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Meta-analysis |

Mortality Rates in Patients With Anorexia Nervosa and Other Eating Disorders:  A Meta-analysis of 36 Studies FREE

Jon Arcelus, LMS, MSc, FRCPsych, PhD; Alex J. Mitchell, MRCPsych; Jackie Wales, BA; Søren Nielsen, MD
[+] Author Affiliations

Author Affiliations: Loughborough University Centre for Research into Eating Disorders, Loughborough University (Dr Arcelus), Brandon Unit, Eating Disorders Service (Dr Arcelus and Ms Wales), and Department of Psycho-Oncology (Dr Mitchell), Leicester Partnership Trust, Leicester General Hospital, and Department of Cancer and Molecular Medicine, Leicester Royal Infirmary, University of Leicester (Dr Mitchell), Leicester, England; and Region Sjælland, Child and Adolescent Psychiatric Services, Næstved, Denmark (Dr Nielsen).


Arch Gen Psychiatry. 2011;68(7):724-731. doi:10.1001/archgenpsychiatry.2011.74.
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Context Morbidity and mortality rates in patients with eating disorders are thought to be high, but exact rates remain to be clarified.

Objective To systematically compile and analyze the mortality rates in individuals with anorexia nervosa (AN), bulimia nervosa (BN), and eating disorder not otherwise specified (EDNOS).

Data Sources A systematic literature search, appraisal, and meta-analysis were conducted of the MEDLINE/PubMed, PsycINFO, and Embase databases and 4 full-text collections (ie, ScienceDirect, Ingenta Select, Ovid, and Wiley-Blackwell Interscience).

Study Selection English-language, peer-reviewed articles published between January 1, 1966, and September 30, 2010, that reported mortality rates in patients with eating disorders.

Data Extraction Primary data were extracted as raw numbers or confidence intervals and corrected for years of observation and sample size (ie, person-years of observation). Weighted proportion meta-analysis was used to adjust for study size using the DerSimonian-Laird model to allow for heterogeneity inclusion in the analysis.

Data Synthesis From 143 potentially relevant articles, we found 36 quantitative studies with sufficient data for extraction. The studies reported outcomes of AN during 166 642 person-years, BN during 32 798 person-years, and EDNOS during 22 644 person-years. The weighted mortality rates (ie, deaths per 1000 person-years) were 5.1 for AN, 1.7 for BN, and 3.3 for EDNOS. The standardized mortality ratios were 5.86 for AN, 1.93 for BN, and 1.92 for EDNOS. One in 5 individuals with AN who died had committed suicide.

Conclusions Individuals with eating disorders have significantly elevated mortality rates, with the highest rates occurring in those with AN. The mortality rates for BN and EDNOS are similar. The study found age at assessment to be a significant predictor of mortality for patients with AN. Further research is needed to identify predictors of mortality in patients with BN and EDNOS.

Figures in this Article

Eating disorders are increasingly recognized as an important cause of morbidity and mortality in young individuals. The lifetime risk of anorexia nervosa (AN) in women is estimated to be 0.3% to 1%, with a greater number of patients having bulimia nervosa (BN).1,2 Anorexia nervosa is a serious psychiatric illness characterized by an inability to maintain an adequate, healthy body weight. Bulimia nervosa is characterized by recurrent episodes of binge eating in combination with some form of unhealthy compensatory behavior. Eating disorder not otherwise specified (EDNOS) is a catchall DSM-IV diagnosis for patients with significant features of eating disorders that do not meet the criteria for AN or BN.3 Despite EDNOS being a common presentation in eating disorders services, few published data exist regarding mortality rates in patients given this diagnosis.4,5 Anorexia nervosa is a serious illness in the young population, and outcome is often poor. Steinhausen6 showed that only 46% of patients fully recovered from AN, a third improved with only partial or residual features of the disorder, and 20% remained chronically ill for the long term. A low body mass index (BMI), a greater severity of social and psychological problems, self-induced vomiting, and purgative abuse have been identified as predictors of poor outcome in this disorder.7

Most mortality research in the eating disorders literature has focused on AN. Some authors have suggested that the mortality risk for BN is low.8 This conclusion is surprising, given the medical complications associated with self-induced vomiting, laxative abuse, and other purging behaviors. The ratio of observed to expected deaths (ie, the standardized mortality ratio [SMR]) for AN has been reported to be between 0.719 and 12.8.10 Also, it often has been reported that suicide is a particularly common cause of death in AN.11,12 Muir and Palmer13 suggested that official death certification may underestimate the incidence of suicide associated with this disorder. The wide variation of SMRs for eating disorders partly may depend on the length of follow-up. For example, Nielsen14 reported an SMR of 9.6 after approximately 10 years of follow-up, as opposed to 3.7 in 4 studies with a mean follow-up period ranging from 20 to 36 years. Other factors that correlate with a higher estimate of mortality are age, case severity, study period, and whether other eating disorders with a lower mortality rate were evaluated separately.15

Given this debate, the primary aim of our study was systematically to compile and to analyze mortality rates in individuals with eating disorders, taking into account variations in sampling, diagnosis, and length of follow-up of the study. Our hypothesis was that mortality rates would be elevated in all types of eating disorders. We also aimed to explore factors associated with mortality among individuals with AN, BN, and EDNOS.

SEARCH STRATEGY

A systematic literature search, appraisal, and meta-analysis were conducted. The MEDLINE/PubMed, PsycINFO, and Embase abstract databases were searched from 1966 through September 30, 2010. Also, 4 full-text collections, ScienceDirect, Ingenta Select, Ovid Full text, and Wiley-Blackwell Interscience, were searched, and an article published online ahead of print was included.16 A broad range of subject headings was used to identify the relevant disorders and diagnoses. For each database search, 7 main search components (eating disorders, anorexia nervosa, bulimia nervosa, eating disorder not otherwise specified [EDNOS], mortality, death, and survival) were created by combining subject headings with the“OR” operator, and the same components then were combined by using the“AND” operator. Studies that followed up patients for a minimum of 1 year and included 15 or more participants at the time of analysis were included. Relevance was determined by screening titles and abstracts. Reference lists of relevant articles were screened for further potentially relevant studies, and citation searches were conducted. The results are reported for the exposure groups for AN, BN, and EDNOS (eTable 1).

