Feily Amir, Dormanesh Benafshe, Ghorbani Ali Reza, Moosavi Zahra, Kouchak Maryam, Cheraghian Bahman, Mousavi Seyed Seifollah Beladi, Mehrabian Abolfath, Ranjbari Nastaran
AJA University of Medical Sciences, Tehran, Iran.
Int J Clin Pharmacol Ther. 2012 Jul;50(7):510-3. doi: 10.5414/cp201629.
Chronic kidney disease (CKD)-associated pruritus is a significant clinical symptom affecting more than 50% of patients on hemodialysis. The availability of effective therapeutic options for management of CKD-associated pruritus remains a treatment challenge.
The aim of this study was to compare cromolyn sodium cream 4% with placebo for the treatment of renal pruritus.
A randomized, double-blind, prospective, 4-week study was designed. 60 patients with ESRD in our dialysis ward were randomly allocated to cromolyn sodium cream 4% or placebo. All of them completed the study period and their pruritus levels were evaluated 5 times (before the start of the study and at the end of each week for 4 weeks) using a Visual Analogue Scale (VAS).
The average pruritus score before administration of the drug in cromolyn sodium 4% and placebo group had been 2.5 ± 1.1 and 2.7 ± 1.3, respectively. In the cromolyn sodium 4% group the average score of pruritus gradually reduced to 0.3 ± 1.3 and in the placebo group it gradually decreased to 1.3 ± 1.4 at the end of Week 4. Method of t-test repeat analytical measurement indicated that there is no significant difference between reduction of pruritus in cromolyn 4% and placebo groups in the first and second week of the study, but in third and fourth week there were significant differences in reducing pruritus in favor of cromolyn sodium 4% (p < 0.04).
According to our study cromolyn sodium cream 4% was more effective than placebo in reducing pruritus in uremic patients. We suggest to our colleagues to consider this treatment when facing a patient suffering from this symptom.
慢性肾脏病(CKD)相关瘙痒是一种严重的临床症状,影响超过50%的血液透析患者。对于CKD相关瘙痒的管理,有效的治疗选择仍然是一个治疗挑战。
本研究的目的是比较4%色甘酸钠乳膏与安慰剂治疗肾性瘙痒的效果。
设计了一项随机、双盲、前瞻性、为期4周的研究。将我们透析病房的60例终末期肾病患者随机分配至4%色甘酸钠乳膏组或安慰剂组。所有患者均完成研究期,并使用视觉模拟量表(VAS)在5个时间点(研究开始前以及之后4周每周结束时)评估其瘙痒程度。
4%色甘酸钠组和安慰剂组在用药前的平均瘙痒评分别为2.5±1.1和2.7±1.3。在4%色甘酸钠组,瘙痒平均评分在第4周结束时逐渐降至0.3±1.3,而在安慰剂组则逐渐降至1.3±1.4。采用t检验重复分析测量方法表明,在研究的第一周和第二周,4%色甘酸钠组和安慰剂组在瘙痒减轻方面无显著差异,但在第三周和第四周,4%色甘酸钠组在减轻瘙痒方面存在显著差异(p<0.04)。
根据我们的研究,4%色甘酸钠乳膏在减轻尿毒症患者瘙痒方面比安慰剂更有效。我们建议同事们在面对有此症状的患者时考虑这种治疗方法。