eMedicine Specialties > Psychiatry > Adult

Bulimia: Treatment & Medication

Author: Raj K Kalapatapu, MD, Fellow, Addiction Psychiatry, Columbia University College of Physicians and Surgeons
Coauthor(s): Kelda Harris Walsh, MD, Assistant Professor of Clinical Psychiatry, Section of Child and Adolescent Psychiatry, Department of Psychiatry, Indiana University School of Medicine; Chief, Obsessive-Compulsive/Tourette/Anxiety Disorders Clinic, Riley Hospital for Children; Gabriel I Uwaifo, MBBS, Clinical and Research Attending, Assistant Professor of Medicine and Endocrinology, MedStar Clinical Research Center, MedStar Research Institute and Washington Hospital Center; Robert C Daly, MB, ChB, MPH, BCh, Senior Fellow, Department of Behavioral Endocrinology, National Institute of Mental Health, National Institutes of Health
Contributor Information and Disclosures

Updated: Aug 12, 2008

Treatment

Medical Care

The proper management of bulimia is with a multidisciplinary approach. The minimum of care providers who should be involved in the care of these patients are the primary care provider, psychiatrist, psychotherapist, and a dietitian. Involvement of a psychotherapist with expertise in the management of eating disorders is strongly recommended. Dietary review and nutritional rehabilitation counseling should be provided by a nutritionist/registered dietitian. Depending on circumstances and complications, those with bulimia may also require the services of an endocrinologist or surgeon.

  • The goals of treatment are as follows:67
    • Reduce and, where possible, eliminate binge eating and purging
    • Treat physical complications
    • Enhance patients' motivation to cooperate in the restoration of healthy eating patterns and participate in treatment
    • Provide education regarding healthy nutrition and eating patterns
    • Help patients reassess and change core dysfunctional thoughts, attitudes, motives, conflicts, and feelings related to bulimia
    • Treat associated psychiatric conditions, including deficits in mood and impulse regulation, self-esteem, and behavior
    • Enlist family support and provide family counseling and therapy where appropriate
    • Prevent relapse

Treatment should be comprehensive and multidisciplinary and may include the following components:67

  • Nutritional rehabilitation counseling: A structured meal plan is a means to reduce the episodes of dietary restriction and the urges to binge and purge. Adequate nutritional intake can prevent craving and promote satiety. Assessing nutritional intake for all patients, even those with a normal body weight (or normal BMI), is important because normal weight does not ensure appropriate nutritional intake or normal body composition. Among patients of normal weight, nutritional counseling is a useful part of treatment and helps reduce food restriction, increase the variety of foods eaten, and promote healthy but not compulsive exercise patterns.
  • Cognitive behavioral psychotherapy (CBT): Distorted or maladaptive cognitions regarding weight and shape are identified and addressed. Irrational beliefs are explored and confronted. Behavioral approaches to avoiding undesirable eating habits are used, including exposure to food. Cognitive distortions are examined to allow better understanding, enhanced self-control, and improved body image. The cognitive component of CBT appears to be the active ingredient for change, as behavioral interventions alone are not as effective.68,69
  • Interpersonal psychotherapy (IPT): Interpersonal psychotherapy works with specific issues in the interpersonal arena that create the context for the patient's symptoms; these fall within the categories of grief, role transition, role conflict, or interpersonal deficits. Brief focused therapy in these areas can be effective in producing improvements in those with mood disturbance and low self-esteem, which may trigger and maintain the symptoms of bulimia. Its efficacy is similar to CBT in reducing binge eating but may be somewhat less effective in curbing purging.
  • Family therapy: Family therapy explores family dynamics, dysfunctional relationships, and factors that may precipitate or perpetuate abnormal eating and bingeing behaviors. This technique often views eating as a means of communication within a family. Family therapy should be considered especially for adolescent patients still living with their parents or older patients with ongoing conflicted interactions with parents.
  • Psychodynamic psychotherapy: Using psychodynamic interventions in conjunction with CBT and other psychotherapies may yield better global outcomes. Some patients, particularly those with concurrent personality pathology or other co-occurring disorders, require lengthy treatment. Clinical reports suggest that psychodynamic and psychoanalytic approaches in individual or group format are useful once bingeing and purging improve.
  • Couples therapy: Patients with marital discord may benefit from couples therapy. Among people with bulimia in married or other cohabiting consensual adult relationships, the research is limited. Overall, these relationships are generally suggested to be suboptimal, with the appearance of impaired levels of intimacy in such relationships and suboptimal communication skills. Self-consciousness and self-silencing during sexual activity, and anxious attachment may be associated with bulimic symptoms.70 Counseling and openness about these problems may assist with the management of the bulimia.
  • Support and self-help groups: Support groups and 12-step programs such as Overeaters Anonymous may be helpful as adjuncts in the initial treatment of bulimia and for subsequent relapse prevention, but they are not recommended as the sole initial treatment approach for bulimia. In the most recent update of the Self-help and guided self-help for eating disorders in the Cochrane Database of Systematic Reviews,71 efficacies of pure self-help (PSH) and guided self-help (GSH) were mixed. PSH/GSH did not significantly differ from waiting list in abstinence from bingeing or purging, although PSH/GSH produced greater improvement on other eating disorder symptoms, psychiatric symptomatology and interpersonal functioning but not depression.
  • Supportive-expressive psychotherapy (SEP) or group therapy: SEP or group therapy may be helpful for patients with bulimia.
  • Bright light therapy has been shown to reduce binge frequency in several controlled trials and may be used as an adjunct when CBT and antidepressant therapy have not been effective in reducing bingeing symptoms.72
  • One study provided some support for guided imagery compared to journaling, although long-term maintenance of treatment effects is unknown.68 Dialectical behavior therapy and integrative cognitive-affective therapy may have an emerging role in treatment.73
  • Self-help support may also be available through books and online.
  • Pharmacotherapy: (see Medication)

