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Analysis of Clinical Utility of Functional MRI in Neurosurgical Decision-Making in Focal Epilepsy

Published online by Cambridge University Press:  05 November 2024

Christopher O’Grady
Affiliation:
Dahousie University Medical School, Halifax, NS, Canada
Antonina Omisade*
Affiliation:
Nova Scotia Health, Halifax, NS, Canada Department of Psychology & Neuroscience, Dalhousie University, Halifax, Canada
*
Corresponding author: Antonina Omisade; Email: [email protected]

Abstract

Background:

Functional MRI (fMRI) has proven valuable in presurgical planning for people with brain tumors. However, it is underutilized for patients with epilepsy, likely due to less data on its added clinical value in this population. We reviewed clinical fMRI referrals at the QEII Health Sciences Center (Halifax, Nova Scotia) to determine the impact of fMRI on surgical planning for patients with epilepsy. We focused on reasons for fMRI referrals, findings and clinical decisions based on fMRI findings, as well as postoperative cognitive outcomes.

Methods:

We conducted a retrospective chart review of patients who underwent fMRI between June 2015 and March 2021.

Results:

Language lateralization represented the primary indication for fMRI (100%), with 7.7% of patients also referred for motor and sensory mapping. Language dominance on the side of resection was observed in 12.8% of patients; in 20.5%, activation was adjacent to the proposed resection site. In 18% of patients, fMRI provided an indication for further invasive testing due to the risk of significant cognitive morbidity (e.g., anterograde amnesia). Further invasive testing was avoided based on fMRI findings in 69.2% of patients. Cognitive outcomes based on combined neuropsychological findings and fMRI-determined language dominance were variable.

Conclusion:

fMRI in epilepsy was most often required to identify hemispheric language dominance. Although fMRI-determined language dominance was not directly predictive of cognitive outcomes, it helped identify patients at low risk of catastrophic cognitive morbidity and those at high risk who required additional invasive testing.

Résumé

RÉSUMÉ

Analyse de l’utilité clinique de l’IRM fonctionnelle dans les cas d’épilepsie focale en ce qui concerne les prises de décision relatives à la neurochirurgie.

Contexte :

L’imagerie par résonance magnétique fonctionnelle (IRMf) se révèle particulièrement utile en phase préopératoire chez les personnes souffrant d’une tumeur cérébrale. Toutefois, cette technique est sous-utilisée chez les patients atteints d’épilepsie, probablement en raison d’une collecte moindre de données sur la valeur clinique ajoutée de l’examen dans cette population. Aussi avons-nous procédé à une analyse clinique des demandes d’IRMf au QEII Health Sciences Center (Halifax, Nouvelle-Écosse) dans le but de déterminer l’incidence de cet examen sur la planification chirurgicale dans les cas d’épilepsie. Ont été retenus les motifs des demandes d’IRMf, les constatations et les décisions cliniques fondées sur les résultats de l’examen ainsi que les résultats cognitifs postopératoires.

Méthode :

Il s’agit d’une étude rétrospective de dossiers de patients qui ont subi une IRMf entre juin 2015 et mars 2021.

Résultats :

La latéralisation du langage constituait le principal motif des demandes d’IRMf (100 %), auquel s’ajoutait une cartographie motrice et sensorielle dans 7,7 % des cas. La zone de domination du langage était du côté de la résection chez 12,8 % des patients, et l’activation, adjacente au siège proposé de résection dans 20,5 % de l’échantillon. Dans 18 % des cas, l’IRMf a fourni des indications d’autres examens effractifs en raison de risques d’une morbidité cognitive grave (p. ex. l’amnésie antérograde). Par contre, les résultats de l’IRMf ont permis d’éviter des examens exploratoires effractifs additionnels chez 69,2 % des patients. Les résultats cognitifs fondés sur l’association d’observations neuropsychologiques et de la zone de domination du langage déterminée par l’IRMf se sont révélés variables.

Conclusion :

Les demandes d’IRMf visaient principalement à déterminer la domination hémisphérique du langage dans les cas d’épilepsie. Bien que la détermination de la latéralité du langage par l’IRMf n’ait pas été associée à une valeur prévisionnelle directe quant aux résultats cliniques, elle a néanmoins permis de repérer les patients à faible risque de morbidité cognitive catastrophique et ceux à risque élevé chez qui d’autres examens effractifs s’imposaient.

Type
Original Article
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of Canadian Neurological Sciences Federation

