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Clinical review: Traumatic brain injury in patients receiving antiplatelet medication
As the population ages, emergency physicians are confronted with a growing number of trauma patients receiving antithrombotic and antiplatelet medication prior to injury. In cases of traumatic brain injury, pre-injury treatment with anticoagulants has been associated with an increased risk of posttr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580675/ https://www.ncbi.nlm.nih.gov/pubmed/22839302 http://dx.doi.org/10.1186/cc11292 |
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author | Beynon, Christopher Hertle, Daniel N Unterberg, Andreas W Sakowitz, Oliver W |
author_facet | Beynon, Christopher Hertle, Daniel N Unterberg, Andreas W Sakowitz, Oliver W |
author_sort | Beynon, Christopher |
collection | PubMed |
description | As the population ages, emergency physicians are confronted with a growing number of trauma patients receiving antithrombotic and antiplatelet medication prior to injury. In cases of traumatic brain injury, pre-injury treatment with anticoagulants has been associated with an increased risk of posttraumatic intracranial haemorrhage. Since high age itself is a well-recognised risk factor in traumatic brain injury, this population is at special risk for increased morbidity and mortality. The effects of antiplatelet medication on coagulation pathways in posttraumatic intracranial haemorrhage are not well understood, but available data suggest that the use of these agents increases the risk of an unfavourable outcome, especially in cases of severe traumatic brain injury. Standard laboratory investigations are insufficient to evaluate platelet activity, but new assays for monitoring platelet activity have been developed. Commonly used interventions to restore platelet activity include platelet transfusion and application of haemostatic drugs. Nevertheless, controlled clinical trials have not been carried out and, therefore, clinical practice guidelines are not available. In addition to the risks of the acute trauma, patients are at risk for cardiac events such as life-threatening stent thrombosis if antiplatelet therapy is withdrawn. In this review article, we summarize the pathophysiologic mechanisms of the most commonly used antiplatelet agents and analyse results of studies on the effects of this treatment on patients with traumatic brain injury. Additionally, we focus on opportunities to counteract antiplatelet effects in those patients as well as on considerations regarding the withdrawal of antiplatelet therapy. In those chronically ill patients, an interdisciplinary approach involving intensivists, neurosurgeons as well as cardiologists is often mandatory. |
format | Online Article Text |
id | pubmed-3580675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35806752013-07-26 Clinical review: Traumatic brain injury in patients receiving antiplatelet medication Beynon, Christopher Hertle, Daniel N Unterberg, Andreas W Sakowitz, Oliver W Crit Care Review As the population ages, emergency physicians are confronted with a growing number of trauma patients receiving antithrombotic and antiplatelet medication prior to injury. In cases of traumatic brain injury, pre-injury treatment with anticoagulants has been associated with an increased risk of posttraumatic intracranial haemorrhage. Since high age itself is a well-recognised risk factor in traumatic brain injury, this population is at special risk for increased morbidity and mortality. The effects of antiplatelet medication on coagulation pathways in posttraumatic intracranial haemorrhage are not well understood, but available data suggest that the use of these agents increases the risk of an unfavourable outcome, especially in cases of severe traumatic brain injury. Standard laboratory investigations are insufficient to evaluate platelet activity, but new assays for monitoring platelet activity have been developed. Commonly used interventions to restore platelet activity include platelet transfusion and application of haemostatic drugs. Nevertheless, controlled clinical trials have not been carried out and, therefore, clinical practice guidelines are not available. In addition to the risks of the acute trauma, patients are at risk for cardiac events such as life-threatening stent thrombosis if antiplatelet therapy is withdrawn. In this review article, we summarize the pathophysiologic mechanisms of the most commonly used antiplatelet agents and analyse results of studies on the effects of this treatment on patients with traumatic brain injury. Additionally, we focus on opportunities to counteract antiplatelet effects in those patients as well as on considerations regarding the withdrawal of antiplatelet therapy. In those chronically ill patients, an interdisciplinary approach involving intensivists, neurosurgeons as well as cardiologists is often mandatory. BioMed Central 2012 2012-07-26 /pmc/articles/PMC3580675/ /pubmed/22839302 http://dx.doi.org/10.1186/cc11292 Text en Copyright ©2012 BioMed Central Ltd |
spellingShingle | Review Beynon, Christopher Hertle, Daniel N Unterberg, Andreas W Sakowitz, Oliver W Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title | Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title_full | Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title_fullStr | Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title_full_unstemmed | Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title_short | Clinical review: Traumatic brain injury in patients receiving antiplatelet medication |
title_sort | clinical review: traumatic brain injury in patients receiving antiplatelet medication |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580675/ https://www.ncbi.nlm.nih.gov/pubmed/22839302 http://dx.doi.org/10.1186/cc11292 |
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