Evidence map›Paper›PMID 40486483›Full record

ArticleCureus2025

Impact of Unilateral Selective Dorsal Rhizotomy (SDR) on Spasticity and Motor Function Improvement in Children With Hemiparetic Cerebral Palsy Caused by Intraventricular Hemorrhage.

Sevgi Sarikaya-Seiwert, Ralf Clauberg, Ina Hainmann, Hartmut Vatter, Hannes Haberl, Ehab Shabo

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sevgi Sarikaya-SeiwertSection of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital Bonn, Bonn, DEU.
Ralf ClaubergDepartment of Neuroradiology, University Hospital Bonn, Bonn, DEU.
Ina HainmannDepartment of Pediatric Hematology and Oncology, University Hospital Bonn, Bonn, DEU.
Hartmut VatterDepartment of Neurosurgery, University Hospital Bonn, Bonn, DEU.
Hannes HaberlSection of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital Bonn, Bonn, DEU.
Ehab ShaboDepartment of Neurosurgery, University Hospital Bonn, Bonn, DEU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Selective dorsal rhizotomy (SDR) is an established surgical treatment for reducing spasticity in children with cerebral palsy (CP). However, its role in cases of hemiparetic spastic CP due to intraventricular hemorrhage (IVH) remains less well defined, especially regarding the potential benefit of unilateral SDR. Moreover, the majority of existing studies primarily focus on the effectiveness of SDR in reducing spasticity based on quantitative scoring systems, with no evaluation of clinically meaningful improvements in motor function. This study investigates the clinical outcomes of unilateral SDR in children with spastic hemiparetic CP resulting from IVH, with a particular focus on both the reduction of spasticity and improvements in motor function at 6 and 12 months following surgery. Materials and methods This retrospective monocentric study included 11 pediatric patients with IVH-induced hemiparetic CP who underwent a unilateral SDR between 2017 and 2023. IVH was classified using Volpe's grading system. Pre- and postoperative assessments included the Gross Motor Function Classification System (GMFCS), Modified Ashworth Scale (MAS), as well as functional motor domains (sitting, standing, and walking) at 6 and 12 months after surgery. Furthermore, an additional analysis was conducted to assess the relationship between IVH severity and postoperative outcomes. Results All patients demonstrated complete resolution of spasticity following surgery, with postoperative MAS scores reduced to 0. In contrast, GMFCS levels remained unchanged in most patients, with improvement observed in only one case. Remarkably, all patients demonstrated improvements in functional motor skills at both the 6- and 12-month follow-ups, with no evidence of regression or recurrence of motor disability. No adverse events were observed. Notably, higher grades of IVH were not significantly associated with presurgical MAS scores (p=1.0) or GMFCS levels (p=0.45), and no meaningful correlation was observed between IVH severity and postoperative clinical outcomes. Conclusion Unilateral SDR is a promising and safe approach for children with hemisymptomatic CP resulting from IVH, leading to significant reductions in spasticity and sustained functional motor gains regardless of IVH severity. Further and larger prospective studies are needed to validate these findings.

Indexed as

cerebral palsyhemiparesisintraventricular hemorrhagemotor functionselective dorsal rhizotomyspasticityunilateral

Identifiers

PMID40486483
PMCPMC12142565

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.