research shows UK doctors’ lack of training on                  eating disorders puts lives at risk

A study revealed that, alarmingly, medical students receive less than two hours of training on eating disorders over four to six years of undergraduate study, which experts and the UK’s eating disorder charities warn is putting patients’ lives at risk.

 

The research, published in the Postgraduate Medical Journal (a specialist journal published by the BMJ), is the first comprehensive analysis of the extent of training on eating disorders in the UK.

 

Surveying all medical schools in the country, it finds that the average teaching and assessment time on eating disorders in undergraduate courses amounts to just 1.8 hours, and one in five medical schools do not offer any training on eating disorders at all.

 

Of the 33 universities offering medical degrees, only six offered placements in specialist eating disorder units for children, and seven in units for adults, and even these placements were limited to six – twelve students. This means just 1% of doctors have the opportunity for clinical experience on eating disorders, and even see how the theory translates to clinical practice.

 

The research also highlights the severe lack of specialist training posts, with just 17 such posts dedicated to training clinicians to treat eating disorders. Sufferers of eating disorders should be referred to specialist services and should not be treated in general mental health units, but the lack of specialist training placements will only add to shortage of specialist clinicians.

 

This research comes in the wake of a 2017 Parliamentary and Health Service Ombudsman (PHSO) inquiry into the deaths of three people with eating disorders, which concluded that lack of training was one of the factors that contributed to the tragedies.

 

The lead author of the research, Dr Agnes Ayton, said: 

Tragedies such as those outlined in the PHSO inquiry should not happen, people should not die from eating disorders and the lack of eating disorder training for our doctors is contributing to the risk to patient safety.

Too often under-trained doctors only look at the physical symptoms like weight, or do not recognise that someone is ill at all. Patients end up not getting the treatment they need and suffer unnecessarily.

“Medical schools are treating eating disorders as a niche subject, despite the fact that they affect 1.25 million people in the UK and cost the NHS hundreds of millions of pounds. Improved training would save lives at a minimal cost to the NHS.

 

People suffering with an eating disorder frequently report to us at AEDRA how doctors’ knowledge of eating disorders, or lack of it, can be the difference between continuing to suffer and recovery.

 

In a survey of 1,700 people in 2017, only 42% felt that their GP understood eating disorders and only 34% believed their GP knew how to help them with their illness.

One sufferer described  to BEAT her first visit to a GP who had clearly had little or no training on eating disorders:

“They told my mum that my not eating was a phase I would grow out of and sent us away with a meal plan cut from the back of a cereal box. […] Since then I've had staff in general psychiatric wards tell me that I don't look like I have an eating disorder, which has been very triggering and difficult.”

 

Others spoke of doctors whose understanding of eating disorders enabled them to make appropriate referrals. One patient described this as: 

“…a huge help to my recovery and a major factor in me not requiring inpatient treatment later on.”

 

 We at AEDRA call for a review training in eating disorders for junior doctors as recommended by PHSO. 

 

 It is widely known that the best way of dealing with an eating disorder is early treatment. All doctors should leave medical school equipped to recognise eating disorders and stop them in their tracks by making appropriate referrals.

 

Only with adequate training covering the psychological and physical aspects of these serious and enduring mental illnesses can doctors hope to protect patient safety.

 

 

The full paper is available here.

 

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The December 2017 report by the Parliamentary and Health Service Ombudsman, titled Ignoring the alarms: How NHS eating disorder services are failing patients, concluded that lack of understanding of eating disorders among NHS staff was amongst a number of failings which led to the death of Averil Hart and that the current level of eating disorder training is not enough. It also concluded, as one of its main recommendations: "The General Medical Council (GMC) should conduct a review of training for all junior doctors on eating disorders to improve understanding of these complex mental health conditions.”

Anorexia Nervosa has a higher mortality rate than any other any mental health condition. Other eating disorders also have high mortality rates."

 

 

                        Research Students

Participation:

Participating in research is a chance to have your voice heard which might help influence how support is offered to others in the future.

Research requiring you to focus on personal experience can be emotionally provoking. If you have any concerns about participating in a research study make sure you read all the information provided and contact the researcher if you need to ask further questions. It may be important to discuss what support you can access if you find any of the experience triggering.

The research projects listed below are recruiting participants:

A step-by-step guide for friends & family to become recovery mentors

You are invited to take part in a research project evaluating a new DVD –' How to Care for Someone with an Eating Disorder' –which has been written, produced and directed by carers, patients and clinicians who have experience of eating disorders. The DVD has been produced to train family and friends to become recovery mentors.

Aim

We wish to assess whether the DVD, as an adjunct to treatment as usual, is effective for improving eating disorder symptoms. We also aim to test whether the DVD has an impact on distress in friends and family.

What’s involved

Individuals receiving treatment for an eating disorder, and friends and family members who have a supportive role in recovery, can take part in this study. 

We will ask participants to complete a series of questionnaires (at the beginning of your involvement, two months later and then six months later). Family and friends will be randomly allocated to start training to be recovery mentors –immediately or after a short waiting period.

Interested in taking part?

Friends, family members and partners should visit: 
www.surveymonkey.com/s/recoverymentor1

 

People with an eating disorder should visit: 
www.surveymonkey.com/s/patients1

Contact

charlotte.c.rhind@kcl.ac.uk 
+44 (0) 20 7848 5963

New meta-analysis from Jess Kerr-Gaffney finds lowered cognitive empathy in anorexia nervosa. Check out the paper here to learn more about cognitive empathy and its implications in eatingdisorders