Faculty of Medicine, Tanta University, Tanta, Gharbia, Egypt.
Faculty of Medicine, University of Algiers 1, Algiers, Algeria.
Ren Fail. 2024 Dec;46(2):2384590. doi: 10.1080/0886022X.2024.2384590. Epub 2024 Aug 1.
Chronic kidney disease-associated pruritus (CKD-ap) is a common complication that negatively affects the quality of life. Difelikefalin has emerged as a novel FDA-approved drug to manage CKD-ap. This systematic review and meta-analysis will assess the efficacy and safety of Difelikefalin versus placebo to manage CKD-ap.
PubMed, Scopus, WOS, Central, and Embase were systematically searched until November 2023. RevMan was used to perform meta-analysis. Quality assessment was conducted using the Cochrane RoB 2.0 tool. Results were reported as risk ratio (RR) and mean difference (MD) with a 95% confidence interval (CI). PROSPERO ID: (CRD42023485979).
Five RCTs with a total of 896 participants were included. Difelikefalin significantly decreased the weekly mean WI-NRS score (MD: -0.99 [-1.22, -0.75], ˂ .00001), 5-D itch scale total score (MD: -1.51 [-2.26, -0.76], > .0001), and Skindex-10 total score (MD: -7.39 [-12.51, -2.28], = .005), but showed significantly higher adverse events (RR: 1.26 [1.03, 1.55], = .03), versus placebo. However, there was no significant difference between both groups in serious adverse events (RR: 1.42 [0.78, 2.57], = .25) or death (RR: 0.81 [0.19, 3.34], = .77).
Difelikefalin appears to be a promising agent for the management of CKD-induced pruritus in patients with end-stage renal disease. However, evidence is still underpowered due to the paucity of the current data; therefore, more robust RCTs are required to confirm the benefit of Difelikefalin.
慢性肾脏病相关性瘙痒(CKD-ap)是一种常见的并发症,会对生活质量产生负面影响。地氟可来是一种新型美国食品药品监督管理局批准的药物,可用于治疗 CKD-ap。本系统评价和荟萃分析将评估地氟可来与安慰剂相比治疗 CKD-ap 的疗效和安全性。
系统检索了 PubMed、Scopus、WOS、CENTRAL 和 Embase 数据库,检索时间截至 2023 年 11 月。使用 RevMan 进行荟萃分析。使用 Cochrane RoB 2.0 工具进行质量评估。结果以风险比(RR)和均数差(MD)表示,95%置信区间(CI)。PROSPERO 注册号:(CRD42023485979)。
纳入了 5 项 RCT,共 896 名参与者。地氟可来可显著降低每周平均 WI-NRS 评分(MD:-0.99[-1.22,-0.75],<0.00001)、5-D 瘙痒量表总分(MD:-1.51[-2.26,-0.76],>.0001)和 Skindex-10 总分(MD:-7.39[-12.51,-2.28],=0.005),但与安慰剂相比,不良反应发生率显著升高(RR:1.26[1.03,1.55],=0.03)。然而,两组间严重不良反应发生率(RR:1.42[0.78,2.57],=0.25)或死亡率(RR:0.81[0.19,3.34],=0.77)无显著差异。
地氟可来似乎是治疗终末期肾病患者 CKD 引起的瘙痒的一种有前途的药物。然而,由于目前数据有限,证据仍然不足;因此,需要更多的高质量 RCT 来证实地氟可来的疗效。