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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people.

Body Dysmorphic Disorder (BDD)

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Body Dysmorphic Disorder (BDD) is a preoccupation with an imagined defect in appearance, or excessive concern over a slight physical anomaly. It is characterised by time-consuming behaviours such as mirror gazing, comparing one's appearance with others, excessive camouflaging to hide the defect, skin picking and seeking reassurance. One study suggested that patients with BDD pay more attention to facial appearance in others, compared to controls.1

Epidemiology

Population surveys produce different results from audits of clinical samples and seem to suggest a predominance of females. 0.5-0.7% is reported in audits of of clinical samples, but population surveys suggest a higher figure of 1-2%. One study found that 10% of patients presenting to a maxillofacial clinic had BDD. Another found a prevalence of 5-15% of patients seeking cosmetic surgery or dermatological treatment to enhance their appearance.2

Differences between BDD and obsessive compulsive disorder (OCD)3

Although there are many similarities between the two conditions - which often co-exist - some differences have been identified. Patients with BDD have significantly poorer insight than those with OCD and are more likely to be delusional. They are also significantly more likely to have lifetime suicidal ideation, as well as lifetime major depressive disorder and a lifetime substance use disorder. See also our dedicated record on OCD.

The GP's role4

NICE recommend referral to a specialist multi-discipline team offering age-appropriate care. This is unlikely to be available in many areas due to lack of resources, but it is worth getting in touch with local mental health trusts to see what is currently available. The GP's role depends on expertise but it should be remembered that drug management should be part of a package which includes psychological care.
In all patients, however, the GP will need to:

  • Identify cases.
  • For patients at risk of BDD (depression, social phobia, substance misuse, OCD,5 eating disorder, mild disfigurement or blemish seeking dermatology or cosmetic surgery referral) ask the following questions:
    • Do you worry a lot about the way you look and wish you could think about it less?
    • What specific concerns do you have about your appearance?
    • On a typical day, how many hours a day is your appearance on your mind? (More than 1 hour a day is considered excessive).
    • What effect does it have on your life?
    • Does it make it hard to do your work or be with friends?
  • Assess severity - i.e. how much it is affecting the patient's ability to function in everyday life.
  • Assess risk of self-harm or suicide and presence of co-morbidity such as depression.
  • Arrange referral to appropriate secondary care provision.
  • Ensure continuity of care to avoid multiple assessments, gaps in service and a smooth transition from child to adult services (many patients have lifelong symptoms).
  • Promote understanding - make patients/families aware of involuntary nature of symptoms. Consider patient information leaflets, contact numbers of self-help groups, etc.
  • Consider the bigger picture - cultural, social, emotional and mental health needs.
  • If patient is a parent, consider child protection issues.
Management in adults4

Patients with mild functional impairment can be managed with low intensity psychological treatment. This may involve:

  • Individual Cognitive Behaviour Therapy (CBT) plus Exposure and Response Prevention (ERP)*
  • Individual CBT and ERP by telephone
  • Group CBT

*ERP is a technique in which patients are repeatedly exposed to the situation causing them anxiety (e.g. exposure to dirt) and are prevented from performing repetitive actions which lessens that anxiety (e.g. washing their hands). This method is only used after extensive counselling and discussion with the patient who knows fully what to expect. After an initial increase in anxiety, the level gradually decreases. This is extremely therapeutic, as the patient feels that they have confronted their worse fears without anything terrible happening.

  • Adults with mild symptoms should be offered an selective serotonin reuptake inhibitor (SSRI) if they cannot engage in low-intensity psychological treatment, if such treatment has failed, or if they opt not to have more intensive psychological treatment.
  • Adults with moderate symptoms or where low-intensity psychological treatment has failed should be offered high-intensity CBT and ERP (more than 10 hours per patient) or an SSRI.
  • Adults with severe symptoms - offer high-intensity psychological therapy plus an SSRI.
Management in children4
  • Mild dysfunction - offer guided self help. As for moderate to severe if this fails.
  • Moderate to severe - offer CBT ERP as for adults but involve family/carers: individual or group depending on the preference of the patient.
  • If psychological treatment fails, factors which might require other interventions may be involved, e.g. co-existence of comorbid conditions, learning disorders, persisting psychosocial risk factors such as family discord, presence of parental mental health problems. In children over the age of 8, adding SSRI might be appropriate,following multidisciplinary review (but see below concerning safety issues).

