Cargando…
Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage?
PURPOSE: Patients with glioblastoma (GBM) or brain metastases (MET) and atrial fibrillation (AF) might be at an increased risk of intracranial hemorrhage (ICH) due to anticoagulation (AC). Our aim was to assess this risk. METHODS: Our institution’s database (from 2005 to 2017) was screened for patie...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084835/ https://www.ncbi.nlm.nih.gov/pubmed/33674992 http://dx.doi.org/10.1007/s11060-021-03716-8 |
_version_ | 1783686235951202304 |
---|---|
author | Burth, Sina Ohmann, Mona Kronsteiner, Dorothea Kieser, Meinhard Löw, Sarah Riedemann, Lars Laible, Mona Berberich, Anne Drüschler, Katharina Rizos, Timolaos Wick, Antje Winkler, Frank Wick, Wolfgang Nagel, Simon |
author_facet | Burth, Sina Ohmann, Mona Kronsteiner, Dorothea Kieser, Meinhard Löw, Sarah Riedemann, Lars Laible, Mona Berberich, Anne Drüschler, Katharina Rizos, Timolaos Wick, Antje Winkler, Frank Wick, Wolfgang Nagel, Simon |
author_sort | Burth, Sina |
collection | PubMed |
description | PURPOSE: Patients with glioblastoma (GBM) or brain metastases (MET) and atrial fibrillation (AF) might be at an increased risk of intracranial hemorrhage (ICH) due to anticoagulation (AC). Our aim was to assess this risk. METHODS: Our institution’s database (from 2005 to 2017) was screened for patients with GBM or MET and AF with an indication for AC according to their CHA(2)DS(2)VASc stroke risk score (≥ 2). Required follow-up was at least 3 months. AC was either performed with heparins, phenprocoumon or non-Vitamin K antagonist oral anticoagulants. Applying the propensity score approach, patient cohorts (matched according to primary tumor, age, sex) were generated (GBM [or MET] with AF ± AC, GBM [or MET] without AF/AC, no GBM [or MET] but AF on AC). ICH was defined as clinical deterioration caused by new blood on imaging. A log rank test was performed to compare the risk for ICH between the three groups. RESULTS: In total, 104 patients were identified of which 49 with GBM (37% on AC) and 37 with MET (46% on AC) were successfully matched. Median follow up was 8.6 and 7.2 months, respectively. ICH occurred in 10.2% of GBM + AF and 12.2% GBM-AF, whereas 8% of patients with AF on AC suffered ICH (p = 0.076). 13.5% of patients with MET + AF had ICHs, in the controls it was 16% for MET-AF and 8% for AF on AC (p = 0.11). CONCLUSION: AC did not seem to influence the incidence of ICH in patients with glioblastoma or brain metastases within follow up of just under 9 months. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-021-03716-8. |
format | Online Article Text |
id | pubmed-8084835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-80848352021-05-05 Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? Burth, Sina Ohmann, Mona Kronsteiner, Dorothea Kieser, Meinhard Löw, Sarah Riedemann, Lars Laible, Mona Berberich, Anne Drüschler, Katharina Rizos, Timolaos Wick, Antje Winkler, Frank Wick, Wolfgang Nagel, Simon J Neurooncol Clinical Study PURPOSE: Patients with glioblastoma (GBM) or brain metastases (MET) and atrial fibrillation (AF) might be at an increased risk of intracranial hemorrhage (ICH) due to anticoagulation (AC). Our aim was to assess this risk. METHODS: Our institution’s database (from 2005 to 2017) was screened for patients with GBM or MET and AF with an indication for AC according to their CHA(2)DS(2)VASc stroke risk score (≥ 2). Required follow-up was at least 3 months. AC was either performed with heparins, phenprocoumon or non-Vitamin K antagonist oral anticoagulants. Applying the propensity score approach, patient cohorts (matched according to primary tumor, age, sex) were generated (GBM [or MET] with AF ± AC, GBM [or MET] without AF/AC, no GBM [or MET] but AF on AC). ICH was defined as clinical deterioration caused by new blood on imaging. A log rank test was performed to compare the risk for ICH between the three groups. RESULTS: In total, 104 patients were identified of which 49 with GBM (37% on AC) and 37 with MET (46% on AC) were successfully matched. Median follow up was 8.6 and 7.2 months, respectively. ICH occurred in 10.2% of GBM + AF and 12.2% GBM-AF, whereas 8% of patients with AF on AC suffered ICH (p = 0.076). 13.5% of patients with MET + AF had ICHs, in the controls it was 16% for MET-AF and 8% for AF on AC (p = 0.11). CONCLUSION: AC did not seem to influence the incidence of ICH in patients with glioblastoma or brain metastases within follow up of just under 9 months. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-021-03716-8. Springer US 2021-03-05 2021 /pmc/articles/PMC8084835/ /pubmed/33674992 http://dx.doi.org/10.1007/s11060-021-03716-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Study Burth, Sina Ohmann, Mona Kronsteiner, Dorothea Kieser, Meinhard Löw, Sarah Riedemann, Lars Laible, Mona Berberich, Anne Drüschler, Katharina Rizos, Timolaos Wick, Antje Winkler, Frank Wick, Wolfgang Nagel, Simon Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title | Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title_full | Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title_fullStr | Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title_full_unstemmed | Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title_short | Prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
title_sort | prophylactic anticoagulation in patients with glioblastoma or brain metastases and atrial fibrillation: an increased risk for intracranial hemorrhage? |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084835/ https://www.ncbi.nlm.nih.gov/pubmed/33674992 http://dx.doi.org/10.1007/s11060-021-03716-8 |
work_keys_str_mv | AT burthsina prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT ohmannmona prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT kronsteinerdorothea prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT kiesermeinhard prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT lowsarah prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT riedemannlars prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT laiblemona prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT berberichanne prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT druschlerkatharina prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT rizostimolaos prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT wickantje prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT winklerfrank prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT wickwolfgang prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage AT nagelsimon prophylacticanticoagulationinpatientswithglioblastomaorbrainmetastasesandatrialfibrillationanincreasedriskforintracranialhemorrhage |