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Affective disorders
Depression
part – 1
BY ,
MOGALATHURTHI TEJASHREE
PHARM D 4TH YEAR
Contents
 INTRODUCTION ON AFFECTIVE DISORDERS
 INTRODUCTION ON DEPRESSION
 EPIDEMIOLOGY
 Types of depression
 Etiology
 Biochemical factors
 Stress mechanism
 PATHOPHYSIOLOGY
 CLINICAL MANIFESTATIONS
 DIAGNOSIS
 TREATMENT
INTRODUCTION ON AFFECTIVE
DISORDERS
 DEFINITION: Affect refers mood or emotional state.
 Affective disorders are a set of psychiatric disorders, also called mood disorders.
 This includes :
 Depression
 Bipolar and unipolar disorder
 Mania and hypomania
DEPRESSION
 Term depression describes a general feeling of being low in mood and negative feelings.
 It is affective and mental disorder that presents with loss of interest Or pleasure mood feeling
of guilty or self-worth, disturbed sleep or appetite with low energy and poor concentration.
 It is a common serious illness.
 This feeling is a short lived and pass within a couple of days.
EPIDEMIOLOGY
 Globally more than 350 million people of all ages suffer from depression. (WHO)
 For the age group 15-44 major depression is the leading cause of disability in the U.S.
 Women are nearly twice as likely to suffer from a major depressive disorder than men are.
 With age the symptoms of depression become even more severe.
 About thirty percent of people with depressive illnesses attempt suicide.
Types of depression
 Major depressive disorder : recurrence of long episodes of low moods, or one extended episode that
seems to be ‘never-ending.
 Atypical depression
 Post partum depression
 Catatonic depression
 Seasonal affective disorder
 Melancholic depression
 Manic depression (bipolar disorder) Four ‘Episodes’ of Bipolar Disorder
 depressive episode
 manic episodes
 hypomanic episode
 mixed-mood states
 Dysthymic depression - lasts a long time but involves less severe symptoms.
 lead a normal life, but we may not be functioning well or feeling good .
 Situational depression
 Psychotic depression
 Endogenous depression
Etiology
 Genetic cause
 Environmental factors
 Biochemical factors : Biochemical theory of depression postulates a deficiency of neurotransmitters in certain areas of the
brain (noradrenaline, serotonin, and dopamine).
 Dopaminergic activity : reduced in case of depression, over activity in mania.
 Endocrine factors - hypothyroidism, cushing’s syndrome etc
 Abuse of Drugs or Alcohol
 Hormone Level Changes
 Physical illness and side effects of medications
 DRUGS
 Analgesics
 Antidepressants
 Antihypertensives
 Anticonvulsants
 Benzodiazipine withdrawal
 Antipsychotics
Biochemical factors
Stress mechanism
PHYSICAL ILLNESS
 Viral illness
 Carcinoma
 Neurological disorders
 Thyroid disease
 Multiple sclerosis
 Pernicious anaemia
 Diabetes
 Systemic lupus erythematosus
 Addison’s disease
PATHOPHYSIOLOGY
 The Biogenic Amine Hypothesis
 The Receptor Sensitivity Hypothesis
 The Serotonin-only Hypothesis
 The Permissive Hypothesis
 The Electrolyte Membrane Hypothesis
 The Neuroendocrine Hypothesis
 The Biogenic Amine Hypothesis
 caused by a deficiency of monoamines, particularly noradrenaline and serotonin.
 cannot explain the delay in time of onset of clinical relief of depression of up to 6-8 weeks.
 The Receptor Sensitivity Hypothesis
 depression is the result of a pathological alteration (supersensitivity and up-regulation) in
receptor sites.
 TCAs (tyricylase antidepressants) receptors or MAOIs(monoamine oxidase inhibitors)
receptors causes desensitization (the uncoupling of receptor sites)
 possibly down regulation (a decrease in the number of receptor sites).
 The Serotonin-only Hypothesis
 emphasizes the role of serotonin in depression and
downplays noradrenaline.
 But the serotonin-only theory has not explained the role of in depression.
 The Permissive Hypothesis
 the control of emotional behavior results from a balance between noradrenaline and serotonin.
 If serotonin and noradrenaline falls to abnormally low levels, the patient becomes depressed.
 If the level of serotonin falls and the level of noradrenaline becomes abnormally high, the patient
becomes manic.