STATISTICAL ANALYSIS

Primary data were extracted as raw numbers or confidence intervals (CIs) and corrected for years of observation and sample size (ie, person-years of observation). Weighted proportion meta-analysis was used to adjust for study size using the DerSimonian-Laird model to allow for heterogeneity inclusion in the analysis. We excluded articles without adequate data such as those in which no raw number was presented (or calculable), those that examined predictors of functional decline only, and those that looked at other aspects of prognosis, such as hospitalization, without information regarding mortality rate. Mantel-Haenszel pooled risk ratios were estimated, with aχ2 test for heterogeneity (I2) used to assess between-study differences in effect.17 Random-effects models were fitted if heterogeneity existed, and risk ratios were presented as a forest plot.18 The forest plot shows study-specific risk ratios (and their 95% CIs) and the relative weighted contribution of each study, as well as the risk ratio estimate pooled across all studies. The analyses were performed with StatsDirect statistical software, version 2.7.7 (StatsDirect Ltd, Cheshire, England).

For the analysis, we collected data regarding the number of participants, the number of participants at follow-up, mean age of the population studied at first assessment, sex, mean BMI at first assessment, whether the population studied was inpatient or outpatient, SMR, the percentage of dead case individuals, diagnosis, and predictors of death, if available. We discuss findings for AN, BN, and EDNOS separately. The outcome of interest was mortality rate.

INCLUDED AND EXCLUDED STUDIES

Two independent assessors (J.A. and J.W.) identified 143 relevant articles that were screened in detail (Figure 1). In some cases, the authors of those articles were contacted to gather further information.1922 After doing so, we excluded 78 articles because of inadequate duration of the study (<1-year follow-up or case series) or inadequate sample size (<15 patients). Review articles also were excluded from the analysis. Of the 65 articles retrieved for more detailed evaluation, 29 were excluded because of lack of description of cases resulting in death, same database used in other studies, or lack of diagnosis of death in cases. When investigators conducted multiple analyses reported in separate articles, we only selected the article with a longer follow-up; 7 studies were excluded for this reason.

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Figure 1. Literature review method used. AN indicates anorexia nervosa; BN, bulimia nervosa; EDNOS, eating disorder not otherwise specified.

SUMMARY OF RELEVANT STUDIES

Thirty-six relevant empirical quantitative studies of mortality in eating disorders were published between January 1, 1966, and September 30, 2010. All but 1 study23 provided data regarding mortality rate in patients with AN. Twelve studies provided information regarding patients with BN, and 6 studies described mortality rate in patients with a diagnosis of EDNOS. Twenty-five studies provided sufficient data for analysis of SMR in AN. Across 36 studies, 17 272 unique patients had eating disorders. Reported deaths totalled 755. Considerable differences existed among the studies regarding design, group size, and methods. Few studies were prospectively organized. Diagnostic categories changed considerably during the period of the studies. In some cases, duration of follow-up also was difficult to compute from the original studies. Besides missing data, this problem occurred due to variations in the definition of the starting point or the general practice of providing only ranges instead of precise group parameters.

A general lack of control conditions and a scarcity of precise information regarding treatment was observed in these studies. Different treatment and psychotherapeutic approaches were used. The diversity of interventions precluded any definite evaluation of treatment effects.24 Most outcome studies for AN reported crude mortality rates and SMRs. The crude mortality rates may have been inflated slightly; not all studies reported the cause of death, so causes other than the eating disorder might have led to patient death.

ANOREXIA NERVOSA
Mortality Rate per Person-years

Thirty-five studies described the mortality rates of patients with AN (eTable 2). The mean (SD) follow-up period of the studies was 12.82 (7.39) years, with a maximum mean time of follow-up period of 36.2 years.25 The mean (SD) sample size was 360.7 (954.1), with a maximum sample size at follow-up of 6009 cases.26 The 35 studies subjected to bias assessment (eFigure 1) followed up a total of 12 808 individuals and reported 639 total deaths. The total follow-up time was 166 642 person-years. Overall, the weighted annual mortality for AN was 5.10 deaths (95% CI, 3.99-6.14) per 1000 person-years (Figure 2), of which 1.3 deaths resulted from suicide. We analyzed 14 studies that included only female patients with AN and found that the weighted annual mortality rate was 5.39 (95% CI, 3.57-7.59) per 1000 person-years. The weighted mortality rate was lower for studies (n = 11) that selected inpatients (4.55; 95% CI, 3.09-6.28).

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Figure 2. Annual mortality rate per 1000 person-years in anorexia nervosa. Studies include male and female patients.

Standardized Mortality Ratio

Twenty-five studies involving 12 189 patients with AN examined SMRs compared with a reference population (eFigure 2). The mean follow-up period was 14.2 years. Heterogeneity was high (I2 = 91.2%; 95% CI, 88.9%-92.9%). The overall SMR using random-effects meta-analysis was 5.86 (95% CI, 4.17-8.26).

Predictors of Mortality

Meta-regression analysis was used to identify risk factors of death in AN. A priori (based in the literature), we assumed that interstudy differences in age at assessment, sex, BMI, and comorbid conditions, such as alcohol intake, could be related to mortality in AN. Not enough studies reported comorbid conditions, and no studies observed male patients. Therefore, meta-regression analysis only could be conducted for age and BMI. This analysis showed significant positive correlation with age (r = 0.1, P = .01) and nonsignificant correlation with BMI on assessment (r = 0.9, P = .11). Results of the literature review regarding mortality in AN are presented in eTable 2.

BULIMIA NERVOSA
Mortality Rate per Person-years

Since the first study was reported in 1988, 12 studies described the mortality rates of patients with this diagnosis (eFigure 3 and eTable 3). Twelve studies followed up 2585 individuals with BN and reported 57 deaths. The mean (SD) sample size was 200.7 (252.6), and the mean (SD) follow-up period was 9.34 (3.8) years. The total person-years of follow-up was 32 798 years. The mean follow-up period was 9.74 years. The mortality rate for BN was lower than that reported for AN, with a relative risk of mortality of 2.11 (95% CI, 1.40-3.20). The weighted mortality rate was 1.74 (95% CI, 1.09-2.44) per 1000 person-years. We examined separately 5 studies that reported on a female population only. The analysis found a weighted mortality rate of 2.22 (95% CI, 0.73-4.72) per 1000 person-years of follow-up. No male-only studies were found.

