Kleijnen Systematic Reviews Ltd, York, UK.
Grünenthal GmbH, Aachen, Germany.
Curr Med Res Opin. 2020 Jan;36(1):101-115. doi: 10.1080/03007995.2019.1662687. Epub 2019 Sep 12.
Neuropathic pain prevalence is estimated between 7% and 10% of the population. International guidelines recommend a variety of drugs at different therapy lines for pain relief. However, side effect profiles, for example, prompted the UK government recently to classify pregabalin and gabapentin as class C drugs. Lidocaine 700 mg medicated plaster (LMP) might be a safer alternative. A systematic review assessed how LMP and pregabalin compared in terms of efficacy and safety. The review focused on pain reduction, quality of life and adverse events in peripheral neuropathic pain (PNP) i.e. post-herpetic neuralgia, diabetic peripheral neuropathy, post-surgical/trauma, or other PNP conditions. Electronic databases were searched as well as a number of other sources up to November 2018. Sensitive strategies were used, with no restriction by language or publication status. Two independent reviewers screened records and extracted data with consensus determining final decisions. Risk of bias was assessed using the Cochrane Collaboration 2011 checklist for RCTs. Full network meta-analysis was conducted to compare LMP to pregabalin 300/600 mg in terms of pain reduction, quality of life, as well as serious adverse events and selected adverse events. Trials with enriched enrolment design were excluded. Searches retrieved 7,104 records. In total 111 references pertaining to 43 RCTs were included for data extraction. Bayesian network meta-analysis of several pain outcomes showed no clear difference in efficacy between treatments However, LMP was clearly advantageous in terms of dizziness and any adverse event vs. pregabalin 600 mg/day and discontinuations vs. pregabalin 300 mg/day or 600 mg/day, as well as being associated with improved quality of life (albeit in this case based on weak evidence). LMP was found to be similar to pregabalin in reducing pain in all populations but had a better adverse events profile.
神经病理性疼痛的患病率估计为人群的 7%至 10%。国际指南建议在不同的治疗线上使用多种药物来缓解疼痛。然而,副作用概况,例如,促使英国政府最近将普瑞巴林和加巴喷丁列为 C 类药物。700mg 利多卡因贴剂(LMP)可能是一种更安全的替代药物。一项系统评价评估了 LMP 和普瑞巴林在疗效和安全性方面的差异。该评价主要集中在周围神经病理性疼痛(PNP)即带状疱疹后神经痛、糖尿病周围神经病变、术后/创伤后或其他 PNP 疾病的疼痛减轻、生活质量和不良事件方面。电子数据库以及其他一些来源都进行了搜索,检索截至 2018 年 11 月。使用了敏感策略,没有语言或出版状态的限制。两名独立的审查员进行了记录筛选和数据提取,共识决定最终决策。使用 Cochrane 协作组 2011 年 RCT 偏倚风险评估工具评估了偏倚风险。采用全网络荟萃分析比较 LMP 与普瑞巴林 300/600mg 在疼痛减轻、生活质量以及严重不良事件和选定不良事件方面的疗效。排除了具有丰富入组设计的试验。检索到 7104 条记录。共有 111 篇参考文献涉及 43 项 RCT 被纳入数据提取。几种疼痛结局的贝叶斯网络荟萃分析显示,治疗之间的疗效没有明显差异。然而,与普瑞巴林 600mg/天相比,LMP 明显在头晕和任何不良事件方面具有优势,与普瑞巴林 300mg/天或 600mg/天相比,停药率也更低,同时生活质量也得到改善(尽管在这种情况下,证据较弱)。LMP 在所有人群中减轻疼痛的效果与普瑞巴林相似,但不良事件谱更好。