Literature DB >> 21092798

Does the dilated ascending aorta in an adult with congenital heart disease require intervention?

John M Stulak1, Joseph A Dearani, Harold M Burkhart, Thoralf M Sundt, Heidi M Connolly, Hartzell V Schaff.   

Abstract

OBJECTIVES: There is increasing attention to prophylactic replacement of the moderately dilated ascending aorta at aortic valve surgery. Moderate ascending aortic dilatation is common in adult patients with conotruncal anomalies. There are no data outlining actual risk of progressive ascending aortic dilatation or dissection to provide management guidelines.
METHODS: From December 1973 through January 2008, 81 consecutive adults (median age, 34 years; range, 18--59 years) with conotruncal anomalies underwent operation on the aortic root, ascending aorta, or aortic valve. Primary cardiac diagnoses included tetralogy of Fallot with or without pulmonary atresia in 60 patients, truncus arteriosus in 12, double-outlet right ventricle in 6, and other in 3. Indications for operation included aortic regurgitation in 69 patients, supracoronary ascending aneurysm in 16, aortic stenosis in 5, and other in 8. Median ascending aortic size was 45 mm (23--80 mm).
RESULTS: Operations included isolated aortic valve repair/replacement in 63 patients, combined aortic valve replacement and reduction aortoplasty in 9, aortic root replacement in 7, and isolated ascending aortic replacement in 2. Four patients required reoperation during a median follow-up of 3.8 years (maximum 31 years). There were no ascending aortic reoperations after previous reduction aortoplasties or supracoronary ascending aortic grafts, and there were no late aortic dissections.
CONCLUSIONS: Moderate ascending aortic enlargement is common among patients with conotruncal anomalies coming to operation, but aortic dissection is rare, as is subsequent need for aortic reoperation. Despite current enthusiasm for prophylactic operations on the ascending aorta in patients with acquired disease, these data suggest that the moderately dilated aorta in this setting may be observed.
Copyright © 2010 The American Association for Thoracic Surgery. Published by Mosby, Inc. All rights reserved.

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Year:  2010        PMID: 21092798     DOI: 10.1016/j.jtcvs.2010.08.052

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  7 in total

Review 1.  Aortic dilatation in complex congenital heart disease.

Authors:  Koichiro Niwa
Journal:  Cardiovasc Diagn Ther       Date:  2018-12

2.  Correlation Between Total Repair Timing and Late Aortic Root Dilatation in Repaired Tetralogy of Fallot.

Authors:  Hyung Tae Sim; Jeong-Won Kim; Seong Ho Kim; Su-Jin Park; So-Ick Jang; Chang-Ha Lee
Journal:  Pediatr Cardiol       Date:  2020-07-29       Impact factor: 1.655

3.  Tetralogy of Fallot and Aortic Dissection: Implications in Management.

Authors:  Sumeet S Vaikunth; Joshua L Chan; Jennifer P Woo; Michael R Bykhovsky; George K Lui; Michael Ma; Anitra W Romfh; John Lamberti; Domenico Mastrodicasa; Dominik Fleischmann; Michael P Fischbein
Journal:  JACC Case Rep       Date:  2022-05-18

4.  Pulmonic regurgitation and management challenges in the adult with tetralogy of fallot.

Authors:  Emily Ruckdeschel; Joseph D Kay
Journal:  Curr Treat Options Cardiovasc Med       Date:  2014-06

Review 5.  Aortopathy associated with congenital heart disease: A current literature review.

Authors:  Katrien Francois
Journal:  Ann Pediatr Cardiol       Date:  2015 Jan-Apr

Review 6.  Molecular and Genetic Insights into Thoracic Aortic Dilation in Conotruncal Heart Defects.

Authors:  W Aaron Kay
Journal:  Front Cardiovasc Med       Date:  2016-06-07

7.  Primary and secondary aortopathy associated with adult congenital heart disease - retrospective study.

Authors:  Ingrid Schusterova; Alžbeta Banovcinova; Marianna Vachalcova; Marta Jakubova; Panagiotis Artemiou
Journal:  J Cardiothorac Surg       Date:  2020-09-10       Impact factor: 1.637

  7 in total

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