Risk factors for postoperative cerebellar mutism syndrome in pediatric patients: a systematic review and meta-analysis

Author:

Pettersson Samuel D.1,Kitlinski Michael1,Miękisiak Grzegorz2,Ali Shan3,Krakowiak Michał4,Szmuda Tomasz4

Affiliation:

1. Scientific Circle of Neurology and Neurosurgery, Neurosurgery Department, Medical University of Gdansk;

2. Institute of Medicine, Opole University, Opole;

3. Neurology Department, Mayo Clinic, Jacksonville, Florida

4. Neurosurgery Department, Medical University of Gdansk, Poland; and

Abstract

OBJECTIVE A review article assessing all the risk factors reported in the literature for postoperative cerebellar mutism syndrome (pCMS) among children remains absent. The authors sought to perform a systematic review and meta-analysis to evaluate this issue. METHODS PubMed, Embase, and Web of Science were queried to systematically extract potential references. The articles relating to pCMS were required to be written in the English language, involve pediatric patients (≤ 18 years of age), and provide extractable data, which included a comparison group of patients who did not develop pCMS. The quality of the included studies was evaluated using the Newcastle-Ottawa Scale. Data were pooled using RevMan 5.4, and publication bias was assessed by visual inspection for funnel plot asymmetry. The study protocol was registered through PROSPERO (ID: CRD42021256177). RESULTS Overall, 28 studies involving 2276 patients were included. Statistically significant risk factors identified from univariate analysis were brainstem invasion (OR 4.28, 95% CI 2.23–8.23; p < 0.0001), fourth ventricle invasion (OR 12.84, 95% CI 4.29–38.44; p < 0.00001), superior cerebellar peduncle invasion (OR 6.77, 95% CI 2.35–19.48; p = 0.0004), diagnosis of medulloblastoma (OR 3.26, 95% CI 1.93–5.52; p < 0.0001), medulloblastoma > 50 mm (OR 8.85, 95% CI 1.30–60.16; p = 0.03), left-handedness (OR 6.57, 95% CI 1.25–34.44; p = 0.03), and a vermis incision (OR 5.44, 95% CI 2.09–14.16; p = 0.0005). On the other hand, a tumor located in the cerebellar hemisphere (OR 0.23, 95% CI 0.06–0.92; p = 0.04), cerebellar hemisphere compression (OR 0.23, 95% CI 0.11–0.45; p < 0.0001), and intraoperative imaging (OR 0.36, 95% CI 0.18–0.72; p = 0.004) reduced the risk of pCMS. CONCLUSIONS This study provides the largest and most reliable review of risk factors associated with pCMS. Although some risk factors may be dependent on one another, the data may be used by surgeons to better identify patients at risk for pCMS and for intervention planning.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference94 articles.

1. Establishing reproducible predictors of cerebellar mutism syndrome based on pre-operative imaging;Zhang;Childs Nervous Syst,2019

2. Single photon emission tomography following posterior fossa surgery in patients with and without mutism;Erşahin;Childs Nervous Syst,2002

3. Neuropsychological profile in children with posterior fossa tumors with or without postoperative cerebellar mutism syndrome (CMS);Cámara;Cerebellum,2020

4. Intraoperative MRI-guided resection in pediatric brain tumor surgery: a meta-analysis of extent of resection and safety outcomes;Wach;J Neurol Surg A Cent Eur Neuorsurg,2020

5. Tumour type and size are high risk factors for the syndrome of "cerebellar" mutism and subsequent dysarthria;Catsman-Berrevoets;J Neurol Neurosurg Psychiatry,1999

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