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Cited 13 time in webofscience Cited 16 time in scopus
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Role of perfusion-weighted imaging in a diffusion-weighted-imaging-negative transient ischemic attack

Authors
Lee, Sang-HunNah, Hyun WookKim, Bum JoonAhn, Sung HoKim, Jong S.Kang, Dong WhaKwon, Sun U.
Issue Date
Apr-2017
Publisher
Korean Neurological Association
Keywords
Focal perfusion abnormality; Perfusion-weighted imaging; Transient ischemic attacks
Citation
Journal of Clinical Neurology, v.13, no.2, pp 129 - 137
Pages
9
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Clinical Neurology
Volume
13
Number
2
Start Page
129
End Page
137
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/43432
DOI
10.3988/jcn.2017.13.2.129
ISSN
1738-6586
2005-5013
Abstract
Background and Purpose The absence of acute ischemic lesions in diffusion-weighted imaging (DWI) in transient ischemic attack (TIA) patients makes it difficult to diagnose the true vascular etiologies. Among patients with DWI-negative TIA, we investigated whether the presence of a perfusion-weighted imaging (PWI) abnormality implied a true vascular event by identifying new acute ischemic lesions in follow-up magnetic resonance imaging (MRI) in areas corresponding to the initial PWI abnormality. Methods The included patients underwent DWI and PWI within 72 hours of TIA and also follow-up DWI at 3 days after the initial MRI. These patients had visited the emergency room between July 2009 and May 2015. Patients who demonstrated initial DWI lesions were excluded. The initial PWI abnormalities in the corresponding vascular territory were visually classified into three patterns: no abnormality, focal abnormality, and territorial abnormality. Results No DWI lesions were evident in initial MRI in 345 of the 443 TIA patients. Followup DWI was applied to 87 of these 345 DWI-negative TIA patients. Initial PWI abnormalities were significantly associated with follow-up DWI abnormalities: 8 of 43 patients with no PWI abnormalities (18.6%) had new ischemic lesions, whereas 13 of 16 patients with focal perfusion abnormalities (81.2%) had new ischemic lesions in the areas of initial PWI abnormalities [odds ratio (OR)=15.1, 95% confidence interval (CI)=3.6–62.9], and 14 of 28 patients with territorial perfusion abnormalities (50%) had new lesions (OR=3.7, 95% CI=1.2– 11.5). Conclusions PWI is useful in defining whether or not the transient neurological symptoms in DWI-negative TIA are true vascular events, and will help to improve the understanding of the pathomechanism of TIA. © 2017 Korean Neurological Association.
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Lee, Sang-Hun
Ansan Hospital (Department of Neurology, Ansan Hospital)
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