Anxiety disorders, such as generalized anxiety disorder (GAD), panic disorder and social phobia, are the most prevalent psychiatric disorders in the United States,1 and patients with these disorders are more likely to seek treatment from a primary care physician than from a psychiatrist.2 Patients with anxiety disorders are more likely than other patients to make frequent medical appointments, to undergo extensive diagnostic testing,3 to report their health as poor and to smoke cigarettes and abuse other substances.4
Anxiety disorders, particularly panic disorder, occur more frequently in patients with chronic medical illnesses (e.g., hypertension, chronic obstructive pulmonary disease, irritable bowel syndrome, diabetes) than in the general population.5 Conversely, patients with anxiety disorders are more likely than others to develop a medical illness,6,7 and the presence of an anxiety disorder may prolong the course of a medical illness.2 Patients with anxiety disorders have higher rates of mortality from all causes.4
Characteristics of Generalized Anxiety Disorder
The definition of GAD has changed over time. Originally, little distinction was made between panic disorder and GAD. As panic disorder became better understood and specific treatments were developed, GAD was defined in the Diagnostic and Statistical Manual of Mental Disorders, 3d ed. (DSM-III)8 as a disorder without panic attacks or symptoms of major depression. This definition had little reliability,9 and current diagnostic criteria (Table 1)10 for GAD in the Diagnostic and Statistical Manual of Mental Disorders, 4th ed. (DSM-IV)10 emphasize the psychic component (e.g., the worry) rather than the somatic (e.g., muscle tension) or autonomic symptoms (e.g., diaphoresis, increased arousal). In addition to the DSM-IV framework, the symptoms of GAD can be conceptualized as being contained in three categories: excessive physiologic arousal, distorted cognitive processes and poor coping strategies.11 The symptoms associated with each of these categories are listed in Table 2.10,11
|Excessive physiologic arousal
|Distorted cognitive processes
|Unrealistic assessment of problems
|Poor coping strategies
|Poor problem-solving skills
To make the diagnosis of GAD by DSM-IV10 criteria, the worry and other associated symptoms must be present for at least six months and must adversely affect the patient's life (e.g., the patient misses work days or cannot maintain daily responsibilities).10 The diagnosis can be challenging because the difference between normal anxiety and GAD is not always distinct12 and because GAD often coexists with other psychiatric disorders (e.g., major depression, dysthymia, panic disorder, substance abuse).13
The lifetime prevalence of GAD is 4.1 to 6.6 percent,14 which is higher than that of the other anxiety disorders. The prevalence of GAD in patients visiting physicians' offices is twice that found in the community.15 It is more prevalent in women than in men,1 with the median age of onset occurring during the early 20s.13 The onset of symptoms is usually gradual, although GAD can be precipitated by stressful life events. The condition tends to be chronic with periods of exacerbation and remission.13
The evaluation process for patients with anxiety is outlined in Figure 1.
After obtaining a patient history, the physician should try to categorize the anxiety as acute (or brief or intermittent) or persistent (or chronic).15,16 Acute anxiety lasts from hours to weeks (in contrast, panic attacks last for minutes) and is usually preceded by a stressor. Often, comorbid conditions (e.g., major depression) are not present.15 Persistent anxiety lasts for months to years and can include what is called “trait anxiety.” Trait anxiety can be viewed as part of a patient's temperament; for instance, a patient may say, “I've always been nervous, but I don't know about what.”
Although there is usually not a precipitating stressor in most cases of persistent anxiety, a stressor can exacerbate the patient's baseline level of anxiety. This situation is called “double anxiety” (i.e., acute anxiety superimposed on persistent anxiety).15 GAD is a form of persistent anxiety and can occur in patients with or without trait anxiety.
Patients with GAD present with a wide variety of symptoms and range of severity.12 Some patients may emphasize a special symptom (e.g., insomnia) and not report other symptoms that are usually associated with GAD.12 Some patients may not complain of anxiety or specific worries but present with exclusively somatic symptoms such as diarrhea, palpitations, dyspnea, abdominal pain, headache or chest pain.2 These patients warrant a full medical evaluation because there may be no indication that GAD is the etiology. Conversely, physicians should include a psychiatric disorder in the differential diagnosis when symptoms are vaguely described, do not conform to known pathophysiologic mechanisms, persist after a negative work-up and are not resolved by reassurance. Patients with this clinical profile should be asked as early in the evaluation as possible about worries, “nerves,” or anxiety, acute or chronic stressors, and about the presence of symptoms listed in Tables 110 and 2.10,11
EVALUATION FOR MEDICAL DISORDERS
Nonpsychiatric disorders must be ruled out before GAD can be diagnosed as the etiology of a patient's complaint of anxiety. Neurologic and endocrine diseases, such as hyperthyroidism and Cushing's disease, are the most frequently cited medical causes of anxiety.17 Other medical conditions commonly associated with anxiety include mitral valve prolapse, carcinoid syndrome and pheochromocytoma.17 It must be stressed that these conditions, although often cited, are clinically uncommon, and all patients who present with the complaint of anxiety do not require an extensive work-up to exclude these other medical conditions. Medications such as steroids, over-the-counter sympathomimetics, selective serotonin reuptake inhibitors (SSRIs), digoxin, thyroxine and theophylline may cause anxiety.17 The physician should also inquire about the use of herbal products or vitamins. If possible, all exogenous substances should be removed before initiating treatment of patients with GAD.
