Improving the Reporting of Primary Care Research: Consensus Reporting Items for Studies in Primary Care-the CRISP Statement

被引:0
作者
Phillips, William R. [1 ,8 ]
Sturgiss, Elizabeth [2 ]
Glasziou, Paul [3 ]
Hartman, Tim C. olde [4 ]
Orkin, Aaron M. [5 ]
Prathivadi, Pallavi [6 ]
Reeve, Joanne [7 ]
Russell, Grant M. [6 ]
van Weel, Chris [4 ]
机构
[1] Univ Washington, Seattle, WA USA
[2] Monash Univ, Sch Primary & Allied Hlth Care, Melbourne, Vic, Australia
[3] Bond Univ, Robina, Qld, Australia
[4] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Nijmegen, Netherlands
[5] Univ Toronto, Toronto, ON, Canada
[6] Monash Univ, Melbourne, Vic, Australia
[7] Univ Hull, Kingston Upon Hull, England
[8] Univ Washington, Dept Family Med, Box 356390, Seattle, WA 98195 USA
基金
英国医学研究理事会;
关键词
GUIDELINES; WASTE;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Primary care (PC) is a unique clinical specialty and research discipline with its own perspec-tives and methods. Research in this field uses varied research methods and study designs to investigate myriad topics. The diversity of PC presents challenges for reporting, and despite the proliferation of reporting guidelines, none focuses specifically on the needs of PC. The Consensus Reporting Items for Studies in Primary Care (CRISP) Checklist guides reporting of PC research to include the information needed by the diverse PC community, including practitioners, patients, and communities. CRISP complements current guidelines to enhance the reporting, dissemination, and application of PC research findings and results. Prior CRISP studies documented opportunities to improve research reporting in this field. Our surveys of the international, interdisciplinary, and interprofessional PC community identi-fied essential items to include in PC research reports. A 2-round Delphi study identified a consensus list of items considered necessary. The CRISP Checklist contains 24 items that describe the research team, patients, study participants, health conditions, clinical encoun-ters, care teams, interventions, study measures, settings of care, and implementation of findings/results in PC. Not every item applies to every study design or topic. The CRISP guidelines inform the design and reporting of (1) studies done by PC researchers, (2) studies done by other investigators in PC populations and settings, and (3) studies intended for appli-cation in PC practice. Improved reporting of the context of the clinical services and the pro-cess of research is critical to interpreting study findings/results and applying them to diverse populations and varied settings in PC.
引用
收藏
页码:549 / 555
页数:7
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