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Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period

The radial artery is increasingly used as a second arterial conduit for myocardial revascularization. However, the radial artery is susceptible to vasospasm, which is thought to be the principal cause of graft failure. The radial artery is harvested as a skeletonized or a non-skeletonized graft, but...

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Autores principales: Maruyama, Takuto, Kohno, Hiroki, Ishida, Keiichi, Ishizaka, Toru, Funabashi, Nobusada, Kobayashi, Yoshio, Matsumiya, Goro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820472/
https://www.ncbi.nlm.nih.gov/pubmed/25656931
http://dx.doi.org/10.1007/s00380-015-0639-3
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author Maruyama, Takuto
Kohno, Hiroki
Ishida, Keiichi
Ishizaka, Toru
Funabashi, Nobusada
Kobayashi, Yoshio
Matsumiya, Goro
author_facet Maruyama, Takuto
Kohno, Hiroki
Ishida, Keiichi
Ishizaka, Toru
Funabashi, Nobusada
Kobayashi, Yoshio
Matsumiya, Goro
author_sort Maruyama, Takuto
collection PubMed
description The radial artery is increasingly used as a second arterial conduit for myocardial revascularization. However, the radial artery is susceptible to vasospasm, which is thought to be the principal cause of graft failure. The radial artery is harvested as a skeletonized or a non-skeletonized graft, but the effect of different harvesting technique remains unknown. In this study, we compared the early- and mid-term angiographic findings to elucidate its influence on the graft luminal diameter. We harvested 39 radial arteries either as a skeletonized (n = 18) or a non-skeletonized graft (n = 21) using an ultrasonic scalpel. We constructed a composite straight graft by combining a right internal thoracic artery and a radial artery. All the radial artery grafts were sequentially anastomosed to coronary arteries. We measured the diameters of the radial arteries before the operation, within 1 month and 1 year after the operation. At early postoperative period, graft diameter was significantly larger in skeletonized grafts. Graft diameter at the point before the first and the second anastomosis was similar in skeletonized grafts, although that was significantly smaller before the second anastomosis in non-skeletonized grafts. However, 1 year after the operation, the graft diameter was comparable and equally reduced after the first anastomosis in both groups. Skeletonization with an ultrasonic scalpel increases the luminal diameter of the radial artery graft at early postoperative period, which, however, reduces possibly as adaptation to graft flow 1 year after the operation.
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spelling pubmed-48204722016-04-11 Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period Maruyama, Takuto Kohno, Hiroki Ishida, Keiichi Ishizaka, Toru Funabashi, Nobusada Kobayashi, Yoshio Matsumiya, Goro Heart Vessels Original Article The radial artery is increasingly used as a second arterial conduit for myocardial revascularization. However, the radial artery is susceptible to vasospasm, which is thought to be the principal cause of graft failure. The radial artery is harvested as a skeletonized or a non-skeletonized graft, but the effect of different harvesting technique remains unknown. In this study, we compared the early- and mid-term angiographic findings to elucidate its influence on the graft luminal diameter. We harvested 39 radial arteries either as a skeletonized (n = 18) or a non-skeletonized graft (n = 21) using an ultrasonic scalpel. We constructed a composite straight graft by combining a right internal thoracic artery and a radial artery. All the radial artery grafts were sequentially anastomosed to coronary arteries. We measured the diameters of the radial arteries before the operation, within 1 month and 1 year after the operation. At early postoperative period, graft diameter was significantly larger in skeletonized grafts. Graft diameter at the point before the first and the second anastomosis was similar in skeletonized grafts, although that was significantly smaller before the second anastomosis in non-skeletonized grafts. However, 1 year after the operation, the graft diameter was comparable and equally reduced after the first anastomosis in both groups. Skeletonization with an ultrasonic scalpel increases the luminal diameter of the radial artery graft at early postoperative period, which, however, reduces possibly as adaptation to graft flow 1 year after the operation. Springer Japan 2015-02-06 2016 /pmc/articles/PMC4820472/ /pubmed/25656931 http://dx.doi.org/10.1007/s00380-015-0639-3 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Maruyama, Takuto
Kohno, Hiroki
Ishida, Keiichi
Ishizaka, Toru
Funabashi, Nobusada
Kobayashi, Yoshio
Matsumiya, Goro
Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title_full Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title_fullStr Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title_full_unstemmed Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title_short Change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
title_sort change of luminal diameter of skeletonized and non-skeletonized radial artery graft at early and late postoperative period
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820472/
https://www.ncbi.nlm.nih.gov/pubmed/25656931
http://dx.doi.org/10.1007/s00380-015-0639-3
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