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Inhibition of platelet aggregation by aspirin progressively decreases in long-term treated patients.

作者信息

Pulcinelli Fabio M, Pignatelli Pasquale, Celestini Andrea, Riondino Silvia, Gazzaniga Pier Paolo, Violi Francesco

机构信息

Department of Experimental Medicine and Pathology, University La Sapienza, Viale Regina Elena 324, 00161 Rome, Italy.

出版信息

J Am Coll Cardiol. 2004 Mar 17;43(6):979-84. doi: 10.1016/j.jacc.2003.08.062.

DOI:10.1016/j.jacc.2003.08.062
PMID:15028353
Abstract

OBJECTIVES

We sought to investigate, during a two-year follow-up period, the effects of aspirin on platelet aggregation.

BACKGROUND

The platelets of patients given aspirin may be less sensitive to antiplatelet treatment, although the extent of such phenomenon over long-term follow-up is unclear.

METHODS

Adenosine diphosphate (ADP) and collagen-induced platelet aggregation was periodically monitored before and after 2, 6, 12, and 24 months of treatment with aspirin (n = 150) or ticlopidine (n = 80) in patients matched for gender, age, and risk factors for atherothrombosis.

RESULTS

Compared with baseline values, two months of aspirin treatment significantly inhibited platelet aggregation; thereafter, this inhibitory effect progressively decreased. At 24-month follow-up, collagen-induced platelet aggregation was significantly higher than that observed at two months (p < 0.05); a more pronounced difference was observed when collagen-induced lag phase was considered (p < 0.01). Restoration of platelet aggregation was less evident when ADP was used as an agonist. Conversely, the inhibition induced by ticlopidine was constant throughout follow-up with both agonists.

CONCLUSIONS

The study demonstrates that a long-term treatment with aspirin is associated with a progressive reduction in platelet sensitivity to this drug.

摘要

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