Literature DB >> 16266423

Consumer-driven health care: building partnerships in research.

Beverley Shea1, Nancy Santesso, Ann Qualman, Turid Heiberg, Amye Leong, Maria Judd, Vivian Robinson, George Wells, Peter Tugwell.   

Abstract

Over the past four decades, there has been a widespread movement to increase the involvement of patients and the public in health care. Strategies to effectively foster consumer participation are occurring within all research activities from research priority setting to utilization. One of the ten principles of the Cochrane Collaboration is to 'enable wide participation', and this includes consumers. The Cochrane Musculoskeletal Group (CMSG) is a review group of 50 within the Collaboration that has been working to increase consumer participation since its inception in 1993. Based in Canada, the CMSG has embraced the concept of knowledge translation as advocated by the Canadian Institutes of Health Research. The emphasis in knowledge translation is on interactions or partnerships between researchers and users to facilitate the use of relevant research in decision making. While the CMSG recognizes the importance of reaching all users, much of its work has focused on developing relationships with people with musculoskeletal diseases to enhance consumer participation in research. The CMSG has built a network of consumer members who guide research priorities, peer review systematic reviews and also promote and facilitate consumer-appropriate knowledge dissemination. Consumers were recruited through links with other arthritis organizations and the recruitment continues. Specific roles were established for the consumer team and responsibilities of the CMSG staff developed. The continuing development of a diversified team of consumer participants enables the CMSG to produce and promote access to high quality relevant systematic reviews and summaries of those reviews to the consumer.

Entities:  

Mesh:

Year:  2005        PMID: 16266423      PMCID: PMC5060309          DOI: 10.1111/j.1369-7625.2005.00347.x

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


  3 in total

1.  A consumer involvement model for health technology assessment in Canada.

Authors:  Jayne Pivik; Elisabeth Rode; Christopher Ward
Journal:  Health Policy       Date:  2004-08       Impact factor: 2.980

Review 2.  Involving consumers in research and development agenda setting for the NHS: developing an evidence-based approach.

Authors:  S Oliver; L Clarke-Jones; R Rees; R Milne; P Buchanan; J Gabbay; G Gyte; A Oakley; K Stein
Journal:  Health Technol Assess       Date:  2004-04       Impact factor: 4.014

3.  Towards the measurement of community participation.

Authors:  W Bichmann; S B Rifkin; M Shrestha
Journal:  World Health Forum       Date:  1989
  3 in total
  26 in total

1.  Involvement of the consumer voice.

Authors:  Hazel Thornton; Michael Baum; Mike Clarke
Journal:  Health Expect       Date:  2006-03       Impact factor: 3.377

2.  Practical Guidance for Involving Stakeholders in Health Research.

Authors:  Thomas W Concannon; Sean Grant; Vivian Welch; Jennifer Petkovic; Joseph Selby; Sally Crowe; Anneliese Synnot; Regina Greer-Smith; Evan Mayo-Wilson; Ellen Tambor; Peter Tugwell
Journal:  J Gen Intern Med       Date:  2018-12-18       Impact factor: 5.128

Review 3.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

4.  Consumer involvement in systematic reviews of comparative effectiveness research.

Authors:  Julia Kreis; Milo A Puhan; Holger J Schünemann; Kay Dickersin
Journal:  Health Expect       Date:  2012-03-06       Impact factor: 3.377

5.  Patient-expert partnerships in research: how to stimulate inclusion of patient perspectives.

Authors:  Janneke E Elberse; J Francisca Caron-Flinterman; Jacqueline E W Broerse
Journal:  Health Expect       Date:  2010-12-22       Impact factor: 3.377

Review 6.  A systematic review of the impact of patient and public involvement on service users, researchers and communities.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Patient       Date:  2014       Impact factor: 3.883

7.  Do different stakeholder groups share mental health research priorities? A four-arm Delphi study.

Authors:  Christabel Owens; Ann Ley; Peter Aitken
Journal:  Health Expect       Date:  2008-12       Impact factor: 3.377

Review 8.  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

9.  Do not forget the professional--the value of the FIRST model for guiding the structural involvement of patients in rheumatology research.

Authors:  Maarten P T de Wit; Janneke E Elberse; Jacqueline E W Broerse; Tineke A Abma
Journal:  Health Expect       Date:  2013-01-31       Impact factor: 3.377

10.  PartecipaSalute, an Italian project to involve lay people, patients' associations and scientific-medical representatives in the health debate.

Authors:  Paola Mosconi; Cinzia Colombo; Roberto Satolli; Alessandro Liberati
Journal:  Health Expect       Date:  2007-06       Impact factor: 3.377

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.