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Heng et al. Vessel Plus 2023;7:31                                          Vessel Plus
               DOI: 10.20517/2574-1209.2023.97



               Review                                                                        Open Access



               The biomechanics and prevention of vein graft

               failure in coronary revascularization


                                                                               2,3
                           1,2
                                                               1,2
                                         1,2
               Elbert E. Heng , Hanjay Wang , Oluwatomisin Obafemi , Alison Marsden , Y. Joseph Woo 1,2,3 , Jack H.
               Boyd 1,2
               1
                Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
               2
                Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
               3
                Department of Bioengineering, Stanford University, Stanford, CA 94035, USA.
               Correspondence to: Dr. Jack H. Boyd, Department of Cardiothoracic Surgery, Stanford University, 870 Quarry Road Extension,
               Palo Alto, CA 94305, USA. E-mail: jackboyd@stanford.edu
               How to cite this article: Heng EE, Wang H, Obafemi O, Marsden A, Woo YJ, Boyd JH. The biomechanics and prevention of vein
               graft failure in coronary revascularization. Vessel Plus 2023;7:31. https://dx.doi.org/10.20517/2574-1209.2023.97
               Received: 1 Aug 2023  First Decision: 19 Sep 2023   Revised: 31 Oct 2023  Accepted: 8 Dec 2023  Published: 15 Dec 2023
               Academic Editors: Jerzy Beltowski, Antonio Calafiore  Copy Editor: Fangyuan Liu  Production Editor: Fangyuan Liu


               Abstract
               Saphenous vein grafts (SVGs) are the most widely used conduit in coronary artery bypass grafting (CABG)
               surgery; however, SVG failures due to neointimal hyperplasia present a significant long-term limitation to the
               effectiveness of myocardial revascularization. This review will provide a comprehensive overview of the biological
               mechanisms of vein graft failure, including compensatory endothelial proliferation, extracellular matrix deposition,
               and adventitial disruption. We will discuss historical and emerging strategies for vein graft failure prevention with a
               focus on the role of mechanical vein graft support using external stenting. Finally, we will highlight the results of
               preclinical and human trials and discuss future directions for investigation.

               Keywords: Coronary artery bypass grafting, saphenous vein, vein graft failure, neointimal hyperplasia, external
               stenting, vein graft remodeling



               INTRODUCTION
               Coronary artery bypass grafting (CABG) is the gold-standard treatment for increasing survival in patients
               with multivessel coronary artery disease (CAD), and saphenous vein grafts (SVGs) remain the most widely
               used conduit in over 350,000 surgeries performed annually in the United States . Despite advances in
                                                                                      [1]
               surgical care and technique, SVG failure following CABG remains a significant cause of morbidity in the






                           © The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing,
                           adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
               long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and
               indicate if changes were made.

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