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You are in: eMedicine Specialties >
Psychiatry > Adult
Anxiety Disorders
Article Last Updated: Aug 23, 2007
AUTHOR AND EDITOR INFORMATION
Section 1 of 11
Author: William R Yates, MD, Professor of Research, Department of Psychiatry, University of Oklahoma College of Medicine at Tulsa
William R Yates is a member of the following medical societies: Academy of Psychosomatic Medicine, American Academy of Family Physicians, and American Psychiatric Association
Editors: Denis F Darko, MD, Executive Director, Clinical Research and Development, Neuroscience Global Licensing Medical Director, Clinical Neuroscience Therapy Area and CNS and Pain Control Research Area, AstraZeneca LP; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Eduardo Dunayevich, MD, Adjunct Assistant Professor, Department of Psychiatry, University of Cincinnati; Clinical Research Physician, Neuroscience, Lilly Research Laboratories; 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; Stephen Soreff, MD, President of Education Initiatives, Nottingham, NH; Faculty, Metropolitan College of Boston University, Boston, MA
Author and Editor Disclosure
Synonyms and related keywords:
generalized anxiety disorder, panic disorder, phobia, agoraphobia, obsessive-compulsive disorder, OCD, stress, anxiety neurosis, nervousness, posttraumatic stress disorder, PTSD, substance-induced anxiety disorder, specific phobias, social phobia, adjustment disorder, acute stress disorder, major depression, separation anxiety, substance abuse disorder, recurrent distressing dreams, recurrent distressing nightmares, difficulty staying asleep, exaggerated startle response, hypervigilance, difficulty concentrating, anger outbursts, irritability, difficulty falling asleep, sweaty palms, restlessness
Background
Anxiety disorders are common psychiatric disorders. Many patients with anxiety disorders experience physical symptoms related to anxiety and subsequently visit their primary care physicians. Despite the high prevalence rates of these anxiety disorders, they often are underrecognized and undertreated clinical problems. The Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) classifies the anxiety disorders into the following categories:4
Pathophysiology
Anxiety disorders appear to be caused by an interaction of biopsychosocial factors, including genetic vulnerability, which interact with situations, stress, or trauma to produce clinically significant syndromes. In the central nervous system, the major mediators of the symptoms of anxiety disorders appear to be norepinephrine and serotonin. Other neurotransmitters and peptides, such as corticotropin-releasing factor, may be involved. Peripherally, the autonomic nervous system, especially the sympathetic nervous system, mediates many of the symptoms.
Frequency
United States
Two major studies in the United States have estimated the prevalence rates for a variety of anxiety disorders. These 2 studies are the Epidemiological Catchment Area (ECA) study1 and the National Comorbidity Survey (NCS) study2. Using these and other studies, the estimated lifetime prevalence rates for individual anxiety disorders are panic disorder (2.3-2.7%), generalized anxiety disorder (4.1-6.6%), OCD (2.3-2.6%), PTSD (1-9.3%), and social phobia (2.6-13.3%).
International
The prevalence of specific anxiety disorders appears to vary between countries and cultures. A cross-national study of the prevalence of panic disorder found lifetime prevalence rates ranging from 0.4% in Taiwan to 2.9% in Italy. A cross-cultural study of the prevalence of OCD found lifetime prevalence rates ranging from 0.7% in Taiwan to 2.5% in Puerto Rico.3
Mortality/Morbidity
- Anxiety disorders may contribute to morbidity and mortality through neuroendocrine and neuroimmune mechanisms or by direct neural stimulation, eg, hypertension or cardiac arrhythmia.
- Severe anxiety disorders may be complicated by suicide, with or without secondary mood disorders (eg, depression). Anxiety disorders have high rates of comorbidity with major depression and alcohol and drug abuse. Some of the increased morbidity and mortality associated with anxiety disorders may be related to this high rate of comorbidity. The ECA study found that panic disorder was associated with suicide attempts (odds ratio=18 compared to populations without psychiatric disorders). How much of the association of panic disorder with suicide is mediated through the association of panic disorder with mood and substance abuse disorders is unclear. Acute stress may play a role in producing suicidal behavior. Suicide attempts can be precipitated by adverse life events such as divorce or financial disaster. The effects of acute stress in producing suicidal behavior are increased in those with underlying mood, anxiety, and substance abuse problems.
