eMedicine Specialties > Psychiatry > Psychosomatic
Somatoform Disorders: Treatment & Medication
Updated: Feb 4, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
- Emergency department care: Somatoform disorders may present to the emergency room for assessment and treatment during periods of acute increase in symptom severity.
- Electroconvulsive therapy is not effective for somatoform disorders, but it may successfully treat depression occurring in the context of a somatoform disorder.
- Obtain necessary studies to rule out physical causes such as myocardial infarction or appendicitis.
- Intravenous or oral acute sedation with benzodiazepines may be used.
- Avoid long-term benzodiazepines for somatoform disorders.
- Avoid acute or long-term narcotic analgesics for somatoform disorders.
- Treatment of conversion disorder in the emergency room: Conversion disorder may be interpreted by the patient and family as a sign of an acute and potentially catastrophic medical condition. ER personnel should quickly rule out potential life-threatening, disabling, or treatable causes for the symptoms. Emotional support should be provided to patient's family members. Early consultation with a psychiatrist may limit unnecessary medical or surgical interventions. Referral to psychiatrist may be prefaced by stating that the cause for the medical symptoms have not been found and that in similar cases, assessment of the role of stress by a medical psychiatrist may be helpful in reducing the discomfort experienced by the patient.
- Psychosocial interventions (primary care management)
- Randomized trials have demonstrated the value of physician education in the management of the patient with somatization.2,3
- Cognitive-behavioral psychotherapy strategies may be specifically helpful in reducing distress and high medical use.
- Psychosocial interventions directed by physicians form the basis for successful treatment.
- A strong relationship between the patient and the primary care physician can assist in long-term management.
- Psychoeducation can be helpful by letting the patient know that physical symptoms may be exacerbated by anxiety or other emotional problems. However, be careful because patients are likely to resist suggestions that their condition is due to emotional rather than physical problems.
- The primary care physician should inform the patient that the symptoms do not appear to be due to a life-threatening, disabling, medical condition and should schedule regular visits for reassessment and reinforcement of the lacking severity of ongoing symptoms.
- The patient also may be told that some patients with similar symptoms have had spontaneous improvement, implying that spontaneous improvement may occur.
- However, the physician should accept the patient's physical symptoms and not pursue a goal of symptom resolution.
- Indeed, regular, noninvasive, medical assessment reduces anxiety and limits health care–seeking behavior; this may be facilitated by regularly scheduled visits with the patient's primary care physician.
- Encourage patients to remain active and limit the effect of target symptoms on the quality of life and daily functioning.
- Family members should not become preoccupied with the patients physical symptoms or medical care.
- Family members should direct the patient to report symptoms to their primary care physician.
- Psychosocial interventions for specific somatoform disorders
- Somatization disorder: Patients may resist suggestions for individual or group psychotherapy because they view their illness as a medical problem. Patients who accept psychotherapy may be able to reduce health care utilization. Psychosocial interventions that focus on maintaining social and occupational function despite chronic medical symptoms may be helpful.
- Conversion disorder: Limited studies about specific psychotherapy exist for conversion disorder. Behavior therapy or hypnosis may be effective. Symptoms often resolve spontaneously.
- Hypochondriasis: Physicians should attempt to answer questions and reduce the patient's fear of a specific illness. Group psychotherapy may provide social support and reduce anxiety. Cognitive therapy strategies may help by focussing on distorted disease-related cognitions. Individual insight-oriented psychotherapy has not been proven effective.
- Pain disorder: Behavior therapy, including biofeedback, can be helpful. Hypnosis also may be considered for chronic pain syndromes. Some outcome data supports the effectiveness of individual psychotherapy. Exploration of interpersonal effects of chronic pain may reduce social complications of pain.
Consultations
- Psychiatrist
Medication
Somatization disorder: For people with somatization disorder, medication approaches rarely are successful. Physicians should search for evidence of psychiatric comorbidity, such as depression or an anxiety disorder. If present, medication interventions specific to the diagnosis can be attempted. Successful treatment of a major depression or an anxiety disorder, such as panic disorder, also may produce significant reduction in somatization disorder. Nonmedication strategies are the most successful. See psychosocial treatment in Medical Care for more details.
