Literature DB >> 27280411

Lay and professional stakeholder involvement in scoping palliative care issues: Methods used in seven European countries.

Louise Brereton1, Christine Ingleton2, Clare Gardiner2, Elizabeth Goyder1, Kati Mozygemba3, Kristin Bakke Lysdahl4, Marcia Tummers5, Dario Sacchini6, Wojciech Leppert7, Aurelija Blaževičienė8, Gert Jan van der Wilt5, Pietro Refolo6, Martina De Nicola6, James Chilcott1, Wija Oortwijn9.   

Abstract

BACKGROUND: Stakeholders are people with an interest in a topic. Internationally, stakeholder involvement in palliative care research and health technology assessment requires development. Stakeholder involvement adds value throughout research (from prioritising topics to disseminating findings). Philosophies and understandings about the best ways to involve stakeholders in research differ internationally. Stakeholder involvement took place in seven countries (England, Germany, Italy, Lithuania, the Netherlands, Norway and Poland). Findings informed a project that developed concepts and methods for health technology assessment and applied these to evaluate models of palliative care service delivery. AIMS: To report on stakeholder involvement in the INTEGRATE-HTA project and how issues identified informed project development.
DESIGN: Using stakeholder consultation or a qualitative research design, as appropriate locally, stakeholders in seven countries acted as 'advisors' to aid researchers' decision making. Thematic analysis was used to identify key issues across countries. SETTING/PARTICIPANTS: A total of 132 stakeholders (82 professionals and 50 'lay' people) aged ⩾18 participated in individual face-to-face or telephone interviews, consultation meetings or focus groups.
RESULTS: Different stakeholder involvement methods were used successfully to identify key issues in palliative care. A total of 23 issues common to three or more countries informed decisions about the intervention and comparator of interest, sub questions and specific assessments within the health technology assessment.
CONCLUSION: Stakeholders, including patients and families undergoing palliative care, can inform project decision making using various involvement methods according to the local context. Researchers should consider local understandings about stakeholder involvement as views of appropriate and feasible methods vary. Methods for stakeholder involvement, especially consultation, need further development.

Entities:  

Keywords:  Patient involvement; health technology assessment; palliative care

Mesh:

Year:  2016        PMID: 27280411     DOI: 10.1177/0269216316649154

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  8 in total

1.  Designing and Implementing Deliberative Processes for Health Technology Assessment: A Good Practices Report of a Joint HTAi/ISPOR Task Force.

Authors:  Wija Oortwijn; Don Husereau; Julia Abelson; Edwine Barasa; Diana Dana Bayani; Vania Canuto Santos; Anthony Culyer; Karen Facey; David Grainger; Katharina Kieslich; Daniel Ollendorf; Andrés Pichon-Riviere; Lars Sandman; Valentina Strammiello; Yot Teerawattananon
Journal:  Int J Technol Assess Health Care       Date:  2022-06-03       Impact factor: 2.406

2.  Designing and Implementing Deliberative Processes for Health Technology Assessment: A Good Practices Report of a Joint HTAi/ISPOR Task Force.

Authors:  Wija Oortwijn; Don Husereau; Julia Abelson; Edwine Barasa; Diana Dana Bayani; Vania Canuto Santos; Anthony Culyer; Karen Facey; David Grainger; Katharina Kieslich; Daniel Ollendorf; Andrés Pichon-Riviere; Lars Sandman; Valentina Strammiello; Yot Teerawattananon
Journal:  Value Health       Date:  2022-06       Impact factor: 5.101

3.  How to specify healthcare process improvements collaboratively using rapid, remote consensus-building: a framework and a case study of its application.

Authors:  Jan W van der Scheer; Matthew Woodward; Akbar Ansari; Tim Draycott; Cathy Winter; Graham Martin; Karolina Kuberska; Natalie Richards; Ruth Kern; Mary Dixon-Woods
Journal:  BMC Med Res Methodol       Date:  2021-05-11       Impact factor: 4.615

4.  Building Strong Clinician-Researcher Collaborations for Successful Hospice and Palliative Care Research.

Authors:  Susan Lysaght Hurley; Susan DeSanto-Madeya; Christine A Fortney; Seiko Izumi; Veerawat Phongtankuel; Joan G Carpenter
Journal:  J Hosp Palliat Nurs       Date:  2022-02-01       Impact factor: 1.918

Review 5.  Patient and carer involvement in palliative care research: An integrative qualitative evidence synthesis review.

Authors:  Eleni Chambers; Clare Gardiner; Jill Thompson; Jane Seymour
Journal:  Palliat Med       Date:  2019-06-28       Impact factor: 4.762

6.  EMTReK: An Evidence-based Model for the Transfer & Exchange of Research Knowledge-Five Case Studies in Palliative Care.

Authors:  Cathy Payne; Mary J Brown; Suzanne Guerin; W George Kernohan
Journal:  SAGE Open Nurs       Date:  2019-07-26

7.  Stakeholder-engaged process for refining the design of a clinical trial in home hospice.

Authors:  Jennifer Tjia; Margaret Clayton; Germán Chiriboga; Brooke Staples; Geraldine Puerto; Lynley Rappaport; Susan DeSanto-Madeya
Journal:  BMC Med Res Methodol       Date:  2021-04-30       Impact factor: 4.615

8.  Potential Barriers of Patient Involvement in Health Technology Assessment in Central and Eastern European Countries.

Authors:  Maria Dimitrova; Ivett Jakab; Zornitsa Mitkova; Maria Kamusheva; Konstantin Tachkov; Bertalan Nemeth; Antal Zemplenyi; Dalia Dawoud; Diana M J Delnoij; François Houýez; Zoltan Kalo
Journal:  Front Public Health       Date:  2022-07-28
  8 in total

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