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让患者伙伴参与KRESCENT同行评审:目的、过程、挑战与机遇

Involving Patient Partners in the KRESCENT Peer Review: Intent, Process, Challenges, and Opportunities.

作者信息

Fowler Elisabeth A, Bell Karin, Burns Kevin, Chiazzese Angela, DeSerres Sacha A, Foster Bethany J, Hartwig Sunny, Herrington Gwen, James Matthew T, Jensen Victor, Jones Nina, Kidston Sandi, Lemay Serge, Levin Adeera, MacPhee Anne, McCutcheon Shanda, Ravani Pietro, Samuel Susan, Scholey James, Takano Tomoko, Tangri Navdeep, Verdin Nancy, Alexander R Todd, Clase Catherine M

机构信息

Kidney Foundation of Canada, Montreal, QC, Canada.

Patient Partner and Member of Canadians Seeking Solutions and Innovations to Overcome Chronic Kidney Disease (Can-SOLVE CKD), Vancouver, BC, Canada.

出版信息

Can J Kidney Health Dis. 2022 Nov 15;9:20543581221136402. doi: 10.1177/20543581221136402. eCollection 2022.

DOI:10.1177/20543581221136402
PMID:36406869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9669682/
Abstract

PURPOSE OF REVIEW

The Kidney Research Scientist Core Education and National Training (KRESCENT) is a national Canadian training program for kidney scientists, funded by the Kidney Foundation of Canada (KFOC), the Canadian Institutes of Health Research (CIHR), and the Canadian Society of Nephrology (CSN). We describe our first year of incorporating patient partners into a scientific peer-review committee, the 2017 committee to select senior research trainees and early-career kidney researchers for funding and training, in the hope that it will be helpful to others who wish to integrate the perspective of people with lived experience into the peer-review process.

SOURCES OF INFORMATION

Other peer-review committees, websites, journal articles, patient partners, Kidney Foundation of Canada Research Council, Canadians Seeking Solutions and Innovations to Overcome Chronic Kidney Disease (Can-SOLVE CKD) Patient Council, participants in the 2017 Kidney Foundation of Canada KRESCENT peer-review panel.

METHODS

We describe our motivation, rationale, guiding principles, plans, feedback, implementation, and response.

KEY FINDINGS

We disseminated a "call for patient partners" 8 weeks before the meeting, seeking patients or their care givers to partner with the KRESCENT peer-review panel; we defined these people with lived experience of kidney disease as patient partners. Eight patient partners came forward and all participated as reviewers. Patient partners first participated in a webinar to learn about the function, structure, and processes of a peer-review committee. They practiced reviewing plain language summaries and giving feedback. In a subsequent teleconference, they shared and discussed their reviews. Plain language summaries were scored, overall, on the same 0-5 quality scale used by scientific reviewers. Three patient reviewers participated in some or all of the 6-hour meeting, which was conducted as usual, for this panel, by teleconference (initially audio only; from 2020 onwards by videoconference). In the meeting, the 2 assigned scientific reviewers first gave their scores, followed by the patient reviewers giving their scores, and discussion (mostly scientific, and conducted in usual scientific language). Scientific reviewers then negotiated a consensus score based on their initial scores, the discussion, patient reviewers' scores and statements, and the scientific officer's notes. Patient reviewers, scientific reviewers, and the Kidney Foundation of Canada (KFOC) were generally positive about the process. The increased length of the meeting (estimated at 1 hour) was generally thought to be acceptable. Patient reviewers also provided feedback on the methods used to incorporate patients into the research under review. These comments were concrete, insightful, and helpful. The patients did not uniformly recommend that basic scientists involve patients in their work. We did not detect bias against preclinical science, work that did not involve patients, or rarer diseases. Some patients found participation inspiring and enlightening. All participants appreciated the idea of patient partners as community witnesses to a group process committed to fairness and supportiveness. We discussed assigning formal meaningful weight to patient reviewers' assessments. Most, but not all, patients thought that the scientific reviewers were ultimately the best judges of the allocation of scarce research resources.

