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首页> 外文期刊>Current medical research and opinion >Efficacy and safety of combination therapy with 5% lidocaine medicated plaster and pregabalin in post-herpetic neuralgia and diabetic polyneuropathy.
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Efficacy and safety of combination therapy with 5% lidocaine medicated plaster and pregabalin in post-herpetic neuralgia and diabetic polyneuropathy.

机译:5%利多卡因药膏和普瑞巴林联合治疗疱疹后神经痛和糖尿病多发性神经病的疗效和安全性。

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摘要

OBJECTIVE: Neuropathic pain is often difficult to treat due to a complex pathophysiology. This study evaluated the efficacy, tolerability and safety of combination therapy with 5% lidocaine medicated plaster and pregabalin for neuropathic pain in patients with post-herpetic neuralgia (PHN) or painful diabetic polyneuropathy (DPN). METHODS: Patients completing 4-week monotherapy with 5% lidocaine medicated plaster or pregabalin were enrolled in an 8-week combination phase. Patients with adequate response to monotherapy (recalled average pain intensity of 4 or less on 11-point numeric rating scale in the previous 3 days [NRS-3 score]) continued their previous therapy, whereas those with insufficient response received combination therapy. Efficacy endpoints included change in NRS-3 from combination phase baseline, Patient and Clinical Global Impression of Change (PGIC/CGIC), and patient's satisfaction with treatment. Safety evaluation included adverse events (AEs), drug-related AEs (DRAEs), and withdrawal due to AEs. CLINICAL TRIAL REGISTRATION: EudraCT No. 2006-003132-29. RESULTS: Of 229 patients in the per-protocol set (PPS: 68 PHN and 161 DPN), 71 received 5% lidocaine medicated plaster monotherapy, 57 had pregabalin added to 5% lidocaine medicated plaster, 57 pregabalin monotherapy and 44 received 5% lidocaine medicated plaster in addition to continued pregabalin treatment. There were no meaningful differences in demographic data between the treatment groups. Patients continuing on monotherapy demonstrated additional decreases in NRS-3 scores. Patients receiving combination therapy achieved clinically relevant reduction in NRS-3 values in addition to improvement achieved during the 4 weeks of monotherapy. Improvement was similar between the two combination therapy groups. Considerable improvements in patients' treatment satisfaction were reported. Incidences of AEs were in line with previous reports for the two treatments and combination therapy was generally well tolerated. CONCLUSIONS: In patients with PHN and painful DPN failing to respond to monotherapy, combination therapy with 5% lidocaine medicated plaster and pregabalin provides additional clinically relevant pain relief and is safe and well-tolerated.
机译:目的:由于病理生理复杂,神经性疼痛通常难以治疗。这项研究评估了5%利多卡因药膏和普瑞巴林联合治疗带状疱疹后神经痛(PHN)或疼痛性糖尿病多发性神经病(DPN)患者的神经性疼痛的疗效,耐受性和安全性。方法:采用5%利多卡因药膏或普瑞巴林完成4周单药治疗的患者进入8周联合治疗阶段。对单一疗法有足够反应的患者(在过去3天内,使用11点数字评分表测得的平均疼痛强度为4或更低[NRS-3评分])继续接受先前的治疗,而对反应不足的患者则接受联合治疗。疗效终点包括NRS-3相对于联合阶段基线的变化,患者和临床整体变化印象(PGIC / CGIC)以及患者对治疗的满意度。安全性评估包括不良事件(AE),与药物相关的AE(DRAE)和因AE引起的停药。临床试验注册:EudraCT号2006-003132-29。结果:按照协议,在229例患者中(PPS:68 PHN和161 DPN),71例接受5%利多卡因药膏的单药治疗,57例使用普瑞巴林加5%利多卡因药膏的人,57例普瑞巴林单药治疗和44例使用5%利多卡因的药除继续进行普瑞巴林治疗外,还应使用药膏。治疗组之间的人口统计学数据没有有意义的差异。继续接受单一疗法的患者证明NRS-3得分进一步降低。接受联合治疗的患者除了在单药治疗的4周内获得的改善外,还实现了NRS-3值的临床相关降低。两个联合治疗组之间的改善相似。据报道,患者的治疗满意度得到了显着改善。两种疗法的不良事件发生率均与以前的报道相符,并且联合治疗的耐受性普遍良好。结论:对于PHN和疼痛性DPN对单药治疗无效的患者,联合5%利多卡因药膏和普瑞巴林的联合治疗可进一步缓解临床相关疼痛,并且安全且耐受性良好。

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