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首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Comparative study of safety and efficacy of pregabalin and gabapentin in management of neuropathic pain associated with chronic lumbar radiculopathy
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Comparative study of safety and efficacy of pregabalin and gabapentin in management of neuropathic pain associated with chronic lumbar radiculopathy

机译:普瑞巴林和加巴喷丁治疗慢性腰椎神经根神经痛相关的安全性和有效性比较研究

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Background: Chronic lumbar radiculopathy a clinical condition in which there is back and leg pain associated with sensory, reflex, or motor deficits in the area of nerve root distribution lasting for more than 12 weeks. The prevalence of lumbar radiculopathy has been reported to be 5.3% in men and 3.7% in women. Pregabalin and gabapentin, which fit in to a new category of drugs called as alpha-2-delta (α2δ) modulators, have been discovered to be effective in the treatment of neuropathic pain related with multiple conditions. So this study was done to compare safety and efficacy of pregabalin and gabapentin in management of pain associated with chronic lumbar radiculopathy. Methods: This was a randomized two arm comparative prospective study. Total 160 patients were enrolled and randomized equally into 2 groups. Group A patients were given capsule pregabalin 75 mg two times a day orally, Group B patients were given tablet gabapentin 300 mg two times a day. Pain intensity was assessed at the start of study i.e. at baseline (0 week), at 6 weeks and at 12 weeks of starting the treatment using numeric pain rating scale. Results: There was significant reduction in pain at the end of 12 weeks in both the groups (p0.0001), but there was no significant difference between these two groups. The incidence of adverse effects was also more in group A. Conclusions: Both the drugs are having comparable efficacy but gabapentin is more tolerable in such cases.
机译:背景:慢性腰椎神经根病是一种临床状况,其中,在神经根分布区域持续12周以上,伴有背部和腿部疼痛,并伴有感觉,反射或运动功能障碍。腰椎神经根病的患病率据报道男性为5.3%,女性为3.7%。已发现普瑞巴林和加巴喷丁适用于称为α-2-δ(α2δ)调节剂的新型药物,可有效治疗与多种疾病相关的神经性疼痛。因此,本研究旨在比较普瑞巴林和加巴喷丁在治疗慢性腰椎神经根痛相关的疼痛方面的安全性和有效性。方法:这是一项随机的两臂比较性前瞻性研究。共有160名患者入组,并随机分为2组。 A组患者每天两次口服普瑞巴林胶囊75 mg,B组患者每天两次口服加巴喷丁片剂300 mg。在研究开始时,即在基线(0周),开始治疗时的6周和12周时,使用数字疼痛等级量表评估疼痛强度。结果:两组在12周结束时疼痛均明显减轻(p <0.0001),但两组之间无显着差异。不良反应的发生率在A组中也更高。结论:两种药物的疗效相当,但在这种情况下加巴喷丁的耐受性更高。

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