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dc.contributor.authorPadma, Vasantha
dc.contributor.authorFisher, Marc
dc.contributor.authorMoonis, Majaz
dc.date2022-08-11T08:09:26.000
dc.date.accessioned2022-08-23T16:31:08Z
dc.date.available2022-08-23T16:31:08Z
dc.date.issued2006-05-24
dc.date.submitted2008-04-17
dc.identifier.citationExpert Rev Cardiovasc Ther. 2006 May;4(3):405-15. <a href="http://dx.doi.org/10.1586/14779072.4.3.405">Link to article on publisher's site</a>
dc.identifier.issn1744-8344 (Electronic)
dc.identifier.doi10.1586/14779072.4.3.405
dc.identifier.pmid16716101
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37574
dc.description.abstractThe numerous large-scale randomized clinical trials performed during the last decade on either unfractionated heparin, or low molecular weight heparin have not been able to demonstrate undisputed benefits in patients with acute ischemic stroke, compared with no treatment or aspirin. However, a large number of these trials, including the International Stroke Trial and Chinese Acute Stroke Trial, exhibit severe methodological limitations and need to be interpreted with caution. Knowledge of thromboembolism pathophysiology and clinical experience leads to the theory that heparins will prevent red thrombus formation, propagation and embolism. Heparins effectively prevent venous thrombosis and pulmonary embolism. More trials are needed to test heparins in patients whose cardiocerebrovascular lesions are better defined by newer neuroimaging techniques. The efficacy of heparins has not been adequately tested in patients with defined stroke subtypes and occlusive vascular lesions. Heparins should not be indiscriminately given to all patients with acute ischemic stroke. High-quality, randomized trials that adequately study heparin use in patients using modern technology for vascular lesions and stroke subtypes are lacking, and need to be performed.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16716101&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1586/14779072.4.3.405
dc.subjectAcute Disease
dc.subjectAnticoagulants
dc.subjectBrain Ischemia
dc.subjectHeparin
dc.subjectHeparin, Low-Molecular-Weight
dc.subjectHumans
dc.subjectIntracranial Thrombosis
dc.subjectRecurrence
dc.subjectStroke
dc.subjectVenous Thrombosis
dc.subjectNeurology
dc.subjectNeuroscience and Neurobiology
dc.titleRole of heparin and low-molecular-weight heparins in the management of acute ischemic stroke
dc.typeJournal Article
dc.source.journaltitleExpert review of cardiovascular therapy
dc.source.volume4
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/113
dc.identifier.contextkey492219
html.description.abstract<p>The numerous large-scale randomized clinical trials performed during the last decade on either unfractionated heparin, or low molecular weight heparin have not been able to demonstrate undisputed benefits in patients with acute ischemic stroke, compared with no treatment or aspirin. However, a large number of these trials, including the International Stroke Trial and Chinese Acute Stroke Trial, exhibit severe methodological limitations and need to be interpreted with caution. Knowledge of thromboembolism pathophysiology and clinical experience leads to the theory that heparins will prevent red thrombus formation, propagation and embolism. Heparins effectively prevent venous thrombosis and pulmonary embolism. More trials are needed to test heparins in patients whose cardiocerebrovascular lesions are better defined by newer neuroimaging techniques. The efficacy of heparins has not been adequately tested in patients with defined stroke subtypes and occlusive vascular lesions. Heparins should not be indiscriminately given to all patients with acute ischemic stroke. High-quality, randomized trials that adequately study heparin use in patients using modern technology for vascular lesions and stroke subtypes are lacking, and need to be performed.</p>
dc.identifier.submissionpathneuro_pp/113
dc.contributor.departmentDepartment of Neurology
dc.source.pages405-15


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