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Cunningham M, France EF, Ring N, et al. Developing a reporting guideline to improve meta-ethnography in health research: the eMERGe mixed-methods study. Southampton (UK): NIHR Journals Library; 2019 Feb. (Health Services and Delivery Research, No. 7.4.)

Cover of Developing a reporting guideline to improve meta-ethnography in health research: the eMERGe mixed-methods study

Developing a reporting guideline to improve meta-ethnography in health research: the eMERGe mixed-methods study.

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Scientific summary

Background

Meta-ethnography is a widely used and thorough qualitative synthesis method in which researchers select, analyse and interpret qualitative studies to answer focused questions on a specific topic (e.g. people’s experiences of having, and being treated for, arthritis). Meta-ethnography is suited to developing theory and can lead to new conceptual understandings of complex health-care issues.

Findings from high-quality meta-ethnographies have been used in clinical guidelines. However, the reporting quality of published meta-ethnographies varies and is often poor. The analytic synthesis process is particularly poorly described. Users of research evidence need clear reporting of the methods, analysis and findings to be able to asses, use and have confidence in the output of meta-ethnographies. A generic guideline for reporting qualitative evidence synthesis exists. However, meta-ethnography has unique, complex analytic synthesis processes that are not covered by the generic guideline, and bespoke guidelines are required to improve the completeness and clarity of meta-ethnography reporting.

A systematic, mixed-methods approach is recommended for good practice in developing reporting guidance including literature reviews, workshops involving methodological experts, consensus studies, and developing a guidance statement and an accompanying explanatory document. The meta-ethnography reporting guidance (eMERGe) project followed this approach to create evidence-based meta-ethnography reporting guidance.

Objectives

The eMERGe project aimed to create evidence-based meta-ethnography reporting guidance, by answering the following research questions:

  • What are the existing recommendations and guidance for conducting and reporting each process in a meta-ethnography, and why?
  • What good practice principles can we identify in meta-ethnography conduct and reporting to inform recommendations and guidance?
  • From these good practice principles, what standards can we develop in meta-ethnography conduct and reporting to inform recommendations and guidance?
  • What is the consensus of experts and other stakeholders on key standards and domains for reporting meta-ethnography in an abstract and main report/publication?

Methods of guidance development

The project included four key stages, conducted by the project team, in consultation with one of the originators of meta-ethnography, Professor George Noblit, and supported by a Project Advisory Group of national and international academics, policy experts and lay advisors who had an active role in the development of the guidance and whose contribution was central throughout the project.

Stage 1 involved a systematic review of methodological guidance using comprehensive literature searches, from which we identified good practice principles and recommendations for conducting and reporting meta-ethnographies.

Stage 2 involved a review and audit of published meta-ethnographies. There were three parts to this stage of the project: (2.1a) documentary analysis of a sample of both seminal and poorly reported published meta-ethnographies, (2.1b) exploration of professional end-user views on the utility of seminal and poorly reported meta-ethnographies for policy and practice and (2.2) an audit of published health- or social care-related meta-ethnographies to identify the extent to which they met the good practice principles and recommendations identified in stages 1, 2.1a and 2.1b.

Stage 3 involved finding consensus on the reporting items through an online workshop and two identical eDelphi (Version 1, Duncan E, Swinger K, University of Stirling, Stirling, UK) consensus studies that were run in parallel: one with meta-ethnography method expert participants and another with key stakeholders who use synthesised evidence (i.e. professional evidence users and patient and public representatives). These groups were separated, as each brings specific expertise and could have potentially different views on the importance of specific items.

Stage 4 covered the development of the guidance table, reporting criteria, explanatory notes and extensions to the guidance, along with training materials to support the use of the guidance. This process was iterative, and involved input from the project team and the wider Project Advisory Group.

Results

Fifty-seven papers that gave methodological guidance about meta-ethnography reporting or conduct were included in the stage 1 systematic review. The analysis of these papers identified that more clarity is required in reporting the methods for selecting a qualitative evidence synthesis methodology, and in how the reading, translation and synthesis phases (4–6) of meta-ethnography are conducted.

The documentary analysis of 29 seminal and poorly reported meta-ethnographies (stage 2.1a), together with the interviews of potential end-users of meta-ethnographies (stage 2.1b), enabled us to identify good practice principles and contributed towards our development of standards in the reporting of meta-ethnographies.

From the results of stages 1, 2.1a and 2.1b, we identified good practice principles and standards that we then developed into an audit tool of 109 measurable provisional standards. After applying these standards to 19 published meta-ethnography papers in an audit, we reviewed and refined the provisional standards to create 69 reporting items for the eDelphi studies.

Sixty-two people (39 experts and 23 professional/lay people) completed all three rounds of the eDelphi studies (stage 3). Four items failed to reach consensus in both eDelphi studies and so were excluded from the final guidance. Participants reached consensus that 65 out of 69 items should be included in the guidance.

The final reporting criteria for the guidance were developed from the 65 items that met consensus in the eDelphi studies. A small writing group was formed to write the guidance table and explanatory notes. During the writing process, the writing group sought regular feedback from the wider project team and the Project Advisory Group. The guidance was developed through a series of iterations, with feedback being sought on specific issues, namely the structure of the guidance, merging related items, readability and usability of the guidance, and checking against the eDelphi items. Members of the Project Advisory Group and project team reviewed and agreed the final guidance table and explanatory notes.

The project team developed training materials to support use of the guidance, including four short films about meta-ethnography reporting and a webinar about how to use the guidance material. The training material is freely available online at www.emergeproject.org (accessed 26 March 2018).

Conclusions

The eMERGe meta-ethnography reporting guidance has been developed following a rigorous and systematic mixed-methods approach, as recommended in guidelines for developing health research reporting guidelines. The guidance was developed to improve the clarity and completeness of meta-ethnography reporting, and to maximise the value and utility of meta-ethnography for informing policy and practice decisions. In future, the guidance may need to be refined or updated to encompass methodological advances and accommodate changes identified after evaluation of the impact of the guidance.

Study registration

This study is registered as PROSPERO CRD42015024709 for the stage 1 systematic review.

Copyright © Queen’s Printer and Controller of HMSO 2019. This work was produced by Cunningham et al. under the terms of a commissioning contract issued by the Secretary of State for Health and Social Care. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK.
Bookshelf ID: NBK537417

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