- Chronic anxiety may be associated with increased risk for cardiovascular morbidity and mortality.
Race
- The ECA study found no difference in rates of panic disorder among white, African American, or Hispanic populations in the United States.
- Some studies have found higher rates of PTSD in minority populations. Some of this association may be due to higher rates of specific traumatic events (ie, assault) in minority populations.
Sex
- The female-to-male ratio for any lifetime anxiety disorder is 3:2.
Age
- Most anxiety disorders begin in childhood, adolescence, and early adulthood. Separation anxiety is an anxiety disorder of childhood that often includes anxiety related to going to school. This disorder may be a precursor for adult anxiety disorders. Panic disorder demonstrates a bimodal age of onset in the NCS study in the age groups of 15-24 years and 45-54 years. The median age of onset of social phobia in the NCS study was 16 years. The age of onset for OCD appears to be in the mid 20s to early 30s.
- New-onset anxiety symptoms in older adults should prompt a search for an unrecognized general medical condition, a substance abuse disorder, or major depression with secondary anxiety symptoms.
History
Symptoms vary depending on the specific anxiety disorder. To rule out anxiety disorders secondary to general medical or substance abuse conditions, a detailed history and review of symptoms is essential. Review use of caffeine-containing beverages (coffee, tea, colas, Mountain Dew), over-the-counter medications (aspirin with caffeine, sympathomimetics), herbal "medications," or street drugs. Ask the patient's sleep partner about apneic episodes or myoclonic limb jerks. Concurrent depressive symptoms are common in all of the anxiety disorders. Severe anxiety disorders may produce agitation, suicidal ideation, and increased risk of completed suicide. Always ask about suicidal ideation or suicidal intent. - Panic disorder is characterized by recurrent panic attacks (ie, periods of intense fear of abrupt onset peaking in intensity within 10 min). Four of the following must be present for a panic attack:
- Palpitations, pounding heart, or accelerated heart rate
- Sweating
- Trembling or shaking
- Shortness of breath or dyspnea
- Sensation of choking
- Chest pain or discomfort
- Nausea or abdominal distress
- Feeling dizzy, unsteady, lightheaded, or faint
- Derealization or depersonalization
- Fear of losing control or going crazy
- Fear of dying
- Paresthesias
- Chills or hot flashes
- Although not a diagnostic feature, suicidal ideation and completed suicide have been associated with panic disorder.
- Generalized anxiety disorder is characterized by excessive anxiety and worry. Worrying is difficult to control. Anxiety and worry are associated with at least 3 of the following symptoms:
- Restlessness or feeling keyed-up or on edge
- Being easily fatigued
- Difficulty concentrating or mind going blank
- Irritability
- Muscle tension
- Sleep disturbance
- Although not a diagnostic feature, suicidal ideation and completed suicide have been associated with generalized anxiety disorder.
- OCD is characterized by obsessions or compulsions. Obsessions or compulsions must be recognized as unreasonable or excessive and must cause marked distress.
- Obsessions include all of the following:
- Recurrent and persistent thoughts, impulses, or images that are intrusive and knowingly inappropriate and cause anxiety or distress
- Thoughts, impulses, or images that are not simply excessive worries about real-life problems
- Attempts are made to ignore or suppress thoughts.
- Thoughts, impulses, or images are recognized as being the product of the mind and not imposed from an outside force.
- Compulsions include the following:
- Repetitive behaviors, such as handwashing, ordering, and checking, that people feel are driven and must be carried out and occur to such an extreme that a person's ability to function is impaired.
- Behaviors or mental acts are done to reduce distress or anxiety.
- Social phobia
- Marked and persistent fear of social or performance situations to the extent that a person's ability to function at work or in school is impaired.
- Exposure to social or performance situation always produces anxiety.
- Fear/anxiety recognized as excessive
- Social or performance situations are avoided or endured with intense anxiety.
- Avoidance behavior, anticipation, or distress in the feared social or performance setting produces significant impairment in functioning.
- PTSD is a severe trauma that is experienced that includes (1) actual or threatened death or serious injury or threat to personal integrity of self or others and (2) responses that include intense fear, helplessness, or horror. (Life-threatening experiences and the attendant loss of control are key elements.)
