week 10 - mood disorders Flashcards

1
Q

The Episodes

A
The Episodes
Manic Episode
Major Depressive Episode
Mixed Episode
Hypomanic Episode
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2
Q

The Disorders

A

Bipolar I disorder
Major Depressive Disorder
–Description, Diagnosis (and DDx), Case Examples, Statistics, Formulation Models, Treatments

Dysthymic Disorder
Bipolar II disorder

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3
Q

Manic Episode

A

A distinct period of abnormal, persistently elevated, expansive or irritable mood, lasting at least one week.

During the mood disturbance, three or more of the following are present.
Inflated self esteem or grandiosity
Decreased need for sleep
More talkative or pressure of speech
Flight of ideas or subjective experience of racing thoughts
Distractibility
Increased goal-directed activity
Excessive involvement in pleasant activities with potential for negative consequences.

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4
Q

Manic Episode

course/onset

A

Mean age of onset for first Manic Episode is in early 20s, although cases in adolescence and old-age are observed.

Manic episodes typically begin suddenly, with rapid escalation of symptoms over only a few days.

Episodes tend to last weeks to months

  • –Onset and end are more abrupt than Major Depressive Episodes
  • –Episodes tend to be more brief than Major Depressive Episodes

Onset of Manic Episode follows a Major Depressive
Episode in 50-60% of cases.

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5
Q

Major Depressive Episode

A

Five or more of the following over at least two weeks, representing a change from previous functioning

At least one of the symptoms present must be depressed mood or anhedonia.

Depressed mood
Diminished interest or pleasure
Significant weight loss
Insomnia or hypersomnia
Psychomotor agitation or retardation
Fatigue or anergia
Feelings of worthlessness or excessive guilt
Diminished ability to think or concentrate
Recurrent thoughts of death or suicide.
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6
Q

MDE - course

A

Course
Symptoms typically develop over days to weeks and when untreated Major Depressive Episodes tend to last around four months or longer.

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7
Q

Mixed Episode

A

Criteria for both Major Depressive Episode and Manic Episode are met nearly every day during a one week period

One week time-period for Manic Episode is not required.

Course:

May evolve from MDE or Manic Episode, or arise on own.

May last weeks to several months

Far less common for Mixed Episodes to evolve into Manic Episodes.

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8
Q

Bipolar I Disorder

A

Diagnosis
Occurrence of one or more Manic Episodes or Mixed Episodes
Additional episodes may be present (e.g. Major Depressive Episode)
The disorder is not better accounted for by other psychological conditions, medical conditions, or substance use.
Significant distress or impact on functioning

Differential Diagnosis
Other mood disorders and Psychotic Disorders

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9
Q

Bipolar I disorder - specifiers

A

Specifiers (Continued)
“With Rapid Cycling”
Four or more episodes occur within the previous 12 months
Episodes are demarcated by either full or partial remission for at least two months, or a switch to an episode of opposite polarity.

NOTE: Patients who describe rapid mood swings in which they are “happy one minute and deeply depressed the next” are usually not Bipolar, but are more accurately described as having ‘labile mood’.

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10
Q

bipolar 1 - stats

A

Statistics
Gender Differences
Epidemiological data from USA indicates no difference in prevalence between males and females.

Prevalence
Lifetime prevalence rates range from 0.4% to 1.6%

Elevated Suicide Risk
Completed suicide occurs in 10-15% of Bipolar I Disorders
More likely when patient is in Mixed or Depressed state

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11
Q

Bipolar I Disorder - course & onset

A

Average age of onset for males and females is 20 years.
Typical course is chronic, lifelong.
More than 90% of those who experience a single Manic Episode will experience future episodes.
60-70% of Manic Episodes occur immediately following a MDE.
—A specific pattern of episode may be evident
Untreated Bipolar I Disorder patients experience an average of four episodes per decade.
5-15% meet criteria for Rapid Cycling specifier
Around 20-30% suffer residual interepisode mood symptoms
10-15% of adolescents diagnosed with Major Depressive Disorder will go on to develop Bipolar I Disorder

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12
Q

Bipolar Disorders:

Etiology / Formulation – Biological

A

Genetic factors
Stronger genetic component in Bipolar than in Unipolar mood disorders.
Some studies identifying specific genes (e.g. Chromosome II, X Chromosome) need further investigation.
MZ Twin concordance is 33 to 90 percent.

