[Efficacy analysis of lidocaine plaster combined with gabapentin in the treatment of herpes zoster neuralgia]

Zhonghua Yi Xue Za Zhi. 2022 Nov 1;102(40):3186-3191. doi: 10.3760/cma.j.cn112137-20220419-00852.
[Article in Chinese]

Abstract

Objective: To evaluate the efficacy and safety of lidocaine plaster combined with gabapentin in the treatment of herpes zoster neuralgia (HZN). Methods: A total of 93 patients diagnosed with HZN from June 4, 2021 to January 5, 2022 in the Department of Pain Clinic of Nanjing Drum Tower Hospital were selected, and their gender was not limited. They were divided into 3 groups by random number table method: group A (n=32) prescribed gabapentin alone, group B (n=30) lidocaine plaster alone, and group C (n=31) lidocaine plaster combined with gabapentin. After excluding patients who did not meet the criteria, there were 28 cases in group A, 28 cases in group B, and 29 cases in group C. The visual analogue scale (VAS), the short-form McGill pain questionnaire (SF-MPQ) score, and drug dosage and adverse reaction in each group at pre-treatment (T0), post-treatment in one week (T1), in two weeks (T2), in four weeks (T4), and in 12 weeks (T12) were recorded and evaluated; Pittsburgh Sleep Quality Index (PSQI) score and Medical Outcomes Study short-form 36 (SF-36) score at T0, T4, and T12 were recorded. Adverse reactions and drug dosage in each group were documented. Repeated measures ANOVA was used to compare the curative effects of the three groups at different time points before and after treatment. Results: The ages of the three groups of patients were (67.8±10.0), (60.9±11.4) and (63.5±12.5) years old respectively (P=0.318), and the proportions of men were 46.4 % (13 cases), 35.7% (10 cases) and 44.8 % (13 cases), respectively (P=0.472). After treatment, the VAS scores and SF-MPQ scores of patients in the three groups were decreased at each time point compared with those before treatment (all P<0.05), the VAS and SF-MPQ scores of patients in group C at T12 time point were 1.2±0.4 and 5.2±2.4 respectively, which were lower than those of patients in groups A and B (both P<0.05). The dosages of gabapentin and lidocaine plaster in group C were lower than those in groups A and B at each time point after treatment (all P<0.05). The PSQI scores of patients in the three groups at T4 and T12 were lower than those before treatment (all P<0.05). The PSQI scores of patients in group C at T4 and T12 were 5.7±1.2 and 4.5±1.2, which were lower than those of patients in groups A and B. (all P<0.05), The SF-36 scores of patients in three groups at T4 and T12 were higher than those before treatment (all P<0.05), and the SF-36 scores of group C at T4 and T12 were 91.7±8.5, 93.1±6.3, which were higher than that of patients in groups A and B (both P<0.05). The incidence of adverse reactions in the three groups were 35.7% (9 cases), 10.7% (3 cases), and 13.8% (4 cases) respectively (P<0.05), the adverse reactions in groups B and C were less than those in group A (P<0.05), and there was no statistical difference between groups B and C (P>0.05). Conclusion: Lidocaine plaster combined with gabapentin has better analgesic effect in the treatment of HZN, with less incidence of adverse reactions, and can reduce the dosage of systemic drugs, improve patients' sleep and quality of life, and thus could provide a safe and effective method for the treatment of HZN.

目的: 评价利多卡因凝胶贴膏联合加巴喷丁治疗带状疱疹神经痛(HZN)的有效性和安全性。 方法: 选择南京鼓楼医院疼痛科2021年6月4日至2022年1月5日确诊为HZN的93例患者为研究对象,采用随机数字表法分为3组:A组(32例)单用加巴喷丁,B组(30例)单用利多卡因凝胶贴膏,C组(31例)利多卡因贴膏联合加巴喷丁;剔除不符合要求的患者后,A组28例,B组28例,C组29例。记录治疗前(T0)和治疗后1周(T1)、2周(T2)、4周(T4)及12周(T12)的疼痛视觉模拟评分(VAS)、简式McGill疼痛问卷评分(SF-MPQ)、各组药物用量和不良反应;T0、T4、T12的匹兹堡睡眠质量指数(PSQI)评分和简明健康状况调查表(SF-36)评分;采用重复测量方差分析比较3组患者治疗前后不同时间点的疗效。 结果: 3组患者的年龄分别为(67.8±10.0)、(60.9±11.4)和(63.5±12.5)岁(P=0.318),男性构成分别为46.4 %(13例)、35.7%(10例)和44.8%(13例)(P=0.472)。治疗后,3组患者疼痛VAS评分和SF-MPQ评分在各时间点较治疗前降低(均P<0.05),C组患者T12时间点VAS评分和SF-MPQ评分分别为(1.2±0.4)、(5.2±2.4)分,低于A和B组患者(均P<0.05)。治疗后各时间点C组加巴喷丁及利多卡因凝胶贴膏用量低于A和B组患者(均P<0.05)。3组患者PSQI评分在T4、T12时间点较治疗前降低(均P<0.05),C组患者在T4、T12时间点PSQI评分为(5.7±1.2)、(4.5±1.2)分,均低于A和B组患者(均P<0.05);3组患者SF-36评分在T4、T12时间点较治疗前提高(均P<0.05),C组在T4、T12时间点SF-36评分为(91.7±8.5)、(93.1±6.3)分,均高于A和B组(均P<0.05);3组患者不良反应发生率分别为35.7%(9例)、10.7%(3例)、13.8%(4例)(P<0.05),B组及C组不良反应均少于A组(均P<0.05),B组和C组之间差异无统计学意义(P>0.05)。 结论: 利多卡因凝胶贴膏联合加巴喷丁治疗HZN镇痛效果较好,可减少系统用药量,改善患者的睡眠和生活质量,且不良反应发生率较低,为治疗HZN提供了一种安全有效的临床方案。.

Publication types

  • English Abstract

MeSH terms

  • Aged
  • Female
  • Gabapentin / adverse effects
  • Herpes Zoster* / chemically induced
  • Herpes Zoster* / drug therapy
  • Humans
  • Lidocaine
  • Male
  • Middle Aged
  • Neuralgia* / chemically induced
  • Neuralgia* / drug therapy
  • Quality of Life
  • Treatment Outcome

Substances

  • Gabapentin
  • Lidocaine