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Mood Disorders

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2 views67 pages

Mood Disorders

Uploaded by

Shaan
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPT, PDF, TXT or read online on Scribd
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 MOOD is a pervasive and a sustained

feeling tone that is experienced internally


and that influences a person’s behaviour
and perception of the world.

 AFFECT is the external manifestation of


mood.

 Mood Disorders are a group of clincal


conditions characterized by loss of sense
of control and subjective experience of
distress.
HISTORY
 HIPPOCRATES(400BC) used the term
MANIA and MELANCHOLIA to
describe mental disturbances.
 JULES FALRET(1854)- la folie
circulaire
 Karl Kahlbaum(1882)- used the term
CYCLOTHYMIA
 Emil Kraeplin(1899)- Manic
Depressive Psychosis.
Differentiated it from Dementia
Praecox(Schiz)
CLASSIFICATION
 MAJOR DEPRESSIVE DISORDER(MDD
 MANIA & HYPOMANIA
 BIPOLAR DISORDER I
 BIPOLAR DISORDER II
 DYSTHYMIC DISORDER
 CYCLOTHYMIC DISORDER
 ATYPICAL BIPOLAR OR DEPRESSIVE
DISORDER
 RAPID CYCLERS
OTHERS :

 MINOR DEPRESSIVE DISORDER


 RECURRENT BRIEF DEPRESSIVE
DISORDER
 PRE MENSTRUAL DYSPHORIC
DISORDER
 MOOD DISORDER DUE TO MEDICAL
CONDITIONS AND SUBSTANCE
ABUSE
EPIDEMIOLOGY
 Life Time Prevalance of

MDD 12%
BIPOLAR DISORDERS 0-4.8%
SEX :
M:F
MDD 1:2
BIPOLAR DISORDERS 1:1
Mania more in men and MDD more in
women
 AGE :
Years
MDD 20-50
BIPOLAR 30 (mean age)

MARITAL STATUS :
Divorced or seperated, single.
COMORBIDITY:
1.ALCOHOL ABUSE
2.PANIC DISORDER
3. OCD
4. SOCIAL ANXIETY DISORDER
ETIOLOGY

 I. BILOGICAL FACTORS
 II. GENETIC FACTORS
 III. PSYCHOSOCIAL FACTORS
 IV. PSYCHODYNAMIC FACTORS
 V. COGNITIVE THEORIES
I.BIOLOGICAL FACTORS :

1.BIOGENIC AMINES:
A. NOREPINEPHRINE :
Decreased sensitivity of Beta
Adrenergic receptors and clinical
antidepressant response indicates
direct role of Nor adrenergic system
in Depression.
B.SERETONIN
C.DOPAMINE :
Its activity may be decreased in
Depression and increased in Mania.
D.ACETYLCHOLINE
E.GABA
F. AMINO ACIDS : GLUTAMATE &
GLYCINE
 G. Alterations of Hormonal Regulation:
Increased HPA activity is asso with
Depression.

 H. Thyroid dysfunction in Depression :


Elevated TSH.

 I. Growth Hormone

 L. Prolactin
M.SLEEP NEUROPHYSIOLOGY :
Reduction in total sleep time,
Increased REM, Increased body temp

N.Immunological disturbances.

O.Brain structural changes :


CT & MRI – Abnormal
Hyperintensities in Sub cortical
regions.
Ventricular enlargement
Cortical atrophy.
 PET SCAN : Decreased Anterior Brain
Metabolism on left side.

 Decreased Cerebral blood flow.


 GENETIC FACTORS :

FAMILY STUDIES
ADOPTION STUDIES
TWIN STUDIES
These studies have long documented the
heritability of Modd disorders.
LINKAGE STUDIES : Chromosomes 18q &
22q are the two regions with strongest
evidence for linkage to bipolar disorder.
This disease is said to be Genetically linked
 PSYCHOSOCIAL FACTORS :
Life events
Environmental stress

 PERSONALITY FACTORS :
OCD, HISTRIONIC, BORDERLINE
Personlaities – Risk for Depression
 PSYCHODYNAMIC FACTORS :

Disturbances in the Infant-Mother


relationships during Oral Phase(Below
1yr).
Real or imagined object loss.
Introjection of departed objects is a
defense mechanism.
The lost object- feelings of anger are
directed inward at the self.
Mania is a defensive reaction to
depression.
COGNITIVE FACTORS :
Depression results from specific
Cognitive distortions.

