Intraoperative Functional Mapping and Neurophysiological Monitoring in the Resection of Supratentorial Gliomas in Eloquent Areas: A Critical Narrative Review and Algorithm for Responding to Alerts

Authors

DOI:

https://doi.org/10.70577/9rtdgv20

Keywords:

intraoperative neurophysiological monitoring; brain mapping; glioma; motor evoked potentials; direct electrical stimulation; awake craniotomy; functional preservation.

Abstract

Introduction. Resection of supratentorial gliomas located near the cortex or functionally relevant tracts requires balancing the oncological benefit of extensive resection with the risk of persistent neurological disability. Functional mapping and intraoperative neurophysiological monitoring provide distinct and complementary information: the former locates functional tissue; the latter monitors the integrity of neural systems during surgery.

Objective. To critically analyze the rationale, indications, technical parameters, alarm criteria, limitations, and clinical utility of the main mapping and monitoring modalities used in supratentorial gliomas in eloquent locations, and to propose a structured algorithm for responding to neurophysiological changes.

Methods. A structured critical narrative review was conducted, guided by the SANRA quality domains. The search was updated through June 19, 2026, in PubMed/MEDLINE; PubMed Central was used to retrieve full-text articles, and the identification process was supplemented by reference tracking. Priority was given to guidelines and position statements, systematic reviews and meta-analyses, prospective studies, large cohort studies, and case series with direct relevance to supratentorial glioma surgery. The synthesis was organized by function at risk, modality, alarm criteria, and clinical applicability.

Results. The most robust strategy is multimodal and is defined by the vulnerable function, not by a fixed combination of tests. In motor surgery, motor evoked potentials obtained through transcranial or direct cortical stimulation should be integrated with cortical and subcortical mapping. Persistent loss of response constitutes the most serious warning sign; a reduction in amplitude of more than 50%, threshold elevation, and low subcortical thresholds are paradigm-dependent indicators and not universal rules. The approximate ratio of 1 mA per 1 mm is a valid heuristic only under comparable technical conditions. Somatosensory evoked potentials provide localization through phase inversion and sensory monitoring, but they do not replace motor assessment. For speech, direct electrical stimulation with the patient awake remains the gold standard when clinical selection allows; cortico-cortical evoked potentials are complementary and still lack standardized alarm criteria. Visual monitoring shows promise, although it exhibits technical variability and is supported by limited evidence. Any alert requires ruling out technical, anesthetic, and physiological causes before attributing it to surgical injury.

Conclusions. Intraoperative neurophysiology should be used as a predefined, individualized, and documented clinical decision-making system. Its usefulness depends on consistency across modalities, anesthetic stability, expert interpretation, and an immediate response from the team. The available evidence supports an association with greater functional safety and improved extent of resection, but it comes primarily from observational studies and does not justify attributing causality to any single modality.

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References

1. Baethge C, Goldbeck-Wood S, Mertens S. SANRA-a scale for the quality assessment of narrative review articles. Res Integr Peer Rev. 2019;4:5. doi:10.1186/s41073-019-0064-8. DOI: https://doi.org/10.1186/s41073-019-0064-8

2. Weller M, van den Bent M, Preusser M, et al. EANO guidelines on the diagnosis and treatment of diffuse gliomas of adulthood. Nat Rev Clin Oncol. 2021;18(3):170-186. doi:10.1038/s41571-020-00447-z. DOI: https://doi.org/10.1038/s41571-020-00447-z

3. Mirza AB, Vastani A, Suvarna R, Rashed S, Al-Omari A, Mthunzi E, et al. Preoperative and intraoperative neuromonitoring and mapping techniques impact oncological and functional outcomes in supratentorial function-eloquent brain tumours: a systematic review and meta-analysis. EClinicalMedicine. 2025;80:103055. doi:10.1016/j.eclinm.2024.103055. DOI: https://doi.org/10.1016/j.eclinm.2024.103055

4. de Witt Hamer PC, Gil Robles S, Zwinderman AH, Duffau H, Berger MS. Impact of intraoperative stimulation brain mapping on glioma surgery outcome: a meta-analysis. J Clin Oncol. 2012;30(20):2559-2565. doi:10.1200/JCO.2011.38.4818. DOI: https://doi.org/10.1200/JCO.2011.38.4818

5. Gerritsen JKW, Arends L, Klimek M, Dirven CMF, Vincent AJPE. Impact of intraoperative stimulation mapping on high-grade glioma surgery outcome: a meta-analysis. Acta Neurochir (Wien). 2019;161(1):99-107. doi:10.1007/s00701-018-3732-4. DOI: https://doi.org/10.1007/s00701-018-3732-4

