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Turbidimetry on Human Washed Platelets: The Effect of the Pannexin1-inhibitor Brilliant Blue FCF on Collagen-induced Aggregation
Published on: April 6, 2017
Platelet-suppressant therapy in patients with coronary artery disease
Insights
Platelet survival is shortened in most men with coronary artery disease and graft occlusion. Platelet-suppressant drugs improved survival and graft patency in these patients.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Medical Research
Background:
- Platelets play a role in atherosclerosis and its complications like myocardial infarction and graft occlusion.
- Shortened platelet survival is observed in patients with coronary artery disease.
Purpose of the Study:
- To investigate the relationship between platelet survival and coronary artery disease complications.
- To evaluate the effect of platelet-suppressant drugs on platelet survival and graft patency.
Main Methods:
- Chromium-51 labeling was used to measure platelet survival in men with coronary artery disease.
- Platelet survival was compared between patients with and without saphenous vein graft occlusion.
- The impact of sulfinpyrazone, clofibrate, and dipyridamole on platelet survival and graft patency was assessed.
Main Results:
- Platelet survival was significantly shortened in 68% of men with coronary artery disease.
- Shortened platelet survival was strongly associated with saphenous vein graft occlusion.
- Platelet-suppressant drugs increased platelet survival and were linked to improved graft patency.
Conclusions:
- Shortened platelet survival is a significant factor in coronary artery disease and graft occlusion.
- Platelet-suppressant medications show potential in improving outcomes for patients with coronary artery disease and graft issues.
Abstract:
Platelets may contribute to the pathogenesis of atherosclerosis and to the complications of coronary atherosclerosis, acute myocardial infarction, unstable angina, and sudden cardiac death. In addition, platelets may contribute to saphenous vein aortocoronary graft occlusion. Of 104 men with coronary artery disease, platelet survival (SURV) (chromium51 labeling) was shortened in 68% (3.1+/-0.03 days [average+/-SEM]; normal, 3.7+/-0.03 days; P greater than .001). Three platelet-suppressant drugs, sulfinpyrazone, clofibrate, and dipyridamole increased SURV. Saphenous vein graft occlusion was associated with shortened SURV. Of 36 men with occlusion of at least one graft, SURV was shortened in 35 (2.5+/-0.08 days), whereas in 19 with all grafts open, SURV was shortened in six (3.5+/-0.10 days; P less than .01). These drugs increased SURV (2.3 +/- 0.08 to 2.7 +/- 0.11 days; P less than 0.1) and were associated with improved graft patency (four of 32 grafts after initial bypass vs 30 of 34 grafts open after second operation).
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