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加巴喷丁与多塞平治疗尿毒症瘙痒的比较:一项随机交叉临床试验。

Comparison of gabapentin and doxepin in the management of uremic pruritus: A randomized crossover clinical trial.

机构信息

Department of Dermatology, Saint George Hospital University Medical Center, Beirut, Lebanon.

Faculty of Medicine, Balamand University, Beirut, Lebanon.

出版信息

Dermatol Ther. 2020 Nov;33(6):e14522. doi: 10.1111/dth.14522. Epub 2020 Nov 23.

Abstract

Gabapentin and doxepin are well-known treatments of uremic pruritus in hemodialysis patients but no head-to-head studies were conducted to date. The aim of this trial is to compare the efficacy and the tolerability of gabapentin and doxepin in the treatment of uremic pruritus in hemodialysis patients. A single-blind crossover randomized trial was conducted that included hemodialysis patients with uremic pruritus. Patients were randomized to receive 10 mg doxepin daily or 100 mg gabapentin for 4 weeks and the two groups were treated conversely for another 4 weeks after a 4-week washout period. Eighty-five patients were screened for eligibility. Thirty-one met the inclusion criteria and four were excluded. Sixteen patients agreed and signed the consent and two withdrew from the study. VAS scores at baseline were 6.71 and 6.14, and dropped to 0.57 and 2.35 at week 4 in the gabapentin and doxepin groups, respectively. Mean scores of the 5-Domain Itch Scale (5-D) at baseline were 14.71 and 14.64, and dropped to 5.78 and 7.57 at week 4 in the gabapentin and doxepin groups, respectively. Mean scores of the Dermatology Life Quality Index (DLQI) at baseline were 9.6429 and 8.7857, and dropped to 0.71 and 3.35 at week 4 in the gabapentin and doxepin groups, respectively. Reductions in Visual Analog Scale (VAS), 5-D and DLQI were statistically significant (P < .05). No serious side effects were recorded. Limitations of this study include single-blind design, small number of included cases and lack of placebo control. Gabapentin was more effective than doxepin in decreasing uremic pruritus severity and improving quality of life of these patients.

摘要

加巴喷丁和多塞平是血液透析患者尿毒症瘙痒的常用治疗方法,但迄今为止尚未进行过头对头研究。本试验旨在比较加巴喷丁和多塞平治疗血液透析患者尿毒症瘙痒的疗效和耐受性。进行了一项单盲交叉随机试验,纳入了患有尿毒症瘙痒的血液透析患者。患者随机接受 10 毫克多塞平每日或 100 毫克加巴喷丁治疗 4 周,两组在 4 周洗脱期后再分别治疗 4 周。对 85 名患者进行了筛选以确定其是否符合条件。31 名符合纳入标准,4 名被排除。16 名患者同意并签署了同意书,2 名患者退出了研究。加巴喷丁组和多塞平组的基线视觉模拟评分(VAS)分别为 6.71 和 6.14,第 4 周时分别降至 0.57 和 2.35。基线时 5 域瘙痒量表(5-D)的平均评分分别为 14.71 和 14.64,第 4 周时分别降至 5.78 和 7.57。基线时皮肤病生活质量指数(DLQI)的平均评分分别为 9.6429 和 8.7857,第 4 周时分别降至 0.71 和 3.35。VAS、5-D 和 DLQI 的评分降低具有统计学意义(P <.05)。未记录到严重的副作用。本研究的局限性包括单盲设计、纳入病例数少以及缺乏安慰剂对照。加巴喷丁在降低尿毒症瘙痒严重程度和改善这些患者的生活质量方面比多塞平更有效。

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