Standardized Mortality Ratio

All 12 studies reported SMRs (although 3 studies reported no deaths) (Figure 3). Heterogeneity was low (I2 = 0%), and the overall SMR using random-effects meta-analysis was 1.93 (95% CI, 1.44-2.59), a significant differences from 1.00 (P = .002).

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Figure 3. Standardized mortality ratios (95% confidence intervals) in patients with bulimia nervosa.

EDNOS Mortality Rate
Mortality Rate per Person-years

Only 6 studies described the mortality rate of patients with EDNOS (Figure 4). The difficulties defining EDNOS makes it more complicated to study this group. Despite the relatively small number of studies, the examination of this group is important to the inclusivity of the study, given that these patients represent such a large proportion of patients observed in practice. The mean (SD) sample size was 313 (391.7) patients, and the mean follow-up period of the studies was 9.1 (7.7) years. A total of 1879 individuals were followed up, and the reported total number of deaths was 59. The total person-years of follow-up was 22 644. Overall, the weighted annual mortality rate for EDNOS was 3.31 deaths (95% CI, 1.48-5.75) per 1000 person-years.

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Figure 4. Mortality rates per person-years in patients with eating disorder not otherwise specified.

Standardized Mortality Ratio

Only 4 studies involving 1812 individuals with EDNOS reported SMRs with CIs (eTable 4). The mean follow-up period was 10.9 years. Heterogeneity was low (I2 = 0%), and the overall SMR using random-effects meta-analysis was 1.92 (95% CI, 1.46-2.52), a significant difference from 1 (P < .001).

Because of the small number of studies, multiregression analysis was not used to explore prognostic factors for mortality rate in patients with BN and EDNOS. No difference in observed mortality (per 1000 person-years of follow-up) between BN and EDNOS was found, but AN had a 2.7-fold higher mortality rate than BN. Time series analysis showed no statistically significant effect for AN and BN but a negative correlation for EDNOS (adjusted R2 = 0.66, P = .01), suggesting a smaller effect in more recent studies.

The aim of this study was to measure mortality rate in patients with eating disorders using meta-analysis. The existing literature regarding mortality rate from eating disorders has several limitations. First, length of follow-up has varied considerably. A second and probably more important limitation is low ascertainment rates. For example, in the BN studies reviewed by Keel and Mitchell,49 some had ascertainment rates as low as 50%. Other limitations include the relatively small numbers of study patients with BN or EDNOS, the classification used in the study, and the population studied. A further limitation is that many studies have focused on indirect SMRs. Two major approaches to standardization, direct and indirect, have been used. Direct standardization is used when the study population is large enough that age-specific rates within the population are stable. When the population is small (or the outcome is rare), the number of events observed can be small. In that circumstance, indirect standardization methods can be used to produce an SMR. The indirect SMR presents a comparison with the general population, but it is unclear whether this population is comparable with that of individuals with eating disorders. Indeed, it is equally useful to present the actual death rate per person-year.

The issue of diagnostic crossover also is important. A range of rates have been reported in the literature. For individuals with AN, it has been suggested that 20% to 50% will develop BN over time.10,11,50 A study by Eddy et al51 showed that one-third of patients with an intake diagnosis of AN crossed over to BN during 7 years of follow-up. This finding did not prevent patients from crossing back (ie, relapsing) into AN. Movement from an initial diagnosis of BN to AN is less common. A review by Keel and Mitchell49 put this figure at less than 10%; Eddy et al51 found this rate to be 14.06% during a 7-year follow-up period. This finding is important when examining SMRs for the eating disorder groups because patients who had been diagnosed as having AN on assessment may have had BN by the time they died. Diagnostic crossover may have occurred; therefore, we cannot imply stability of diagnosis.

As hypothesized, we found an overall elevated mortality rate for patients with all types of eating disorders. This risk of death was highest for those with AN, with a weighted annual mortality rate of 5 per 1000 person-years (slightly higher in studies of females only), followed by patients with EDNOS at 3 per 1000 person-years of follow-up and BN at 1.7 per 1000 person-years of follow-up. The mortality rate, particularly for AN, was considerably lower for those studies that had a long follow-up period, such as that by Korndörfer et al,9 which showed an SMR for AN of 0.71 and had 27.1 years of follow-up, or the study by Crow et al,21 with an SMR of 1.7 and a follow-up of 18.13 years. Studies15,19,40 with fewer years of follow-up generally showed a high SMR. Given the crossover observed between diagnoses, the actual duration of follow-up may be less important than the duration of illness.

The causes of patient deaths were not always available, and it is likely that many of the people who died may not have had AN or an eating disorder at the time of death. However, the rates of suicide were examined separately because this was mentioned in a number of studies. Twelve studies described deaths from suicide in patients with AN, and analysis showed that the weighted annual mortality due to suicide in AN was 1.39, which means that 1 in 5 individuals with AN who died had committed suicide.

The SMR values for BN and EDNOS are lower than for AN (ie, 5.86), giving individuals with EDNOS and BN SMRs of 1.92 and 1.93, respectively. It can be argued that reviews of SMR in BN can be highly selective because they only may include those studies that have found deaths at follow-up. In the present meta-analysis, we included all follow-up studies of patients with BN. Three of the studies did not find any case individuals who died, and 4 studies gave an SMR higher than 2. The low SMR suggests that a diagnosis of BN per se does not render an individual at increased risk of premature death, but this finding does not necessarily justify complacency, given that comorbid affective disorder and related behaviors may often accompany bulimic symptoms.

Little has been reported regarding the morbidity or mortality associated with EDNOS because this was not an accepted diagnosis until the DSM-IV criteria were published, although atypical eating disorders were noted before then. Our results for EDNOS suggest a possibly higher mortality risk than in BN. The SMR (ie, 1.92) reported in this meta-analysis is higher that that reported in the study by Birmingham et al,32 which found that SMR for patients with EDNOS was only 1.1. Eating disorder not otherwise specified is a mixture of atypical AN and atypical BN in International Statistical Classification of Diseases, 10th Revision (ICD-10)52 terms; therefore, those findings can be difficult to interpret. The question also exists of whether patients with EDNOS had previously been or were likely to become patients with AN. Based on the study by Eddy et al,51 this would appear to be so. The authors' depiction of the longitudinal course and crossover diagnoses for patients with an intake diagnosis of AN highlighted that some patients could be classified as having partial recovery. These figures ranged from 75% to 85% during the 7-year follow-up period, depending on subtype. Agras et al53 examined the course of EDNOS and found that only 18% of this group had never had or did not develop another diagnosed ED during the 4-year study. Thus, any elevated mortality risk of EDNOS partly could be explained by the assertion that EDNOS sometimes reflected the earlier stages of AN. Further studies are required before firm conclusions can be drawn.

