The Diagnosis and Treatment of Anxiety Disorders

*Charité – Universitätsmedizin Berlin, corporate member of the Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health Department of Psychiatry and Psychotherapy Klinik für Psychiatrie und Psychotherapie, Campus Charité Mitte Charitéplatz 1, 10117 Berlin, Germany ed.etirahc@elheorts.saerdna

Abstract

Background

Anxiety disorders are the most common type of mental illness in Europe, with a 12-month prevalence of 14% among persons aged 14 to 65. Their onset is usually in adolescence or early adulthood. The affected patients often develop further mental or somatic illnesses (sequential comorbidity).

Methods

This review is based on pertinent publications retrieved by a selective search in PubMed.

Results

The group of anxiety disorders includes generalized anxiety disorder (GAD), phobic disorders, panic disorders, and two disorders that are often restricted to childhood—separation anxiety and selective mutism. A comprehensive differential diagnostic evaluation is essential, because anxiety can be a principal manifestation of other types of mental or somatic illness as well. Psychotherapy and treatment with psychoactive drugs are the therapeutic strategies of first choice. Of all types of psychotherapy, cognitive behavioral therapy has the best documented efficacy. Modern antidepressants are the drugs of first choice for the treatment of panic disorders, agoraphobia, social phobia, and GAS; pregabalin is a further drug of first choice for GAS.

Conclusion

In general, anxiety disorders can now be effectively treated. Patients should be informed of the therapeutic options and should be involved in treatment planning. Current research efforts are centered on individualized and therefore, it is hoped, even more effective treatment approaches than are available at present.

Anxiety is a a normal and necessary basic emotion without which individual survival would be impossible. Pathologically increased anxiety can arise not only in anxiety disorders per se, but also in most other types of mental illness. Anxiety can also be a warning signal of potential harm in somatic illnesses, such as myo-cardial infarction or hypoglycemia in a diabetic patient; it naturally requires an entirely different therapeutic approach in such situations. For any patient presenting with pathologically increased anxiety, a thorough psychiatric and somatic evaluation is needed so that an underlying pulmonary (e1), cardiovascular (e2), neurological (e3), or endocrine disease (e.g., of the thyroid gland) (e4) can be ruled out. Anxiety reactions as such are important indicators of a possible threat to homeostasis; anxiety is considered a disease requiring treatment when it arises in the absence of any threat, or in disproportionate relation to a threat, and keeps the affected individual from leading a normal life.

Anxiety disorders

Anxiety is considered a disease requiring treatment when it arises in the absence of any threat, or in disproportionate relation to a threat, and keeps the affected individual from leading a normal life.

Learning objectives

After reading this article, the reader should

know that anxiety disorders are common mental illnesses of early onset that elevate the risk of developing further mental illnesses;

Sex ratio

Women are affected two to three times as commonly as men.

Methods

This review is based on pertinent publications retrieved by a selective search in PubMed.

Epidemiology

Anxiety disorders are the most common type of mental illness in the European Union, Switzerland, Iceland, and Norway (figures for the year 2010). With a 12-month prevalence of 14% and approximately 61.5 million affected persons, they are more common than any other mental illness among persons in Europe aged 14 to 65. Women are affected two to three times as commonly as men (1).

Anxiety disorders often begin in childhood or adolescence (e5). This is particularly true for specific phobias and social phobia. Selective mutism can arise as early as a child’s third year. Most children go through a transient phase of non-pathological aversion to strangers, often beginning at the age of eight or nine months. In 2–3% of children, marked separation anxiety persists into the preschool or school-age years. Treatment is indicated if separation anxiety impairs the normal development of the child, e.g., by making it impossible for the child to have important social experiences.

The World Health Organization (WHO) reported that, in 2015, anxiety disorders ranked in sixth place among all mental and somatic illnesses worldwide as a cause of so-called years lived with disability (YLD), and in fourth place in highly developed countries; they are thus among the chronic illnesses with the greatest impact on patients’ lives (2). Specific phobias are the most common type of anxiety disorder.