- Persistent reexperience of the event occurs by at least 1 of the following:
- Recurrent and intrusive recollections
- Recurrent distressing dreams/nightmares
- Feelings of reliving traumatic event, ie, flashbacks
- Intense psychologic distress with internal or external cues to the trauma
- Physiological reactivity on exposure to trauma cues
- Persistent avoidance of stimuli of trauma and numbing/avoidance behavior demonstrated by at least 3 of the following:
- Avoidance of thoughts or conversation related to the trauma
- Avoidance of activities, places, or people related to the trauma
- Amnesia for important trauma-related events
- Decreased participation in significant activities
- Feeling detached or estranged from others
- Restricted affect
- Foreshortened sense of the future
- Persistent symptoms of increased arousal demonstrated by 2 or more of the following:
- Difficulty staying or falling asleep
- Irritability or anger outbursts
- Difficulty concentrating
- Hypervigilance
- Exaggerated startle response
- Although not a diagnostic feature, suicidal and homicidal ideation have been associated with PTSD.
Physical
- Tremor
- Tachycardia
- Tachypnea
- Sweaty palms
- Restlessness
Causes
- First, evaluate for anxiety due to a known or unrecognized medical condition.
- Most presenting anxiety disorders are functional psychiatric disorders.
- Substance-induced anxiety disorder (over-the-counter medications, herbal medications, substances of abuse) is a diagnosis that often is missed.
Acute Respiratory Distress Syndrome
Addison Disease
Adrenal Crisis
Alcohol-Related Psychosis
Alcoholism
Amphetamine-Related Psychiatric Disorders
Anaphylaxis
Androgen Excess
Anorexia Nervosa
Apnea, Sleep
Asthma
Atrial Fibrillation
Atrial Tachycardia
Body Dysmorphic Disorder
Brief Psychotic Disorder
Bulimia
Caffeine-Related Psychiatric Disorders
Cannabis Compound Abuse
Cardiogenic Shock
Conversion Disorders
Delirium
Delirium Tremens
Delusional Disorder
Depression
Diabetes Mellitus, Type 1
Diabetic Ketoacidosis
Digitalis Toxicity
Dissociative Disorders
Dysthymic Disorder
Encephalopathy, Dialysis
Encephalopathy, Hepatic
Encephalopathy, Hypertensive
Encephalopathy, Uremic
Epilepsy Surgery
Esophageal Motility Disorders
Esophageal Spasm
Euthyroid Hyperthyroxinemia
Factitious Disorder
Fibromyalgia
Folic Acid Deficiency
Food Poisoning
Gastritis, Acute
Gastritis, Chronic
Goiter
Goiter, Diffuse Toxic
Hallucinogens
Hyperaldosteronism, Primary
Hypercalcemia
Hyperparathyroidism
Hyperprolactinemia
Hypersensitivity Reactions, Delayed
Hypersensitivity Reactions, Immediate
Inhalant-Related Psychiatric Disorders
Injecting Drug Use
Insomnia
Irritable Bowel Syndrome
Lyme Disease
Malingering
Meningitis
Multifocal Atrial Tachycardia
Personality Disorders
Phobic Disorders
Premenstrual Dysphoric Disorder
Primary Hypersomnia
Primary Insomnia
Schizoaffective Disorder
Schizophrenia
Shared Psychotic Disorder
Sleep Disorder, Geriatric
Sleep Disorders
Somatoform Disorders
Stimulants
Syndrome of Inappropriate Secretion of Antidiuretic Hormone
Thyroiditis, Subacute
Tourette Syndrome
Undifferentiated Connective-Tissue Disease
Unstable Angina
Other Problems to be Considered
Adult respiratory distress syndrome (ARDS)
AIDS
Thyrotoxicosis
Anxiety disorders have one of the longest differential diagnosis lists of all psychiatric disorders. Anxiety is a nonspecific syndrome and can be due to a variety of medical or psychiatric syndromes. A variety of anxiety symptoms, such as panic, worry, rumination, and obsessions, can present in a variety of psychiatric illnesses including mood disorders, psychotic disorders, personality disorders, somatoform disorders, and cognitive impairment disorders (eg, delirium). Anxiety also can be observed as part of a drug withdrawal or drug intoxication effect.
Other important causes in the differential include medication-induced anxiety (ie, due to epinephrine or other sympathomimetics, theophylline or other neurostimulant bronchodilators, analgesics containing caffeine, corticosteroids, antivirals, others); migraine, seizure disorders, or other CNS-based disorders; and sleep disorders such as restless legs syndrome, sleep apnea, and periodic limb movement. Heroin abuse also should be considered in the differentials.
