Department of Clinical Neurosciences and the University of Calgary, Calgary, AB, Canada.
J Pain Res. 2010 Apr 1;3:33-49. doi: 10.2147/jpr.s8675.
Although many therapies are used in the management of neuropathic pain (NeP) due to polyneuropathy (PN), few comparison studies exist. We performed a prospective, non-randomized, unblended, efficacy comparison of the serotonin-norepinephrine reuptake inhibitor venlafaxine, as either monotherapy or adjuvant therapy, with a first-line medication for NeP, gabapentin, in patients with PN-related NeP. VAS pain scores were assessed after 3 and 6 months in intervention groups and in a cohort of patients receiving no pharmacotherapy. In a total of 223 patients, we analyzed pain quantity and quality (visual analogue scale [VAS] score, Brief Pain Inventory [BPI]), quality of life and health status measures [EuroQol 5 Domains, EQ-5D], Medical Outcomes Sleep Study Scale [MOSSS], Hospital Anxiety and Depression Scale [HADS] and Short Form 36 Health Survey [SF-36]) after 6 months of therapy. Significant improvements in VAS pain scores occurred for all treatment groups after 6 months. Improvements in aspects of daily life and anxiety were identified in all treatment groups. Our data suggest that monotherapy or adjuvant therapy with venlafaxine is comparable to gabapentin for NeP management. We advocate for head-to-head, randomized, double-blinded studies of current NeP therapies.
尽管有许多疗法可用于治疗多发性神经病相关的神经病理性疼痛(NeP),但很少有比较研究。我们进行了一项前瞻性、非随机、非盲、疗效比较研究,比较了作为单药或辅助治疗的 5-羟色胺-去甲肾上腺素再摄取抑制剂文拉法辛与一线治疗药物加巴喷丁在治疗多发性神经病相关 NeP 患者中的疗效。在干预组和未接受药物治疗的患者队列中,分别在 3 个月和 6 个月时评估视觉模拟评分(VAS)疼痛评分。在总共 223 名患者中,我们在 6 个月的治疗后分析了疼痛量和质量(VAS 评分、简明疼痛量表[BPI])、生活质量和健康状况测量(欧洲五维健康量表[EQ-5D]、医学结局睡眠研究量表[MOSSS]、医院焦虑抑郁量表[HADS]和简明健康状况量表[SF-36])。所有治疗组在 6 个月后 VAS 疼痛评分均显著改善。所有治疗组在日常生活和焦虑方面均有改善。我们的数据表明,文拉法辛单药或辅助治疗与加巴喷丁治疗 NeP 的疗效相当。我们提倡对当前 NeP 治疗进行头对头、随机、双盲研究。