Taxonomy and manifestations

The anxiety disorders, as classified in the International Classification of Diseases (ICD-10) (3), comprise the phobic disorders, including agoraphobia with (F40.00) or without panic disorder (F40.01), social phobia (F40.1), and the specific phobias (F40.2), as well as other anxiety disorders, including panic disorder (F41.0), generalized anxiety disorder (F41.1), and mixed anxiety and depression (F41.2) ( table 1 ). In the current edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (e6), which is the main reference text for the taxonomy of mental illnesses in the USA, separation anxiety disorder and selective mutism are newly classified as anxiety disorders. These were previously considered illnesses restricted to childhood and adolescence, but are now held to be relevant in adulthood as well. The upcoming ICD-11 can be previewed in a beta version that is available online. In this classification, too, separation anxiety disorder and selective mutism will appear for the first time among the (adult) anxiety disorders (4).

Table 1

Age of presentation

Anxiety disorders often begin in childhood, adolescence, or early adulthood.

Separation anxiety disorder is characterized by persistent and excessive anxiety associated with separation from the patient’s most significant other(s), to an inappropriate extent from the developmental psychological point of view. Its lifetime prevalence is 4.8%. It is usually initially diagnosed in childhood, but recent studies have shown that it is increasingly common in adulthood as well. For instance, an evaluation of the World Mental Health Survey conducted by the World Health Organization (WHO) revealed that, among 38 993 adults in 18 different countries, the age of onset of separation anxiety disorder was over 18 years in 43.1% of cases (5, 6).

Selective mutism is a rare anxiety disorder that usually presents in childhood or adolescence. The diagnostic evaluation for this disorder often takes place only after the child has started school. Persons suffering from selective mutism are persistently unable to speak in certain situations, even though they can do so in other situations, usually when with their families. If the patient emits no phonetic expressions of any kind (e.g., coughing, crying, laughing, or speaking) in any situation whatsoever, the term “total mutism” is used. According to the DSM-5 (e6), the point prevalence of selective mutism lies between 0.03% and 1%. No data are yet available from representative epidemiological studies of entire populations; the wide disparity of prevalence estimates is presumably due to the diversity of settings in which the data were acquired (hospitals, schools, the population at large) (e6). Approximately one-third of sufferers have persistent symptoms into adulthood (7). Unfortunately, no valid data are available on the frequency of this disorder as a function of age.

Sequential comorbidity

Sequential comorbidity

Anxiety disorders elevate the risk of developing other mental illnesses.

Anxiety disorders are associated with high parallel comorbidity with other anxiety disorders. In addition, individuals with an anxiety disorder are at elevated risk of developing further anxiety disorders over time. A meta-analysis of 20 studies revealed that, among children with separation anxiety, the risk of developing a panic disorder later on is more than three times higher than in children without separation anxiety (8). The epidemiological term for such longitudinal associations is “sequential comorbidity” ( Figure ). This exists not only within the anxiety disorders among themselves, but beyond them as well: anxiety disorders elevate the risk of developing other mental illnesses such as depression or substance-related disorders (9). For example, a Danish study on a cohort of 3 380 059 persons showed that patients with anxiety disorders, in comparison to the general population, have an adjusted incidence rate ratio (IRR) of 3.0 for a depressive episode (95% confidence interval [CI]: [2.8; 3.1]) and an IRR of 5.0 for a recurrent depressive disorder (95% CI: [4.8; 5.2]) (10).

Anxiety disorders presenting early in life increase the risk of developing other mental illnesses later on in life (sequential comorbidity) (modified from [e7] and reprinted with the kind permission of John Wiley, publishers)

Anxiety disorders also play a major role in the development and prognosis of somatic diseases. In a longitudinal study of 293 persons (median age: 55 years) who were in good cardiovascular and autoimmune health, amygdalar activation on 18 F-fluorodexoyglucose positron emission tomography/computed tomography ( 18 F-PET-CT)—a key radiological finding that is typical of anxiety disorders—was found to be associated with an elevated risk of developing cardiovascular disease in a subsequent observation period of 3.7 years (median duration). There were a total of 22 new cases of cardiovascular disease and a calculated hazard ratio (HR) of 1.6 (95% CI: [1.27; 1.98]), i.e., a 60% elevation of the risk of developing a cardiovascular disease for each increase of the amygdalar signal by one standard deviation. This association seems to be mediated by elevated bone-marrow activity and arterial inflammation. When interpreting these results, one must bear in mind that amygdalar activation is a general measure of emotional processes and is not specific for anxiety or for anxiety disorders (11).

