Bb. Bhakta et al., Impact of botulinum toxin type A on disability and carer burden due to armspasticity after stroke: a randomised double blind placebo controlled trial, J NE NE PSY, 69(2), 2000, pp. 217-221
Objectives-After stroke, abnormal arm posture due to spasticity in a functi
onally useless arm may interfere with self care tasks. In these patients bo
tulinum toxin treatment presents an opportunity to reduce disability. The p
urpose was to investigate whether reduction in spasticity after botulinum t
oxin treatment translates into reduction in disability and carer burden.
Methods-Forty patients with stroke with spasticity in a functionally useles
s arm (median duration 3.1 years) were randomised to receive intramuscular
botulinum toxin type A (BT-A; Dysport) (n=20) or placebo (n=20) in a total
dose of 1000 MU divided between elbow, wrist, and finger flexors. Spasticit
y (using the modified Ashworth scale), muscle power, joint movement, and pa
in were assessed. Disability and carer burden were measured using an eight
item and a four item scale respectively. Two baseline and three posttreatme
nt assessments (weeks 2, 6, and 12) were made. Concurrent treatments as far
as possible remained unchanged and not optimised.
Results-Disability improved at week 6 with BT-A compared with placebo. This
effect, present at week 2, wore off by week 12. Reduction in carer burden
was seen at week 6 with BT-A and continued for at least 12 weeks. Forearm f
lexor spasticity was reduced with BT-A up to 12 weeks after treatment. Alth
ough significant improvement in elbow flexor spasticity was seen at week 2
with BT-A compared with placebo, this effect was not evident at weeks 6 and
12. Arm pain was not improved after BT-A. Grip strength was reduced with B
T-A. No serious BT-A related adverse effects were reported.
Conclusion--BT-A is useful for treating patients with stroke who have self
care difficulties due to arm spasticity. The decision to treat should also
include relief of carer burden. As muscle weakness may occur, its potential
impact on functional activities must be assessed before intervention.