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Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial
Endovascular treatment (EVT) is the main treatment for peripheral artery disease (PAD). Despite advances in device development, the restenosis rate remains high in patients with femoropopliteal lesions (FP). This study aimed to evaluate the effectiveness of exercise training in reducing the 1-year i...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349080/ https://www.ncbi.nlm.nih.gov/pubmed/35396952 http://dx.doi.org/10.1007/s00380-022-02060-9 |
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author | Kato, Tamon Miura, Takashi Yamamoto, Shuhei Miyashita, Yusuke Hashizume, Naoto Shoin, Kyoko Sasaki, Shinya Kanzaki, Yusuke Yui, Hisanori Maruyama, Shusaku Nagae, Ayumu Sakai, Takahiro Saigusa, Tatsuya Ebisawa, Soichiro Okada, Ayako Motoki, Hirohiko Ikeda, Uichi Kuwahara, Koichiro |
author_facet | Kato, Tamon Miura, Takashi Yamamoto, Shuhei Miyashita, Yusuke Hashizume, Naoto Shoin, Kyoko Sasaki, Shinya Kanzaki, Yusuke Yui, Hisanori Maruyama, Shusaku Nagae, Ayumu Sakai, Takahiro Saigusa, Tatsuya Ebisawa, Soichiro Okada, Ayako Motoki, Hirohiko Ikeda, Uichi Kuwahara, Koichiro |
author_sort | Kato, Tamon |
collection | PubMed |
description | Endovascular treatment (EVT) is the main treatment for peripheral artery disease (PAD). Despite advances in device development, the restenosis rate remains high in patients with femoropopliteal lesions (FP). This study aimed to evaluate the effectiveness of exercise training in reducing the 1-year in-stent restenosis rate of bare metal nitinol stents for FPs. This prospective, randomized, open-label, multicenter study was conducted from January 2017 to March 2019. We randomized 44 patients who had claudication with de novo stenosis or occlusion of the FP into an intensive exercise group (n = 22) and non-intensive exercise group (n = 22). Non-intensive exercise was defined as walking for less than 30 min per session, fewer than three times a week. We assessed exercise tolerance using an activity meter at 1, 3, 6, and 12 months, and physiotherapists ensured maintenance of exercise quality every month. The primary endpoint was instant restenosis defined as a peak systolic velocity ratio > 2.5 on duplex ultrasound imaging. Kaplan–Meier analysis was used to evaluate the data. There were no significant differences in background characteristics between the groups. Six patients dropped out of the study within 1 year. In terms of the primary endpoint, intensive exercise significantly improved the patency rate of bare nitinol stents at 12 months. The 1-year freedom from in-stent restenosis rates were 81.3% in the intensive exercise group and 47.6% in the non-intensive exercise group (p = 0.043). No cases of stent fracture were observed in the intensive exercise group. Intensive exercise is safe and reduces in-stent restenosis in FP lesions after endovascular therapy for PAD. Clinical trial registration: University Hospital Medical Information Network Clinical Trials Registry (No. UMIN 000025259). |
format | Online Article Text |
id | pubmed-9349080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-93490802022-08-05 Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial Kato, Tamon Miura, Takashi Yamamoto, Shuhei Miyashita, Yusuke Hashizume, Naoto Shoin, Kyoko Sasaki, Shinya Kanzaki, Yusuke Yui, Hisanori Maruyama, Shusaku Nagae, Ayumu Sakai, Takahiro Saigusa, Tatsuya Ebisawa, Soichiro Okada, Ayako Motoki, Hirohiko Ikeda, Uichi Kuwahara, Koichiro Heart Vessels Original Article Endovascular treatment (EVT) is the main treatment for peripheral artery disease (PAD). Despite advances in device development, the restenosis rate remains high in patients with femoropopliteal lesions (FP). This study aimed to evaluate the effectiveness of exercise training in reducing the 1-year in-stent restenosis rate of bare metal nitinol stents for FPs. This prospective, randomized, open-label, multicenter study was conducted from January 2017 to March 2019. We randomized 44 patients who had claudication with de novo stenosis or occlusion of the FP into an intensive exercise group (n = 22) and non-intensive exercise group (n = 22). Non-intensive exercise was defined as walking for less than 30 min per session, fewer than three times a week. We assessed exercise tolerance using an activity meter at 1, 3, 6, and 12 months, and physiotherapists ensured maintenance of exercise quality every month. The primary endpoint was instant restenosis defined as a peak systolic velocity ratio > 2.5 on duplex ultrasound imaging. Kaplan–Meier analysis was used to evaluate the data. There were no significant differences in background characteristics between the groups. Six patients dropped out of the study within 1 year. In terms of the primary endpoint, intensive exercise significantly improved the patency rate of bare nitinol stents at 12 months. The 1-year freedom from in-stent restenosis rates were 81.3% in the intensive exercise group and 47.6% in the non-intensive exercise group (p = 0.043). No cases of stent fracture were observed in the intensive exercise group. Intensive exercise is safe and reduces in-stent restenosis in FP lesions after endovascular therapy for PAD. Clinical trial registration: University Hospital Medical Information Network Clinical Trials Registry (No. UMIN 000025259). Springer Japan 2022-04-09 2022 /pmc/articles/PMC9349080/ /pubmed/35396952 http://dx.doi.org/10.1007/s00380-022-02060-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Kato, Tamon Miura, Takashi Yamamoto, Shuhei Miyashita, Yusuke Hashizume, Naoto Shoin, Kyoko Sasaki, Shinya Kanzaki, Yusuke Yui, Hisanori Maruyama, Shusaku Nagae, Ayumu Sakai, Takahiro Saigusa, Tatsuya Ebisawa, Soichiro Okada, Ayako Motoki, Hirohiko Ikeda, Uichi Kuwahara, Koichiro Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title | Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title_full | Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title_fullStr | Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title_full_unstemmed | Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title_short | Intensive exercise therapy for restenosis after superficial femoral artery stenting: the REASON randomized clinical trial |
title_sort | intensive exercise therapy for restenosis after superficial femoral artery stenting: the reason randomized clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349080/ https://www.ncbi.nlm.nih.gov/pubmed/35396952 http://dx.doi.org/10.1007/s00380-022-02060-9 |
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