EVALUATION FOR SUBSTANCE ABUSE
Use of and withdrawal from addictive substances can cause anxiety. The physician should inquire about the patient's use of alcohol, caffeine, nicotine and other commonly used substances (including those given by prescription). Corroborative history from family members may be necessary.17
EVALUATION FOR OTHER PSYCHIATRIC DISORDERS
The evaluation for other psychiatric disorders is probably the most challenging aspect of patient evaluation because the symptoms of GAD overlap with those of other psychiatric disorders (e.g., major depression, substance abuse, panic disorder) and because these disorders often occur concomitantly with GAD. Generally, GAD should be considered a diagnosis of exclusion after other psychiatric disorders have been ruled out. Because of the overlap and comorbidity associated with other psychiatric disorders, some authors have questioned whether GAD is a distinct entity and have posited that it is a variant of panic disorder or major depression.18,19
Symptoms of GAD can occur before, during or after the onset of the symptoms of major depression or panic disorder.12 Some patients have symptoms of anxiety and depression but do not meet the full criteria as delineated in DSM-IV,10 for GAD, panic disorder or major depression. In these cases, the term “mixed anxiety-depressive disorder” can be applied, although it is not yet part of the official nosology. Despite the confusion, anxious patients should be asked about the symptoms of panic attacks and the neurovegetative symptoms (including suicidal ideation) that are associated with major depression. When more than one psychiatric condition exists, an attempt should be made to determine which disorder occurred first. Some distinguishing characteristics of GAD, panic disorder and major depression are listed in Table 3.10,19
|Age of onset
|Course of illness
|Generalized anxiety disorder
|Worry about a specific concern
|Restlessness, motor tension, fatigue
|Generalized anxiety disorder, panic disorder, alcohol abuse
|Intense, brief, acute anxiety; frequency of attacks variable; often no precipitant
|Bimodal onset (late adolescence, mid-30s)
|Rapid heart rate, trembling, diaphoresis, dyspnea
|Variable periods of remissions and relapses
|Panic disorder, major depression, alcohol abuse
|Persistently low mood; may be accompanied by persistent anxiety
|Neurovegetative symptoms (e.g., insomnia, lack of appetite, guilt)
|Symptoms remit but may recur
|Major depression, alcohol abuse
Obsessive-compulsive disorder and social phobia should also be considered in the evaluation for comorbid disorders. The key symptom of obsessive-compulsive disorder is recurring, intrusive thoughts or actions. Social phobia is characterized by intense anxiety provoked by social or performance situations.10 Because patients with GAD may present with mostly somatic complaints, somatization disorder is also a consideration. The distinguishing feature of this disorder is chronic, multiple physical complaints that involve several organ systems. Patients with exclusively GAD have a much more limited range of physical complaints.
Nonpharmacologic modalities should be the initial treatment for patients with mild anxiety4 to address the three categories of symptoms of GAD (Table 2).10,11 Relaxation techniques and biofeedback are used to decrease arousal.11 Cognitive therapy helps patients to limit cognitive distortions by viewing their worries more realistically, enabling them to make better plans to manage their anxiety. In cognitive therapy, patients may be taught to record their worries, listing evidence that justifies or contradicts the extent of their concerns.20 Patients also learn that “worrying about worry” maintains anxiety and that avoidance and procrastination are not effective ways to solve problems.20
A small number of studies have found that cognitive therapy is more effective than behavior therapy21, psychodynamic psychotherapy22 and pharmacotherapy,23,24 but more research needs to be conducted before the superiority of cognitive therapy is firmly established.20 Patients with personality disorders, those with chronic social stressors and those who expect little benefit from psychologic treatments do not respond well to psychotherapeutic techniques for the treatment of anxiety.25 Often, psychotherapy and pharmacotherapy are necessary.
