• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

成人寰枕减压并硬脑膜成形术治疗 Chiari 畸形 I 型:297 例系列研究。

Long-term outcomes of foramen magnum decompression with duraplasty for Chiari malformation type I in adults: a series of 297 patients.

机构信息

1Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, People's Republic of China; and.

2China National Clinical Research Center for Neurological Diseases, Beijing, People's Republic of China.

出版信息

Neurosurg Focus. 2023 Mar;54(3):E5. doi: 10.3171/2022.12.FOCUS22627.

DOI:10.3171/2022.12.FOCUS22627
PMID:36857791
Abstract

OBJECTIVE

Foramen magnum decompression with duraplasty (FMDD) is one of the most frequently utilized surgical treatments for Chiari malformation type I (CMI) in adults. However, its long-term outcomes remain controversial. The object of this study was to evaluate the long-term outcomes of FMDD in adults with CMI.

METHODS

In total, 297 adults with CMI who had undergone FMDD at the authors' institution between 2011 and 2020 were included in this retrospective study. Long-term (> 1 year) outcomes were evaluated using the Chicago Chiari Outcome Scale (CCOS), visual analog scale (VAS), and Japanese Orthopaedic Association (JOA) scale.

RESULTS

The median patient age was 44 years (range 18-65 years). The mean clinical follow-up period was 67 months (range 14-123 months). Compared with preoperative conditions, the postoperative syringomyelia regression rate was 91.3% (242/265), and the cerebellar tonsil ascended in 18.2% of patients (54/297), was stable in 64.3% (191/297), and continuously descended in 17.5% (52/297). Long-term clinical follow-up data were acquired from 267 patients. According to the CCOS score, the patient's condition improved in 62.5% of cases (167/267), was stable in 31.8% (85/267), and worsened in 5.6% (15/267). According to the VAS score, the patient's condition improved in 59.5% of cases (110/185), remained unchanged in 27.6% (51/185), and worsened in 13.0% (24/185) among the follow-up patients with relevant data. According to the JOA score, the patient's condition improved in 40.1% of cases (107/267), remained unchanged in 50.2% (134/267), and worsened in 9.7% (26/267). Notably, there was no association between clinical outcomes and syringomyelia regression (p = 0.227) or changes in the cerebellar tonsillar position (p = 0.323).

CONCLUSIONS

FMDD is a simple, safe, and effective surgical procedure for adult CMI that yields significant and sustained improvement in clinical and radiological outcomes. However, clinical improvement does not always correlate with syringomyelia regression and cerebellar tonsillar shift.

摘要

目的

寰枕减压硬脑膜成形术(FMDD)是成人 Chiari 畸形 I 型(CMI)最常采用的手术治疗方法之一。然而,其长期疗效仍存在争议。本研究旨在评估 FMDD 治疗成人 CMI 的长期疗效。

方法

回顾性分析 2011 年至 2020 年在作者所在机构接受 FMDD 的 297 例 CMI 成人患者的临床资料。采用芝加哥 Chiari 结局量表(CCOS)、视觉模拟评分(VAS)和日本矫形协会(JOA)评分评估长期(>1 年)疗效。

结果

患者中位年龄为 44 岁(18-65 岁)。平均临床随访时间为 67 个月(14-123 个月)。与术前相比,术后脊髓空洞症消退率为 91.3%(242/265),小脑扁桃体上移占 18.2%(54/297),稳定占 64.3%(191/297),持续下移占 17.5%(52/297)。267 例患者获得长期临床随访资料。根据 CCOS 评分,167 例(62.5%)患者病情改善,85 例(31.8%)病情稳定,15 例(5.6%)病情恶化。根据 VAS 评分,110 例(59.5%)患者病情改善,51 例(27.6%)病情无变化,24 例(13.0%)病情恶化。根据 JOA 评分,107 例(40.1%)患者病情改善,134 例(50.2%)病情稳定,26 例(9.7%)病情恶化。值得注意的是,临床疗效与脊髓空洞症消退(p=0.227)或小脑扁桃体位置变化(p=0.323)无显著相关性。

结论

FMDD 是治疗成人 CMI 的一种简单、安全、有效的手术方法,可显著改善临床和影像学结局,并具有持续疗效。然而,临床改善并不总是与脊髓空洞症消退和小脑扁桃体移位相关。

