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Article: Magnesium therapy within 48 hours of an aneurysmal subarachnoid hemorrhage: Neuro-panacea

TitleMagnesium therapy within 48 hours of an aneurysmal subarachnoid hemorrhage: Neuro-panacea
Authors
KeywordsCerebral vasospasm
Intracranial aneurysm
Magnesium
Subarachnoid hemorrhage
Issue Date2006
Citation
Neurological Research, 2006, v. 28, n. 4, p. 431-435 How to Cite?
AbstractWhereas advances in neurosurgical treatment and intensive care management improve the results from many of the devastating complications associated with aneurysmal subarachnoid hemorrhage, cerebral vasospasm remains a major cause of neurological morbidity and mortality. Experimental studies suggested that MgSO4 inhibits excitatory amino acid release, blocks N-methyl-D-aspartate (NMDA) receptors and prevents calcium entry into the cell. Magnesium also increases red blood cell deformability. These changes may reduce the occurrence of cerebral vasospasm and minimize neuronal injury during episodes of cerebral vasospasm. Our group is currently hosting the intravenous magnesium sulfate to improve outcome after aneurysmal subarachnoid hemorrhage (IMASH) trial, which is a randomized, placebo-controlled, double-blinded, multicentered trial to evaluate the effect of magnesium sulfate infusion on the clinical outcome of patients with aneurysmal subarachnoid hemorrhage since 2002. The pilot result showed a trend towards decreased clinical vasospasm and better patient outcome. Magnesium sulfate infusion may prove to be an effective and inexpensive way to reduce the morbidity and mortality associated with aneurysmal subarachnoid hemorrhage, which is a major breakthrough in the current management. © 2006 W. S. Maney & Son Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/324936
ISSN
2023 Impact Factor: 1.7
2023 SCImago Journal Rankings: 0.586
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWong, George K.C.-
dc.contributor.authorChan, Matthew T.V.-
dc.contributor.authorPoon, Wai S.-
dc.contributor.authorBoet, Ronald-
dc.contributor.authorGin, Tony-
dc.date.accessioned2023-02-27T07:28:23Z-
dc.date.available2023-02-27T07:28:23Z-
dc.date.issued2006-
dc.identifier.citationNeurological Research, 2006, v. 28, n. 4, p. 431-435-
dc.identifier.issn0161-6412-
dc.identifier.urihttp://hdl.handle.net/10722/324936-
dc.description.abstractWhereas advances in neurosurgical treatment and intensive care management improve the results from many of the devastating complications associated with aneurysmal subarachnoid hemorrhage, cerebral vasospasm remains a major cause of neurological morbidity and mortality. Experimental studies suggested that MgSO4 inhibits excitatory amino acid release, blocks N-methyl-D-aspartate (NMDA) receptors and prevents calcium entry into the cell. Magnesium also increases red blood cell deformability. These changes may reduce the occurrence of cerebral vasospasm and minimize neuronal injury during episodes of cerebral vasospasm. Our group is currently hosting the intravenous magnesium sulfate to improve outcome after aneurysmal subarachnoid hemorrhage (IMASH) trial, which is a randomized, placebo-controlled, double-blinded, multicentered trial to evaluate the effect of magnesium sulfate infusion on the clinical outcome of patients with aneurysmal subarachnoid hemorrhage since 2002. The pilot result showed a trend towards decreased clinical vasospasm and better patient outcome. Magnesium sulfate infusion may prove to be an effective and inexpensive way to reduce the morbidity and mortality associated with aneurysmal subarachnoid hemorrhage, which is a major breakthrough in the current management. © 2006 W. S. Maney & Son Ltd.-
dc.languageeng-
dc.relation.ispartofNeurological Research-
dc.subjectCerebral vasospasm-
dc.subjectIntracranial aneurysm-
dc.subjectMagnesium-
dc.subjectSubarachnoid hemorrhage-
dc.titleMagnesium therapy within 48 hours of an aneurysmal subarachnoid hemorrhage: Neuro-panacea-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1179/016164106X115035-
dc.identifier.pmid16759446-
dc.identifier.scopuseid_2-s2.0-33745653507-
dc.identifier.volume28-
dc.identifier.issue4-
dc.identifier.spage431-
dc.identifier.epage435-
dc.identifier.isiWOS:000238656600007-

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