GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research

被引:726
作者
Staniszewska, S. [1 ]
Brett, J. [2 ]
Simera, I. [3 ,4 ]
Seers, K. [1 ]
Mockford, C. [5 ]
Goodlad, S. [6 ]
Altman, D. G. [7 ]
Moher, D. [8 ]
Barber, R. [9 ]
Denegri, S. [10 ]
Entwistle, A. [5 ]
Littlejohns, P. [11 ]
Morris, C. [12 ]
Suleman, R. [5 ]
Thomas, V. [13 ]
Tysall, C. [5 ]
机构
[1] Univ Warwick, Warwick Res Nursing, Warwick Med Sch, Coventry CV4 7AL, W Midlands, England
[2] Oxford Brookes Univ, Fac Hlth & Life Sci, Oxford, England
[3] Univ Oxford, Ctr Trop Med & Global Hlth, Oxford, England
[4] Univ Oxford, UK EQUATOR Ctr, Oxford, England
[5] Warwick Med Sch, Coventry, W Midlands, England
[6] Coventry Univ, Coventry, W Midlands, England
[7] Univ Oxford, Ctr Stat Med, Oxford, England
[8] Ottawa Hosp Res Inst, Ctr Journalol, Clin Epidemiol Program, Ottawa, ON, Canada
[9] Univ Sheffield, Sch Hlth & Related Res, Sect Publ Hlth, Sheffield, S Yorkshire, England
[10] UCL Sch Life & Med Sci, Natl Inst Hlth Res, London, England
[11] Kings Coll London, London, England
[12] Univ Exeter, Sch Med, Exeter, Devon, England
[13] Natl Inst Hlth & Care Excellence, Publ Involvement Programme, London, England
来源
BMJ-BRITISH MEDICAL JOURNAL | 2017年 / 358卷
关键词
CARE RESEARCH; HEALTH-CARE; IMPACT;
D O I
10.1136/bmj.j3453
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. OBJECTIVE To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research partners at all stages in the development of GRIPP2. METHODS The EQUATOR method for developing reporting guidelines was used. The original GRIPP (Guidance for Reporting Involvement of Patients and the Public) checklist was revised, based on updated systematic review evidence. A three round Delphi survey was used to develop consensus on items to be included in the guideline. A subsequent face-to-face meeting produced agreement on items not reaching consensus during the Delphi process. RESULTS 143 participants agreed to participate in round one, with an 86% (123/143) response for round two and a 78% (112/143) response for round three. The Delphi survey identified the need for long form (LF) and short form (SF) versions. GRIPP2-LF includes 34 items on aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections and is suitable for studies where the main focus is PPI. GRIPP2SF includes five items on aims, methods, results, outcomes, and critical perspective and is suitable for studies where PPI is a secondary focus. CONCLUSIONS GRIPP2-LF and GRIPP2-SF represent the first international evidence based, consensus informed guidance for reporting patient and public involvement in research. Both versions of GRIPP2 aim to improve the quality, transparency, and consistency of the international PPI evidence base, to ensure PPI practice is based on the best evidence. In order to encourage its wide dissemination this article is freely accessible on The BMJ and Research Involvement and Engagement journal websites.
引用
收藏
页数:7
相关论文
共 21 条
[1]   Towards complete and accurate reporting of studies of diagnostic accuracy: The STARD initiative [J].
Bossuyt, PM ;
Reitsma, JB ;
Bruns, DE ;
Gatsonis, CA ;
Glasziou, PP ;
Irwig, LM ;
Lijmer, JG ;
Moher, D ;
Rennie, D ;
de Vet, HCW .
CLINICAL CHEMISTRY, 2003, 49 (01) :1-6
[2]  
Braun V, 2006, QUAL RES PSYCHOL, V3, DOI [DOI 10.1191/1478088706QP063OA, 10.1191/1478088706qp063oa]
[3]  
Brett J, BMJ OPEN IN PRESS
[4]   A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities [J].
Brett, Jo ;
Staniszewska, Sophie ;
Mockford, Carole ;
Herron-Marx, Sandra ;
Hughes, John ;
Tysall, Colin ;
Suleman, Rashida .
PATIENT-PATIENT CENTERED OUTCOMES RESEARCH, 2014, 7 (04) :387-395
[5]   Mapping the impact of patient and public involvement on health and social care research: a systematic review [J].
Brett, Jo ;
Staniszewska, Sophie ;
Mockford, Carole ;
Herron-Marx, Sandra ;
Hughes, John ;
Tysall, Colin ;
Suleman, Rashida .
HEALTH EXPECTATIONS, 2014, 17 (05) :637-650
[6]   Patient engagement in research: a systematic review [J].
Domecq, Juan Pablo ;
Prutsky, Gabriela ;
Elraiyah, Tarig ;
Wang, Zhen ;
Nabhan, Mohammed ;
Shippee, Nathan ;
Brito, Juan Pablo ;
Boehmer, Kasey ;
Hasan, Rim ;
Firwana, Belal ;
Erwin, Patricia ;
Eton, David ;
Sloan, Jeff ;
Montori, Victor ;
Asi, Noor ;
Abu Dabrh, Abd Moain ;
Murad, Mohammad Hassan .
BMC HEALTH SERVICES RESEARCH, 2014, 14
[7]   Introducing patients' and the public's perspectives to health technology assessment: A systematic review of international experiences [J].
Gagnon, Marie-Pierre ;
Desmartis, Marie ;
Lepage-Savary, Dolores ;
Gagnon, Johanne ;
St-Pierre, Michele ;
Rhainds, Marc ;
Lemieux, Renald ;
Gauvin, Francois-Pierre ;
Pollender, Hugo ;
Legare, France .
INTERNATIONAL JOURNAL OF TECHNOLOGY ASSESSMENT IN HEALTH CARE, 2011, 27 (01) :31-42
[8]  
Kuhn T.S., 2012, The structure of scientific revolutions, DOI [10.7208/chicago/9780226458144.001.0001, DOI 10.7208/CHICAGO/9780226458144.001.0001]
[9]   STrengthening the REporting of Genetic Association Studies (STREGA) - An Extension of the STROBE Statement [J].
Little, Julian ;
Higgins, Julian P. T. ;
Ioannidis, John P. A. ;
Moher, David ;
Gagnon, France ;
von Elm, Erik ;
Khoury, Muin J. ;
Cohen, Barbara ;
Davey-Smith, George ;
Grimshaw, Jeremy ;
Scheet, Paul ;
Gwinn, Marta ;
Williamson, Robin E. ;
Zou, Guang Yong ;
Hutchings, Kim ;
Johnson, Candice Y. ;
Tait, Valerie ;
Wiens, Miriam ;
Golding, Jean ;
van Duijn, Cornelia ;
McLaughlin, John ;
Paterson, Andrew ;
Wells, George ;
Fortier, Isabel ;
Freedman, Matthew ;
Zecevic, Maja ;
King, Richard ;
Infante-Rivard, Claire ;
Stewart, Alex F. R. ;
Birkett, Nick .
PLOS MEDICINE, 2009, 6 (02) :151-163
[10]   The impact of patient and public involvement on UK NHS health care: a systematic review [J].
Mockford, Carole ;
Staniszewska, Sophie ;
Griffiths, Frances ;
Herron-Marx, Sandra .
INTERNATIONAL JOURNAL FOR QUALITY IN HEALTH CARE, 2012, 24 (01) :28-38