Iskra D A, Kovalenko A P, Koshkarev M A, Frunza D N
Kirov Medical-Military Academy, St-Petersburg, Russia.
Branch N 5 Vishnevsky 3th Central Military Clinical Hospital, Sergiev Posad, Russia.
Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(12. Vyp. 2):51-57. doi: 10.17116/jnevro201911912251.
To study the electromiographic (EMG) parameters and to evaluate the therapeutic efficacy of a combination of central (baclofen, baclosan) and peripheral (incobotulotoxinA, xeomin) muscle relaxants in the treatment of post-stroke spasticity (PSS).
Ninety-six patients with PSS of upper and lower limbs were divided into 2 groups: the first group (n=56) was treated with xeomin and the second (n=40) received combined therapy of xeomin and baclofen. Xeomin was administered according to the pattern of spasticity. The total dosage reached 800 U. Baclofen was used orally in a dose of 10 mg 3 times a day. The scales of paresis and spasticity assessment (MRCS, MAS and Tardieu), activity and participation of patients in everyday life (Bartel, Rankin, Rivermead mobility Index, comfortable walking test, LASIS) were used. EMG and transcranial magnetic stimulation (TMS) were performed. M-response, H-reflex, F-wave, central conduction time were determined. The total duration of the study was 120 days. Patients were assessed at 4 points.
Potentiation of peripheral and central muscle relaxants and prolongation of the effect of xeomin was revealed (it was expressed in the reduction of the number of injection sessions from 7-8 to 5-6). The use of xeomin in a total dosage of up to 800 U has shown its efficacy and safety for the treatment of spasticity of the upper and lower limbs. The results of EMG and TMS shed a light on the mechanisms of the therapeutic effect of combined (xeomin+baclosan) and monotherapy (xeomin) spasticity.
研究肌电图(EMG)参数,并评估中枢性(巴氯芬、巴氯沙明)和外周性(incobotulotoxinA、Xeomin)肌肉松弛剂联合使用治疗脑卒中后痉挛(PSS)的疗效。
96例上下肢PSS患者分为2组:第一组(n = 56)接受Xeomin治疗,第二组(n = 40)接受Xeomin与巴氯芬联合治疗。Xeomin根据痉挛模式给药,总剂量达800 U。巴氯芬口服,剂量为10 mg,每日3次。使用轻瘫和痉挛评估量表(MRCS、MAS和Tardieu)、患者在日常生活中的活动及参与情况量表(Bartel、Rankin、Rivermead运动指数、舒适步行测试、LASIS)。进行EMG和经颅磁刺激(TMS)检查,测定M波反应、H反射、F波、中枢传导时间。研究总时长为120天,患者在4个时间点接受评估。
发现外周和中枢肌肉松弛剂联合使用有增效作用,且Xeomin的作用时间延长(表现为注射次数从7 - 8次减少至5 - 6次)。总剂量达800 U的Xeomin已显示出其治疗上下肢痉挛的有效性和安全性。EMG和TMS结果揭示了联合治疗(Xeomin + 巴氯沙明)和单一疗法(Xeomin)治疗痉挛的作用机制。