Cardiac and vascular imaging with labeled platelets and leukocytes.

The contribution of platelets in atherosclerosis and thrombosis in animal models and in clinical studies has been quantified with 111In-platelet scintigraphy. New in vitro quantitative techniques have been developed using 111In-labeled platelets to determine the number of adherent platelets on deendothelialized surfaces of damaged vessel walls and synthetic vascular grafts. In vivo imaging techniques are semi-quantitative in nature; in these studies 111In radioactivity on thrombotic vessels or graft surfaces of iliac, femoral, or popliteal arteries is compared with contralateral vessels. Background 111In radioactivity in the circulating blood pool of venous and capillary networks and radioactivity in marrow decreases the sensitivity of these techniques. Despite these limitations, the dynamic process of platelet deposition in most of the denuded, atherosclerotic vessels and prostheses in the circulatory system can be recorded. This ongoing thrombosis and embolization has been observed in 5-10-year-old vascular grafts of Teflon and Dacron biomaterials. Currently used platelet function inhibitor drugs, eg, aspirin, Persantine, sulfinpyrazone, and Motrin, have a demonstrable effect on platelet deposition. Slight changes in reduction of platelet deposition on these surfaces due to medical intervention have been observed by noninvasive imaging with 111In-platelets. Subtraction of blood pool radioactivity with 99mTc-labeled autologous red cells and calculation of 111In radioactivity associated with platelet thrombus on vessel walls also have been performed for coronary, carotid, and femoral arteries. Although platelet concentrates are used frequently after open heart surgery (one to six per patient), consumption of platelets in the artificial lung or oxygenator, lysis of platelets during pumping, and suction of blood only recently have been quantified with the use of 111In-labeled platelets. These studies also demonstrated far less trauma to platelets with the use of a membrane rather than a bubble oxygenator. Further reduction in platelet consumption and trauma was observed with the use of prostacyclin, a short-acting drug with significant beneficial effect on platelet thrombus reduction and disaggregation of aggregated platelets. The role of polymorphonuclear leukocytes in inflammation, infection and myocardial infarction, and in vivo evaluation with 111In-leukocyte scintigraphy in animals and humans has been described.(ABSTRACT TRUNCATED AT 400 WORDS)