Vigneri Simone, Sindaco Gianfranco, La Grua Marco, Zanella Matteo, Ravaioli Laura, Paci Valentina, Pari Gilberto
Department of Experimental Biomedicine and Clinical Neurosciences, University of Palermo, Palermo; Advanced Algology Research and Pain Medicine Unit, Santa Maria Maddalena Hospital, Occhiobello, RO, Italy.
Advanced Algology Research and Pain Medicine Unit, Santa Maria Maddalena Hospital, Occhiobello, RO, Italy.
J Pain Res. 2016 Nov 21;9:1081-1087. doi: 10.2147/JPR.S113996. eCollection 2016.
The aim of this study was to investigate the therapeutic effectiveness of epidural morphine and bupivacaine in patients with chronic lumbosacral radicular neuropathic pain after the cessation of treatment.
Twenty-two patients with chronic lumbosacral pain with neuropathic features were enrolled. An indwelling catheter was placed into the epidural space, and each patient received an epidural injection of morphine chlorhydrate and bupivacaine up to three times a day. The medication was administered for 4 weeks. The pain intensity score on a 0-10 numeric rating scale (NRS), the total pain rating index rank (PRIr-T), and its coefficients were evaluated before treatment and 1 month after catheter removal. -value <0.05 was considered statistically significant.
NRS and PRIr-T were significantly reduced at follow-up (=0.001 and =0.03, respectively), whereas the parallel evolution of the two scores (=0.75 and <0.001, respectively) confirmed significant pain relief lasting up to 1 month after treatment cessation. None of the four pain rating coefficients was significantly modified compared to the others in either responders or nonresponders. Successful clinical outcome (pain reduction >30% in NRS) was reached and maintained in half of the patients at follow-up.
Combined epidural morphine and bupivacaine seems to be effective in the treatment of neuropathic pain.
本研究旨在调查硬膜外注射吗啡和布比卡因对慢性腰骶部神经根性神经病理性疼痛患者停止治疗后的疗效。
纳入22例具有神经病理性特征的慢性腰骶部疼痛患者。将一根留置导管置入硬膜外腔,每位患者每天接受多达3次的硬膜外注射吗啡和布比卡因。用药持续4周。在治疗前及拔除导管1个月后评估0至10数字评分量表(NRS)上的疼痛强度评分、总疼痛评分指数等级(PRIr-T)及其系数。P值<0.05被认为具有统计学意义。
随访时NRS和PRIr-T显著降低(分别为P = 0.001和P = 0.03),而两个评分的平行变化(分别为P = 0.75和P<0.001)证实治疗停止后长达1个月疼痛持续显著缓解。在有反应者或无反应者中,四个疼痛评分系数与其他系数相比均无显著改变。随访时半数患者达到并维持了成功的临床结局(NRS疼痛减轻>30%)。
硬膜外联合应用吗啡和布比卡因似乎对神经病理性疼痛有效。