Our study found that the mortality rates in patients with eating disorders are high. In some cases (ie, those involving AN), they are much higher than for other psychiatric disorders. Studies in other psychiatric disorders have found SMRs of 2.8 and 2.5 in males and females with schizophrenia,54 1.9 and 2.1 in males and females with bipolar disorder, and 1.5 and 1.6 in males and females with unipolar disorder, respectively.55

PREDICTION OF DEATH

Our secondary objective was to examine the factors associated with mortality rate among the different diagnoses. Information regarding factors that predict outcomes was drawn from only a handful of studies and occasionally was conflicting. We anticipated that we would analyze predictors of death in the varying diagnoses. However, because an insufficient number of studies identified risk factors by meta-regression analysis for the EDNOS and BN groups, this was examined for the AN studies only. Few studies specifically examined predictors of mortality; instead, many examined predictors of poorer outcome. Based on the information from different studies, factors highlighted for poorer outcome, including mortality, in patients with AN included older age at first presentation,31,36,40 alcohol misuse,22,34,55 and low BMI at presentation.25,34,46 Other strong predictors of mortality involved comorbid disorders, such as affective disorder, suicidal behavior or self-harm, alcohol abuse, and a history of hospitalization for such mental health problems. Button et al22 found that only BMI at assessment and alcohol misuse reliably predicted mortality status, although evidence of an affective disorder almost was significant. Some studies24,46 also have found evidence of an association between alcohol misuse and increased mortality in AN. One of them26 found that younger age and longer hospital stay at first hospitalization were associated with better outcome, and psychiatric and somatic comorbidity worsened the outcome of patients with eating disorders.

Unfortunately, because of the small number of studies that recorded different prognostic factors (such as somatic comorbidity, alcohol and drug abuse, and psychiatric comorbidity), meta-regression analysis for these factors was not possible. However, the studies selected in this meta-analysis allow examination of the influence of weight and age at presentation on the SMR. One study included in the meta-analysis22 found that when SMR is used as an index of mortality, an inverse trend seems to occur, namely, higher SMR with lower weight at presentation. In view of this, some studies have suggested low BMI on assessment as a predictor of death. However, meta-regression analysis of the studies did not show a significant correlation between mortality and BMI on assessment. Because age at presentation is known, this point frequently is used as a proxy variable for age at illness onset. Age at onset is difficult to determine with any precision in most cases. Most of the studies included in this meta-analysis indicated effect of age at presentation, which for most studies was a highly significant effect. Most studies report too few deaths in the younger age groups and too many deaths in those presenting for treatment at age 20 years or older. A clear pattern can be observed across ages: an SMR of approximately 3 in the youngest, approximately 10 in those aged 15 to 19 years, close to 18 in those aged 20 to 29 years, and approximately 6 in those who present for treatment at age 30 years or older.19,47,55,56

LIMITATIONS AND FUTURE STUDIES

This analysis has a number of limitations. Notably, we relied on the quality and nonrepetition of primary publications. We sought to ensure data integrity by excluding small studies with less than 1 year of follow-up and fewer than 15 patients. The possibility exists of counting some individuals twice, especially when several related publications are derived from 1 group. We attempted to deal with duplicate data from the same authors by excluding studies in which the population characteristics were nearly identical to those already entered. The study is limited by the number of available published data for these diagnoses, and although these were reasonably robust for AN, fewer were available for the other diagnoses. Through the years, investigators used many diagnostic and outcome assessment measures; these measures reflected numerous definitions (ie, diagnoses) of illness. The lack of consistency of measures makes comparisons across studies difficult. Consolidation of measures, standardized definitions, and reporting guidelines are critical to the further advancement of the field. In addition, although we have used the values published in the relevant studies, it is possible that not all deaths reported were due to the eating disorder itself because comorbid physical conditions were not reported. Despite the number of studies examined, it is impossible to conclude whether patient death is a direct result of eating disorders. Future studies only will be able to investigate cause and predictive factors of death in patients with eating disorders by developing large national or international databases containing information that should include psychiatric and physical comorbidity, drug and alcohol abuse, and personality factors, as well as the psychopathologic features of eating disorders. The study showed that mortality rates in individuals with eating disorders are high not only for those with AN but also for those with EDNOS and BN, which highlights the seriousness of these conditions. Future, robust studies should inform physicians of the predictive factors associated with mortality rate in patients with EDNOS and BN; so far, late presentation of AN appears to be the only clear predictor of death among these disorders.55,56

Correspondence: Jon Arcelus, LMS, MSc, MRCPsych, PhD, Brandon Unit, Eating Disorders Service, Leicester Partnership Trust, Leicester General Hospital, Gwendolen Road, Leicester LE5 4PW, England (J.Arcelus@lboro.ac.uk).

Submitted for Publication: July 22, 2010; final revision received October 1, 2010; accepted December 28, 2010.

Author Contributions:Study concept and design: Arcelus. Acquisition of data: Arcelus, Mitchell, Wales, and Nielsen. Analysis and interpretation of data: Mitchell and Nielsen. Drafting of themanuscript: Arcelus, Mitchell, Wales, and Nielsen. Critical revision of the manuscript for important intellectual content: Arcelus, Mitchell, Wales, and Nielsen. Statistical analysis: Mitchell and Nielsen. Administrative, technical, and material support: Arcelus and Wales. Study supervision: Arcelus.

Financial Disclosure: None reported.

