Moulin Dwight, Boulanger Aline, Clark A J, Clarke Hance, Dao Thuan, Finley G A, Furlan Andrea, Gilron Ian, Gordon Allan, Morley-Forster Patricia K, Sessle Barry J, Squire Pamela, Stinson Jennifer, Taenzer Paul, Velly Ana, Ware Mark A, Weinberg Erica L, Williamson Owen D
Pain Res Manag. 2014 Nov-Dec;19(6):328-35. doi: 10.1155/2014/754693.
Neuropathic pain (NeP), redefined as pain caused by a lesion or a disease of the somatosensory system, is a disabling condition that affects approximately two million Canadians.
To review the randomized controlled trials (RCTs) and systematic reviews related to the pharmacological management of NeP to develop a revised evidence-based consensus statement on its management.
RCTs, systematic reviews and existing guidelines on the pharmacological management of NeP were evaluated at a consensus meeting in May 2012 and updated until September 2013. Medications were recommended in the consensus statement if their analgesic efficacy was supported by at least one methodologically sound RCT (class I or class II) showing significant benefit relative to placebo or another relevant control group. Recommendations for treatment were based on the degree of evidence of analgesic efficacy, safety and ease of use.
Analgesic agents recommended for first-line treatments are gabapentinoids (gabapentin and pregabalin), tricyclic antidepressants and serotonin noradrenaline reuptake inhibitors. Tramadol and controlled-release opioid analgesics are recommended as second-line treatments for moderate to severe pain. Cannabinoids are now recommended as third-line treatments. Recommended fourth-line treatments include methadone, anticonvulsants with lesser evidence of efficacy (eg, lamotrigine, lacosamide), tapentadol and botulinum toxin. There is support for some analgesic combinations in selected NeP conditions.
These guidelines provide an updated, stepwise approach to the pharmacological management of NeP. Treatment should be individualized for each patient based on efficacy, side-effect profile and drug accessibility, including cost. Additional studies are required to examine head-to-head comparisons among analgesics, combinations of analgesics, long-term outcomes and treatment of pediatric, geriatric and central NeP.
神经病理性疼痛(NeP)被重新定义为由躯体感觉系统的损伤或疾病引起的疼痛,是一种致残性疾病,影响着约两百万加拿大人。
回顾与神经病理性疼痛药物治疗相关的随机对照试验(RCT)和系统评价,以制定关于其治疗的修订后的循证共识声明。
在2012年5月的一次共识会议上对神经病理性疼痛药物治疗的随机对照试验、系统评价和现有指南进行了评估,并更新至2013年9月。如果至少一项方法学合理的随机对照试验(I类或II类)表明相对于安慰剂或另一个相关对照组有显著益处,则在共识声明中推荐使用这些药物。治疗建议基于镇痛疗效、安全性和易用性的证据程度。
推荐用于一线治疗的镇痛药有加巴喷丁类药物(加巴喷丁和普瑞巴林)、三环类抗抑郁药和5-羟色胺去甲肾上腺素再摄取抑制剂。曲马多和控释阿片类镇痛药被推荐作为中重度疼痛的二线治疗药物。大麻素类药物现在被推荐作为三线治疗药物。推荐的四线治疗药物包括美沙酮、疗效证据较少的抗惊厥药(如拉莫三嗪、拉科酰胺)、他喷他多和肉毒毒素。在某些神经病理性疼痛情况下支持一些镇痛联合用药。
这些指南为神经病理性疼痛的药物治疗提供了一种更新的、逐步的方法。应根据疗效、副作用情况和药物可及性(包括成本)为每位患者制定个体化治疗方案。需要进行更多研究以检验镇痛药之间的直接比较、镇痛药联合用药、长期疗效以及儿科、老年和中枢性神经病理性疼痛的治疗。