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Serial Changes Of Platelet Function In Acute Myocardial Infarction Treated By Primary Percutaneous Transluminal Coronary Angioplasty

Posted on:2002-03-01Degree:MasterType:Thesis
Country:ChinaCandidate:Y X MaFull Text:PDF
GTID:2144360032956158Subject:Internal Medicine
Abstract/Summary:PDF Full Text Request
Objective To observe the serial change of platelet function before and early after primary percutaneous transluminal coronary angioplasty (P-PTCA)in patients with acute myocardial infarction(AMI) to provide an evidence to antiplatelet therapy for patients treated by P-PTCA. Methods 33 Patients with AMI undergoing P-PTCA successfully within 6 hours after the onset of symptom were included. Venous blood samples were obtained according to schedule. CD62P,PAC-1 and CD61b were tested by flow cytometric analysis. 10 sex and age matched healthy subjects were chosen as control group. Results 33 patients with AMI before P-PTCA, CD62P was 3.68±1.57 and PAC-1 was 1.82±0.73,they were significantly higher than control group (P<0.01); CD62P and PAC-1 decreased gradually and reached the lowest at 8 hours after PTCA,CD62p was1.85±0.71and PAC-1 was 1.35±0.66, significantly lower than that before P-PTCA; and then CD62p and PAC-1 increased gradually, reached the peak at 24hours after PTCA,CD62p was 3.98±1.52 and PAC-1 was 2.28±0.87,significantly higher than before( P<0.01); 72 hours later,CD62P and PAC-1 decreased again and reduced to the normal level 168 hours after P-PTCA. CD61b did not show significant change before P-PTCA compared with control group (P>0.05). CD61b of different time after P-PTCA did not show significant difference either (P>0.05). Conclusion P-PTCA in patients with AMI can recanalize infarction related artery(IRA)earlier but activate platelet meanwhile, the risk of acute and subacute thrombosis increased. The present data provide a basis for more effective antiplatelet strategies in AMI patients treated by P-PTCA.
Keywords/Search Tags:acute myocardial infarction, primary percutaneous transluminal coronary angioplasty, membrane glycoproteins, platelet activation
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