Lab Studies
- When the index of suspicion for anxiety being produced by a medical disorder is low (lack of physical findings, younger age, typical anxiety disorder presentation), initial lab studies might be limited to the following:
- CBC count
- Chemistry profile
- Thyroid function tests
- Urinalysis
- Urine drug screen
- For presentations with a higher index of suspicion for other medical causes of anxiety (ie, atypical anxiety disorder presentation, older age, specific physical examination abnormalities), more detailed evaluations may be indicated as follows:
- Rule out CNS disorder using electroencephalogram, lumbar puncture, or brain CT scan, as indicated by history and associated clinical findings.
- Rule out cardiac disorder using ECG or treadmill ECG.
- Rule out infectious causes using rapid plasma reagent test, lumbar puncture (CNS infections), or HIV testing.
Imaging Studies
- Diagnostic imaging studies are not indicated in the diagnosis of primary anxiety disorders unless specific general medical conditions need to be ruled out.
- Imaging studies may be helpful, however, to rule out anxiety due to a general medical condition, eg, cephalic CT scan or MRI to evaluate for pathological intracranial processes.
Procedures
- Psychosurgery is used in rare cases of severe treatment-refractory OCD.
- Electroconvulsive therapy is not effective for anxiety disorders but may successfully treat comorbid conditions, such as severe major depression, and is especially indicated when the patient is at high risk for suicide.
Medical Care
Patients with panic disorder frequently present to the emergency department with chest pain or dyspnea, fearing that they are dying of myocardial infarction. Anxiety symptoms often accompany or can exacerbate respiratory conditions such as asthma and chronic obstructive pulmonary disease.
- If clinically indicated, obtain necessary studies to rule out myocardial infarction and pulmonary embolism (ECG, chest x-ray).
- Intravenous or oral acute sedation with benzodiazepines may be used. Untreated panic attacks can subside spontaneously within 20-30 minutes, especially with reassurance and a calming environment.
- If possible, avoid long-term benzodiazepines for chronic anxiety disorders. If this approach seems necessary, obtaining a confirming opinion from a consulting psychiatrist may be helpful.
Consultations
- Most often, psychiatrists are consulted.
- In anxiety disorders secondary to a general medical condition, specialty consultation may be indicated.
Diet
- Discontinue (or decrease to a low reasonable level) caffeine-containing products such as coffee, tea, colas, and Mountain Dew.
- Over-the-counter preparations and herbal remedies should be reviewed with special caution because ephedrine and other herbal compounds may precipitate or exacerbate anxiety symptoms.
Activity
- If no medical contraindication exists, recommend at least a mild-to-moderate daily exercise program.
The management of individual anxiety disorders is dependent on the specific diagnosis. Selective serotonin reuptake inhibitors (SSRIs) are helpful in a variety of anxiety disorders, including generalized anxiety disorder, panic disorder, OCD, and social phobia. Antidepressant agents are the drugs of choice in the treatment of anxiety disorders, particularly the newer agents that have a safer adverse effect profile and higher ease of use than the older tricyclic agents; however, benzodiazepines often are used as adjunct treatment. Some anticonvulsant medications, such as divalproex and gabapentin, may have a role in the treatment of anxiety disorders, especially in patients with high potential for abusing benzodiazepines. Older antidepressants, such as tricyclic antidepressants and monoamine oxidase inhibitors (MAOIs) also are effective in the treatment of some anxiety disorders. Caution in their use is warranted due to their higher toxicity and potential lethality in overdose. Their use should be limited to cases where SSRIs are ineffective or cannot be afforded. MAOIs may be especially indicated in treatment-refractory panic disorder. Clomipramine (Anafranil, a tricyclic agent) has a US Food and Drug Administration (FDA) indication in the treatment of OCD and is the only tricyclic agent effective in the treatment of this condition. Indeed, it can be effective in cases refractory to treatment with SSRI agents. MAOI agents also may have a role in the treatment of certain subtypes of OCD refractory to conventional treatment, such as patients with symmetry obsessions or associated panic attacks. The FDA has granted specific indications to the following disorders and agents: generalized anxiety disorder (venlafaxine, buspirone, escitalopram, paroxetine, duloxetine), social phobia (paroxetine, sertraline, venlafaxine), OCD (fluoxetine, sertraline, paroxetine, fluvoxamine), and PTSD (sertraline, paroxetine). All SSRIs may be equal in the treatment of anxiety disorders; however, higher doses may be necessary in the treatment of OCD. Antidepressants that are not FDA-approved for the treatment of a given anxiety disorder, such as nefazodone and mirtazapine, still may be beneficial. Patients with panic disorder may be more sensitive to treatment with antidepressants and frequently need lower initial doses and slower titration to accomplish successful therapy. Benzodiazepines are especially useful in the management of acute situational anxiety disorder and adjustment disorder where the duration of pharmacotherapy is anticipated to be 6 weeks or less and for the rapid control of panic attacks. If long-term use of benzodiazepines seems necessary, obtaining a confirmatory opinion from a second physician may be helpful because chronic benzodiazepine use may be associated with tolerance, withdrawal, and treatment-emergent anxiety.
