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The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan
BACKGROUND: Proximal protection devices, such as the Mo.Ma system provides better neurological outcomes than the distal filter system in the carotid artery stenting (CAS) procedure. This study first evaluated the safety and efficacy of the Mo.Ma system during CAS in a single tertiary referral hospit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522320/ https://www.ncbi.nlm.nih.gov/pubmed/36186979 http://dx.doi.org/10.3389/fcvm.2022.926513 |
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author | Cheng, Cheng-Chung Lin, Chin-Sheng Yin, Wei-Hsian Lin, Chin Liu, I-Fan Lee, Yu-Feng Liu, Wei-Ting Fu, Hao-Neng Huang, Chien-Lung Tsao, Tien-Ping |
author_facet | Cheng, Cheng-Chung Lin, Chin-Sheng Yin, Wei-Hsian Lin, Chin Liu, I-Fan Lee, Yu-Feng Liu, Wei-Ting Fu, Hao-Neng Huang, Chien-Lung Tsao, Tien-Ping |
author_sort | Cheng, Cheng-Chung |
collection | PubMed |
description | BACKGROUND: Proximal protection devices, such as the Mo.Ma system provides better neurological outcomes than the distal filter system in the carotid artery stenting (CAS) procedure. This study first evaluated the safety and efficacy of the Mo.Ma system during CAS in a single tertiary referral hospital from Taiwan. The outcomes of distal vs. proximal embolic protection devices were also studied. METHODS: A total of 294 patients with carotid artery stenosis who underwent the CAS procedure were retrospectively included and divided into two groups: 152 patients in the distal filter system group and 142 patients in the Mo.Ma system. The outcomes of interest were compared between the two groups. The factors contributing to occlusion intolerance (OI) in the Mo.Ma system were evaluated. RESULTS: The procedure success rates were more than 98% in both groups. No major stroke occurred in this study. The minor stroke rates were 2.8% (4/142) and 4.6% (7/152) in the Mo.Ma system and filter system, respectively (p = 0.419). Patients with hypoalbuminemia significantly predicted the risk of stroke with an odds ratio of 0.08 [95% confidence interval (CI), 0.01–0.68, p = 0.020] per 1 g/day of serum albumin in the filter group. A total of 12 patients developed OI in the Mo.Ma system (12/142, 8%). Low occlusion pressure predicted the occurrence of OI in the Mo.Ma group with the hazard ratios of 0.88 (95% CI: 0.82–0.96) and 0.90 (95% CI: 0.84–0.98) per 1 mmHg of occlusion systolic pressure (OSP) and diastolic pressure (ODP), respectively. We further indicated that patients with an OSP of ≥60 mmHg or an ODP of ≥44 mmHg could tolerate the procedure of occlusion time up to 400 s, while patients with an OSP of <49 mmHg or an ODP of <34 mmHg should undergo the procedure of occlusion time less than 300 s to prevent the occurrence of OI. CONCLUSION: We have demonstrated the safety and effectiveness of the Mo.Ma system during CAS in an Asia population. By reducing the occlusion time, our study indicated a lower risk of OI in the Mo.Ma system and proposed the optimal occlusion time according to occlusion pressure to prevent OI during the CAS procedure. Further large-scale and prospective studies are needed to verify our results. |
format | Online Article Text |
id | pubmed-9522320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95223202022-09-30 The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan Cheng, Cheng-Chung Lin, Chin-Sheng Yin, Wei-Hsian Lin, Chin Liu, I-Fan Lee, Yu-Feng Liu, Wei-Ting Fu, Hao-Neng Huang, Chien-Lung Tsao, Tien-Ping Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Proximal protection devices, such as the Mo.Ma system provides better neurological outcomes than the distal filter system in the carotid artery stenting (CAS) procedure. This study first evaluated the safety and efficacy of the Mo.Ma system during CAS in a single tertiary referral hospital from Taiwan. The outcomes of distal vs. proximal embolic protection devices were also studied. METHODS: A total of 294 patients with carotid artery stenosis who underwent the CAS procedure were retrospectively included and divided into two groups: 152 patients in the distal filter system group and 142 patients in the Mo.Ma system. The outcomes of interest were compared between the two groups. The factors contributing to occlusion intolerance (OI) in the Mo.Ma system were evaluated. RESULTS: The procedure success rates were more than 98% in both groups. No major stroke occurred in this study. The minor stroke rates were 2.8% (4/142) and 4.6% (7/152) in the Mo.Ma system and filter system, respectively (p = 0.419). Patients with hypoalbuminemia significantly predicted the risk of stroke with an odds ratio of 0.08 [95% confidence interval (CI), 0.01–0.68, p = 0.020] per 1 g/day of serum albumin in the filter group. A total of 12 patients developed OI in the Mo.Ma system (12/142, 8%). Low occlusion pressure predicted the occurrence of OI in the Mo.Ma group with the hazard ratios of 0.88 (95% CI: 0.82–0.96) and 0.90 (95% CI: 0.84–0.98) per 1 mmHg of occlusion systolic pressure (OSP) and diastolic pressure (ODP), respectively. We further indicated that patients with an OSP of ≥60 mmHg or an ODP of ≥44 mmHg could tolerate the procedure of occlusion time up to 400 s, while patients with an OSP of <49 mmHg or an ODP of <34 mmHg should undergo the procedure of occlusion time less than 300 s to prevent the occurrence of OI. CONCLUSION: We have demonstrated the safety and effectiveness of the Mo.Ma system during CAS in an Asia population. By reducing the occlusion time, our study indicated a lower risk of OI in the Mo.Ma system and proposed the optimal occlusion time according to occlusion pressure to prevent OI during the CAS procedure. Further large-scale and prospective studies are needed to verify our results. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9522320/ /pubmed/36186979 http://dx.doi.org/10.3389/fcvm.2022.926513 Text en Copyright © 2022 Cheng, Lin, Yin, Lin, Liu, Lee, Liu, Fu, Huang and Tsao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Cheng, Cheng-Chung Lin, Chin-Sheng Yin, Wei-Hsian Lin, Chin Liu, I-Fan Lee, Yu-Feng Liu, Wei-Ting Fu, Hao-Neng Huang, Chien-Lung Tsao, Tien-Ping The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title | The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title_full | The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title_fullStr | The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title_full_unstemmed | The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title_short | The safety and efficacy of the Mo.Ma system device for carotid artery stenting: A single-center experience from Taiwan |
title_sort | safety and efficacy of the mo.ma system device for carotid artery stenting: a single-center experience from taiwan |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522320/ https://www.ncbi.nlm.nih.gov/pubmed/36186979 http://dx.doi.org/10.3389/fcvm.2022.926513 |
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