首页> 外文期刊>Indian journal of palliative care >Comparison of safety and efficacy of pregabalin versus gabapentin for the treatment of uremic pruritus in patients with chronic kidney disease on maintenance haemodialysis
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Comparison of safety and efficacy of pregabalin versus gabapentin for the treatment of uremic pruritus in patients with chronic kidney disease on maintenance haemodialysis

机译:Prababalin对慢性肾疾病患者尿毒剂瘙痒症治疗血液透析患者尿毒剂瘙痒症的安全性和疗效的比较

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Background: Uremic pruritus (UP) affects many patients suffering from chronic kidney disease (CKD) and has a negative impact on the quality of life. The severity of UP ranges from sporadic discomfort to complete restlessness during both day and night time. It has become increasingly evident that central transmission and sensitization processes similar to those observed in chronic pain are important mechanisms of pruritus. Methodology: This was a randomized single-blind prospective-interventional study carried out for 6 weeks. Male and female patients aged between 20 and 85 years with end-stage renal disease undergoing maintenance hemodialysis and who had substantial pruritus defined as persistent were included in our study. Informed consent was obtained from each patient before enrolling in the study. Patients were randomly divided into two groups (Group A and B), with Group A receiving pregabalin 25 mg and Group B receiving gabapentin 100 mg. The efficacy and safety of drugs were assessed after 6 weeks using visual analog scale and 5D itch scale. Results: We used gabapentin 100 mg or pregabalin 25 mg for 42 consecutive patients with CKD on maintenance hemodialysis with a mean age of patients in Group A (pregabalin 25 mg) 55.29 ± 14.58 and B (gabapentin 100 mg) 58.10 ± 11.09. Both gabapentin and pregabalin produced a significant difference in itching intensity with P 0.001; however, there was no statistically significant difference between the effectiveness of two drugs in reducing itch. While receiving gabapentin, 11 of 21 patients (52.38%) reported fatigue, dizziness, somnolescence, which was statistically significant (P ≤ 0.001) and 4 of these patients discontinued use of the drug due to excessive somnolence, all after the first dose. A statistically significant difference was found in each domain of 5D-Pruritus scale after gabapentin and pregabalin therapy.
机译:背景:尿毒症瘙痒(UP)影响许多患有慢性肾病(CKD)的患者,对生活质量产生负面影响。在一天和夜间的时间内,散发性不适的巨大范围的严重程度。它越来越明显,类似于慢性疼痛中观察到的中枢传输和敏化过程是瘙痒的重要机制。方法论:这是一项随机单盲预期 - 介入研究,进行了6周。在我们的研究中纳入了经历血液透析的末期肾病和患有大量瘙痒症的男性和女性患者患者患者患者和女性和女性患者。在注册研究之前,每位患者获得知情同意。患者随机分为两组(A和B组),其中A组接受蛋白蛋白25毫克和B组接受加巴帕坦100mg。使用视觉模拟规模和5D瘙痒尺度在6周后评估药物的功效和安全性。结果:我们使用加巴亨坦100毫克或普瑞巴林25毫克连续42例CKD维持血液透析患者(Praetabalin 25mg)55.29±14.58和B(加巴普蛋白100mg)58.10±11.09患者的平均年龄。 Gabapentin和Prababalin都产生了瘙痒强度的显着差异,P <0.001;然而,两种药物在减少瘙痒时的有效性之间没有统计学意义。在接受加巴亨坦素的同时,21例患者中的11名(52.38%)报告疲劳,头晕,生长学,这些患者的统计学意义(p≤0.001)和4名患者中的4名患者由于过度嗜睡而在第一次剂量之后终止使用药物。在加巴亨坦素和普瑞巴林疗法后,在5D-PRURITUS规模的每个结构域中发现了统计学意义。

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