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Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack
BACKGROUND: The TARDIS trial assessed the safety and efficacy of intensive versus guideline antiplatelet agents given for one month in patients with acute stroke or TIA. The aim of this substudy was to assess the effect of antiplatelet agents taken at baseline on platelet function reactivity and act...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463170/ https://www.ncbi.nlm.nih.gov/pubmed/28630782 http://dx.doi.org/10.1155/2017/7365684 |
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author | Bath, Philip M. May, Jane Flaherty, Katie Woodhouse, Lisa J. Dovlatova, Natalia Fox, Sue C. England, Timothy J. Krishnan, Kailash Robinson, Thompson G. Sprigg, Nikola Heptinstall, Stan Investigators, TARDIS |
author_facet | Bath, Philip M. May, Jane Flaherty, Katie Woodhouse, Lisa J. Dovlatova, Natalia Fox, Sue C. England, Timothy J. Krishnan, Kailash Robinson, Thompson G. Sprigg, Nikola Heptinstall, Stan Investigators, TARDIS |
author_sort | Bath, Philip M. |
collection | PubMed |
description | BACKGROUND: The TARDIS trial assessed the safety and efficacy of intensive versus guideline antiplatelet agents given for one month in patients with acute stroke or TIA. The aim of this substudy was to assess the effect of antiplatelet agents taken at baseline on platelet function reactivity and activation. METHODS: Platelet function, assessed by remotely measured surface expression of P-selectin, was assessed in patients at their time of randomisation. Data are median fluorescence values. RESULTS: The aspirin P-selectin test demonstrated that platelet expression was lower in 494 patients taking aspirin than in 162 patients not: mean 210 (SD 188) versus 570 (435), difference 360.3 (95% CI 312.2–408.4) (2p < 0.001). Aspirin did not suppress P-selectin levels below 500 units in 23 (4.7%) patients. The clopidogrel test showed that platelet reactivity was lower in 97 patients taking clopidogrel than in 585 patients not: 655 (296) versus 969 (315), difference 314.5 (95% CI 247.3–381.7) (2p < 0.001). Clopidogrel did not suppress P-selectin level below 860 units in 24 (24.7%) patients. CONCLUSIONS: Aspirin and clopidogrel suppress stimulated platelet P-selectin, although one-quarter of patients on clopidogrel have high on-treatment platelet reactivity. Platelet function testing may be performed remotely in the context of a large multicentre trial. Trial registration ISRCTN47823388. |
format | Online Article Text |
id | pubmed-5463170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54631702017-06-19 Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack Bath, Philip M. May, Jane Flaherty, Katie Woodhouse, Lisa J. Dovlatova, Natalia Fox, Sue C. England, Timothy J. Krishnan, Kailash Robinson, Thompson G. Sprigg, Nikola Heptinstall, Stan Investigators, TARDIS Stroke Res Treat Clinical Study BACKGROUND: The TARDIS trial assessed the safety and efficacy of intensive versus guideline antiplatelet agents given for one month in patients with acute stroke or TIA. The aim of this substudy was to assess the effect of antiplatelet agents taken at baseline on platelet function reactivity and activation. METHODS: Platelet function, assessed by remotely measured surface expression of P-selectin, was assessed in patients at their time of randomisation. Data are median fluorescence values. RESULTS: The aspirin P-selectin test demonstrated that platelet expression was lower in 494 patients taking aspirin than in 162 patients not: mean 210 (SD 188) versus 570 (435), difference 360.3 (95% CI 312.2–408.4) (2p < 0.001). Aspirin did not suppress P-selectin levels below 500 units in 23 (4.7%) patients. The clopidogrel test showed that platelet reactivity was lower in 97 patients taking clopidogrel than in 585 patients not: 655 (296) versus 969 (315), difference 314.5 (95% CI 247.3–381.7) (2p < 0.001). Clopidogrel did not suppress P-selectin level below 860 units in 24 (24.7%) patients. CONCLUSIONS: Aspirin and clopidogrel suppress stimulated platelet P-selectin, although one-quarter of patients on clopidogrel have high on-treatment platelet reactivity. Platelet function testing may be performed remotely in the context of a large multicentre trial. Trial registration ISRCTN47823388. Hindawi 2017 2017-05-24 /pmc/articles/PMC5463170/ /pubmed/28630782 http://dx.doi.org/10.1155/2017/7365684 Text en Copyright © 2017 Philip M. Bath et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Bath, Philip M. May, Jane Flaherty, Katie Woodhouse, Lisa J. Dovlatova, Natalia Fox, Sue C. England, Timothy J. Krishnan, Kailash Robinson, Thompson G. Sprigg, Nikola Heptinstall, Stan Investigators, TARDIS Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title | Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title_full | Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title_fullStr | Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title_full_unstemmed | Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title_short | Remote Assessment of Platelet Function in Patients with Acute Stroke or Transient Ischaemic Attack |
title_sort | remote assessment of platelet function in patients with acute stroke or transient ischaemic attack |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463170/ https://www.ncbi.nlm.nih.gov/pubmed/28630782 http://dx.doi.org/10.1155/2017/7365684 |
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