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J Cardiovasc Pharmacol ; 75(2): 180-184, 2020 02.
Article in English | MEDLINE | ID: mdl-32023227

ABSTRACT

Rivaroxaban is a direct oral anti-factor Xa anticoagulant. It has recently been suggested that rivaroxaban may affect platelet function in vitro; however, little is known about the clinical impact of this likely antiplatelet effect and whether this probable phenomenon is dose-dependent. Our aim was to determine whether rivaroxaban at 4 different doses inhibits direct platelet aggregation. We included adult patients of both sexes and who were allocated to one of the following groups depending on the prescribed daily dose of rivaroxaban: 5, 10, 15, and 20 mg. In 80 patients (20 patients/group), the percentage of platelet aggregation was determined by means of platelet aggregometry tests before and after rivaroxaban use. Basal samples were obtained before starting rivaroxaban and 1 month after treatment, both 2 and 24 hours after the last dose of the drug (12 hours after in the case of rivaroxaban 5 mg). We used 5 platelet agonists: adenosine diphosphate, epinephrine, arachidonic acid, collagen, and thrombin. There were no significant changes in the percentage of platelet aggregation before and after rivaroxaban use independently of the dose administered and the agonist used. Our results have clearly shown that rivaroxaban, even at a high dose, does not directly affect platelet aggregation.


Subject(s)
Factor Xa Inhibitors/administration & dosage , Platelet Aggregation/drug effects , Rivaroxaban/administration & dosage , Adolescent , Adult , Aged , Factor Xa Inhibitors/adverse effects , Female , Humans , Longitudinal Studies , Male , Middle Aged , Platelet Function Tests , Prospective Studies , Rivaroxaban/adverse effects , Time Factors , Treatment Outcome , Young Adult
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