» Articles » PMID: 30954551

Efficacy of Post-dilatation During Carotid Artery Stenting for Unstable Plaque Using Closed-cell Design Stent Evaluated by Optical Coherence Tomography

Overview
Journal J Neuroradiol
Specialties Neurology
Radiology
Date 2019 Apr 8
PMID 30954551
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background And Purpose: This study aimed to use optical coherence tomography (OCT) to evaluate the efficacy of post-dilatation (PD) after stent placement for unstable plaques during carotid artery stenting (CAS) using closed-cell design stent.

Materials And Methods: Twelve unstable carotid plaque lesions diagnosed by magnetic resonance imaging were evaluated by OCT during CAS. Pre-procedural minimum lumen diameter and area were 1.5 ± 0.6 mm and 2.6 ± 1.6 mm, respectively. The lesion was pre-dilated with balloon catheters (diameter 4.8 ± 0.3 mm), and closed-cell stent was deployed. PD was performed with balloon catheters of the same size as those used for pre-dilatation. Minimum lumen diameter/area and in-stent tissue prolapse volume after stent placement and after PD were calculated by 2-dimensional cross section images. The number of the stent cells showing tissue prolapse and malapposition after stent-placement and after PD were calculated by 3-dimensional analysis.

Results: Compared to after stent placement, in-stent tissue prolapse volume (0.18 ± 0.10 to 0.22 ± 0.07 mm/slice, P < 0.01), number of stent cells with any tissue prolapse (12.7 ± 8.2 to 21.0 ± 11.8%, P < 0.001) were significantly increased after PD; stent cells with ≥ 500-µm tissue prolapse (1.6 ± 1.1 to 0.7 ± 0.8%, P < 0.01) and stent malapposition (17.4 ± 7.2 to 14.0 ± 6.3%, P < 0.01) were significantly decreased.

Conclusions: PD after carotid stent placement caused increase in in-stent tissue prolapse volume and small tissue prolapse, however, the in-stent large tissue prolapse decreased, as the in-stent tissue prolapse may have been crushed into debris.

Citing Articles

Carotid artery stenting for symptomatic carotid near occlusions: Feasibility, safety and outcome analysis.

Celebioglu E, Dabus G, Uludag S, Cetinkaya O, Unal S, Bengisun U Interv Neuroradiol. 2024; :15910199241292387.

PMID: 39431297 PMC: 11559908. DOI: 10.1177/15910199241292387.


Optical coherence tomography findings of balloon angioplasty/stenting for in-stent restenosis after carotid artery stenting.

Yamada S, Harada K, Baba D, Oshima T, Tanaka K Interv Neuroradiol. 2024; :15910199241232465.

PMID: 38347719 PMC: 11571311. DOI: 10.1177/15910199241232465.


Debris generated by laser and/or balloon cause cerebral infarction with different severity.

Yang K, Tan J, Deng Y, Jiang S, Tang J, Shi W Lasers Med Sci. 2023; 39(1):15.

PMID: 38135785 DOI: 10.1007/s10103-023-03904-0.


Novel Imaging-Based Biomarkers for Identifying Carotid Plaque Vulnerability.

Fernandez-Alvarez V, Linares-Sanchez M, Suarez C, Lopez F, Guntinas-Lichius O, Makitie A Biomolecules. 2023; 13(8).

PMID: 37627301 PMC: 10452902. DOI: 10.3390/biom13081236.


Efficacy of Post-Dilatation during Carotid Artery Stenting for Unstable Plaque Using a Double-Layer Stent Evaluated by OFDI.

Kiyosawa R, Saito T, Yamada S, Harada K J Neuroendovasc Ther. 2023; 16(8):395-401.

PMID: 37502638 PMC: 10370631. DOI: 10.5797/jnet.oa.2022-0003.