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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6497337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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