DEPRESSION
• Depression is a affective disorder.
• Affective disorders : mental illnesses characterized
by pathological changes in mood.
• Depression : pathologically depressed mood
DEFINITION
• DEPRESSION: Common mental disorder that
presents with depressed mood, loss of interest or
pleasure, feelings of guilt or low self- worth,
disturbed sleep or appetite, low energy, and poor
concentration.
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
- Postpartum depression
- Catatonic depression
- Seasonal affective disorder
- Melancholic depression
• 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
MAJOR DEPRESSIVE DISORDER
 aka unipolar depression
 lifetime prevalence:
up to 21% in women
13% in men
 typical age of onset:
20s, but can occur at any time
SYMPTOMS OF MDD
• Feelings of sadness, tearfulness, emptiness or hopelessness
• Angry outbursts, irritability or frustration, even over small matters
• Loss of interest or pleasure in most or all normal activities, such as sex,
hobbies or sports
• Sleep disturbances, including insomnia or sleeping too much
• Tiredness and lack of energy, so even small tasks take extra effort
• Reduced appetite and weight loss or increased cravings for food and
weight gain
• Anxiety, agitation or restlessness
• Slowed thinking, speaking or body movements
• Feelings of worthlessness or guilt, fixating on past failures or self-blame
• Trouble thinking, concentrating, making decisions and remembering
things
• Frequent or recurrent thoughts of death, suicidal thoughts, suicide
attempts or suicide
• Unexplained physical problems, such as back pain or headaches
ATYPICAL DEPRESSION
Described in DSM-IV
Depression that shares many of the typical
symptoms of the major depression or dysthymia
But is characterized by improved mood in response
to positive events.
It also features significant weight gain or an
increased appetite, hypersomnia, a heavy sensation
in the limbs, and interpersonal rejection sensitivity
that results in significant social or occupational
impairment
POSTPARTUM DEPRESSION
• Also called Postnatal depression
• Associated with childbirth
• Can affect both sexes
• Symptoms may include: extreme sadness, low
energy, anxiety, crying episodes, irritability, and
changes in sleeping or eating patterns
• Onset is typically between one week and one
month following childbirth
• PPD can also negatively affect the newborn child
CATATONIC DEPRESSION
 Catatonic depression affects the individual’s motor skills
 Can be caused by other underlying mental health disorders,
such as schizophrenia, mood disorders, and post-traumatic
stress disorder
 People with catatonia remain still and do not respond to any
events/things around them
 There are three types of catatonia: akinetic, excited and
malignant catatonia
 Akinetic catatonia is the most commonly observed in people
with catatonic depression
 Malignant catatonia can be dangerous, causing severe health
effects
SIGNS AND SYMPTOMS
Automatic obedience – The patient automatically obeys all instructions
given by the doctor
Ambitendency – The patient alternates between cooperating with the
doctor’s instructions and resisting them
Aversion – The patient turns away when he or she is being spoken to
Echopraxia – The patient imitates the activities of the person speaking with
him or her.
Excitement – The patient engages in excessive and purposeless action that is
not driven by outside stimuli
Negativism – The person is always having negative thoughts and feels sad
every day
Stupor – This is one of the common signs of catatonia. It is characterized by
a lack of mobility and speech
Posturing – The person remains in the same posture for a long period of
time
Mutism – The person is verbally unresponsive and refuses to speak
Staring – The individual’s eye is fixed on a particular space and open for
long periods of time.
SEASONAL DEPRESSION
 More than just "the winter blues"
 Seasonal depression is often called seasonal affective disorder
(SAD)
 Occurs at the same time each year
 Linked to reduced exposure to sunlight during the shorter
autumn and winter days (production of Melatonin, Serotonin
and Circadian rhythm)
Symptoms:
• A persistent low mood
• A loss of pleasure or interest in normal everyday activities
• Irritability
• Feelings of despair, guilt and worthlessness
• Feeling lethargic (lacking in energy) and sleepy during the day
• Sleeping for longer than normal and finding it hard to wake up
• Craving carbohydrates and gaining weight
MELANCHOLIC DEPRESSION
 Melancholic depression, or depression with
melancholic features
 Is a DSM-IV and DSM-5 subtype of clinical
depression
Signs and Symptoms
• Requiring at least one of the following symptoms:
• Anhedonia
• Lack of mood reactivity
• And at least three of the following:
• Depression that is subjectively different from grief or loss
• Severe weight loss or loss of appetite
• Psychomotor agitation or retardation
• Early morning awakening
• Guilt that is excessive
• Worse mood in the morning
Double Depression
Dysthymic disorder with episodes of
major depression
Prognosis more negative
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.
