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首页> 外文期刊>Current medical research and opinion >Efficacy and tolerability of a 5% lidocaine medicated plaster for the topical treatment of post-herpetic neuralgia: results of a long-term study.
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Efficacy and tolerability of a 5% lidocaine medicated plaster for the topical treatment of post-herpetic neuralgia: results of a long-term study.

机译:5%利多卡因药膏对疱疹后神经痛的局部治疗的疗效和耐受性:一项长期研究的结果。

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OBJECTIVE: Evaluation of long-term efficacy and safety of the 5% lidocaine medicated plaster for neuropathic pain symptoms in patients with post-herpetic neuralgia (PHN). MATERIALS AND METHODS: Design - a 12-month, open-label, phase III study with an open-label extension conducted at 34 outpatient clinics in 12 European countries. Patients - aged >or=50 years, newly recruited (average pain intensity >or=4) or pre-treated with the 5% lidocaine medicated plaster in a previous study. Interventions - application of up to three 5% lidocaine medicated plasters dependent upon size of the painful area for up to 12 hours per day. Outcome measures - efficacy measures included patients' recall of pain relief and pain intensity in the previous week. Adverse events (AEs) were also reported. RESULTS: 249 patients participated in the 12-month study, 247 were analysed (full analysis set, FAS). Newly recruited patients had a mean average pain intensity (11-point numerical rating scale [NRS]) of 5.9 +/- 1.4 at baseline, which decreased to 3.9 +/- 1.6 at week 12 and remained stable at 3.9 +/- 2.3 until the end of the 12-month study. In pre-treated patients, pain intensity decreased further from baseline (3.9 +/- 1.9) to study end (3.4 +/- 2.0). Pain relief values were consistent with pain intensity reductions and were sustained in patients continuing treatment in the extension phase (mainly >or=24 months treatment in total). The most common AEs tended to be infections such as bronchitis and nasopharyngitis. Forty-eight drug-related adverse events (DRAEs), mainly mild to moderate localised skin reactions, occurred in 31 (12.4%) patients in the first 12 months. The profile of DRAEs was similar in the extension phase. CONCLUSIONS: This study suggests that long-term treatment with the 5% lidocaine medicated plaster may provide substantial and maintained reductions in pain intensity, and that it is continuously well tolerated in patients suffering from peripheral neuropathic pain associated with previous herpes zoster infection. These findings support the use of the 5% lidocaine medicated plaster as one of the first-line therapies in this population.
机译:目的:评价5%利多卡因药膏对疱疹后神经痛(PHN)患者神经性疼痛症状的长期疗效和安全性。材料与方法:设计-在12个欧洲国家/地区的34个门诊进行的为期12个月的开放标签III期研究,并进行了开放标签扩展。患者-年龄大于或等于50岁,新入组(平均疼痛强度大于或等于4)或在先前的研究中使用5%利多卡因含药的石膏进行了预先治疗。干预-每天最多12个小时,根据疼痛部位的大小,使用多达3个5%利多卡因的药膏。结果指标-疗效指标包括患者前一周的疼痛缓解和疼痛强度回想。还报告了不良事件(AE)。结果:249位患者参加了为期12个月的研究,其中247位接受了分析(完整分析集,FAS)。新招募的患者在基线时的平均平均疼痛强度(11点数字评分标准[NRS])为5.9 +/- 1.4,在第12周时降至3.9 +/- 1.6,并保持稳定在3.9 +/- 2.3,直到12个月的研究结束。在预先治疗的患者中,疼痛强度从基线(3.9 +/- 1.9)到研究结束(3.4 +/- 2.0)进一步降低。疼痛缓解值与疼痛强度的降低相一致,并且在延长阶段继续接受治疗的患者(主要是≥24个月的总治疗时间)得以维持。最常见的AE往往是感染,如支气管炎和鼻咽炎。在最初的12个月中,有31名(12.4%)患者发生了48次与药物相关的不良事件(DRAE),主要是轻度至中度的局部皮肤反应。在扩展阶段,DRAE的配置文件相似。结论:这项研究表明,使用5%利多卡因药膏的长期治疗可以使疼痛强度显着并保持降低,并且在患有先前带状疱疹感染相关的周围神经性疼痛的患者中,其耐受性得到了持续良好的耐受。这些发现支持使用5%利多卡因药膏作为该人群的一线疗法。

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