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13
Q

Bipolar disorders:
Etiology/Formulation – Biological
Neurotransmitter Dysregulation

A

The usual suspects
5HT, NE, DA
Brain Imaging Studies
A significant group of male Bipolar patients show enlarged cerebral ventricles.
Ventricular enlargement is much less common in unipolar depression than in bipolar disorder.

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14
Q

bipolar disorders model

A

other life stress > family stress
|||
rhythm dysregulartion(sleep)»<

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15
Q

Bipolar Disorders
Etiology/Formulation – Biopsychosocial
Expressed Emotion

A

Critical comments, Hostility, and Emotional overinvolvement.
Several studies link high-EE families with greater relapse risk in depression.
The relationship between EE and Bipolar is complex and not simply reflective of an underlying vulnerability to interpersonal stress.

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16
Q

bipolar disorders -= Treatment, Pharmacological

A

Lithium Carbonate
Anticonvulsants

Antipsychotics

generally not Antidepressants as they may push client over edge

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17
Q

Bipolar Disorders treatment, psychosocial

A

Treatment, Psychosocial
Why bother with psychosocial interventions?
Cochran (1984)
Investigated 28 patients treated with Lithium
–Lithium Carbonate alone
—Lithium Carbonate with 6wks Cognitive Therapy aimed at restructuring cognitions associated with medication nonadherance.

A 6m follow-up, those receiving CBT showed

  • -Better medication compliance
  • –Fewer hospitalisations
  • -Fewer mood episodes from non-compliance
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18
Q

bipolar disorders & misdiagnosis

A

69 percent of patients with bipolar disorder are misdiagnosed initially
40 percent are initially diagnosed with unipolar depression
Many others with Borderline Personality Disorder, Histrionic Personality Disorder or Adult ADHD.

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19
Q

misdiagnosis may be because:

A
  1. Lack of insight
    E.g., It was not Mania It was great!
  2. Lack of available information
    E.g., I do not remember anyone telling me that I was manic
  3. Lack of appropriate assessment tools used
    E.g., 13-item Mood Disorder Questionnaire is good…typical depression inventories are not
  4. The overlap in apparent signs with other disorders
    E.g., many health workers are confused about what Borderline vs Bipolar is
  5. The high percentage of comorbidity with other disorders
    E.g., You could have Bipolar with comorbid personality disorder and unipolar depression…that is confusing to diagnose!
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20
Q

Major Depressive Disorder

A

Major Depressive Disorder, Single Episode
Presence of a single Major Depressive Episode (MDE)
The MDE is not better accounted for by Schizoaffective Disorder, and is not superimposed on another psychotic disorder.
There has never been a Manic Episode, Mixed Episode, or Hypomanic Episode.

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21
Q

Major Depressive Disorder - recurrent

A

Presence of two or more Major Depressive Episodes (MDEs)
The MDEs are not better accounted for by a psychotic disorder.
There has never been a Manic Episode, Mixed Episode or Hypomanic Episode.

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22
Q

Major Depressive Disorder

A

Severity Specifiers (Continued)

Severe, with psychotic features
-Delusions or hallucinations are present. Where -possible, specify whether or not the delusions are mood-congruent.

In Partial Remission
-Symptoms of a MDE are present, but full criteria are not met.

In Full Remission
-No significant symptoms of MDE over the past two months

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23
Q

Major Depressive Disorder

differential Diagnosis

A

Differential Diagnosis
Bipolar Disorder
—Have there been mixed, manic or hypomanic episodes?

General Medical Conditions
–Numerous medical conditions present with depression symptoms

Dysthymic Disorder (Now called Persistent Depressive Disorder)
Severity, chronicity, persistence

Schizoaffective Disorder
Have there been >2wks of delusions/hallucinations in the absence of mood symptoms

Dementia

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24
Q

Major Depressive Disorder - stats, gender differences , family patterm

A

Age Differences
Younger people may be at greater risk for “atypical features”
Older adults may be more at risk for “melancholic features”
Gender Differences

In adults and adolescents, females present twice as often with Major Depressive Disorder (WHY?)
In childhood, males and females appear equally affected.

Family Pattern
1.5 to 3.0 times more common in 1st degree relatives
Increased risk of alcohol dependence in 1st degree relatives
Increased risk of anxiety disorder in 1st degree relatives

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25
Q

MDD stats - prevalence

A

Prevalence
Different studies have presented varying data on prevalence
Lifetime risk in community samples: 10% to 25% for women
Lifetime risk in community samples: 5% to 12% for men
Point-prevalence in adult community sample
—5% to 9% of females, 2% to 3% for males
Prevalence appears unrelated to ethnicity, income, education or marital status.

