Literature DB >> 15858088

Vessel wall damage caused by cerebral protection devices: ex vivo evaluation in porcine carotid arteries.

Stefan Müller-Hülsbeck1, Paul Stolzmann, Carsten Liess, Jürgen Hedderich, Friedrich Paulsen, Thomas Jahnke, Martin Heller.   

Abstract

PURPOSE: To determine the extent of vessel wall damage caused by cerebral protection devices designed for carotid angioplasty by using ex vivo porcine carotid arteries.
MATERIALS AND METHODS: The local animal experimentation committee did not require its approval for this study. With a benchtop vascular model (flow rate, 470 mL/min; dicrotic pulsatile flow, 76 pulses per minute; pressure, 115/67 mm Hg [mean pressure, 91 mm Hg]) into which 85 porcine internal carotid arteries (ICAs) were inserted, five different protection devices (Angioguard [Cordis/Johnson & Johnson, Miami, Fla], Filterwire EX [Boston Scientific, Natick, Mass], Trap [Microvena, White Bear Lake, Minn], Neuroshield [Abbott Laboratories, Redwood City, Calif], and Percusurge [Abbott Laboratories]) were evaluated. Adverse movement (1 cm up, 2 cm down, and 1 cm up again) of the activated devices (deployed filters or inflated balloons [Percusurge only]) was simulated, and the device was retrieved. For each of these steps (deployment, movement, retrieval) the amount of debris from the vessel wall in the effluent of the ICA was determined by using a 100-microm filter. The Mann-Whitney test was used to test for differences, and a correction for multiple comparisons was made. P < .05 was considered to indicate a significant difference. The authors attempted to determine whether there was a notable association between the total amount of debris captured and the classification of damage at microscopy. Carotid arteries were analyzed histologically with light and scanning electron microscopy.
RESULTS: All examined protection devices caused dislodged debris, which was captured in the effluent filter. There were significant differences among the devices in terms of the total amount of debris captured in the filters (lowest amounts of debris, 4.75 mg [Angioguard] and 5.02 mg [Filterwire EX]; highest amount, 7.51 mg [Trap]; P < or = .001 for all). All devices caused histologically visible wall damage, with the degree of intimal denudation correlating with the mass of the debris. The Trap device caused the most severe intimal and subintimal wall damage. Adverse movement resulted in no increased debris dislodgment as compared with the debris dislodged during deployment and retrieval of the devices.
CONCLUSION: On the basis of the data obtained, cerebral protection devices themselves have a potential influence on embolization rates by causing debris to be dislodged during carotid stent placement. (c) RSNA, 2005.

Entities:  

Mesh:

Year:  2005        PMID: 15858088     DOI: 10.1148/radiol.2352031968

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  12 in total

1.  Carotid Stenting without Angioplasty and without Protection: The Advantages of a Less Invasive Procedure.

Authors:  M Leonardi; M Dall'olio; L Raffi; P Cenni; L Simonetti; R Marasco; F Giagnorio
Journal:  Interv Neuroradiol       Date:  2008-06-30       Impact factor: 1.610

2.  Diffusion-weighted MR imaging lesions after filter-protected stenting of high-grade symptomatic carotid artery stenoses.

Authors:  R du Mesnil de Rochemont; S Schneider; B Yan; A Lehr; M Sitzer; J Berkefeld
Journal:  AJNR Am J Neuroradiol       Date:  2006 Jun-Jul       Impact factor: 3.825

Review 3.  The Angioguard embolic protection device.

Authors:  Gail M Siewiorek; Mark K Eskandari; Ender A Finol
Journal:  Expert Rev Med Devices       Date:  2008-05       Impact factor: 3.166

4.  Carotid intervention 3: the evidence for cerebral protection.

Authors:  Fabrizio Fanelli; Mario Bezzi; Emanuele Boatta; Roberto Passariello
Journal:  Semin Intervent Radiol       Date:  2007-06       Impact factor: 1.513

5.  In vitro performance assessment of distal protection filters: pulsatile flow conditions.

Authors:  Gail M Siewiorek; Mark H Wholey; Ender A Finol
Journal:  J Endovasc Ther       Date:  2009-12       Impact factor: 3.487

6.  New ischemic brain lesions on diffusion-weighted MRI after carotid artery stenting with filter protection: frequency and relationship with plaque morphology.

Authors:  D Stojanov; M Ilic; P Bosnjakovic; M Zivkovic; S Jolic; N Vukasinovic; A Ignjatovic; B Ilic; D Benedeto-Stojanov
Journal:  AJNR Am J Neuroradiol       Date:  2011-12-22       Impact factor: 3.825

7.  Initial experience of using the filter protection device during carotid artery stenting in Japan.

Authors:  Katsutoshi Takayama; Hiroyuki Nakagawa; Satoru Iwasaki; Toshiaki Taoka; Toshiteru Miyasaka; Kaoru Myouchin; Takeshi Wada; Masahiko Sakamoto; Akio Fukusumi; Ichiro Nakagawa; Shinichiro Kurokawa; Kimihiko Kichikawa
Journal:  Radiat Med       Date:  2008-08-03

8.  Spasm induced by protection balloon during carotid artery stenting.

Authors:  Masanori Tsutsumi; Kiyoshi Kazekawa; Masanari Onizuka; Hiroshi Aikawa; Kouhei Nii; Tomonobu Kodama; Minoru Iko; Makoto Tomokiyo; Shuko Matsubara; Akira Tanaka
Journal:  Radiat Med       Date:  2007-08-27

9.  Endovascular catheter for magnetic navigation under MR imaging guidance: evaluation of safety in vivo at 1.5T.

Authors:  S W Hetts; M Saeed; A J Martin; L Evans; A F Bernhardt; V Malba; F Settecase; L Do; E J Yee; A Losey; R Sincic; P Lillaney; S Roy; R L Arenson; M W Wilson
Journal:  AJNR Am J Neuroradiol       Date:  2013-07-11       Impact factor: 3.825

10.  Lesion load in unprotected carotid artery stenting.

Authors:  I Q Grunwald; P Papanagiotou; C Roth; K Fassbender; K Karp; C Krick; H Schieber; M Müller; A Haass; W Reith
Journal:  Neuroradiology       Date:  2009-02-06       Impact factor: 2.804

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