Bryant et al. Journal of Eating Disorders (2022) 10:78
https://doi.org/10.1186/s40337-022-00597-8
REVIEW
Screening, assessment and diagnosis
in the eating disorders: findings from a rapid
review
Emma Bryant
1*
, Karen Spielman
1
, Anvi Le
3
, Peta Marks
1
, National Eating Disorder Research Consortium,
Stephen Touyz
1
and Sarah Maguire
1,2
Abstract
Background: Limited screening practices, minimal eating disorder training in the healthcare professions, and barriers
related to help-seeking contribute to persistent low rates of eating disorder detection, significant unmet treatment
need, and appreciable associated disease burden. The current review sought to broadly summarise the literature
and identify gaps relating to the screening, assessment, and diagnosis of eating disorders within Western healthcare
systems.
Methods: This paper forms part of a Rapid Review series scoping the evidence base for the field of eating disorders,
conducted to inform the Australian National Eating Disorders Research and Translation Strategy 2021–2031, funded
and released by the Australian Government. ScienceDirect, PubMed and Ovid/Medline were searched for studies
published between 2009 and mid 2021 in English. High-level evidence such as meta-analyses, large population stud-
ies and Randomised Control Trials were prioritised through purposive sampling. Data from selected studies relating
to Screening, Assessment and Diagnosis of eating disorders were synthesised and are disseminated in the current
review.
Results: Eighty seven studies were identified, 38% relating to screening and 62% to assessment and diagnosis.
The majority of screening studies were conducted in university student samples, showing high prevalence but only
modest improvements in help-seeking in those studies that followed up post-screen. In healthcare settings, clinicians
continue to have difficulty identifying eating disorder presentations, particularly Binge Eating Disorder, Other Speci-
fied Feeding or Eating Disorders, and sub-threshold eating disorders. This is preceded by inadequate and frequently
homogenous screening mechanisms and exacerbated by considerable personal and health-system barriers, includ-
ing self-stigma and lack of resourcing. While all groups are at risk of delayed or no diagnosis, those at particular risk
include LGBTQ+ and gender diverse individuals, individuals living in larger bodies, and males.
Conclusions: A majority of individuals with eating disorders remain undiagnosed and untreated despite a high
prevalence of these conditions and increased advocacy in recent years. Research into improving detection and clini-
cian diagnostic skill is extremely limited. Innovative empirical research is strongly recommended to address significant
individual and health-system barriers currently preventing appropriate and timely intervention for many.
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Open Access
*Correspondence: emma.bryant@sydney.edu.au
1
InsideOut Institute for Eating Disorders, Faculty of Medicine and Health,
University of Sydney, Sydney, NSW, Australia
Full list of author information is available at the end of the article