Long-term views on chronic kidney disease research priorities among stakeholders engaged in a priority-setting partnership: A qualitative study

被引:4
|
作者
Elliott, Meghan J. [1 ,2 ]
Sale, Joanna E. M. [3 ,4 ]
Goodarzi, Zahra [1 ,5 ]
Wilhelm, Linda [6 ]
Laupacis, Andreas [3 ,4 ,7 ]
Hemmelgarn, Brenda R. [1 ,2 ]
Straus, Sharon E. [3 ,4 ,7 ]
机构
[1] Univ Calgary, Dept Med, Calgary, AB, Canada
[2] Univ Calgary, Dept Community Hlth Sci, Calgary, AB, Canada
[3] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[4] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[5] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[6] Canadian Arthrit Patient Alliance, Toronto, ON, Canada
[7] Univ Toronto, Dept Med, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
chronic kidney disease; patient engagement; patient-oriented research; qualitative research; research priorities; RANDOMIZED CONTROLLED-TRIALS; PUBLIC INVOLVEMENT; PATIENT; IMPACT; PARTICIPATION; HEALTH;
D O I
10.1111/hex.12818
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Patients and stakeholders are increasingly engaging in health research to help address evidence-practice gaps and improve health-care delivery. We previously engaged patients, caregivers, health-care providers (HCPs) and policymakers in identifying priorities for chronic kidney disease (CKD) research. Objective: We aimed to explore participants' views on the research priorities and prioritization process 2 years after the exercise took place. Design: In this qualitative descriptive study, individual interviews were conducted and analysed using an inductive, thematic analysis approach. Setting/participants: Participants resided across Canada. We purposively sampled across stakeholder groups (CKD patients, caregivers, HCPs and policymakers) and types of engagement (wiki, workshop and/or steering committee) from the previous CKD priority-setting project. Results: Across 23 interviews, participants discussed their research priorities over time, views on the prioritization process and perceived applicability of the priorities. Even though their individual priorities may have changed, participants remained in agreement overall with the previously identified priorities, and some perceived a distinction between patient and HCP priorities. They tended to balance individual priorities with their broader potential impact and viewed the prioritization process as systematic, collaborative and legitimate. However, participants acknowledged challenges to applying the priorities and emphasized the importance of communicating the project's outcomes upon its completion. Conclusion: Two years after engaging in CKD research prioritization, stakeholder participants remained in agreement with the previously identified priorities, which they felt reflected group deliberation and consensus. Rapport and communication were highlighted as key elements supporting effective engagement in research prioritization.
引用
收藏
页码:1142 / 1149
页数:8
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