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Society of University Surgeons| Volume 74, ISSUE 2, P263-275, August 1973

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Utility of anticoagulant drugs in vascular thrombosis: Electron microscopic and biophysical study

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      Abstract

      Studies in dogs demonstrated that injuries produced by Fogarty catheterization, electricity, and crushing were different, as evaluated by the interface potential and scanning electron microscope. Fogarty catheterization destroyed the integrity of the vascular potential, evulsing the intima from underlying media usually with much platelets and cells sticking to underlying collagen and causing progressive thrombosis. The positively charged electrode caused much destruction, “building block” surface thrombosis, and obvious geographical destruction. These results were more or less reversed by heparin so that the normal rugae were still discernible. Crushing physically destroyed the integrity of blood vessel walls, markedly reducing normal negative interface potentials. The damaged crevices filled in by what appears to be a smooth platelet fibrin layer. Thrombi under each condition have both different appearance and different cellular structure. All of this is reversed by heparin and promoted by protamine. The thrombotic response to injury is modulated by the mechanism of damage, the order of magnitude of injury, and the coagulant status of the blood and the vascular tree. The effects of injury are modified by heparin and other anticoagulant agents. In the face of continuing blood flow, their application appear to limit the effects of injury.
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