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 orAlcohol
• Hormone Level Changes
• Physical illness and side effects of medications
DRUGS
• Analgesics
• Antidepressants
• Antihypertensives
• Anticonvulsants
• Benzodiazipine withdrawal
• Antipsychotics
PHYSICAL ILLNESS
• Viral illness
• Carcinoma
• Neurological disorders
• Thyroid disease
• Multiple sclerosis
• Pernicious anaemia
• Diabetes
• Systemic lupus erythematosus
• Addison’s disease
PATHOPHYSIOLOGY
• The BiogenicAmine Hypothesis
• The Receptor Sensitivity Hypothesis
• The Serotonin-only Hypothesis
• The Permissive Hypothesis
• The Electrolyte Membrane Hypothesis
• The Neuroendocrine Hypothesis
• The BiogenicAmine 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 or MAOIs causes desensitization (the
uncoupling of receptor sites) and 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
shortcomings:
- it does not explain why there is a delay
in onset of clinical relief
- it does not explain the role of NA
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
or contributed to by altered endocrine function.
CLINICAL MANIFESTATIONS
• DEPRESSIONS
o Thinking is pessimistic and in some cases suicidal.
o In severe cases psychotic symptoms such as
hallucinations or delusions may be present.
o Insomnia or hypersomnia, libido, weight loss, loss of
appetite.
o Intellectual or cognitive symptoms include a
decreased ability to concentrate, slowed thinking, & a
poor memory for recent events.
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.
COMMONSYMPTOMS
• 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.
MODERATEDEPRESSIVE 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 severeintensity.
INVESTIGATIONS
• RATING SCALES
o Beck depression inventory
o Hamilton depression rating scale
• DEXAMETHASONE SUPPRESSION TEST
TREATMENT
ANTIDEPRESSANTS
1. MAO inhibitors:
• Irreversible: Isocarboxazid, Iproniazid, Phenelzine and
Tranylcypromine.
• Reversible: Moclobemide and Clorgyline.
2. Tricyclic antidepressants (TCAs)
• NAand 5 HT reuptake inhibitors : Imipramine,
Amitryptiline, Doxepin, Dothiepin and
Clomipramine.
• NAreuptake inhibitors : Desimipramine,
Nortryptyline,Amoxapine.
3. Selective Serotonin reuptake inhibitors:
• Fluoxetine, Fluvoxamine, Sertraline and
Citalopram
4.Atypical antidepressants:
• Trazodone, Mianserin, Mirtazapine,
Venlafaxine, Duloxetine, Bupropion and
Tianeptine
MAO Inhibitors
• Drugs act by increasing the local availability of NA
or 5 HT.
• MAO is a Mitochondrial Enzyme involved
in Oxidative deamination of these amines.
o MAO-A: Peripheral nerve endings, Intestine
and Placenta (5-HT and NA).
o MAO-B: Brain and in Platelets (Dopamine).
o Selective MAO-A inhibitors (RIMA) have
antidepressant property
(eg:Moclobemide).
• Side effects : postural hypotension,
weight gain, atropine like effects and
CNS stimulation.
• Severe hypertensive response to tyramine
containing foods-cheese reaction
• Drug interaction : Ephedrine, Reserpine.
TCAs
• NA, 5 HT and Dopamine are present in Nerve
endings
• Normally, there are reuptake mechanism and
termination of action.
• TCAs inhibit reuptake and make more monoamines
available for action.
• In most TCA, other receptors (incl. those outside the
CNS) are also affected: blockade of H1-receptor,
Alpha-receptors, M-receptors.
SSRIs
• First line drug in depression.
• Relatively safe and better patient acceptability.
• Some patients not responding to TCAs may
respond with SSRIs.
• SSRIs inhibit the reuptake mechanism and
make more 5 HT available for action.
