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J Thorac Cardiovasc Surg 2004;127:1766-1772
© 2004 The American Association for Thoracic Surgery


Cardiopulmonary support and physiology

A bioabsorbable (polyglactin), nonrestrictive, external sheath inhibits porcine saphenous vein graft thickening

Jamie Y. Jeremy, PhDa,*, Richard Bulbulia, FRCSb, Jason L. Johnson, MSca, Patricia Gadsdon, BScc, Vikram Vijayan, FRCSb, Nilima Shukla, PhDa, Frank C. T. Smith, FRCSb, Gianni D. Angelini, FRCSa

a The Bristol Heart Institute, Bristol Royal Infirmary, University of Bristol, Bristol, UK
b Vascular Studies Unit, Bristol Royal Infirmary, University of Bristol, Bristol, United Kingdom
c School of Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom

Received for publication June 18, 2003; revisions received September 19, 2003; accepted for publication September 23, 2003.

* Address for reprints: Dr Jamie Y Jeremy, Bristol Heart Institute, Bristol Royal Infirmary, University of Bristol, Bristol BS2 8HW, United Kingdom
j.y.jeremy{at}bris.ac.uk

OBJECTIVE: External, nonrestrictive, macro-porous polyester stents prevent neointima formation in porcine vein grafts and have been proposed as a therapeutic approach to the prevention of late vein graft failure. These stents are nonbiodegradable and therefore may promote long-term foreign body problems including infection and inflammation. The effect of external macro-porous biodegradable (polyglactin) sheaths on neointimal and medial thickening in porcine vein grafts was therefore investigated.

METHODS: Bilateral saphenous vein–carotid artery interposition grafting was performed in white Landrace pigs (n = 8) with external placement of polyglactin (Vicryl) sheaths (8 mm in diameter) on 1 side, with the contralateral side acting as a control. One month after surgery, grafts were explanted and wall dimensions measured on histological sections using computer-aided planimetry, and an immunocytochemical appraisal was carried out.

RESULTS: All grafts were patent at explantation. Polyglactin sheaths significantly reduced intimal thickness, medial thickness, and the percentage of proliferating cells compared with unsheathed controls. There was a pronounced accumulation of macrophages, giant cells, endothelial cells, and microvessels within and surrounding the biodegradable sheath compared with controls.

CONCLUSIONS: A nonrestrictive, biodegradable (polyglactin), external sheath reduces medial and intimal thickening in experimental saphenous vein grafts, possibly through inflammatory cell–mediated angiogenesis. If subsequent long-term studies confirm preservation of this beneficial effect, once the sheath biodegrades, this approach may have an advantage over the permanent polyester stent when applied clinically.





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