 The Electrolyte Membrane Hypothesis
 hypocalcemia may be associated with mania.
 hypercalcemia is associated with depression.
 The Neuroendocrine Hypothesis
 pathological mood states are explained by altered endocrine function.
CLINICAL MANIFESTATIONS
 Thinking is pessimistic(evil or worst believe) and in some cases suicidal.
 In severe cases psychotic symptoms
 hallucinations or delusions.
 Insomnia or hypersomnia,
 libido (sexual desire),
 weight loss,
 loss of appetite.
 Intellectual or cognitive symptoms
 decreased ability to concentrate,
 slowed thinking,
 a poor memory for recent events.
SITUATIONS –
loss, isolation, conflict,
stress
THOUGHTS –
negative thinking habits, harsh
self-criticism, unfair and
unrealistic thoughts
EMOTIONS-
Discouragement,
sadness, irritability/anger,
numbness, anxiety
PHYSICAL STATUS –
Altered sleep, low
energy/fatigue, agitation,
change in brain
chemistry
ACTIONS-
Social withdrawal,
reduced activity
level, poor self-
care
DIAGNOSIS
 ICD 10 Diagnostic criteria for a depressive episode {who}
 USUAL SYMPTOMS
 Depressed mood.
 Loss of interest and enjoyment.
 Reduced energy leading to increased fatiguability and diminished activity.
 COMMON SYMPTOMS
 Reduced concentration and attention.
 Reduced self esteem and self confidence.
 Ideas of guilt and unworthiness.
 Bleak and pessimistic views of future .
 Ideas or acts of self harm or suicide.
 Disturbed sleep.
 Diminished appetite.
 MILD DEPRESSIVE EPISODE
 For at least 2 weeks, at least two of the usual symptoms of a depressive
episode plus at least two common symptoms.
 MODERATE DEPRESSIVE EPISODE
 For at least 2 weeks, at least two or three of the usual symptoms of a
depressive episode plus at least three of the common symtoms.
 SEVERE DEPRESSIVE EPISODE
 For at least 2 weeks all three of the usual symptoms of a depressive
episode plus at least 4 of the common symptoms some of which should be
of severe intensity.
 RATING SCALES
 Beck depression inventory
 Hamilton depression rating scale
 DEXAMETHASONE SUPPRESSION TEST
NON – PHARMACOLOGIC THERAPY
 LIFESTYLE CHANGES
 Stress reduction
 Social support o Sleep
 PSYCHOTHERAPY
 Cognitive behavioral therapy
 Interpersonal therapy
 Psychodynamic therapy
 ELECTROCONVULSIVE THERAPY – ECT o Safe & effective disorder for all
subtypes of major depressive disorder.
 ADR : Cognitive dysfunction, cardiovascular dysfunction, prolonged apnoea
etc.
TREATMENT
 ANTIDEPRESSANT
 MAO inhibitors:
 Irreversible: Isocarboxazid, Iproniazid, Phenelzine and Tranylcypromine.
 Reversible: Moclobemide and Clorgyline.
 Tricyclic antidepressants (TCAs) NA and 5 HT reuptake inhibitors :
Imipramine, Amitryptiline, Doxepin, Dothiepin and Clomipramine.
 Imipramine (depsonil) : 50- 200 mg/day - antidepressant action starts after few
weeks.
