Leukoaraiosis May Confound the Interpretation of CT Perfusion in Patients Treated with Mechanical Thrombectomy for Acute Ischemic Stroke.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
08 2019
Historique:
received: 22 03 2019
accepted: 19 06 2019
pubmed: 28 7 2019
medline: 7 5 2020
entrez: 27 7 2019
Statut: ppublish

Résumé

Leukoaraiosis frequently coexists in patients with acute stroke. We studied whether leukoaraiosis could confound the interpretation of CTP findings in patients treated with mechanical thrombectomy. We analyzed 236 patients with stroke treated with mechanical thrombectomy and studied with CTP, of whom 127 (53.8%) achieved complete reperfusion. Periventricular white matter hyperintensities on MR imaging and hypodensities on NCCT were assessed through the Fazekas score. CTP-predicted nonviable tissue was defined as relative CBF <30%, and final infarct volume was quantified in DWI. We estimated mean MTT, CBV, and CBF in the asymptomatic hemisphere. In patients achieving complete reperfusion, we assessed the accuracy of nonviable tissue to predict final infarct volume using the intraclass correlation coefficient across periventricular hyperintensity/hypodensity Fazekas scores and variable relative CBF cutoffs. MTT was longer (Spearman ρ = 0.279, In patients with stroke, the presence of leukoaraiosis confounds the interpretation of CTP despite proper adjustment of CBF thresholds.

Sections du résumé

BACKGROUND AND PURPOSE
Leukoaraiosis frequently coexists in patients with acute stroke. We studied whether leukoaraiosis could confound the interpretation of CTP findings in patients treated with mechanical thrombectomy.
MATERIALS AND METHODS
We analyzed 236 patients with stroke treated with mechanical thrombectomy and studied with CTP, of whom 127 (53.8%) achieved complete reperfusion. Periventricular white matter hyperintensities on MR imaging and hypodensities on NCCT were assessed through the Fazekas score. CTP-predicted nonviable tissue was defined as relative CBF <30%, and final infarct volume was quantified in DWI. We estimated mean MTT, CBV, and CBF in the asymptomatic hemisphere. In patients achieving complete reperfusion, we assessed the accuracy of nonviable tissue to predict final infarct volume using the intraclass correlation coefficient across periventricular hyperintensity/hypodensity Fazekas scores and variable relative CBF cutoffs.
RESULTS
MTT was longer (Spearman ρ = 0.279,
CONCLUSIONS
In patients with stroke, the presence of leukoaraiosis confounds the interpretation of CTP despite proper adjustment of CBF thresholds.

Identifiants

pubmed: 31345941
pii: ajnr.A6139
doi: 10.3174/ajnr.A6139
pmc: PMC7048478
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1323-1329

Informations de copyright

© 2019 by American Journal of Neuroradiology.

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Auteurs

S Rudilosso (S)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

C Laredo (C)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

C Vivancos (C)

Neurosurgery Service (C.V.), Universitary Hospital La Paz, Madrid, Spain.

X Urra (X)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

L Llull (L)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

A Renú (A)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

V Obach (V)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

Y Zhao (Y)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.

J L Moreno (JL)

Department of Radiology (J.L.M., A.L.-R.), Hospital Clínic, University of Barcelona, Barcelona, Spain.

A Lopez-Rueda (A)

Department of Radiology (J.L.M., A.L.-R.), Hospital Clínic, University of Barcelona, Barcelona, Spain.

S Amaro (S)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain achamorro@clinic.ub.es samaro@clinic.cat.

Á Chamorro (Á)

From the Department of Neuroscience (S.R., C.L., X.U., L.L., A.R., V.O., Y.Z., S.A., Á.C.)., Comprehensive Stroke Center, Hospital Clinic, University of Barcelona and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain achamorro@clinic.ub.es samaro@clinic.cat.
Medicine Department (Á.C.), School of Medicine, University of Barcelona, Barcelona, Spain.

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