Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729618
Title: Assessment of individual responses to antiplatelet therapy in cardiovascular disease : insights with short thrombelastography
Author: Khanna, Vikram
ISNI:       0000 0004 6496 1425
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2016
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Abstract:
The pivotal role of platelets in atherogenesis and thrombosis is well established. Consequently, suppression of platelet function with antiplatelet therapy (APT) is an important therapeutic target for the prevention of cardiovascular events in high-risk populations, particularly in patients treated with percutaneous coronary intervention (PCI). Based on various ex vivo platelet function assays (PFAs), studies have consistently shown heterogeneity in responses to APT. This is especially important given that platelet reactivity has been associated with both atherothrombotic events and bleeding complications at opposite ends of the spectrum. Personalised APT based on assessing individual responses has therefore emerged as a logical solution to the dilemma of optimising clinical outcomes in PCI and CVD, however this has yet to be proven. Furthermore, a number of important questions regarding the delivery of this strategy remain outstanding before it can be implemented in clinical practice. The studies presented in this thesis have universally employed Short Thrombelastography (s-TEG) to: (i) determine whether VerifyNow, a point of care PFA, overestimates the functional effects of clopidogrel compared to s-TEG, based on the inclusion of prostaglandin E1 as agonist; (ii) to evaluate whether responses to APT remain stable over time following hospital discharge thereby obviating the need for serial testing; and (iii) to compare the antiplatelet and anticoagulant effects of unfractionated heparin and bivalirudin, two adjunctive anticoagulant agents used commonly in the setting of primary PCI. Furthermore, there is anecdotal evidence suggesting that arachidonic acid (AA), a substrate of the cyclooxygenase-1 (COX-1) pathway blocked by aspirin, can stimulate clotting via alternative pathway(s). We therefore sought to investigate potential COX-1-independent mechanisms for AA-mediated clotting in a population of patients undergoing major vascular surgery on aspirin. Studies in this thesis raise concerns about the stability of responses to APT over time and highlight the importance of an accurate and reliable assay of platelet function for the successful implementation of a personalised APT strategy. Furthermore, they offer important mechanistic insights into the contrasting pharmacodynamic effects of anticoagulant agents commonly used as adjuncts in PCI. Collectively, these studies could form the basis of larger clinical trials that may influence how these agents are prescribed in the future.
Supervisor: Curzen, Nicholas ; Englyst, Nicola Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.729618  DOI: Not available
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