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      Saphenous Vein Graft Failure: From Pathophysiology to Prevention and Treatment Strategies

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          Abstract

          Saphenous vein grafts (SVGs) remain the most frequently used conduits in coronary artery bypass graft surgery (CABG). Despite advances in surgical techniques and pharmacotherapy, SVG failure rates remain high, often leading to repeat coronary revascularization. The no-touch SVG harvesting technique (minimal graft manipulation with preservation of vasa vasorum and nerves) reduces the risk of SVG failure, whereas the effect of the off-pump technique on SVG patency remains unclear. Use of buffered storage solutions, intraoperative graft flow measurement, careful selection of the target vessels, and physiological assessment of the native coronary circulation before CABG may also reduce the incidence of SVG failure. Perioperative aspirin and high-intensity statin administration are the cornerstones of secondary prevention after CABG. Dual antiplatelet therapy is recommended for off-pump CABG and in patients with a recent acute coronary syndrome. Intermediate (30%–60%) SVG stenoses often progress rapidly. Stenting of intermediate SVG stenoses failed to improve outcomes; hence, treatment focuses on strict control of coronary artery disease risk factors. Redo CABG is associated with higher perioperative mortality compared with percutaneous coronary intervention (PCI); hence, the latter is preferred for most patients requiring repeat revascularization after CABG. SVG PCI is limited by high rates of no-reflow and a high incidence of restenosis during follow-up. Drug-eluting and bare metal stents provide similar long-term outcomes in SVG PCI. Embolic protection devices reduce no-reflow and should be used when feasible. PCI of the corresponding native coronary artery is associated with better short- and long-term outcomes and is preferred over SVG PCI, if technically feasible.

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          Most cited references99

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          2018 ESC/EACTS Guidelines on myocardial revascularization

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            Cardiovascular Risk Reduction with Icosapent Ethyl for Hypertriglyceridemia

            Patients with elevated triglyceride levels are at increased risk for ischemic events. Icosapent ethyl, a highly purified eicosapentaenoic acid ethyl ester, lowers triglyceride levels, but data are needed to determine its effects on ischemic events.
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              2011 ACCF/AHA/SCAI Guideline for Percutaneous Coronary Intervention: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions.

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                Author and article information

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                Journal
                Circulation
                Circulation
                Ovid Technologies (Wolters Kluwer Health)
                0009-7322
                1524-4539
                August 31 2021
                August 31 2021
                : 144
                : 9
                : 728-745
                Affiliations
                [1 ]Center for Coronary Artery Disease, Minneapolis Heart Institute and Minneapolis Heart Institute Foundation, Abbott Northwestern, MN (I.X., I.N., E.V., J.K., M.N.B., V.N.B., E.S.B.).
                [2 ]Second Department of Cardiology, Attikon University Hospital, National and Kapodistrian University of Athens Medical School, Greece (I.X., D.A.).
                [3 ]Division of Cardiac Surgery, Veterans Affairs Boston Healthcare System and Harvard Medical School, Boston, MA (M.A.Z.).
                [4 ]Heart and Vascular Center, Brigham and Women’s Hospital, Harvard Medical School, MA (D.L.B.).
                [5 ]Durham VA Medical Center, Duke University, NC (S.R.).
                [6 ]Quebec Heart and Lung Institute, Laval University, Quebec City, Canada (J.R.-C.).
                [7 ]Hospital Clinic of Barcelona, Barcelona, Spain (J.R.-C.).
                [8 ]Sarver Heart Center, University of Arizona, Tucson (S.G.).
                [9 ]San Francisco VA Medical Center, University of California, San Francisco (K.S.).
                [10 ]Atlanta VA Medical Center, Emory University, GA (K.M.).
                [11 ]VA North Texas Health Care System, University of Texas Southwestern Medical School, Dallas (S.B.).
                [12 ]Henry Ford Hospital, Detroit, MI (K.A.).
                [13 ]Yale School of Medicine, Yale New Haven Hospital (I.N., E.V.).
                Article
                10.1161/CIRCULATIONAHA.120.052163
                34460327
                9d1fd425-d382-4c7c-b011-b113a497d61b
                © 2021
                History

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