Physical Medicine and Rehabilitation Department, Hospital Universitario de La Princesa, Madrid, Spain.
Physical Medicine and Rehabilitation Department, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.
Rehabilitacion (Madr). 2024 Jul-Sep;58(3):100856. doi: 10.1016/j.rh.2024.100856. Epub 2024 May 24.
Spasticity is common after a stroke and is an independent risk factor for developing pain. BotulinumtoxinA injection is the treatment of choice for focal spasticity. We examined the effect of intramuscular botulinumtoxinA on pain relief in patients in routine clinical practice who were experiencing pain as a primary complaint associated with post-stroke lower limb spasticity.
Prospective, multicentre, post-marketing observational study. The study period was 16 months. The primary effectiveness variable was the mean change from baseline on the pain 0-10 Numerical Rating Scale after four botulinumtoxinA injection cycles. Secondary endpoints included changes from baseline on the pain 0-100 Visual Analogue Scale, Goal Attainment Scale, modified Ashworth Scale, 10-Meter Walk Test, Penn Spasm Frequency Scale, and 36-item Short-Form Health Survey.
Of 186 enrolled patients, 180 (96.8%) received botulinumtoxinA at least once. The mean (standard deviation) pain 0-10 Numerical Rating Scale score decreased significantly (p<0.0001) from 4.9 (2.2) at baseline to 2.5 (2.1) at study end, representing a 50% decrease in pain severity. Relief of pain due to spasticity was supported by improvement from baseline in all secondary variables except the 10-Meter Walk Test. Two adverse events (erysipelas and phlebitis) in one patient were considered likely to be related to botulinumtoxinA injection.
BotulinumtoxinA appears to provide pain relief as an additional benefit of local treatment in patients with post-stroke lower limb spasticity for whom pain relief is a primary therapeutic goal (a Lay Abstract has been provided as Appendix A).
痉挛是中风后的常见并发症,也是导致疼痛的独立危险因素。肉毒毒素 A 注射是治疗局灶性痉挛的首选方法。我们研究了在常规临床实践中,因下肢痉挛性疼痛而接受肉毒毒素 A 肌内注射的中风患者,其疼痛缓解的效果。
前瞻性、多中心、上市后观察性研究。研究期间为 16 个月。主要有效性变量是四次肉毒毒素 A 注射周期后,疼痛 0-10 数字评分量表从基线的平均变化。次要终点包括疼痛 0-100 视觉模拟量表、目标实现量表、改良 Ashworth 量表、10 米步行测试、宾夕法尼亚痉挛频率量表和 36 项简明健康调查问卷的基线变化。
186 名入组患者中,180 名(96.8%)至少接受过一次肉毒毒素 A 注射。疼痛 0-10 数字评分量表的平均(标准差)从基线时的 4.9(2.2)显著下降(p<0.0001)至研究结束时的 2.5(2.1),表示疼痛严重程度降低了 50%。除 10 米步行测试外,所有次要变量均显示基线时的改善,表明痉挛引起的疼痛得到缓解。除 10 米步行测试外,所有次要变量均显示基线时的改善,表明痉挛引起的疼痛得到缓解。除 10 米步行测试外,所有次要变量均显示基线时的改善,表明痉挛引起的疼痛得到缓解。除 10 米步行测试外,所有次要变量均显示基线时的改善,表明痉挛引起的疼痛得到缓解。除 10 米步行测试外,所有次要变量均显示基线时的改善,表明痉挛引起的疼痛得到缓解。
肉毒毒素 A 似乎为中风后下肢痉挛患者提供了疼痛缓解的额外益处,这些患者的主要治疗目标是缓解疼痛(作为附录 A 提供了一份简化摘要)。