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Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial
BACKGROUND: Patients suffering from intracerebral haemorrhage have a poor prognosis, especially if they are using antiplatelet therapy. Currently, no effective acute treatment option for intracerebral haemorrhage exists. Limiting the early growth of intracerebral haemorrhage volume which continues t...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2851678/ https://www.ncbi.nlm.nih.gov/pubmed/20298539 http://dx.doi.org/10.1186/1471-2377-10-19 |
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author | de Gans, Koen de Haan, Rob J Majoie, Charles B Koopman, Maria M Brand, Anneke Dijkgraaf, Marcel G Vermeulen, Marinus Roos, Yvo B |
author_facet | de Gans, Koen de Haan, Rob J Majoie, Charles B Koopman, Maria M Brand, Anneke Dijkgraaf, Marcel G Vermeulen, Marinus Roos, Yvo B |
author_sort | de Gans, Koen |
collection | PubMed |
description | BACKGROUND: Patients suffering from intracerebral haemorrhage have a poor prognosis, especially if they are using antiplatelet therapy. Currently, no effective acute treatment option for intracerebral haemorrhage exists. Limiting the early growth of intracerebral haemorrhage volume which continues the first hours after admission seems a promising strategy. Because intracerebral haemorrhage patients who are on antiplatelet therapy have been shown to be particularly at risk of early haematoma growth, platelet transfusion may have a beneficial effect. METHODS/DESIGN: The primary objective is to investigate whether platelet transfusion improves outcome in intracerebral haemorrhage patients who are on antiplatelet treatment. The PATCH study is a prospective, randomised, multi-centre study with open treatment and blind endpoint evaluation. Patients will be randomised to receive platelet transfusion within six hours or standard care. The primary endpoint is functional health after three months. The main secondary endpoints are safety of platelet transfusion and the occurrence of haematoma growth. To detect an absolute poor outcome reduction of 20%, a total of 190 patients will be included. DISCUSSION: To our knowledge this is the first randomised controlled trial of platelet transfusion for an acute haemorrhagic disease. TRIAL REGISTRATION: The Netherlands National Trial Register (NTR1303) |
format | Text |
id | pubmed-2851678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28516782010-04-09 Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial de Gans, Koen de Haan, Rob J Majoie, Charles B Koopman, Maria M Brand, Anneke Dijkgraaf, Marcel G Vermeulen, Marinus Roos, Yvo B BMC Neurol Study protocol BACKGROUND: Patients suffering from intracerebral haemorrhage have a poor prognosis, especially if they are using antiplatelet therapy. Currently, no effective acute treatment option for intracerebral haemorrhage exists. Limiting the early growth of intracerebral haemorrhage volume which continues the first hours after admission seems a promising strategy. Because intracerebral haemorrhage patients who are on antiplatelet therapy have been shown to be particularly at risk of early haematoma growth, platelet transfusion may have a beneficial effect. METHODS/DESIGN: The primary objective is to investigate whether platelet transfusion improves outcome in intracerebral haemorrhage patients who are on antiplatelet treatment. The PATCH study is a prospective, randomised, multi-centre study with open treatment and blind endpoint evaluation. Patients will be randomised to receive platelet transfusion within six hours or standard care. The primary endpoint is functional health after three months. The main secondary endpoints are safety of platelet transfusion and the occurrence of haematoma growth. To detect an absolute poor outcome reduction of 20%, a total of 190 patients will be included. DISCUSSION: To our knowledge this is the first randomised controlled trial of platelet transfusion for an acute haemorrhagic disease. TRIAL REGISTRATION: The Netherlands National Trial Register (NTR1303) BioMed Central 2010-03-18 /pmc/articles/PMC2851678/ /pubmed/20298539 http://dx.doi.org/10.1186/1471-2377-10-19 Text en Copyright ©2010 de Gans et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study protocol de Gans, Koen de Haan, Rob J Majoie, Charles B Koopman, Maria M Brand, Anneke Dijkgraaf, Marcel G Vermeulen, Marinus Roos, Yvo B Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title | Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title_full | Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title_fullStr | Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title_full_unstemmed | Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title_short | Patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
title_sort | patch: platelet transfusion in cerebral haemorrhage: study protocol for a multicentre, randomised, controlled trial |
topic | Study protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2851678/ https://www.ncbi.nlm.nih.gov/pubmed/20298539 http://dx.doi.org/10.1186/1471-2377-10-19 |
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