Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset.

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Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset. / Cheng, Bastian; Brinkmann, Mathias; Forkert, Nils D; Treszl, Andras; Ebinger, Martin; Köhrmann, Martin; Wu, Ona; Kang, Dong-Wha; Liebeskind, David S; Tourdias, Thomas; Singer, Oliver C; Christensen, Soren; Luby, Marie; Warach, Steven; Fiehler, Jens; Fiebach, Jochen B; Gerloff, Christian; Thomalla, Götz; STIR/VISTA Imaging Collaboration.

In: J CEREBR BLOOD F MET, Vol. 33, No. 1, 1, 2013, p. 76-84.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Cheng, B, Brinkmann, M, Forkert, ND, Treszl, A, Ebinger, M, Köhrmann, M, Wu, O, Kang, D-W, Liebeskind, DS, Tourdias, T, Singer, OC, Christensen, S, Luby, M, Warach, S, Fiehler, J, Fiebach, JB, Gerloff, C, Thomalla, G & STIR/VISTA Imaging Collaboration 2013, 'Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset.', J CEREBR BLOOD F MET, vol. 33, no. 1, 1, pp. 76-84. https://doi.org/10.1038/jcbfm.2012.129

APA

Cheng, B., Brinkmann, M., Forkert, N. D., Treszl, A., Ebinger, M., Köhrmann, M., Wu, O., Kang, D-W., Liebeskind, D. S., Tourdias, T., Singer, O. C., Christensen, S., Luby, M., Warach, S., Fiehler, J., Fiebach, J. B., Gerloff, C., Thomalla, G., & STIR/VISTA Imaging Collaboration (2013). Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset. J CEREBR BLOOD F MET, 33(1), 76-84. [1]. https://doi.org/10.1038/jcbfm.2012.129

Vancouver

Bibtex

@article{cb3bc62517f5475591bfcca72ccca0a2,
title = "Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset.",
abstract = "In acute stroke magnetic resonance imaging, a 'mismatch' between visibility of an ischemic lesion on diffusion-weighted imaging (DWI) and missing corresponding parenchymal hyperintensities on fluid-attenuated inversion recovery (FLAIR) data sets was shown to identify patients with time from symptom onset ≤4.5 hours with high specificity. However, moderate sensitivity and suboptimal interpreter agreement are limitations of a visual rating of FLAIR lesion visibility. We tested refined image analysis methods in patients included in the previously published PREFLAIR study using refined visual analysis and quantitative measurements of relative FLAIR signal intensity (rSI) from a three-dimensional, segmented stroke lesion volume. A total of 399 patients were included. The rSI of FLAIR lesions showed a moderate correlation with time from symptom onset (r=0.382, P<0.001). A FLAIR rSI threshold of <1.0721 predicted symptom onset ≤4.5 hours with slightly increased specificity (0.85 versus 0.78) but also slightly decreased sensitivity (0.47 versus 0.58) as compared with visual analysis. Refined visual analysis differentiating between 'subtle' and 'obvious' FLAIR hyperintensities and classification and regression tree algorithms combining information from visual and quantitative analysis also did not improve diagnostic accuracy. Our results raise doubts whether the prediction of stroke onset time by visual image judgment can be improved by quantitative rSI measurements.",
keywords = "Humans, Male, Aged, Female, Sensitivity and Specificity, Predictive Value of Tests, Time Factors, Algorithms, Data Interpretation, Statistical, Image Interpretation, Computer-Assisted, *Diffusion Magnetic Resonance Imaging, Stroke/*diagnosis, Cerebrovascular Circulation/*physiology, Blood Volume/physiology, Brain/*blood supply, Microvessels/physiology, Symptom Assessment/*methods, Humans, Male, Aged, Female, Sensitivity and Specificity, Predictive Value of Tests, Time Factors, Algorithms, Data Interpretation, Statistical, Image Interpretation, Computer-Assisted, *Diffusion Magnetic Resonance Imaging, Stroke/*diagnosis, Cerebrovascular Circulation/*physiology, Blood Volume/physiology, Brain/*blood supply, Microvessels/physiology, Symptom Assessment/*methods",
author = "Bastian Cheng and Mathias Brinkmann and Forkert, {Nils D} and Andras Treszl and Martin Ebinger and Martin K{\"o}hrmann and Ona Wu and Dong-Wha Kang and Liebeskind, {David S} and Thomas Tourdias and Singer, {Oliver C} and Soren Christensen and Marie Luby and Steven Warach and Jens Fiehler and Fiebach, {Jochen B} and Christian Gerloff and G{\"o}tz Thomalla and {STIR/VISTA Imaging Collaboration}",
year = "2013",
doi = "10.1038/jcbfm.2012.129",
language = "English",
volume = "33",
pages = "76--84",
journal = "J CEREBR BLOOD F MET",
issn = "0271-678X",
publisher = "SAGE Publications",
number = "1",

}

RIS

TY - JOUR

T1 - Quantitative measurements of relative fluid-attenuated inversion recovery (FLAIR) signal intensities in acute stroke for the prediction of time from symptom onset.

