Evidence map›Paper›PMID 41423601›Full record

ArticleJournal of neuroengineering and rehabilitation2025

Non-invasive assessment of muscle spasticity in children with cerebral palsy undergoing botulinum toxin treatment using near-infrared spectroscopy.

Mehdi Nourizadeh, Maria Juricic, Jocelyn Begin, Leila Bektash, Stacey Miller, Kishore Mulpuri, Babak Shadgan

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Article in Journal of neuroengineering and rehabilitation, 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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mehdi NourizadehInternational Collaboration on Repair Discoveries, Vancouver, Canada.
Maria JuricicDepartment of Orthopaedics, University of British Columbia, Vancouver, Canada.
Jocelyn BeginInternational Collaboration on Repair Discoveries, Vancouver, Canada.
Leila BektashInternational Collaboration on Repair Discoveries, Vancouver, Canada.
Stacey MillerDepartment of Orthopaedic Surgery, BC Children's Hospital, University of British, Columbia, Canada.
Kishore Mulpuri *Department of Orthopaedics, University of British Columbia, Vancouver, Canada.
Babak Shadgan *International Collaboration on Repair Discoveries, Vancouver, Canada. babak.shadgan@ubc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpasticity is a common and debilitating feature of cerebral palsy (CP), often treated with botulinum toxin A (BoNT-A). Standard assessments, such as the Modified Ashworth Scale (MAS), are subjective and prone to inter-rater variability. Near-infrared spectroscopy (NIRS) is a non-invasive method that measures muscle oxygenation and hemodynamics. In CP, spastic muscles exhibit impaired perfusion and abnormal oxygen consumption due to sustained contraction and elevated intramuscular pressure. Prior studies suggest that reducing spastic overactivity improves local tissue oxygenation, indicating that NIRS-derived metrics could objectively reflect spasticity severity and treatment response.

objectiveTo evaluate the feasibility of using NIRS as a biomarker for spasticity severity and treatment response in children with CP receiving BoNT-A and to assess the correlation between NIRS-derived tissue oxygenation index (TOI%) and MAS scores over time.

methodsIn this prospective pilot study, eight children (aged 2–17 years) with CP undergoing BoNT-A treatment were assessed. Muscle oxygenation was recorded using a portable NIRS device at baseline, 2–4 weeks, 6–10 weeks, 3 months, and 6 months post-injection. Spasticity was measured concurrently using MAS. Temporal changes in TOI% and MAS were analyzed using repeated-measures ANOVA, and associations between the two were evaluated with Pearson correlation.

resultsTOI% increased significantly after injection, peaking at 6–10 weeks and 3 months (p < 0.001), then declined toward baseline by 6 months. MAS scores showed a similar trend, with reduced spasticity during peak effect. A moderate, significant negative correlation between TOI% and MAS (r = − 0.409, p < 0.05) indicated higher oxygenation was associated with lower spasticity.

conclusionNIRS is a feasible, non-invasive tool for assessing muscle spasticity and monitoring BoNT-A response in children with CP. Its correlation with MAS supports physiological relevance and suggests NIRS may offer a more objective measure of spasticity. Larger studies are warranted to validate these findings and support clinical use.

Indexed as

Botulinum Toxins, Type ACerebral PalsyMuscle SpasticityNeuromuscular AgentsAdolescentChildChild, PreschoolFemaleHumansMalePilot ProjectsProspective StudiesSpectroscopy, Near-InfraredTreatment OutcomeBotulinum Toxins, Type ANeuromuscular AgentsBotulinum toxin (BoNT-A)Cerebral palsyMuscle spasticityNear-Infrared spectroscopy (NIRS)Spasticity assessmentTissue oxygenation index (TOI%)

Identifiers

PMID41423601
PMCPMC12751561

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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.