Affiliation:
1. University Medical Centre, Department of Vascular Diseases, Ljubljana, Slovenia
Abstract
The clinical efficacy of antiplatelet therapy (aspirin, P2Y12 and
glycoprotein IIb/IIIa receptor antagonists) to prevent occlusive arterial
events in patients with atherothrombotic disease is well established. Despite
the proven benefits of antiplatelet therapy, many patients continue to
experience arterial events. Many factors may influence the response of
platelets to antiplatelet therapy and some patients with adequate compliance
to the treatment may exhibit failure of platelet inhibition as determined by
ex vivo laboratory tests, a phenomenon termed ?resistance?to antiplatelet
therapy. Platelet function can be measured by numerous platelet function
tests, with which various parameters of platelet activation, secretion,
adhesion and aggregation can be determined. These tests include light
transmission (optical) and whole blood aggregometry, point-of-care devices,
such as platelet function analyzers PFA-100?, and VerifyNow?, flow cytometry,
serum thromboxane B2 and urinary levels of the thromboxane B2 metabolite
11-dehyro-thromboxane B2. Other tests, such as whole blood platelet
aggregation measured by platelet counting, thrombelastography and devices
such as the cone and plate(let) analyzer, Plateletworks and thrombotic status
analyzer have also been used to determine platelet inhibition by antiplatelet
drugs, but their use is not widespread and therefore experience is limited.
Further studies need to be carried out to answer basic questions on the
clinical utility and cost-effectiveness of laboratory monitoring of
antiplatelet therapy before it can be recommended in clinical practice.
Publisher
National Library of Serbia
Cited by
7 articles.
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