AU - Cheng, Bastian

AU - Brinkmann, Mathias

AU - Forkert, Nils D

AU - Treszl, Andras

AU - Ebinger, Martin

AU - Köhrmann, Martin

AU - Wu, Ona

AU - Kang, Dong-Wha

AU - Liebeskind, David S

AU - Tourdias, Thomas

AU - Singer, Oliver C

AU - Christensen, Soren

AU - Luby, Marie

AU - Warach, Steven

AU - Fiehler, Jens

AU - Fiebach, Jochen B

AU - Gerloff, Christian

AU - Thomalla, Götz

AU - STIR/VISTA Imaging Collaboration

PY - 2013

Y1 - 2013

N2 - In acute stroke magnetic resonance imaging, a 'mismatch' between visibility of an ischemic lesion on diffusion-weighted imaging (DWI) and missing corresponding parenchymal hyperintensities on fluid-attenuated inversion recovery (FLAIR) data sets was shown to identify patients with time from symptom onset ≤4.5 hours with high specificity. However, moderate sensitivity and suboptimal interpreter agreement are limitations of a visual rating of FLAIR lesion visibility. We tested refined image analysis methods in patients included in the previously published PREFLAIR study using refined visual analysis and quantitative measurements of relative FLAIR signal intensity (rSI) from a three-dimensional, segmented stroke lesion volume. A total of 399 patients were included. The rSI of FLAIR lesions showed a moderate correlation with time from symptom onset (r=0.382, P<0.001). A FLAIR rSI threshold of <1.0721 predicted symptom onset ≤4.5 hours with slightly increased specificity (0.85 versus 0.78) but also slightly decreased sensitivity (0.47 versus 0.58) as compared with visual analysis. Refined visual analysis differentiating between 'subtle' and 'obvious' FLAIR hyperintensities and classification and regression tree algorithms combining information from visual and quantitative analysis also did not improve diagnostic accuracy. Our results raise doubts whether the prediction of stroke onset time by visual image judgment can be improved by quantitative rSI measurements.

AB - In acute stroke magnetic resonance imaging, a 'mismatch' between visibility of an ischemic lesion on diffusion-weighted imaging (DWI) and missing corresponding parenchymal hyperintensities on fluid-attenuated inversion recovery (FLAIR) data sets was shown to identify patients with time from symptom onset ≤4.5 hours with high specificity. However, moderate sensitivity and suboptimal interpreter agreement are limitations of a visual rating of FLAIR lesion visibility. We tested refined image analysis methods in patients included in the previously published PREFLAIR study using refined visual analysis and quantitative measurements of relative FLAIR signal intensity (rSI) from a three-dimensional, segmented stroke lesion volume. A total of 399 patients were included. The rSI of FLAIR lesions showed a moderate correlation with time from symptom onset (r=0.382, P<0.001). A FLAIR rSI threshold of <1.0721 predicted symptom onset ≤4.5 hours with slightly increased specificity (0.85 versus 0.78) but also slightly decreased sensitivity (0.47 versus 0.58) as compared with visual analysis. Refined visual analysis differentiating between 'subtle' and 'obvious' FLAIR hyperintensities and classification and regression tree algorithms combining information from visual and quantitative analysis also did not improve diagnostic accuracy. Our results raise doubts whether the prediction of stroke onset time by visual image judgment can be improved by quantitative rSI measurements.

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Sensitivity and Specificity

KW - Predictive Value of Tests

KW - Time Factors

KW - Algorithms

KW - Data Interpretation, Statistical

KW - Image Interpretation, Computer-Assisted

KW - Diffusion Magnetic Resonance Imaging

KW - Stroke/diagnosis

KW - Cerebrovascular Circulation/physiology

KW - Blood Volume/physiology

KW - Brain/blood supply

KW - Microvessels/physiology

KW - Symptom Assessment/methods

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Sensitivity and Specificity

KW - Predictive Value of Tests

KW - Time Factors

KW - Algorithms

KW - Data Interpretation, Statistical

KW - Image Interpretation, Computer-Assisted

KW - Diffusion Magnetic Resonance Imaging

KW - Stroke/diagnosis

KW - Cerebrovascular Circulation/physiology

KW - Blood Volume/physiology

KW - Brain/blood supply

KW - Microvessels/physiology

KW - Symptom Assessment/methods

U2 - 10.1038/jcbfm.2012.129

DO - 10.1038/jcbfm.2012.129

M3 - SCORING: Journal article

C2 - 23047272

VL - 33

SP - 76

EP - 84

JO - J CEREBR BLOOD F MET

JF - J CEREBR BLOOD F MET

SN - 0271-678X

IS - 1

M1 - 1

ER -