Literature DB >> 25194573

Patient and public engagement in health-related quality of life and patient-reported outcomes research: what is important and why should we care? Findings from the first ISOQOL patient engagement symposium.

Kirstie Haywood1, Jo Brett, Sam Salek, Nancy Marlett, Colin Penman, Svetlana Shklarov, Colleen Norris, Maria Jose Santana, Sophie Staniszewska.   

Abstract

PURPOSE: Recent years have witnessed growing international interest in the active involvement, or engagement [patient engagement (PE)], of patients and the public in health services research. However, there is limited evidence of the extent or impact of PE in health-related quality of life (HRQL) and patient-reported outcomes (PRO) research. Therefore, in October 2013, the International Society for Quality of Life research (ISOQOL) hosted its first symposium, which sought to explore the potential for PE in this field.
METHODS: A 'World Café' format encouraged the exploration of three 'menu' questions' in small groups at round tables. Views, opinions and concerns were captured. A thematic analysis was undertaken, and key themes listed.
RESULTS: Sixty conference attendees participated in the 'PE Café', which lasted for 90 min. A diversity of experience was communicated, with most participants positive about the potential for PE. Similarities and differences in approaches, barriers and solutions were identified. However, a key message focused on the uncertainty about how to effectively engage with patients throughout the research process. Moreover, the lack of evidence-base demonstrating the impact of PE was a significant concern. No patient partners participated in the meeting.
CONCLUSION: This study describes the first international exploration of PE in HRQL and PRO research. Discussions highlighted that, in the absence of good practice guidelines, a framework or toolkit of how to embed PE within HRQL and PRO research is required. Moreover, this framework should support the rigorous evaluation of PE impact. ISOQOL should be instrumental in taking these ideas forward, actively engaging with patient partners towards shaping a future ISOQOL PE strategy.

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Year:  2014        PMID: 25194573     DOI: 10.1007/s11136-014-0796-3

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  21 in total

1.  A new taxonomy for stakeholder engagement in patient-centered outcomes research.

Authors:  Thomas W Concannon; Paul Meissner; Jo Anne Grunbaum; Newell McElwee; Jeanne-Marie Guise; John Santa; Patrick H Conway; Denise Daudelin; Elaine H Morrato; Laurel K Leslie
Journal:  J Gen Intern Med       Date:  2012-04-13       Impact factor: 5.128

2.  The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research.

Authors:  Sophie Staniszewska; Jo Brett; Carole Mockford; Rosemary Barber
Journal:  Int J Technol Assess Health Care       Date:  2011-10       Impact factor: 2.188

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.  Stakeholder participation in comparative effectiveness research: defining a framework for effective engagement.

Authors:  Patricia A Deverka; Danielle C Lavallee; Priyanka J Desai; Laura C Esmail; Scott D Ramsey; David L Veenstra; Sean R Tunis
Journal:  J Comp Eff Res       Date:  2012-03       Impact factor: 1.744

Review 5.  Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review.

Authors:  Kirstie L Haywood; Sophie Staniszewska; Sarah Chapman
Journal:  Qual Life Res       Date:  2011-05-18       Impact factor: 4.147

Review 6.  A practice-based tool for engaging stakeholders in future research: a synthesis of current practices.

Authors:  Jeanne-Marie Guise; Christen O'Haire; Melissa McPheeters; Carole Most; Lia Labrant; Kathy Lee; Erika K Barth Cottrell; Elaine Graham
Journal:  J Clin Epidemiol       Date:  2013-03-13       Impact factor: 6.437

7.  Progress on incorporating the patient perspective in outcome assessment in rheumatology and the emergence of life impact measures at OMERACT 9.

Authors:  John R Kirwan; Stanton Newman; Peter S Tugwell; George A Wells; Sarah Hewlett; Leanne Idzera; Britta Laslo; Lyn M March; Patricia Minnock; Pam Montie; Jo Nicklin; Tamara Rader; Pamela Richards; Tessa C Sanderson; Maria Suarez-Almazor; Elizabeth Tanjong-Ghogomu; Erin Ueffing; Vivian Welch
Journal:  J Rheumatol       Date:  2009-09       Impact factor: 4.666

8.  A model for incorporating patient and stakeholder voices in a learning health care network: Washington State's Comparative Effectiveness Research Translation Network.

