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dc.contributor.authorFisher, Marc
dc.contributor.authorBogousslavsky, Julien
dc.date2022-08-11T08:09:26.000
dc.date.accessioned2022-08-23T16:31:06Z
dc.date.available2022-08-23T16:31:06Z
dc.date.issued1998-05-02
dc.date.submitted2008-04-17
dc.identifier.citationJAMA. 1998 Apr 22-29;279(16):1298-303. <a href="http://dx.doi.org/10.1001/jama.279.16.1298">Link to article on publisher's website</a>
dc.identifier.issn0098-7484 (Print)
dc.identifier.doi10.1001/jama.279.16.1298
dc.identifier.pmid9565012
dc.identifier.urihttp://hdl.handle.net/20.500.14038/37568
dc.description.abstractThe effective treatment of acute ischemic stroke remains an important goal of modern medicine and substantive advances are occurring. Recently, thrombolytic therapy with tissue-type plasminogen activator was approved for selected patients with acute ischemic stroke when therapy is started within 3 hours of onset. Streptokinase therapy for acute ischemic stroke has not been shown to be effective and is associated with an increased risk of hemorrhage, although it was not evaluated as early after stroke onset as tissue-type plasminogen activator. Various types of neuroprotective interventions are effective in animal models, but none has yet been proven effective in patients. In the future, combinations of thrombolytic and neuroprotective drugs may be used to attempt maximum rates of recovery after acute ischemic stroke. For combination therapy to achieve its maximum potential, patients with acute ischemic stroke will have to be carefully selected and treated.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9565012&dopt=Abstract ">Link to article in PubMed</a>
dc.relation.urlhttp://jama.ama-assn.org/content/279/16/1298.full.pdf+html
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectBrain Ischemia
dc.subjectCalcium Channel Blockers
dc.subjectFibroblast Growth Factor 2
dc.subjectGABA Agents
dc.subjectHumans
dc.subjectIntracranial Embolism and Thrombosis
dc.subjectNeuroprotective Agents
dc.subjectPatient Selection
dc.subjectPlasminogen Activators
dc.subjectRandomized Controlled Trials as Topic
dc.subjectStreptokinase
dc.subject*Thrombolytic Therapy
dc.subjectTissue Plasminogen Activator
dc.subjectNeurology
dc.subjectNeuroscience and Neurobiology
dc.titleFurther evolution toward effective therapy for acute ischemic stroke
dc.typeJournal Article
dc.source.journaltitleJAMA : the journal of the American Medical Association
dc.source.volume279
dc.source.issue16
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/neuro_pp/107
dc.identifier.contextkey492213
html.description.abstract<p>The effective treatment of acute ischemic stroke remains an important goal of modern medicine and substantive advances are occurring. Recently, thrombolytic therapy with tissue-type plasminogen activator was approved for selected patients with acute ischemic stroke when therapy is started within 3 hours of onset. Streptokinase therapy for acute ischemic stroke has not been shown to be effective and is associated with an increased risk of hemorrhage, although it was not evaluated as early after stroke onset as tissue-type plasminogen activator. Various types of neuroprotective interventions are effective in animal models, but none has yet been proven effective in patients. In the future, combinations of thrombolytic and neuroprotective drugs may be used to attempt maximum rates of recovery after acute ischemic stroke. For combination therapy to achieve its maximum potential, patients with acute ischemic stroke will have to be carefully selected and treated.</p>
dc.identifier.submissionpathneuro_pp/107
dc.contributor.departmentDepartment of Neurology
dc.source.pages1298-303


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