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Theander S. Anorexia nervosa: a psychiatric investigation of 94 female patients.  Acta Psychiatr Scand Suppl. 1970;214:1-194
PubMed
Papadopoulos FC, Ekbom A, Brandt L, Ekselius L. Excess mortality, causes of death and prognostic factors in anorexia nervosa.  Br J Psychiatry. 2009;194(1):10-17
PubMed   |  Link to Article
Joergensen J. The epidemiology of eating disorders in Fyn County, Denmark, 1977-1986.  Acta Psychiatr Scand. 1992;85(1):30-34
PubMed   |  Link to Article
Tanaka H, Kiriike N, Nagata T, Riku K. Outcome of severe anorexia nervosa patients receiving inpatient treatment in Japan: an 8-year follow-up study.  Psychiatry Clin Neurosci. 2001;55(4):389-396
PubMed   |  Link to Article
Pagsberg AK, Wang AR. Epidemiology of anorexia nervosa and bulimia nervosa in Bornholm County, Denmark, 1970-1989.  Acta Psychiatr Scand. 1994;90(4):259-265
PubMed   |  Link to Article
Dancyger IF, Sunday SR, Eckert ED, Halmi KA. A comparative analysis of Minnesota Multiphasic Personality Inventory profiles of anorexia nervosa at hospital admission, discharge, and 10-year follow-up.  Compr Psychiatry. 1997;38(3):185-191
PubMed   |  Link to Article
Deter H-C, Herzog W. Anorexia nervosa in a long-term perspective: results of the Heidelberg-Mannheim Study.  Psychosom Med. 1994;56(1):20-27
PubMed
Birmingham CL, Su J, Hlynsky JA, Goldner EM, Gao M. The mortality rate from anorexia nervosa.  Int J Eat Disord. 2005;38(2):143-146
PubMed   |  Link to Article
Fichter MM, Quadflieg N, Hedlund S. Twelve-year course and outcome predictors of anorexia nervosa.  Int J Eat Disord. 2006;39(2):87-100
PubMed   |  Link to Article
Ben-Tovim DI, Walker K, Gilchrist P, Freeman R, Kalucy R, Esterman A. Outcome in patients with eating disorders: a 5-year study.  Lancet. 2001;357(9264):1254-1257
PubMed   |  Link to Article
Crisp AH, Callender JS, Halek C, Hsu LK. Long-term mortality in anorexia nervosa: a 20-year follow-up of the St George's and Aberdeen cohorts.  Br J Psychiatry. 1992;161:104-107
PubMed   |  Link to Article
Crisp A, Gowers S, Joughin N, McClelland L, Rooney B, Nielsen S, Bowyer C, Halek C, Hartman D, Tattersall M, Hugo P, Robinson D, Atkinson R, Clifton A. Death, survival and recovery in anorexia nervosa: a thirty five year study.  Eur Eat Disord Rev. 2006;14(3):168-175
Link to Article
Tolstrup K, Brinch M, Isager T, Nielsen S, Nystrup J, Severin B, Olesen NS. Long-term outcome of 151 cases of anorexia nervosa: The Copenhagen Anorexia Nervosa Follow-Up Study.  Acta Psychiatr Scand. 1985;71(4):380-387
PubMed   |  Link to Article
Hebebrand J, Himmelmann GW, Herzog W, Herpertz-Dahlmann BM, Steinhausen H-C, Amstein M, Seidel R, Deter H-C, Remschmidt H, Schäfer H. Prediction of low body weight at long-term follow-up in acute anorexia nervosa by low body weight at referral.  Am J Psychiatry. 1997;154(4):566-569
PubMed
Patton GC. Mortality in eating disorders.  Psychol Med. 1988;18(4):947-951
PubMed   |  Link to Article
Lee S, Chan YYL, Hsu LKG. The intermediate-term outcome of Chinese patients with anorexia nervosa in Hong Kong.  Am J Psychiatry. 2003;160(5):967-972
PubMed   |  Link to Article
Franko DL, Keel PK, Dorer DJ, Blais MA, Delinsky SS, Eddy KT, Charat V, Renn R, Herzog DB. What predicts suicide attempts in women with eating disorders?  Psychol Med. 2004;34(5):843-853
PubMed   |  Link to Article
Signorini A, De Filippo E, Panico S, De Caprio C, Pasanisi F, Contaldo F. Long-term mortality in anorexia nervosa: a report after an 8-year follow-up and a review of the most recent literature.  Eur J Clin Nutr. 2007;61(1):119-122
PubMed   |  Link to Article
Morgan HG, Purgold J, Welbourne J. Management and outcome in anorexia nervosa: a standardized prognostic study.  Br J Psychiatry. 1983;143:282-287
PubMed   |  Link to Article
Millar HR, Wardell F, Vyvyan JP, Naji SA, Prescott GJ, Eagles JM. Anorexia nervosa mortality in Northeast Scotland, 1965–1999.  Am J Psychiatry. 2005;162(4):165-172
PubMed   |  Link to Article
Sullivan PF, Bulik CM, Fear JL, Pickering A. Outcome of anorexia nervosa: a case-control study.  Am J Psychiatry. 1998;155(7):939-946
PubMed
Lindblad F, Lindberg L, Hjern A. Improved survival in adolescent patients with anorexia nervosa: a comparison of two Swedish national cohorts of female inpatients.  Am J Psychiatry. 2006;163(8):1433-1435
PubMed   |  Link to Article
Halvorsen I, Andersen A, Heyerdahl S. Good outcome of adolescent onset anorexia nervosa after systematic treatment: intermediate to long-term follow-up of a representative county-sample.  Eur Child Adolesc Psychiatry. 2004;13(5):295-306
PubMed   |  Link to Article
Wentz E, Gillberg IC, Anckarsäter H, Gillberg C, Råstam M. Adolescent-onset anorexia nervosa: 18-year outcome.  Br J Psychiatry. 2009;194(2):168-174
PubMed   |  Link to Article
Keel PK, Mitchell JE. Outcome in bulimia nervosa.  Am J Psychiatry. 1997;154(3):313-321
PubMed
Bulik CM, Sullivan PF, Fear J, Pickering A. Predictors of the development of bulimia nervosa in women with anorexia nervosa.  J Nerv Ment Dis. 1997;185(11):704-707
PubMed   |  Link to Article
Eddy KT, Dorer DJ, Franko DL, Tahilani K, Thompson-Brenner H, Herzog DB. Diagnostic crossover in anorexia nervosa and bulimia nervosa: implications for DSM-V.  Am J Psychiatry. 2008;165(2):245-250
PubMed   |  Link to Article
World Health Organization.  International Statistical Classification of Diseases, 10th Revision (ICD-10). Geneva, Switzerland: World Health Organization; 1992
Agras WS, Crow S, Mitchell JE, Halmi KA, Bryson S. A 4-year prospective study of Eating Disorder NOS compared with full eating disorder syndromes.  Int J Eat Disord. 2009;42(6):565-570
PubMed   |  Link to Article
Ösby U, Correia N, Brandt L, Ekbom A, Sparén P. Mortality and causes of death in schizophrenia in Stockholm County, Sweden.  Schizophr Res. 2000;45(1):21-28
PubMed   |  Link to Article
Deter HC, Schellberg D, Köpp W, Friederich HC, Herzog W. Predictability of a favorable outcome in anorexia nervosa.  Eur Psychiatry. 2005;20(2):165-172
PubMed   |  Link to Article
Ösby U, Brandt L, Correia N, Ekbom A, Sparén P. Excess mortality in bipolar and unipolar disorder in Sweden.  Arch Gen Psychiatry. 2001;58(9):844-850
PubMed   |  Link to Article

Figures

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Figure 1. Literature review method used. AN indicates anorexia nervosa; BN, bulimia nervosa; EDNOS, eating disorder not otherwise specified.

