Literature DB >> 21176014

Patients' and clinicians' research priorities.

Ruth J Stewart1, Jenny Caird, Kathryn Oliver, Sandy Oliver.   

Abstract

BACKGROUND: If research addresses the questions of relevance to patients and clinicians, decision-makers will be better equipped to design and deliver health services which meet their needs. To this end, a number of initiatives have engaged patients and clinicians in setting research agendas. This paper aimed to scope the research literature addressing such efforts.
METHODS: A systematic search strategy combined electronic searches of bibliographic databases with handsearching and contacting key authors. Two researchers, initially working independently, described the relevant reports.
FINDINGS: Over 250 studies addressed patients' or clinicians' priorities for research and outcomes for assessment. This literature described different routes for patients and clinicians to contribute to research agendas. Two-thirds of the studies addressing patients' or clinicians' research questions were applicable across health care, with the remainder focussed on specific health conditions. The 27 formal studies of patient involvement revealed a literature that has grown in the last decade. Although only nine studies engaged patients and clinicians in identifying research questions together, they show that methods have advanced over time, with all of them engaging participants directly and repeatedly in facilitated debate and most employing formal decision-making procedures.
CONCLUSION: A sizeable literature is available to inform priorities for research and the methods for setting research agendas with patients and clinicians. We recommend that research funders and researchers draw on this literature to provide relevant research for health service decision-makers.
© 2010 Blackwell Publishing Ltd.

Entities:  

Mesh:

Year:  2010        PMID: 21176014      PMCID: PMC5060597          DOI: 10.1111/j.1369-7625.2010.00648.x

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  25 in total

1.  Suggestions in maternal and child health for the National Technology Assessment Programme: a consideration of consumer and professional priorities.

Authors:  R Johanson; C Rigby; M Newburn; M Stewart; P Jones
Journal:  J R Soc Promot Health       Date:  2002-03

2.  The way forward: identifying palliative nursing research priorities within a hospice.

Authors:  L Daniels; C Howlett
Journal:  Int J Palliat Nurs       Date:  2001-09

3.  OMERACT 6 brings new perspectives to rheumatology measurement research.

Authors:  Kenneth G Saag
Journal:  J Rheumatol       Date:  2003-04       Impact factor: 4.666

4.  Illinois's child welfare research agenda: an approach to building consensus for practice-based research.

Authors:  Michelle A Johnson; Susan J Wells; Mark F Testa; Jess McDonald
Journal:  Child Welfare       Date:  2003 Jan-Feb

Review 5.  Priorities for antiretroviral therapy research in sub-Saharan Africa: a 2002 consensus conference in Zambia.

Authors:  Isaac Zulu; Paula Schuman; Rosemary Musonda; Elwyn Chomba; Kasonde Mwinga; Moses Sinkala; Maureen Chisembele; Peter Mwaba; Dorothy Kasonde; Sten H Vermund
Journal:  J Acquir Immune Defic Syndr       Date:  2004-07-01       Impact factor: 3.731

6.  Public involvement in setting a national research agenda: a mixed methods evaluation.

Authors:  Sandy Oliver; David G Armes; Gill Gyte
Journal:  Patient       Date:  2009-09-01       Impact factor: 3.883

7.  The progress of lay involvement in the NHS Research and Development Programme.

Authors:  S Oliver
Journal:  J Eval Clin Pract       Date:  1996-11       Impact factor: 2.431

Review 8.  Outcomes from the Patient Perspective Workshop at OMERACT 6.

Authors:  John Kirwan; Turid Heiberg; Sarah Hewlett; Rod Hughes; Tore Kvien; Monica Ahlmèn; Maarten Boers; Patricia Minnock; Kenneth Saag; Beverley Shea; Maria Suarez Almazor; Erik Taal
Journal:  J Rheumatol       Date:  2003-04       Impact factor: 4.666

9.  Health researchers' attitudes towards public involvement in health research.

Authors:  Jill Thompson; Rosemary Barber; Paul R Ward; Jonathan D Boote; Cindy L Cooper; Christopher J Armitage; Georgina Jones
Journal:  Health Expect       Date:  2009-04-22       Impact factor: 3.377

