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Antiplatelet medication
Antiplatelet medication










antiplatelet medication antiplatelet medication

Nowadays, physicians can choose from multiple antithrombotic treatment regimens including the more potent P2Y12 inhibitors prasugrel ( 5) and ticagrelor ( 6) next to clopidogrel, and the widespread availability of direct oral anticoagulants (DOACs) in addition to vitamin K antagonists (VKA). A delicate balance between limiting ischemic risk while preventing bleeding emerges in patients on antithrombotic treatment. In patients with comorbidities, such as atrial fibrillation or a mechanic valve, the P2Y12 inhibitor is often combined with an anticoagulant ( 3, 4). Patients with coronary artery disease (CAD) undergoing percutaneous coronary intervention (PCI) are generally prescribed dual antiplatelet therapy (DAPT), consisting of aspirin and a P2Y12 inhibitor (P2Y12i), for 6-12 months to prevent recurrent atherothrombotic events ( 1, 2).

antiplatelet medication

Furthermore, the ability of EXTEM CT to identify patients at risk for bleeding may be promising and warrants further research. 62, p = 0.030).Ĭonclusion: ROTEM CT has high potential for identifying anticoagulants and tPA ROTEM could detect a diminished fibrinolytic potential in patients using DAPT. Furthermore, EXTEM CT was significantly prolonged in DAPT patients with bleeding complications during follow-up (68 vs.

antiplatelet medication

Patients receiving anticoagulants had prolonged clotting times (CT) when compared to the control and DAPT group EXTEM and FIBTEM CT could best discriminate between patients (not) using anticoagulants (AUC > 0.97). All post-PCI patients had elevated ROTEM clot stiffness values, but only the DAPT group additionally presented with a decreased fibrinolytic potential as measured with tPA ROTEM. Patients were stratified by antithrombotic regimen consisting of a P2Y12 inhibitor with either aspirin (dual antiplatelet therapy DAPT, n = 323), a vitamin K antagonist (VKA, n = 69) or a direct oral anticoagulant (DOAC, n = 48). Laboratory assessment, including (tPA) ROTEM, was performed one month post-PCI and bleeding/ischemic complications were collected over a five-month follow-up. Methods and Results: In this prospective cohort, 440 patients treated with double antithrombotic therapy after recent PCI and with ≥3 risk factors for either ischemic or bleeding complications were included and compared with a control group ( n = 95) consisting of perioperative patients not using antithrombotic medication. We aimed to explore routine and tissue plasminogen activated (tPA) ROTEM results in a post-PCI population on dual antithrombotic treatment.

  • 4Thrombosis Expert Centre Maastricht, Maastricht University Medical Center+, Maastricht, NetherlandsĪims: Patients using antithrombotic drugs after percutaneous coronary intervention (PCI) are at risk for bleeding and recurrent ischemia.
  • 3Department of Internal Medicine, Maastricht University, Maastricht, Netherlands.
  • 2Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, Netherlands.
  • 1Central Diagnostic Laboratory, Maastricht University Medical Center+, Maastricht, Netherlands.
  • van der Meijden 2, Hugo ten Cate 2,3,4 and Yvonne M.












    Antiplatelet medication