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一种用于预测小儿术后小脑缄默综合征风险的术前评分系统的开发。

Development of a pre-operative scoring system for predicting risk of post-operative paediatric cerebellar mutism syndrome.

作者信息

Liu Jo-Fen, Dineen Robert A, Avula Shivaram, Chambers Tom, Dutta Manali, Jaspan Tim, MacArthur Donald C, Howarth Simon, Soria Daniele, Quinlan Philip, Harave Srikrishna, Ong Chan Chang, Mallucci Conor L, Kumar Ram, Pizer Barry, Walker David A

机构信息

a Children's Brain Tumour Research Centre , University of Nottingham , Nottingham , UK.

b Radiological Sciences, Division of Clinical Neuroscience , University of Nottingham , Nottingham , UK.

出版信息

Br J Neurosurg. 2018 Feb;32(1):18-27. doi: 10.1080/02688697.2018.1431204. Epub 2018 Feb 12.

Abstract

BACKGROUND

Despite previous identification of pre-operative clinical and radiological predictors of post-operative paediatric cerebellar mutism syndrome (CMS), a unifying pre-operative risk stratification model for use during surgical consent is currently lacking. The aim of the project is to develop a simple imaging-based pre-operative risk scoring scheme to stratify patients in terms of post-operative CMS risk.

METHODS

Pre-operative radiological features were recorded for a retrospectively assembled cohort of 89 posterior fossa tumour patients from two major UK treatment centers (age 2-23yrs; gender 28 M, 61 F; diagnosis: 38 pilocytic astrocytoma, 32 medulloblastoma, 12 ependymoma, 1 high grade glioma, 1 pilomyxoid astrocytoma, 1 atypical teratoid rhabdoid tumour, 1 hemangioma, 1 neurilemmoma, 2 oligodendroglioma). Twenty-six (29%) developed post-operative CMS. Based upon results from univariate analysis and C4.5 decision tree, stepwise logistic regression was used to develop the optimal model and generate risk scores.

RESULTS

Univariate analysis identified five significant risk factors and C4.5 decision tree analysis identified six predictors. Variables included in the final model are MRI primary location, bilateral middle cerebellar peduncle involvement (invasion and/or compression), dentate nucleus invasion and age at imaging >12.4 years. This model has an accuracy of 88.8% (79/89). Using risk score cut-off of 203 and 238, respectively, allowed discrimination into low (38/89, predicted CMS probability <3%), intermediate (17/89, predicted CMS probability 3-52%) and high-risk (34/89, predicted CMS probability ≥52%).

CONCLUSIONS

A risk stratification model for post-operative paediatric CMS could flag patients at increased or reduced risk pre-operatively which may influence strategies for surgical treatment of cerebellar tumours. Following future testing and prospective validation, this risk scoring scheme will be proposed for use during the surgical consenting process.

摘要

背景

尽管先前已确定小儿小脑缄默综合征(CMS)术后的术前临床和影像学预测指标,但目前仍缺乏一种在手术知情同意过程中使用的统一术前风险分层模型。该项目的目的是开发一种基于影像学的简单术前风险评分方案,以根据术后CMS风险对患者进行分层。

方法

记录了来自英国两个主要治疗中心的89例后颅窝肿瘤患者(年龄2 - 23岁;性别:男性28例,女性61例;诊断:38例毛细胞型星形细胞瘤,32例髓母细胞瘤,12例室管膜瘤,1例高级别胶质瘤,1例毛黏液样星形细胞瘤,1例非典型畸胎样横纹肌样肿瘤,1例血管瘤,1例神经鞘瘤,2例少突胶质细胞瘤)回顾性队列的术前影像学特征。其中26例(29%)出现了术后CMS。基于单因素分析结果和C4.5决策树,采用逐步逻辑回归来开发最优模型并生成风险评分。

结果

单因素分析确定了五个显著风险因素,C4.5决策树分析确定了六个预测指标。最终模型纳入的变量包括MRI主要位置、双侧小脑中脚受累(侵犯和/或压迫)、齿状核侵犯以及影像学检查时年龄>12.4岁。该模型的准确率为88.8%(79/89)。分别使用风险评分临界值203和238,可将患者分为低风险(38/89,预测CMS概率<3%)、中度风险(17/89,预测CMS概率3 - 52%)和高风险(34/89,预测CMS概率≥52%)。

结论

小儿CMS术后风险分层模型可以在术前识别风险增加或降低的患者,这可能会影响小脑肿瘤的手术治疗策略。在未来进行测试和前瞻性验证后,将提议在手术知情同意过程中使用这种风险评分方案。

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