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June 13, 2017; 88 (24) Article

MR perfusion lesions after TIA or minor stroke are associated with new infarction at 7 days

Jun Lee, Manabu Inoue, Michael Mlynash, Sharanpal K. Mann, Carlo W. Cereda, Michael Ke, Gregory W. Albers, Jean M. Olivot
First published May 12, 2017, DOI: https://doi.org/10.1212/WNL.0000000000004039
Jun Lee
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Manabu Inoue
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Michael Mlynash
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Sharanpal K. Mann
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Carlo W. Cereda
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Michael Ke
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Gregory W. Albers
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Jean M. Olivot
From Yeungnam University Medical Center (J.L.), Daegu, South Korea; Department of Vascular Medicine (M.I.), National Cerebral and Cardiovascular Center, Suita, Japan; Stanford Stroke Center (M.M., G.W.A.), Stanford University, CA; Division of Neurology (S.K.M.), University of British Columbia, Vancouver, Canada; Stroke Center Neurocenter of Southern Switzerland (C.W.C.), Ospedale Civico, Switzerland; California Pacific Medical Center (M.K.), San Francisco; and Toulouse Neuroimaging Center UMR 1214 (J.M.O.), Stroke Unit, Toulouse University Hospital, France.
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Citation
MR perfusion lesions after TIA or minor stroke are associated with new infarction at 7 days
Jun Lee, Manabu Inoue, Michael Mlynash, Sharanpal K. Mann, Carlo W. Cereda, Michael Ke, Gregory W. Albers, Jean M. Olivot
Neurology Jun 2017, 88 (24) 2254-2259; DOI: 10.1212/WNL.0000000000004039

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Abstract

Objective: To investigate the relationship between acute perfusion-weighted imaging (PWI) lesions occurring within the first hours after a TIA or a minor brain infarction (BI) and the incidence of new BI detected on a systematic MRI at 1 week.

Methods: Consecutive patients who experienced a TIA or BI with a neurologic deficit that lasted <24 hours, did not receive any revascularization therapy (thrombolysis/thrombectomy), and underwent DWI/PWI at baseline and fluid-attenuated inversion recovery (FLAIR)/DWI 1 week after symptom onset were enrolled. Investigators blinded to clinical information independently assessed the presence of acute ischemic lesions on baseline DWI/PWI and follow-up DWI and FLAIR. Baseline and follow-up MRIs were then compared to determine the occurrence and location of new infarctions.

Results: Sixty-four patients met the inclusion criteria. Median (IQR) ABCD2 score was 4 (3–5). Median delay from onset to baseline and follow-up MRI was 5 (2–10) hours and 6 (5–7) days, respectively. MRI revealed an acute ischemic lesion on DWI and/or PWI in 38 patients. Nine patients (14%) had a new infarction on follow-up MRI. Each had a PWI and 4 had a DWI lesion on baseline MRI. All new BIs except one were asymptomatic and in the same location as the acute PWI lesion.

Conclusions: Our results showed that 30% of the acute focal PWI lesions detected after a TIA are associated with a new BI at 1 week. Those new BIs may result from the progression of the initial ischemic injury.

GLOSSARY

ADC=
apparent diffusion coefficient;
BI=
brain infarction;
CI=
confidence interval;
DWI=
diffusion-weighted imaging;
FLAIR=
fluid-attenuated inversion recovery;
IQR=
interquartile range;
MR=
magnetic resonance;
MTT=
mean transit time;
NIHSS=
NIH Stroke Scale;
PWI=
perfusion-weighted imaging;
SNIL=
silent new ischemic lesion;
TTP=
time to peak

Footnotes

  • ↵* These authors contributed equally to this work.

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received December 17, 2016.
  • Accepted in final form March 24, 2017.
  • © 2017 American Academy of Neurology
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