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隐性脊柱裂相关脊髓栓系综合征的评估和管理:国际儿童尿控协会的建议。

Evaluation and management of tethered cord syndrome in occult spinal dysraphism: Recommendations from the international children's continence society.

机构信息

Institute of Brain Protection Science, Division of Pediatric Neurosurgery, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.

Department of Paediatric Neurosurgery, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.

出版信息

Neurourol Urodyn. 2018 Mar;37(3):890-903. doi: 10.1002/nau.23382. Epub 2017 Aug 9.

Abstract

AIMS

As awareness and frequency of tethered spinal cord (TSC) related to occult spinal dysraphism (OSD) has increased with magnetic resonance imaging (MRI), variability exists in its evaluation and management. Due to no published level I data, we summarize the current International Children's Continence Society (ICCS) recommendations for diagnosis and treatment of OSD.

METHODS

Guidelines were formulated based on analysis of pertinent literature and consensus among authors. This document was vetted by the multidisciplinary members of the ICCS via its website before submission for peer review publication.

RESULTS

The more frequent diagnosis of OSD is associated with increased operative intervention. Spinal cord untethering (SCU) has a highly variable risk profile, largely dependent on the specific form of OSD. Progressive neurological deterioration attributed to "tethered cord" may occur, with or without surgery, in selected forms of OSD whereas other cohorts do well.

CONCLUSION

Infants with classic cutaneous markers of OSD, with progressive neurologic, skeletal, and/or urologic findings, present no diagnostic or therapeutic dilemma: they routinely undergo MRI and SCU. Conversely, in asymptomatic patients or those with fixed, minor abnormalities, the risk profile of these OSD cohorts should be carefully considered before SCU is performed. Irrespective of whether or not SCU is performed, patients at risk for progression should be followed carefully throughout childhood and adolescence by a multidisciplinary team.

摘要

目的

随着磁共振成像(MRI)对隐性脊柱裂相关脊髓栓系(TSC)认识和检出率的提高,其评估和管理方法存在差异。由于缺乏一级数据,我们总结了目前国际儿童尿控协会(ICCS)对隐性脊柱裂相关脊髓栓系的诊断和治疗建议。

方法

根据相关文献分析和作者共识制定指南。本文件在提交同行评议出版前,由 ICCS 的多学科成员在其网站上进行了审查。

结果

隐性脊柱裂的更频繁诊断与手术干预的增加相关。脊髓松解(SCU)的风险特征差异很大,主要取决于隐性脊柱裂的具体形式。与手术与否相关,某些形式的隐性脊柱裂可能会出现“脊髓栓系”导致的进行性神经功能恶化,而其他亚组则预后良好。

结论

具有隐性脊柱裂典型皮肤标志、进行性神经、骨骼和/或泌尿系统表现的婴儿,不存在诊断或治疗方面的难题:他们通常会接受 MRI 和 SCU 检查。相反,对于无症状患者或存在固定、轻微异常的患者,在进行 SCU 之前,应仔细考虑这些隐性脊柱裂亚组的风险特征。无论是否进行 SCU,有进展风险的患者都应由多学科团队在整个儿童期和青春期进行密切随访。

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