Sharma Julia, Bonfield Christopher, Steinbok Paul
Division of Neurosurgery, Department of Surgery, University of British Columbia, Vancouver, BC, Canada.
Vanderbilt University Medical Center, Nashville, USA.
Childs Nerv Syst. 2016 Aug;32(8):1489-94. doi: 10.1007/s00381-016-3122-2. Epub 2016 Jun 16.
The aim of this study was to determine the outcomes for children who underwent selective dorsal rhizotomy (SDR) for the treatment of spasticity related to spinal pathology.
We performed a retrospective review of all cases of SDR at our institution over the last 30 years and identified patients in whom spasticity was attributed to spinal rather than cerebral pathology. We gathered demographic information and recorded functional status and spasticity scores pre-operatively and over long-term follow-up.
We identified four patients who underwent SDR for spinal-related spasticity. All four had hereditary spastic paraparesis (HSP). All patients had reduced spasticity in the lower limbs after SDR, which was maintained over long-term follow-up. Two patients had a more severe and progressive subtype of HSP, and both these patients exhibited functional decline despite improvement in tone.
Our findings suggest SDR is a reasonable option to consider for relief of spinal-related spasticity in uncomplicated hereditary spastic paraparesis. However, SDR for the treatment of complicated HSP seems to carry more risks and have a less predictable outcome. Overall, SDR is probably best reserved for pathologies that are relatively stable in their disease course.
本研究旨在确定接受选择性背根切断术(SDR)治疗与脊柱病变相关痉挛的儿童的治疗结果。
我们对本机构过去30年中所有SDR病例进行了回顾性研究,确定痉挛归因于脊柱而非脑部病变的患者。我们收集了人口统计学信息,并记录了术前和长期随访期间的功能状态和痉挛评分。
我们确定了4例因脊柱相关痉挛接受SDR治疗的患者。所有4例均患有遗传性痉挛性截瘫(HSP)。所有患者在SDR后下肢痉挛均减轻,并在长期随访中得以维持。2例患者患有更严重且进行性的HSP亚型,尽管肌张力有所改善,但这2例患者均出现了功能衰退。
我们的研究结果表明,对于单纯性遗传性痉挛性截瘫中脊柱相关痉挛的缓解,SDR是一个值得考虑的合理选择。然而,SDR治疗复杂性HSP似乎风险更大,预后更难预测。总体而言,SDR可能最适合疾病进程相对稳定的病变。