Revue systématique sur la fréquence et la qualité de la déclaration de la participation des patients et du public dans la recherche sur la sécurité des patients

Titre original en anglais : Systematic review on the frequency and quality of reporting patient and public involvement in patient safety research

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Hammoud, S., Alsabek, L., Rogers, L., & McAuliffe, É. (2024). Systematic review on the frequency and quality of reporting patient and public involvement in patient safety research. BMC Health Services Research, 24(1), 532-532. https://doi.org/10.1186/s12913-024-11021-z

Date de publication: 26/04/2024 Ajout dans AutiHub: 18/07/2026 Type: Article Langue de l’article: Anglais
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Auteurs

Auteur·ices des publications
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Auteur·ices de la publication identifié·es comme autistes
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  1. Sahar Hammoud
  2. Laith Alsabek
  3. Lisa Rogers
  4. Éilish McAuliffe

Résumé

Résumé Contexte Ces dernières années, la participation des patients et du public (PPI) à la recherche a considérablement augmenté ; cependant, la déclaration de la PPI demeure insuffisante. Le Guide pour la déclaration de la participation des patients et du public (GRIPP2) a été élaboré afin d'améliorer la qualité et la cohérence de la déclaration de la PPI. L'objectif de cette revue systématique est d'identifier la fréquence et la qualité de la déclaration de la PPI dans la recherche sur la sécurité des patients (PS) à l'aide de la liste de contrôle GRIPP2. Méthodes Des recherches ont été effectuées dans Ovid MEDLINE, EMBASE, PsycINFO et CINAHL de 2018 à décembre 2023. Les études portant sur la PPI dans la recherche sur la PS ont été incluses. Nous avons inclus des études empiriques qualitatives, quantitatives, à méthodes mixtes et des études de cas. Seuls les articles publiés en anglais dans des revues évaluées par les pairs ont été inclus. La qualité de la déclaration de la PPI a été évaluée à l'aide de la version courte de la liste de contrôle (GRIPP2-SF). Résultats Au total, 8561 études ont été obtenues à partir des recherches dans les bases de données, des mises à jour et des vérifications des références, parmi lesquelles 82 répondaient aux critères d'éligibilité et ont été incluses dans cette revue. Les principaux thèmes de PS étaient liés à la sécurité des médicaments, à la PS générale et à la prévention des chutes. Les représentants des patients, les défenseurs, les groupes consultatifs de patients, les patients, les usagers des services et les consommateurs de soins de santé étaient les plus impliqués. La principale participation dans l'ensemble des études consistait à commenter ou à élaborer des matériels de recherche. Seules 6,1 % (n = 5) des études ont déclaré la PPI conformément à la liste de contrôle GRIPP2. Concernant la qualité de la déclaration selon les critères GRIPP2-SF, nos résultats montrent une déclaration sous-optimale, principalement en raison de l'absence de : réflexion critique sur la PPI dans l'étude ; déclaration de l'objectif de la PPI dans l'étude ; et déclaration de la mesure dans laquelle la PPI a influencé l'étude dans son ensemble. Conclusions Notre revue montre une faible fréquence de déclaration de la PPI dans la recherche sur la PS à l'aide de la liste de contrôle GRIPP2. En outre, elle révèle une qualité sous-optimale de la déclaration de la PPI selon les éléments du GRIPP2-SF. Les chercheurs, les financeurs, les éditeurs et les revues doivent promouvoir une déclaration cohérente et transparente de la PPI conformément à des lignes directrices de déclaration élaborées à l'échelle internationale, telles que le GRIPP2. Les lignes directrices fondées sur des données probantes pour la déclaration de la PPI devraient être encouragées et soutenues, car elles aident les futurs chercheurs à planifier et à déclarer la PPI plus efficacement. Enregistrement de l'essai Le protocole de la revue est enregistré auprès de PROSPERO (CRD42023450715).

Abstract Background In recent years, patient and public involvement (PPI) in research has significantly increased; however, the reporting of PPI remains poor. The Guidance for Reporting Involvement of Patients and the Public (GRIPP2) was developed to enhance the quality and consistency of PPI reporting. The objective of this systematic review is to identify the frequency and quality of PPI reporting in patient safety (PS) research using the GRIPP2 checklist. Methods Searches were performed in Ovid MEDLINE, EMBASE, PsycINFO, and CINAHL from 2018 to December, 2023. Studies on PPI in PS research were included. We included empirical qualitative, quantitative, mixed methods, and case studies. Only articles published in peer-reviewed journals in English were included. The quality of PPI reporting was assessed using the short form of the (GRIPP2-SF) checklist. Results A total of 8561 studies were retrieved from database searches, updates, and reference checks, of which 82 met the eligibility criteria and were included in this review. Major PS topics were related to medication safety, general PS, and fall prevention. Patient representatives, advocates, patient advisory groups, patients, service users, and health consumers were the most involved. The main involvement across the studies was in commenting on or developing research materials. Only 6.1% (n = 5) of the studies reported PPI as per the GRIPP2 checklist. Regarding the quality of reporting following the GRIPP2-SF criteria, our findings show sub-optimal reporting mainly due to failures in: critically reflecting on PPI in the study; reporting the aim of PPI in the study; and reporting the extent to which PPI influenced the study overall. Conclusions Our review shows a low frequency of PPI reporting in PS research using the GRIPP2 checklist. Furthermore, it reveals a sub-optimal quality in PPI reporting following GRIPP2-SF items. Researchers, funders, publishers, and journals need to promote consistent and transparent PPI reporting following internationally developed reporting guidelines such as the GRIPP2. Evidence-based guidelines for reporting PPI should be encouraged and supported as it helps future researchers to plan and report PPI more effectively. Trial registration The review protocol is registered with PROSPERO (CRD42023450715).

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