Oskarsson Björn, Moore Dan, Mozaffar Tahseen, Ravits John, Wiedau-Pazos Martina, Parziale Nicholas, Joyce Nanette C, Mandeville Ross, Goyal Namita, Cudkowicz Merit E, Weiss Michael, Miller Robert G, McDonald Craig M
University of California, Davis, Sacramento, California, USA.
Pacific Medical Center, San Francisco, California, USA.
Muscle Nerve. 2018 Mar 6. doi: 10.1002/mus.26117.
More than 90% of amyotrophic lateral sclerosis (ALS) patients have muscle cramps, but evidence-based treatments have not been available.
A multicenter, double-blind, placebo-controlled crossover trial of mexiletine 150 mg twice daily was conducted in ALS patients requesting treatment of symptomatic muscle cramps.
Muscle cramp frequency was reduced in 18 of 20 patients; 13 reductions were attributed to treatment (P < 0.05). The average reduction, based on t tests, was 1.8 cramps per day (a reduction from 5.3 with placebo to 3.5 with mexiletine). The estimated reduction of cramp severity was 15 units on a 100-unit scale (P = 0.01) from a baseline average of 46. No effect on fasciculations was noted. One patient discontinued the study because of dizziness, and another patient discontinued the study to start open-label mexiletine therapy. No serious adverse event occurred.
Mexiletine is a well tolerated and effective medication for controlling the symptom of muscle cramps in ALS. Muscle Nerve, 2018.
超过90%的肌萎缩侧索硬化症(ALS)患者会出现肌肉痉挛,但尚无循证治疗方法。
对有症状性肌肉痉挛治疗需求的ALS患者进行一项多中心、双盲、安慰剂对照的美西律交叉试验,美西律剂量为每日两次,每次150毫克。
20名患者中有18名患者的肌肉痉挛频率降低;13次降低归因于治疗(P<0.05)。根据t检验,平均降低幅度为每天1.8次痉挛(从安慰剂组的5.3次降至美西律组的3.5次)。在100分制中,痉挛严重程度估计从基线平均46分降低了15分(P=0.01)。未观察到对肌束震颤有影响。一名患者因头晕退出研究,另一名患者退出研究以开始接受美西律开放标签治疗。未发生严重不良事件。
美西律是一种耐受性良好且有效的药物,可控制ALS患者的肌肉痉挛症状。《肌肉与神经》,2018年