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Author Notes:

Correspondance: Renu Virmani, MD, Medical Director, CVPath Institute, Inc., 19 Firstfield, Road, Gaithersburg, MD 20878, Phone (301) 208–3570, Fax (301) 208–3745, rvirmani@cvpath.org

Dr. Virmani is a consultant for Medtronic AVE, Abbott Vascular, W.L. Gore, Atrium Medical, Arsenal Medical, Atrium, and Lutonix.

Subjects:

Research Funding:

Dr. Finn is supported by the NIH grant HL096970-01A1, the Carlyle Fraser Heart Center at Emory University, sponsored research agreement with Medtronic and St. Jude Medical, and is a consultant for Abbott Vascular and Cordis.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cardiac & Cardiovascular Systems
  • Cardiovascular System & Cardiology
  • bare-metal stent(s)
  • drug-eluting stent(s)
  • pathology
  • saphenous vein bypass graft
  • CORONARY-ARTERY-DISEASE
  • BALLOON ANGIOPLASTY
  • FOLLOW-UP
  • SIROLIMUS
  • IMPLANTATION
  • THROMBOSIS
  • INTERVENTION
  • PREDICTORS
  • RESTENOSIS
  • PLACEMENT

Pathology of Drug-Eluting Versus Bare-Metal Stents in Saphenous Vein Bypass Graft Lesions

Tools:

Journal Title:

JACC: Cardiovascular Interventions

Volume:

Volume 5, Number 6

Publisher:

, Pages 666-674

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Objectives: The purpose of this study was to assess the pathological responses of atherosclerotic saphenous vein bypass grafts (SVBGs) to drug-eluting stents (DES) versus bare-metal stents (BMS). Background: Repeat bypass surgery is typically associated with a high rate of morbidity and mortality. Percutaneous coronary interventions have emerged as the preferred treatment; however, only limited data are available on SVBGs pathological responses to DES and BMS. Methods: Formalin-fixed SVBG of > 2 years duration (n = 31) were collected to histologically characterize advanced atherosclerotic lesions in native SVBG. In a separate group, SVBGs treated with DES (n = 9) and BMS (n = 9) for > 30 days duration were assessed for morphological and morphometric changes. Results: Necrotic core lesions were identified in 25% of SVBG sections, and plaque rupture with luminal thrombosis was observed in 6.3% of histological sections (32% [10 of 31] vein grafts examined). Morphometry of DES demonstrated reduction in neointimal thickening versus BMS (0.13 mm [interquartile range: 0.06 to 0.16 mm] vs. 0.30 mm [interquartile range: 0.20 to 0.48 mm], p = 0.004). DES lesions also showed greater delayed healing characterized by increased peristrut fibrin deposition, higher percentage of uncovered struts, and less endothelialization compared with BMS. Stent fractures (DES 56% vs. BMS 11%, p = 0.045) and late stent thrombosis (DES 44% vs. BMS 0%, p = 0.023) were more common in DES versus BMS. Conclusions: Advanced SVBG atherosclerotic lesions are characterized by large hemorrhagic necrotic cores. Stenting of such lesions is associated with delayed vascular healing and late thrombosis particularly following DES implantation, which may help explain the higher rates of cardiovascular events observed in SVBG stenting as compared with native coronary arteries.

Copyright information:

© 2012 American College of Cardiology Foundation.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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