6. MacDonald DB, Skinner S, Shils J, Yingling C. Intraoperative motor evoked potential monitoring: a position statement by the American Society of Neurophysiological Monitoring. Clin Neurophysiol. 2013;124(12):2291-2316. doi:10.1016/j.clinph.2013.07.025. DOI: https://doi.org/10.1016/j.clinph.2013.07.025

7. Legatt AD, Emerson RG, Epstein CM, MacDonald DB, Deletis V, Bravo RJ, López JR. ACNS guideline: transcranial electrical stimulation motor evoked potential monitoring. J Clin Neurophysiol. 2016;33(1):42-50. doi:10.1097/WNP.0000000000000253. DOI: https://doi.org/10.1097/WNP.0000000000000253

8. MacDonald DB, Dong C, Quatrale R, Sala F, Skinner S, Soto F, Szelényi A. Recommendations of the International Society of Intraoperative Neurophysiology for intraoperative somatosensory evoked potentials. Clin Neurophysiol. 2019;130(1):161-179. doi:10.1016/j.clinph.2018.10.008. DOI: https://doi.org/10.1016/j.clinph.2018.10.008

9. Toleikis JR, Pace C, Jahangiri FR, Hemmer LB, Toleikis SC. Intraoperative somatosensory evoked potential (SEP) monitoring: an updated position statement by the American Society of Neurophysiological Monitoring. J Clin Monit Comput. 2024;38(5):1003-1042. doi:10.1007/s10877-024-01201-x. DOI: https://doi.org/10.1007/s10877-024-01201-x

10. Asimakidou E, Álvarez Abut P, Raabe A, Seidel K. Motor evoked potential warning criteria in supratentorial surgery: a scoping review. Cancers (Basel). 2021;13(11):2803. doi:10.3390/cancers13112803. DOI: https://doi.org/10.3390/cancers13112803

11. You H, Qiao H. Intraoperative neuromonitoring during resection of gliomas involving eloquent areas. Front Neurol. 2021;12:658680. doi:10.3389/fneur.2021.658680. DOI: https://doi.org/10.3389/fneur.2021.658680

12. Morshed RA, Young JS, Lee AT, Hervey-Jumper SL. Functional mapping for glioma surgery, part 2: intraoperative mapping tools. Neurosurg Clin N Am. 2021;32(1):75-81. doi:10.1016/j.nec.2020.09.001. DOI: https://doi.org/10.1016/j.nec.2020.09.001

13. Plans G, Fernández-Conejero I, Rifà-Ros X, et al. Evaluation of the high-frequency monopolar stimulation technique for mapping and monitoring the corticospinal tract in patients with supratentorial gliomas: a proposal for intraoperative management based on neurophysiological data analysis in a series of 92 patients. Neurosurgery. 2017;81(4):585-594. doi:10.1093/neuros/nyw087. DOI: https://doi.org/10.1093/neuros/nyw087

14. Seidel K, Beck J, Stieglitz L, Schucht P, Raabe A. The warning-sign hierarchy between quantitative subcortical motor mapping and continuous motor evoked potential monitoring during resection of supratentorial brain tumors. J Neurosurg. 2013;118(2):287-296. doi:10.3171/2012.10.JNS12895. DOI: https://doi.org/10.3171/2012.10.JNS12895

15. Raabe A, Beck J, Schucht P, Seidel K. Continuous dynamic mapping of the corticospinal tract during surgery of motor eloquent brain tumors: evaluation of a new method. J Neurosurg. 2014;120(5):1015-1024. doi:10.3171/2014.1.JNS13909. DOI: https://doi.org/10.3171/2014.1.JNS13909

16. Seidel K, Schucht P, Beck J, Raabe A. Continuous dynamic mapping to identify the corticospinal tract in motor eloquent brain tumors: an update. J Neurol Surg A Cent Eur Neurosurg. 2020;81(2):105-110. doi:10.1055/s-0039-1698384. DOI: https://doi.org/10.1055/s-0039-1698384

17. Seidel K, Wagner N, Wermelinger J, Álvarez Abut P, et al. Motor evoked potential monitoring and continuous dynamic mapping: warning criteria during surgery on motor eloquent intra-axial brain tumors. Clin Neurophysiol. 2025;178:2110979. doi:10.1016/j.clinph.2025.2110979. DOI: https://doi.org/10.1016/j.clinph.2025.2110979

18. El Mohamad A, Msheik A, Krishnan R, Al Ghazou M, Eid A, Alhajjali A, et al. Continuous dynamic subcortical mapping of corticospinal tract: a systematic review and meta-analysis. Surg Neurol Int. 2026;17:90. doi:10.25259/SNI_747_2025. DOI: https://doi.org/10.25259/SNI_747_2025

