Elsevier

The Lancet

Volume 357, Issue 9264, 21 April 2001, Pages 1254-1257
The Lancet

Articles
Outcome in patients with eating disorders: a 5-year study

https://doi.org/10.1016/S0140-6736(00)04406-8Get rights and content

Summary

Background

Eating disorders are disabling, unpredictable, and difficult to treat. We did a prospective 5-year investigation of a representative sample of patients with eating disorders. Our aim was to identify predictors of outcome and to assess effects of available treatments.

Methods

We prospectively investigated 95 patients with anorexia nervosa, 88 with bulimia nervosa, and 37 with eating disorders not otherwise specified (EDNOS), who sought treatment in Adelaide, South Australia. We divided patients into those who had, and had not, received treatment in specialist units and reached a safe body weight. Individuals were then further classified dependent on intensity of any treatment received. We assessed clinical symptoms, body-related attitudes, and psychosocial function.

Findings

216 (98%) patients were available for follow-up after 5 years. Three patients with anorexia nervosa and two with EDNOS died. 65 (74%) bulimic, 29 (78%) EDNOS, and 53 (56%) anorexic patients had no diagnosable eating disorder. A small proportion of patients in every group had poor Morgan-Russell-Hayward scores at outcome. Final outcome was predicted by extent and intensity, but not duration, of initial symptoms in patients with anorexia nervosa, and by initial body-related attitudes and impaired psychosocial functioning in bulimia patients. We were unable to predict EDNOS outcome. Treatment did not affect outcome for any group.

Interpretation

Deaths in the study confirm the serious nature of eating disorders. However, our results suggest that the efficacy of existing interventions is questionable.

Introduction

Studies of the outcome of patients with eating disorders, such as those with anorexia nervosa or bulimia nervosa, have been limited by technical and sampling difficulties.1, 2, 3, 4, 5 Our aim was to investigate whether or not predictors of patient outcome could be identified from measures obtained at the point that individuals first make contact with secondary or tertiary health services, alone or in combination with measures from a subsequent assessment 6 months later.

Section snippets

Methods

We enrolled women aged 15 years or older, who were living in Adelaide, South Australia, and who were either making first contact with secondary or tertiary services for treatment of an eating disorder, or were recontacting such services after a treatment break of at least 6 months. The study protocol was agreed by the Flinders Medical Centre ethics committee and all patients gave informed consent.

We did the initial research assessment within 48 h of index contact with the patient, and we

Results

Agreement to participate was obtained from all identifiable specialist service providers in Adelaide, apart from one psychiatrist in individual practice. Recruitment took 27 months. We excluded ten of the patients screened because they did not have a clinical eating disorder. 235 patients who fulfilled the recruitment criteria were seen at participating centres. 220 agreed to take part in our study. The study cohort contained 95 patients with anorexia, 88 with bulimia, and 37 with EDNOS. Table 1

Discussion

Our results provide strong support for separate identities for anorexia and bulimia.21, 22 We report clear differences in overall outcomes of these two groups and in the characteristics that predicted those outcomes. There was also little crossover between the conditions.

The size, relative isolation, and diversity of resources available for treatment of eating disorders in Adelaide made this city well suited to a study of a more representative sample of patients than has previously been

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