Wright J M, Oki J C, Graves L
School of Medicine, University of Missouri, Kansas City 64108, USA.
Ann Pharmacother. 1997 Jan;31(1):29-34. doi: 10.1177/106002809703100103.
To evaluate the efficacy and safety of mexiletine in the symptomatic treatment of diabetic peripheral neuropathy (DPN).
In this prospective, double-blind study, 29 patients were randomized to receive mexiletine 600 mg/d or matching placebo for 3 weeks. A four-item symptom score (FIS), which rated pain, dysesthesias, paresthesias, and nightly exacerbations of symptoms, and a 100-mm visual analog scale (VAS), which rated pain intensity, were completed by patients before and after treatment. At the end of treatment independent patient and investigator global assessments were made. Patients reported adverse effects after 1 and 3 weeks of treatment.
Treatment groups were similar at baseline. The difference between the median changes in FIS scores (mexiletine = 5.5, placebo = 2) was not statistically significant. Overall symptom response was similar in both treatment groups as demonstrated by both global assessments (p = 0.19). The mean change in VAS score from baseline to posttreatment was determined for both groups and the difference between these mean scores was 16.5 mm (95% CI, -7.1 to 40.2 mm) (p = 0.16). Inadequate statistical power (1-beta = 0.40) may have resulted from small sample size, small magnitude of effect, or variability in the measured effect. Adverse effects were more common in the mexiletine group, though not statistically significant. One patient receiving mexiletine was hospitalized for palpitations.
Because of conflicting reports of mexiletine's efficacy in the treatment of symptomatic DPN, this drug should be reserved for patients unresponsive or intolerant to standard therapy, without evidence of heart disease, and with sensations of burning heat, formication, or stabbing pain.
评估美西律对症治疗糖尿病周围神经病变(DPN)的疗效和安全性。
在这项前瞻性、双盲研究中,29例患者被随机分为两组,分别接受600mg/d美西律或匹配的安慰剂治疗3周。患者在治疗前后完成一项四项症状评分(FIS),该评分对疼痛、感觉异常、感觉迟钝和夜间症状加重情况进行评分,以及一项100mm视觉模拟量表(VAS),该量表对疼痛强度进行评分。治疗结束时,进行独立的患者和研究者整体评估。患者在治疗1周和3周后报告不良反应。
治疗组在基线时相似。FIS评分的中位数变化之间的差异(美西律=5.5,安慰剂=2)无统计学意义。两项整体评估均显示,两个治疗组的总体症状反应相似(p=0.19)。两组均测定了从基线到治疗后的VAS评分平均变化,这些平均评分之间的差异为16.5mm(95%CI,-7.1至40.2mm)(p=0.16)。样本量小、效应量小或测量效应的变异性可能导致统计效能不足(1-β=0.40)。美西律组的不良反应更常见,尽管无统计学意义。一名接受美西律治疗的患者因心悸住院。
由于关于美西律治疗症状性DPN疗效的报道相互矛盾,该药应保留给对标准治疗无反应或不耐受、无心脏病证据且有灼热感、蚁走感或刺痛感的患者。