Abstract

Botulinum Neurotoxin type-A (BoNT-A) injections are widely used as first-line spasticity treatment in spastic cerebral palsy (SCP). Despite improved clinical outcomes, concerns regarding harmful effects on muscle morphology have been raised. Yet, the risk of initiating BoNT-A to reduce muscle growth remains unclear. This study investigated medial gastrocnemius (MG) morphological muscle growth in children with SCP (n = 26, median age of 5.2 years (3.5)), assessed by 3D-freehand ultrasound prior to and six months post-BoNT-A injections. Post-BoNT-A MG muscle growth of BoNT-A naive children (n = 11) was compared to (a) muscle growth of children who remained BoNT-A naive after six months (n = 11) and (b) post-BoNT-A follow-up data of children with a history of BoNT-A treatment (n = 15). Six months after initiating BoNT-A injection, 17% decrease in mid-belly cross-sectional area normalized to skeletal growth and 5% increase in echo-intensity were illustrated. These muscle outcomes were only significantly altered when compared with children who remained BoNT-A naive (+4% and −3%, respectively, p < 0.01). Muscle length growth persevered over time. This study showed reduced cross-sectional growth post-BoNT-A treatment suggesting that re-injections should be postponed at least beyond six months. Future research should extend follow-up periods investigating muscle recovery in the long-term and should include microscopic analysis.

Highlights

  • Starting from an early age, the medial gastrocnemius (MG) muscle morphology is impaired in children with spastic cerebral palsy (SCP) [1,2]

  • Absolute muscle atrophy was not determined, the current study revealed hampered medial gastrocnemius muscle growth six months post-botulinum neurotoxin type-A (BoNT-A) injection

  • The hampered muscle growth was primarily attributed to the cross-sectional muscle dimension, while growth in the longitudinal muscle dimension remained preserved

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Summary

Introduction

Starting from an early age, the medial gastrocnemius (MG) muscle morphology is impaired in children with spastic cerebral palsy (SCP) [1,2]. The injection of botulinum neurotoxin type-A (BoNT-A) is widely used within the conventional management of spasticity. This treatment is already prescribed from the ages of two to four years, aiming to reduce focal muscle hyper-excitability [7]. Beneficial outcomes such as reduced muscle spasticity, increased ankle joint range of motion and improved gait have been described when BoNT-A injections are combined with concurrent therapies (e.g., serial casting, ankle–foot orthoses and physiotherapy) [8,9,10,11]

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