相似文献

1
Long-term outcomes of foramen magnum decompression with duraplasty for Chiari malformation type I in adults: a series of 297 patients.成人寰枕减压并硬脑膜成形术治疗 Chiari 畸形 I 型:297 例系列研究。
Neurosurg Focus. 2023 Mar;54(3):E5. doi: 10.3171/2022.12.FOCUS22627.
2
Is atlantoaxial instability the cause of Chiari malformation? Outcome analysis of 65 patients treated by atlantoaxial fixation.寰枢椎不稳是 Chiari 畸形的病因吗?65 例寰枢椎固定治疗患者的疗效分析。
J Neurosurg Spine. 2015 Feb;22(2):116-27. doi: 10.3171/2014.10.SPINE14176. Epub 2014 Nov 21.
3
A points-based algorithm for prognosticating clinical outcome of Chiari malformation Type I with syringomyelia: results from a predictive model analysis of 82 surgically managed adult patients.一种用于预测伴脊髓空洞症的Ⅰ型Chiari畸形临床结局的积分算法:82例接受手术治疗的成年患者预测模型分析结果
J Neurosurg Spine. 2018 Jan;28(1):23-32. doi: 10.3171/2017.5.SPINE17264. Epub 2017 Nov 10.
4
Treatment failure of syringomyelia associated with Chiari I malformation following foramen magnum decompression: how should we proceed?寰枕减压术后伴 Chiari I 畸形的脊髓空洞症治疗失败:我们应该如何处理?
Neurosurg Rev. 2019 Sep;42(3):705-714. doi: 10.1007/s10143-018-01066-0. Epub 2018 Dec 15.
5
Surgical outcomes after posterior fossa decompression with and without duraplasty in Chiari malformation-I.Chiari畸形I型行后颅窝减压术伴或不伴硬脑膜成形术的手术结果。
Clin Neurol Neurosurg. 2014 Oct;125:182-8. doi: 10.1016/j.clineuro.2014.07.027. Epub 2014 Aug 12.
6
Elucidating the pathophysiology of syringomyelia.阐明脊髓空洞症的病理生理学。
J Neurosurg. 1999 Oct;91(4):553-62. doi: 10.3171/jns.1999.91.4.0553.
7
Chiari I malformation with and without basilar invagination: a comparative study.伴或不伴基底凹陷的Chiari I型畸形:一项对比研究。
Neurosurg Focus. 2015 Apr;38(4):E12. doi: 10.3171/2015.1.FOCUS14783.
8
Surgical results of arachnoid-preserving posterior fossa decompression for Chiari I malformation with associated syringomyelia.保留蛛网膜的后颅窝减压术治疗 Chiari I 畸形伴脊髓空洞症的手术效果。
J Clin Neurosci. 2012 Apr;19(4):557-60. doi: 10.1016/j.jocn.2011.06.034. Epub 2012 Feb 1.
9
Pediatric and adult Chiari malformation Type I surgical series 1965-2013: a review of demographics, operative treatment, and outcomes.1965年至2013年儿童及成人I型Chiari畸形手术系列研究:人口统计学、手术治疗及结果综述
J Neurosurg Pediatr. 2015 Feb;15(2):161-77. doi: 10.3171/2014.10.PEDS14295. Epub 2014 Dec 5.
10
When is duraplasty required in the surgical treatment of Chiari malformation type I based on tonsillar descending grading scale?基于扁桃体下疝分级标准,Chiari 畸形 I 型的手术治疗中何时需要硬脑膜成形术?
World Neurosurg. 2011 Feb;75(2):307-13. doi: 10.1016/j.wneu.2010.09.005.

引用本文的文献

1
Fourth ventricular stenting in foramen magnum decompression for type 1 Chiari malformations with syringomyelia.第四脑室支架置入术用于伴脊髓空洞症的Ⅰ型Chiari畸形的枕大孔减压。
Surg Neurol Int. 2025 Jul 4;16:271. doi: 10.25259/SNI_40_2025. eCollection 2025.
2
Difference in clinical presentation and surgical outcomes in pediatric and adult patients with Chiari malformation type 1: a single center retrospective study.1型Chiari畸形小儿与成人患者的临床表现及手术结果差异:一项单中心回顾性研究
Acta Neurochir (Wien). 2025 Apr 24;167(1):120. doi: 10.1007/s00701-025-06534-3.
3
Surgical Outcomes in Chiari 1 and Chiari 1.5 Malformation Treated by Posterior Fossa Reconstruction: A Comprehensive Analysis of 110 Pediatric Cases and Literature Review.
后颅窝重建治疗Chiari 1型和Chiari 1.5型畸形的手术结果:110例儿科病例综合分析及文献综述
J Clin Med. 2024 Jun 30;13(13):3852. doi: 10.3390/jcm13133852.
4
Evaluating the Need for Durotomy and Duraplasty in Adults Undergoing Suboccipital Craniectomy for Chiari Decompression: A Case Series Analysis of Radiographic and Clinical Outcomes.评估行枕下颅骨切除术治疗Chiari减压的成人患者中硬脑膜切开术和硬脑膜成形术的必要性:影像学和临床结果的病例系列分析
Cureus. 2024 May 20;16(5):e60694. doi: 10.7759/cureus.60694. eCollection 2024 May.
5
Preoperative estimation of intracranial compliance in symptomatic children with Chiari malformation type 1: impact on outcome and risk of complications.Chiari 畸形 1 型有症状儿童颅内顺应性的术前评估:对结局和并发症风险的影响。
Acta Neurochir (Wien). 2024 Jan 18;166(1):22. doi: 10.1007/s00701-024-05897-3.
6
Individualized Functional Decompression Options for Adult Chiari Malformation With Syringomyelia and A Novel Scale for Syringomyelia Resolution: A Single-Center Experience.成人Chiari畸形合并脊髓空洞症的个体化功能减压方案及脊髓空洞症缓解新量表:单中心经验
Neurospine. 2023 Dec;20(4):1501-1512. doi: 10.14245/ns.2346626.313. Epub 2023 Dec 31.
7
A long-term follow-up study of adults with Chiari malformation type I combined with syringomyelia.一项关于成年I型Chiari畸形合并脊髓空洞症患者的长期随访研究。
Front Neurol. 2023 Dec 1;14:1274971. doi: 10.3389/fneur.2023.1274971. eCollection 2023.