|
|
AAFP Home Page >
News & Publications >
Journals >
American Family Physician® >
Vol. 62/No. 7 (October 1, 2000)
Generalized Anxiety Disorder
- MICHAEL F. GLIATTO, M.D.
- Philadelphia Veterans Affairs Medical Center, Philadelphia,
Pennsylvania
|
|
Patients with generalized anxiety
disorder experience worry or anxiety and a number of physical and psychologic
symptoms. The disorder is frequently difficult to diagnose because of the
variety of presentations and the common occurrence of comorbid medical or
psychiatric conditions. The lifetime prevalence is approximately 4 to 6 percent
in the general population and is more common in women than in men. It is often
chronic, and patients with this disorder are more likely to be seen by family
physicians than by psychiatrists. Treatment consists of pharmacotherapy and
various forms of psychotherapy. The benzodiazepines are used for short-term
treatment, but because of the frequently chronic nature of generalized anxiety
disorder, they may need to be continued for months to years. Buspirone and
antidepressants are also used for the pharmacologic management of patients with
generalized anxiety disorder. Patients must receive an appropriate
pharmacologic trial with dosage titrated to optimal levels as judged by the
control of symptoms and the tolerance of side effects. Psychiatric consultation
should be considered for patients who do not respond to an appropriate trial of
pharmacotherapy. (Am Fam Physician
2000;62:1591-600,1602.)
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
|
TABLE 1 Diagnostic
Criteria for 300.02 Generalized Anxiety Disorder |
Excessive anxiety and worry
(apprehensive expectation), occurring more days than not for at least six
months, about a number of events or activities (such as work or school
performance).
The person finds it
difficult to control the worry.
- The anxiety and worry
are associated with three (or more) of the following six symptoms (with at
least some symptoms present for more days than not for the past six months).
NOTE: Only one item is required in children.
- Restlessness or feeling
keyed up or on edge
Being easily fatigued Difficulty concentrating or
mind going blank Irritability Muscle tension Sleep disturbance
(difficulty falling or staying asleep, or restless unsatisfying
sleep)
The focus of the anxiety
and worry is not confined to features of an Axis I disorder, e.g., the anxiety
or worry is not about having a panic attack (as in Panic Disorder), being
embarrassed in public (as in Social Phobia), being contaminated (as in
Obsessive-Compulsive Disorder), being away from home or close relatives (as in
Separation Anxiety Disorder), gaining weight (as in Anorexia Nervosa), having
multiple physical complaints (as in Somatization Disorder), or having a serious
illness (as in Hypochondriasis), and the anxiety and worry do not occur
exclusively during Post-traumatic Stress Disorder.
The anxiety, worry or
physical symptoms cause clinically significant distress or impairment in
social, occupational or other important areas of functioning.
The disturbance is not due
to the direct physiological effects of a substance (e.g., a drug of abuse, a
medication) or a general medical condition (e.g., hyperthyroidism) and does not
occur exclusively during a Mood Disorder, a Psychotic Disorder, or a Pervasive
Developmental Disorder. |
Reprinted with permission
from the American Psychiatric Association. Diagnostic and statistical manual of
mental disorders. 4th ed. Washington, D.C.: American Psychiatric Association,
1994:435-6. |
|
|
Characteristics of Generalized Anxiety
Disorder
|
TABLE 2 Symptoms and
Behaviors Associated with Generalized Anxiety Disorder |
Excessive physiologic
arousal Muscle
tension Irritability Fatigue Restlessness Insomnia
Distorted cognitive
processes Poor concentration Unrealistic assessment of
problems Worries
Poor coping
strategies Avoidance Procrastination Poor problem-solving
skills |
Information from American
Psychiatric Association. Diagnostic and statistical manual of mental disorders.