 Amitryptyline (tryptomer) : 50- 200 mg/day
 NA reuptake inhibitors : Desimipramine, Nortryptyline, Amoxapine
 Selective Serotonin reuptake inhibitors: Fluoxetine(5-20MG), Fluvoxamine,
Sertraline 50mg and Citalopram (20-40mg)
 Atypical antidepressants: Trazodone, Mianserin, Mirtazapine, Venlafaxine,
Duloxetine, Bupropion and Tianeptine
Diagnosis of MDD
Antidepressants therapy with psychotherapy
Tricyclic antideppressant
Nortriptyline
Doxepin
Desipramine
clomipramine
SSRI antidepressant
Fluoxetine
Sertraline
paroxetine
Fluvoxamine
citalopram
 MILD DEPRESSION
 Pharmacological interventions
 Antidepressants, a short term benzodiazepine as adjunct
OR
 Non-pharmacological interventions
 Counseling, problem solving, psychotherapy
 MODERATE DEPRESSION
 Pharmacological interventions + Non-pharmacological interventions
 SEVERE DEPRESSION
 Pharmacological interventions + Non-pharmacological interventions +/ ECT

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Affective disorders part 1

  • 1. Affective disorders Depression part – 1 BY , MOGALATHURTHI TEJASHREE PHARM D 4TH YEAR
  • 2. Contents  INTRODUCTION ON AFFECTIVE DISORDERS  INTRODUCTION ON DEPRESSION  EPIDEMIOLOGY  Types of depression  Etiology  Biochemical factors  Stress mechanism  PATHOPHYSIOLOGY  CLINICAL MANIFESTATIONS  DIAGNOSIS  TREATMENT
  • 3. INTRODUCTION ON AFFECTIVE DISORDERS  DEFINITION: Affect refers mood or emotional state.  Affective disorders are a set of psychiatric disorders, also called mood disorders.  This includes :  Depression  Bipolar and unipolar disorder  Mania and hypomania
  • 4. DEPRESSION  Term depression describes a general feeling of being low in mood and negative feelings.  It is affective and mental disorder that presents with loss of interest Or pleasure mood feeling of guilty or self-worth, disturbed sleep or appetite with low energy and poor concentration.  It is a common serious illness.  This feeling is a short lived and pass within a couple of days.
  • 5. EPIDEMIOLOGY  Globally more than 350 million people of all ages suffer from depression. (WHO)  For the age group 15-44 major depression is the leading cause of disability in the U.S.  Women are nearly twice as likely to suffer from a major depressive disorder than men are.  With age the symptoms of depression become even more severe.  About thirty percent of people with depressive illnesses attempt suicide.
  • 6. Types of depression  Major depressive disorder : recurrence of long episodes of low moods, or one extended episode that seems to be ‘never-ending.  Atypical depression  Post partum depression  Catatonic depression  Seasonal affective disorder  Melancholic depression  Manic depression (bipolar disorder) Four ‘Episodes’ of Bipolar Disorder  depressive episode  manic episodes  hypomanic episode  mixed-mood states  Dysthymic depression - lasts a long time but involves less severe symptoms.  lead a normal life, but we may not be functioning well or feeling good .  Situational depression  Psychotic depression  Endogenous depression
  • 7. Etiology  Genetic cause  Environmental factors  Biochemical factors : Biochemical theory of depression postulates a deficiency of neurotransmitters in certain areas of the brain (noradrenaline, serotonin, and dopamine).  Dopaminergic activity : reduced in case of depression, over activity in mania.  Endocrine factors - hypothyroidism, cushing’s syndrome etc  Abuse of Drugs or Alcohol  Hormone Level Changes  Physical illness and side effects of medications  DRUGS  Analgesics  Antidepressants  Antihypertensives  Anticonvulsants  Benzodiazipine withdrawal  Antipsychotics
  • 10. PHYSICAL ILLNESS  Viral illness  Carcinoma  Neurological disorders  Thyroid disease  Multiple sclerosis  Pernicious anaemia  Diabetes  Systemic lupus erythematosus  Addison’s disease
  • 11. PATHOPHYSIOLOGY  The Biogenic Amine Hypothesis  The Receptor Sensitivity Hypothesis  The Serotonin-only Hypothesis  The Permissive Hypothesis  The Electrolyte Membrane Hypothesis  The Neuroendocrine Hypothesis
  • 12.  The Biogenic Amine Hypothesis  caused by a deficiency of monoamines, particularly noradrenaline and serotonin.  cannot explain the delay in time of onset of clinical relief of depression of up to 6-8 weeks.  The Receptor Sensitivity Hypothesis  depression is the result of a pathological alteration (supersensitivity and up-regulation) in receptor sites.  TCAs (tyricylase antidepressants) receptors or MAOIs(monoamine oxidase inhibitors) receptors causes desensitization (the uncoupling of receptor sites)  possibly down regulation (a decrease in the number of receptor sites).
  • 13.  The Serotonin-only Hypothesis  emphasizes the role of serotonin in depression and downplays noradrenaline.  But the serotonin-only theory has not explained the role of in depression.  The Permissive Hypothesis  the control of emotional behavior results from a balance between noradrenaline and serotonin.  If serotonin and noradrenaline falls to abnormally low levels, the patient becomes depressed.  If the level of serotonin falls and the level of noradrenaline becomes abnormally high, the patient becomes manic.  The Electrolyte Membrane Hypothesis  hypocalcemia may be associated with mania.  hypercalcemia is associated with depression.  The Neuroendocrine Hypothesis  pathological mood states are explained by altered endocrine function.