 Relative advantages:
– No sedation, so no
cognitive or
psychomotor function
interference
– No anicholinergic
effects
– No alpha-blocking
action, so no postural
hypotension and suits
for elderly
– No seizure induction
– No arrhythmia
 Drawbacks:
– Nausea is common
– Interfere with
ejaculation
– Insomnia, dyskinesia,
headache and
diarrhoea
– Impairment of platelet
function – epistaxis
SSRIs – Pharmacokinetic comparison
Atypical antidepressants
1. Trazodone:
• Weak 5-HT uptake block, α – block, 5-HT2 antagonist
• No arrhythmia
• No seizure
• ADRs: Postural Hypotension
2. Venlafaxine:
• SNRI (Serotonin and NAuptake inhibitor)
• Fast in action
• No cholinergic, adrenergic and histaminic interference
• Raising of BP
3. Mianserin
• Not inhibiting either NA or 5 HT uptake, but blocks
presynaptic alpha-2 receptors- increase release of
NA in brain.
• ADR : Blood dyscrasias, liver dysfunction.
4. Bupropion
• Inhibitor of DAand NA uptake (NDRI)
• Non-sedative but excitant property
• Used in depression and cessation of smoking
• Seizure may precipitated
Serotonin Syndrom
• A group of symptoms that may occur with the use of
certain serotonergic medications or drugs
• The degree of symptoms can range from mild to severe,
including a potentiality of death
• Symptoms in mild cases include high blood pressure and
a fast heart rate; usually without a fever
• Symptoms in moderate cases include: fever,
agitation, increased reflexes, tremor, sweating, dilated
pupils, and diarrhea
• In severe cases body temperature can increase to greater
than 41.1 °C. Complications may include seizures
and extensive muscle breakdown, kidney failure and
unconsciousness
Causes of Serotonin Syndrom
• Selective serotonin reuptake inhibitors
• Serotonin and norepinephrine reuptake inhibitors Bupropion an
antidepressant and tobacco-addiction medication
• Tricyclic antidepressants
• Monoamine oxidase inhibitors
• Anti-migraine medications, such as carbamazepine, valproic acid and
triptans
• Pain medications, such as opioid pain medications including codeine,
fentanyl, oxycodone
• Lithium a mood stabilizer
• Illicit drugs, including LSD, ecstasy, cocaine and amphetamines
• Herbal supplements, including St. John's wort, ginseng and nutmeg
• Over-the-counter cough and cold medications containing
dextromethorphan
• Anti-nausea medications such as granisetron, metoclopramide and etc.
• Linezolid an antibiotic
• Ritonavir an anti-retroviral medication used to treat HIV
Treatment of Serotonin Syndrom
Depending on your symptoms, you may receive the following
treatments:
 Muscle relaxants. Benzodiazepines, they can help control
agitation, seizures and muscle stiffness.
 Serotonin-production blocking agents
 Oxygen and intravenous (IV) fluids. Breathing oxygen
through a mask helps maintain normal oxygen levels in your
blood, and IV fluids are used to treat dehydration and fever.
 Drugs that control heart rate and blood pressure.
 A breathing tube and machine and medication to paralyze
your muscles. You may need this treatment if you have a
high fever.
NON– PHARMACOLOGIC THERAPY
• LIFESTYLE CHANGES
o Stress reduction
o Social support
o Sleep
• PSYCHOTHERAPY
o Cognitive behavioral therapy
o Interpersonal therapy
o Psychodynamic therapy
Comparing Treatments
Studies compare CBT and IPT to antidepressant
meds and other control conditions
results
CBT, IPT, and meds are equally effective
CBT, IPT, and meds are more effective than
placebo conditions
brief psychodynamic treatments
other control conditions
50-70% of people benefit from treatment to a
significant extent, compared to 30% in placebo or
control conditions
Combined Treatments
 Meds work more quickly
 Psychosocial treatments:
 Increase long-range social
functioning
 Prevent relapse
• ELECTROCONVULSIVE THERAPY
– ECT
o Safe & effective disorder for all subtypes
of major depressive disorder.
o ADR : Cognitive dysfunction,
cardiovascular dysfunction, prolonged
apnoea etc.
CONCLUSION
• Affective disorders remain one of the most
commonly occurring mental illnesses in adults.
• It is often undiagnosed and untreated.
• Both pharmacological and nonpharmacological
interventions acts as cornerstone in the treatment
of affective
disorders.
• Pharmacist plays an important role in
accomplishing these treatment goals.

Depression psychiatry

  • 1.
    DEPRESSION • Depression isa affective disorder. • Affective disorders : mental illnesses characterized by pathological changes in mood. • Depression : pathologically depressed mood
  • 2.
    DEFINITION • DEPRESSION: Commonmental disorder that presents with depressed mood, loss of interest or pleasure, feelings of guilt or low self- worth, disturbed sleep or appetite, low energy, and poor concentration.
