Saphenous Vein Grafts With Multiple Versus Single Distal Targets in Patients Undergoing Coronary Artery Bypass Surgery

  • Rajendra H. Mehta
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • T. Bruce Ferguson
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Renato D. Lopes
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Gail E. Hafley
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Michael J. Mack
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Nicholas T. Kouchoukos
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • C. Michael Gibson
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Robert A. Harrington
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Robert M. Califf
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • Eric D. Peterson
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).
  • John H. Alexander
    From the Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.H.M., R.D.L., G.E.H., R.A.H., R.M.C., E.D.P., J.H.A.); The Brody School of Medicine, East Carolina University, Greensville, NC (B.F.); Medical City Hospital, Dallas, TX (M.J.M.); Missouri Baptist Medical Center, St. Louis, MO (N.T.K); and Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).

書誌事項

タイトル別名
  • One-Year Graft Failure and Five-Year Outcomes From the Project of Ex-Vivo Vein Graft Engineering via Transfection (PREVENT) IV Trial

抄録

<jats:sec> <jats:title>Background—</jats:title> <jats:p>Limited information exists on the intermediate-term graft patency and 5-year clinical outcomes of patients receiving saphenous vein grafts with multiple (m-SVG) versus single distal targets (s-SVG) during coronary artery bypass graft (CABG) surgery in the current era.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods and Results—</jats:title> <jats:p>We studied the association of the use of m-SVG versus s-SVG conduits with 1-year SVG failure (defined as ≥75% angiographic stenosis) and 5-year clinical events (death; death or myocardial infarction [MI]; and death, MI, or revascularization) in 3014 patients undergoing their first CABG surgery enrolled in the Project of Ex-vivo Vein Graft Engineering via Transfection (PREVENT) IV. Of 3014 patients enrolled in PREVENT IV, 1045 (34.7%) had ≥1 m-SVGs during CABG. Vein graft failure at 1-year was higher for m-SVG compared with s-SVG (adjusted odds ratio 1.24, 95% confidence interval 1.03 to 1.48). At 5 years, the adjusted composite of death, MI (including perioperative MI), or revascularization (hazard ratio 1.15, 95% confidence interval 1.00 to 1.31) and death or MI (hazard ratio 1.21, 95% confidence interval 1.03 to 1.43) were significantly higher in patients receiving m-SVGs.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions—</jats:title> <jats:p>In patients undergoing first CABG surgery, the use of m-SVG was associated with a higher 1-year vein graft failure rate and trends toward worse clinical outcomes. Additional studies are needed to better understand the most appropriate conduit to improve long-term graft patency and clinical outcomes of patients undergoing CABG surgery. In the meantime, these data should encourage the use of s-SVG over m-SVG when feasible.</jats:p> </jats:sec>

収録刊行物

  • Circulation

    Circulation 124 (3), 280-288, 2011-07-19

    Ovid Technologies (Wolters Kluwer Health)

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