Thromb Haemost 1985; 53(03): 332-336
DOI: 10.1055/s-0038-1661309
Original Article
Schattauer GmbH Stuttgart

The Effect of Ticlopidine on Platelet Functions in Acute Myocardial Infarction

A Double Blind Controlled Trial
J Bjerre Knudsen
1   The Coagulation Laboratory, the Municipal Hospital, Copenhagen, Denmark
,
E Kjøller
2   The Medical Department II, the Municipal Hospital, Copenhagen, Denmark
,
K Skagen
2   The Medical Department II, the Municipal Hospital, Copenhagen, Denmark
,
J Gormsen
1   The Coagulation Laboratory, the Municipal Hospital, Copenhagen, Denmark
› Author Affiliations
Further Information

Publication History

Received 27 February 1984

Accepted 28 February 1985

Publication Date:
18 July 2018 (online)

Summary

A group of 43 consecutive patients with AMI were randomized to treatment with a novel platelet inhibitor, ticlopidine, or placebo in a double blind study. Treatment was started within 12 hr after onset of precordial pain. Patients who had taken drugs with known platelet inhibitory effect prior to the onset of therapy were excluded.

Platelet survival time (PS) was measured 24–36 hr after onset of precordial pain and after 3 months of treatment in both groups. In the early phase of AMI CK-MB and ASAT were taken twice daily for estimation of infarction size. Platelet function, coagulation factors and fibrinolysis parameters were followed sequentially for 21 days and repeated after 3 months.

In the placebo group a significant reduction in PS (5.62 ± 1.63 S. D. days) was measured in the acute phase of AMI compared to PS 3 months after infarction (8.03 ± 1.20 S.D. days). In the ticlopidine group PS was normal during the acute phase (8.35 ± 1.82 S.D. days). After 3 months of treatment PS was normal in both groups. During the first two weeks after AMI significant changes in coagulation parameters and fibrinolysis indicated an increased risk of thrombosis in both groups. These parameters were unaffected by the platelet inhibitory therapy. Estimated by peak CK-MB and ASAT, infarction size was significantly reduced in the ticlopidine group.

 
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