The risk of addiction potential with benzodiazepines should be carefully considered before use in the anxiety disorders. Avoid use in patients with a prior history of alcohol or other drug abuse. Closely monitor for evidence of unauthorized dose escalation or obtaining benzodiazepine prescriptions from multiple sources.
Drug Category: Benzodiazepines
Several drugs in the benzodiazepine class can be used for the short-term (£6 wk) control of anxiety. Drugs in this class include lorazepam, diazepam, clonazepam, and chlordiazepoxide.
| Drug Name | Lorazepam (Ativan) |
| Description | Sedative hypnotic in the benzodiazepine class that has a short onset of effect and a relatively long half-life. By increasing action of gamma-aminobutyric acid (GABA), which is a major inhibitory neurotransmitter in the brain, may depress all levels of the CNS, including limbic and reticular formation. Available for PO, IV, or IM use. |
| Adult Dose | 0.5-6 mg PO/IV/IM in divided doses |
| Pediatric Dose | 0.25-2 mg PO/IV/IM in divided doses |
| Contraindications | Documented hypersensitivity; preexisting CNS depression, hypotension, and narrow-angle glaucoma |
| Interactions | Toxicity of benzodiazepines in CNS increases when used concurrently with alcohol, phenothiazines, barbiturates, and MAOIs |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
|
| Precautions | Be aware of the occasional patient (frequency depends on practice setting) with benzodiazepine drug-seeking behavior, ie, malingering In renal or hepatic impairment, myasthenia gravis, organic brain syndrome, or Parkinson disease, use shorter-acting benzodiazepines (eg, lorazepam, oxazepam) to avoid accumulation of active metabolites and drowsiness |
Drug Category: Serotonin and norepinephrine reuptake inhibitors
Pharmacologic agents with both reuptake inhibition of serotonin and norepinephrine may be helpful in a variety of mood and anxiety disorders.
| Drug Name | Venlafaxine (Effexor XR) |
| Description | FDA-approved for generalized anxiety disorder, panic disorder and social anxiety disorder in adults. May be helpful for other anxiety disorders. |
| Adult Dose | 37.5-300 mg extended-release formulation PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; patients taking MAOIs or those who have taken them within 14 days of initiating therapy |
| Interactions | Cimetidine, MAOIs, sertraline, fluoxetine class I-C antiarrhythmics, tricyclic antidepressants, and phenothiazine may increase effects |
| 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 | Patients may experience hypertension; fatal reaction may occur if taken concurrently with a MAOI; exercise caution in patients with cardiovascular disorders |
| Drug Name | Duloxetine (Cymbalta) |
| Description | Potent inhibitor of neuronal serotonin and norepinephrine reuptake. Indicated for generalized anxiety disorder. |
| Adult Dose | 30-60 mg PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; uncontrolled narrow-angle glaucoma; within 14 d of stopping MAOI use (do not initiate MAOIs within 5 d of stopping duloxetine) |
| Interactions | Metabolized by CYP1A2 and CYP2D6; coadministration with drugs that inhibit CYP1A2 (eg, fluvoxamine, cimetidine, ciprofloxacin, enoxacin) may increase duloxetine blood levels and toxicity; coadministration with drugs that inhibit CYP2D6 (eg, paroxetine, fluoxetine, quinidine) may increase duloxetine blood levels and toxicity; duloxetine moderately inhibits CYP2D6 and may decrease elimination of CYP2D6 substrates (eg, tricyclic antidepressants, phenothiazines [eg, thioridazine], type 1C antiarrhythmics [eg, propafenone, flecainide]); coadministration with MAOIs or triptans serotonin syndrome consisting of serious, sometimes fatal reactions that include hyperthermia, rigidity, myoclonus, autonomic instability, mental status changes including extreme agitation, delirium, and coma (see contraindications) |
| 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 | Observe closely for clinical worsening and suicidality when initiating treatment or following dosage change; gradually decrease dose when discontinuing, do not abruptly discontinue; caution with hepatic impairment or end-stage renal disease; recommended not to prescribe to patients with substantial alcohol use or evidence of chronic liver disease; may cause slight blood pressure increase; may activate mania or hypomania; common adverse effects include nausea, dry mouth, constipation, decreased appetite, fatigue, somnolence and increased sweating; may cause serotonin syndrome (ie, changes in mental status [agitation, hallucinations, coma], autonomic instability [tachycardia, labile blood pressure, hyperthermia], neuromuscular abnormalities [hyperreflexia, incoordination], and/or gastrointestinal tract symptoms |
Drug Category: Antianxiety agents
Buspirone is a novel antianxiety agent with no other members in its class.