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26
Q

Major Depressive Disorder - Course: /Onset

A

May have onset at any age, mean onset in 20s
–Some evidence that age of onset is decreasing

Course of Recurrent MDD is variable and idiosyncratic

Naturalistic Course - One Year Post-Diagnosis Follow-Up

  • –40% have symptoms that still meet MDE criteria
  • –20% have residual symptoms, but do not meet MDE criteria
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27
Q

Major Depressive Disorder relapse risk

A

Relapse Risk
After one episode, 60% will experience a second
After two episodes, 70% will experience a third
After three episodes, 90% will experience a fourth

That means that 60% of the 60% (that initially got better) will experience a second episode! So they are not healthy after all

28
Q

mdd remittance

A

So 63% never get better with management as usual!

potentially

29
Q

MDD ETIOLOGY /FORMULATION

A
Etiology / Formulation
Numerous systems are implied in etiology of Major 
Depressive Disorder.
Understanding of mood disorders remains incomplete.
-
Biological Factors
Genetic Factors
Dynamic Factors
Interpersonal Factors
Cognitive Factors
Behavioural Factors

It is important to remember that each of these factors interacts, and changes in one system can effect changes in others.

30
Q

Major Depressive Disorder - Etiology (Continued)

Biological Factors

A

The Monoamine Hypothesis of Depression
Idea that depression is caused by a deficiency of catecholamines
—Norepinephrine (NE), Serotonin (5HT), Dopamine (DA)
—-All effective antidepressants operate on monoamine systems through various mechanisms.
—-Drugs that deplete monoamines (e.g. reserpine) have a depressogenic effect

See after end of slides for more in depth discussion about the biological factors!

31
Q

Major Depressive Disorder genetic factors

A

Literature indicates a significant genetic contribution in depression.
Genetic factors appear slightly less important in Major Depression, compared with Bipolar Disorder.
Those with a first-degree relative with Major Depressive Disorder are at 1.5-3.0 times the normal risk for developing depression.
Biological children of depressed parents remain at risk even when reared in a different family.
Concordance rate in monozygotic twins is 50%
Concordance rate in dizygotic twins is 10-25%

32
Q

Suicide Risk? from mdd

A

As many as between 2 to 9% of those experiencing depression commit suicide.

30% to 70% of those committing suicide suffer from depression!

33
Q

Major Depressive Disorder
Etiology (Continued)
Behavioural Factors

A

Learning Theory / Social Skills
Loss of reinforcer effectiveness (Costello, 1972)
Also, reduced reinforcers present (e.g., not engaging in rewarding activities anymore!)

Briefly stated: Depression is reduced activity and consequently reduced reward and treatment is increasing activity and reward (i.e., behavioural activation)

34
Q

Major Depressive Disorder
Cognitive Factors
Aaron Beck’s cognitive model of depression

A

early experience> dysfuncitonal assumptions>criticalincident> ANTS >symptoms

Briefly stated: Depression is automatic negative thoughts and treatment is changing those thoughts and assumptions

35
Q

History of Mood Disorders

A
Depression recognized since antiquity
Biblical Examples
--King Saul (I Samuel 16, 14-23)
The suicide of Ajax in Homer’s Iliad
Hippocrates description of Melancholia and Mania (400BC)
Further examples throughout history

DSM-I Psychoneurotic Disorders / Affective Reactions
Manic Depressive Reaction
Depressive Reaction
Psychotic Depressive Reaction

36
Q

History of Mood Disorders II

A

DSM-III and DSM-III-R conceptualization of “Affective Disorders”
–Relationship to Anxiety Disorders

Bipolar mood disorders also recognized historically

  • Hippocrates (400BC) description of Mania.
  • Bonet (1686) description of Maniaco-Melancholicus
  • Falret (1854) description of Folie Circulaire
  • Kahlbaum (1882) first use of term Cyclothymia
  • Kraepelin (1899) description of Manic-Depression
37
Q

