Intramuscular Injection of Botulinum Toxin for the Treatment of Wrist and Finger Spasticity after a Stroke
Allison Brashear, M.D., Mark F. Gordon, M.D., Elie Elovic, M.D., V. Daniel Kassicieh, D.O., Christina Marciniak, M.D., Mai Do, B.S., Chia-Ho Lee, M.S., Stephen Jenkins, M.D., Catherine Turkel, Pharm.D., for the Botox Post-Stroke Spasticity Study Group
Background Spasticity is a disabling complication of stroke,and it is uncertain whether intramuscular injections of botulinumtoxin type A reduce disability in persons with spasticity ofthe wrist and fingers after a stroke.
Methods We performed a randomized, double-blind, placebo-controlled,multicenter trial to assess the efficacy and safety of one-timeinjections of botulinum toxin A (200 to 240 units) in 126 subjectswith increased flexor tone in the wrist and fingers after astroke. The primary outcome measure was self-reported disabilityin four areas: personal hygiene, dressing, pain, and limb position(on a four-point scale ranging from no disability to severedisability) at six weeks; at base line, each subject selectedone of these areas in which there was moderate-to-severe disabilityas the principal target of treatment.
Results Subjects who received botulinum toxin A had greaterimprovement in flexor tone in the wrist and fingers at all follow-upvisits through 12 weeks than did subjects who received placebo(P<0.001 for all comparisons). Subjects treated with botulinumtoxin A had greater improvement in the principal target of treatmentat weeks 4, 6, 8, and 12 (P<0.001, P<0.001, P=0.03, andP=0.02, respectively); at week 6, 40 of the 64 subjects in thebotulinum-toxin group (62 percent), as compared with 17 of the62 in the placebo group (27 percent), reported improvement ofat least one point on the Disability Assessment Scale in theprincipal target of treatment (P<0.001). There were no majoradverse events associated with injection of botulinum toxinA.
Conclusions Intramuscular injections of botulinum toxin A reducespasticity of the wrist and finger muscles and associated disabilityin patients who have had a stroke.
Source Information
From the Department of Neurology, Indiana University School of Medicine, Indianapolis (A.B.); the Department of Neurology and Psychiatry, Long Island Jewish Medical Center, New Hyde Park, N.Y. (M.F.G.); Traumatic Brain Injury Research Laboratory, Kessler Medical Rehabilitation Research Education Corporation, West Orange, N.J. (E.E.); the Neurological Research Institute of Sarasota, Sarasota, Fla. (V.D.K.); the Rehabilitation Institute of Chicago, Chicago (C.M.); and Allergan, Irvine, Calif. (M.D., C.-H.L., S.J., C.T.).
Address reprint requests to Dr. Brashear at Indiana University Hospital, Department of Neurology, 550 University Blvd., Rm. 6620, Indianapolis, IN 46202, or at abrashea{at}iupui.edu.
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