Ultimately, improving the way researchers report meta-ethnographies, will help to ensure that the best use is made of research evidence for the benefit of people who use health and social care services.
The new guidance has 19 specific reporting criteria, supported by detailed explanatory notes. It includes recommendations on all aspects of meta-ethnography conduct and reporting, from selecting studies to analysing data.
The guidance will be free to use and is aimed predominantly at researchers, journal editors, and academics who review research articles to guide how meta-ethnographies should be reported. It will also be used by researchers and students looking to understand how to conduct a meta-ethnography.
“We have developed guidance to assist researchers in carrying out quality meta-ethnographies and reporting them to a high standard, meaning this rich information can be used to create better decision-making and improve outcomes for patients,” Dr France explained.
“The guidance will help to provide new insights and conclusions regarding specific health topics, for example, people’s experiences of being treated for a certain type of illness.
“Ultimately, improving the way researchers report meta-ethnographies, will help to ensure that the best use is made of research evidence for the benefit of people who use health and social care services.”
The study, Improving reporting of Meta-Ethnography: The eMERGe Reporting Guidance, is published in the Journal of Advanced Nursing; BMC Medical Research Methodology; Review of Education; and Psycho-oncology.
Find out more about the eMERGe project.