Goodchild Colin S, Nelson Joanne, Cooke Ian, Ashby Michael, Jackson Kate
Department of Anaesthesia and Perioperative Medicine, Monash University, Clayton, Victoria, Australia.
Pain Med. 2008 Oct;9(7):939-49. doi: 10.1111/j.1526-4637.2008.00512.x.
This study is a case series that was designed to provide data on the efficacy and the incidence and duration of adverse effects of flupirtine in the treatment of cancer-related neuropathic pain.
This was an 8-day, open-label study of palliative care patients with neuropathic pain despite maximal opioid treatment. They received an initial dose of flupirtine 100 mg orally four times daily (QID) that could be titrated. Efficacy measures included: a neuropathic pain discriminant score; scales measuring average pain and quality of life activities; and a score of percentage pain relief.
Ten patients were recruited. Only one patient was withdrawn because of side effects. Several pain measurements were used. All patients were able to participate in these measurements apart from two who did not understand the concept of percentage pain relief. There were significant reductions of average pain (P < 0.01) and neuropathic pain discriminant scores (P < 0.01), as well as an increase in percentage pain relief (P < 0.01). There was no statistically significant change in overall opioid use but 8/10 patients had some reduction in opioid use and three of those required substantially reduced doses of opioid when flupirtine was added to their treatment regime. Eight patients elected to continue to take flupirtine after the trial, two taking 200 mg QID and the others 100 mg QID. Of these eight, six said that flupirtine was of considerable help and two said it helped a little. All of these continued to take flupirtine with very good pain control until death, one of which was 18 months after the trial course.
These results in humans follow animal studies that suggest a role for flupirtine in the treatment of neuropathic pain. This short duration open-label study in 10 subjects suggests that flupirtine may be useful in the treatment of neuropathic pain when used in combination with opioids.
本研究为病例系列研究,旨在提供氟吡汀治疗癌症相关神经性疼痛的疗效、不良反应发生率及持续时间的数据。
这是一项针对尽管接受了最大剂量阿片类药物治疗仍患有神经性疼痛的姑息治疗患者的为期8天的开放标签研究。他们接受初始剂量为每日4次、每次口服100mg氟吡汀(每日4次),该剂量可进行滴定。疗效指标包括:神经性疼痛鉴别评分;测量平均疼痛和生活质量活动的量表;以及疼痛缓解百分比评分。
招募了10名患者。仅1名患者因副作用退出。使用了几种疼痛测量方法。除两名不理解疼痛缓解百分比概念的患者外,所有患者均能够参与这些测量。平均疼痛(P<0.01)和神经性疼痛鉴别评分(P<0.01)均显著降低,疼痛缓解百分比增加(P<0.01)。总体阿片类药物使用量无统计学显著变化,但10名患者中有8名阿片类药物使用量有所减少,其中3名在治疗方案中添加氟吡汀后所需阿片类药物剂量大幅减少。8名患者在试验后选择继续服用氟吡汀,2名患者每日服用200mg,其余患者每日服用100mg。在这8名患者中,6名表示氟吡汀有很大帮助,2名表示有一点帮助。所有这些患者在疼痛得到很好控制的情况下继续服用氟吡汀直至死亡,其中1例在试验疗程后18个月死亡。
这些人体研究结果与动物研究一致,提示氟吡汀在治疗神经性疼痛中发挥作用。这项针对10名受试者的短期开放标签研究表明,氟吡汀与阿片类药物联合使用时可能对治疗神经性疼痛有用。