Initial care may be on an inpatient or outpatient basis, depending on the clinical presentation. Factors that may indicate a need for inpatient care include significant metabolic abnormalities, medical complications, risk of suicide, failed outpatient treatment, inability to care for self, and diagnostic uncertainty.

  • Inpatient care for the patient with bulimia should be considered when any of the following are present, alone or in combination:67
    • Diagnostic uncertainty
    • Associated secondary infections
    • Medical comorbidities (eg, arrhythmias, significant electrolyte derangements, dehydration, organ compromise requiring acute treatment)
    • Suicidality with specific plan with high lethality or intent
    • Absence of a support structure at home
    • Severe impairments in the patient's capacity to function in regular daily activities (ie, severe psychosocial impairment)
    • Failed outpatient treatment
    • Significant concerns over follow-up (whether patient or program related)
    • Any existing psychiatric disorder that would require hospitalization

Surgical Care

Major medical treatment requiring surgical intervention is rare, but medical care providers should be familiar with potential serious complications.

  • Patients may develop an acute gastric obstruction and/or gastric dilatation74 (possibly resulting in gastric perforation leading to acute peritonitis), which presents with severe, continuous projectile vomiting that occurs soon after any oral intake. This should be considered in individuals with known bulimia who present complaining of uncontrollable vomiting. Consumption of nonfood material during binges or soon after should be considered, as well.
    • When the potential for gastric dilatation, outlet obstruction, or both is considered, an urgent surgical consultation is indicated for possible surgical management.
    • These conditions are surgical emergencies and, although uncommon, are the major cause of bulimia-related mortality.
  • Emergency surgical review is also required if symptoms suggestive of esophageal tear (Mallory-Weiss syndrome) develop or in case of esophageal rupture, which can precipitate acute mediastinitis. (See Media files 2-9). For more information, see eMedicine articles Mallory-Weiss Syndrome and Esophageal Rupture.

Consultations

Dental professionals can play a unique role in opening a dialogue with patients about eating disorders. They can help with early recognition and refer patients to professionals specializing in the evaluation and treatment of eating disorders. The dental professional can become an important contributor to the recovery and long-term treatment of the patient with an eating disorder.56,75

Diet

As the disorder is treated, patient education regarding balanced diets, exercise, and long-term maintenance of a healthy weight is important and may reduce the risk of relapse or development of chronic symptoms.

