Prognostic analysis of posterior fossa decompression with or without cerebellar tonsillectomy for Chiari malformation type I: a multicenter retrospective study

Author:

Cai Yuankun1,Wang Chaobin23,Chai Songshan14,Li Guo1,Zhang Tingbao1,Liu Zheng1,Yi Dongye4,Chen Jincao1,Hu Juntao3,Liu Kui1,Xiong Nanxiang1

Affiliation:

1. Department of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan, Hu Bei;

2. Department of Neurosurgery, Taihe Hospital, Jinzhou Medical University Union Training Base, Shiyan, Hu Bei;

3. Department of Neurosurgery, Taihe Hospital, Hubei University of Medicine, Shiyan, Hu Bei; and

4. Department of Neurosurgery, Wuhan Union Hospital, Wuhan, Hu Bei, China

Abstract

OBJECTIVE The purpose of this study was to compare the prognosis of patients with Chiari malformation type I (CM-I) treated with posterior fossa decompression with duraplasty (PFDD) and posterior fossa decompression with resection of tonsils (PFDRT). METHODS The clinical data of patients with CM-I treated using these two procedures in three medical centers between January 2016 and June 2021 were retrospectively analyzed and divided into PFDD and PFDRT groups according to the procedures. The Chicago Chiari Outcome Scale (CCOS) was used to score the patients and compare the prognosis of the two groups. RESULTS A total of 125 patients with CM-I were included, of whom 90 (72.0%) were in the PFDD group, and 35 (28.0%) were in the PFDRT group. There was no significant difference in the overall essential characteristics of the two groups. Moreover, there was no significant difference in complication rates (3.3% vs 8.6%, p = 0.348), CCOS scores (13.5 ± 1.59 vs 14.0 ± 1.21, p = 0.111), and the probability of poor prognosis (25.6% vs 11.4%, p = 0.096) between the two groups. Nevertheless, a subgroup of patients who had CM-I combined with syringomyelia (SM) revealed higher CCOS scores (13.91 ± 1.12 vs 12.70 ± 1.64, p = 0.002) and a lower probability of poor prognosis (13.0% vs 40.4%, p = 0.028) in the PFDRT than in the PFDD group. Also, SM relief was more significant in patients in the PFDRT compared to the PFDD group. A logistic multifactor regression analysis of poor prognosis in patients with CM-I and SM showed that the PFDRT surgical approach was a protective factor compared to PFDD. Furthermore, by CCOS analysis, it was found that the main advantage of PFDRT in treating patients with CM-I and SM was to improve patients’ nonpain and functionality scores. CONCLUSIONS Compared with PFDD, PFDRT is associated with a better prognosis for patients with CM-I and SM and is a protective factor for poor prognosis. Therefore, the authors suggest that PFDRT may be considered for patients with CM-I and SM.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Neurology (clinical),General Medicine,Surgery

Reference19 articles.

1. Management of Chiari malformations: opinions from different centers—a review;Hersh DS,2019

2. Syringomyelia and Chiari Syndrome Registry: advances in epidemiology, clinical phenotypes and natural history based on a North Western Italy cohort;Ciaramitaro P,2020

3. A morphometric assessment of type I Chiari malformation above the McRae line: a retrospective case-control study in 302 adult female subjects;Houston JR,2018

4. Headache characteristics and postoperative course in Chiari I malformation;Thunstedt DC,2022

5. Diagnosis and treatment of Chiari malformation and syringomyelia in adults: international consensus document;Ciaramitaro P,2022

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