Literature DB >> 30165980

External Aortic Root Support to Prevent Aortic Dilatation in Patients With Marfan Syndrome.

Cemil Izgi1, Simon Newsome2, Francisco Alpendurada3, Eva Nyktari1, Maria Boutsikou1, John Pepper4, Tom Treasure5, Raad Mohiaddin6.   

Abstract

BACKGROUND: Personalized external aortic root support (PEARS) was introduced in 2004 for prevention of aortic root dilatation in Marfan patients. The individual's aortic root is replicated by 3-dimensional printing. A polymer mesh sleeve is manufactured, which is implanted with the aim to support and stabilize the aortic wall.
OBJECTIVES: The aim of this study was to assess effectiveness of PEARS for prevention of aortic root dilatation in Marfan patients.
METHODS: A total of 24 consecutive Marfan patients operated 2004 to 2012 were prospectively monitored with magnetic resonance imaging. Following a pre-defined protocol, baseline and follow-up aorta measurements were made in a blinded random sequence.
RESULTS: The mean age of the patients was 33 ± 13.3 years (range: 16 to 58 years), and the mean aortic root diameter was 45 ± 2.8 mm (range: 41 to 52 mm). Follow-up was 6.3 ± 2.6 years. There was no increase in the aortic root and ascending aorta diameters, but there was a tendency toward reduction: annulus diameter 28.9 ± 2.3 mm to 28.5 ± 2.4 mm (change -0.39 mm, 95% confidence interval [CI]: -1.05 to 0.27 mm), sinus of Valsalva diameter 44.9 ± 2.9 mm to 44.5 ± 3.0 mm (change -0.37 mm, 95% CI: -1.23 to 0.51 mm), and ascending aorta diameter 32.4 ± 3.6 mm to 32.3 ± 3.7 mm (change -0.10 mm, 95% CI: -0.92 to 0.74 mm). In the same period, the descending aorta diameter increased from 22.9 ± 2.4 mm to 24.2 ± 3.0 mm (change 1.32 mm, 95% CI: 0.70 to 1.94 mm; p < 0.001) with a tendency toward increase in aortic arch diameter 24.1 ± 2.0 mm to 24.5 ± 2.8 mm (change 0.41 mm, 95% CI: -0.56 to 1.37 mm).
CONCLUSIONS: PEARS is effective in stabilizing the aortic root and preventing its dilatation. It is a viable alternative for prevention of aortic root dissection in Marfan patients.
Copyright © 2018 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Marfan syndrome; aneurysm; aorta; dissection; magnetic resonance

Mesh:

Year:  2018        PMID: 30165980     DOI: 10.1016/j.jacc.2018.06.053

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  4 in total

Review 1.  Pathophysiology and Pathogenesis of Marfan Syndrome.

Authors:  Sanford M Zeigler; Brandon Sloan; Jeffrey A Jones
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 2.  Marfan syndrome.

Authors:  Dianna M Milewicz; Alan C Braverman; Julie De Backer; Shaine A Morris; Catherine Boileau; Irene H Maumenee; Guillaume Jondeau; Arturo Evangelista; Reed E Pyeritz
Journal:  Nat Rev Dis Primers       Date:  2021-09-02       Impact factor: 65.038

Review 3.  Understanding Pulmonary Autograft Remodeling After the Ross Procedure: Stick to the Facts.

Authors:  Lucas Van Hoof; Peter Verbrugghe; Elizabeth A V Jones; Jay D Humphrey; Stefan Janssens; Nele Famaey; Filip Rega
Journal:  Front Cardiovasc Med       Date:  2022-02-09

4.  A contemporary approach to a young female patient with Loeys-Dietz syndrome and an uncomplicated type B aortic dissection: a case report.

Authors:  Petko Prodanov; Hana Linkova; Robert Petr; Richard Fojt; Zuzana Motovska; Jiri Knot; Filip Rohac; Boris Koznar; Mariwan Majid; Petr Widimsky; Petr Kacer
Journal:  J Cardiothorac Surg       Date:  2020-08-31       Impact factor: 1.637

  4 in total

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