Major Depressive Disorder - other specifiiers used in dsm 5

A

Chronic
Where full criteria for a MDE are met continuously for >2yrs

With Catatonic Features
Where the clinical picture is dominated by two of the following
-Motoric immobility / Catalepsy / Stupor
-Excessive motor activity
-Extreme negativism or mutism
-Peculiarities of voluntary movement as evidenced by -posturing, stereotypies, mannerisms or prominent grimacing.
-Echolalia or echopraxia

38
Q

mdd with other specifiers - melancholic

A

With Melancholic Features
Either
Loss of pleasure in all / almost all activities
Lack of reactivity to normally pleasurable stimuli

Three or more of the following–
Distinctly depressed mood
Diurnal mood variation, depression worse in morning
Early morning awakening
Marked psychomotor agitation or retardation
Significant loss of appetite or weight loss
Excessive or inappropriate guilt

39
Q

mdd specifiers - atypical features

postpartum onset

A

With Atypical Features

  • Mood remains reactive
  • Two or more of the following
  • -Significant weight gain or increase in appetite
  • -Hypersomnia
  • –Leaden paralysis
  • -Long-standing pattern of sensitivity to interpersonal rejection leading to significant social impairment.

With Postpartum Onset
–Onset of the MDE is within four weeks postpartum

40
Q

more specifiers
interepisode recover,

seasonal patter (SAD?)

A

With Interepisode Recovery
When full remission is attained between the two most recent MDEs

Without Interepisode Recovery
When full remission is not attained between the two most recent mood episodes

With Seasonal Pattern
There is a regular temporal relationship between MDE onset and a time of year.
–Two episodes conform to this pattern with none outside this pattern in the last two years
–Seasonally related episodes outnumber non-seasonally related episodes.

41
Q

Hypomanic Episode

A

A distinct period of persistently elevated, expansive or irritable mood, lasting >4days, that is clearly different from normal non-depressed mood.
Clear change in functioning from normal character when asymptomatic.
Change in mood disturbance is objectively observable.

Symptoms do not cause marked impairment in functioning, and psychotic features are absent.
Three or more of the following are present
Inflated self-esteem
Decreased need for sleep
Pressure of speech
Flight of ideas / Racing thoughts
Distractibility
Increased goal-directed activity
Increase in pleasant activity with potential for harm

42
Q

Hypomanic Episode Course

A

Typically sudden onset, with rapid escalation of symptoms over 24-48 hours

Episodes may last weeks to months

Hypomanic episodes tend to have more abrupt onset and cessation of symptoms than MDEs

Hypomanic episodes tend to be shorter in duration than MDEs

5-15% of Hypomanic Episodes will evolve into a full Manic Episode.

43
Q

etiology of MDD receptor based hypotheses

A

Receptor Based Hypotheses of Depression
Almost all antidepressants effect a decrease in the post-synaptic sensitivity of B-adrenergic and serotonergic-type II receptors

This down-regulation that occurs with treatment is consistent with the treatment response times seen in antidepressants.

Similar down-regulation is seen as a result of atypical antidepressant (e.g mianserin) treatment, and electroconvulsive therapy.

44
Q

MDD bio factors - beuroendocrine dysfunction

A

Neuroendocrine Dysfunction
Unlikely to be root cause of mood dysfunction, but indicators of other underlying pathology

No neuroendocrine markers are perfectly sensitive or specific to presence of depression.

Adrenal Axis

  • -Depressive symptoms are correlated with hypersecretion of cortisol.
  • -Dexamethasone Suppression Test (DST) - Approximately 50% of depressed patients show abnormal cortisol suppression in response to dexamethasone administration.
45
Q

Major Depressive Disorder biofactors
thyroid axis,
growth hormone
other neuroendrocine

A

Neuroendocrine Dysfunction
Thyroid Axis
-Abnormal thyroid regulation with depression
-About 33% of depressed patients with normal thyroid function may show abnormal (reduced TSH) responses to thyrotropin-releasing hormone.

Growth Hormone
Depressed patients may show reduced nocturnal release of growth hormone.

Other neuroendocrine markers exists
e.g. Reduced nocturnal melatonin release

46
Q

MDD
Etiology (Continued)
Cognitive Factors (Continued)

A

Learned Helplessness/Hopelessness (Seligman)
-People prone to depression expect that they are helpless to control aversive outcomes, and behave accordingly.

