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加巴喷丁用于带状疱疹后神经痛患者的起始剂量——一项剂量反应研究。

Starting dose of gabapentin for patients with post-herpetic neuralgia--a dose-response study.

作者信息

Jean Wei-Horng, Wu Chia-Chan, Mok Martin S, Sun Wei-Zen

机构信息

Department Anaesthesiology, Far Eastern Memorial Hospital, Taipei, Taiwan, ROC.

出版信息

Acta Anaesthesiol Taiwan. 2005 Jun;43(2):73-7.

Abstract

BACKGROUND

Gabapentin has been shown to provide pain relief for post-herpetic neuralgia at dosage of 1200 to 2400 mg/day. However, the initial dosing strategy has not been thoroughly investigated. The purpose of this study was to establish the initial dosing strategy in the treatment of the gabapentin-naive patients with post-herpetic neuralgia.

METHODS

This clinical study was an open-label, randomized, time-sequence and controlled trial. Each gabapentin-naive subject was allocated to receive either 200 mg (100 mg, twice daily), 400 mg (100 mg, four times daily), or 600 mg (200 mg, three times daily) of gabapentin for three days. The analgesic effect and occurrence of dizziness, drowsiness, and fatigue were assessed at day 0 and day 3.

RESULTS

A total of 61 subjects (32 male/29 female) were enrolled in this study. The intensity of pain was greatly improved in all three groups after three days of treatment (visual analog scale decreased from 6.5 +/- 1.6 to 4.5 +/- 2.1, P < 0.05). There was no statistically significant difference among subjects taking 200 mg, 400 mg, or 600 mg with respect to dizziness, drowsiness or fatigue.

CONCLUSIONS

This study shows that elderly gabapentin-naive subjects no matter whether receiving 200, 400 or 600 mg/day of gabapentin benefited a moderate pain relief with minimal side effects at the first three days of treatment. Since starting with a minimal dose of 200 mg/day did not offer a better reduction of side effects, we suggest that 600 mg/day gabapentin could be a safe and effective starting dose for patients with post-herpetic neuralgia.

摘要

背景

加巴喷丁已被证明以1200至2400毫克/天的剂量可为带状疱疹后神经痛提供疼痛缓解。然而,初始给药策略尚未得到充分研究。本研究的目的是确定治疗初用加巴喷丁的带状疱疹后神经痛患者的初始给药策略。

方法

本临床研究为开放标签、随机、时间序列和对照试验。每位初用加巴喷丁的受试者被分配接受200毫克(100毫克,每日两次)、400毫克(100毫克,每日四次)或600毫克(200毫克,每日三次)的加巴喷丁,为期三天。在第0天和第3天评估镇痛效果以及头晕、嗜睡和疲劳的发生情况。

结果

本研究共纳入61名受试者(32名男性/29名女性)。治疗三天后,所有三组的疼痛强度均有显著改善(视觉模拟评分从6.5±1.6降至4.5±2.1,P<0.05)。服用200毫克、400毫克或600毫克的受试者在头晕、嗜睡或疲劳方面无统计学显著差异。

结论

本研究表明,初用加巴喷丁的老年受试者无论接受200、400或600毫克/天的加巴喷丁,在治疗的前三天都能获得适度的疼痛缓解且副作用最小。由于从最低剂量200毫克/天开始并未更好地减少副作用,我们建议600毫克/天的加巴喷丁可能是带状疱疹后神经痛患者安全有效的起始剂量。

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