Thromb Haemost 1985; 54(02): 528-532
DOI: 10.1055/s-0038-1657890
Original Article
Schattauer GmbH Stuttgart

Equal Antiplatelet Effects of Aspirin 50 or 324 mg/Day in Patients After Acute Myocardial Infarction

Authors

  • R De Caterina

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • D Giannessi

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • A Boem

    *   The Division of Cardiovascular Medicine, Spedali Riuniti di S. Chiara, Pisa, Italy
  • W Bernini

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • D Battaglia

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • C Michelassi

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • F Dell’Amico

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • A L’Abbate

    The C.N.R. Institute of Clinical Physiology, Pisa, Italy
  • P Patrignani

    **   The Institute of Pharmacology, Universitá Cattolica del Sacro Cuore, Roma, Italy
  • C Patrono

    **   The Institute of Pharmacology, Universitá Cattolica del Sacro Cuore, Roma, Italy
Weitere Informationen

Publikationsverlauf

Received 14. März 1985

Accepted 18. Juni 1985

Publikationsdatum:
18. Juli 2018 (online)

Preview

Summary

This study explores the effects on some hematological parameters of a low-dose aspirin regimen (50 mg/day) versus a conventional aspirin treatment with reported antithrombotic efficacy (324 mg/day), in patients with acute myocardial infarction. Fifteen patients were randomized into 3 equal groups receiving 50 mg or 324 mg aspirin or placebo, daily for 21 days. Compared with placebo, bleeding time was significantly and similarly prolonged with both aspirin doses (+ 71 ± 22% and + 69 ± 20%, mean ± S.D.). Aspirin 50 mg/day suppressed arachidonate-induced platelet aggregation and secondary phase aggregation after ADP and adrenaline. Collagen aggregation was inhibited by 44 ± 15%. In no case were differences in the antiplatelet effects of the two doses observed. The effects of 50 mg/day persisted without attenuation during the observation period. Platelet thromboxane B2 generation during arachidonate-induced aggregation was inhibited by 95 ± 2 and 99 ± 1% compared to placebo group after 50 and 324 mg/day, respectively (P between doses <0.05). No change was observed with any treatment in coagulation time, prothrombin time or plasma thromboplastin time. Thus, in patients with acute myocardial infarction, the antiplatelet effects of aspirin 50 mg/day are stable over time and superimposable on those of 324 mg/day. The antithrombotic efficacy of aspirin 50 mg/day remains to be tested clinically.