Medication

  • Antidepressants as a group are the mainstay of pharmacotherapy.67 These may be helpful for patients with substantial concurrent symptoms of depression, anxiety, obsessions, or certain impulse disorder symptoms or for patients who have not benefited from or had only a suboptimal response to appropriate psychosocial therapy.
  • Selective serotonin reuptake inhibitors (SSRIs) have the most evidence for efficacy and the fewest difficulties with adverse side effects.76,67 Only fluoxetine (Prozac) is approved by the Food and Drug Administration (FDA) for treatment of bulimia. Sertraline is the only other SSRI that has been shown to be effective, as demonstrated in a small, randomized controlled trial. Fluvoxamine77 and citalopram78 have also shown benefit. The exact mechanism underlying the efficacy of antidepressants in bulimia is unclear, but the effects may be mediated through their salutary impact on cerebral serotonin systems.
  • Bupropion (Wellbutrin) is relatively contraindicated in the treatment of bulimia nervosa because of a higher risk of seizures induced by the medication.67
  • Tricyclic antidepressants79 and monoamine oxidase inhibitors (MAOIs) have been used in patients with bulimia, although rarely, but are not recommended as initial treatments.67
  • Small controlled trials have demonstrated efficacy of the anticonvulsant topiramate, but because adverse reactions to this medication are common, it should be used only when other medications have proven ineffective. Also, because patients tend to lose weight on topiramate, its use is problematic for normal or underweight patients.67,80
  • Lithium and valproic acid, both mood stabilizers, are prone to induce weight gain in patients and may be less acceptable to patients who are weight preoccupied. Lithium is not recommended for patients with bulimia because it is ineffective. In patients with co-occurring bipolar disorder and bulimia nervosa, treatment with lithium is more likely to be associated with toxicity.67,81
  • Reports suggest the use of ondansetron,82 baclofen,83 and an antiandrogenic oral contraceptive84 as alternative pharmacotherapeutic options in the management of bulimia nervosa. Trials investigating naltrexone (ReVia) and venlafaxine have shown no significant benefit.
  • Clinicians must be aware of the black box warnings relating to antidepressants and discuss the potential benefits and risks of antidepressant treatment with patients and families if such medications are to be prescribed. See the statement on Antidepressant Use in Children, Adolescents, and Adults by the Food and Drug Administration.
  • Case reports indicate that methylphenidate may be helpful for patients with bulimia nervosa and concurrent ADHD. Methylphenidate should be used only for patients who have a very clear diagnosis of ADHD.67
  • The most recent update of Antidepressants versus placebo for people with bulimia nervosa in the Cochrane Database of Systematic Reviews included tricyclic antidepressants (TCAs), SSRIs, MAOIs, and other classes of drugs (mianserin, trazodone, bupropion). Similar results were obtained in terms of efficacy for these different groups of drugs. Patients with TCAs depressed out due to any cause more frequently than patients with placebo, and the opposite was found for fluoxetine.85

Antidepressants

SSRIs are the most commonly prescribed medications. Doses are higher than those typically used for depression management.


Fluoxetine (Prozac)

Selectively inhibits presynaptic serotonin reuptake with minimal effect in the reuptake of norepinephrine or dopamine. The antidepressant, anti-obsessive-compulsive, and antibulimic actions are presumed to be linked to inhibition of CNS neuronal uptake of serotonin. Efficacy was demonstrated in two 8-wk and one 16-wk multicenter parallel group studies of adult outpatients meeting DSM-III-R criteria for bulimia. Patients in the 8-wk studies received either 20 mg/d or 60 mg/d of fluoxetine or placebo in the morning. Patients in the 16-wk study received a fixed fluoxetine dose of 60 mg/d or placebo. Patients in these 3 studies had moderate-to-severe bulimia with median binge eating and vomiting frequencies ranging from 7-10 episodes per wk and 5-9 episodes per wk, respectively. Fluoxetine 60 mg (but not 20 mg) was superior to placebo in reducing the number of binge-eating and vomiting episodes per wk.

