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Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors
Although intracranial hemorrhage (ICH) is frequent in the setting of brain metastases, there are limited data on the influence of antiplatelet agents on the development of brain tumor–associated ICH. To evaluate whether the administration of antiplatelet agents increases the risk of ICH, we performe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905695/ https://www.ncbi.nlm.nih.gov/pubmed/35086145 http://dx.doi.org/10.1182/bloodadvances.2021006470 |
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author | Miller, Eric J. Patell, Rushad Uhlmann, Erik J. Ren, Siyang Southard, Hannah Elavalakanar, Pavania Weber, Griffin M. Neuberg, Donna Zwicker, Jeffrey I. |
author_facet | Miller, Eric J. Patell, Rushad Uhlmann, Erik J. Ren, Siyang Southard, Hannah Elavalakanar, Pavania Weber, Griffin M. Neuberg, Donna Zwicker, Jeffrey I. |
author_sort | Miller, Eric J. |
collection | PubMed |
description | Although intracranial hemorrhage (ICH) is frequent in the setting of brain metastases, there are limited data on the influence of antiplatelet agents on the development of brain tumor–associated ICH. To evaluate whether the administration of antiplatelet agents increases the risk of ICH, we performed a matched cohort analysis of patients with metastatic brain tumors with blinded radiology review. The study population included 392 patients with metastatic brain tumors (134 received antiplatelet agents and 258 acted as controls). Non–small cell lung cancer was the most common malignancy in the cohort (74.0%), followed by small cell lung cancer (9.9%), melanoma (4.6%), and renal cell cancer (4.3%). Among those who received an antiplatelet agent, 86.6% received aspirin alone and 23.1% received therapeutic anticoagulation during the study period. The cumulative incidence of any ICH at 1 year was 19.3% (95% CI, 14.1-24.4) in patients not receiving antiplatelet agents compared with 22.5% (95% CI, 15.2-29.8; P = .22, Gray test) in those receiving antiplatelet agents. The cumulative incidence of major ICH was 5.4% (95% CI, 2.6-8.3) among controls compared with 5.5% (95% CI, 1.5-9.5; P = .80) in those exposed to antiplatelet agents. The combination of anticoagulation plus antiplatelet agents did not increase the risk of major ICH. The use of antiplatelet agents was not associated with an increase in the incidence, size, or severity of ICH in the setting of brain metastases. |
format | Online Article Text |
id | pubmed-8905695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-89056952022-03-09 Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors Miller, Eric J. Patell, Rushad Uhlmann, Erik J. Ren, Siyang Southard, Hannah Elavalakanar, Pavania Weber, Griffin M. Neuberg, Donna Zwicker, Jeffrey I. Blood Adv Clinical Trials and Observations Although intracranial hemorrhage (ICH) is frequent in the setting of brain metastases, there are limited data on the influence of antiplatelet agents on the development of brain tumor–associated ICH. To evaluate whether the administration of antiplatelet agents increases the risk of ICH, we performed a matched cohort analysis of patients with metastatic brain tumors with blinded radiology review. The study population included 392 patients with metastatic brain tumors (134 received antiplatelet agents and 258 acted as controls). Non–small cell lung cancer was the most common malignancy in the cohort (74.0%), followed by small cell lung cancer (9.9%), melanoma (4.6%), and renal cell cancer (4.3%). Among those who received an antiplatelet agent, 86.6% received aspirin alone and 23.1% received therapeutic anticoagulation during the study period. The cumulative incidence of any ICH at 1 year was 19.3% (95% CI, 14.1-24.4) in patients not receiving antiplatelet agents compared with 22.5% (95% CI, 15.2-29.8; P = .22, Gray test) in those receiving antiplatelet agents. The cumulative incidence of major ICH was 5.4% (95% CI, 2.6-8.3) among controls compared with 5.5% (95% CI, 1.5-9.5; P = .80) in those exposed to antiplatelet agents. The combination of anticoagulation plus antiplatelet agents did not increase the risk of major ICH. The use of antiplatelet agents was not associated with an increase in the incidence, size, or severity of ICH in the setting of brain metastases. American Society of Hematology 2022-03-04 /pmc/articles/PMC8905695/ /pubmed/35086145 http://dx.doi.org/10.1182/bloodadvances.2021006470 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
spellingShingle | Clinical Trials and Observations Miller, Eric J. Patell, Rushad Uhlmann, Erik J. Ren, Siyang Southard, Hannah Elavalakanar, Pavania Weber, Griffin M. Neuberg, Donna Zwicker, Jeffrey I. Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title | Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title_full | Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title_fullStr | Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title_full_unstemmed | Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title_short | Antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
title_sort | antiplatelet medications and risk of intracranial hemorrhage in patients with metastatic brain tumors |
topic | Clinical Trials and Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905695/ https://www.ncbi.nlm.nih.gov/pubmed/35086145 http://dx.doi.org/10.1182/bloodadvances.2021006470 |
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