|
|
||||||||
Eur J Cardiothorac Surg 1999;15:735-741
© 1999 Elsevier Science NL
The Heart Unit, Birmingham Children's Hospital, Steelhouse Lane, Birmingham, UK
Received 23 September 1998; received in revised form 22 February 1999; accepted 11 March 1999.
Corresponding author. Tel.: +44-121-3339437; fax: +44-121-3339441
Objective: Total anomalous pulmonary venous connection (TAPVC) can be corrected with low mortality and good outcome. If complicated by pulmonary vein stenosis (PVS), either at presentation or secondary to the repair, the long-term outcome is compromised. We have evaluated an institutional experience with TAPVC, with particular regard to the evolving management of PVS. Methods: Retrospective analysis of 85 consecutive patients with non-isomeric TAPVC undergoing surgical correction over a 10-year period (19881997). In addition, three patients were referred to us with secondary PVS, having had their primary procedure elsewhere. Attention was focused on incidence of PVS, and strategies for management. Results: Median age at first operation was 33 days (range 1533). Site of drainage was supracardiac (43/88), infracardiac (20/88), cardiac (17/88), and mixed (8/88). On presentation, 35% of patients were ventilated. Early mortality was 7% (6/85), with one late non-cardiac death. 82% of the original patients (70/85) are currently well at a median follow-up of 64 months (range 6119). The incidence of PVS requiring intervention was 11% (9/85). Median time to PVS was 41 days. In these patients, 18 balloon angioplasties, four endovascular stent placements (in two patients), and a further 23 surgical procedures were performed. Of the nine patients undergoing re-intervention after initial surgery at our institution, five (56%) survived. Two of these have no residual obstruction and right ventricular pressure (RVP) <50% systemic, two have unilateral obstruction and RVP <50% systemic, and one has bilateral obstruction and RVP 80% systemic. Of the three patients referred to us with secondary PVS, two are alive and well, and one died early after the first re-operation. Conclusions: Intrinsic obstruction (endocardial sclerosis or thickening) is associated with worse prognosis and earlier re-intervention than extrinsic (anatomical) obstruction. We advocate an early, aggressive approach to the management of patients with TAPVC, especially in the presence of PVS. This complication is most appropriately managed by a combination of re-operation and repeated balloon dilatation.
Key Words: Total anomalous pulmonary venous connection Pulmonary vein stenosis
This article has been cited by other articles:
![]() |
E. Buitrago, A. L. Panos, and M. Ricci Primary repair of infracardiac total anomalous pulmonary venous connection using a modified sutureless technique. Ann. Thorac. Surg., July 1, 2008; 86(1): 320 - 322. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Hirsch and E. L. Bove Total anomalous pulmonary venous connection MMCTS, May 7, 2007; 2007(0507): 2253. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Karamlou, R. Gurofsky, E. Al Sukhni, J. G. Coles, W. G. Williams, C. A. Caldarone, G. S. Van Arsdell, and B. W. McCrindle Factors Associated With Mortality and Reoperation in 377 Children With Total Anomalous Pulmonary Venous Connection Circulation, March 27, 2007; 115(12): 1591 - 1598. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. J. Devaney, A. C. Chang, R. G. Ohye, and E. L. Bove Management of Congenital and Acquired Pulmonary Vein Stenosis. Ann. Thorac. Surg., March 1, 2006; 81(3): 992 - 996. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Ando, Y. Takahashi, and T. Kikuchi Total anomalous pulmonary venous connection with dysmorphic pulmonary vein: a risk for postoperative pulmonary venous obstruction Interactive CardioVascular and Thoracic Surgery, December 1, 2004; 3(4): 557 - 561. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Michielon, R. M. Di Donato, L. Pasquini, S. Giannico, G. Brancaccio, E. Mazzera, C. Squitieri, and G. Catena Total anomalous pulmonary venous connection: long-term appraisal with evolving technical solutions Eur. J. Cardiothorac. Surg., August 1, 2002; 22(2): 184 - 191. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Lange, C. Schreiber, T. Gunther, M. Wottke, F. Haas, F. Meisner, J. Hess, and K. Holper Results of biventricular repair of congenital cardiac malformations: definitive corrective surgery? Eur. J. Cardiothorac. Surg., December 1, 2001; 20(6): 1207 - 1213. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Shah, S. Shah, S. Shankargowda, U. Krishnan, and K. M. Cherian L->R shunt: a serious consequence of TAPVC repair without ligation of vertical vein Ann. Thorac. Surg., September 1, 2000; 70(3): 971 - 973. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |