Does botulinum neurotoxin A make walking easier in children with cerebral palsy? A randomized clinical trial

Author:

Brændvik Siri Merete12ORCID,Ross Raftemo Anne Elisabeth34,Roeleveld Karin1,Andersen Guro Lillemoen34,Ramstad Kjersti5,Follestad Turid67,Aarli Ånen8,Bonikowski Marcin9,Vik Torstein4,

Affiliation:

1. Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology, NTNU Trondheim Norway

2. Rehabilitation Clinic St. Olavs University Hospital Trondheim Norway

3. Vestfold Hospital Trust Tønsberg Norway

4. Department of Laboratory Medicine, Children's and Women's Health, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology, NTNU Trondheim Norway

5. Oslo University Hospital Oslo Norway

6. Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology, NTNU Trondheim Norway

7. Clinical Research Unit Central Norway St. Olavs Hospital Trondheim Norway

8. Haukeland University Hospital Bergen Norway

9. Mazovian Neuropsychiatry Center, Neuro Rehabilitation Department Movement Analysis Laboratory Poland

Abstract

AbstractAimTo assess the effect of single botulinum neurotoxin A (BoNT‐A) injections into the calf muscles on the gross energy cost of walking in children with cerebral palsy (CP) and to evaluate the effect of BoNT‐A on walking capacity, physical activity, perceived changes in mobility, and pain.MethodThis was an industry‐independent, randomized, quadruple‐blind, placebo‐controlled, multicentre trial (ClinicalTrials.gov registration: NCT02546999). Sixty‐one children (33 male, median age [range] = 8 years [4–16 years]) with spastic CP and classified in Gross Motor Function Classification System (GMFCS) levels I and II allocated to single injections of either BoNT‐A or 0.9% saline into the calf muscles. The main outcome was gross energy cost (J/kg/m); secondary outcomes were walking capacity, habitual physical activity, perceived change in mobility tasks, and calf pain at baseline, 4 weeks (P1), 12 weeks (P2), and 24 weeks (P3) after the injection.ResultsThe mean change in energy cost did not differ significantly between groups at the primary time point P2 (−0.27 J/kg/m, 95% confidence interval − 0.91 to 0.36, p = 0.404), nor at P1 or P3. Regarding the secondary outcomes, there was some evidence of a larger reduction in pain intensity in the group given BoNT‐A (p = 0.043).InterpretationOne treatment with BoNT‐A was not superior to placebo in making walking easier in children with CP classified in GMFCS levels I and II, at least in the short term. BoNT‐A may have a pain‐reducing effect.

Funder

Fakultet for medisin og helsevitenskap, Norges Teknisk-Naturvitenskapelige Universitet

Publisher

Wiley

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