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The MOVEMENT Trial

BACKGROUND: Morphine administration is a strong predictor of delayed onset of action of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction, likely because of impaired gastrointestinal motility. The aim of this study was to evaluate whether the peripheral opioi...

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Autores principales: Holm, Manne, Tornvall, Per, Henareh, Loghman, Jensen, Ulf, Golster, Nanna, Alström, Patrik, Santos‐Pardo, Irene, Witt, Nils, Fedchenko, Nikolai, Venetsanos, Dimitrios, Beck, Olof, van der Linden, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497337/
https://www.ncbi.nlm.nih.gov/pubmed/30636504
http://dx.doi.org/10.1161/JAHA.118.010152
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author Holm, Manne
Tornvall, Per
Henareh, Loghman
Jensen, Ulf
Golster, Nanna
Alström, Patrik
Santos‐Pardo, Irene
Witt, Nils
Fedchenko, Nikolai
Venetsanos, Dimitrios
Beck, Olof
van der Linden, Jan
author_facet Holm, Manne
Tornvall, Per
Henareh, Loghman
Jensen, Ulf
Golster, Nanna
Alström, Patrik
Santos‐Pardo, Irene
Witt, Nils
Fedchenko, Nikolai
Venetsanos, Dimitrios
Beck, Olof
van der Linden, Jan
author_sort Holm, Manne
collection PubMed
description BACKGROUND: Morphine administration is a strong predictor of delayed onset of action of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction, likely because of impaired gastrointestinal motility. The aim of this study was to evaluate whether the peripheral opioid antagonist methylnaltrexone could improve pharmacodynamics and pharmacokinetics of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction receiving morphine. METHODS AND RESULTS: The MOVEMENT (Methylnaltrexone to Improve Platelet Inhibition of Ticagrelor in Morphine‐Treated Patients With ST‐Segment Elevation Myocardial Infarction) trial was a multicenter, prospective, randomized, controlled trial in patients with ST‐segment–elevation myocardial infarction treated with morphine and ticagrelor. Upon arrival to the catheterization laboratory, patients were randomized to a blinded intravenous injection of either methylnaltrexone (8 or 12 mg according to weight) or 0.9% sodium chloride. The proportion of patients with high on‐treatment platelet reactivity and plasma concentrations of ticagrelor and AR‐C124910XX were assessed at baseline (arrival in the catheterization laboratory) and 1 and 2 hours later. A total of 82 patients received either methylnaltrexone (n=43) or placebo (n=39). Median (interquartile range) time from ticagrelor administration to randomization was 41 (31–50) versus 45.5 (37–60) minutes (P=0.16). Intravenous methylnaltrexone administration did not significantly affect prevalence of high on‐treatment platelet reactivity at 2 hours after inclusion, the primary end point, when compared with placebo (54% versus 51%, P=0.84). Plasma concentrations of ticagrelor and its active metabolite, the prespecified secondary end points, did not differ significantly between the groups over time. There was no significant difference in patient self‐estimated pain between the groups. CONCLUSIONS: Methylnaltrexone did not significantly improve platelet reactivity or plasma concentrations of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction receiving morphine. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT02942550.
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spelling pubmed-64973372019-05-07 The MOVEMENT Trial Holm, Manne Tornvall, Per Henareh, Loghman Jensen, Ulf Golster, Nanna Alström, Patrik Santos‐Pardo, Irene Witt, Nils Fedchenko, Nikolai Venetsanos, Dimitrios Beck, Olof van der Linden, Jan J Am Heart Assoc Original Research BACKGROUND: Morphine administration is a strong predictor of delayed onset of action of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction, likely because of impaired gastrointestinal motility. The aim of this study was to evaluate whether the peripheral opioid antagonist methylnaltrexone could improve pharmacodynamics and pharmacokinetics of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction receiving morphine. METHODS AND RESULTS: The MOVEMENT (Methylnaltrexone to Improve Platelet Inhibition of Ticagrelor in Morphine‐Treated Patients With ST‐Segment Elevation Myocardial Infarction) trial was a multicenter, prospective, randomized, controlled trial in patients with ST‐segment–elevation myocardial infarction treated with morphine and ticagrelor. Upon arrival to the catheterization laboratory, patients were randomized to a blinded intravenous injection of either methylnaltrexone (8 or 12 mg according to weight) or 0.9% sodium chloride. The proportion of patients with high on‐treatment platelet reactivity and plasma concentrations of ticagrelor and AR‐C124910XX were assessed at baseline (arrival in the catheterization laboratory) and 1 and 2 hours later. A total of 82 patients received either methylnaltrexone (n=43) or placebo (n=39). Median (interquartile range) time from ticagrelor administration to randomization was 41 (31–50) versus 45.5 (37–60) minutes (P=0.16). Intravenous methylnaltrexone administration did not significantly affect prevalence of high on‐treatment platelet reactivity at 2 hours after inclusion, the primary end point, when compared with placebo (54% versus 51%, P=0.84). Plasma concentrations of ticagrelor and its active metabolite, the prespecified secondary end points, did not differ significantly between the groups over time. There was no significant difference in patient self‐estimated pain between the groups. CONCLUSIONS: Methylnaltrexone did not significantly improve platelet reactivity or plasma concentrations of orally administered ticagrelor in patients with ST‐segment–elevation myocardial infarction receiving morphine. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT02942550. John Wiley and Sons Inc. 2019-01-13 /pmc/articles/PMC6497337/ /pubmed/30636504 http://dx.doi.org/10.1161/JAHA.118.010152 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Holm, Manne
Tornvall, Per
Henareh, Loghman
Jensen, Ulf
Golster, Nanna
Alström, Patrik
Santos‐Pardo, Irene
Witt, Nils
Fedchenko, Nikolai
Venetsanos, Dimitrios
Beck, Olof
van der Linden, Jan
The MOVEMENT Trial
title The MOVEMENT Trial
title_full The MOVEMENT Trial
title_fullStr The MOVEMENT Trial
title_full_unstemmed The MOVEMENT Trial
title_short The MOVEMENT Trial
title_sort movement trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497337/
https://www.ncbi.nlm.nih.gov/pubmed/30636504
http://dx.doi.org/10.1161/JAHA.118.010152
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