
Vol. 27, No. 5, 2009
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Original Paper
Classification of Stroke Subtypes
P. Amarencoa, J. Bogousslavskyb, L.R. Caplanc, G.A. Donnand, M.G. Hennericie
aDepartment of Neurology and Stroke Center, INSERM U-698 and Paris-Diderot University, Bichat University Hospital, Paris, France; bDepartment of Neurology, Genolier Swiss Medical Network, Valmont-Genolier, Glion-sur-Montreux, Switzerland; cDivision of Cerebrovascular/Stroke, Beth Israel Deaconess Medical Center, Boston, Mass., USA; dNational Stroke Research Institute, Austin Health, University of Melbourne, Melbourne, Vic., Australia; eDepartment of Neurology, University of Heidelberg, Universitätsklinikum Mannheim, Mannheim, Germany
Address of Corresponding Author
Cerebrovasc Dis 2009;27:493-501 (DOI: 10.1159/000210432)
Key Words
- Stroke
- Classification systems
- Review
Abstract
This article reviews published stroke subtype classification systems and offers rules and a basis for a new way to subtype stroke patients. Stroke subtyping can have different purposes, e.g. describing patients' characteristics in a clinical trial, grouping patients in an epidemiological study, careful phenotyping of patients in a genetic study, and classifying patients for therapeutic decision-making in daily practice. The classification should distinguish between ischemic and hemorrhagic stroke, subarachnoid hemorrhage, cerebral venous thrombosis, and spinal cord stroke. Regarding the 4 main categories of etiologies of ischemic stroke (i.e. atherothrombotic, small vessel disease, cardioembolic, and other causes), the classification should reflect the most likely etiology without neglecting the vascular conditions that are also found (e.g. evidence of small vessel disease in the presence of severe large vessel obstructions). Phenotypes of large cohorts can also be characterized by surrogate markers or intermediate phenotypes (e.g. presence of internal carotid artery plaque, intima-media thickness of the common carotid artery, leukoaraiosis, microbleeds, or multiple lacunae). Parallel classifications (i.e. surrogate markers) may serve as within-study abnormalities to support research findings. Copyright © 2009 S. Karger AG, Basel
Author Contacts Prof. Pierre Amarenco, MD Department of Neurology and Stroke Centre, Bichat University Hospital 46, rue Henri Huchard FR-75018 Paris (France) Tel. +33 1 4025 8726, Fax +33 1 4025 7198, E-Mail pierre.amarenco@bch.aphp.fr
Article Information
Received: October 2, 2008
Accepted: February 2, 2009
Published online: April 3, 2009
Number of Print Pages : 9
Number of Figures : 0, Number of Tables : 3, Number of References : 13 |
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