5%利多卡因局部用药贴剂治疗带状疱疹后神经痛:一项双盲、安慰剂对照、多国疗效与安全性试验的结果
Topical 5% lidocaine (lignocaine) medicated plaster treatment for post-herpetic neuralgia: results of a double-blind, placebo-controlled, multinational efficacy and safety trial.
作者信息
Binder Andreas, Bruxelle Jean, Rogers Peter, Hans Guy, Bösl Irmgard, Baron Ralf
机构信息
Division of Neurological Pain Research and Therapy, Department of Neurology, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.
出版信息
Clin Drug Investig. 2009;29(6):393-408. doi: 10.2165/00044011-200929060-00003.
BACKGROUND AND OBJECTIVE
Post-herpetic neuralgia (PHN) is a distressing neuropathic pain condition mainly affecting elderly patients. Neuropathic pain symptoms can be of a burning, shooting and stabbing nature, and may continue for prolonged periods and are often poorly controlled by polymedication. The aim of this study was to evaluate the analgesic efficacy and safety of topical analgesic treatment (5% lidocaine [lignocaine] medicated plaster) compared with placebo plaster in patients with PHN.
METHODS
This was a double-blind, placebo plaster-controlled, parallel-group, multicentre study employing enriched enrolment with randomized withdrawal methodology. After an initial 8-week open-label, active run-in phase, responders entered a 2-week randomized, double-blind, placebo-controlled phase. The study was conducted at 33 outpatient investigational centres in 12 European countries. Patients with PHN were selected who were aged >/=50 years, had experienced neuropathic pain persisting for >/=3 months after rash healing, and had a mean pain intensity of >/=4 on an 11-point numerical rating scale. A total of 265 patients entered the open-label phase and subsequently a pre-defined number of 71 patients entered the randomized phase. Patients applied up to three 5% lidocaine medicated plasters for up to 12 hours per day. The primary endpoint of the study was time-to-exit due to a >/=2-point reduction in pain relief on two consecutive days of plaster application using a 6-point verbal rating scale.
RESULTS
Of the 265 patients entering the run-in phase, 51.7% achieved at least moderate pain relief. In the double-blind phase (full analysis set, n = 71), median times-to-exit were 13.5 (range 2-14) and 9.0 (range 1-14) days for lidocaine and placebo plaster groups, respectively (p = 0.151). For per-protocol patients (n = 34), median time-to-exit was 14.0 (range 3-14) and 6.0 (range 1-14) days for lidocaine and placebo plaster groups, respectively (p = 0.0398). Drug-related adverse events occurred in 13.6% of patients. Treatment with 5% lidocaine medicated plaster was associated with improvements in pain, allodynia, quality of life and sleep measures.
CONCLUSIONS
This study adds to a growing body of evidence that the 5% lidocaine medicated plaster can be considered a valuable treatment option for patients with PHN, providing beneficial effects on pain, allodynia, quality of life and sleep, with minimal adverse effects.
背景与目的
带状疱疹后神经痛(PHN)是一种令人痛苦的神经性疼痛疾病,主要影响老年患者。神经性疼痛症状可能具有烧灼样、电击样和刺痛样性质,可能持续较长时间,并且通常通过多种药物联合治疗难以得到有效控制。本研究的目的是评估局部镇痛治疗(5%利多卡因[盐酸利多卡因]药用贴剂)与安慰剂贴剂相比,对PHN患者的镇痛疗效和安全性。
方法
这是一项双盲、安慰剂贴剂对照、平行组、多中心研究,采用富集入组和随机撤药方法。在最初为期8周的开放标签、活性导入期后,反应者进入为期2周的随机、双盲、安慰剂对照期。该研究在12个欧洲国家的33个门诊研究中心进行。入选的PHN患者年龄≥50岁,皮疹愈合后神经性疼痛持续≥3个月,且在11点数字评分量表上的平均疼痛强度≥4。共有265例患者进入开放标签期,随后预先确定数量的71例患者进入随机期。患者每天最多使用3片5%利多卡因药用贴剂,最长使用12小时。该研究的主要终点是使用6点言语评分量表,在连续两天使用贴剂后疼痛缓解降低≥2分而退出研究的时间。
结果
在进入导入期的265例患者中,51.7%至少实现了中度疼痛缓解。在双盲期(全分析集,n = 71),利多卡因和安慰剂贴剂组的中位退出时间分别为13.5(范围2 - 14)天和9.0(范围1 - 14)天(p = 0.151)。符合方案集患者(n = 34)中,利多卡因和安慰剂贴剂组的中位退出时间分别为14.0(范围3 - 14)天和6.0(范围1 - 14)天(p = 0.0398)。13.6%的患者发生了与药物相关的不良事件。使用5%利多卡因药用贴剂治疗与疼痛、痛觉过敏、生活质量和睡眠指标的改善相关。
结论
本研究增加了越来越多的证据,表明5%利多卡因药用贴剂可被视为PHN患者的一种有价值的治疗选择,对疼痛、痛觉过敏、生活质量和睡眠具有有益作用,且不良反应最小。