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References

Amaro, E, Barker, GJ. Study design in fMRI: basic principles. Brain Cognition. 2006;60:220–32. https://doi.org/10.1016/j.bandc.2005.11.009.CrossRefGoogle ScholarPubMed
Ogawa, S, Lee, TM, Kay, AR, Tank, DW. Brain magnetic resonance imaging with contrast dependent on blood oxygenation. Proc Natl Acad Sci USA. 1990;87:9868–72. DOI: https://doi.org/10.1073/pnas.87.24.9868.CrossRefGoogle ScholarPubMed
Dimou, S, Battisti, RA, Hermens, DF, Lagopoulos, J. A systematic review of functional magnetic resonance imaging and diffusion tensor imaging modalities used in presurgical planning of brain tumour resection. Neurosurg Rev. 2013;36:205–14. DOI: https://doi.org/10.1007/s10143-012-0436-8.CrossRefGoogle ScholarPubMed
Lau, JC, Kosteniuk, SE, Bihari, F, Megyesi, JF. Functional magnetic resonance imaging for preoperative planning in brain tumour surgery. Can J Neurol Sci. 2017;44:5968. DOI: https://doi.org/10.1017/cjn.2016.306.CrossRefGoogle ScholarPubMed
Lolli, VE, Coolen, T, Sadeghi, N, Voordecker, P, Lefranc, F. BOLD fMRI and DTI fiber tracking for preoperative mapping of eloquent cerebral regions in brain tumor patients: impact on surgical approach and outcome. Neurol Sci. 2023;44:2903–14. DOI: https://doi.org/10.1007/s10072-023-06667-2.CrossRefGoogle ScholarPubMed
Benjamin, CF, Walshaw, PD, Hale, K et al. Presurgical language fMRI: mapping of six critical regions. Hum Brain Mapp. 2017;38:4239–55. DOI: https://doi.org/10.1002/hbm.23661.CrossRefGoogle ScholarPubMed
Cox, RW. AFNI: software for analysis and visualization of functional magnetic resonance neuroimages. Comput Biomed Res. 1996;29:162–73. DOI: https://doi.org/10.1006/cbmr.1996.0014.CrossRefGoogle ScholarPubMed
Friston, KJ, Holmes, AP, Worsley, KJ, Poline, J, Frith, CD, Frackowiak, RSJ. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Mapp. 1994;2:189–210. DOI: https://doi.org/10.1002/hbm.460020402.CrossRefGoogle Scholar
Omisade, A, O’Grady, CB, Schmidt, MH, Fisk, JD. Visual and auditory fMRI paradigms for presurgical language mapping: convergent validity and relationship to individual variables. Neurol Res Intl. 2019;2019:19. DOI: https://doi.org/10.1155/2019/6728120.CrossRefGoogle ScholarPubMed
Wengenroth, M, Blatow, M, Guenther, J, Akbar, M, Tronnier, VM, Stippich, C. Diagnostic benefits of presurgical fMRI in patients with brain tumours in the primary sensorimotor cortex. Eur Radiol. 2011;21:1517–25. DOI: https://doi.org/10.1007/s00330-011-2067-9.CrossRefGoogle ScholarPubMed
Hamberger, MJ, Cole, J. Language organization and reorganization in epilepsy. Neuropsychol Rev. 2011;21:240–51. DOI: https://doi.org/10.1007/s11065-011-9180-z.CrossRefGoogle ScholarPubMed
Springer, JA, Binder, JR, Hammeke, TA et al. Language dominance in neurologically normal and epilepsy subjects. Brain. 1999;122:2033–46. DOI: https://doi.org/10.1093/brain/122.11.2033.CrossRefGoogle ScholarPubMed
Andelman, F, Kipervasser, S, Maimon, S, Fried, I, Parmet, Y, Neufeld, MY. A revised intracarotid etomidate memory (Wada) procedure. Acta Neurol Scand. 2013;127:97102. DOI: https://doi.org/10.1111/j.1600-0404.2012.01685.x .CrossRefGoogle ScholarPubMed
Goodglass, H, Kaplan, E. Boston naming test (BNT). Philadelphia: Lea and Febiger: APA PsycTests; 1983.Google Scholar
Wechsler, D. Wechsler Memory Scale – Fourth Edition (WMS-IV) San Antonio: The Psychological Corporation, 2009.Google Scholar
Schmidt, M. Rey auditory verbal learning test: a handbook. Los Angeles, CA: Western Psychological Services; 1996.Google Scholar
Majdan, A, Sziklas, V, Jones-Gotman, M. Performance of healthy subjects and patients with resection from the anterior temporal lobe on matched tests of verbal and visuoperceptual learning. J Clin Exp Neuropsyc. 1996;18:416–30. DOI: https://doi.org/10.1080/01688639608408998.CrossRefGoogle ScholarPubMed
Crane, J, Milner, B. Do I know you? Face perception and memory in patients with selective amygdalo-hippocampectomy. Neuropsychologia. 2002;40:530–538.https://doi.org/10.1016/s0028-3932(01)00131-2.CrossRefGoogle ScholarPubMed
Sherman, EMS, Wiebe, S, Fay-McClymont, TB et al. Neuropsychological outcomes after epilepsy surgery: systematic review and pooled estimates. Epilepsia. 2011;52:857–69. DOI: https://doi.org/10.1111/j.1528-1167.2011.03022.x.CrossRefGoogle ScholarPubMed
Joo, EY, Han, HJ, Lee, EK et al. Resection extent versus postoperative outcomes of seizure and memory in mesial temporal lobe epilepsy. Seizure. 2005;14:541–51. DOI: https://doi.org/10.1016/j.seizure.2005.08.011.CrossRefGoogle ScholarPubMed
Foesleitner, O, Sigl, B, Schmidbauer, V, et al. Language network reorganization before and after temporal lobe epilepsy surgery. J Neurosurg. 2021;134:1694–702. DOI: https://doi.org/10.3171/2020.4.JNS193401.CrossRefGoogle ScholarPubMed
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