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Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage
Aneurysmal subarachnoid hemorrhage (aSAH) continues to be associated with significant morbidity and mortality despite advances in care and aneurysm treatment strategies. Cerebral vasospasm continues to be a major source of clinical worsening in patients. We intended to review the clinical and experi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776745/ https://www.ncbi.nlm.nih.gov/pubmed/31583833 http://dx.doi.org/10.1111/cns.13222 |
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author | Daou, Badih J. Koduri, Sravanthi Thompson, B. Gregory Chaudhary, Neeraj Pandey, Aditya S. |
author_facet | Daou, Badih J. Koduri, Sravanthi Thompson, B. Gregory Chaudhary, Neeraj Pandey, Aditya S. |
author_sort | Daou, Badih J. |
collection | PubMed |
description | Aneurysmal subarachnoid hemorrhage (aSAH) continues to be associated with significant morbidity and mortality despite advances in care and aneurysm treatment strategies. Cerebral vasospasm continues to be a major source of clinical worsening in patients. We intended to review the clinical and experimental aspects of aSAH and identify strategies that are being evaluated for the treatment of vasospasm. A literature review on aSAH and cerebral vasospasm was performed. Available treatments for aSAH continue to expand as research continues to identify new therapeutic targets. Oral nimodipine is the primary medication used in practice given its neuroprotective properties. Transluminal balloon angioplasty is widely utilized in patients with symptomatic vasospasm and ischemia. Prophylactic “triple‐H” therapy, clazosentan, and intraarterial papaverine have fallen out of practice. Trials have not shown strong evidence supporting magnesium or statins. Other calcium channel blockers, milrinone, tirilazad, fasudil, cilostazol, albumin, eicosapentaenoic acid, erythropoietin, corticosteroids, minocycline, deferoxamine, intrathecal thrombolytics, need to be further investigated. Many of the current experimental drugs may have significant roles in the treatment algorithm, and further clinical trials are needed. There is growing evidence supporting that early brain injury in aSAH may lead to significant morbidity and mortality, and this needs to be explored further. |
format | Online Article Text |
id | pubmed-6776745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67767452019-10-07 Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage Daou, Badih J. Koduri, Sravanthi Thompson, B. Gregory Chaudhary, Neeraj Pandey, Aditya S. CNS Neurosci Ther Review Articles Aneurysmal subarachnoid hemorrhage (aSAH) continues to be associated with significant morbidity and mortality despite advances in care and aneurysm treatment strategies. Cerebral vasospasm continues to be a major source of clinical worsening in patients. We intended to review the clinical and experimental aspects of aSAH and identify strategies that are being evaluated for the treatment of vasospasm. A literature review on aSAH and cerebral vasospasm was performed. Available treatments for aSAH continue to expand as research continues to identify new therapeutic targets. Oral nimodipine is the primary medication used in practice given its neuroprotective properties. Transluminal balloon angioplasty is widely utilized in patients with symptomatic vasospasm and ischemia. Prophylactic “triple‐H” therapy, clazosentan, and intraarterial papaverine have fallen out of practice. Trials have not shown strong evidence supporting magnesium or statins. Other calcium channel blockers, milrinone, tirilazad, fasudil, cilostazol, albumin, eicosapentaenoic acid, erythropoietin, corticosteroids, minocycline, deferoxamine, intrathecal thrombolytics, need to be further investigated. Many of the current experimental drugs may have significant roles in the treatment algorithm, and further clinical trials are needed. There is growing evidence supporting that early brain injury in aSAH may lead to significant morbidity and mortality, and this needs to be explored further. John Wiley and Sons Inc. 2019-10-03 /pmc/articles/PMC6776745/ /pubmed/31583833 http://dx.doi.org/10.1111/cns.13222 Text en © 2019 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Daou, Badih J. Koduri, Sravanthi Thompson, B. Gregory Chaudhary, Neeraj Pandey, Aditya S. Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title | Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title_full | Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title_fullStr | Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title_full_unstemmed | Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title_short | Clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
title_sort | clinical and experimental aspects of aneurysmal subarachnoid hemorrhage |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776745/ https://www.ncbi.nlm.nih.gov/pubmed/31583833 http://dx.doi.org/10.1111/cns.13222 |
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