| Literature DB >> 30453344 |
Joanna Sikora1, Piotr Niezgoda2, Malwina Barańska2, Katarzyna Buszko3, Natalia Skibińska2, Wiktor Sroka4, Krzysztof Pstrągowski2, Jolanta Siller-Matula5, Jilma Bernd6, Diana Gorog7, Eliano Pio Navarese1,8,9, Michał Piotr Marszałł4, Jacek Kubica2.
Abstract
Extensive search for methods of overcoming morphine-related delay of the absorption and onset of action of oral P2Y12 inhibitors in patients presenting with acute coronary syndrome is on-going. The aim of the trial was to investigate whether metoclopramide co-administration could reduce this delay and improve the pharmacokinetics (PKs) and pharmacodynamics (PDs) of ticagrelor and its active metabolite AR-C124900XX. Plasma concentration of both compounds and platelet reactivity were evaluated in nine pre-defined time points within 6 hours after administration of ticagrelor loading dose. The results of our study show that mean platelet activity within the first hour was noticeably higher in metoclopramide-naive patients. Moreover, ticagrelor mean plasma concentration was significantly higher within the initial four time points (15, 30, 45, 60 minutes) in patients receiving metoclopramide (p = 0.039; p = 0.009; p = 0.005; p = 0.008, respectively). To conclude, the co-administration of metoclopramide in patients presenting with unstable angina and treated with morphine, has a beneficial effect on the PK/PD profile of ticagrelor and its metabolite; however, its impact on ST-elevation myocardial infarction patients requires further investigation. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2018 PMID: 30453344 DOI: 10.1055/s-0038-1675605
Source DB: PubMed Journal: Thromb Haemost ISSN: 0340-6245 Impact factor: 5.249