Evidence map›Paper›PMID 39102668›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2024

How to mobilise users' experiential knowledge in the evaluation of advanced technologies and practices in Quebec? The example of the permanent users' and relatives' panel.

Marie-Pascale Pomey, Sandra Pelaez, Enora Le Roux, Oliver Demers-Payette, Marie-Claude Sirois, Louis Lochhead, Isabelle Ganache, Louise Normandin, Audrey L'Espérance, Michèle de Guise

Abstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Marie-Pascale PomeyResearch Centre of the University of Montreal Hospital Centre, Montréal, Québec, Canada.ORCID 0000-0001-5180-8139
Sandra PelaezInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.
Enora Le RouxResearch Centre of the University of Montreal Hospital Centre, Montréal, Québec, Canada.
Oliver Demers-PayetteInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.
Marie-Claude SiroisInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.
Louis LochheadInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.
Isabelle GanacheInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.
Louise NormandinResearch Centre of the University of Montreal Hospital Centre, Montréal, Québec, Canada.
Audrey L'EspéranceCentre d'excellence sur le partenariat avec les patients et le public, Montréal, Québec, Canada.
Michèle de GuiseInstitut national d'excellence en santé et services sociaux (INESSS), Montréal, Québec, Canada.

Funding

Fonds de Recherche du Québec - Santé
6 · The paper itself

Abstract

introductionWith the purpose of supporting scientific professionals and helping them to better integrate the expertise of users in their work, a users' and relatives' panel (URP) was set up at the National Institute for Excellence in Health and Social Services in Quebec (INESSS), Canada for the social services and mental health directorate. URPs are advisory structures that mobilise the experiential knowledge of people affected by various issues.

objectivesThe objective of this study is to assess from a diverse stakeholders' perceptions: (1) the experience of developing and implementing the URP within the context of an Agencies for Health Technology Assessment and Assessment of Social Services (AHTAASS), (2) the contribution of such a URP, (3) the challenges encountered and (4) the perspectives of improvement for the following years. METHODOLOGY: We conducted a qualitative descriptive evaluation study. Nineteen interviews were conducted: six with URP members and 13 with staff representatives. The documents related to the creation of the panel, the URP minutes summarising the discussions and the reports published during that period were collected and analysed. Following a preliminary round of data analysis, a debriefing meeting was conducted with a few participants to validate the results.

resultsThe panel was set up as part of the INESSS' desire to better integrate experiential knowledge into its recommendations. Twelve projects were presented to the panel on various themes. The URP enabled health professionals to consider dimensions they had not identified, to better integrate the experiential data collected from users into their work and to develop recommendations that made more sense to users. Panel members and INESSS professionals learned to work together, moving the working methods from consultation to collaboration and even coconstruction. Based on the panel's significant contribution, the INESSS decided to maintain it and to strengthen its place in its system to better integrate the experiential knowledge of users into its work.

conclusionThis research illustrates how AHTAASS can set up a URP composed exclusively of users, and how it can contribute and be evaluated. It shows that URPs are structures that value the sharing of experiential knowledge of its members, humanise decision-making and give meaning to the work done by scientific professionals. PATIENT OR PUBLIC CONTRIBUTION: One patient-researcher has contributed to the preparation and writing of this manuscript.

Indexed as

Qualitative ResearchTechnology Assessment, BiomedicalFamilyHumansInterviews as TopicQuebecSocial Workevaluationhealth technology assessment agencysocial servicesusers' experiencesusers' panelusers' perspective

Identifiers

PMID39102668
PMCPMC10767678

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.