Generalized anxiety disorder

This type of anxiety disorder manifests itself with anxious worrying, tension, and fears about everyday events and problems.

In a meta-analysis of 16 cohort studies (Health Survey for England [HSE], Scottish Health Survey [SHS]) involving a total of 163 363 men and women who stated that they did not have cancer at the time of inclusion in the study, it was found, after correction for age, sex, level of education, smoking status, and alcohol consumption, that persons with a high anxiety/depression score at the time of inclusion were significantly more likely to die of cancer in an ensuing observation period of 9.5 years (mean duration; 4353 deaths overall; multivariable adjusted hazard ratio 1.32, 95% CI: [1.18; 1.48]), compared to persons with a low anxiety/depression score (GHQ-12: 0–6). This was particularly the case for colorectal, prostatic, pancreatic, and esophageal cancer and for leukemia. Aside from other, possibly overlooked confounding variables, it cannot be ruled out that persons with a high anxiety/depression score at the time of inclusion already had an as yet undetected subclinical malignancy, leading to increased mental stress in the sense of what epidemiologists call “reverse causality.” To limit the influence of initially occult malignancies on the study findings, patients who died in the first five years of the observation period were excluded from the analysis (12).

The early detection and treatment of anxiety disorders may thus have a secondary preventive effect against further mental and somatic diseases as well as a beneficial influence on the course of somatic disease. The association between early detection and prevention remains to be examined in randomized controlled trials.

Etiology

Panic disorders are characterized by:

Repeated and unexpected panic attacks (anxiety attacks) with both physical manifestations (palpitations, dyspnea, diaphoresis, paresthesiae, nausea) and mental ones (fear ranging to mortal fear, fear of losing control, feeling of alienation).

Anxiety disorders are among the so-called complex genetic diseases characterized by a complex pathogenetic interaction of environmental factors with multiple genetic variants at different chromosomal loci. Family studies have shown that first-degree relatives of patients with panic disorders have a three- to fivefold elevation of the risk of developing such a disorder themselves, compared to the general population. Familial clustering is also seen in generalized anxiety disorder and in the specific phobias. The heritability of anxiety disorders, i.e., the degree of participation of genetic factors in their development, lies in the range of 30–67%, with the remainder of the variation accounted for by individual negative environmental factors, such as life events (13). These include, for example (14):

On the other hand, positive environmental factors, effective coping strategies, secure bonding styles, supportive learning experiences, and a good social support network can increase resilience, even in the presence of a genetic risk-factor constellation. Meanwhile, the role of epigenetic mechanisms in the causation of anxiety disorders is gaining increased attention. Epigenetic mechanisms are biochemical processes, such as, for example, DNA methylation or histone acetylation, that act on DNA or its spatial structure without changing the DNA sequence per se. They play an important role in the regulation of gene activity and display marked temporal plasticity, being alterable by life events or even by psychotherapeutic intervention. Epigenetic processes may, therefore, play a key role in tipping the balance between risk factors and resilience, leading to an adaptive or maladaptive outcome: it is perhaps the integration of the genetic risk together with the environmentally determined risk by way of epigenetic processes that ultimately determines whether an anxiety disorder will arise. Individual epigenetic effects, like individual genetic effects, are small (15). Initial epigenetic pilot studies on small groups of patients with anxiety disorders have revealed altered patterns of DNA methylation in risk genes for these disorders, and it seems that successful psychotherapy or pharmacotherapy leads to the normalization of these altered epigenetic patterns (16).

Genetic factors

The heritability of anxiety disorders, i.e., the degree of participation of genetic factors in their development, lies in the range of 30–67%, with the remainder of the variation accounted for by individual negative environmental factors, such as life events.