Theory reformulated in light of some inconsistent findings to one of attributions of causes of events
—Internal, stable, global attributions re negative events
“I failed the Abnormal Psych exam because I am stupid (internal), I will always fail/be stupid (stable) at everything (global)”

–External, unstable, specific attributions re positive events
“I only passed the Abnormal Psych exam because Sally helped me (external). It doesn’t mean I will always (unstable) pass everything (specific)”

47
Q

Persistent Depressive Disorder

A

Depressed mood, most of the day, more days than not, for at least two years.
When depressed, two or more of the following:

Poor appetite or overeating
Insomnia or hypersomnia
Low energy or fatigue
Low self-esteem
Poor concentration or difficulty in making decisions
Feelings of hopelessness

The above symptoms have never been absent for more than two months
No Major Depressive Episode has been present during the first two years of mood disturbance
No history of manic or hypomanic episodes

48
Q

Persistent Depressive Disorder

Specifiers

A
Specifiers
With Atypical Features
See previous slide for Major Depressive Disorder
Early Onset
Onset is before age 21
Late Onset
Onset is after age 21
49
Q

Persistent Depressive Disorder

DDx

A

Major Depressive Disorder

  • -Chronic versus generally episodic course
  • -“Double-depression”
  • —-Major Depressive Disorder superimposed on Dysthymic Disorder

Mood Disorder Due to a General Medical Condition

Substance Induced Mood Disorder

Personality Disorder

50
Q

persistant depression stats

A

Statistics
Gender Differences
Equally common in male and female children
In adulthood, women 2-3 times more likely to be diagnosed as males

Family Pattern
Increased prevalence of DD when a first degree relative had MDD
Increased prevalence of DD and MDD when a first degree relative has DD

Prevalence
Lifetime prevalence rates: 6%
Point prevalence rate: 3%

Course
Typically early, insidious onset, with chronic course

51
Q

Persistant

Etiology / Formulation

A

Relationship to other disorders remains unclear (e.g. Major Depressive Disorder, Borderline Personality Disorder, etc.)

Some have suggested that while the symptoms of DD and MDD may be similar, they may be due to different underlying pathology.
-Differences in response to Dexamethasone
Suppression Test.
-But both show abnormalities (decreased latency, increased intensity) to that seen in Major Depression.

Psychosocial models for Dysthymic Disorder are similar to those for major depressive disorder

52
Q

Persistent Depressive Disorder

Treatment - Psychosocial & pharma

A

Prognosis has been generally regarded as poor in comparison with Major Depression.
-Early studies suggested recovery in only 10 to 15 percent of patients one-year after diagnosis.

-Some emerging evidence for effectiveness of cognitive and behavioural interventions, as well as IPT.

Treatment - Pharmacological
Treatment regimes generally follow that of Major Depressive Disorder
—SSRIs, Tricyclics, MAOIs, venlafaxine

53
Q

Disruptive Mood Dysregulation Disorder

A

Severe recurrent temper outbursts that are grossly out of proportion
Outbursts are inconsistent with developmental level
Outbursts occur on average 3+ times per week
Persistent irritable or angry mood, even between outbursts
Duration of 12 months, with no periods of >3 months asymptomatic
Occurring in at least 2 settings

54
Q

Bipolar I Disorder course continued

A

Substance use/abuse is associated with increased frequency of hospitalisation and poorer prognosis.
Onset after 40 is rare and other Differential Diagnoses should be considered.
Mixed Episodes are much more common in adolescents and young adults than older adults

55
Q

Bipolar I Disorder

specifiers

A
Specifiers
Use of specifiers is dependent on the current state of the illness (e.g. a person cannot be “In partial remission” if they still meet criteria for a mood episode, etc.)
Mild
Moderate
Severe
Severe with Psychotic Features
With Catatonic Features
With Postpartum Onset
In partial remission
In full remission
Chronic
With Melancholic Features
With Atypical Features
With Full Interepisode Recovery
Without Full Interepisode Recovery
With Seasonal Pattern

With Rapid Cycling

56
Q

bipolar I

Specifiers (Continued)

A

The most recent episode is specified in the diagnosis and DSM-IV-TR coding of the illness
Bipolar I Disorder, Single Manic Episode
Bipolar I Disorder, Most Recent Episode Hypomanic
Bipolar I Disorder, Most Recent Episode Manic
Bipolar I Disorder, Most Recent Episode Mixed
Bipolar I Disorder, Most Recent Episode Depressed
Bipolar I Disorder, Most Recent Episode Unspecified

Example
296.53: Bipolar I Disorder, Most Recent Episode Depressed, Severe, With Melancholic Features, Without Full Interepisode Recovery

