Abstract
Occlusion of saphenous vein grafts is a major problem after coronary artery bypass grafting (CABG). Five to ten percent of patients undergo repeat CABG, mostly because of vein graft occlusion.1,2 The understanding of the pathogenesis of saphenous vein graft occlusion is extrapolated from studies on the atherogenesis in arteries. In the previous chapter the acute histopathological changes were described occurring in human saphenous vein grafts in the first week after implantation. A significant loss of medial smooth muscle cells (SMC) was demonstrated, especially in the circular layer of the media. The extensive loss of endothelial cells was a second remarkable feature. We were interested in the further evolution of these lesions and therefore removed the occluded vein grafts during repeat CABG for further study. Of specific interest were the integrity of the endothelium, the cell composition of the thickened intima and the repair of the media.
Adapted with permission of Blackwell Science Ltd from Kockx et al. Histopathology 1994; 25:365-371.
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References
Foster ED. Reoperation for coronary artery disease. Circulation 1985; 72 (suppl V): 59–64.
Lawrie MD, Morris GC, Calhoon JH, Safi H, Zamora JL, Beltengady M, Baron A, Silvers A, Chapman DW. Clinical results of coronary bypass in 500 patients at least 10 years after operation. Circulation 1982; 66 (suppl I): 1–5.
Smith HS, Geer JC. Morphology of saphenous vein-coronary artery bypass grafts. Arch Pathol Lab Med 1983; 107: 13–18.
Curtiss LK, Black AS, Takagi Y, Plow EF. New mechanism for foam cell generation in atherosclerotic lesions. J Clin Invest 1987; 80: 367–73.
Boerboom LE, Olinger GN, Tie-Zhu L, Rodriguez ER, Ferrans VJ, Kissebah AH. Histologic, morphometric and biochemical evaluation of vein bypass grafts in a nonhuman primate model II. Modification of early changes by platelet inhibition with aspirin and dipyridamole. J Thorac Cardiovasc Surg 1990; 99: 107–12.
Kerr JFR, Wyllie AH, Currie AR. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Brit J Cancer 1972; 26: 239–57.
Ross R, Wight TN, Strandness E, Thiele B. Human atherosclerosis I. Cell constitution and characteristics of advanced lesions of the superficial femoral artery. Am J Pathol 1984; 114: 79–83.
Kockx MM, Cambier BA, Bortier HE, De Meyer GRY, Van Cauwelaert PA. The modulation of smooth muscle cell phenotype is an early event in human aorto-coronary saphenous vein grafts. Virchows Archiv A Pathol Anat 1992; 420: 155–162.
Kockx MM, Wuyts FL, Buyssens N, Van den Bossche RM, De Meyer GRY, Bult H, Herman AG. Longitudinally orientated smooth muscle cells in rabbit arteries. Virchows Archiv A Path Anat 1993; 422: 293–299.
Schwartz SM, Campbell GR, Campbell JH. Replication of smooth muscle cells in vascular disease. Circ Res 1986; 58: 427–44.
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© 1995 Springer-Verlag Berlin Heidelberg
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Kockx, M.M. (1995). The Thickened Intima in Long-Standing Aorto-Coronary Saphenous Vein Grafts. In: Spontaneous and Induced Intima Formation in Blood Vessels. Medical Intelligence Unit. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-22430-4_8
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DOI: https://doi.org/10.1007/978-3-662-22430-4_8
Publisher Name: Springer, Berlin, Heidelberg
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