Adult

60-80 mg PO qd

Pediatric

Not established

Increases toxicity of diazepam, alprazolam, midazolam, flecainide, vinblastine, TCAs, and trazodone by decreasing clearance; also increases toxicity of MAOIs, haloperidol, clozapine, phenytoin, carbamazepine, and highly protein-bound drugs (eg, warfarin, digoxin); monitor lithium levels (levels reported to increase or decrease with concurrent use)

Documented hypersensitivity; current use of MAOIs or use within previous 2 wk

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in hepatic impairment and history of seizures; MAOIs should be discontinued at least 14 d before initiating fluoxetine therapy; adverse effects include anxiety, nervousness, insomnia, mania/hypomania, and anorexia


Desipramine (Norpramin)

Secondary-amine tricyclic that may increase synaptic concentration of norepinephrine in CNS by inhibiting reuptake by presynaptic neuronal membrane. May have effects in the desensitization of adenyl cyclase, down-regulation of beta-adrenergic receptors, and down-regulation of serotonin receptors.

Adult

100-300 mg PO qd

Pediatric

Not established

Decreases antihypertensive effects of clonidine and guanethidine but increases effects of sympathomimetics, cimetidine, and benzodiazepines; effects of desipramine increase with phenytoin, phenothiazines, carbamazepine, and barbiturates

Documented hypersensitivity; narrow-angle glaucoma, recent postmyocardial infarction; current use of MAOIs or fluoxetine or use within previous 2 wk

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in cardiovascular disease, conduction disturbances, seizure disorders, urinary retention, glaucoma, hyperthyroidism, and thyroid replacement therapy; may impair mental and/or physical abilities


Amitriptyline (Elavil)

Inhibits reuptake of serotonin and/or norepinephrine at presynaptic neuronal membrane, which increases concentration in CNS. May increase or prolong neuronal activity since reuptake of these biogenic amines is important physiologically in terminating transmitting activity.

Adult

25-150 mg PO qd

Pediatric

Not established

Phenobarbital may decrease effects; coadministration with CYP2D6 enzyme (debrisoquin hydroxylase) system inhibitors (eg, cimetidine, quinidine) may increase amitriptyline levels; inhibits hypotensive effects of guanethidine; may interact with thyroid medications, SSRIs, alcohol, CNS depressants, barbiturates, and disulfiram; if given with anticholinergic agents or sympathomimetic drugs, including epinephrine combined with local anesthetics, close supervision and careful adjustment of dosages is required; hyperpyrexia reported with concurrent use of anticholinergic agents or with neuroleptic drugs, particularly during hot weather; caution if patients receive large doses of ethchlorvynol concurrently (transient delirium has been reported)

Documented hypersensitivity; MAOIs in past 14 d; acute phase after MI; history of seizures, cardiac arrhythmias, glaucoma, or urinary retention

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in cardiac conduction disturbances and history of hyperthyroidism, seizures, urinary retention, angle-closure glaucoma or increased intraocular pressure, and hepatic or renal impairment; avoid using in elderly persons


Imipramine (Tofranil)

Dibenzazepine antidepressant, referred to as a tricyclic because of its chemical structure. Metabolized to desipramine, which is marketed separately.
Inhibits reuptake of norepinephrine or serotonin (5-hydroxytryptamine, 5-HT) at presynaptic neuron.
Use parenteral administration for starting therapy only in patients unable or unwilling to use oral medication.
Has demonstrated clear superiority over placebo in double-blind trials for treating specific symptoms of bulimia nervosa.

Adult

25 mg PO tid initially and increase 25-50 mg at weekly intervals prn to 200 mg/d; not to exceed 300 mg/d

Pediatric

<6 years: Not established
6-12 years: 10-30 mg/d PO or 1-5 mg/kg/d PO in divided doses
>12 years: Administer as in adults

Increases toxicity of sympathomimetic agents such as isoproterenol and epinephrine by potentiating effects and inhibiting antihypertensive effects of clonidine; coadministration with or use within 2 wk of MAOIs or fluoxetine may cause serotonin syndrome or hypertensive crisis

Documented hypersensitivity; narrow-angle glaucoma; acute recovery phase following myocardial infarction; current use of MAOIs or fluoxetine or use within previous 2 wk

