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    Role of heparin and low-molecular-weight heparins in the management of acute ischemic stroke

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    Authors
    Padma, Vasantha
    Fisher, Marc
    Moonis, Majaz
    UMass Chan Affiliations
    Department of Neurology
    Document Type
    Journal Article
    Publication Date
    2006-05-24
    Keywords
    Acute Disease
    Anticoagulants
    Brain Ischemia
    Heparin
    Heparin, Low-Molecular-Weight
    Humans
    Intracranial Thrombosis
    Recurrence
    Stroke
    Venous Thrombosis
    Neurology
    Neuroscience and Neurobiology
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    Link to Full Text
    http://dx.doi.org/10.1586/14779072.4.3.405
    Abstract
    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.
    Source
    Expert Rev Cardiovasc Ther. 2006 May;4(3):405-15. Link to article on publisher's site
    DOI
    10.1586/14779072.4.3.405
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/37574
    PubMed ID
    16716101
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1586/14779072.4.3.405
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