Family members should participate in the treatment plan of patients with GAD. Initially they can provide additional historical information and contribute to the formulation of the treatment plan. Because patients with this disorder tend to be vigilant for signs of danger and may misinterpret information,26 family members can provide another perspective on the patient's problems. In addition, family members should be included in efforts to help the patient develop problem-solving skills and can also help decrease the social isolation of patients with GAD by providing structured activities to promote interaction with others and lessen rumination about problems. Another source of structured activity includes day programs provided by community mental health centers. If substance abuse is prominent, the patient should be referred to a rehabilitation facility. Patients and their families can be referred to the Anxiety Disorders Association of America (301–231–9350) for further information about available resources.
Pharmacologic therapy should be considered for patients whose anxiety results in significant impairment in daily functioning. Study results have not revealed an optimal duration of pharmacologic treatment for patients with GAD.27 While 25 percent of patients relapse within one month of discontinuing drug therapy and 60 to 80 percent relapse within one year,16 patients treated for at least six months have a lower relapse rate than those treated for shorter time periods.16
Benzodiazepines. The anxiolytics most frequently used are the benzodiazepines4 (Table 4).12,28 All of the benzodiazepines are of equal efficacy29 and all act on the γ-amino-butyric acid (GABA)/benzodiazepine (BZ) receptor complex, causing sedation, problems in concentrating and anterograde amnesia.4 Benzodiazepines do not decrease worrying per se, but act to lower anxiety by decreasing vigilance and by eliminating somatic symptoms such as muscle tension. Tolerance to the sedation, impaired concentration and amnesia effects of these drugs develop within several weeks,27 although tolerance to the anxiolytic effects occurs much more slowly—if at all.4 Benzodiazepine therapy can begin with 2 mg of diazepam, or its equivalent, three times daily. The dosage can be increased by 2 mg per day every two to three days until the symptoms abate, side effects develop4 or a daily dose of 40 mg is reached.28 Diazepam does not have to be used as the initial agent; several alternatives are available. In the elderly patient, benzodiazepine therapy should begin at the lowest possible dosage and increased slowly.30
|Dosage range (per day)*
|1 to 4 mg
|0.25 to 0.5 mg four times daily
|$15 to 19
|15 to 40 mg
|5 to 10 mg three times daily
|0.5 to 4.0 mg
|0.5 to 1.0 mg twice daily
|10 to 12
|15 to 60 mg
|7.5 to 15.0 mg twice daily
|18 to 25
|6 to 40 mg
|2 to 5 mg three times daily
|1 to 2
|1 to 6 mg
|0.5 to 1.0 mg three times daily
|13 to 17
|30 to 90 mg
|15 to 30 mg three times daily
|15 to 21
Agents with short half-lives, such as oxazepam (Serax), are easily metabolized and do not cause excessive sedation. These agents should be used in the elderly and in patients with liver disease. They are also suitable for use on an “as-needed” basis. Agents with long half-lives, such as clonazepam (Klonopin), should be used in younger patients who do not have concomitant medical problems. In addition to improved compliance, the longer acting agents offer several advantages: they can be taken less frequently during the day, patients are less likely to experience anxiety between doses and withdrawal symptoms are less severe when the medication is discontinued. When a benzodiazepine is prescribed, the patient should be warned about driving and operating heavy machinery while taking this medication.
Use of benzodiazepines in therapeutic dosages does not lead to abuse, and addiction is rare.12 The benzodiazepines most likely to be abused are those that are rapidly absorbed such as diazepam, lorazepam (Ativan) and alprazolam (Xanax).27 Alprazolam should be prescribed only for patients with panic disorder. When abused, benzodiazepines are usually abused with other substances, particularly opiates.31 The patients most likely to abuse benzodiazepines are those who have a previous history of alcohol or drug abuse, and those with a personality disorder.28
All benzodiazepine therapy can lead to dependence; that is, withdrawal symptoms occur once the medications are discontinued. Withdrawal symptoms include anxiety, irritability and insomnia, and it can be difficult to differentiate between withdrawal symptoms and the recurrence of anxiety. Seizures occur rarely during withdrawal.28 Withdrawal symptoms tend to be more severe with higher dosages, with agents that have short half-lives, with rapidly tapered dosages, and in patients with current tobacco use or with a history of illegal drug use.15 The risk of dependence increases as the dosage and the duration of treatment increases, but it can occur even when appropriate dosages are used continuously for three months.4,27
Withdrawal symptoms begin six to 12 hours after the last dose of an agent with a short half-life and 24 to 48 hours after the last dose of an agent with a longer half-life.27 In patients who have taken a benzodiazepine for more than six weeks, the dosage should be decreased by 25 percent or less per week to prevent withdrawal symptoms.4 Patients may experience rebound anxiety (akin to the rebound hypertension that occurs when some antihypertensives are discontinued) once the tapering process is completed, but this is transient and ends within 48 to 72 hours.28 Once the rebound anxiety ends, a patient may re-experience the original symptoms of anxiety, referred to as recurrent anxiety.