Aaron Beck postulated COGNITIVE


TRIAD of Depression :
1. Views about the self – Negative
self precept
2. About the environment – Hostile
and demanding
3. About the future – Expectation of
suffering & failure.
CLINICAL FEATURES
 MAJOR DEPRESSIVE DISORDER :
Five or more of the following, most of
the day and/or nearly every day,
including at least symptom 1 or 2:
 1. Depressed mood

• Sad, empty, weepy; irritable, angry


 2. Loss of interest or pleasure in
previously enjoyable
activities(Anhedonia)
 3. Change in weight or appetite
 4. Sleep changes
 5. Noticeable change in movement
 6. Fatigue
 7. Feelings of worthlessness or guilt
 8. Impaired cognition or volition
 9. Repeated thoughts of death or suicide,
or planned or attempted suicide
The five symptoms must occur in the
same two weeks
MANIC EPISODE
 One week of persistently high,
expansive, or irritable mood, and 3
of:
 Grandiose self-esteem
 Lower sleep need
 Overly talkative
 Racing thoughts
 Easily distracted
 Increased activity or agitation
 High risk activities
MANIC EPISODE
Mixed episode
 One week of both manic and major
depressive symptoms with rapidly
alternating moods
 Common symptoms:
• Agitation
• Insomnia
• Irregular appetite (binge-fast)
• Delusions
• Thoughts of suicide
Hypomanic episode
 Mood disturbance does not critically
impair ability to work or maintain
social responsibilities

 Response pattern is uncharacteristic

 Not euthymia
Bipolar disorders
 Bipolar I Disorder
• One or more manic or mixed episodes
• Usually one or more major depressive
episodes
• Subcategorized based on the character
of the most recent episode
 Most recent episode depressed
 Most recent episode manic

 Most recent episode mixed


Bipolar disorders…
 Bipolar II Disorder
• One or more major depressive episodes
• One or more hypomanic episodes
• NO manic or mixed episode
 Cyclothymic Disorder
• Two years of alternating hypomanic and
depressive symptoms
• No remission of more than two months
• NO major depressive, manic, or mixed
episodes
 Dysthymic Disorder
• Two years of chronically depressed mood
• Two additional depression symptoms
(appetite, sleep, energy, concentration, low
self-esteem, hopeless feelings)

RAPID CYCLING –
Rapid cycling Bipolar I disorder
Female
Atleast 4 episodes of Modd Disturbance within
12 month period.
Mood Disorder Specifiers
These specifiers may be applied to mood
disorder diagnoses, where appropriate:

• Mild/moderate/severe w/o psychotic features


• With:psychotic/ catatonic/ melancholic/
atypical features (m-older, a-younger)
• In remission/chronic/seasonal pattern
• With postpartum onset- Symptoms within
4weeks of postpartum, inclde Psychotic
symptoms(postpartum psychosis)
Mood Disorder Specifiers
These specifiers may be applied to mood
disorder diagnoses, where appropriate:

• Mild/moderate/severe w/o psychotic features


• With:psychotic/ catatonic/ melancholic/
atypical features (m-older, a-younger)
• In remission/chronic/seasonal pattern
• With postpartum onset- Symptoms within
4weeks of postpartum, inclde Psychotic
symptoms(postpartum psychosis)
TREATMENT

 TREATMENT OF MDD
 Various antidepressants altering levels of
central neurotransmitters are available to
treat depression.
 Their overall effectiveness: 65-70%
 Mild to moderate depressive episode:
SSRIs.
 Severe depression: antidepressants with
broader spectrum of effects, like SNRI or
TCA and E.C.T
 ANTIDEPRESSANTS
 NE Reuptake Inhibitors
Desipramine
75-300mg
Drowsiness, insomnia, OSH, agitation,
CA, weight gain anticholinergic,
Overdose may be fatal.
Dose titration is needed..
Nortriptyline
 40-200mg

 Drowsiness, , Ortho static

Hypeotension, weight gain, Cardiac


Arrhythmias,
 Overdose may be fatal. Dose titration

is needed.
 5-HT Reuptake Inhibitors
Citalopram
 20-60mg.