Using SSRIs4,6

See our record Selective Serotonin Re-uptake Inhibitors and below:

  • SSRIs in Adults - evidence for use of SSRIs in OCD is stronger than for BDD. Caution is advised in view of increased risk of suicidal thoughts and self-harm in people with depression. It is unclear whether this applies to people with OCD or BDD in absences of other co-morbidity; further guidance is awaited.

    When prescribing, discuss the following and provide written supporting material:
    • Craving and tolerance do not occur.
    • There is a risk of discontinuation/withdrawal symptoms on stopping the drug, missing doses, or reducing the dose.
    • There is a range of potential side effects, (see individual drugs) including worsening anxiety, suicidal thoughts and self-harm, which need to be carefully monitored, especially in the first few weeks of treatment.
    • There is commonly a delay in onset up to 12 weeks, although depressive symptoms improve more quickly.
    • In high risk patients, prescribe limited quantities, keep in contact especially during first few weeks and actively monitor for akathisia (restlessness and the urge to move), suicidal ideation, increased anxiety, agitation.
    • Monitor all patients around time of dosage changes.
    • NICE recommends fluoxetine as there is more supporting evidence than for other SSRIs.
    • If there is no response to a standard dose, check compliance, check interaction with drugs and alcohol, then consider titrating to maximum dose according to the Product Characteristics.
    • Continue for at least twelve months, withdraw gradually.
  • SSRIs in Children and young people (8-18 years)
    • Caution is advised as there is a risk of self-harm or suicide in patients with depression. Only prescribed by specialists, in conjunction with psychological therapy following assessment by child and adolescent psychiatrist who should also be involved in dosage changes and discontinuation.
    • Fluoxetine is the first-line SSRI for BDD. In the presence of depression, follow NICE guidance for treatment of childhood depression.
    • Discuss adverse effects, dosage, monitoring etc with patient/family/carers as per adults (see above).

Treatment failures (applicable to adults, children and young people)4,7,8

The following in conjunction with specialist assessment and multi-disciplinary review:

  • Try another SSRI.
  • Change to clonidine - but greater tendency to produce adverse effects. Do baseline ECG and check BP, start with small dose, titrate according to response, monitor regularly.
  • Antipsychotics - sometimes used to augment effect of SSRI.
  • In-patient treatment - for 'last resort' treatment failures.
  • Residential/supportive care - for patients with chronic severe dysfunction.
  • Patients with BDD do not usually benefit from surgical treatment.9


Document references
  1. Stangier U, Adam-Schwebe S, Muller T, et al; Discrimination of facial appearance stimuli in body dysmorphic disorder. J Abnorm Psychol. 2008 May;117(2):435-43. [abstract]
  2. Sarwer DB, Crerand CE; Body dysmorphic disorder and appearance enhancing medical treatments. Body Image. 2008 Mar;5(1):50-8. Epub 2008 Feb 5. [abstract]
  3. Phillips KA, Pinto A, Menard W, et al; Obsessive-compulsive disorder versus body dysmorphic disorder: a comparison study of two possibly related disorders. Depress Anxiety. 2007;24(6):399-409. [abstract]
  4. Obsessive Compulsive Disorder, NICE (2005); (Core interventions in the treatment of obsessive compulsive disorder and body dysmorphic disorder)
  5. Stewart SE, Stack DE, Wilhelm S; Severe obsessive-compulsive disorder with and without body dysmorphic disorder: clinical correlates and implications. Ann Clin Psychiatry. 2008 Jan-Mar;20(1):33-8. [abstract]
  6. Depression in children and young people, NICE (2005); (Identification and management in primary, community and secondary care)
  7. Hewlett WA, Vinogradov S, Agras WSC; lomipramine, clonazepam, and clonidine treatment of obsessive-compulsive disorder. J Clin Psychopharmacol. 1992 Dec;12(6):420-30. [abstract]
  8. Matthews K, Eljamel MS; Status of neurosurgery for mental disorder in Scotland. Selective literature review and overview of current clinical activity. Br J Psychiatry. 2003 May;182:404-11. [abstract]
  9. Pavan C, Simonato P, Marini M, et al; Psychopathologic aspects of body dysmorphic disorder: a literature review. Aesthetic Plast Surg. 2008 May;32(3):473-84. [abstract]

Internet and further reading Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2008.
DocID: 8743
Document Version: 1
DocRef: bgp26145
Last Updated: 6 Nov 2008
Review Date: 6 Nov 2010

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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