Co-design workshops to develop evidence synthesis summary formats for use by clinical guideline development groups

Author:

Murray Ruairi1,Magendran Erindaa2,Chander Neya2,Lynch Rosarie3,O’Neill Michelle1,Devane Declan4,Smith Susan M.5,Mahtani Kamal6,Ryan Máirín1,Clyne Barbara2,Sharp Melissa K2ORCID

Affiliation:

1. HIQA: Health Information and Quality Authority

2. RCSI University of Medicine and Health Sciences: RCSI Dublin

3. Department of Health National Patient Safety Office

4. University of Galway School of Nursing and Midwifery

5. Trinity College Dublin Faculty of Health Sciences

6. University of Oxford Nuffield Department of Clinical Medicine: University of Oxford Nuffield Department of Medicine

Abstract

Abstract Background: Evidence synthesis is used by decision-makers in various ways, such as developing evidence-based recommendations for clinical guidelines. Clinical guideline development groups (GDGs) typically discuss evidence synthesis findings in a multidisciplinary group, including patients, healthcare providers, policymakers, etc. A recent mixed methods systematic review (MMSR) identified no gold standard format for optimally presenting evidence synthesis findings to these groups. However, it provided 94 recommendations to help produce more effective summary formats for general evidence syntheses (e.g., systematic reviews). To refine the MMSR recommendations to create more actionable guidance for summary producers, we aimed to explore these 94 recommendations with participants involved in evidence synthesis and guideline development. Methods: We conducted a descriptive qualitative study using online focus group workshops in February and March 2023. These groups used a participatory co-design approach with interactive voting activities to identify preferences for a summary format's essential content and style. We created a topic guide focused on recommendations from the MMSR with mixed methods support, ≥3 supporting studies, and those prioritised by an expert advisory group via a pragmatic prioritisation exercise using the MoSCoW method (Must, Should, Could, and Will not haves). Eligible participants must be/have been involved in GDGs and/or evidence synthesis. Groups were recorded and transcribed. Two independent researchers analysed transcripts using directed content analysis with 94 pre-defined codes from the MMSR. Results: Thirty individuals participated in six focus groups. We coded 79 of the 94 pre-defined codes. Participants suggested a “less is more” structured approach that minimises methodological steps and statistical data, promoting accessibility to all audiences by judicious use of links to further information in the full report. They emphasised concise, consistently-presented formats which highlight key messages, flag readers to indicators of trust in the producers (i.e., logos, websites, and conflict of interest statements), and highlight the certainty of evidence (without extenuating details). Conclusions: This study identified guidance based on the preferences of guideline developers and evidence synthesis producers about the format of evidence synthesis summaries to support decision-making. Next steps involve developing and user-testing prototype formats through one-on-one semi-structured interviews to optimise evidence synthesis summaries and support decision-making.

Publisher

Research Square Platform LLC

Reference28 articles.

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5. Richter Sundberg L, Me RG. N. Reaching Beyond the Review of Research Evidence: A Qualitative Study of Decision Making During the Development of Clinical Practice Guidelines for Disease Prevention in Healthcare. BMC health services research [Internet]. 2017 May 11 [cited 2020 Jul 7];17(1). Available from: https://pubmed.ncbi.nlm.nih.gov/28490325/.

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