Letter to the editor: health professionals’ attitudes toward individuals with eating disorders: who do we think they are?
© The Author(s). 2017
Received: 7 April 2017
Accepted: 25 April 2017
Published: 17 July 2017
Health professionals are not immune to stigmatizing attitudes and stereotypes found in society-at-large. Along with patients and their loved ones, treatment providers are important stakeholders – and gatekeepers – in the successful delivery of mental healthcare. Prevailing attitudes among professionals can facilitate timely recognition, enable access to care and uptake of evidence-based practices, or undermine help-seeking and therapeutic engagement. At an interactive activity at the 2016 Nordic Eating Disorders Society (NEDS) meeting, we asked health professionals to describe individuals with eating disorders. The most common descriptive term used was “anxiety” followed by “thin”, “sad”, “control”, "female", and "suffering/pain". Further research on professionals’ attitudes toward individuals with eating disorders is necessary to inform education, awareness, and advocacy efforts following the diagnostic revisions in the DSM-5.
Health professionals play a vital role in connecting science to service, and bridging bench-to-bedside gaps in the delivery of care, yet they are not immune to lay stereotypes or stigmatizing beliefs found in the community . Individuals with eating disorders (ED) have been viewed by society-at-large as attention-seeking, blameworthy, or as having a trivial, self-imposed problem , and viewed by professionals as vain, manipulative, or difficult [3, 4]. These findings are particularly worrying in light of studies of patient perspectives on treatment-seeking and engagement in ED. Individuals with ED highly value clinician attributes such as acceptance, empathy, warmth, and openness, whereas negative clinical encounters are characterized by a judgmental stance, disregard, or prejudice by health professionals . Frequency of stigma exposure is associated with numerous adverse effects on health and well-being for those with ED, including greater ED symptomology, depression, and lower self-esteem . Perceived stigma, or fear thereof, is consistently recognized as a prominent barrier to help-seeking for ED , diminishing our ability to identify and effectively treat all who may benefit .
Traditional views that ED are afflictions of “thin, affluent, young, white women” , render higher-weight individuals, older individuals, males, and ethnic minorities highly susceptible to bias and under-detection. Symptoms may go unrecognized, misinterpreted, or dismissed due to health professionals’ expectations about the presentation of an ED. The DSM-5 criteria for ED have recently undergone changes with the removal of female-centric criteria (i.e., amenorrhea) and pejorative terminology (i.e., “refusal” to maintain weight). How these diagnostic changes might affect provider attitudes toward individuals with ED is unclear. More research is also needed to understand professionals’ attitudes toward newly added diagnostic labels, including avoidant-restrictive food intake disorder and binge eating disorder, as well as atypical presentations such as muscle dysmorphia .
Putting it into words: who do we think they are?
Whether thinness and female-centric words reflect lingering stereotypes of ED, or simply reflect the clientele treated by this group of professionals is unclear, yet findings deserve further investigation given the implications for potential bias and ascertainment. Encouragingly, and in contrast to some prior indications from the literature , little evidence of stigmatizing or pejorative terms was observed; rather, we noted several empathic or humanizing adjectives reflecting strength and individual differences. Research with a variety of professional categories is needed, as this line of investigation would almost certainly prove fruitful to help direct our education, awareness, and advocacy efforts. In particular, targeting primary care professionals is important for early detection, given their likelihood of encountering an undiagnosed eating disorder along the initial pathway-to-care.
We would like to acknowledge the Nordic Eating Disorders Society.
DLR conceived of the paper and participated in its design and coordination. JL and KG were speakers for the NEDS plenary session, “Who do we think they are? Confronting myths in the treatment of eating disorders.” RI served as the chairman of the Nordic Eating Disorders Society. JL, KG, and RI provided analytical input and helped draft and edit the manuscript. All authors read and approved the final manuscript.
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