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OnabotulinumtoxinA Improves Pain in Patients With Post-Stroke Spasticity: Findings From a Randomized, Double-Blind, Placebo-Controlled Trial

Wissel, Joerg (författare)
Vivantes Klinikum Spandau, Germany
Ganapathy, Vaidyanathan (författare)
Sunovion Pharmaceut Inc, MA USA
Ward, Anthony B. (författare)
Haywood Hospital, England
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Borg, Jorgen (författare)
Karolinska Institutet
Ertzgaard, Per (författare)
Linköpings universitet,Medicinska fakulteten,Avdelningen för samhällsmedicin,Region Östergötland, Rehabiliteringsmedicinska kliniken
Herrmann, Christoph (författare)
Asklepios Kliniken Schildautal, Germany
Häggstrom, Anders (författare)
Örebro University Hospital, Sweden
Sakel, Mohamed (författare)
East Kent University Hospital NHS, England
Ma, Julia (författare)
Allergan Plc, CA 92612 USA
Dimitrova, Rozalina (författare)
Allergan Plc, CA 92612 USA
Fulford-Smith, Antony (författare)
Marlow Int, England
Gillard, Patrick (författare)
Allergan Plc, CA 92612 USA
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 (creator_code:org_t)
ELSEVIER SCIENCE INC, 2016
2016
Engelska.
Ingår i: Journal of Pain and Symptom Management. - : ELSEVIER SCIENCE INC. - 0885-3924 .- 1873-6513. ; 52:1, s. 17-26
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Context. Patients with post-stroke spasticity (PSS) commonly experience pain in affected limbs, which may impact quality of life. Objectives. To assess onabotulinumtoxinA for pain in patients with PSS from the BOTOX (R) Economic Spasticity Trial, a multicenter, randomized, double-blind, placebo-controlled trial. Methods. Patients with PSS (N = 273) were randomized to 22- to 34-week double-blind treatment with onabotulinumtoxinA + standard care (SC) or placebo injection + SC and were eligible to receive open-label onabotulinumtoxinA up to 52 weeks. Assessments included change from baseline on the 11-point pain numeric rating scale, proportion of patients with baseline pain amp;gt;= 4 achieving amp;gt;= 30% and amp;gt;= 50% improvement in pain, and pain interference with work at Week 12, end of double-blind treatment, and Week 52. Results. At baseline, most patients (74.3%) experienced pain and 47.4% had pain amp;gt;= 4 (pain subgroup). Mean pain reduction from baseline at Week 12 was significantly greater with onabotulinumtoxinA + SC (-0.77, 95% CI -1.14 to -0.40) than placebo + SC (-0.13, 95% CI -0.51 to 0.24; P amp;lt; 0.05). Higher proportions of patients in the pain subgroup achieved amp;gt;= 30% and amp;gt;= 50% reductions in pain at Week 12 with onabotulinumtoxinA + SC (53.7% and 37.0%, respectively) compared with placebo (28.8% and 18.6%, respectively; P amp;lt; 0.05). Reductions in pain were sustained through Week 52. Compared with placebo + SC, onabotulinumtoxinA consistently reduced pain interference with work. Conclusion. This is the first randomized, placebo-controlled trial demonstrating statistically significant and clinically meaningful reductions in pain and pain interference with work with onabotulinumtoxinA in patients with PSS. (C) 2016 The Authors. Published by Elsevier Inc. on behalf of American Academy of Hospice and Palliative Medicine. This is an open access article under the CC BY-NC-ND license.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Annan medicin och hälsovetenskap -- Övrig annan medicin och hälsovetenskap (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Other Medical and Health Sciences -- Other Medical and Health Sciences not elsewhere specified (hsv//eng)

Nyckelord

OnabotulinumtoxinA; pain; post-stroke spasticity; disability

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