Hypochondriasis: Hypochondriasis may be a feature of a mood or anxiety disorder. Pharmacologic treatment of the mood or anxiety disorder may reduce hypochondriacal symptoms. If a mood or anxiety disorder is present, see Medical Care. Group psychotherapy is very effective in a medical setting.
Conversion disorder: No specific pharmacological interventions have been shown to be effective for conversion disorder.
Pain disorder: Analgesic therapy often is ineffective for somatoform disorders characterized a pain disorder. Tricyclic antidepressants and selective serotonin reuptake inhibitors (SSRI) may be helpful.
Body dysmorphic disorder: Randomized controlled trials demonstrate that selective serotonin reuptake inhibitors reduce symptoms in as many as one half of individuals with body dysmorphic disorders. Case reports have suggested improvement with other agents, including monoamine oxidase inhibitors, tricyclic antidepressants, and the pimozide (an antipsychotic).
Antidepressants
Imipramine is a tricyclic antidepressant that has demonstrated clear superiority over the placebo in double-blind trials for treating specific symptoms of bulimia nervosa. However, SSRIs (eg, fluoxetine) probably should be first-line agents.
SSRIs are greatly preferred over the other classes of antidepressants. Because the adverse effect profile of SSRIs is less prominent, improved compliance is promoted. SSRIs do not have the cardiac arrhythmia risk associated with tricyclic antidepressants. Arrhythmia risk is especially pertinent in overdose, and suicide risk must always be considered when treating a child or adolescent with mood disorder.
Physicians are advised to be aware of the following information and use appropriate caution when considering treatment with SSRIs in the pediatric population.
In December 2003, the UK Medicines and Healthcare Products Regulatory Agency (MHRA) issued an advisory that most SSRIs are not suitable for use by persons younger than 18 years for treatment of "depressive illness." After review, this agency decided that the risks to pediatric patients outweigh the benefits of treatment with SSRIs, except fluoxetine (Prozac), which appears to have a positive risk-benefit ratio in the treatment of depressive illness in patients younger than 18 years.
In October 2003, the US Food and Drug Administration (FDA) issued a public health advisory regarding reports of suicidality in pediatric patients being treated with antidepressant medications for major depressive disorder. This advisory reported suicidality (both ideation and attempts) in clinical trials of various antidepressant drugs in pediatric patients. The FDA has asked that additional studies be performed because suicidality occurred in both treated and untreated patients with major depression and thus could not be definitively linked to drug treatment.
Imipramine (Tofranil)
Inhibits reuptake of norepinephrine or serotonin (5-hydroxytryptamine, 5-HT), at presynaptic neuron. One of the oldest agents available for the treatment of depression and has established efficacy in the treatment of panic disorder. Geriatric and adolescent patients may need lower dosing or slower titration.
Adult
50-75 mg PO qd initial; titrate gradually to 150 mg qd according to tolerance; range, 75-300 mg/d hs or in divided doses
Pediatric
Not established
Increases toxicity of sympathomimetic agents (eg, isoproterenol, epinephrine) by potentiating effects and inhibiting antihypertensive effects of clonidine
Documented hypersensitivity; narrow-angle glaucoma; acute recovery phase following myocardial infarction; history of bipolar disorders; avoid in patients taking MAOIs or fluoxetine or in patients who took them in the 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
May impair mental or physical abilities required for performance of potentially hazardous tasks; caution in cardiovascular disease, conduction disturbances, seizure disorders, urinary retention, hyperthyroidism, or patients receiving thyroid replacement; an ECG prior to initiation of therapy with imipramine may be warranted, also repeating once on a stable dose, to monitor any potential widening of QRS
Fluoxetine (Prozac)
Selectively inhibits presynaptic serotonin reuptake with minimal or no effect in the reuptake of norepinephrine or dopamine.
