awake_surgery_for_insular_glioma

Awake surgery for insular glioma

Predictors of Awake Surgery Failure for Insular Glioma

Awake craniotomy is a key strategy for maximizing safe resection in insular glioma surgery, especially when tumors are close to eloquent areas. However, several factors can predict failure of awake protocols, such as conversion to general anesthesia, incomplete mapping, or interruption of surgery.

  • High anxiety or psychiatric disorders
    • Risk of panic attacks or inability to tolerate awake conditions.
  • Low cognitive reserve or baseline neuropsychological deficits
    • Impaired cooperation with intraoperative tasks (e.g., language or attention testing).
  • Poor understanding or low motivation
    • Inadequate preoperative education may lead to intraoperative refusal or confusion.
  • Obstructive sleep apnea, obesity, or other comorbidities
    • Increased risk of hypoxia or airway compromise under sedation.
  • Language barrier
    • Non-native speakers may struggle during language mapping tasks.
  • Tumor location in posterior insula (zones III–IV)
    • More difficult access, increased discomfort, or higher risk of neurological deficit.
  • Involvement of operculum or internal capsule
    • Associated with greater surgical complexity and higher stress on the patient.
  • High-grade gliomas or extensive edema
    • May lead to intraoperative seizures or neurological deterioration.
  • Large tumor volume
    • Longer duration of mapping, leading to fatigue and reduced cooperation.
  • Inadequate preoperative simulation or training
    • Lack of rehearsal of tasks may cause confusion during awake mapping.
  • Inexperienced surgical or anesthetic team
    • Increases risk of technical errors and poor sedation control.
  • Suboptimal sedation management
    • Undersedation: anxiety or movement; oversedation: decreased arousal.
  • Intraoperative seizures
    • May lead to interruption of mapping and switch to general anesthesia.
  • Prolonged surgical time
    • Fatigue and patient discomfort contribute to poor cooperation.

Basal ganglionic involvement, which means the high-intensity area on Fluid Attenuated Inversion Recovery imaging is found in the basal ganglia consisting of the striatum and globus pallidus, was significantly associated with AS failure. AS contributes significantly to the maximal resection of IG. Basal ganglionic involvement is a potential predictor of AS failure for IG 4).

2017

Of the 52 identified patients, 24 had awake surgery and 28 had surgery under GA. The extent of resection was similar for the two anesthesia techniques: the median extent of resection was 61.4% (IQR: 37.8-74.3%) in the WHO grade <4 AC group vs. 50.5% (IQR: 35.0-71.2%) in the grade <4 GA group and 73.4% (IQR: 54.8-87.2%) in the grade 4 AC group vs. 88.6% (IQR: 61.2-93.0%) in the grade 4 GA group. Consistent with literature, there were more early neurological deficits after an AC, while the GA group showed more new late neurological deficits; however, these trends were not significant. Survival was similar between the two groups, with 100% 1- and 2-year survival in the grade <4 groups.

The results showed that the extent of resection, neurological outcomes, and survival were similar using the two anesthesia techniques. Since AC is more challenging for the patient and for his or her caregiver after surgery, this finding has implications for clinical decision-making 5).


Motomura et al. retrospectively reviewed the records of 33 consecutive patients with glial tumors in the eloquent brain areas who underwent awake surgery using iMRI. Volumetric analysis of MRI studies was performed. The pre-, intra-, and postoperative tumor volumes were measured in all cases using MRI studies obtained before, during, and after tumor resection. RESULTS Intraoperative MRI was performed to check for the presence of residual tumor during awake surgery in a total of 25 patients. Initial iMRI confirmed no further tumor resection in 9 patients (36%) because all observable tumors had already been removed. In contrast, intraoperative confirmation of residual tumor during awake surgery led to further tumor resection in 16 cases (64%) and eventually an EOR of more than 90% in 8 of 16 cases (50%). Furthermore, EOR benefiting from iMRI by more than 15% was found in 7 of 16 cases (43.8%). Interestingly, the increase in EOR as a result of iMRI for tumors associated mainly with the insular lobe was significantly greater, at 15.1%, than it was for the other tumors, which was 8.0% (p = 0.001).

This study revealed that combining awake surgery with iMRI was associated with a favorable surgical outcome for intrinsic brain tumors associated with eloquent areas. In particular, these benefits were noted for patients with tumors with complex anatomy, such as those associated with the insular lobe 6).


1)
Berger MS, Ojemann GA: Intraoperative brain mapping techniques in neuro-oncology. Stereotact Funct Neurosurg 58: 153–161, 1992
2)
Berger MS, Ojemann GA, Lettich E: Neurophysiological monitoring during astrocytoma surgery. Neurosurg Clin N Am 1:65–80, 1990
3)
Berger MS, Rostomily RC: low-grade glioma s: functional mapping resection strategies, extent of resection, and outcome. J Neurooncol 34:85–101, 1997
4)
Takada S, Hattori EY, Sano N, Sawada M, Tanji M, Mineharu Y, Kikuchi T, Arakawa Y. Potential predictors of awake surgery failure for insular glioma. Sci Rep. 2025 May 23;15(1):17953. doi: 10.1038/s41598-025-03219-w. PMID: 40410264; PMCID: PMC12102373.
5)
Gravesteijn BY, Keizer ME, Vincent AJPE, Schouten JW, Stolker RJ, Klimek M. Awake craniotomy versus craniotomy under general anesthesia for the surgical treatment of insular glioma: choices and outcomes. Neurol Res. 2017 Nov 23:1-10. doi: 10.1080/01616412.2017.1402147. [Epub ahead of print] PubMed PMID: 29168669.
6)
Motomura K, Natsume A, Iijima K, Kuramitsu S, Fujii M, Yamamoto T, Maesawa S, Sugiura J, Wakabayashi T. Surgical benefits of combined awake craniotomy and intraoperative magnetic resonance imaging for gliomas associated with eloquent areas. J Neurosurg. 2017 Jan 6:1-8. doi: 10.3171/2016.9.JNS16152. [Epub ahead of print] PubMed PMID: 28059650.
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