Home

search

Subjectguide
Journals
Books / Serials / Multimedia
Services
Services

Login for Subscribers
Logout

Sitemap
Help
Contacts


Logo






Vol. 112, No. 1, 2009   

Free Abstract     Article (Fulltext)     Article (PDF 171 KB)     

Original Research

Mortality and Restenosis Rate of Surgical Coarctation Repair in Infancy: A Study of 191 Patients
Alfred Hagera, Christian Schreiberb, Silvia Nützlb, John Hessa

aDepartment of Pediatric Cardiology and Congenital Heart Disease, and
bDepartment of Cardiovascular Surgery, Deutsches Herzzentrum München, Technische Universität München, München, Germany

Address of Corresponding Author

Cardiology 2009;112:36-41 (DOI: 10.1159/000137697)


 goto top of page Key Words

  • Congenital heart disease
  • Coarctation of the aorta
  • Long-term follow-up
  • Restenosis

 goto top of page Abstract

Study Design: This is a retrospective cross-sectional study to analyze mortality and the rate of restenosis in the follow-up of patients after surgical repair of isolated aortic coarctation in infancy. Patients and Methods: From 1974 to 2003, 191 patients underwent surgical repair of aortic coarctation in infancy. Follow-up data of 2,432 patient-years were extracted from the clinical files of our outpatient department or from family practitioners. Results: Five patients died (total mortality 2.6%): 1 patient intraoperatively and 2 within 30 days after surgery (early mortality 1.6%). The other 2 patients died within 3 months. All deaths were contributed to patients that underwent surgery in the years up to 1981 and within the first 43 days of life. Of the surviving 186 patients, 31 had reintervention because of restenosis and another 11 patients had a noninvasive brachial-ankle systolic blood pressure gradient >20 mm Hg, suggesting current restenosis. Risk factors for death or restenosis were a hypoplastic aortic arch and a low body length at surgery. Conclusions: Nowadays, surgical repair of coarctation can be performed in infancy with minimal risk. The restenosis rate is considerably high (23%). It is mainly caused by the size of the whole aortic arch, but can also develop during later follow-up.

Copyright © 2008 S. Karger AG, Basel


 goto top of page Author Contacts

Alfred Hager
Department of Pediatric Cardiology and Congenital Heart Disease
Deutsches Herzzentrum München, Technische Universität München
Lazarettstrasse 36, DE-80636 München (Germany)
Tel. +49 89 1218 3015, Fax +49 89 1218 3003, E-Mail a-hager@web.de


 goto top of page Article Information

Some of the results of this study were previously presented at the 73rd Annual Meeting of the German Cardiac Society, April 2007, Mannheim, Germany.

Received: December 19, 2007
Accepted after revision: January 25, 2008
Published online: June 26, 2008
Number of Print Pages : 6
Number of Figures : 2, Number of Tables : 2, Number of References : 25

 
Journal Home
Journal Content
Guidelines
Editorial Board
Aims and Scope
Subscriptions
Medline Abstract (ID 18580057)
Download Citation

This journal is part of the third subject package of the Karger

Journal Archive Collection

Information on packages (PDF)
Free sample issues


For non-native English speakers and international authors who would like assistance with their writing before submission, we suggest American Journal Experts for their scientific editing service.





copyright  © 2009 S. Karger AG, Basel