BackgroundCerebellar mutism (CM) is characterized by a signi cant loss of speech in children following posterior fossa (PF) surgery. The biological origin of CM remains unclear and is the subject of ongoing debate.Signi cant recovery from CM is less likely than previously described despite rigorous multidisciplinary neuro-rehabilitational efforts.
MethodsA national multi-centered retrospective review of all children undergoing PF resection in 4 midsized Canadian academic pediatric institutions was undertaken. Patient, tumor, and surgical factors associated with the post-operative development of CM were reviewed. Retrospective identi cation of PF surgery patients including those developing and those that did not (internal control).
ResultsThe study identi ed 258 patients across the 4 centers between 2010-2020 (mean age 6.73 years; 42.2 female). Overall, CM was experienced in 19.5% of patients (N = 50). Amongst children who developed CM histopathology included medulloblastoma (35.7%), pilocytic astrocytoma (32.6%), and ependymoma (17.1%). Intraoperative impression of adherence to the oor of the 4th ventricle was positive in 36.8%.Intraoperative abrupt changes in blood pressure and/or heart rate were identi ed in 19.4% and 17.8% of cases. The clinical resolution of CM was rated to be complete, signi cant resolution, slight improvement, no improvement, and deterioration in 56.0%, 8.0%, 20.0%, 14.0%, 2.0%, respectively. In the cohort of children who experienced post-operative CM as compared to their no-CM counterpart, proportionally more tumors were felt to be adherent to the oor of the 4th ventricle (56.0% vs 49.5%), intraoperative extent of resection was a GTR (74% vs 68.8%), and changes in heart rate were noted (≥ 20% from baseline) (26.0% vs 15.9%). However, a logistic regression for experiencing CM identi ed only intraoperative impression of adherence to the oor of the 4th ventricle (OR 2.32, p = 0.011), abrupt changes in intraoperative HR (> 20% from baseline) (OR 2.34, p = 0.028), and medulloblastoma histology (OR 3.77, p = 0.001) to signi cantly associated with development of post-operative CM.
ConclusionAs a devastating surgical complication, identifying and understanding the biological origin of CM is the rst step to complication avoidance. Maximal safe resection irrespective of intraoperative pathology remains the strategy to minimize the devastating post-operative development of CM.