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Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection
BACKGROUND: Cervical artery dissection (CeAD) patients with or without stroke are frequently treated with either antiplatelet agents or vitamin K antagonists (VKAs), but few data are reported on the use of nonvitamin K oral anticoagulants (NOACs). METHODS: Between November 2011 and January 2014, we...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559015/ https://www.ncbi.nlm.nih.gov/pubmed/26356074 http://dx.doi.org/10.1002/brb3.349 |
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author | Mustanoja, Satu Metso, Tiina M Putaala, Jukka Heikkinen, Noora Haapaniemi, Elena Salonen, Oili Tatlisumak, Turgut |
author_facet | Mustanoja, Satu Metso, Tiina M Putaala, Jukka Heikkinen, Noora Haapaniemi, Elena Salonen, Oili Tatlisumak, Turgut |
author_sort | Mustanoja, Satu |
collection | PubMed |
description | BACKGROUND: Cervical artery dissection (CeAD) patients with or without stroke are frequently treated with either antiplatelet agents or vitamin K antagonists (VKAs), but few data are reported on the use of nonvitamin K oral anticoagulants (NOACs). METHODS: Between November 2011 and January 2014, we recorded data from patients with a stroke due to vertebral (VAD) or internal carotid artery dissection (ICAD). Patients using oral anticoagulants were included in the study and were divided into two treatment groups: patients using NOACs and those using VKAs. Excellent outcome was defined on modified Rankin Scale (mRS) ≤1 at 6 months. RESULTS: Of 68 stroke patients (67% male; median age 45 [39–53]), six (8.8%; two with VAD and four with ICAD) were treated with NOACs: three with direct thrombin inhibitor dabigatran and three with direct factor Xa inhibitor rivaroxaban. National Institutes of Health Stroke Scale score at baseline was 4 (3–7) in the NOAC versus 2 (1–7) in the VKA groups. Complete recanalization at 6 months was seen in most patients in the NOAC (n = 5; 83%) and VKA (n = 34; 55%) groups. All the patients using NOACs had mRS ≤1 at 6 months and none had an intracerebral hemorrhage (ICH). In the VKA group most patients (n = 48; 77%) had mRS ≤1, one patient (1.7%) had an ICH and one died. CONCLUSIONS: In this small, consecutive single-center patient sample treating ischemic stroke patients with CeAD with NOACs did not bring up safety concerns and resulted in similar, good outcomes compared to patients using VKAs. |
format | Online Article Text |
id | pubmed-4559015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45590152015-09-09 Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection Mustanoja, Satu Metso, Tiina M Putaala, Jukka Heikkinen, Noora Haapaniemi, Elena Salonen, Oili Tatlisumak, Turgut Brain Behav Original Research BACKGROUND: Cervical artery dissection (CeAD) patients with or without stroke are frequently treated with either antiplatelet agents or vitamin K antagonists (VKAs), but few data are reported on the use of nonvitamin K oral anticoagulants (NOACs). METHODS: Between November 2011 and January 2014, we recorded data from patients with a stroke due to vertebral (VAD) or internal carotid artery dissection (ICAD). Patients using oral anticoagulants were included in the study and were divided into two treatment groups: patients using NOACs and those using VKAs. Excellent outcome was defined on modified Rankin Scale (mRS) ≤1 at 6 months. RESULTS: Of 68 stroke patients (67% male; median age 45 [39–53]), six (8.8%; two with VAD and four with ICAD) were treated with NOACs: three with direct thrombin inhibitor dabigatran and three with direct factor Xa inhibitor rivaroxaban. National Institutes of Health Stroke Scale score at baseline was 4 (3–7) in the NOAC versus 2 (1–7) in the VKA groups. Complete recanalization at 6 months was seen in most patients in the NOAC (n = 5; 83%) and VKA (n = 34; 55%) groups. All the patients using NOACs had mRS ≤1 at 6 months and none had an intracerebral hemorrhage (ICH). In the VKA group most patients (n = 48; 77%) had mRS ≤1, one patient (1.7%) had an ICH and one died. CONCLUSIONS: In this small, consecutive single-center patient sample treating ischemic stroke patients with CeAD with NOACs did not bring up safety concerns and resulted in similar, good outcomes compared to patients using VKAs. John Wiley & Sons, Ltd 2015-08 2015-05-30 /pmc/articles/PMC4559015/ /pubmed/26356074 http://dx.doi.org/10.1002/brb3.349 Text en © 2015 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Mustanoja, Satu Metso, Tiina M Putaala, Jukka Heikkinen, Noora Haapaniemi, Elena Salonen, Oili Tatlisumak, Turgut Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title | Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title_full | Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title_fullStr | Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title_full_unstemmed | Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title_short | Helsinki experience on nonvitamin K oral anticoagulants for treating cervical artery dissection |
title_sort | helsinki experience on nonvitamin k oral anticoagulants for treating cervical artery dissection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559015/ https://www.ncbi.nlm.nih.gov/pubmed/26356074 http://dx.doi.org/10.1002/brb3.349 |
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