  • 3.
    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 - Postpartum depression - Catatonic depression - Seasonal affective disorder - Melancholic depression
  • 4.
    • 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
  • 5.
    MAJOR DEPRESSIVE DISORDER aka unipolar depression  lifetime prevalence: up to 21% in women 13% in men  typical age of onset: 20s, but can occur at any time
  • 6.
    SYMPTOMS OF MDD •Feelings of sadness, tearfulness, emptiness or hopelessness • Angry outbursts, irritability or frustration, even over small matters • Loss of interest or pleasure in most or all normal activities, such as sex, hobbies or sports • Sleep disturbances, including insomnia or sleeping too much • Tiredness and lack of energy, so even small tasks take extra effort • Reduced appetite and weight loss or increased cravings for food and weight gain • Anxiety, agitation or restlessness • Slowed thinking, speaking or body movements • Feelings of worthlessness or guilt, fixating on past failures or self-blame • Trouble thinking, concentrating, making decisions and remembering things • Frequent or recurrent thoughts of death, suicidal thoughts, suicide attempts or suicide • Unexplained physical problems, such as back pain or headaches
  • 7.
    ATYPICAL DEPRESSION Described inDSM-IV Depression that shares many of the typical symptoms of the major depression or dysthymia But is characterized by improved mood in response to positive events. It also features significant weight gain or an increased appetite, hypersomnia, a heavy sensation in the limbs, and interpersonal rejection sensitivity that results in significant social or occupational impairment
  • 8.
    POSTPARTUM DEPRESSION • Alsocalled Postnatal depression • Associated with childbirth • Can affect both sexes • Symptoms may include: extreme sadness, low energy, anxiety, crying episodes, irritability, and changes in sleeping or eating patterns • Onset is typically between one week and one month following childbirth • PPD can also negatively affect the newborn child
  • 9.
    CATATONIC DEPRESSION  Catatonicdepression affects the individual’s motor skills  Can be caused by other underlying mental health disorders, such as schizophrenia, mood disorders, and post-traumatic stress disorder  People with catatonia remain still and do not respond to any events/things around them  There are three types of catatonia: akinetic, excited and malignant catatonia  Akinetic catatonia is the most commonly observed in people with catatonic depression  Malignant catatonia can be dangerous, causing severe health effects
  • 10.
    SIGNS AND SYMPTOMS Automaticobedience – The patient automatically obeys all instructions given by the doctor Ambitendency – The patient alternates between cooperating with the doctor’s instructions and resisting them Aversion – The patient turns away when he or she is being spoken to Echopraxia – The patient imitates the activities of the person speaking with him or her. Excitement – The patient engages in excessive and purposeless action that is not driven by outside stimuli Negativism – The person is always having negative thoughts and feels sad every day Stupor – This is one of the common signs of catatonia. It is characterized by a lack of mobility and speech Posturing – The person remains in the same posture for a long period of time Mutism – The person is verbally unresponsive and refuses to speak Staring – The individual’s eye is fixed on a particular space and open for long periods of time.
  • 11.
    SEASONAL DEPRESSION  Morethan just "the winter blues"  Seasonal depression is often called seasonal affective disorder (SAD)  Occurs at the same time each year  Linked to reduced exposure to sunlight during the shorter autumn and winter days (production of Melatonin, Serotonin and Circadian rhythm) Symptoms: • A persistent low mood • A loss of pleasure or interest in normal everyday activities • Irritability • Feelings of despair, guilt and worthlessness • Feeling lethargic (lacking in energy) and sleepy during the day • Sleeping for longer than normal and finding it hard to wake up • Craving carbohydrates and gaining weight
  • 12.
    MELANCHOLIC DEPRESSION  Melancholicdepression, or depression with melancholic features  Is a DSM-IV and DSM-5 subtype of clinical depression Signs and Symptoms • Requiring at least one of the following symptoms: • Anhedonia • Lack of mood reactivity • And at least three of the following: • Depression that is subjectively different from grief or loss • Severe weight loss or loss of appetite • Psychomotor agitation or retardation • Early morning awakening • Guilt that is excessive • Worse mood in the morning
  • 13.
    Double Depression Dysthymic disorderwith episodes of major depression Prognosis more negative
  • 14.
    EPIDEMIOLOGY • Globally morethan 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.
  • 15.
    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
  • 16.