| Drug Name | Buspirone (BuSpar) |
| Description | FDA-approved for generalized anxiety disorder in adults. Does not appear to be helpful as primary treatment for panic disorder or OCD. |
| Adult Dose | 15-60 mg PO qd/bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Toxicity increased with MAOIs, phenothiazines, and CNS depressants; increases toxicity of digoxin and haloperidol |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
|
| Precautions | Caution in hepatic or renal impairment |
Drug Category: Tricyclic antidepressants
A complex group of drugs that have central and peripheral anticholinergic effects, as well as sedative effects.
| Drug Name | Imipramine (Tofranil) |
| Description | Tricyclic antidepressant that has norepinephrine and serotonin reuptake-inhibition properties. One of the oldest agents available for the treatment of depression and has established efficacy in the treatment of panic disorder. Elderly and adolescent patients may need lower dosing or slower titration. |
| Adult Dose | Initial: 50-75 mg PO qd titrated gradually to 150 mg qd according to tolerance Dose range: 75-300 mg qd, administered either hs or divided doses |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma; acute recovery phase following myocardial infarction; history of bipolar disorders; patients taking MAOIs or fluoxetine or those who took them in the previous 2 wk |
| Interactions | Increases toxicity of sympathomimetic agents such as isoproterenol and epinephrine by potentiating effects and inhibiting antihypertensive effects of clonidine |
| 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 those receiving thyroid replacement; an ECG may be warranted prior to initiation of therapy with imipramine, repeat after dose stabilized to monitor any potential widening of QRS |
Drug Category: Antidepressant, Serotonin Reuptake Inhibitor
These agents specifically inhibit presynaptic reuptake or serotonin but not noradrenaline.
| Drug Name | Paroxetine (Paxil) |
| Description | FDA-approved for panic disorder, depression, social anxiety disorder, generalized anxiety disorder, posttraumatic stress disorder, and OCD. |
| Adult Dose | 10-60 mg PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; concurrent administration with MAOIs or administering within 14 days of discontinuing an MAOI |
| Interactions | Phenobarbital and phenytoin decrease effects; alcohol, cimetidine, sertraline, phenothiazines, and warfarin increase toxicity |
| 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 history of seizures, mania, renal disease, and cardiac disease |
| Drug Name | Escitalopram (Lexapro) |
| Description | FDA approved for generalized anxiety disorder. SSRI and S-enantiomer of citalopram. Used for the treatment of depression. Mechanism of action is thought to be potentiation of serotonergic activity in central nervous system resulting from inhibition of CNS neuronal reuptake of serotonin. Onset of depression relief may be obtained after 1-2 wk, which is sooner than other antidepressants. |
| Adult Dose | 10 mg PO qd initially; if needed, may increase to 20 mg/d after 1 wk
|
| Pediatric Dose | Not established
|
| Contraindications | Documented hypersensitivity; administration within 14 d of receiving MAOI |
| Interactions | Primarily metabolized by CYP450 3A4 and 2C19; coadministration with alcohol or other centrally acting drugs increases CNS depression; cimetidine increases AUC and maximum serum concentration; coadministration with sumatriptan and SSRIs has caused weakness and hyperreflexia |
| 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 with history of seizures, mania, suicide; common adverse effects include insomnia, ejaculation disorder (primarily ejaculatory delay), nausea, sweating, fatigue, and somnolence |
| Drug Name | Sertraline (Zoloft) |
| Description | FDA-approved for panic disorder, PTSD, social phobia, and OCD. May be helpful for other anxiety disorders. |
| Adult Dose | 50-200 mg PO; initiate at 25 mg/d and increase as tolerated, not to exceed 200 mg/d |
| Pediatric Dose | 25-100 mg PO qd |