4th ed. Washington, D.C.: American Psychiatric Association, 1994:435-6, and
Gelder M. Psychological treatment for anxiety disorders. In: the clinical
management of anxiety disorders. Coryell W, Winokur G, eds. New York: Oxford
University Press, 1991:10-27. |
|
|
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
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
Evaluation
The evaluation process for patients with anxiety is outlined in
Figure 1.
|
Assessment of Patients with Anxiety |
*--If some symptoms of major depression and GAD are present but do
not meet the full criteria for either, treat for mixed anxiety-depressive
disorder. |
FIGURE 1. Algorithm for evaluating patients with complaints of
anxiety. (GAD = generalized anxiety disorder) |
|
|
Initial Assessment 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."
|
Generalized
anxiety disorder is distinguished from other medical and psychiatric conditions
and normal worrying principally by the long duration of the anxiety and the
resultant impairment in daily functioning. |
|
|
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
|
TABLE
3 Distinguishing Characteristics of Generalized Anxiety Disorder, Panic
Disorder and Major Depression |
Disorder
|
Distinguishing feature
|
Age
of onset
|
Associated symptoms
|
Course of illness
|
Family history
|
Generalized
anxiety disorder |
Worry about
a specific concern |
Early
20s |
Restlessness, motor tension, fatigue |
Chronic |
Generalized
anxiety disorder, panic disorder, alcohol abuse |
Panic
disorder |
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 |
Major
depression |
Persistently low mood; may be accompanied by persistent
anxiety |
Mid-20s |
Neurovegetative symptoms (e.g., insomnia, lack of appetite,
guilt) |
Symptoms
remit but may recur |
Major
depression, alcohol abuse |
|
Information from American
Psychiatric Association. Diagnostic and statistical manual of mental disorders.
4th ed. Washington, D.C.: American Psychiatric Association, 1994:436, and Noyes
R, Woodman C, Garvey MJ, Cook BL, Suelzer M, Clancy J, et al. Generalized
anxiety disorder vs. panic disorder. Distinguishing characteristics and
patterns of comorbidity. J Nerv Ment Dis 1992;180:369-79. |
|
|
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.
Treatment
Psychologic Treatments 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
|
Patients with
generalized anxiety disorder may respond to psychologic or pharmacologic
therapies or a combination of both approaches. |
|
|
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 Treatment 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 g-aminobutyric
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
|
TABLE
4 Benzodiazepines Commonly Prescribed for Anxiety Disorders
|
Name
|
Half-life (hours)
|
Dosage range (per day)*
|
Initial dosage
|
Weekly cost†
|
Alprazolam
(Xanax) |
14 |
1 to 4
mg |
0.25 to 0.5
mg four times daily |
$15 to
19 |
Chlordiazepoxide (Librium) |
20 |
15 to 40
mg |
5 to 10 mg
three times daily |
2 |
Clonazepam
(Klonopin) |
50 |
0.5 to 4.0
mg |
0.5 to 1.0
mg twice daily |
10 to
12 |
Clorazepate
(Tranxene) |
60 |
15 to 60
mg |
7.5 to 15.0
mg twice daily |
18 to
25 |
Diazepam
(Valium) |
40 |
6 to 40
mg |
2 to 5 mg
three times daily |
1 to
2 |
Lorazepam
(Ativan) |
14 |
1 to 6
mg |
0.5 to 1.0
mg three times daily |
13 to
17 |
Oxazepam
(Serax) |
9 |
30 to 90
mg |
15 to 30 mg
three times daily |
15 to
21 |
|
*--For elderly patients, use
one half of the dosage listed. †--Estimated cost to the pharmacist
based on average wholesale prices in Red Book. Montvale, N.J.: Medical
Economics Data, 1999. Cost to the patient will be higher, depending on
prescription filling fee. Information from Hoehn-Saire R, McLeod DR.
Clinical management of generalized anxiety disorder. In: the clinical
management of anxiety disorders. Coryell W, Winokur G, eds. New York: Oxford
University Press, 1991:79-100, and Schatzberg AF, Cole JO, DeBattista C. Manual
of clinical psychopharmacology. 3rd ed. Washington, D.C.: American Psychiatric
Press Inc., 1997. |
|
|
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
|
Benzodiazepines remain the most widely used pharmacologic agents
for the treatment of patients with generalized anxiety disorder, but buspirone
is commonly used as a treatment modality. |
|
|
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
The initial dosage of buspirone is 5 mg three times daily with a
gradual dose titration until symptoms remit or the maximum dosage of 20 mg
three times daily is reached.15 If the dosage
is titrated too quickly, headaches or dizziness may occur.15 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.
This article exemplifies the AAFP 2000
Annual Clinical Focus on mental health.