  • 14. CLINICAL MANIFESTATIONS  Thinking is pessimistic(evil or worst believe) and in some cases suicidal.  In severe cases psychotic symptoms  hallucinations or delusions.  Insomnia or hypersomnia,  libido (sexual desire),  weight loss,  loss of appetite.  Intellectual or cognitive symptoms  decreased ability to concentrate,  slowed thinking,  a poor memory for recent events.
  • 15. SITUATIONS – loss, isolation, conflict, stress THOUGHTS – negative thinking habits, harsh self-criticism, unfair and unrealistic thoughts EMOTIONS- Discouragement, sadness, irritability/anger, numbness, anxiety PHYSICAL STATUS – Altered sleep, low energy/fatigue, agitation, change in brain chemistry ACTIONS- Social withdrawal, reduced activity level, poor self- care
  • 16. DIAGNOSIS  ICD 10 Diagnostic criteria for a depressive episode {who}  USUAL SYMPTOMS  Depressed mood.  Loss of interest and enjoyment.  Reduced energy leading to increased fatiguability and diminished activity.  COMMON SYMPTOMS  Reduced concentration and attention.  Reduced self esteem and self confidence.  Ideas of guilt and unworthiness.  Bleak and pessimistic views of future .  Ideas or acts of self harm or suicide.  Disturbed sleep.  Diminished appetite.
  • 17.  MILD DEPRESSIVE EPISODE  For at least 2 weeks, at least two of the usual symptoms of a depressive episode plus at least two common symptoms.  MODERATE DEPRESSIVE EPISODE  For at least 2 weeks, at least two or three of the usual symptoms of a depressive episode plus at least three of the common symtoms.  SEVERE DEPRESSIVE EPISODE  For at least 2 weeks all three of the usual symptoms of a depressive episode plus at least 4 of the common symptoms some of which should be of severe intensity.  RATING SCALES  Beck depression inventory  Hamilton depression rating scale  DEXAMETHASONE SUPPRESSION TEST
  • 18. NON – PHARMACOLOGIC THERAPY  LIFESTYLE CHANGES  Stress reduction  Social support o Sleep  PSYCHOTHERAPY  Cognitive behavioral therapy  Interpersonal therapy  Psychodynamic therapy  ELECTROCONVULSIVE THERAPY – ECT o Safe & effective disorder for all subtypes of major depressive disorder.  ADR : Cognitive dysfunction, cardiovascular dysfunction, prolonged apnoea etc.
  • 19. TREATMENT  ANTIDEPRESSANT  MAO inhibitors:  Irreversible: Isocarboxazid, Iproniazid, Phenelzine and Tranylcypromine.  Reversible: Moclobemide and Clorgyline.  Tricyclic antidepressants (TCAs) NA and 5 HT reuptake inhibitors : Imipramine, Amitryptiline, Doxepin, Dothiepin and Clomipramine.  Imipramine (depsonil) : 50- 200 mg/day - antidepressant action starts after few weeks.  Amitryptyline (tryptomer) : 50- 200 mg/day  NA reuptake inhibitors : Desimipramine, Nortryptyline, Amoxapine  Selective Serotonin reuptake inhibitors: Fluoxetine(5-20MG), Fluvoxamine, Sertraline 50mg and Citalopram (20-40mg)  Atypical antidepressants: Trazodone, Mianserin, Mirtazapine, Venlafaxine, Duloxetine, Bupropion and Tianeptine
  • 20. Diagnosis of MDD Antidepressants therapy with psychotherapy Tricyclic antideppressant Nortriptyline Doxepin Desipramine clomipramine SSRI antidepressant Fluoxetine Sertraline paroxetine Fluvoxamine citalopram
  • 21.  MILD DEPRESSION  Pharmacological interventions  Antidepressants, a short term benzodiazepine as adjunct OR  Non-pharmacological interventions  Counseling, problem solving, psychotherapy  MODERATE DEPRESSION  Pharmacological interventions + Non-pharmacological interventions  SEVERE DEPRESSION  Pharmacological interventions + Non-pharmacological interventions +/ ECT