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Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol
INTRODUCTION: To advance person- and family-centred healthcare, government initiatives have supported the engagement of patients and family caregivers in decision-making in healthcare systems. There is, however, no consensus on how to define success for such initiatives. This scoping review aims to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858224/ https://www.ncbi.nlm.nih.gov/pubmed/31699750 http://dx.doi.org/10.1136/bmjopen-2019-032788 |
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author | Hamilton, Clayon Snow, M Elizabeth Clark, Nancy Gibson, Shannon Dehnadi, Maryam Lui, Michelle Koster, Andrew McLean, Janet Li, Linda C |
author_facet | Hamilton, Clayon Snow, M Elizabeth Clark, Nancy Gibson, Shannon Dehnadi, Maryam Lui, Michelle Koster, Andrew McLean, Janet Li, Linda C |
author_sort | Hamilton, Clayon |
collection | PubMed |
description | INTRODUCTION: To advance person- and family-centred healthcare, government initiatives have supported the engagement of patients and family caregivers in decision-making in healthcare systems. There is, however, no consensus on how to define success for such initiatives. This scoping review aims to identify the key elements for defining the quality of patient and family caregiver engagement in decision-making across the engagement domains (individual, community/organisation, system) of British Columbia’s healthcare system. We will use those elements to develop a conceptual evaluation framework. METHODS AND ANALYSIS: This scoping review follows Arskey and O’Malley’s methodology. (1) The research question was identified through team discussions. (2) Articles for data source will be identified using a librarian-informed search strategy for seven bibliographic databases as well as grey literature sources. (3) Selected articles will be relevant to the evaluation of patient and family caregiver engagement in healthcare systems. (4) Two researchers will independently extract data into predefined and emerging categories. (5) The researchers will reconcile and organise the identified elements. The research team’s collective perspective will then refine the elements, and select, interpret and summarise the results. (6) Persons from key stakeholder groups will be consulted to refine the emergent conceptual framework. ETHICS AND DISSEMINATION: We will seek ethics approval for the stakeholder consultation. This study follows an integrated knowledge translation approach. The results will inform evaluation of the Patients as Partners Initiative of the British Columbia Ministry of Health, and will be disseminated as a scientific article, a research brief, and presentations at conferences and stakeholder meetings. |
format | Online Article Text |
id | pubmed-6858224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-68582242019-12-03 Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol Hamilton, Clayon Snow, M Elizabeth Clark, Nancy Gibson, Shannon Dehnadi, Maryam Lui, Michelle Koster, Andrew McLean, Janet Li, Linda C BMJ Open Health Policy INTRODUCTION: To advance person- and family-centred healthcare, government initiatives have supported the engagement of patients and family caregivers in decision-making in healthcare systems. There is, however, no consensus on how to define success for such initiatives. This scoping review aims to identify the key elements for defining the quality of patient and family caregiver engagement in decision-making across the engagement domains (individual, community/organisation, system) of British Columbia’s healthcare system. We will use those elements to develop a conceptual evaluation framework. METHODS AND ANALYSIS: This scoping review follows Arskey and O’Malley’s methodology. (1) The research question was identified through team discussions. (2) Articles for data source will be identified using a librarian-informed search strategy for seven bibliographic databases as well as grey literature sources. (3) Selected articles will be relevant to the evaluation of patient and family caregiver engagement in healthcare systems. (4) Two researchers will independently extract data into predefined and emerging categories. (5) The researchers will reconcile and organise the identified elements. The research team’s collective perspective will then refine the elements, and select, interpret and summarise the results. (6) Persons from key stakeholder groups will be consulted to refine the emergent conceptual framework. ETHICS AND DISSEMINATION: We will seek ethics approval for the stakeholder consultation. This study follows an integrated knowledge translation approach. The results will inform evaluation of the Patients as Partners Initiative of the British Columbia Ministry of Health, and will be disseminated as a scientific article, a research brief, and presentations at conferences and stakeholder meetings. BMJ Publishing Group 2019-11-06 /pmc/articles/PMC6858224/ /pubmed/31699750 http://dx.doi.org/10.1136/bmjopen-2019-032788 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Health Policy Hamilton, Clayon Snow, M Elizabeth Clark, Nancy Gibson, Shannon Dehnadi, Maryam Lui, Michelle Koster, Andrew McLean, Janet Li, Linda C Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title | Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title_full | Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title_fullStr | Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title_full_unstemmed | Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title_short | Quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
title_sort | quality of patient, family, caregiver and public engagement in decision-making in healthcare systems: a scoping review protocol |
topic | Health Policy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858224/ https://www.ncbi.nlm.nih.gov/pubmed/31699750 http://dx.doi.org/10.1136/bmjopen-2019-032788 |
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