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基线瘙痒严重程度对接受维持性血液透析的中重度瘙痒成人使用地肤法林治疗结局的影响:一项探索性分析。

Influence of Baseline Itch Severity on Treatment Outcomes With Difelikefalin in Adults With Moderate-to-Severe Pruritus Receiving Maintenance Haemodialysis: An Exploratory Analysis.

作者信息

McCafferty Kieran, Schaufler Thilo, Molina Pablo, Lowe Murray, Wen Warren, Weiner Daniel E

机构信息

Barts Health NHS Trust, London, UK.

CSL Vifor, Glattbrugg, Switzerland.

出版信息

J Ren Care. 2025 Jun;51(2):e70017. doi: 10.1111/jorc.70017.

Abstract

BACKGROUND

Difelikefalin is well-tolerated and reduces itch among adults undergoing haemodialysis (HD), with chronic kidney disease-associated pruritus (CKD-aP).

OBJECTIVE

This study aims to explore the influence of baseline itch severity on difelikefalin treatment outcomes.

DESIGN

Study 3105 (NCT03998163) was a 12-week, phase 3, single-arm, open-label trial assessing safety and effectiveness of difelikefalin 0.5 µg/kg. We report key endpoints from 3105 by baseline itch severity, determined using the Worst Itching Intensity Numerical Rating Scale (WI-NRS [moderate: WI-NRS < 7; severe: WI-NRS ≥ 7]).

PARTICIPANTS

Adult participants undergoing maintenance HD (n = 222) with mild-to-moderate CKD-aP (WI-NRS score ≥ 5 at baseline).

MEASUREMENTS

The primary endpoint of 3105 was safety; secondary endpoints included reduction in itch intensity (WI-NRS), and improvements in itch-related quality of life (QoL; 5-D itch scale) and sleep quality (Sleep Quality Numerical Rating Scale).

FINDINGS

Mean (SD) age was 57.1 (13.3) years; mean (SD) baseline WI-NRS scores were 6.0 (0.5) and 8.3 (0.9) for participants with moderate (n = 70/222) or severe (n = 152/222) itch, respectively. No treatment-related deaths occurred, and there were no safety concerns according to baseline itch severity. By week 12, both groups reported residual 'mild itch' according to mean (SD) WI-NRS scores (moderate: 2.9 [2.2]; severe: 3.1 [2.3]). Approximately one in four participants demonstrated 'complete response' in itch reduction (moderate: 27.1%; severe: 25.0%). Clinically relevant improvements in itch-related QoL and sleep quality occurred among both subgroups.

CONCLUSIONS

Difelikefalin was well-tolerated and effective in reducing itch in participants with moderate and severe baseline itch, supporting its broad use in a range of individuals on HD with CKD-aP.

摘要

背景

地肤利法林耐受性良好,可减轻接受血液透析(HD)且患有慢性肾脏病相关瘙痒(CKD-aP)的成年人的瘙痒症状。

目的

本研究旨在探讨基线瘙痒严重程度对地肤利法林治疗效果的影响。

设计

研究3105(NCT03998163)是一项为期12周的3期单臂开放标签试验,评估0.5μg/kg地肤利法林的安全性和有效性。我们根据基线瘙痒严重程度报告研究3105的关键终点,使用最严重瘙痒强度数字评定量表(WI-NRS[中度:WI-NRS<7;重度:WI-NRS≥7])进行判定。

参与者

患有轻至中度CKD-aP(基线WI-NRS评分≥5)的维持性HD成年参与者(n = 222)。

测量指标

研究3105的主要终点是安全性;次要终点包括瘙痒强度降低(WI-NRS),以及瘙痒相关生活质量(QoL;5-D瘙痒量表)和睡眠质量改善(睡眠质量数字评定量表)。

研究结果

平均(标准差)年龄为57.1(13.3)岁;中度瘙痒(n = 70/222)或重度瘙痒(n = 152/222)参与者的平均(标准差)基线WI-NRS评分分别为6.0(0.5)和8.3(0.9)。未发生与治疗相关的死亡,根据基线瘙痒严重程度也无安全问题。到第12周时,两组根据平均(标准差)WI-NRS评分均报告有残留的“轻度瘙痒”(中度:2.9[2.2];重度:3.1[2.3])。约四分之一的参与者在瘙痒减轻方面表现出“完全缓解”(中度:27.1%;重度:25.0%)。两个亚组的瘙痒相关QoL和睡眠质量均出现了具有临床意义的改善。

结论

地肤利法林耐受性良好,对减轻中度和重度基线瘙痒的参与者的瘙痒有效,支持其在一系列患有CKD-aP的HD个体中广泛使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5cb/12054700/10acf32fa070/JORC-51-0-g004.jpg

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