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加巴喷丁对保守治疗的慢性肾脏病患者尿毒症瘙痒和不安腿综合征的疗效及安全性

Efficacy and safety of gabapentin for uremic pruritus and restless legs syndrome in conservatively managed patients with chronic kidney disease.

作者信息

Cheikh Hassan Hicham I, Brennan Frank, Collett Gemma, Josland Elizabeth A, Brown Mark A

机构信息

Department of Renal Medicine, St. George Hospital, Sydney, New South Wales, Australia; University of New South Wales, Sydney, New South Wales, Australia.

Department of Renal Medicine, St. George Hospital, Sydney, New South Wales, Australia; University of New South Wales, Sydney, New South Wales, Australia.

出版信息

J Pain Symptom Manage. 2015 Apr;49(4):782-9. doi: 10.1016/j.jpainsymman.2014.08.010. Epub 2014 Sep 8.

Abstract

CONTEXT

Pruritus and restless legs syndrome (RLS) frequently affect patients with chronic kidney disease (CKD) and end-stage kidney disease (ESKD), impacting the quality of life. Gabapentin (1-aminomethyl cyclohexane acetic acid) alleviates these symptoms in hemodialysis (HD) patients, but data are lacking for patients on the conservative pathway.

OBJECTIVES

To determine the safety and effectiveness of gabapentin for pruritus or RLS in conservatively managed patients (n = 34) with CKD and ESKD.

METHODS

This was a single-center retrospective cohort study. We compared dosing and side effects in 34 CKD/ESKD patients with similar patients receiving HD (n = 15).

RESULTS

Forty-four percent of conservatively managed patients complained of RLS and/or pruritus; 18% were excluded for a nonuremic cause of symptom. Thirty-four patients were included in the final analysis. The most common starting daily dose of gabapentin was the equivalent of 50 mg (44.1%) or 100 mg (38.2%) daily, with the median daily dose of 100 mg (range 39-455 mg). Side effects occurred in 47% of patients, with 17% discontinuing gabapentin. Gabapentin reduced symptoms of pruritus (P < 0.001) and RLS (P < 0.05). There was no statistical difference when comparing HD and conservatively managed patients for daily starting dose (P = 0.88), median dose (P = 0.84), and final dose (P = 0.18). Patients conservatively managed were more likely to manifest side effects compared with HD patients (47.1% vs. 14.3%, P = 0.023). Dose was not found to be a factor associated with side effects in univariate analysis.

CONCLUSION

Gabapentin is a viable treatment for conservatively managed CKD and ESKD patients with pruritus and/or RLS, but side effects are common. Gabapentin should be used with caution although higher doses do not appear to be a factor associated with side effects.

摘要

背景

瘙痒症和不宁腿综合征(RLS)经常影响慢性肾脏病(CKD)和终末期肾病(ESKD)患者,对生活质量产生影响。加巴喷丁(1-氨基甲基环己烷乙酸)可缓解血液透析(HD)患者的这些症状,但对于接受保守治疗的患者,相关数据尚缺。

目的

确定加巴喷丁对接受保守治疗的CKD和ESKD患者(n = 34)的瘙痒症或RLS的安全性和有效性。

方法

这是一项单中心回顾性队列研究。我们比较了34例CKD/ESKD患者与接受HD治疗的类似患者(n = 15)的用药剂量和副作用。

结果

44%接受保守治疗的患者抱怨有RLS和/或瘙痒症;18%因非尿毒症性症状原因被排除。最终分析纳入34例患者。加巴喷丁最常见的起始日剂量相当于每日50 mg(44.1%)或100 mg(38.2%),日中位剂量为100 mg(范围39 - 455 mg)。47%的患者出现副作用,17%的患者停用加巴喷丁。加巴喷丁减轻了瘙痒症(P < 0.001)和RLS(P < 0.05)的症状。比较HD患者和接受保守治疗的患者的起始日剂量(P = 0.88)、中位剂量(P = 0.84)和最终剂量(P = 0.18)时,无统计学差异。与HD患者相比,接受保守治疗的患者更易出现副作用(47.1%对14.3%,P = 0.023)。在单因素分析中,未发现剂量是与副作用相关的因素。

结论

加巴喷丁是治疗接受保守治疗的伴有瘙痒症和/或RLS的CKD和ESKD患者的一种可行疗法,但副作用常见。尽管较高剂量似乎不是与副作用相关的因素,但使用加巴喷丁时仍应谨慎。

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