 All SSRIs may cause insomnia, agitation,

sedation, GI distress, and sexual


dysfunction Many SSRIs inhibit various
cytochrome P450 isoenzymes.
 They are better tolerated than tricyclics

and have high safety in overdose.


 Shorter half-life SSRIs may be associated

with discontinuation symptoms when


abruptly stopped.
 OTHER SSRIs

 Escitalopram 10-20mg
 Fluoxetine 10-40mg
 Fluvoxamine 100-300mg
 Paroxetine 20-50mg
 Sertraline 50-150mg
 NE and 5-HT Reuptake Inhibitors
Amitriptyline
 75-300mg

 Drowsiness, OSH, CA, weight gain,

anticholinergic,
 Overdose may be fatal. Dose

titration is needed.
Imipramine
 75-300mg

 Drowsiness, insomnia and agitation,

OSH, CA, GI distress, weight gain,


anticholinergica Overdose may be
Venlafaxine / Desvenlafaxine(50-100)
 150-375mg mg
 Sleep changes, GI distress,

discontinuation syndrome Higher


doses may cause hypertension.
 Dose titration is needed.

 Abrupt discontinuation may result in

discontinuation symptoms.

Duloxetine 30-60mg
 GI distress, discontinuation

syndrome
 Pre- and Postsynaptic Active
Agents
 Mirtazapine
 15-30mg
 Sedation, weight gain,
 No sexual dysfunction.
Dopamine Reuptake Inhibitor
Bupropion :
 200-400mg

 Insomnia or agitation, GI distress

Twice-a-day dosing with sustained


release.
 No sexual dysfunction or weight gain
 Mixed Action Agents
Amoxapine 100-600mg
 Drowsiness, insomnia/agitation, CA,

weight gain, OSH, anticholinergic


Movement disorders may occur. Dose
titration is needed.
Clomipramine 75-300mg
Drowsiness, weight gain,
Dose titration is needed.
Trazodone
 150-600mg Drowsiness, OSH, CA, GI

distress, weight gain, Priapism is possible.


Treatment of Depression

 Onset of Action – Takes atleast 5 to 7 days for the


drug to act

First episode of depression - the drug should be


continued for another 16-20 weeks after the patient
is thought to be well (continuation treatment to
prevent recurrence).

The medication should be tapered gradually because


many patients experience some mild withdrawal
effects.

Educate the patient and family members about the


side effects
Treatment of Acute Mania
DOSE BLOOD
LEVELS
• Lithium 900-1200mg 0.6-1.2mEq/l

• carbamazepine 600-1200mg 4-12 microgm/l

• valproate 750-2500mg

• Clonazepam/Lorazepam

• Typical & Atypical Antipsychotics


 Atypical Antipsychotics :

OLANZEPINE
RISPERIDONE
QUITIEPINE
ZIPRASIDONE
ARIPIPRAZOLE
TREATMENT OF
ACUTE BIPOLAR DEPRESSION
 ANTIDEPRESSANTS
 AD + MOOD STABILIZER ( or Anti
Psychotic)
 ECT

OTHERS :
Calcium channel Antagonists –
Verapamil
Gabapentin, Topiramate etc.
MAINTAINANCE TREATMENT

 LITHIUM
 CARBAMAZEPINE
 VALPROATE
 LAMOTRIGINE- Prophylactic
Antidepressant
 Thyroid Supplementation
OTHER THERAPIES :

1. COGNITIVE THERAPY
2. INTERPERSONAL THERAPY
3.BEHAVIOURAL THERAPY
4.FAMILY THERAPY
5.SLEEP DEPRIVATION
6.PHOTO THERAPY or LIGHT THERAPY
(SAD)
7.ECT
8.TRANS CRANIAL MAGNETIC STIMULATION
Postpartum “Baby Blues”
 Time of Onset – 3 to 5 daysafter
Delivery
 Symptoms : Mood Lability
Sadness
Dysphoria
Subjective Confusion
Tearfulness
 Due to :
1.Rapid changes in women’s
2.Hormonal levels
3.Stress of Child birth
4.Awareness of increased
responsibility that motherhood
brings

 No professional treatment is required

 Education and support for the new


Mother
POSTPARTUM DEPRESSION

Onset : Within 12weeks after


Delivery
Symptoms : Depressed Mood
Excessive Anxiety
Insomnia
Change in Weight

 Increases the risk of MDD


 Syndrome described in Fathers is
characterized by Mood changes during
wife’s Pregnancy or delivery.
 Fathers are effected by added
responsibility, diminished sexual outlet,
decreased attention from wife.