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Graphic Jump Location

Figure 2. Annual mortality rate per 1000 person-years in anorexia nervosa. Studies include male and female patients.

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Graphic Jump Location

Figure 3. Standardized mortality ratios (95% confidence intervals) in patients with bulimia nervosa.

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Graphic Jump Location

Figure 4. Mortality rates per person-years in patients with eating disorder not otherwise specified.

Tables

References

Hoek HW, van Hoeken D. Review of the prevalence and incidence of eating disorders.  Int J Eat Disord. 2003;34(4):383-396
PubMed   |  Link to Article
Preti A, de Girolamo G, Vilagut G, Alonso J, Graaf R, Bruffaerts R, Demyttenaere K, Pinto-Meza A, Haro JM, Morosini P.ESEMeD-WMH Investigators.  The epidemiology of eating disorders in six European countries: results of the ESEMeD-WMH project.  J Psychiatr Res. 2009;43(14):1125-1132
PubMed   |  Link to Article
American Psychiatric Association.  Diagnostic and Statistical Manual of Mental Disorders. ed 4. Washington, DC: American Psychiatric Association; 1994
Button EJ, Benson E, Nollett C, Palmer RL. Don't forget EDNOS (eating disorder not otherwise specified): patterns of service use in an eating disorders service.  Psychiatr Bull. 2005;29:134-136
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Fairburn CG, Cooper Z, Bohn K, O’Connor ME, Doll HA, Palmer RL. The severity and status of eating disorder NOS: implications for DSM-V.  Behav Res Ther. 2007;45(8):1705-1715
PubMed   |  Link to Article
Steinhausen H-C. Outcome of eating disorders.  Child Adolesc Psychiatr Clin N Am. 2009;18(1):225-242
PubMed   |  Link to Article
Löwe B, Zipfel S, Buchholz C, Dupont Y, Reas DL, Herzog W. Long-term outcome of anorexia nervosa in a prospective 21-year follow-up study.  Psychol Med. 2001;31(5):881-890
PubMed
Herzog DB, Greenwood DN, Dorer DJ, Flores AT, Ekeblad ER, Richards A, Blais MA, Keller MB. Mortality in eating disorders: a descriptive study.  Int J Eat Disord. 2000;28(1):20-26
PubMed   |  Link to Article
Korndörfer SR, Lucas AR, Suman VJ, Crowson CS, Krahn LE, Melton LJ III. Long-term survival of patients with anorexia nervosa: a population-based study in Rochester, Minn.  Mayo Clin Proc. 2003;78(3):278-284
PubMed   |  Link to Article
Eckert ED, Halmi KA, Marchi P, Grove W, Crosby R. Ten-year follow-up of anorexia nervosa: clinical course and outcome.  Psychol Med. 1995;25(1):143-156
PubMed   |  Link to Article
Strober M, Freeman R, Morrell W. The long-term course of severe anorexia nervosa in adolescents: survival analysis of recovery, relapse, and outcome predictors over 10-15 years in a prospective study.  Int J Eat Disord. 1997;22(4):339-360
PubMed   |  Link to Article
Pompili M, Mancinelli I, Girardi P, Ruberto A, Tatarelli R. Suicide in anorexia nervosa: a meta-analysis.  Int J Eat Disord. 2004;36(1):99-103
PubMed   |  Link to Article
Muir A, Palmer RL. An audit of a British sample of death certificates in which anorexia nervosa is listed as a cause of death.  Int J Eat Disord. 2004;36(3):356-360
PubMed   |  Link to Article
Nielsen S. Epidemiology and mortality of eating disorders.  Psychiatr Clin North Am. 2001;24(2):201-214
PubMed   |  Link to Article
Keel PK, Dorer DJ, Eddy KT, Franko D, Charatan DL, Herzog DB. Predictors of mortality in eating disorders.  Arch Gen Psychiatry. 2003;60(2):179-183
PubMed   |  Link to Article
Rosling AM, Sparén P, Norring C, von Knorring A-L. Mortality of eating disorders: a follow up study of treatment in a specialist unit 1974-2000.  Int J Eat Disord. 2011;44(4):304-310
PubMed   |  Link to Article
Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease.  J Natl Cancer Inst. 1959;22(4):719-748
PubMed
Egger M, Smith GD, Phillips AN. Meta-analysis: principles and procedures.  BMJ. 1997;315(7121):1533-1537
PubMed   |  Link to Article
Møller-Madsen S, Nystrup J, Nielsen S. Mortality in anorexia nervosa in Denmark during the period 1970-1987.  Acta Psychiatr Scand. 1996;94(6):454-459
PubMed   |  Link to Article
Crow S, Praus B, Thuras P. Mortality from eating disorders: a 5- to 10-year record linkage study.  Int J Eat Disord. 1999;26(1):97-101
PubMed   |  Link to Article
Crow SJ, Peterson CB, Swanson SA, Raymond NC, Specker S, Eckert ED, Mitchell JE. Increased mortality in bulimia nervosa and other eating disorders.  Am J Psychiatry. 2009;166(12):1342-1346
PubMed   |  Link to Article
Button EJ, Chadalavada B, Palmer RL. Mortality and predictors of death in a cohort of patients presenting to an eating disorders service.  Int J Eat Disord. 2010;43(5):387-392
PubMed
Fichter MM, Quadflieg N. Twelve-year course and outcome of bulimia nervosa.  Psychol Med. 2004;34(8):1395-1406
PubMed   |  Link to Article
Steinhausen H-C. The outcome of anorexia nervosa in the 20th century.  Am J Psychiatry. 2002;159(8):1284-1293
PubMed   |  Link to Article
Theander S. Anorexia nervosa: a psychiatric investigation of 94 female patients.  Acta Psychiatr Scand Suppl. 1970;214:1-194
PubMed
Papadopoulos FC, Ekbom A, Brandt L, Ekselius L. Excess mortality, causes of death and prognostic factors in anorexia nervosa.  Br J Psychiatry. 2009;194(1):10-17
PubMed   |  Link to Article
Joergensen J. The epidemiology of eating disorders in Fyn County, Denmark, 1977-1986.  Acta Psychiatr Scand. 1992;85(1):30-34
PubMed   |  Link to Article
Tanaka H, Kiriike N, Nagata T, Riku K. Outcome of severe anorexia nervosa patients receiving inpatient treatment in Japan: an 8-year follow-up study.  Psychiatry Clin Neurosci. 2001;55(4):389-396