| Contraindications | Documented hypersensitivity; within 14 d of taking an MAOI |
| Interactions | Increases toxicity of MAOIs, diazepam, tolbutamide, and warfarin |
| 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 preexisting seizure disorders and those who have experienced a recent myocardial infarction, have unstable heart disease, and hepatic or renal impairment |
| Drug Name | Fluoxetine (Prozac) |
| Description | FDA-approved for OCD and panic disorder. May be helpful for other anxiety disorders. |
| Adult Dose | 10-60 mg PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; concurrently taking MAOIs or took them in the last 2 wk |
| Interactions | Increases toxicity of diazepam and trazodone by decreasing clearance; increases toxicity of MAOIs and highly protein-bound drugs |
| 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 hepatic impairment and history of seizures; MAOIs should be discontinued at least 14 d before initiating therapy |
| Drug Name | Fluvoxamine (Luvox) |
| Description | FDA approved for OCD in children (8-17 y) and adults. May be helpful for other anxiety disorders. |
| Adult Dose | 50-300 mg PO qd |
| Pediatric Dose | 25-200 mg PO qd |
| Contraindications | Documented hypersensitivity; patients currently receiving MAOIs or those who took them in previous 2 wk |
| Interactions | Risk of a hypertensive crisis increases with coadministration with MAOIs; potentiates effect of triazolam and alprazolam and thus, when taking them concurrently, dose should be reduced by at least 50%; also reduce dose of theophylline by one third and monitor plasma levels if taking it concurrently with fluvoxamine; alcohol, cimetidine, sertraline, phenothiazines, and warfarin increase toxicity |
| 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 liver dysfunction or cardiovascular disease and history of seizures or suicidal tendencies |
Further Inpatient Care
- Inpatient care rarely is needed for the management of anxiety disorders unless complicated by comorbid conditions such as affective or substance abuse disorders or general medical conditions.
- Inpatient care should be considered if suicide is a risk or detoxification is needed for comorbid substance dependence.
Further Outpatient Care
- Anxiety disorders often are chronic and require ongoing medical/psychiatric care, including psychosocial therapies and medication (pharmacotherapy).
- Psychosocial interventions in anxiety disorder
- Cognitive-behavioral therapy often is efficacious and is the treatment of choice for specific phobias. It often is used alone or in combination with pharmacotherapy in the treatment of OCD and panic disorder.
- Other psychotherapeutic approaches, such as interpersonal therapy or psychodynamic therapy, also may be helpful in the treatment of anxiety disorders.
- Marital therapy, family therapy, or group therapy may be helpful adjunct therapies in the long-term management of severe anxiety disorders. Educating families and friends enables them to cope with their loved one's disease.
In/Out Patient Meds
- See Medication for recommendations for specific anxiety disorders.
- Generalized anxiety disorder
- Panic disorder
- OCD
- Simple phobia
- Social phobia
- PTSD
- Adjustment disorder with anxious mood
Complications
- Agoraphobia
- Major depression
- Suicide
- Homicide (especially in patients with PTSD)
- Alcohol abuse and dependence
- Sedative abuse and dependence
- Social dysfunction and withdrawal
- Occupational impairment
- Marital and familiar dysfunction, divorce
Prognosis
- Anxiety disorders can range from mild and transient to severe and chronic.
- Early treatment improves prognosis and limits social and occupational impairment.
Patient Education
- Education can be obtained through books, newsletters, support groups, and Internet sites.
- A helpful Internet resource for patient education regarding anxiety disorders is MentalHelp.net.
- For excellent patient education resources, visit eMedicine's Mental Health and Behavior Center, Anxiety Center, and Muscle Disorders Center. Also, see eMedicine's patient education articles Stress, Anxiety, Panic Attacks, and Hyperventilation.