LIMITATIONS

Patient participants tended to be Caucasian, middle class, and well educated. Because of the difficulties of travel for some people living with or supporting those living with kidney disease, our findings may not generalize fully to peer-review meetings that are conducted face to face. This is explicitly a supportive panel, committed to reviewing junior scientists with kindness as well as rigor; our findings may not generalize to panels conducted differently. We did not use formal qualitative methodology.

IMPLICATIONS

Inclusion of patient partners as patient reviewers for the KRESCENT program peer-review panel was feasible, added value for scientific and patient reviewers, and for the funding stakeholders (CIHR, KFOC, and CSN). We were glad that we had taken this step and continue to refine the process with each successive competition.

摘要

综述目的:肾脏研究科学家核心教育与国家培训项目(KRESCENT)是加拿大一项面向肾脏科学家的全国性培训项目,由加拿大肾脏基金会(KFOC)、加拿大卫生研究院(CIHR)和加拿大肾脏病学会(CSN)资助。我们描述了将患者合作伙伴纳入科学同行评审委员会的第一年情况,即2017年选拔高级研究学员和早期肾脏研究人员以提供资金和培训的委员会,希望能对其他希望将有实际经验者的观点融入同行评审过程的人有所帮助。

信息来源:其他同行评审委员会、网站、期刊文章、患者合作伙伴、加拿大肾脏基金会研究委员会、加拿大慢性肾脏病解决方案与创新探索组织(Can - SOLVE CKD)患者委员会、2017年加拿大肾脏基金会KRESCENT同行评审小组的参与者。

方法:我们描述了动机、基本原理、指导原则、计划、反馈、实施情况及回应。

主要发现:我们在会议前8周发布了“招募患者合作伙伴”的通知,寻找患者或其护理人员与KRESCENT同行评审小组合作;我们将这些有肾脏疾病实际经验的人定义为患者合作伙伴。8位患者合作伙伴挺身而出并全部作为评审员参与。患者合作伙伴首先参加了一个网络研讨会,了解同行评审委员会的职能、结构和流程。他们练习评审通俗易懂的摘要并提供反馈。在随后的电话会议中,他们分享并讨论了自己的评审意见。通俗易懂的摘要总体上按照科学评审员使用的相同的0 - 5质量等级进行评分。3位患者评审员参加了部分或全部6小时的会议,该会议像往常一样通过电话会议进行(最初仅音频;从2020年起通过视频会议)。在会议中,2位指定的科学评审员首先给出他们的分数,接着患者评审员给出分数,然后进行讨论(大多是科学性的,用通常的科学语言进行)。科学评审员随后根据他们的初始分数、讨论情况、患者评审员的分数和陈述以及科学官员的记录协商出一个共识分数。患者评审员、科学评审员和加拿大肾脏基金会(KFOC)总体上对这个过程持积极态度。会议延长的时长(估计为1小时)通常被认为是可以接受的。患者评审员还对将患者纳入所评审研究的方法提供了反馈。这些意见具体、有见地且很有帮助。患者并没有一致建议基础科学家让患者参与他们的工作。我们没有发现对临床前科学、不涉及患者的工作或罕见疾病存在偏见。一些患者觉得参与很有启发性。所有参与者都赞赏患者合作伙伴作为群体过程的社区见证者这一理念,该过程致力于公平和支持。我们讨论了给予患者评审员的评估正式且有意义的权重。大多数但并非所有患者认为科学评审员最终是稀缺研究资源分配的最佳评判者。

局限性:患者参与者往往是白人、中产阶级且受过良好教育。由于一些患有肾脏疾病或照顾患有肾脏疾病者的人出行困难,我们的研究结果可能无法完全推广到面对面进行的同行评审会议。这明确是一个支持性小组,致力于以友善且严谨的态度评审初级科学家;我们的研究结果可能不适用于以不同方式进行的小组。我们没有使用正式的定性方法。

启示:将患者合作伙伴纳入KRESCENT项目同行评审小组作为患者评审员是可行的,对科学评审员、患者评审员以及资助利益相关者(CIHR、KFOC和CSN)都有价值。我们很高兴采取了这一步骤,并将在后续的每次竞争中不断完善这个过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/9669682/e03dea25d119/10.1177_20543581221136402-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/9669682/e03dea25d119/10.1177_20543581221136402-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233e/9669682/e03dea25d119/10.1177_20543581221136402-fig1.jpg

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