Adult
10-20 mg/d PO initial; 20-60 mg PO maintenance
Pediatric
10-20 mg/d PO
Increases toxicity of diazepam and trazodone by decreasing clearance; also increases toxicity of MAOIs and highly protein-bound drugs
Documented hypersensitivity; patients concurrently taking MAOIs or patients who took them in the last 2 wk
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Some patients may experience increased anxiety and agitation, especially with first dose; caution in preexisting seizure disorders, recent myocardial infarction, unstable heart disease, and hepatic or renal impairment
More on Somatoform Disorders |
| Overview: Somatoform Disorders |
| Differential Diagnoses & Workup: Somatoform Disorders |
Treatment & Medication: Somatoform Disorders |
| Follow-up: Somatoform Disorders |
| Multimedia: Somatoform Disorders |
| References |
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References
Baruffol E, Thilmany MC. Anxiety, depression, somatization and alcohol abuse. Prevalence rates in a general Belgian community sample. Acta Psychiatr Belg. May-Jun 1993;93(3):136-53. [Medline].
Martin A, Rauh E, Fichter M, Rief W. A one-session treatment for patients suffering from medically unexplained symptoms in primary care: a randomized clinical trial. Psychosomatics. Jul-Aug 2007;48(4):294-303. [Medline].
Smith GR Jr, Monson RA, Ray DC. Psychiatric consultation in somatization disorder. A randomized controlled study. N Engl J Med. May 29 1986;314(22):1407-13. [Medline].
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. Fourth Edition. Text Revision. Washington, DC, American Psychiatric Association. 2000.
Barsky AJ, Ahern DK. Cognitive behavior therapy for hypochondriasis: a randomized controlled trial. JAMA. Mar 24 2004;291(12):1464-70. [Medline].
Baumeister H, Härter M. Prevalence of mental disorders based on general population surveys. Soc Psychiatry Psychiatr Epidemiol. May 21 2007;[Medline].
Bleichhardt G, Timmer B, Rief W. Cognitive-behavioural therapy for patients with multiple somatoform symptoms--a randomised controlled trial in tertiary care. J Psychosom Res. Apr 2004;56(4):449-54. [Medline].
Chioqueta AP, Stiles TC. Suicide risk in patients with somatization disorder. Crisis. 2004;25(1):3-7. [Medline].
de Waal MW, Arnold IA, Eekhof JA, van Hemert AM. Somatoform disorders in general practice: prevalence, functional impairment and comorbidity with anxiety and depressive disorders. Br J Psychiatry. Jun 2004;184:470-6. [Medline].
Dickinson WP, Dickinson LM, deGruy FV. A randomized clinical trial of a care recommendation letter intervention for somatization in primary care. Ann Fam Med. Nov-Dec 2003;1(4):228-35. [Medline].
Fink P, Sorensen L, Engberg M. Somatization in primary care. Prevalence, health care utilization, and general practitioner recognition. Psychosomatics. Jul-Aug 1999;40(4):330-8. [Medline].
Kroenke K, Spitzer RL, deGruy FV 3rd. A symptom checklist to screen for somatoform disorders in primary care. Psychosomatics. May-Jun 1998;39(3):263-72. [Medline].
Morriss RK, Gask L, Ronalds C. Clinical and patient satisfaction outcomes of a new treatment for somatized mental disorder taught to general practitioners. Br J Gen Pract. Apr 1999;49(441):263-7. [Medline].
Phillips KA. Body dysmorphic disorder: diagnostic controversies and treatment challenges. Bull Menninger Clin. Winter 2000;64(1):18-35. [Medline].
Phillips KA, Albertini RS, Rasmussen SA. A randomized placebo-controlled trial of fluoxetine in body dysmorphic disorder. Arch Gen Psychiatry. Apr 2002;59(4):381-8. [Medline].
Smith GR Jr, Rost K, Kashner TM. A trial of the effect of a standardized psychiatric consultation on health outcomes and costs in somatizing patients. Arch Gen Psychiatry. Mar 1995;52(3):238-43. [Medline].
Smith RC, Gardiner JC, Lyles JS, et al. Exploration of DSM-IV criteria in primary care patients with medically unexplained symptoms. Psychosom Med. Jan-Feb 2005;67(1):123-9. [Medline].
Werring DJ, Weston L, Bullmore ET. Functional magnetic resonance imaging of the cerebral response to visual stimulation in medically unexplained visual loss. Psychol Med. May 2004;34(4):583-9. [Medline].
Further Reading
Keywords
somatization, body dysmorphic disorder, conversion disorder, hypochondriasis, somatization disorder, somatoform disorder NOS, somatoform disorder not otherwise specified, unexplained physical symptoms
Treatment & Medication: Somatoform Disorders