- Family members should receive information about the effect of anxiety disorders on mood, behavior, and relationships. Family members can assist in care by reinforcing the need for medical treatment and supervision. Family members may also assist by providing a collaborative resource for monitoring the severity of the patient's anxiety symptoms and response to treatment interventions.
Medical/Legal Pitfalls
- Failure to identify a medical or psychiatric cause for anxiety
- Unnecessary and invasive diagnostic testing for physical symptoms caused by anxiety
- Benzodiazepine prescription use in those with comorbid alcohol or drug dependence
- Failure to recognize cognitive and motor impairment related to chronic high-dose benzodiazepine use
- Failure to recognize factitious disorder with psychological symptoms or malingering to obtain benzodiazepine prescription
| Media file 1:
Chart showing the female-to-male sex ratio for anxiety disorders. Adapted from Kessler et al, 1994. |
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- Robins, LN, Regier, DA. Psychiatric Disorders in America: The Epidemiologic Catchment Area Study. The Free Press; 1990.
- Kessler RC, McGonagle KA, Zhao S, et al. Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey. Arch Gen Psychiatry. Jan 1994;51(1):8-19. [Medline].
- Weissman MM, Bland RC, Canino GJ, Greenwald S, Hwu HG, Lee CK. The cross national epidemiology of obsessive compulsive disorder. The Cross National Collaborative Group. J Clin Psychiatry. Mar 1994;55 Suppl:5-10. [Medline].
- American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Text Revision. Washington, DC: American Psychiatric Association; 2000.
- American Psychiatric Association. Practice guideline for the treatment of patients with panic disorder. Work Group on Panic Disorder. American Psychiatric Association. Am J Psychiatry. May 1998;155(5 Suppl):1-34. [Medline].
- Bernstein GA, Shaw K. Practice parameters for the assessment and treatment of children and adolescents with anxiety disorders. American Academy of Child and Adolescent Psychiatry. J Am Acad Child Adolesc Psychiatry. Oct 1997;36(10 Suppl):69S-84S. [Medline].
- Bisson J, Andrew M. Psychological treatment of post-traumatic stress disorder (PTSD). Cochrane Database Syst Rev. 2005;CD003388. [Medline].
- Breslau N, Peterson EL, Poisson LM, Schultz LR, Lucia VC. Estimating post-traumatic stress disorder in the community: lifetime perspective and the impact of typical traumatic events. Psychol Med. Jul 2004;34(5):889-98. [Medline].
- Connolly SD, Bernstein GA,. Practice parameter for the assessment and treatment of children and adolescents with anxiety disorders. J Am Acad Child Adolesc Psychiatry. Feb 2007;46(2):267-83. [Medline].
- Jenike MA. Clinical practice. Obsessive-compulsive disorder. N Engl J Med. Jan 15 2004;350(3):259-65. [Medline].
- Kroenke K, Spitzer RL, Williams JB, Monahan PO, Löwe B. Anxiety disorders in primary care: prevalence, impairment, comorbidity, and detection. Ann Intern Med. Mar 6 2007;146(5):317-25. [Medline].
- Roy-Byrne PP, Craske MG, Stein MB, et al. A randomized effectiveness trial of cognitive-behavioral therapy and medication for primary care panic disorder. Arch Gen Psychiatry. Mar 2005;62(3):290-8. [Medline].
- Stein MB, Simmons AN, Feinstein JS, Paulus MP. Increased amygdala and insula activation during emotion processing in anxiety-prone subjects. Am J Psychiatry. Feb 2007;164(2):318-27. [Medline].
- Torres AR, Prince MJ, Bebbington PE, Bhugra D, Brugha TS, Farrell M. Obsessive-compulsive disorder: prevalence, comorbidity, impact, and help-seeking in the British National Psychiatric Morbidity Survey of 2000. Am J Psychiatry. Nov 2006;163(11):1978-85. [Medline].
- Weissman MM, Bland RC, Canino GJ, et al. The cross-national epidemiology of panic disorder. Arch Gen Psychiatry. Apr 1997;54(4):305-9. [Medline].
- Yehuda R, Flory JD, Southwick S, Charney DS. Developing an agenda for translational studies of resilience and vulnerability following trauma exposure. Ann N Y Acad Sci. Jul 2006;1071:379-96. [Medline].
Anxiety Disorders excerpt Article Last Updated: Aug 23, 2007
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