Although few controlled studies support the long-term use of benzodiazepines, GAD is a chronic disorder, and some patients will require benzodiazepine therapy for months to years.9 Generally, patients who present with acute anxiety or those with chronic anxiety who undergo a new stressor (“double anxiety”) should receive benzodiazepine therapy for several weeks.13 Patients may be less tolerant of anxiety that recurs when the benzodiazepine is discontinued12 and, if necessary, it may have to be resumed indefinitely. Patients who use benzodiazepines chronically tend to be elderly, to be in psychologic distress and to have multiple medical problems.30
Other Medications. Buspirone (BuSpar) is the drug often used in patients with chronic anxiety and those who relapse after a course of benzodiazepine therapy.13 It is also the initial treatment for anxious patients with a previous history of substance abuse.13 Buspirone appears to be as effective as the benzodiazepines in the treatment of patients with GAD,32 and its use does not result in physical dependence or tolerance.15
Unlike the immediate relief of symptoms that occurs with benzodiazepine therapy, buspirone's onset of action takes two to three weeks.31 Therefore, patients should be informed of the expected delay in relief of symptoms. Buspirone has an opposite effect of the benzodiazepines in that it treats the worry associated with GAD rather than the somatic symptoms.31 However, buspirone may not be as effective in patients who have been treated with a benzodiazepine during the previous 30 days.13
In patients who are taking benzodiazepines at the time of the initiation of buspirone, tapering the benzodiazepine should not begin until the patient reaches a daily dosage of 20 to 40 mg of buspirone.15 In addition to the GABA/BZ complex, research has shown that GAD involves several neurotransmitter systems, including that of norepinephrine and serotonin.9 Pharmacologic agents that affect these neurotransmitters, such as the tricyclic antidepressants and the SSRIs, have been studied in patients with GAD who do not respond to the benzodiazepine therapy or buspirone.
Imipramine (Tofranil) has been shown to be effective in controlling the worrying that is associated with GAD,33 but whether it is as effective as benzodiazepines or buspirone in those patients who have anxiety without depressive symptoms has not been determined.15 Imipramine also has anticholinergic and antiadrenergic side effects that limit its use. Desipramine (Norpramin) and nortriptyline (Pamelor) can be used as alternatives.
Trazodone (Desyrel) is a serotonergic agent, but because of its side effects (sedation and, in men, priapism), it is not an ideal first-line agent.9 Daily dosages of 200 to 400 mg are reported to be helpful in patients who have not responded to other agents.9 Nefazodone (Serzone) has a similar pharmacologic profile to trazodone, but it is better tolerated and is a good alternative.9,31 Paroxetine (Paxil), an SSRI, has also been studied as a treatment for patients with GAD,34 but the trial was small, as has been the case with most of the antidepressants under investigation. Venlafaxine SR (Effexor) is the first medication to be labeled by the U.S. Food and Drug Administration as an anxiolytic and as an antidepressant; thus, it can be used for the treatment of patients with major depression or GAD, or when they occur comorbidly.35
Antihistamines are not potent anxiolytics. Although some antipsychotic drugs have sedating properties, they should rarely be used as therapy for patients with GAD.12 Beta-adrenergic agents are useful for the treatment of patients with performance anxiety (a type of social phobia) because they lower heart rate and decrease tremulousness; they do not however, decrease the worrying or other somatic symptoms associated with GAD.12
Two herbal remedies that are often used for the treatment of anxiety are Valeriana officinalis (valerian), a root extract, and a beverage made from the root of Piper methysticum (kava-kava). Both have sedating properties, but kava has worrisome side effects that include synergy with alcohol and benzodiazepines,36 dyskinesias and dystonia,37 and dermopathy.38 Valerian root has been reported to cause delirium and cardiac failure if abruptly discontinued.39 Further studies are needed before these herbal products can be recommended as therapeutic agents for persons with GAD.
Consultation with a psychiatrist should be considered if a patient with GAD does not respond to an appropriate course of benzodiazepine or buspirone therapy. A psychiatrist can help clarify the diagnosis, determine if a comorbid psychiatric disorder is present and determine which comorbid disorder should be treated as the primary disorder. A psychiatrist can also make recommendations about therapy, including the addition of psychotherapy and changes in medications.