Literature DB >> 30578062

The fate of nonaortic arterial segments in Marfan patients.

Florian S Schoenhoff1, Murat Yildiz2, Bettina Langhammer2, Silvan Jungi2, Thomas R Wyss2, Vladimir Makaloski2, Juerg Schmidli2, Thierry Carrel2.   

Abstract

OBJECTIVES: The aim of this study was to investigate the fate of nonaortic arterial segments in patients with Marfan syndrome (MFS).
METHODS: This was a retrospective analysis of 100 consecutive patients with MFS fulfilling Ghent criteria who underwent 192 interventions on any segment of the arterial tree and were followed over the past 20 years. A review of the available imaging regarding 9 defined regions of interest of the carotid, innominate, subclavian, iliac, and femoral arteries was performed.
RESULTS: Mean follow-up interval was 11.6 ± 7.7 years. Of 600 measurements that were performed, 414 (69%) arterial segments showed dilatation above the upper range of normal. There were no significant sex differences. In 100 patients, 66 dissections in nonaortic arterial segments in 33 patients were identified. Nineteen patients with or without previous dissection underwent 34 interventions. Most interventions were performed on the iliac arteries (56%), followed by the subclavian arteries (21%), the intercostal arteries (9%), the carotid arteries (6%), the visceral arteries (6%), and the innominate artery (3%). Most iliac artery interventions (88%) were caused by dilatations due to previous dissections, whereas this was only the case in 17% of interventions on the subclavian arteries.
CONCLUSIONS: Most patients with MFS presented with at least 2 dilated nonaortic arterial segments. The current data suggest that 20% of MFS patients will need some form of intervention on nonaortic arterial segments 5 to 6 years after their first aortic intervention, referring to the first aortic dissection of the patient if the patient had a history of dissection. Routine long-term follow-up imaging should include the iliac arteries as well as the supra-aortic branches.
Copyright © 2018 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Marfan syndrome; aortic surgery; connective tissue disease

Year:  2018        PMID: 30578062     DOI: 10.1016/j.jtcvs.2018.10.089

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


  3 in total

1.  Thoracoabdominal aortic aneurysm in connective tissue disorder patients.

Authors:  Loschi Diletta; Rinaldi Enrico; Melissano Germano
Journal:  Indian J Thorac Cardiovasc Surg       Date:  2022-02-21

2.  Long-term fate of aortic branches in patients with aortic dissection.

Authors:  Francesco Squizzato; Gustavo S Oderich; Thomas C Bower; Bernardo C Mendes; Manju Kalra; Fahad Shuja; Jill Colglazier; Randall R DeMartino
Journal:  J Vasc Surg       Date:  2021-02-14       Impact factor: 4.860

3.  Magnetic resonance angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome.

Authors:  Julius Matthias Weinrich; Alexander Lenz; Gerhard Schön; Cyrus Behzadi; Isabel Molwitz; Frank Oliver Henes; Bjoern Philip Schoennagel; Gerhard Adam; Yskert von Kodolitsch; Peter Bannas
Journal:  PLoS One       Date:  2022-02-03       Impact factor: 3.240

  3 in total

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