Impact of botulinum toxin type A on disability and carer burden due to arm spasticity after stroke: a randomised double blind placebo controlled trial
Bipin B Bhaktaa, J Alastair Cozensb, M Anne Chamberlaina, John M Bamfordc
a Rheumatology and
Rehabilitation Research Unit, University of Leeds, 36 Clarendon Road,
Leeds LS2 9NZ, UK, b Department of Rehabilitation Medicine, Woodend
Hospital, Aberdeen, UK, c Department of Neurology and Cerebrovascular
Medicine, St James University Hospital, Leeds, UK
Correspondence to: Dr B B Bhakta B.Bhakta{at}leeds.ac.uk
Received 13 December
1999 and in revised form 6 March 2000;
Accepted 23 March
2000
OBJECTIVES
After
stroke, abnormal arm posture due to spasticity in a functionally
useless arm may interfere with self care tasks. In these patients
botulinum toxin treatment presents an opportunity to reduce disability.
The purpose was to investigate whether reduction in spasticity after
botulinum toxin treatment translates into reduction in disability and
carer burden.
METHODS
Forty patients
with stroke with spasticity in a functionally useless 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. Spasticity
(using the modified Ashworth scale), muscle power, joint movement, and
pain were assessed. Disability and carer burden were measured using an
eight item and a four item scale respectively. Two baseline and three
post-treatment 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
flexor spasticity was reduced with BT-A up to 12 weeks after treatment.
Although 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 BT-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.
Keywords: stroke; spasticity; botulinum toxin
© 2000 by Journal of Neurology, Neurosurgery, and Psychiatry
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