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Updated: May 10, 2026

Procedure for Human Saphenous Veins Ex Vivo Perfusion and External Reinforcement
Published on: October 1, 2014
The future of saphenous vein as a coronary artery bypass conduit
1Department of Cardiology, University of Wales College of Medicine, Cardiff, U.K.
Insights
Autologous saphenous vein grafts have poor patency due to platelet activation. Strategies like improved endothelial preservation and better antiplatelet agents may enhance vein graft patency and offer insights into atherosclerosis.
Area of Science:
- Cardiovascular Surgery
- Vascular Biology
- Pharmacology
Background:
- Autologous saphenous vein grafts are widely used for coronary artery bypass grafting (CABG).
- Despite their common use, saphenous vein grafts exhibit suboptimal long-term patency rates.
- Platelet activation is implicated as a primary driver of early and late vein graft occlusion.
Purpose of the Study:
- To review the evidence linking platelet activation to vein graft occlusion.
- To identify key mechanisms contributing to early and late graft failure.
- To propose a comprehensive strategy for improving vein graft patency.
Main Methods:
- Literature review of studies investigating vein graft occlusion.
- Analysis of evidence implicating platelet activation in graft failure.
- Synthesis of findings to propose therapeutic interventions.
Main Results:
- Platelet activation is a significant factor in both early and late saphenous vein graft occlusion.
- Additional mechanisms, beyond platelet activation, likely contribute to late graft occlusions.
- The pathogenesis of vein graft occlusion shares similarities with coronary atherosclerosis.
Conclusions:
- Improving vein graft patency requires a multi-faceted approach.
- Key strategies include enhanced endothelial preservation during surgery.
- Utilizing advanced antiplatelet agents, managing risk factors like high cholesterol, and employing smooth muscle cell proliferation inhibitors (e.g., heparin) are crucial.
- Investigating vein graft patency may provide valuable insights into the broader process of atherogenesis.
Abstract:
Continuing widespread use of autologous saphenous vein for coronary artery bypass grafting seems unavoidable despite its poor-term patency. We review here the evidence that platelet activation is responsible for early and late vein graft occlusion and conclude that other mechanisms probably contribute to late occlusions. We suggest that a rational strategy to improve vein graft patency should include: improved endothelial preservation during surgical implantation; use of better antiplatelet agents, in particular those which prevent platelet adhesion as well as aggregation; reduction of risk factors including serum cholesterol; and application of agents (e.g. heparin) which inhibit smooth muscle cell proliferation directly. We draw parallels between the pathogenesis of vein graft occlusion and coronary atherosclerosis and suggest that testing strategies for improving vein graft patency may also shed light on atherogenesis.
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