AWAKE CRANIOTOMY WITH INTRAOPERATIVE BRAIN MAPPING: PRINCIPLES, TECHNIQUE AND OUTCOMES IN SURGERY FOR TUMORS OF ELOQUENT BRAIN AREAS
Abstract
Background: Surgery for intrinsic brain tumors must balance the extent of resection against the preservation of neurological function. Awake craniotomy with direct electrical stimulation mapping allows the surgeon to identify language, motor and sensory pathways in real time. Aim: To review the history, patient selection, anesthetic management, mapping technique and clinical outcomes of awake craniotomy for tumors located in or near eloquent brain. Methods: Narrative review of key clinical series, meta-analyses and technical reviews. Results: In the largest language-mapping series, only 1.6% of surviving patients (4 of 243) had a persistent language deficit at six months, and most series report a mean extent of resection above 90% or a gross total resection rate above 50%. Failure of the awake procedure is uncommon (0.5–6.4%). Evidence comparing awake surgery with general anesthesia comes almost entirely from non-randomized studies. Conclusion: Awake craniotomy with cortical and subcortical mapping is regarded as the gold standard for the maximal safe resection of tumors in or near eloquent brain.
References
1. Smith JS, Chang EF, Lamborn KR, et al. Role of extent of resection in the long-term outcome of low-grade hemispheric gliomas. J Clin Oncol. 2008;26(8):1338–1345.
2. Sanai N, Polley MY, McDermott MW, Parsa AT, Berger MS. An extent of resection threshold for newly diagnosed glioblastomas. J Neurosurg. 2011;115(1):3–8.
3. Rahman M, Abbatematteo J, De Leo EK, et al. The effects of new or worsened postoperative neurological deficits on survival of patients with glioblastoma. J Neurosurg. 2017;127:123–131.
4. Sanai N, Mirzadeh Z, Berger MS. Functional outcome after language mapping for glioma resection. N Engl J Med. 2008;358(1):18–27.
5. Gogos AJ, Young JS, Morshed RA, Hervey-Jumper SL, Berger MS. Awake glioma surgery: technical evolution and nuances. J Neurooncol. 2020. doi:10.1007/s11060-020-03482-z
6. Hervey-Jumper SL, Li J, Lau D, Molinaro AM, Perry DW, Meng L, Berger MS. Awake craniotomy to maximize glioma resection: methods and technical nuances over a 27-year period. J Neurosurg. 2015;123(2):325–339.
7. De Witt Hamer PC, Robles SG, 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.
8. Lu VM, Phan K, Rovin RA. Comparison of operative outcomes of eloquent glioma resection performed under awake versus general anesthesia: a systematic review and meta-analysis. Clin Neurol Neurosurg. 2018;169:121–127.
9. Gerritsen JKW, et al. Awake craniotomy versus craniotomy under general anesthesia without surgery adjuncts for supratentorial glioblastoma in eloquent areas: a retrospective matched case-control study. Acta Neurochir (Wien). 2019;161:307–315.
10. Bartholow R. Experimental investigations into the functions of the human brain. Am J Med Sci. 1874;67:305–313.
11. Penfield W, Boldrey E. Somatic motor and sensory representation in the cerebral cortex of man as studied by electrical stimulation. Brain. 1937;60(4):389–443.
12. Whitaker HA, Ojemann GA. Graded localisation of naming from electrical stimulation mapping of left cerebral cortex. Nature. 1977;270:50–51.
13. Berger MS, Kincaid J, Ojemann GA, Lettich E. Brain mapping techniques to maximize resection, safety, and seizure control in children with brain tumors. Neurosurgery. 1989. doi:10.1227/00006123-198911000-00015
14. Silbergeld DL, Mueller WM, Colley PS, Ojemann GA, Lettich E. Use of propofol (Diprivan) for awake craniotomies: technical note. Surg Neurol. 1992. doi:10.1016/0090-3019(92)90038-O
15. Southwell DG, Hervey-Jumper SL, Perry DW, Berger MS. Intraoperative mapping during repeat awake craniotomy reveals the functional plasticity of adult cortex. J Neurosurg. 2016;124(5):1460–1469.
16. Molina ES, et al. Conscious sedation with dexmedetomidine compared with asleep-awake-asleep craniotomies in glioma surgery: an analysis of 180 patients. J Neurosurg. 2018;129(5):1223–1230.
17. Goettel N, et al. Dexmedetomidine vs propofol-remifentanil conscious sedation for awake craniotomy: a prospective randomized controlled trial. Br J Anaesth. 2016;116(6):811–821.
18. Ojemann G, Ojemann J, Lettich E, Berger M. Cortical language localization in left, dominant hemisphere: an electrical stimulation mapping investigation in 117 patients. J Neurosurg. 1989;71(3):316–326.
19. Sartorius CJ, Berger MS. Rapid termination of intraoperative stimulation-evoked seizures with application of cold Ringer's lactate to the cortex. J Neurosurg. 1998;88(2). doi:10.3171/jns.1998.88.2.0349
20. Verst SM, et al. Monopolar 250–500 Hz language mapping: results of 41 patients. Clin Neurophysiol Pract. 2019;4:1–8.
21. Chang EF, Raygor KP, Berger MS. Contemporary model of language organization: an overview for neurosurgeons. J Neurosurg. 2015;122(2):250–261.
22. Ries SK, et al. Roles of ventral versus dorsal pathways in language production: an awake language mapping study. Brain Lang. 2019;191:17–27.
23. Nossek E, et al. Failed awake craniotomy: a retrospective analysis in 424 patients undergoing craniotomy for brain tumor. J Neurosurg. 2013;118:243–249.
24. Magill ST, Han SJ, Li J, Berger MS. Resection of primary motor cortex tumors: feasibility and surgical outcomes. J Neurosurg. 2018;129(4):961–972.
25. Swift JR, et al. Passive functional mapping of receptive language areas using electrocorticographic signals. Clin Neurophysiol. 2018. doi:10.1016/j.clinph.2018.09.007