    • Abuse ofDrugs orAlcohol • Hormone Level Changes • Physical illness and side effects of medications DRUGS • Analgesics • Antidepressants • Antihypertensives • Anticonvulsants • Benzodiazipine withdrawal • Antipsychotics
  • 17.
    PHYSICAL ILLNESS • Viralillness • Carcinoma • Neurological disorders • Thyroid disease • Multiple sclerosis • Pernicious anaemia • Diabetes • Systemic lupus erythematosus • Addison’s disease
  • 18.
    PATHOPHYSIOLOGY • The BiogenicAmineHypothesis • The Receptor Sensitivity Hypothesis • The Serotonin-only Hypothesis • The Permissive Hypothesis • The Electrolyte Membrane Hypothesis • The Neuroendocrine Hypothesis
  • 19.
    • The BiogenicAmineHypothesis - 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 or MAOIs causes desensitization (the uncoupling of receptor sites) and possibly down- regulation (a decrease in the number of receptor sites).
  • 20.
    • The Serotonin-onlyHypothesis - emphasizes the role of serotonin in depression and downplays noradrenaline. - But the serotonin-only theory has shortcomings: - it does not explain why there is a delay in onset of clinical relief - it does not explain the role of NA in depression.
  • 21.
    • The PermissiveHypothesis - 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.
  • 22.
    • The ElectrolyteMembrane Hypothesis - hypocalcemia may be associated with mania. - hypercalcemia is associated with depression. • The Neuroendocrine Hypothesis - pathological mood states are explained or contributed to by altered endocrine function.
  • 23.
    CLINICAL MANIFESTATIONS • DEPRESSIONS oThinking is pessimistic and in some cases suicidal. o In severe cases psychotic symptoms such as hallucinations or delusions may be present. o Insomnia or hypersomnia, libido, weight loss, loss of appetite. o Intellectual or cognitive symptoms include a decreased ability to concentrate, slowed thinking, & a poor memory for recent events.
  • 25.
    DIAGNOSIS • ICD 10Diagnostic criteria for a depressive episode (WHO) USUAL SYMPTOMS • Depressed mood. • Loss of interest and enjoyment. • Reduced energy leading to increased fatiguability and diminished activity.
  • 26.
    COMMONSYMPTOMS • Reduced concentrationand 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.
  • 27.
    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. MODERATEDEPRESSIVE 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.
  • 28.
    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 severeintensity.
  • 29.
    INVESTIGATIONS • RATING SCALES oBeck depression inventory o Hamilton depression rating scale • DEXAMETHASONE SUPPRESSION TEST
  • 30.
    TREATMENT ANTIDEPRESSANTS 1. MAO inhibitors: •Irreversible: Isocarboxazid, Iproniazid, Phenelzine and Tranylcypromine. • Reversible: Moclobemide and Clorgyline. 2. Tricyclic antidepressants (TCAs) • NAand 5 HT reuptake inhibitors : Imipramine, Amitryptiline, Doxepin, Dothiepin and Clomipramine. • NAreuptake inhibitors : Desimipramine, Nortryptyline,Amoxapine.
  • 31.
    3. Selective Serotoninreuptake inhibitors: • Fluoxetine, Fluvoxamine, Sertraline and Citalopram 4.Atypical antidepressants: • Trazodone, Mianserin, Mirtazapine, Venlafaxine, Duloxetine, Bupropion and Tianeptine
  • 32.
    MAO Inhibitors • Drugsact by increasing the local availability of NA or 5 HT. • MAO is a Mitochondrial Enzyme involved in Oxidative deamination of these amines. o MAO-A: Peripheral nerve endings, Intestine and Placenta (5-HT and NA). o MAO-B: Brain and in Platelets (Dopamine). o Selective MAO-A inhibitors (RIMA) have antidepressant property (eg:Moclobemide).
  • 33.
    • Side effects: postural hypotension, weight gain, atropine like effects and CNS stimulation. • Severe hypertensive response to tyramine containing foods-cheese reaction • Drug interaction : Ephedrine, Reserpine.
  • 34.
    TCAs • NA, 5HT and Dopamine are present in Nerve endings • Normally, there are reuptake mechanism and termination of action. • TCAs inhibit reuptake and make more monoamines available for action. • In most TCA, other receptors (incl. those outside the CNS) are also affected: blockade of H1-receptor, Alpha-receptors, M-receptors.
  • 36.
    SSRIs • First linedrug in depression. • Relatively safe and better patient acceptability. • Some patients not responding to TCAs may respond with SSRIs. • SSRIs inhibit the reuptake mechanism and make more 5 HT available for action.