19. Viganò L, Callipo V, Lamperti M, et al. Transcranial versus direct electrical stimulation for intraoperative motor-evoked potential monitoring: prognostic value comparison in asleep brain tumor surgery. Front Oncol. 2022;12:963669. doi:10.3389/fonc.2022.963669. DOI: https://doi.org/10.3389/fonc.2022.963669

20. Giampiccolo D, Parisi C, Meneghelli P, et al. Long-term motor deficit in brain tumour surgery with preserved intra-operative motor-evoked potentials. Brain Commun. 2021;3(1):fcaa226. doi:10.1093/braincomms/fcaa226. DOI: https://doi.org/10.1093/braincomms/fcaa226

21. Staub-Bartelt F, Suresh Babu MP, Szelényi A, Rapp M, Sabel M. Establishment of different intraoperative monitoring and mapping techniques and their impact on survival, extent of resection, and clinical outcome in patients with high-grade gliomas: a series of 631 patients in 14 years. Cancers (Basel). 2024;16(5):926. doi:10.3390/cancers16050926. DOI: https://doi.org/10.3390/cancers16050926

22. Ilgaz Aydinlar E, Sari R, Yalinay Dikmen P, Elmaci I. Intraoperative neurophysiologic monitoring improves neurologic outcomes in eloquent brain areas and aids in increasing the volume of resected glioma: current results compared with historical controls. J Clin Neurophysiol. 2025;42(4):343-349. doi:10.1097/WNP.0000000000001127. DOI: https://doi.org/10.1097/WNP.0000000000001127

23. de Zwart B, Ruis C. An update on tests used for intraoperative monitoring of cognition during awake craniotomy. Acta Neurochir (Wien). 2024;166:204. doi:10.1007/s00701-024-06062-6. DOI: https://doi.org/10.1007/s00701-024-06062-6

24. Bu LH, Zhang J, Lu JF, Wu JS. Glioma surgery with awake language mapping versus generalized anesthesia: a systematic review and meta-analysis. Neurosurg Rev. 2021;44(4):1997-2011. doi:10.1007/s10143-020-01418-9. DOI: https://doi.org/10.1007/s10143-020-01418-9

25. Cheon TM, Yoon SH, Kim MJ, Kim KM. Intraoperative language area mapping: cortico-cortical evoked potential. Brain Tumor Res Treat. 2025;13(2):39-44. doi:10.14791/btrt.2025.0008. DOI: https://doi.org/10.14791/btrt.2025.0008

26. Cheon TM, Yoon SH, Kim MJ, Kim KM. Correction of content, table, and funding statement of the article “Intraoperative language area mapping: cortico-cortical evoked potential”. Brain Tumor Res Treat. 2025;13(4):171-172. doi:10.14791/btrt.2025.0008e. DOI: https://doi.org/10.14791/btrt.2025.0008e

27. Conti Nibali M, Leonetti A, Puglisi G, et al. Preserving visual functions during gliomas resection: feasibility and efficacy of a novel intraoperative task for awake brain surgery. Front Oncol. 2020;10:1485. doi:10.3389/fonc.2020.01485. DOI: https://doi.org/10.3389/fonc.2020.01485

28. Shah HA, Begley S, Unadkat P, Hugo K, Schulder M. Direct-cortical visual evoked potential monitoring during brain tumor resection. J Clin Neurosci. 2023;115:1-7. doi:10.1016/j.jocn.2023.06.014. DOI: https://doi.org/10.1016/j.jocn.2023.06.014

29. Adkins GB, Mirallave Pescador A, Koht AH, Gosavi SP. Intraoperative neuromonitoring in intracranial surgery. BJA Educ. 2024;24(5):173-182. doi:10.1016/j.bjae.2024.02.002. DOI: https://doi.org/10.1016/j.bjae.2024.02.002

30. Guzzi G, Della Puppa A, Saladini M. Intraoperative neurophysiological monitoring in neurosurgery. J Clin Med. 2024;13(10):2966. doi:10.3390/jcm13102966. DOI: https://doi.org/10.3390/jcm13102966

31. Chen JS, Bergsneider B, Haddad AF, et al. Intraoperative functional brain mapping for glioma surgery. J Neurooncol. 2026;178:62. doi:10.1007/s11060-026-05664-7. DOI: https://doi.org/10.1007/s11060-026-05664-7

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Published

2026-06-15

How to Cite

Intraoperative Functional Mapping and Neurophysiological Monitoring in the Resection of Supratentorial Gliomas in Eloquent Areas: A Critical Narrative Review and Algorithm for Responding to Alerts. (2026). Salud Medicina E Innovación Journal, 4(2), 74-89. https://doi.org/10.70577/9rtdgv20

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