Centre of Evidence Based Dermatology, School of Medicine, Nottingham, UK.
Institute of Social Medicine and Health Systems Research (ISMHSR), Otto von Guericke University Magdeburg, Magdeburg, Germany.
Br J Dermatol. 2021 Jul;185(1):139-146. doi: 10.1111/bjd.19751. Epub 2021 Feb 8.
The Harmonising Outcome Measures for Eczema (HOME) initiative has established a core outcome set of domains for atopic eczema (AE) clinical trials. Previous consensus meetings have agreed on preferred instruments for clinician-reported signs (Eczema Area and Severity Index, EASI) and patient-reported symptoms (Patient-Oriented Eczema Measure, POEM). This paper reports consensus decisions from the HOME VII meeting.
To complete the core outcome set for AE by agreeing on core outcome instruments for the domains of quality of life (QoL), long-term control and itch intensity.
A face-to-face consensus meeting was held in Tokyo, Japan (8-10 April 2019) including 75 participants (49 healthcare professionals/methodologists, 14 patients, 12 industry representatives) from 16 countries. Consensus decisions were made by presentations of evidence, followed by whole and small group discussions and anonymous voting using predefined consensus rules.
It was agreed by consensus that QoL should be measured using the Dermatology Life Quality Index (DLQI) for adults, the Children's Dermatology Life Quality Index (CDLQI) for children and the Infant's Dermatology Quality of Life Index (IDQoL) for infants. For long-term control, the Recap of Atopic Eczema (RECAP) instrument or the Atopic Dermatitis Control Test (ADCT) should be used. Consensus was not reached over the frequency of data collection for long-term control. The peak itch numerical rating scale (NRS)-11 past 24 h was recommended as an additional instrument for the symptom domain in trials of older children and adults. Agreement was reached that all core outcome instruments should be captured at baseline and at the time of primary outcome assessment as a minimum.
For now, the core outcome set for clinical trials in AE is complete. The specified domains and instruments should be used in all new clinical trials and systematic reviews of eczema treatments.
湿疹结局测量协调(HOME)倡议已经为特应性皮炎(AE)临床试验建立了一个包含领域的核心结局集。之前的共识会议已经就临床医生报告的体征(湿疹面积和严重程度指数,EASI)和患者报告的症状(患者导向的湿疹测量,POEM)的首选工具达成了一致意见。本文报告了 HOME VII 会议的共识决定。
通过就生活质量(QoL)、长期控制和瘙痒强度领域的核心结局工具达成一致,完成 AE 的核心结局集。
2019 年 4 月 8 日至 10 日在日本东京举行了一次面对面的共识会议,来自 16 个国家的 75 名参与者(49 名医疗保健专业人员/方法学家、14 名患者、12 名行业代表)参加了会议。共识决策是通过展示证据,然后进行全体和小组讨论以及使用预设的共识规则进行匿名投票来做出的。
与会者一致认为,成人应使用皮肤病生活质量指数(DLQI)、儿童应使用儿童皮肤病生活质量指数(CDLQI)、婴儿应使用婴儿皮肤病生活质量指数(IDQoL)来测量 QoL。对于长期控制,应使用 RECAP 工具或特应性皮炎控制测试(ADCT)。对于长期控制数据的收集频率,尚未达成共识。建议在年龄较大的儿童和成人的试验中,将过去 24 小时的瘙痒峰值数字评定量表(NRS)-11 作为症状领域的附加工具。与会者一致认为,所有核心结局工具都应至少在基线和主要结局评估时进行采集。
目前,AE 临床试验的核心结局集已经完成。在所有新的临床试验和湿疹治疗的系统评价中,都应使用指定的领域和工具。