Ischemic Lesion Growth in Patients with a Persistent Target Mismatch After Large Vessel Occlusion.

CT perfusion collateral index CT perfusion image Good collateral flow Little core growth Persistent large penumbra

Journal

Clinical neuroradiology
ISSN: 1869-1447
Titre abrégé: Clin Neuroradiol
Pays: Germany
ID NLM: 101526693

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 23 02 2022
accepted: 11 05 2022
pubmed: 6 7 2022
medline: 17 3 2023
entrez: 5 7 2022
Statut: ppublish

Résumé

Failure to reperfuse a cerebral occlusion resulting in a persistent penumbral pattern has not been fully described. We retrospectively reviewed patients with anterior large vessel occlusion who did not receive reperfusion, and underwent repeated perfusion imaging, with baseline imaging < 6 h after onset and follow-up scans from 16-168 h. A persistent target mismatch (PTM) was defined as core volume of < 100 mL, mismatch ratio > 1.2, and mismatch volume > 10 mL on follow-up imaging. Patients were divided into PTM or non-PTM groups. Ischemic core and penumbral volumes were compared between baseline and follow-up imaging between the two groups, and collateral flow status assessed using CT perfusion collateral index. A total of 25 patients (14 PTM and 11 non-PTM) were enrolled in the study. Median core volumes increased slightly in the PTM group, from 22 to 36 ml. There was a much greater increase in the non-PTM group, from 57 to 190 ml. Penumbral volumes were stable in the PTM group from a median of 79 ml at baseline to 88 ml at follow-up, whereas penumbra was reduced in the non-PTM group, from 120 to 0 ml. Collateral flow status was also better in the PTM group and the median collateral index was 33% compared with 44% in the non-PTM group (p = 0.043). Multiple patients were identified with limited core growth and large penumbra (persistent target mismatch) > 16 h after stroke onset, likely due to more favorable collateral flow.

Sections du résumé

BACKGROUND BACKGROUND
Failure to reperfuse a cerebral occlusion resulting in a persistent penumbral pattern has not been fully described.
METHODS METHODS
We retrospectively reviewed patients with anterior large vessel occlusion who did not receive reperfusion, and underwent repeated perfusion imaging, with baseline imaging < 6 h after onset and follow-up scans from 16-168 h. A persistent target mismatch (PTM) was defined as core volume of < 100 mL, mismatch ratio > 1.2, and mismatch volume > 10 mL on follow-up imaging. Patients were divided into PTM or non-PTM groups. Ischemic core and penumbral volumes were compared between baseline and follow-up imaging between the two groups, and collateral flow status assessed using CT perfusion collateral index.
RESULTS RESULTS
A total of 25 patients (14 PTM and 11 non-PTM) were enrolled in the study. Median core volumes increased slightly in the PTM group, from 22 to 36 ml. There was a much greater increase in the non-PTM group, from 57 to 190 ml. Penumbral volumes were stable in the PTM group from a median of 79 ml at baseline to 88 ml at follow-up, whereas penumbra was reduced in the non-PTM group, from 120 to 0 ml. Collateral flow status was also better in the PTM group and the median collateral index was 33% compared with 44% in the non-PTM group (p = 0.043).
CONCLUSION CONCLUSIONS
Multiple patients were identified with limited core growth and large penumbra (persistent target mismatch) > 16 h after stroke onset, likely due to more favorable collateral flow.

Identifiants

pubmed: 35789284
doi: 10.1007/s00062-022-01180-z
pii: 10.1007/s00062-022-01180-z
pmc: PMC10014761
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-48

Informations de copyright

© 2022. The Author(s).

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Auteurs

Shinya Tomari (S)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia. sny5588@gmail.com.

Thomas Lillicrap (T)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.

Carlos Garcia-Esperon (C)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.
Department of Neurology, John Hunter Hospital, Newcastle, Australia.
College of Health, Medicine, and Wellbeing, University of Newcastle, Newcastle, Australia.

Yumi Tomari Kashida (YT)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.

Andrew Bivard (A)

Melbourne Brain Center at the Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia.

Longting Lin (L)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.

Christopher R Levi (CR)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.
Department of Neurology, John Hunter Hospital, Newcastle, Australia.
College of Health, Medicine, and Wellbeing, University of Newcastle, Newcastle, Australia.

Neil J Spratt (NJ)

Hunter Medical Research Institute, University of Newcastle, Newcastle, Australia.
Department of Neurology, John Hunter Hospital, Newcastle, Australia.
College of Health, Medicine, and Wellbeing, University of Newcastle, Newcastle, Australia.

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