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Use of the platelet reactivity index by Grotemeyer, platelet function analyzer, and retention test Homburg to monitor therapy with antiplatelet drugs.

Abstract
In 1974, Wu and Hoak described a method for determining circulating platelet aggregates. This method was modified by Grotemeyer in 1983. The platelet reactivity index (PR) is based on the ratio of platelet aggregates in blood samples obtained in different buffer solutions. Platelet aggregates are resolved when blood is sampled in EDTA-buffer, but remain fixed when EDTA-formalin-buffer is used. Generally, the PR is preferred, because in vitro manipulations of platelets are not necessary, and the results are calculated. PR values above 1.05 are suspicious for elevated platelet aggregation. PR values above 1.2 indicate pathological changes in platelet aggregation. The PR is inexpensive (4.0 euro dollars) and rapid to perform. PR values were used successfully to identify nonresponders to secondary prophylaxis with acetylsalicylic acid (ASA), that is, patients suffering from stroke (33%) and patients after cardiac ischemia (18%). Furthermore, elevated PR values correlated significantly with the incidence of arterial thromboembolic complications. The PR correlated well in our prospective study with values received from the retention test Homburg (RT-H) and the platelet function analyzer (PFA-100). The data indicate that the values of the PR seem to be highly predictive for the evaluation of the ASA therapy. However, the PR is not feasible for the determination of the ASA overdosage.
AuthorsJürgen Koscielny, Tunay Aslan, Oliver Meyer, Holger Kiesewetter, Friedrich Jung, Christof Mrowietz, Reinhard Latza
JournalSeminars in thrombosis and hemostasis (Semin Thromb Hemost) Vol. 31 Issue 4 Pg. 464-9 ( 2005) ISSN: 0094-6176 [Print] United States
PMID16149025 (Publication Type: Journal Article)
Chemical References
  • Platelet Aggregation Inhibitors
  • Formaldehyde
  • Edetic Acid
  • Aspirin
Topics
  • Aspirin (pharmacology)
  • Blood Platelets (drug effects)
  • Clinical Trials as Topic
  • Drug Monitoring (methods)
  • Edetic Acid (pharmacology)
  • Female
  • Flow Cytometry
  • Formaldehyde (pharmacology)
  • Humans
  • Platelet Activation
  • Platelet Adhesiveness
  • Platelet Aggregation
  • Platelet Aggregation Inhibitors (pharmacology)
  • Platelet Count
  • Platelet Function Tests (economics, instrumentation, methods)
  • Pregnancy
  • Prospective Studies
  • Thromboembolism
  • Time Factors

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