Document Detail


Hemorrhagic transformation following ischemic stroke: significance, causes, and relationship to therapy and treatment.
MedLine Citation:
PMID:  11898581     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hemorrhagic transformation (HT) is a frequent consequence of ischemic stroke that becomes more prevalent after thrombolytic therapy. Despite concerns about safety parameters, thrombolytic drugs remain the first course of action available to clinicians for stroke management. However, recent efforts in preclinical studies have attempted to discover other drugs that can lessen the risk of hemorrhage associated with thrombolytic administration. This review focuses on three classes of pharmacologic agents that have shown some promise in animal models of stroke, and can thus be considered as possible candidates for coadministration with thrombolytics in the treatment of stroke. These include the following: 1) spin trap agents, such as alpha-phenyl-N-t-butylnitrone (PBN) that scavenge free radicals; 2) matrix metalloproteinase (MMP) inhibitors, such as BB-94, that prevent membrane and vessel remodeling following ischemia; and 3) the novel glycoprotein (GP) IIb/IIIa platelet receptor antagonist SM-20302. Although these drugs affect different mechanisms, the common denominator seemed to be their effectiveness in reducing the incidence of hemorrhage in response to thrombolytic infusion following an embolic stroke.
Authors:
Paul A Lapchak
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Current neurology and neuroscience reports     Volume:  2     ISSN:  1528-4042     ISO Abbreviation:  Curr Neurol Neurosci Rep     Publication Date:  2002 Jan 
Date Detail:
Created Date:  2002-03-18     Completed Date:  2002-08-28     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  100931790     Medline TA:  Curr Neurol Neurosci Rep     Country:  United States    
Other Details:
Languages:  eng     Pagination:  38-43     Citation Subset:  IM    
Affiliation:
Department of Neuroscience, University of California, San Diego, 9500 Gilman Drive, MTF316, La Jolla, CA 92093-0624, USA. plapchak@ucsd.edu
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MeSH Terms
Descriptor/Qualifier:
Brain Ischemia / complications*
Cerebral Hemorrhage / etiology*,  prevention & control
Humans
Metalloendopeptidases / antagonists & inhibitors
Platelet Aggregation Inhibitors / therapeutic use
Protease Inhibitors / therapeutic use
Spin Labels
Stroke / complications*,  etiology*,  therapy
Thrombolytic Therapy / adverse effects
Chemical
Reg. No./Substance:
0/Platelet Aggregation Inhibitors; 0/Protease Inhibitors; 0/Spin Labels; EC 3.4.24.-/Metalloendopeptidases

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