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制定血液透析试验的核心结局集:一项国际德尔菲调查。

Developing a Set of Core Outcomes for Trials in Hemodialysis: An International Delphi Survey.

机构信息

Sydney School of Public Health, University of Sydney, Sydney, NSW, Australia; Centre for Kidney Research, The Children's Hospital at Westmead, Sydney, NSW, Australia.

Sydney School of Public Health, University of Sydney, Sydney, NSW, Australia; Centre for Kidney Research, The Children's Hospital at Westmead, Sydney, NSW, Australia.

出版信息

Am J Kidney Dis. 2017 Oct;70(4):464-475. doi: 10.1053/j.ajkd.2016.11.029. Epub 2017 Feb 24.

Abstract

BACKGROUND

Survival and quality of life for patients on hemodialysis therapy remain poor despite substantial research efforts. Existing trials often report surrogate outcomes that may not be relevant to patients and clinicians. The aim of this project was to generate a consensus-based prioritized list of core outcomes for trials in hemodialysis.

STUDY DESIGN

In a Delphi survey, participants rated the importance of outcomes using a 9-point Likert scale in round 1 and then re-rated outcomes in rounds 2 and 3 after reviewing other respondents' scores. For each outcome, the median, mean, and proportion rating as 7 to 9 (critically important) were calculated.

SETTING & PARTICIPANTS: 1,181 participants (202 [17%] patients/caregivers, 979 health professionals) from 73 countries completed round 1, with 838 (71%) completing round 3.

OUTCOMES & MEASUREMENTS: Outcomes included in the potential core outcome set met the following criteria for both patients/caregivers and health professionals: median score ≥ 8, mean score ≥ 7.5, proportion rating the outcome as critically important ≥ 75%, and median score in the forced ranking question < 10.

RESULTS

Patients/caregivers rated 4 outcomes higher than health professionals: ability to travel, dialysis-free time, dialysis adequacy, and washed out after dialysis (mean differences of 0.9, 0.5, 0.3, and 0.2, respectively). Health professionals gave a higher rating for mortality, hospitalization, decrease in blood pressure, vascular access complications, depression, cardiovascular disease, target weight, infection, and potassium (mean differences of 1.0, 1.0, 1.0, 0.9, 0.9, 0.8, 0.7, 0.4, and 0.4, respectively).

LIMITATIONS

The Delphi survey was conducted online in English and excludes participants without access to a computer and internet connection.

CONCLUSIONS

Patients/caregivers gave higher priority to lifestyle-related outcomes than health professionals. The prioritized outcomes for both groups were vascular access problems, dialysis adequacy, fatigue, cardiovascular disease, and mortality. This process will inform a core outcome set that in turn will improve the relevance, efficiency, and comparability of trial evidence to facilitate treatment decisions.

摘要

背景

尽管进行了大量研究,但接受血液透析治疗的患者的生存和生活质量仍然很差。现有的试验通常报告替代终点,这些终点可能与患者和临床医生无关。本项目的目的是为血液透析试验生成一个基于共识的优先核心结局清单。

研究设计

在德尔菲调查中,参与者使用 9 分制 Likert 量表在第一轮中对结局的重要性进行评分,然后在第二轮和第三轮中在查看其他受访者的评分后重新对结局进行评分。对于每个结局,计算中位数、平均值和评分 7 至 9(非常重要)的比例。

设置和参与者

来自 73 个国家的 1181 名参与者(202[17%]名患者/照护者,979 名卫生专业人员)完成了第一轮,其中 838 名(71%)完成了第三轮。

结局和测量

纳入潜在核心结局清单的结局满足了患者/照护者和卫生专业人员的以下标准:中位数评分≥8,平均值评分≥7.5,将结局评为非常重要的比例≥75%,以及强制排名问题中的中位数评分<10。

结果

患者/照护者对以下 4 个结局的评分高于卫生专业人员:旅行能力、无透析时间、透析充分性和透析后疲乏(平均差异分别为 0.9、0.5、0.3 和 0.2)。卫生专业人员对死亡率、住院、血压下降、血管通路并发症、抑郁、心血管疾病、目标体重、感染和钾的评分更高(平均差异分别为 1.0、1.0、1.0、0.9、0.9、0.8、0.7、0.4 和 0.4)。

局限性

德尔菲调查是用英语在线进行的,不包括没有计算机和互联网连接的参与者。

结论

患者/照护者比卫生专业人员更重视与生活方式相关的结局。两组患者都优先考虑血管通路问题、透析充分性、疲劳、心血管疾病和死亡率。这一过程将为核心结局集提供信息,进而提高试验证据的相关性、效率和可比性,以促进治疗决策。

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