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Variability of non-response to aspirin in patients with peripheral arterial occlusive disease during long-term follow-up. | LitMetric

Variability of non-response to aspirin in patients with peripheral arterial occlusive disease during long-term follow-up.

Ann Hematol

Department of Internal Medicine, Division of Vascular Medicine, J.W. Goethe University Hospital, Theodor-Stern-Kai 7, D-60590, Frankfurt/Main, Germany.

Published: October 2009

AI Article Synopsis

  • Non-responsiveness to aspirin, as shown through lab tests, may indicate higher risk for future vascular events in patients.
  • The study tracked 98 patients with peripheral arterial occlusive disease over about 17 months to assess the stability of aspirin non-responsiveness.
  • Results found that true non-responsiveness is rare (4.1% to 12.2% based on different tests), and many patients showed varying responses to aspirin over time.

Article Abstract

Non-responsiveness to aspirin as detected by laboratory tests may identify patients at high risk for future vascular events. The aim of this prospective study was to evaluate whether non-responsiveness to aspirin is stable over time. Ninety-eight patients with stable peripheral arterial occlusive disease (PAOD) treated with 100 mg/d aspirin were followed over a median timeframe of 17 months. Platelet function tests were performed initially and at follow-up using arachidonic acid-induced light transmittance aggregometry (LTA) in native platelet-rich plasma with the Behring Coagulation Timer and by measuring the collagen-epinephrine closure time (CT) on a Platelet Function Analyzer (PFA-100). When determining platelet function using LTA, four patients (4.1%) had residual platelet function (i.e., MaxAggr > or =78%) despite aspirin treatment, whereas, according to the PFA-100 results, 12 patients (12.2%) were identified as non-responders (i.e., CT <192 s). Fifty-seven patients who were still under treatment with 100 mg/d aspirin at the time of follow-up provided a second blood sample. Further platelet function tests with the PFA-100 system identified a persistent non-responsiveness to aspirin over time in three patients (5.3%) whereas four (7.0%) and 15 (26.3%) patients had changes in response status when platelet function was assessed by LTA and on the PFA-100(R), respectively. We conclude that true non-responsiveness to aspirin is a rare phenomenon in stable PAOD patients. Furthermore, we conclude that in a number of patients, aspirin non-responsiveness is not stable over time.

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Source
http://dx.doi.org/10.1007/s00277-009-0708-8DOI Listing

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