  • 37.
     Relative advantages: –No sedation, so no cognitive or psychomotor function interference – No anicholinergic effects – No alpha-blocking action, so no postural hypotension and suits for elderly – No seizure induction – No arrhythmia  Drawbacks: – Nausea is common – Interfere with ejaculation – Insomnia, dyskinesia, headache and diarrhoea – Impairment of platelet function – epistaxis
  • 38.
  • 39.
    Atypical antidepressants 1. Trazodone: •Weak 5-HT uptake block, α – block, 5-HT2 antagonist • No arrhythmia • No seizure • ADRs: Postural Hypotension 2. Venlafaxine: • SNRI (Serotonin and NAuptake inhibitor) • Fast in action • No cholinergic, adrenergic and histaminic interference • Raising of BP
  • 40.
    3. Mianserin • Notinhibiting either NA or 5 HT uptake, but blocks presynaptic alpha-2 receptors- increase release of NA in brain. • ADR : Blood dyscrasias, liver dysfunction. 4. Bupropion • Inhibitor of DAand NA uptake (NDRI) • Non-sedative but excitant property • Used in depression and cessation of smoking • Seizure may precipitated
  • 41.
    Serotonin Syndrom • Agroup of symptoms that may occur with the use of certain serotonergic medications or drugs • The degree of symptoms can range from mild to severe, including a potentiality of death • Symptoms in mild cases include high blood pressure and a fast heart rate; usually without a fever • Symptoms in moderate cases include: fever, agitation, increased reflexes, tremor, sweating, dilated pupils, and diarrhea • In severe cases body temperature can increase to greater than 41.1 °C. Complications may include seizures and extensive muscle breakdown, kidney failure and unconsciousness
  • 42.
    Causes of SerotoninSyndrom • Selective serotonin reuptake inhibitors • Serotonin and norepinephrine reuptake inhibitors Bupropion an antidepressant and tobacco-addiction medication • Tricyclic antidepressants • Monoamine oxidase inhibitors • Anti-migraine medications, such as carbamazepine, valproic acid and triptans • Pain medications, such as opioid pain medications including codeine, fentanyl, oxycodone • Lithium a mood stabilizer • Illicit drugs, including LSD, ecstasy, cocaine and amphetamines • Herbal supplements, including St. John's wort, ginseng and nutmeg • Over-the-counter cough and cold medications containing dextromethorphan • Anti-nausea medications such as granisetron, metoclopramide and etc. • Linezolid an antibiotic • Ritonavir an anti-retroviral medication used to treat HIV
  • 43.
    Treatment of SerotoninSyndrom Depending on your symptoms, you may receive the following treatments:  Muscle relaxants. Benzodiazepines, they can help control agitation, seizures and muscle stiffness.  Serotonin-production blocking agents  Oxygen and intravenous (IV) fluids. Breathing oxygen through a mask helps maintain normal oxygen levels in your blood, and IV fluids are used to treat dehydration and fever.  Drugs that control heart rate and blood pressure.  A breathing tube and machine and medication to paralyze your muscles. You may need this treatment if you have a high fever.
  • 46.
    NON– PHARMACOLOGIC THERAPY •LIFESTYLE CHANGES o Stress reduction o Social support o Sleep • PSYCHOTHERAPY o Cognitive behavioral therapy o Interpersonal therapy o Psychodynamic therapy
  • 47.
    Comparing Treatments Studies compareCBT and IPT to antidepressant meds and other control conditions results CBT, IPT, and meds are equally effective CBT, IPT, and meds are more effective than placebo conditions brief psychodynamic treatments other control conditions 50-70% of people benefit from treatment to a significant extent, compared to 30% in placebo or control conditions
  • 48.
    Combined Treatments  Medswork more quickly  Psychosocial treatments:  Increase long-range social functioning  Prevent relapse
  • 49.
    • ELECTROCONVULSIVE THERAPY –ECT o Safe & effective disorder for all subtypes of major depressive disorder. o ADR : Cognitive dysfunction, cardiovascular dysfunction, prolonged apnoea etc.
  • 50.
    CONCLUSION • Affective disordersremain one of the most commonly occurring mental illnesses in adults. • It is often undiagnosed and untreated. • Both pharmacological and nonpharmacological interventions acts as cornerstone in the treatment of affective disorders. • Pharmacist plays an important role in accomplishing these treatment goals.