Stacey Brett R, Dworkin Robert H, Murphy Kevin, Sharma Uma, Emir Birol, Griesing Teresa
Department of Comprehensive Pain Center, Anesthesiology and Peri-Operative Medicine, Oregon Health & Science University, Portland, Oregon 97239, USA.
Pain Med. 2008 Nov;9(8):1202-8. doi: 10.1111/j.1526-4637.2008.00423.x. Epub 2008 Mar 11.
Neuropathic pain associated with postherpetic neuralgia (PHN) and painful diabetic peripheral neuropathy (DPN) can be intractable and may not respond to commonly used treatments, such as tricyclic antidepressants (TCAs) and opioids. This long-term, open-label study was a preliminary evaluation of pregabalin for patients whose pain had been judged refractory to other treatments for neuropathic pain.
Patients had previously participated in double-blind, placebo-controlled, randomized trials of pregabalin in DPN and PHN. They had moderate to severe neuropathic pain despite treatment with gabapentin, a TCA, and a third medication (e.g., other anticonvulsants, opioid, selective serotonin reuptake inhibitor, tramadol). Flexible-dosage pregabalin 150-600 mg/day was taken for 3-month periods followed by 3- to 28-day pregabalin "drug holidays," with an analysis up to 15 months (five treatment cycles). Pain intensity was measured using the visual analog scale of the Short-Form McGill Pain Questionnaire.
In total, 81 patients were included in this analysis. Pregabalin 150-600 mg/day was associated with clinically meaningful and sustained pain reduction during each treatment cycle. During pregabalin "drug holidays," pain quickly returned to baseline levels; it was reduced again when pregabalin was reinstated.
These results suggest that pregabalin may be beneficial in patients with neuropathic pain who have had an unsatisfactory response to treatment with other medications.
与带状疱疹后神经痛(PHN)和疼痛性糖尿病周围神经病变(DPN)相关的神经性疼痛可能难以治疗,且可能对常用治疗方法(如三环类抗抑郁药(TCA)和阿片类药物)无反应。这项长期、开放标签研究是对普瑞巴林用于疼痛被判定对其他神经性疼痛治疗无效的患者的初步评估。
患者此前参加了普瑞巴林治疗DPN和PHN的双盲、安慰剂对照、随机试验。尽管接受了加巴喷丁、一种TCA和第三种药物(如其他抗惊厥药、阿片类药物、选择性5-羟色胺再摄取抑制剂、曲马多)治疗,他们仍有中度至重度神经性疼痛。患者服用灵活剂量的普瑞巴林,150 - 600毫克/天,为期3个月,随后有3至28天的普瑞巴林“停药期”,分析长达15个月(五个治疗周期)。使用简化麦吉尔疼痛问卷的视觉模拟量表测量疼痛强度。
本分析共纳入81例患者。每天150 - 600毫克的普瑞巴林在每个治疗周期均与具有临床意义的持续疼痛减轻相关。在普瑞巴林“停药期”,疼痛迅速恢复至基线水平;重新使用普瑞巴林时疼痛再次减轻。
这些结果表明,普瑞巴林可能对那些对其他药物治疗反应不佳的神经性疼痛患者有益。