Volume 67, Issue 6 pp. 812-820
ORIGINAL ARTICLE

Effect of selective dorsal rhizotomy on neuromuscular symptoms, muscle morphology, and motor function in children with spastic cerebral palsy

Ineke Verreydt

Corresponding Author

Ineke Verreydt

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

Correspondence

Ineke Verreydt, Weligerveld 1, 3212 Pellenberg, Belgium.

Email: [email protected]

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Britta Hanssen

Britta Hanssen

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

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Guy Molenaers

Guy Molenaers

Department of Development and Regeneration, Faculty of Medicine, KU Leuven, Leuven, Belgium

Paediatric Orthopaedics, Department of Orthopaedics, University Hospitals Leuven, Leuven, Belgium

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Nathalie De Beukelaer

Nathalie De Beukelaer

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

Department of Surgery, Faculty of Medicine, University of Geneva, Geneva, Switzerland

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Ines Vandekerckhove

Ines Vandekerckhove

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

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Eirini Papageorgiou

Eirini Papageorgiou

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

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Catherine Huenaerts

Catherine Huenaerts

Clinical Motion Analysis Laboratory, University Hospitals Leuven, Leuven, Belgium

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Els Ortibus

Els Ortibus

Department of Development and Regeneration, Faculty of Medicine, KU Leuven, Leuven, Belgium

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Anja Van Campenhout

Anja Van Campenhout

Department of Development and Regeneration, Faculty of Medicine, KU Leuven, Leuven, Belgium

Paediatric Orthopaedics, Department of Orthopaedics, University Hospitals Leuven, Leuven, Belgium

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Kaat Desloovere

Kaat Desloovere

Department of Rehabilitation Sciences, KU Leuven, Leuven, Belgium

Clinical Motion Analysis Laboratory, University Hospitals Leuven, Leuven, Belgium

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First published: 18 November 2024
Citations: 1

Abstract

Aim

To investigate the effect of selective dorsal rhizotomy (SDR) on an integrated outcome set 1-year post-SDR, in a cohort of children with spastic cerebral palsy (CP).

Method

Fifteen children with bilateral spastic CP (median age 8 years 8 months [interquartile range 3 years 3 months], 11 males, four females, eight in Gross Motor Function Classification System (GMFCS) level II, seven in GMFCS level III) were measured pre- and 1-year post-SDR. Clinical scales and goniometry assessed plantar flexor spasticity, range of motion, strength, and selectivity. Spasticity was also quantified via an instrumented assessment. Medial gastrocnemius macroscopic muscle morphology (absolute and normalized muscle belly, tendon and muscle-tendon unit length, cross-sectional area, muscle volume) was assessed using ultrasound. Gait profile score, ankle and knee gait variable scores, walking speed, cadence, and step length were extracted from gait analysis. Gross motor function was assessed using the Gross Motor Function Measure-66 item set. Wilcoxon signed-rank test was used to analyse pre- and post-SDR changes. A reference database was used to qualitatively judge muscle growth post-SDR with respect to muscle growth of children with spastic CP without SDR intervention.

Results

Significant changes (p < 0.05) were seen for spasticity, selectivity, all absolute morphology parameters, normalized tendon and muscle-tendon unit length, and all gait parameters, except walking speed and cadence. Muscle growth of children with and without SDR was comparable.

Interpretation

SDR is an effective spasticity reducing treatment and does not adversely affect natural muscle growth in spastic CP.

Graphical Abstract

DATA AVAILABILITY STATEMENT

Data available on request from the authors.

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