The neuronal structures that participate in the anxiety network include the amygdala, whose efferent fibers to the hypothalamus, the locus ceruleus, and the periaqueductal gray play a role in the regulation of the central and peripheral manifestations of the anxiety response, and areas of prefrontal cortex and the anterior cingulate gyrus that exert an inhibitory effect on the amygdala (17, 18). Further brain areas belonging to the anxiety network are the insula, which integrates interoceptive signals, and the bed nucleus of the stria terminalis, which has recently been ascribed a central role in what is called “sustained anxiety”—a typical feature of generalized anxiety disorder, panic disorder, and social anxiety disorder (19).

Learning plays a major role in the development and maintenance of anxiety disorders, as well as in their treatment. Classical and operant conditioning exert their effects, and avoidant behavior contributes to the maintenance of the disorder. There also seems to be an evolutionarily determined capacity to mount an excessive anxiety reaction to the objects of the specific phobias, encouraging the development of these phobias; Seligman introduced the term “preparedness” for this capacity (e8). Personality traits, too, especially neuroticism, are related to the development of anxiety disorders (e9). Extinction learning via in-vivo exposure is now considered to be a form of relearning, rather than the erasure (unlearning) of previously acquired content.

Treatment

As recommended in the S3 guideline on the treatment of anxiety disorders issued in May 2014 (20), psychotherapy and pharmacotherapy should both be offered, and the two are considered comparably effective. Decisions about treatment should be made in the light of the severity of the disorder, the preference of the informed patient, the expected latency and durability of the treatment effect, the expected side effects, and the availability of the treatment in question. If one form of treatment proves to be ineffective, the other (or a combination of both) should be tried. Only for the specific phobias is there very good evidence, and therefore a very strong recommendation, for psychotherapy alone; drugs are not indicated in the treatment of the specific phobias.

Treatment

Anxiety disorders can be treated with psychotherapy, drugs, or both.

For all types of anxiety disorder, cognitive behavioral therapy is the type of psychotherapy for which there is the strongest evidence and which receives the highest-level recommendation (Ia; A). Initial randomized controlled trials have confirmed the clinical efficacy of psychodynamic therapies, e.g., in social phobia (21). Nonetheless, psychodynamic therapy receives evidence level IIa in the current German guidelines because of the incomplete state of the data from clinical trials, along with the recommendation that this type of psychotherapy should be offered if cognitive behavioral therapy has been ineffective or is unavailable, or if an informed patient expresses a preference for it (20). The specifics of cognitive behavioral therapy vary depending on the particular anxiety disorder being treated, with the common element that the patient must make the experience that his or her situationally induced anxiety is unfounded and the situation actually harmless. This is best achieved through exposure under the supervision of a therapist (22), in the course of which the patient must experience habituation of the anxiety response, so that the central fear underlying it is refuted. Exposure in virtual reality is now increasingly a part of cognitive-behavioral therapeutic interventions (23).

Psychotherapy

Cognitive behavioral therapy is the tpe of psychotherapy of first choice in the treatment of the anxiety disorders.

Cognitive behavioral therapy has been found to have a moderately strong beneficial effect against all types of anxiety disorder compared to a placebo drug (Cohen’s d = 0.57); the same is true of pharmacotherapy (e.g., sertraline, d = 0.54; venlafaxine, d = 0.50) (24). If only the before vs after changes are studied, remarkably strong effects are found for pharmacotherapy (selective serotonin and norepinephrine reuptake inhibitors [SNRI], d = 2.25) compared to cognitive behavioral therapy (d = 1.30) (24). Combining pharmacotherapy with psychotherapy is usually not superior to monotherapy with either one of the two options alone (20). In a meta-analysis of the few available studies with long follow-up periods, Bandelow et al. (25) concluded that further symptomatic improvement took place 26–104 weeks after the end of cognitive behavioral therapy. After pharmacotherapy, there was no worsening in the follow-up period, but this difference compared to cognitive behavioral therapy did not reach statistical significance.

The drugs with the highest level of supporting evidence are the selective serotonin reuptake inhibitors (SSRI) and SNRI, as well as the calcium-channel modulator pregabalin for generalized anxiety disorder ( table 2 ).

Table 2

* 1 according to the German guidelines

* 2 Case studies indicate that pregabalin has a potential for abuse. mainly in patients with substance-related disorders and above all in opiate-dependent patients (26). It is accordingly recommended in the German guidelines that patients with substance-related disorders. and particularly those who are addicted to multiple drugs. should not be treated with pregabalin. If a patient does not respond to a drug or cannot tolerate it. the next step may be a switch from one standard drug to another (e.g.. from an SSRI to an SSNRI; in generalized anxiety disorder. from an SSRI to pregabalin) or a switch to a nonstandard drug. such as one with a lower evidence level or recommendation grade (e.g.. moclobemide in social phobia). or to one that is not approved for the treatment of anxiety disorders. but has ?nonetheless been reported to be clinically effective (e.g.. quetiapine. agomelatine. lavender oil. and. in some cases. mirtazapine).

CCP = clinical consensus point; SSRI = selective serotonin reuptake inhibitors; SNRI = selective serotonin and norepinephrine reuptake inhibitors;

MAO = monoamine oxidase; TZA = tricyclic antidepressants

Treatment with psychoactive drugs

The drugs most commonly used are the selective serotonin reuptake inhibitors (SSRI) and the selective noradrenaline ruptake inhibitors (SNRI).

In the informed-consent discussion, the patient should not only be informed of the specific side effects of the drug class(es) to be prescribed, but should also be told that the effect of antidepressant drugs may be delayed by a latency of approximately two weeks (range: 1–6 weeks), and that these drugs may, in fact, initially worsen nervousness, agitation, and anxiety. They should therefore be given at a low dose at first, with gradual upward titration (box).

BOX

The off-label use of drugs that have not been approved for the treatment of anxiety disorders

The atypical antipsychotic drug quetiapine has not been approved for the treatment of anxiety disorders. Still, a meta-analysis of three randomized, double-blind, placebo-controlled trials of this drug for the treatment of generalized anxiety disorder (GAD), given for a period of 10 weeks in each trial, showed that it is significantly more effective than placebo in the 50 to 300 mg/day dose range, albeit with an unfavorable profile of metabolic side effects (e10).

Agomelatine acts as an agonist at melatonin MT1- and MT2-receptors and as an antagonist at the serotonin 2C receptor. Multiple studies published from 2008 onward have shown it to be well tolerated and highly effective against GAD in the 25–50 mg/day dose range (e11), yet this drug has not been approved for the treatment of anxiety disorders either.

Silexan, a patented active substance derived from lavender oil, has been approved since 2009 in Germany for the treatment of subsyndromal anxiety and tension states at a daily dose of 80 mg, but not for the treatment of anxiety disorders. Nonetheless, randomized controlled trials (RCTs) have shown its effectiveness against GAS and so-called mixed anxiety and depression (e12).

A common question in clinical practice is how long drug therapy should be continued in order to prevent a relapse. The response rates are generally high (ca. 80%), but too early discontinuation of medication is associated with non-negligible relapse rates. Among patients with panic disorder, for example, a relapse is seen in 15–50% within 6–12 months of the discontinuation of tricyclic antidepressants, SSRI, or venlafaxine. It is therefore recommended that maintenance therapy with SSRI or SNRI be continued for at least 6–12 months after the end of the acute phase, at the effective final dose that was attained. Any attempt to discontinue medication should be gradual, e.g., over the course of 12 weeks if the duration of treatment until now has been 40 weeks (27).

Benzodiazepines are approved in Germany for the acute treatment of “states of tension, excitation, and anxiety.” Nonetheless, the German guidelines on the treatment of anxiety disorders discuss the use of benzodiazepines for this purpose in decidedly critical terms: “Benzodiazepines are effective against panic disorder/agoraphobia/generalized anxiety disorder/social phobia (Ia; guideline adaptation). They should nonetheless not be offered to patients with panic disorder/agoraphobia/generalized anxiety disorder/social phobia because of their serious side effects (development of dependence, etc.). They can be used for a limited time after careful evaluation of the risks and benefits in exceptional cases, e.g., patients with severe cardiac disease, contraindications for standard drugs, suicidality, and other conditions.“ The discontinuation of benzodiazepines after they have been taken for months or years, as is often the case, is a special challenge in the treatment of patients with anxiety disorders (28). Drug discontinuation must often take place in an inpatient setting, and only a few of the pertinent treatment recommendations are supported by adequate evidence.

Benzodiazepines

Benzodiazepines are approved in Germany for the acute treatment of “states of tension, excitation, and anxiety.” Nonetheless, the German guidelines on the treatment of anxiety disorders discuss the use of benzodiazepines for this purpose in decidedly critical terms because of their marked side effects.

While cognitive behavioral therapy and psychopharmacotherapy are considered first-line treatments for anxiety disorders, further treatment strategies have been studied and applied in routine clinical practice in recent years, such as the following:

Noninvasive stimulation techniques, such as repetitive transcranial magnetic stimulation (rTMS) or transcranial direct-current stimulation (tDCS) (32)

A systematic review of the literature is needed so that the relevance of new studies for the guideline recommendations can be appropriately assessed.

We find the use of physical activity and exercise as a treatment of anxiety disorders to be particularly interesting. This mode of treatment is inexpensive and has few undesired effects; it should be applied in combination with the first-line therapies (not as the sole intervention) and is used much too rarely in routine clinical practice (33). Very strong pre/post effect strengths of g = -1.23 (24) seem impressive but have not been reproduced in studies with active control groups (34). Even single units of endurance training can have an anxiolytic effect (e13– e15) or perhaps reinforce the effect of exposure therapy (35).

Aside from drug therapy of the types discussed, clinical practice guidelines also contain recommendations for psychological treatments of anxiety disorders in the primary medical care setting. The essential building-blocks of treatment are (20):

The essential components of the treatment of panic disorder with agoraphobia are:

The primary care physician and the patient work jointly to develop a gradually intensifying treatment plan (participative decision-making). With the primary care physician’s attentive personal support and counseling, the patient carries out specific anxiety-reducing exercises (36). Anxiety-confronting exercises are performed in controlled fashion according to the principles of cognitive behavioral therapy (CBT). Patients with panic disorder, in particular, are confronted with so-called interoceptive stimuli (as an exercise, including, for instance, 60 seconds of hyperventilation under supervision); patients with agoraphobia are confronted with so-called situational stimuli (e.g., taking a train ride by oneself). It is important for the patient to discuss the exercise afterward with the physician in order to reinforce the new experience and solidify the associated learning achievement. The stimuli that were originally felt to be anxiety-producing are now judged more appropriately. Trained medical practice assistants can serve as case managers to help the patient carry out these exercises: they telephone the patient regularly to record the patient’s current disease manifestations with the aid of a brief symptom checklist. This list is at the center of communication between the physician, the patient, and the practice assistant (37); it permits rapid assessment of the patient’s situation and reliable transmission of this information to the physician, who can then respond in timely fashion. If the symptoms fail to improve rapidly under the care of the primary care physician, a psychiatrist or psychotherapist should be consulted without delay. It has been shown that the ambulatory treatment of patients with panic disorder and agoraphobia with exposure therapy is more effective when carried out under direct supervision than when carried out by the patient alone according to directions (22). Supervision of the exposure places a heavy psychological demand on the therapist as well (38); this can be observed in the activation of the stress hormone system, particularly with massive exposure (flooding) (39).

Exercise therapy

Exercise has an anxiolytic effect and is therapeutically useful in both the short term and the long term.

Panic disorders

Patients with panic disorder, in particular, are confronted with so-called interoceptive stimuli (as an exercise, including, for instance, 60 seconds of hyperventilation under supervision); patients with agoraphobia are confronted with so-called situational stimuli (e.g., taking a train ride by oneself).

Prevention

Exposure under the supervision of a therapist

It has been shown that the outpatient treatment of patients with panic disorder and agoraphobia with exposure therapy is more effective when carried out under direct supervision than when carried out by the patient alone.

The development and assessment of preventive measures against anxiety disorders should have a high priority in view of these disorders’ high prevalence and chronicity, the severity of the suffering that they cause, their high socioeconomic costs, and their role as precursors of depression and substance-abuse disorders and as complicating factors in somatic disease (40). Universal preventive measures, applied regardless of the risk status of the individual, might prevent many cases of clinically manifest anxiety disorders, even if their individual effects were not very strong; yet their application to large, unselected target groups would be both very expensive and very labor-intensive. The alternative lies in targeted programs, or, in other words, selective primary preventive measures, such as the Cool Little Kids program or the Friends program. These measures are particularly effective in preventing the development of clinically overt anxiety disorders in high-risk groups in the critical temporal window of childhood and adolescence. For example, a longitudinal randomized controlled trial showed that the Cool Little Kids program was significantly superior to control (no treatment) in a population of 3- to 5-year-old preschool children: the preventive intervention significantly lowered the incidence of anxiety disorders at 12 (p = 0.03), 24 (p = 0.03), and 36 (p = 0.01) months, and even after a further follow-up period of 11 years—but then only among the girls, who were about 15 years old by that time (Cohen’s d = 0.55, p = 0.04) (e16, e17). Targeted prevention in persons who already display subclinical symptoms has been shown to significantly lessen the rate of development of clinically relevant anxiety disorders and is thus probably the most cost-effective primary measure. Meta-analyses have revealed low effect strengths for the prevention of anxiety; targeted measures were found to be somewhat more effective than universal ones right after the intervention (Cohen’s d = 0.26 versus 0.17 [e18, e19]). The prevention manuals now available in the German-speaking countries include, for example, the Friends program; the Separation Anxiety Program for Families (Trennungsangstprogramm für Familien, TAFF); the Being Brave with Til Tiger program (Mutig werden mit Til Tiger); and the Health and Optimism Program (Gesundheits- und Optimismus-Programm). The encouraging initial data imply that preventive measures against mental illnesses, and in particular against anxiety disorders, which are very common and socioeconomically relevant, urgently need to be studied further, systematically, and in detail. If their effects can be confirmed, these measures should be implemented in timely fashion in the healthcare system.

Prevention manuals

The prevention manuals now available in the German-speaking countries include, for example, the Friends program; the Separation Anxiety Program for Families (TAFF); the Being Brave with Til Tiger program; and the Health and Optimism Program.

Further information on CME

Participation in the CME certification program is possible only over the Internet: cme.aerzteblatt.de. This unit can be accessed until 9 December 2018. Submissions by letter, e-mail or fax cannot be considered.

This article has been certified by the North Rhine Academy for Continuing Medical Education. Participants in the CME program can manage their CME points with their 15-digit “uniform CME number” (einheitliche Fortbildungsnummer, EFN), which is found on the CME card (8027XXXXXXXXXXX). The EFN must be stated during registration on www.aerzteblatt.de (“Mein DÄ”) or else entered in “Meine Daten,” and the participant must agree to communication of the results.

CME credit for this unit can be obtained via cme.aerzteblatt.de until 9 December 2018.

Only one answer is possible per question. Please choose the most appropriate answer.

Question 1

What is the approximate 12-month prevalence of anxiety disorders among 14- to 65-year-olds in Europe?

Question 2

What is the most common type of anxiety disorder?

Question 3

What percentage of the development of anxiety disorders is accounted for by genetic factors?

Question 4

What type of psychotherapy is the treatment of first choice for anxiety disorders?

Question 5

What psychoactive drug(s) is/are the first line of drug therapy for anxiety disorders?

Question 6

Which of the following substances is effective against generalized anxiety disorder, according to clinical trials, but not approved for this purpose in Germany?

Question 7

What is a typical feature of a panic disorder?

Question 8

What type of complementary treatment can be used beneficially in patients with anxiety disorders?

Question 9

How long after the end of the acute phase of successful drug treatment for panic disorder should the drug be continued for maintenance therapy?

Question 10

What is a typical feature of selective mutism?

Acknowledgments

Translated from the original German by Ethan Taub, M.D.

Footnotes

Conflict of interest statement

The authors declare that no conflict of interest exists.

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