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

May impair mental or physical abilities required for performance of potentially hazardous tasks including handling machinery, driving; caution in cardiovascular disease, conduction disturbances, seizure disorders, asthma, mental illness, Parkinson disease, increased intraocular pressure or angle-closure glaucoma, benign prostatic hypertrophy, GI disease, gastroesophageal reflux disease (GERD), urinary retention, hyperthyroidism, or receiving thyroid replacement; can induce or exacerbate hiatal hernia, and can cause paralytic ileus or constipation; anticholinergic effects may increase lens discomfort (eg, mydriasis, disturbance of accommodation, dry eyes) for contact lens wearers; avoid abrupt discontinuation (may cause nausea, vomiting, or diarrhea); agranulocytosis, thrombocytopenia, eosinophilia, leukopenia, and purpura reported; photosensitivity may occur with prolonged exposure to sunlight or tanning equipment

More on Bulimia

Overview: Bulimia
Differential Diagnoses & Workup: Bulimia
Treatment & Medication: Bulimia
Follow-up: Bulimia
Multimedia: Bulimia
References
Further Reading

References

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Keywords

bulimia nervosa, BN, binge-eating/purging eating disorder, binge-eating disorder, BED, binging and purging, pathological voracity, cynorexia, kynorexia, morbid hunger, eating disorder, ED, excessive exercise, fasting, dieting, self-induced vomiting, diuretic abuse, laxative abuse, use of appetite suppressants, thyroid hormone, subjective bulimic episode

Contributor Information and Disclosures

Author

Raj K Kalapatapu, MD, Fellow, Addiction Psychiatry, Columbia University College of Physicians and Surgeons
Raj K Kalapatapu, MD is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, American Association for Geriatric Psychiatry, American Medical Association, and American Psychiatric Association
Disclosure: Nothing to disclose.

Coauthor(s)

Kelda Harris Walsh, MD, Assistant Professor of Clinical Psychiatry, Section of Child and Adolescent Psychiatry, Department of Psychiatry, Indiana University School of Medicine; Chief, Obsessive-Compulsive/Tourette/Anxiety Disorders Clinic, Riley Hospital for Children
Kelda Harris Walsh, MD is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry and American Psychiatric Association
Disclosure: Nothing to disclose.

Gabriel I Uwaifo, MBBS, Clinical and Research Attending, Assistant Professor of Medicine and Endocrinology, MedStar Clinical Research Center, MedStar Research Institute and Washington Hospital Center
Gabriel I Uwaifo, MBBS is a member of the following medical societies: American Association of Clinical Endocrinologists, American College of Physicians-American Society of Internal Medicine, American Diabetes Association, American Medical Association, American Society of Hypertension, and Endocrine Society
Disclosure: Nothing to disclose.

Robert C Daly, MB, ChB, MPH, BCh, Senior Fellow, Department of Behavioral Endocrinology, National Institute of Mental Health, National Institutes of Health
Disclosure: Nothing to disclose.

Medical Editor

Sarah C Aronson, MD, Associate Professor, Departments of Psychiatry and Medicine, Case Western Reserve School of Medicine/University Hospitals of Cleveland
Sarah C Aronson, MD is a member of the following medical societies: American Academy of Family Physicians, American Medical Association, and American Psychiatric Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

David Bienenfeld, MD, Vice-Chair, Program Director, Professor, Department of Psychiatry, Wright State University School of Medicine
David Bienenfeld, MD is a member of the following medical societies: American Medical Association, American Psychiatric Association, and Association for Academic Psychiatry
Disclosure: Nothing to disclose.

CME Editor

Harold H Harsch, MD, Program Director of Geropsychiatry, Department of Geriatrics/Gerontology, Associate Professor, Department of Psychiatry and Department of Medicine, Froedtert Hospital, Medical College of Wisconsin
Harold H Harsch, MD is a member of the following medical societies: American Psychiatric Association
Disclosure: lilly Honoraria Speaking and teaching; Forest Labs Honoraria Speaking and teaching; AstraZeneca Honoraria Speaking and teaching; Pfizer Grant/research funds Speaking and teaching; Northstar Grant/research funds Research; Novartis Grant/research funds research; Pfizer  Speaking and teaching; Sanofi-avetis Grant/research funds research; Otsuke Grant/research funds reseach; GlaxoSmithKline Grant/research funds research

Chief Editor

Stephen Soreff, MD, President of Education Initiatives, Nottingham, NH; Faculty, Metropolitan College of Boston University, Boston, MA
Stephen Soreff, MD is a member of the following medical societies: American College of Mental Health Administration and American Psychosomatic Society
Disclosure: Nothing to disclose.

 
 
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