluated by contrast echocardiography at the University of California, San Francisco. The primary cardiac lesion, age at the time of surgery, type of right heart bypass procedure, provision of auxiliary pulmonary blood flow, and changes in oxygen saturation over time were compared. The prevalence of PAVF in children after cavopulmonary anastomosis is 60%, higher than previously reported. The prevalence is significantly higher in infants <6 months old and in those with a heterotaxy syndrome. The provision of an additional source of pulsatile, pulmonary blood flow appears to have little effect on the development of PAVF. Patients who developed PAVF had arterial oxygen saturations at the time of discharge from surgery similar to those who did not develop them. Those with PAVF had significantly lower arterial and pulmonary venous oxygen saturations at follow-up as a result of their intrapulmonary shunt.
Conclusions Contrast echocardiography provides a sensitive method for the detection of PAVF. While the origins, natural history, and ultimate clinical significance of PAVF in children after cavopulmonary anastomosis are unclear, surveillance by contrast echocardiography is indicated for all patients who have had this procedure because PAVF may cause significant intrapulmonary right-to-left shunting in some patients.
Key Words: heart defects, congenital surgery echocardiography microcirculation fistula
This article has been cited by other articles:
![]() |
A. Ikai, R. K. Riemer, X. Ma, O. Reinhartz, F. L. Hanley, and V. M. Reddy Pulmonary expression of the hepatocyte growth factor receptor c-Met shifts from medial to intimal layer after cavopulmonary anastomosis J. Thorac. Cardiovasc. Surg., May 1, 2004; 127(5): 1442 - 1449. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Malhotra, V. M. Reddy, S. Thelitz, Y.-P. He, D. M. McMullan, F. L. Hanley, and R. K. Riemer The role of oxidative stress in the development of pulmonary arteriovenous malformations after cavopulmonary anastomosis J. Thorac. Cardiovasc. Surg., September 1, 2002; 124(3): 479 - 485. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Chu, Q. Y. Wu, and W. M. Wang Pulmonary Blood Distribution After Total Cavopulmonary Connection Asian Cardiovasc Thorac Ann, December 1, 2001; 9(4): 282 - 285. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Malhotra, R. K. Riemer, S. Thelitz, Y.-P. He, F. L. Hanley, and V. M. Reddy Superior cavopulmonary anastomosis suppresses the activity and expression of pulmonary angiotensin-converting enzyme J. Thorac. Cardiovasc. Surg., September 1, 2001; 122(3): 464 - 469. [Abstract] [Full Text] [PDF] |
||||
![]() |
G.S. Haas, H. Hess, M. Black, J. Onnasch, F.W. Mohr, and J.A.M. van Son Extracardiac conduit Fontan procedure: early and intermediate results Eur. J. Cardiothorac. Surg., June 1, 2000; 17(6): 648 - 654. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. B. McElhinney, V. M. Reddy, W. Tworetzky, E. Petrossian, F. L. Hanley, and P. Moore Incidence and implications of systemic to pulmonary collaterals after bidirectional cavopulmonary anastomosis Ann. Thorac. Surg., April 1, 2000; 69(4): 1222 - 1228. [Abstract] [Full Text] [PDF] |
||||
![]() |
R Premsekar, J L Monro, and A P Salmon Diagnosis, management, and pathophysiology of post-Fontan hypoxaemia secondary to Glenn shunt related pulmonary arteriovenous malformation Heart, October 1, 1999; 82(4): 528 - 530. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. Kjeldsen, H. Oxhoj, P. E. Andersen, B. Elle, J. P. Jacobsen, and P. Vase Pulmonary Arteriovenous Malformations: Screening Procedures and Pulmonary Angiography in Patients With Hereditary Hemorrhagic Telangiectasia Chest, August 1, 1999; 116(2): 432 - 439. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. B. McElhinney, S. M. Marianeschi, and V. M. Reddy Additional pulmonary blood flow with the bidirectional Glenn anastomosis: does it make a difference? Ann. Thorac. Surg., August 1, 1998; 66(2): 668 - 672. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Marianeschi, D. B. McElhinney, and V. M. Reddy Pulmonary arteriovenous malformations in and out of the setting of congenital heart disease Ann. Thorac. Surg., August 1, 1998; 66(2): 688 - 691. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. B. McElhinney, V. M. Reddy, P. Moore, and F. L. Hanley Bidirectional Cavopulmonary Shunt in Patients With Anomalies of Systemic and Pulmonary Venous Drainage Ann. Thorac. Surg., June 1, 1997; 63(6): 1676 - 1684. [Abstract] [Full Text] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |