“Anger

Attacks”:

Possible

and Major

Maurizio

Fava,

M.D.,

Keith

Variants

Depressive

Anderson,

Disorders

M.D.,

and Jerrold

strative

The authors report a series of illustrative cases in which patients presented with sudden “spells” of anger with physical features that resembled panic attacks but lacked the affects of fear and anxiety. These spells or “attacks” of anger were experienced as uncharacteristic and were inappropriate to the situations in which they occurred. Since treatment of these attacks with antidepressants produced in each case marked im-

provements

in behavior,

some hypotheses (Am J Psychiatry

the

as to the 1990;

authors

also

nature of these 147:867-870)

and

hen a nonpsychotic isodes of anger

%,v

grossly

out of proportion

stressons,

a personality

derline)

is typically

psychiatric

adult are

that

describes of short

treatments

of

marked

first

organic

considered.

disturbances,

however,

( )

Numerous

may

epand

or

bor-

other

be associated

hypotheses

ogy Unit,

Massachusetts

General

pital, Ottawa, Ont., Canada. Clinical Psychopharmacology tal, 15 Parkman St., ACC81S, Copyright © 1990 American

Am

J

Psychiatry

received

Aug.

the Clinical Hospital, and

1 and

Dec.

20,

PsychopharmacolOttawa Civic Hos-

Address reprint requests to Dr. Fava, Unit, Massachusetts General HospiBoston, MA 02114. Psychiatric Association.

1 47: 7, July

1990

in

attacks

in

as to the

treatment

which

patients

in

each

behavior, nature

case

we

pre-

that were exinappropriate Since specific produced

formulate

of these

episodes

some and

offer

recommendations.

REPORTS

1 Mr.

A, a 45-year-old

.

white

man,

was an attorney

who lived with his wife and referred by his therapist because and thought “in a fragmented problems to stressful life events

three children. He had been he lost his temper frequently way.” Mr. A attributed his over the previous 10 months.

He had

a long

with

lost

his mother

his wife

He denied

and

after

children,

feelings

and

had

of depression

illness, been

and

had

problems

distressed

sleep

at work.

or appetite

dis-

and diminished energy and concentration. He had been in therapy for a couple of years and had found that very helpful, since it had allowed him to deal with the loss of his mother and to turbance

with a tendency to anger 1 : affective disorders, hypochondniasis, schizophrenic disorders, paranoid disorders, and psychoactive substance intoxication or withdrawal. Adult “temper tantrums” have been reported among mentally retarded individuals (2) and in subjects with head trauma, minimal brain dysfunction, epilepsy, brain tumor, infections, cerebral vascular disease, other neurological disease, and endocrine and metabolic disorders (3). When these discrete episodes of loss of control oven aggressive impulses result in assaultive acts or destruction of property, the best diagnostic fit from DSM-III-R may be intermittent explosive disorder. The existence of a discrete disorder is controversial; these behaviors are often viewed as symptomatic of a personality disorder. Six years ago, one of us (K.A.) noted in a patient sudden “spells” of anger with physical features that resembled panic attacks but lacked the affects of fear and anxiety. Since then, we have observed a number of similar cases: we now report some of the most demon-

Received Aug. 2, 1988; revisions 1989; accepted Jan. 25, 1990. From

cases

these

changes

CASE

psychosocial

(e.g.,

illustrative

M.D.

formulate episodes.

repeated duration

to precipitating disorder

F. Rosenbaum,

sented with spells on “attacks” of anger penienced as uncharacteristic and were to the situations in which they occurred.

Case

“ VT

of Panic

but

her.

mourn

tient had his temper

reported

However,

had

yell;

fuse,”

explosive

things

few months,

during enraged and

that

in therapy

patient seizures,

the state

“anger

his heart

quickly, During

rate accelerated, and

his

he would

alien to him and was concerned that he would as a result. He denied having suffered from simin the past. About 12 years earlier he had been for

a short

unremarkable;

time

his

and

At the time for

very

attacks.”

about an hour He felt that these epi-

of arousal.

had no history of or drug or alcohol

alcoholism,

the pa-

which he would lose and yelling at others.

felt out of control

temper

he noticed

from

sodes were lose his job ilar episodes

teria

in

would flush while he felt out of control, after the initial surge, it would take him

to recover

was

interest

for the previous

a “short

an

these attacks face

of

been having episodes in a flash, becoming

He described and

lack

his

because

of

mania, abuse.

hypomania, His past

mother

father

had

had

of his evaluation,

depressive

disorder

a probable

a history

Mr. not

marital

problems.

head medical diagnosis

The injury, history of

of paranoia.

A met

otherwise

DSM-III-R specified;

not appear to have a personality disorder. In addition, a very high hostility score (score of 15; maximum=23)

cri-

he did

he had on

the Kellner Symptom Questionnaire (4), a self-rating scale of distress that contains subscales of anxiety, depression, somatization, and hostility and whose mean±SD hostility subscale score in normal control subjects is 3.7±3.5. Treatment was immediately initiated with desipramine, 10 mg h.s., which was later gradually increased to 200 mg h.s.

867

“ANGER

ATFACKS”

Mr. A was seen on average once every month for pharmacotherapy, and he continued to see his referring psychotherapist once every week. Within 3 weeks, he reported no more feelings of loss of control and cessation of outbursts. It was much harder to get him angry. His hostility score on the Keliner Symptom Questionnaire (4) was 0 two months after his initial evaluation, continued to be 0 two months later, and was 2 after five months of desipramine treatment. The symptoms of temper outbursts and anger did not recur during desipramine treatment. Case 2. Ms. B, a 31-year-old married white woman with no children, was a financial consultant. She had been referred by her family doctor because of chronic depression and burnout. She had been away from work for 3 weeks because of increasing anger in tense negotiations on the job. She felt that she was overreacting, usually in anger. Ms. B and her husband had been fighting a lot, which she attributed to her burnout at work. She reported that in situations “where you cannot do anything about it, like in a bureaucracy,” she would feel a tightness in her chest, her head would get “fuzzy,” she would feel almost dizzy, would feel hot and experience palpitations, would then feel like crying, and would explode in an anger attack. At the time of her evaluation, she denied feeling anxious or panicky and denied any sleep disturbance. She described her appetite as “exuberant,” saying that she had gained 30 pounds in the previous 2 years. She appeared to be mildly depressed without neurovegetative signs and did not meet criteria for personality disorder. The patient’s early childhood was described as “not a good time-I was always left out.” She did well in school until high school; while in high school, she “drank a lot and stayed out.” Ms. B did not have any history of head trauma or seizures. She had an older sister who had been treated for anxiety. She also had a maternal grandmother described as “a nasty old woman who beat her kids.” The patient was started on clomipramine treatment, SO mg h.s., at the time of the evaluation and was seen in follow-up on average once every month by the psychiatrist. Within a few days, she felt much better and in more control and returned to work within 1 week. Since the patient experienced anongasmia, the dose was reduced to 30 mg h.s., and she continued to do well for about 3 months until she decided to stop the medication. Four days later, she had an intense fight with her husband that she described as an anger attack; 2 days later, she had a dispute at work and decided to restart the medication. During the following 14 months of treatment, she did very well and was promoted twice at work. Seventeen months later, while away on a business trip, she called her husband to report that she again was erupting with inappropriate anger. She then recognized that the prescription she had picked up before leaving home looked different from earlier ones. At a pharmacy, she was told that the pills she had been taking for a week were an anti-inflammatory medication

appropriate in 2 days.

made

by the

medication At 2-year

manufacturer

was follow-up,

dispensed,

of clomipramine.

and Ms.

she continued

The

B felt better

to do well

with

clomipramine. Case 3. Ms. C, a 30-year-old single white woman and a registered nurse, had been referred by her psychotherapist, who had seen her for about 1 year. About 28 months before assessment she had become very depressed, and her depression had continued, accompanied by neurovegetative signs and occasional suicidal thoughts, for about 20 months. For this

868

reason,

she

entered

and

continued

psychotherapy.

Her

psychotherapy she

and

had been

her

very helpful

psychotherapist

felt

for her depression,

that

she

needed

but

pharmaco-

logical treatment of her anxiety and anger attacks. During the evaluation, Ms. C reported that she had nervous

been

and

anxious

extremely

situations, ity figures, situation,

since

she

was

a child.

shy and had tended

She

to be afraid

had

been

always

of numerous

such as any social gathering, dealing with authorcrowds, and driving. Especially in this kind of she would have anger attacks; during these epi-

sodes she would hyperventilate, the palms of her hands would begin to sweat, her face would get red, she would become angry and enraged, she would feel like attacking people, and she would want to escape and would feel as if she

was

going

tion.

Because

avoid

those

to lose

of these

control

if she

anger

situations

remained

attacks,

in

which

in that

the patient she

situa-

had begun

might

to

experience

the

attacks. She had been in therapy while she was in high school because of shyness. She had a history of phobia of escalators and elevators. She denied any history of suicide attempts, mania or hypomania, head ical history was unremarkable. of episodic rage, On evaluation, Ms. C appetite, concentration, helpless and hopeless. She histories

of a personality

injury,

or seizures. Her past Her father and brother

without physical violence. reported no difficulty with sleep, and energy. She occasionally felt lacked depressed mood or features

disorder.

In the

3 weeks

before

tion, she had experienced four anger attacks. score on the Kellner Symptom Questionnaire Immediately

after

her

mcdhad

evaluation

was

the

evalua-

Her hostility (4) was 16.

completed,

Ms.

C

started

treatment with clonazepam, 0.5 mg b.i.d., and desipramine, 10 mg h.s.; the latter was gradually increased to 150 mg h.s. There was some improvement in her symptoms in

the

first

few

days

of

the

treatment

in her symptoms

and

marked

improvement

with

ipramine hostility

in addition to the clonazepam. score on the symptom questionnaire

a consistent,

150 mg of des-

At

that point, her dropped to 6.

She reported

no anger attacks for about a month, felt more and was less irritable and “snappy”; she also mentioned that coffee used to have an “enraging” effect on her, but that effect had disappeared. Throughout hen pharmacological treatment, the patient continued to see her inin control,

dividual

psychotherapist.

Her

remission

was

sustained,

and

months later her hostility score was still 6; she continued take desipramine, 200 mg h.s., and clonazepam, 0.5

3

to mg

b.i.d.

Case 4. Mr. D, a 33-year-old by his family doctor because

married white man referred of “bad temper tantrums,” re-

ported that he would get “mad very fast,” especially with his children. His behavior was causing a great deal of marital difficulty. He had a history of quitting many jobs because he would fly into a rage over trivial issues. He had no history of panic

attacks.

He

reported

that

his

childhood

was

“not

great”

because of his mother’s drinking. He did fairly well socially in high school but failed the tenth grade. Since high school, he had had few friends, and “although I wanted to work, I couldn’t seem to hold a job because I would get peed off.” At the time of his referral he was working as a clerk. His mother had been an outgoing, high-strung woman who “abused alcohol and diazepam” to control her nerves. At the time of his evaluation, Mr. D said that he wanted treatment because he was depressed about his work record and he children.

did not like He denied

himself panic

for the way he dealt attacks but did admit

attacks. When these attacks started his heart pounded, he felt lightheaded,

Am

J

Psychiatry

with his to anger

he felt hot and flushed, his hands shook, and

147:7,

July

1990

FAVA,

he perspired. This would culminate in a “rush” of anger and a feeling of being out of control. He denied sleep or appetite disturbance or alcohol injury, or seizures. He

abuse did not

or a history of mania, head appear to have a personality

disorder on interview. neurovegetative signs.

He was

mildly

As soon

as the

evaluation

was

depressed

completed,

recurrence antidepressant symptoms. that anger

but without treatment

was

started with clomipramine, 35 mg h.s.; within a few days Mr. D reported marked improvement, and his wife reported that he was “much easier to live with.” He was initially seen once

every

2 weeks

and

then

once

every

month

during

course of the treatment. He continued to do well for about months. At that time, he failed to renew his prescription was close to payday and he could not afford the medication), and

3 days

“blowup”

after

with

stopping

the

medication,

he

had

the

2 (it

his

first

his children in 2 months. He restarted did well for a month. On a later occasion,

the

medication and he again stopped the medication and 2 days later had a fistfight with a man whom the patient felt was driving too fast near the area where the patient’s children were playing. After restarting treatment, he did very well and had no anger attacks for the next 4 months.

iety

The common feature of these cases is the presence of anger attacks characterized by ego-dystonic episodes of anger that were of short duration and grossly out of proportion to precipitating psychosocial stressons. These episodes were associated with a sudden surge of autonomic arousal including such symptoms as tachycardia, sweating, flushing, and a feeling of being out of control. Although the physical symptoms resemble those of a panic attack, none of the patients described anxious, panicky, or fearful emotions. The intensity of the anger is underscored by the Kellnen Symptom Q uestionnaire (4) hostility scale measures: the two patients administered the questionnaire had a mean pnetreatment scone of 15.5, the mean scone of normal controt subjects is 3.7±3.5. From a psychodynamic point of view, anger or aggression can be seen either as a response to frustration of libidinal wishes (5) or as a separate instinctual entity (6). In both cases anger is, in general, incorporated in the development of the character structure and tends to present as a problem when the patient’s defenses begin to fail in channeling or controlling it. One could postulate that the patients that we describe were all experiencing frustration at some level in their lives on that their instinctual aggressive drives were more intense and/or their defense mechanisms were ineffective. Anger attacks may become a response to feeling helpless or powerless, particularly in individuals with what is simply described as emotional immaturity, on to feeling threatened in some way. A purely psychodynamic explanation of these attacks does not take into account various factors such as the influence of mood on the cognitive appraisal of events as irritating, frustrating, or threatening, the fact that the anger attacks nesponded very well to thymoleptics, that discontinuation of the drug in some of these cases was followed by

sive,

July

1990

attacks, and that nechallenge with was also followed by remission of We would also like to highlight the attacks occurred in our patients in the

hypochondniasis,

Selected may

We

147:7,

of

disorders,

cases

Psychiatry

ROSENBAUM

personality

disorders,

schizophrenic disorders, paranoid disorders, and psychoactive substance intoxication and withdrawal. These conditions as currently defined did not chanacterize our patients, except one, who had a depressive disorder not otherwise specified that was associated with his anger attacks. Although our patients did not have a history of head injury on seizures, we cannot exclude the possibility of a subictal disorder, a clinical diagnosis typically lacking definitive EEG or other evidence.

J

AND

the the fact absence of diagnosable personality disorders; in fact, all patients underwent a comprehensive clinical assessment that included a differential diagnosis for axis II disorders according to DSM-III-R. Fava (1) reviewed the array of psychiatric distunbances most associated with a tendency to anger: affective disorders (particularly bipolar disorders), anx-

DISCUSSION

Am

ANDERSON,

find

be

for quite

two

a single

different,

explanations

common

for

although anger

feeling

these

of panic

not

mutually

exclu-

attacks.

1. Anger attacks may be Deffenbacher et al. (7) have iety is associated with anger of anger; the prodromal arousal during anger attacks attack symptoms. Although subjective

symptom,

heterogeneous.

a variant of panic attacks. observed that general anxin subjects with high levels symptoms of autonomic are similar to some panic our patients denied the

or

anxiety,

one

patient,

who

had a history of simple phobias, developed marked avoidance of settings associated with these attacks, had found caffeine provocative, and had an immediate response to the combination of a benzodiazepine and tnicyclic,

a response

somewhat

similar

to that

a

expected

in panic disorder patients. All of our patients responded to treatments that are considered by clinicians to be effective for panic disorder. For example, in countries where clomipramine is available, it is deemed an excellent antipanic therapy and is frequently observed to be effective at doses lower than those typically necessary for patients with major depression, and often early in treatment (8). That a panic attack may be considered a “false alarm” response, a spontaneous activation of the “fight-flight” reaction usually reserved for life threat, also contributes to this hypothesis. One might expect that fight-flight activation would be, on occasion, cognitively and behaviorally expressed not as fear and flight but as anger and fight. These cases might illustrate this missing link to the fight-flight paradigm. Indeed, the cognitive concomitants of a panic attack do vary, and some sufferers are reported to experience little or no fear or anxiety (9) with their panic attack. 2.

Anger

attacks

may

be an

atypical

depressive disorders. Akiskal et at. (10) the occurrence of irritable-angry-explosive the setting of cyclothymic disorders.

presentation

of

have

described mood in Depressed pa-

869

“ANGER

A1TACKS”

tients are observed to display more hostility than normat control groups (11), and hostility in depressed patients diminishes with recovery after treatment with a tnicyclic (12). There is some evidence of a common biological mechanism, involving senotonengic transmission, for affective disorders and aggression disondens (13). One of our patients also had a depressive disorder, and all patients responded to treatment with tnicyclics, which are commonly used in the treatment of depression. Although Mattes (14), in a review of pharmacological treatments of temper outbursts, noted that carbamazepine, propranolol, and lithium may reduce aggressiveness in patients with temper outbursts and that there was less evidence of beneficial effects on rage outbursts from other drugs, all our patients responded dramatically to tnicyclic antidepressants. We chose to use clomipramine, desipramine, and clonazepam in the treatment of these anger attacks since they are commonly used in the treatment of panic disorder and we thought that anger attacks resembled panic attacks in many respects. In some cases, the presence of comorbid depressive symptoms also played a role in the choice of an antidepressant. In cases 2 and 4, the patients experienced a recurrence of their anger attacks 4 and 3 days, respectively, after discontinuing the antidepressant. Abrupt relapses may appear inconsistent with postulated mechanisms of action of antidepnessants in depression but are consistent with clinical observation of some patients, particularly with panic disorder, who experience a brisk rebound of symptoms in response to decreased intensity of phanmacothenapy. This phenomenon may argue for the primacy of acute and direct effects of these agents, rather than delayed effects involving changes in receptor sensitivity. In conclusion, we report four illustrative cases of patients with anger attacks, which are characterized by short-lived outbursts of anger that are perceived to be excessive and grossly out of proportion to any precipitating psychosocial stressons. In most cases these episodes of anger attacks are associated with tachycardia, sweating, flushing, and a feeling of being out of controt. We have observed that patients with anger attacks respond very well to treatment with tnicyclic antidepressants, and such response may suggest the possibility that anger attacks are variants of panic disorder on depression. The fact that most of our patients reported feelings of helplessness and frustration may be con-

870

sidered further links with both depressive and panic disorders. Finally, recognizing and treating patients with anger attacks may be an important clinical task. Williams et at. (15) and Rosenman (16) have reviewed the consequences of anger for the development of candiovascular disease and support the idea that anger and hostility are the critical components of type A behavior that account for the increased risk of cononary artery disease. Our observations and hypotheses suffer all the limitations of a retrospective case series. However, we believe this to be a fairly prevalent clinical syndrome that is likely to be secondary to either anxiety or depression.

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147:7,

July

1990

"Anger attacks": possible variants of panic and major depressive disorders.

The authors report a series of illustrative cases in which patients presented with sudden "spells" of anger with physical features that resembled pani...
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