Authors:  Emily Beth Devine; Rafael Alfonso-Cristancho; Allison Devlin; Todd C Edwards; Ellen T Farrokhi; Larry Kessler; Danielle C Lavallee; Donald L Patrick; Sean D Sullivan; Peter Tarczy-Hornoch; N David Yanez; David R Flum
Journal:  J Clin Epidemiol       Date:  2013-08       Impact factor: 6.437

9.  Involving patient research partners has a significant impact on outcomes research: a responsive evaluation of the international OMERACT conferences.

Authors:  Maarten de Wit; Tineke Abma; Marije Koelewijn-van Loon; Sarah Collins; John Kirwan
Journal:  BMJ Open       Date:  2013-05-09       Impact factor: 2.692

10.  Facilitating and inhibiting factors for long-term involvement of patients at outcome conferences--lessons learnt from a decade of collaboration in OMERACT: a qualitative study.

Authors:  Maarten de Wit; Tineke Abma; Marije Koelewijn-Van Loon; Sarah Collins; John Kirwan
Journal:  BMJ Open       Date:  2013-08-23       Impact factor: 2.692

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  30 in total

1.  Introduction to special section on patient engagement.

Authors:  Carolyn E Schwartz; Dennis A Revicki
Journal:  Qual Life Res       Date:  2015-05       Impact factor: 4.147

2.  Patient-centered research and practice in the era of genomics: a novel approach.

Authors:  Sam Salek; Esther Oliva; Tatyana Ionova
Journal:  Haematologica       Date:  2016-07       Impact factor: 9.941

3.  Introduction to special section: measuring what matters.

Authors:  Steven I Blum; Sara Ahmed; Emuella Flood; Frans J Oort; Carolyn E Schwartz
Journal:  Qual Life Res       Date:  2018-01       Impact factor: 4.147

Review 4.  Patient-reported outcome measures in older people with hip fracture: a systematic review of quality and acceptability.

Authors:  K L Haywood; J Brett; E Tutton; S Staniszewska
Journal:  Qual Life Res       Date:  2016-10-20       Impact factor: 4.147

5.  Moving towards a more inclusive patient and public involvement in health research paradigm: the incorporation of a trauma-informed intersectional analysis.

Authors:  Carolyn Shimmin; Kristy D M Wittmeier; Josée G Lavoie; Evan D Wicklund; Kathryn M Sibley
Journal:  BMC Health Serv Res       Date:  2017-08-07       Impact factor: 2.655

6.  Successful Stepwise Development of Patient Research Partnership: 14 Years' Experience of Actions and Consequences in Outcome Measures in Rheumatology (OMERACT).

Authors:  Maarten de Wit; John R Kirwan; Peter Tugwell; Dorcas Beaton; Maarten Boers; Peter Brooks; Sarah Collins; Philip G Conaghan; Maria-Antonietta D'Agostino; Cathie Hofstetter; Rod Hughes; Amye Leong; Ann Lyddiatt; Lyn March; James May; Pamela Montie; Pamela Richards; Lee S Simon; Jasvinder A Singh; Vibeke Strand; Marieke Voshaar; Clifton O Bingham; Laure Gossec
Journal:  Patient       Date:  2017-04       Impact factor: 3.883

7.  Patient participation as an integral part of patient-reported outcomes development ensures the representation of the patient voice: a case study from the field of rheumatology.

Authors:  M P T de Wit; T K Kvien; L Gossec
Journal:  RMD Open       Date:  2015-08-05

Review 8.  Patient-Reported Outcomes in Patients with Chronic Kidney Disease and Kidney Transplant-Part 1.

Authors:  Evan Tang; Aarushi Bansal; Marta Novak; Istvan Mucsi
Journal:  Front Med (Lausanne)       Date:  2018-01-15

9.  Satisfaction with quality of ICU care for patients and families: the euroQ2 project.

Authors:  Hanne Irene Jensen; Rik T Gerritsen; Matty Koopmans; Lois Downey; Ruth A Engelberg; J Randall Curtis; Peter E Spronk; Jan G Zijlstra; Helle Ørding
Journal:  Crit Care       Date:  2017-09-07       Impact factor: 9.097

10.  Research Involvement and Engagement: reflections so far and future directions.

Authors:  Richard Stephens; Sophie Staniszewska
Journal:  Res Involv Engagem       Date:  2017-11-08
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