The Author
MICHAEL F. GLIATTO, M.D., is currently an attending psychiatrist in
the Department of Psychiatry at the Philadelphia Veterans Affairs Medical
Center, Philadelphia, and a clinical assistant professor of psychiatry at the
University of Pennsylvania School of Medicine, Philadelphia. He received a
medical degree from the St. Louis University School of Medicine and completed a
residency in internal medicine at Hahnemann University Hospital, Philadelphia,
and a residency in psychiatry at the Hospital of the University of
Pennsylvania, Philadelphia.
Address correspondence to Michael F.
Gliatto, M.D., Department of Psychiatry, Philadelphia Veterans Affairs Medical
Center, 38th and Woodland Ave., Philadelphia, PA 19104. (e-mail:
Gliatto.Michael_Ft@Philadelphia.VA.Gov)
Reprints are not available from the author.
REFERENCES
- Kessler RC, McGonagle KA, Zhao S, Nelson CB, Hughes
M, Eshleman 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 1994;51: 8-19.
- Shear MK, Schulberg HC. Anxiety disorders in
primary care. Bull Menninger Clin 1995;59:A73-85.
- Katon WJ, Von Korff M, Lin E. Panic disorder:
relationship to high medical utilization. Am J Med 1992;92:7S-11S.
- Shader RI, Greenblatt DJ. Use of benzodiazepines in
anxiety disorders. N Engl J Med 1993;328:1398-405.
- Wells KB, Golding JM, Burnam MA. Psychiatric
disorder in a sample of the general population with and without chronic medical
conditions. Am J Psychiatry 1988;145:976-81.
- Rogers MP, White K, Warshaw MG, Yonkers KA,
Rodriguez-Villa F, Chang G, et al. Prevalence of medical illness in patients
with anxiety disorders. Int J Psychiatry Med 1994;24:83-96.
- Wells KB, Golding JM, Burnam MA. Chronic medical
conditions in a sample of the general population with anxiety, affective, and
substance use disorders. Am J Psychiatry 1989;146:1440-6.
- American Psychiatric Association. Diagnostic and
statistical manual of mental disorders. 3d. Washington, D.C.: American
Psychiatric Association, 1980:232-3.
- Connor KM, Davidson JR. Generalized anxiety
disorder: neurobiological and pharmacotherapeutic perspectives. Biol Psychiatry
1998;44:1286-94.
- American Psychiatric Association. Diagnostic and
statistical manual of mental disorders. 4th ed. Washington, D.C.: American
Psychiatric Association, 1994:435-6.
- Gelder M. Psychological treatment for anxiety
disorders. In: the clinical management of anxiety disorders. Coryell W, Winokur
G, eds. New York: Oxford University Press, 1991:10-27.
- Hoehn-Saire R, McLeod DR. Clinical management of
generalized anxiety disorder. In: the clinical management of anxiety disorders.
Coryell W, Winokur G, eds. New York: Oxford University Press, 1991:
79-100.
- Rickels K, Schweizer E. The clinical course and
long-term management of generalized anxiety disorder. J Clin Psychopharmacol
1990;10:101S-10S.
- Robins LN, Regier DA. Psychiatric disorders in
America: the epidemiologic catchment area study. Robins LN, Regier DA, eds;
with a foreword by Freedman DX. New York: Free Press, 1991.
- Schweizer E, Rickels K. Strategies for treatment of
generalized anxiety in the primary care setting. J Clin Psychiatry
1997;58(suppl 3):27-33.
- Hales RE, Hilty DA, Wise MG. A treatment algorithm
for the management of anxiety in primary care practice. J Clin Psychiatry
1997;58(suppl 3): 76-80.
- Wise MG, Griffies WS. A combined treatment approach
to anxiety in the medically ill. J Clin Psychiatry 1995;56(suppl
2):14-9.
- Liebowitz MR, Hollander E, Schneier F, Campeas R,
Fallon B, Welkowitz L, et al. Anxiety and depression: discrete diagnostic
entities? J Clin Psychopharmacol 1990;10:61S-6S.
- Noyes R, Woodman C, Garvey MJ, Cook BL, Suelzer M,
Clancy J, et al. Generalized anxiety disorder vs. panic disorder.
Distinguishing characteristics and patterns of comorbidity. J Nerv Ment Dis
1992;180:369-79.