57
Q

Substance Induced Mood Disorder

A

Numerous drugs are known to be associated with mood symptoms
Depressive:–

Cardiac and antihypertensives
Sedatives and hypnotics
Some Steroids and hormones
Stimulants and appetite suppressants
Some Analgesics and antiinflammatory drugs
Some Antibacterial and antifungal medications
Anti-neoplastic medications
Illicit drugs
Numerous others
58
Q

Cyclothymic Disorder

A

Diagnosis
Two or more years where there have been ‘numerous’ periods with
-Hypomanic symptoms
-Depressive symptoms not meeting criteria for Major Depressive Episode

The person has not been without the symptoms for more than two months during the two year period.

No Major Depressive Episode or Mixed Episode has been present during the first two years of the illness

Rule out other Axis I disorders, substance use or general medical conditions

Impairment of functioning or distress.

59
Q

Cyclothymic Disorder DDx

A
Differential Diagnosis
Other mood disorders
--Have full mood episodes been present?
General medical conditions
Substance use problems
Borderline Personality Disorder
--What other symptoms are the shifts in mood associated with?
60
Q

Cyclothymic Disorder

stats

A

Statistics
Gender Differences
Appears to be equally common in males and females
Women may be more likely to present for treatment than men

Family Pattern
First degree relatives of Cyclothymia patients are at elevated risk for Bipolar I, Bipolar II and Major Depressive Disorder
Some increased risk of substance use problems may be evident also

Prevalence
Lifetime prevalence 0.4 to 1.0%
Prevalence in mood disorder clinics of 3.0 to 5.0%

61
Q

Cyclothymic Disorder - course

A

Course
Onset is typically in late adolescence or early adulthood
Late onset should alert the clinician to differential diagnoses (e.g. general medical conditions)
Onset is often insidious and may be part of a characterological vulnerability to mood disorders
Course is typically chronic and lifelong
15-50% of Cyclothymia patients will go on to develop Bipolar I or Bipolar II Disorder

62
Q

Bipolar II Disorder

specifiers

A
Specifiers
Use of specifiers is dependent on the current state of the illness (e.g. a person cannot be “In partial remission” if they still meet criteria for a mood episode, etc.)
Mild
Moderate
Severe
Severe with Psychotic Features
With Catatonic Features
With Postpartum Onset
In partial remission
In full remission
Chronic
With Melancholic Features
With Atypical Features
With Full Interepisode Recovery
Without Full Interepisode Recovery
With Seasonal Pattern

With Rapid Cycling

63
Q

Bipolar II Disorder

DDx

A

Differential Diagnosis
Other mood disorders
Mood disorder due to a General Medical Condition
Substance Induced Mood Disorder

Psychotic Disorders
Do psychotic symptoms ever occur in the absence of mood features?
What other symptoms of the syndromes are present?
History of mood symptoms / features
Family history

64
Q

Bipolar II Disorder

stats

A

Gender Differences
May be more prevalent in women than men
In men hypomanic episodes equal or exceed the number of depressed episodes, whereas in women the opposite pattern is evident.
Rapid cycling is more common in women than men.

Family Pattern
First degree relatives of Bipolar II patients show increased prevalence of Bipolar I, Bipolar II, and Major Depression.

Prevalence
Community lifetime prevalence rates of 0.5%

65
Q

Bipolar II Disorder course

A

Course
Typical course is chronic and lifelong
60 to 70% of hypomanic episodes occur immediately before or after a Major Depressive Episode.
Individuals may show a specific pattern of episodes.
Number of episodes in Bipolar II is greater than Recurrent Major Depressive Disorder
Interval between episodes reduces with age
5-15% meet criteria for Rapid Cycling (with poor prognosis)
Most show full interepisode recovery, but 5-15% experience residual symptoms between episodes
Psychotic symptoms do not occur in hypomanic episodes and are less common in the MDEs than for Bipolar I Disorder
Over a five year period, 5-15 percent will develop Bipolar I Disorder

66
Q

Bipolar II diagnosis

A

Diagnosis
Presence (or history) of one or more Major Depressive Episodes.
Presence (or history) of one or more Hypomanic Episodes.
Never experienced a Manic or Mixed Episode.
Symptoms not better accounted for by another Axis I disorder, substance use, or general medical condition
Symptoms cause marked impairment in functioning or distress.