10.  OMERACT: an international initiative to improve outcome measurement in rheumatology.

Authors:  Peter Tugwell; Maarten Boers; Peter Brooks; Lee Simon; Vibeke Strand; Leanne Idzerda
Journal:  Trials       Date:  2007-11-26       Impact factor: 2.279

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  50 in total

1.  Public views on participating in newborn screening using genome sequencing.

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Carolyn Barg; Celine Cressman; June C Carroll; Brenda J Wilson; Julian Little; Denise Avard; Michael Painter-Main; Judith Allanson; Yves Giguere; Pranesh Chakraborty
Journal:  Eur J Hum Genet       Date:  2014-02-19       Impact factor: 4.246

2.  Comparative effectiveness topics from a large, integrated delivery system.

Authors:  Kim N Danforth; Carrie D Patnode; Tanya J Kapka; Melissa G Butler; Bernadette Collins; Amy Compton-Phillips; Raymond J Baxter; Jed Weissberg; Elizabeth A McGlynn; Evelyn P Whitlock
Journal:  Perm J       Date:  2013

3.  The top research questions asked by people with lived depression experience in Alberta: a survey.

Authors:  Lorraine J Breault; Katherine Rittenbach; Kelly Hartle; Robbie Babins-Wagner; Catherine de Beaudrap; Yamile Jasaui; Emily Ardell; Scot E Purdon; Ashton Michael; Ginger Sullivan; Aakai'naimsskai'piiaakii Sharon Ryder Unger; Lorin Vandall-Walker; Brad Necyk; Kiara Krawec; Elizabeth Manafò; Ping Mason-Lai
Journal:  CMAJ Open       Date:  2018-09-28

4.  Patients as Agents in Behavioral Health Research and Service Provision: Recommendations to Support the Learning Health System.

Authors:  Hannah K Galvin; Carolyn Petersen; Vignesh Subbian; Anthony Solomonides
Journal:  Appl Clin Inform       Date:  2019-11-06       Impact factor: 2.342

5.  A Critical Discussion of Patient Engagement in Research.

Authors:  Andrea Elaine Bombak; Heather M Hanson
Journal:  J Patient Cent Res Rev       Date:  2017-01-31

Review 6.  Establishing local priorities for a health research agenda.

Authors:  Rebecca Whear; Jo Thompson-Coon; Kate Boddy; Helen Papworth; Julie Frier; Ken Stein
Journal:  Health Expect       Date:  2012-12-06       Impact factor: 3.377

Review 7.  Patient and service user engagement in research: a systematic review and synthesized framework.

Authors:  Nathan D Shippee; Juan Pablo Domecq Garces; Gabriela J Prutsky Lopez; Zhen Wang; Tarig A Elraiyah; Mohammed Nabhan; Juan P Brito; Kasey Boehmer; Rim Hasan; Belal Firwana; Patricia J Erwin; Victor M Montori; M Hassan Murad
Journal:  Health Expect       Date:  2013-06-03       Impact factor: 3.377

8.  A Modified AUGIS Delphi Process to Establish Future Research Priorities in Benign Upper Gastrointestinal Surgery.

Authors:  Michael S J Wilson; P Vaughan-Shaw; C Boyle; G L Yong; S Oglesby; R Skipworth; P Lamb; E A T Griffiths; S E A Attwood
Journal:  World J Surg       Date:  2020-04       Impact factor: 3.352

9.  Patient involvement in research programming and implementation: A responsive evaluation of the Dialogue Model for research agenda setting.

Authors:  Tineke A Abma; Carina A C M Pittens; Merel Visse; Janneke E Elberse; Jacqueline E W Broerse
Journal:  Health Expect       Date:  2014-05-30       Impact factor: 3.377

10.  Comparative analysis of stakeholder experiences with an online approach to prioritizing patient-centered research topics.

Authors:  Dmitry Khodyakov; Sean Grant; Daniella Meeker; Marika Booth; Nathaly Pacheco-Santivanez; Katherine K Kim
Journal:  J Am Med Inform Assoc       Date:  2017-05-01       Impact factor: 4.497

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