TY - JOUR
T1 - An Automatic DWI/FLAIR Mismatch Assessment of Stroke Patients
AU - Johansen, Jacob
AU - Offersen, Cecilie M. rck
AU - Carlsen, Jonathan Frederik
AU - Ingala, Silvia
AU - Hansen, Adam Espe
AU - Nielsen, Michael Bachmann
AU - Darkner, Sune
AU - Pai, Akshay
N1 - Funding Information: This research was funded by Innovationsfonden, grant numbers 0153-00248B, 2103-00090B, and 3109-00079B. Innovationsfonden is a public fond in Denmark which invests in ideas, knowledge and technology which promotes new and innovative ideas which benefit society. Publisher Copyright: © 2023 by the authors.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - DWI/FLAIR mismatch assessment for ischemic stroke patients shows promising results in determining if patients are eligible for recombinant tissue-type plasminogen activator (r-tPA) treatment. However, the mismatch criteria suffer from two major issues: binary classification of a non-binary problem and the subjectiveness of the assessor. In this article, we present a simple automatic method for segmenting stroke-related parenchymal hyperintensities on FLAIR, allowing for an automatic and continuous DWI/FLAIR mismatch assessment. We further show that our method’s segmentations have comparable inter-rater agreement (DICE 0.820, SD 0.12) compared to that of two neuro-radiologists (DICE 0.856, SD 0.07), that our method appears robust to hyper-parameter choices (suggesting good generalizability), and lastly, that our methods continuous DWI/FLAIR mismatch assessment correlates to mismatch assessments made for a cohort of wake-up stroke patients at hospital submission. The proposed method shows promising results in automating the segmentation of parenchymal hyperintensity within ischemic stroke lesions and could help reduce inter-observer variability of DWI/FLAIR mismatch assessment performed in clinical environments as well as offer a continuous assessment instead of the current binary one.
AB - DWI/FLAIR mismatch assessment for ischemic stroke patients shows promising results in determining if patients are eligible for recombinant tissue-type plasminogen activator (r-tPA) treatment. However, the mismatch criteria suffer from two major issues: binary classification of a non-binary problem and the subjectiveness of the assessor. In this article, we present a simple automatic method for segmenting stroke-related parenchymal hyperintensities on FLAIR, allowing for an automatic and continuous DWI/FLAIR mismatch assessment. We further show that our method’s segmentations have comparable inter-rater agreement (DICE 0.820, SD 0.12) compared to that of two neuro-radiologists (DICE 0.856, SD 0.07), that our method appears robust to hyper-parameter choices (suggesting good generalizability), and lastly, that our methods continuous DWI/FLAIR mismatch assessment correlates to mismatch assessments made for a cohort of wake-up stroke patients at hospital submission. The proposed method shows promising results in automating the segmentation of parenchymal hyperintensity within ischemic stroke lesions and could help reduce inter-observer variability of DWI/FLAIR mismatch assessment performed in clinical environments as well as offer a continuous assessment instead of the current binary one.
KW - DWI/FLAIR mismatch
KW - MRI
KW - ischemic stroke
KW - r-tPA
KW - wake-up stroke
UR - http://www.scopus.com/inward/record.url?scp=85181902212&partnerID=8YFLogxK
U2 - https://doi.org/10.3390/diagnostics14010069
DO - https://doi.org/10.3390/diagnostics14010069
M3 - Article
C2 - 38201378
SN - 2075-4418
VL - 14
JO - Diagnostics (Basel, Switzerland)
JF - Diagnostics (Basel, Switzerland)
IS - 1
M1 - 69
ER -