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Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants
BACKGROUND: Point-of-care testing (POCT) of coagulation has been proven to be of great value in accelerating emergency treatment. Specific POCT for direct oral anticoagulants (DOAC) is not available, but the effects of DOAC on established POCT have been described. We aimed to determine the diagnosti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309971/ https://www.ncbi.nlm.nih.gov/pubmed/28196509 http://dx.doi.org/10.1186/s13054-017-1619-z |
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author | Ebner, Matthias Birschmann, Ingvild Peter, Andreas Spencer, Charlotte Härtig, Florian Kuhn, Joachim Blumenstock, Gunnar Zuern, Christine S. Ziemann, Ulf Poli, Sven |
author_facet | Ebner, Matthias Birschmann, Ingvild Peter, Andreas Spencer, Charlotte Härtig, Florian Kuhn, Joachim Blumenstock, Gunnar Zuern, Christine S. Ziemann, Ulf Poli, Sven |
author_sort | Ebner, Matthias |
collection | PubMed |
description | BACKGROUND: Point-of-care testing (POCT) of coagulation has been proven to be of great value in accelerating emergency treatment. Specific POCT for direct oral anticoagulants (DOAC) is not available, but the effects of DOAC on established POCT have been described. We aimed to determine the diagnostic accuracy of Hemochron® Signature coagulation POCT to qualitatively rule out relevant concentrations of apixaban, rivaroxaban, and dabigatran in real-life patients. METHODS: We enrolled 68 patients receiving apixaban, rivaroxaban, or dabigatran and obtained blood samples at six pre-specified time points. Coagulation testing was performed using prothrombin time/international normalized ratio (PT/INR), activated partial thromboplastin time (aPTT), and activated clotting time (ACT+ and ACT-low range) POCT cards. For comparison, laboratory-based assays of diluted thrombin time (Hemoclot) and anti-Xa activity were conducted. DOAC concentrations were determined by liquid chromatography-tandem mass spectrometry. RESULTS: Four hundred and three samples were collected. POCT results of PT/INR and ACT+ correlated with both rivaroxaban and dabigatran concentrations. Insufficient correlation was found for apixaban. Rivaroxaban concentrations at <30 and <100 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.0 and ≤1.1 and ACT+ POCT ≤120 and ≤130 s. Dabigatran concentrations at <30 and <50 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.1 and ≤1.2 and ACT+ POCT ≤100 s. CONCLUSIONS: Hemochron® Signature POCT can be a fast and reliable alternative for guiding emergency treatment during rivaroxaban and dabigatran therapy. It allows the rapid identification of a relevant fraction of patients that can be treated immediately without the need to await the results of much slower laboratory-based coagulation tests. TRIAL REGISTRATION: Unique identifier, NCT02371070. Retrospectively registered on 18 February 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-017-1619-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5309971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53099712017-03-13 Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants Ebner, Matthias Birschmann, Ingvild Peter, Andreas Spencer, Charlotte Härtig, Florian Kuhn, Joachim Blumenstock, Gunnar Zuern, Christine S. Ziemann, Ulf Poli, Sven Crit Care Research BACKGROUND: Point-of-care testing (POCT) of coagulation has been proven to be of great value in accelerating emergency treatment. Specific POCT for direct oral anticoagulants (DOAC) is not available, but the effects of DOAC on established POCT have been described. We aimed to determine the diagnostic accuracy of Hemochron® Signature coagulation POCT to qualitatively rule out relevant concentrations of apixaban, rivaroxaban, and dabigatran in real-life patients. METHODS: We enrolled 68 patients receiving apixaban, rivaroxaban, or dabigatran and obtained blood samples at six pre-specified time points. Coagulation testing was performed using prothrombin time/international normalized ratio (PT/INR), activated partial thromboplastin time (aPTT), and activated clotting time (ACT+ and ACT-low range) POCT cards. For comparison, laboratory-based assays of diluted thrombin time (Hemoclot) and anti-Xa activity were conducted. DOAC concentrations were determined by liquid chromatography-tandem mass spectrometry. RESULTS: Four hundred and three samples were collected. POCT results of PT/INR and ACT+ correlated with both rivaroxaban and dabigatran concentrations. Insufficient correlation was found for apixaban. Rivaroxaban concentrations at <30 and <100 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.0 and ≤1.1 and ACT+ POCT ≤120 and ≤130 s. Dabigatran concentrations at <30 and <50 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.1 and ≤1.2 and ACT+ POCT ≤100 s. CONCLUSIONS: Hemochron® Signature POCT can be a fast and reliable alternative for guiding emergency treatment during rivaroxaban and dabigatran therapy. It allows the rapid identification of a relevant fraction of patients that can be treated immediately without the need to await the results of much slower laboratory-based coagulation tests. TRIAL REGISTRATION: Unique identifier, NCT02371070. Retrospectively registered on 18 February 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-017-1619-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-15 /pmc/articles/PMC5309971/ /pubmed/28196509 http://dx.doi.org/10.1186/s13054-017-1619-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ebner, Matthias Birschmann, Ingvild Peter, Andreas Spencer, Charlotte Härtig, Florian Kuhn, Joachim Blumenstock, Gunnar Zuern, Christine S. Ziemann, Ulf Poli, Sven Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title | Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title_full | Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title_fullStr | Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title_full_unstemmed | Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title_short | Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
title_sort | point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309971/ https://www.ncbi.nlm.nih.gov/pubmed/28196509 http://dx.doi.org/10.1186/s13054-017-1619-z |
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