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Erschienen in: Child's Nervous System 8/2016

16.06.2016 | Original Paper

Selective dorsal rhizotomy for hereditary spastic paraparesis in children

verfasst von: Julia Sharma, Christopher Bonfield, Paul Steinbok

Erschienen in: Child's Nervous System | Ausgabe 8/2016

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Abstract

Purpose

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.

Methods

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.

Results

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.

Conclusions

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.
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Metadaten
Titel
Selective dorsal rhizotomy for hereditary spastic paraparesis in children
verfasst von
Julia Sharma
Christopher Bonfield
Paul Steinbok
Publikationsdatum
16.06.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Child's Nervous System / Ausgabe 8/2016
Print ISSN: 0256-7040
Elektronische ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-016-3122-2

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