 TREATMENT :

 Caution - Risk of transmitting Ads to New


Borns during Lactation.
CHARACTERSTIC BABY BLUES POSTPARTUM DEP

INCIDENCE 30-75% of women 10-15%


who give birth

Time of Onset 3-5days after delivery Within 3-6months

Duration Days to weeks Months to years if


untreated

Asso Stressors NO YES

Sociocultural Influene NO YES


CHARACTERSTIC BABY BLUES POSTPARTUM DEPR

FAMILY HISTORY OF NO YES


MOOD DISORDER

TEARFULNESS YES YES

MOOD LABILITY YES OFTEN PRESENT,


UNIFORMLY DEPRESSED

ANHEDONIA NO OFTEN

SLEEP DISTUBANCE SOMETIMES ALWAYS

SUICIDAL THOUGHTS NO SOMETIMES

THOUGHTS OF RARELY OFTEN


HARMING THE BABY

FEELINGS OF GUILT ABSENT PRESENT


PREMENSTRUAL
DYSPHORIC DISORDER
 Symptoms present during the last
week of LUTEAL PHASE of Menstrual
cycle and Remit after FOLLICULAR
PHASE and absent in the Post
Menses Period.
 SYMPTOMS :

1.Depressed Mood
2.Hopelessness
3.Anxiety
4.Lability of Mood
5.Decreased intrest in activities
6.Anger and irritability
7.Confusion
8.Sleep Disturbances
9.Social withdrawl
10.Breast tenderness
11.Headache , Muscle pain, Abdominal
bloating
12.Weight gain

TREATMENT : SUPPORT & SSRIs


Postpartum Psychosis
(Puerperal Psychosis)
 Onset : Within 2-3 weeks(8 wks of
Delivery)
 Incidence: 1-2/1000 child births

 Symptoms :

1.Fatigue
2.Insomnia
3.Restlessness
4.Emotional lability

5.Depression

6.Delusion

7.Confusion

8.Incoherent/Irrelevant talk

9.Ideas of Suicide or Infanticide


TREATMENT :
Anti depressants
Lithium
Anti Psychotics
Caution : No Anti psychotics to breast
feedin women
Extra care to Suicidal pt

 Psychotherapy
 Increased support from Husband & Family
members
SUICIDE
Epidemology
Indian Statistics
 Death due to suicides >1lakh/year

 Suicide rate in last 2 yrs increased from

7.9 to10.3 per 100,000


 Wide variation in suicide rates within

country- southern states like


kerala,Karnataka, AP & TN, >15 while
northern states of Punjab,UP, Bihar & JK
suicide rate is <3 ( higher literacy, better
reporting, lower external aggression,
higher socio.economic status & higher
expectations are possible explanations)
SUICIDE: A MULTI-FACTORIAL EVENT
Psychiatric Illness
Co-morbidity
Personality Neurobiology
Disorder/Traits
Impulsiveness
Substance
Use/Abuse
Hopelessness
Suicide
Severe Medical
Illness Family History

Access To Weapons Psychodynamics/


Psychological Vulnerability

Life Stressors Suicidal


Behavior
SOMATIC TREATMENTS
ECT Evidence for short-term reduction of
suicide, but not long-term.
Benzodiazepines May reduce risk by treating anxiety
Antidepressants A mainstay treatment of suicidal patients
with depressive illness / symptoms. No
conclusive evidence of suicide reduction
Lithium and Lithium has a demonstrated anti-suicide
Anti-convulsants effect; anticonvulsants do not
Antipsychotics Evidence for Clozapine reducing suicidality
in schizophrenia and schizo-affective
disorders
THANK YOU

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