PubMed   |  Link to Article
Pagsberg AK, Wang AR. Epidemiology of anorexia nervosa and bulimia nervosa in Bornholm County, Denmark, 1970-1989.  Acta Psychiatr Scand. 1994;90(4):259-265
PubMed   |  Link to Article
Dancyger IF, Sunday SR, Eckert ED, Halmi KA. A comparative analysis of Minnesota Multiphasic Personality Inventory profiles of anorexia nervosa at hospital admission, discharge, and 10-year follow-up.  Compr Psychiatry. 1997;38(3):185-191
PubMed   |  Link to Article
Deter H-C, Herzog W. Anorexia nervosa in a long-term perspective: results of the Heidelberg-Mannheim Study.  Psychosom Med. 1994;56(1):20-27
PubMed
Birmingham CL, Su J, Hlynsky JA, Goldner EM, Gao M. The mortality rate from anorexia nervosa.  Int J Eat Disord. 2005;38(2):143-146
PubMed   |  Link to Article
Fichter MM, Quadflieg N, Hedlund S. Twelve-year course and outcome predictors of anorexia nervosa.  Int J Eat Disord. 2006;39(2):87-100
PubMed   |  Link to Article
Ben-Tovim DI, Walker K, Gilchrist P, Freeman R, Kalucy R, Esterman A. Outcome in patients with eating disorders: a 5-year study.  Lancet. 2001;357(9264):1254-1257
PubMed   |  Link to Article
Crisp AH, Callender JS, Halek C, Hsu LK. Long-term mortality in anorexia nervosa: a 20-year follow-up of the St George's and Aberdeen cohorts.  Br J Psychiatry. 1992;161:104-107
PubMed   |  Link to Article
Crisp A, Gowers S, Joughin N, McClelland L, Rooney B, Nielsen S, Bowyer C, Halek C, Hartman D, Tattersall M, Hugo P, Robinson D, Atkinson R, Clifton A. Death, survival and recovery in anorexia nervosa: a thirty five year study.  Eur Eat Disord Rev. 2006;14(3):168-175
Link to Article
Tolstrup K, Brinch M, Isager T, Nielsen S, Nystrup J, Severin B, Olesen NS. Long-term outcome of 151 cases of anorexia nervosa: The Copenhagen Anorexia Nervosa Follow-Up Study.  Acta Psychiatr Scand. 1985;71(4):380-387
PubMed   |  Link to Article
Hebebrand J, Himmelmann GW, Herzog W, Herpertz-Dahlmann BM, Steinhausen H-C, Amstein M, Seidel R, Deter H-C, Remschmidt H, Schäfer H. Prediction of low body weight at long-term follow-up in acute anorexia nervosa by low body weight at referral.  Am J Psychiatry. 1997;154(4):566-569
PubMed
Patton GC. Mortality in eating disorders.  Psychol Med. 1988;18(4):947-951
PubMed   |  Link to Article
Lee S, Chan YYL, Hsu LKG. The intermediate-term outcome of Chinese patients with anorexia nervosa in Hong Kong.  Am J Psychiatry. 2003;160(5):967-972
PubMed   |  Link to Article
Franko DL, Keel PK, Dorer DJ, Blais MA, Delinsky SS, Eddy KT, Charat V, Renn R, Herzog DB. What predicts suicide attempts in women with eating disorders?  Psychol Med. 2004;34(5):843-853
PubMed   |  Link to Article
Signorini A, De Filippo E, Panico S, De Caprio C, Pasanisi F, Contaldo F. Long-term mortality in anorexia nervosa: a report after an 8-year follow-up and a review of the most recent literature.  Eur J Clin Nutr. 2007;61(1):119-122
PubMed   |  Link to Article
Morgan HG, Purgold J, Welbourne J. Management and outcome in anorexia nervosa: a standardized prognostic study.  Br J Psychiatry. 1983;143:282-287
PubMed   |  Link to Article
Millar HR, Wardell F, Vyvyan JP, Naji SA, Prescott GJ, Eagles JM. Anorexia nervosa mortality in Northeast Scotland, 1965–1999.  Am J Psychiatry. 2005;162(4):165-172
PubMed   |  Link to Article
Sullivan PF, Bulik CM, Fear JL, Pickering A. Outcome of anorexia nervosa: a case-control study.  Am J Psychiatry. 1998;155(7):939-946
PubMed
Lindblad F, Lindberg L, Hjern A. Improved survival in adolescent patients with anorexia nervosa: a comparison of two Swedish national cohorts of female inpatients.  Am J Psychiatry. 2006;163(8):1433-1435
PubMed   |  Link to Article
Halvorsen I, Andersen A, Heyerdahl S. Good outcome of adolescent onset anorexia nervosa after systematic treatment: intermediate to long-term follow-up of a representative county-sample.  Eur Child Adolesc Psychiatry. 2004;13(5):295-306
PubMed   |  Link to Article
Wentz E, Gillberg IC, Anckarsäter H, Gillberg C, Råstam M. Adolescent-onset anorexia nervosa: 18-year outcome.  Br J Psychiatry. 2009;194(2):168-174
PubMed   |  Link to Article
Keel PK, Mitchell JE. Outcome in bulimia nervosa.  Am J Psychiatry. 1997;154(3):313-321
PubMed
Bulik CM, Sullivan PF, Fear J, Pickering A. Predictors of the development of bulimia nervosa in women with anorexia nervosa.  J Nerv Ment Dis. 1997;185(11):704-707
PubMed   |  Link to Article
Eddy KT, Dorer DJ, Franko DL, Tahilani K, Thompson-Brenner H, Herzog DB. Diagnostic crossover in anorexia nervosa and bulimia nervosa: implications for DSM-V.  Am J Psychiatry. 2008;165(2):245-250
PubMed   |  Link to Article
World Health Organization.  International Statistical Classification of Diseases, 10th Revision (ICD-10). Geneva, Switzerland: World Health Organization; 1992
Agras WS, Crow S, Mitchell JE, Halmi KA, Bryson S. A 4-year prospective study of Eating Disorder NOS compared with full eating disorder syndromes.  Int J Eat Disord. 2009;42(6):565-570
PubMed   |  Link to Article
Ösby U, Correia N, Brandt L, Ekbom A, Sparén P. Mortality and causes of death in schizophrenia in Stockholm County, Sweden.  Schizophr Res. 2000;45(1):21-28
PubMed   |  Link to Article
Deter HC, Schellberg D, Köpp W, Friederich HC, Herzog W. Predictability of a favorable outcome in anorexia nervosa.  Eur Psychiatry. 2005;20(2):165-172
PubMed   |  Link to Article
Ösby U, Brandt L, Correia N, Ekbom A, Sparén P. Excess mortality in bipolar and unipolar disorder in Sweden.  Arch Gen Psychiatry. 2001;58(9):844-850
PubMed   |  Link to Article