- Clark DM, Phil D, Wells A. Cognitive therapy for
anxiety disorders. In: Dickstein LJ, Riba MB, Oldham JM, eds. Cognitive
therapy. Washington, D.C.: American Psychiatric Press, Inc., 1997.
- Butler G, Fennell M, Robson P, Gelder M. Comparison
of behavior therapy and cognitive behavior therapy in the treatment of
generalized anxiety disorder. J Consult Clin Psychol
1991;59:167-75.
- Durham RC, Murphy T, Allan T, Richard K, Treliving
LR, Fenton GW. Cognitive therapy, analytic psychotherapy and anxiety management
training for generalised anxiety disorder. Br J Psychiatry 1994;
165:315-23.
- Power KG, Jerrom DW, Simpson RJ, Mitchell MJ. A
controlled comparison of cognitive-behaviour therapy, diazepam and placebo in
the management of generalised anxiety. Behav Psychother
1989;17:1-14.
- Power KG, Simpson RJ, Swanson V, Wallace LA, et al.
A controlled comparison of cognitive-behavior therapy, diazepam, and placebo,
alone and in combination, for the treatment of generalized anxiety disorder. J
Anxiety Disord 1990;4:267-92.
- Durham RC, Allan T. Psychological treatment of
generalised anxiety disorder. A review of the clinical significance of results
in outcome studies since 1980. Br J Psychiatry 1993;163:19-26.
- Mathews A. Why worry? The cognitive function of
anxiety. Behav Res Ther 1990;28:455-68.
- Schweizer E. Generalized anxiety disorder.
Longitudinal course and pharmacologic treatment. Psychiatr Clin North Am
1995;18:843-57.
- Schatzberg AF, Cole JO, DeBattista C. Manual of
clinical psychopharmacology. 3d ed. Washington, D.C.: American Psychiatric
Press Inc., 1997.
- Thompson, PM. Generalized anxiety disorder
treatment algorithm. Psychiatric Annals 1996;26:227-32.
- Shorr RI, Robin DW. Rational use of benzodiazepines
in the elderly. Drugs Aging 1994;4:9-20.
- Longo LP. Non-benzodiazepine pharmacotherapy of
anxiety and panic in substance abusing patients. Psychiatr Annals
1998;28:142-53.
- Goa KL, Ward A. Buspirone. A preliminary review of
its pharmacological properties and therapeutic efficacy as an anxiolytic. Drugs
1986;32:114-29.
- Rickels K, Downing R, Schweizer E, Hassman H.
Antidepressants for the treatment of generalized anxiety disorder. A
placebo-controlled comparison of imipramine, trazodone, and diazepam. Arch Gen
Psychiatry 1993;50:884-95.
- Rocca P, Fonzo V, Scotta M, Zanalda E, Ravizza L.
Paroxetine efficacy in the treatment of generalized anxiety disorder. Acta
Psychiatr Scand 1997;95: 444-50.
- Aguiar LM, Haskins T, Rudolph RL, et al.
Double-blind, placebo-controlled study of once daily venlafaxine extended
release of outpatients with GAD [Abstract]. American Psychiatric Association.
1998: 241. Abstract NR643.
- Almeida JC, Grimsley EW. Coma from the health food
store: interaction between kava and alprazolam [Letter]. Ann Intern Med
1996;125:940-1.
- Schelosky L, Raffauf C, Jendroska K, Poewe W. Kava
and dopamine antagonism [Letter]. J Neurol Neurosurg Psychiatry
1995;58:639-40.
- Norton SA, Ruze P. Kava dermopathy. J Am Acad
Dermatol 1994;31:89-97.
- Garges HP, Varia I, Doraiswamy PM. Cardiac
complications and delirium associated with valerian root withdrawal [Letter].
JAMA 1998;280:1566-7.
Copyright © 2000 by the American Academy of
Family Physicians. This content is owned by the AAFP. A person viewing it
online may make one printout of the material and may use that printout only for
his or her personal, non-commercial reference. This material may not otherwise
be downloaded, copied, printed, stored, transmitted or reproduced in any
medium, whether now known or later invented, except as authorized in writing by
the AAFP. Contact afpserv@aafp.org for
copyright questions and/or permission requests.
October 1, 2000
Contents | AFP Home Page |
AAFP Home | Search
|
|
|
|