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Submit a Comment
Exploring heterogeneity
Posted on August 12, 2011
Caroline Huas, MD, PhD
Inserm U669 Paris ; Univ Paris-Sud & Paris Descartes, UMR-S0669; Dept of GP, Univ Tours, France,
Conflict of Interest: None Declared
We read the meta-analysis by Arcelus et al. confirming excess mortality for eating disorders patients, particularly anorexia nervosa (AN), with great interest. We would particularly like to discuss the great heterogeneity evidenced across AN mortality studies when pooling SMRs (I^2=91%), but not mentioned for annual mortality rates. Heterogeneity corresponds to differences across studies and needs to be explored via subgroup, sensitivity or meta-regression analyses before interpreting results.1
Heterogeneity regarding AN mortality could firstly be explained by variations in participant characteristics related to the type of recruitment. Patients in clinical settings may not be representative of all patients with the disorder, because of the 'filtering' effect occurring in the pathways to care.2 Inpatients are usually more severe than outpatients,2 have lower BMI, and present more psychiatric comorbidities,3 all being risk factors for mortality in anorexic patients. In this meta-analysis, the overall weighted annual mortality rate for AN was 5.10 deaths (95% CI: 3.99-6.14), but slightly lower for inpatients (4.55 deaths) (95% CI: 3.09-6.28) in a sensitivity analysis, which seems surprising. Just three studies (Papadopoulos,4 Linbald5 and Halvorsen6) represent 82.7% of all subjects from the 15 inpatients studies, and 72.9% of deaths. These studies however included inpatients with primary and secondary AN diagnoses, so that patients could have been hospitalized for reasons other than AN. Clinical severity indicators (current and minimum BMI, duration of illness, etc.) were not reported, but patients could be less severe than those in tertiary care centers. In line with Rosling et al7 we have shown that ten years on average after their hospitalization in a tertiary center, 539 AN inpatients had a SMR of 10.6 (CI 95% [7.6-14.4]).8 This result from an adult population (mean age= 26.0 (6.8) years) raises questions.
The second explanation for heterogeneity could be age of onset and/or treatment, a link highlighted by the authors. The mortality rates for AN treated during adolescence is lower than in adults.9 Only 20% of ED adolescents will develop a chronic disorder and need care in adulthood, and can explain increased risk for mortality for adults.
The third explanation could be a gender effect. In a recent study, 10 we highlighted a specific excess mortality for males: SMR=6.55; CI95% [2.21 – 15.28]) for 23 AN inpatient men hospitalized between 1988 and 2007, nearly half that for AN inpatient women in the same care unit.8
Another important cause of heterogeneity that requires systematic assessment is the methodological variations across studies.1 This meta- analysis included some studies with large numbers lost to follow-up, which could influence the mortality rates observed.
Finally, we fully agree with the authors concerning the difficulty in interpreting mortality rates cross-sectionally and the need to identify risk factors and potential therapeutic targets. In the previously mentioned sample of AN inpatients, several risk factors were highlighted, such as desired BMI, ED chronicity and suicide attempt; for details see.8 In addition we highlighted two mortality predictive factors for BN inpatients, low minimum lifetime BMI (possibly related to a previous AN diagnosis) and previous suicide attempt. These factors should be taken into account by clinicians as indicators of greater mortality risk to intensify post-hospitalization programs or to adapt treatment.
1. Egger M, Smith GD, Altman DG. Systematic Reviews in Health care: Meta-analysis in Context: BMJ books; 2001.
2. American Psychiatric Association. Treatment of patients with eating disorders, third edition. American Psychiatric Association. Am J Psychiatry. Jul 2006;163(7 Suppl):4-54.
3. Godart NT, Perdereau F, Rein Z, et al. Comorbidity studies of eating disorders and mood disorders. Critical review of the literature. J Affect Disord. Jan 2007;97(1-3):37-49.
4. Papadopoulos FC, Ekbom A, Brandt L, Ekselius L. Excess mortality, causes of death and prognostic factors in anorexia nervosa. Br J Psychiatry. Jan 2009;194(1):10-17.
5. Lindblad F, Lindberg L, Hjern A. Improved survival in adolescent patients with anorexia nervosa: a comparison of two Swedish national cohorts of female inpatients. Am J Psychiatry. Aug 2006;163(8):1433-1435.
6. Halvorsen I, Andersen A, Heyerdahl S. Good outcome of adolescent onset anorexia nervosa after systematic treatment. Intermediate to long-term follow-up of a representative county-sample. Eur Child Adolesc Psychiatry. Oct 2004;13(5):295-306.
7. Rosling AM, Sparen P, Norring C, von Knorring AL. Mortality of eating disorders: a follow-up study of treatment in a specialist unit 1974-2000. Int J Eat Disord. May 2011;44(4):304-310.
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Conflict of Interest: None declared
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