AEFFECTIVE DISORDERS: DEPRESSION Flashcards

1
Q

Which group is most likely to be affected by depression

A

women, more specifically black and mixed race women

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2
Q

depression

A
  • broad and heterogenous diagnosis
  • Central to its depressed mood and/or loss of pleasure in most activities
  • symptoms should be present for at least 2 weeks at sufficient severity for most of every day
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3
Q

diagnostic systems for depression

A

ICD-10/11 and the DSM-5 classification system

severity is determined by both the number and severity of symptoms

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4
Q

bipolar I disorder

A

where a person has had at least one manic episode and periods of significant depression, each usually lasting for an extended period

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5
Q

bipolar II disorder

A

the person has never had a manic episode, but has had at least one hypomanic episode and at least one period of significant depression

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6
Q

cyclothymia

A

similar to bipolar but with lower extremes

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7
Q

euthymia

A

period without mood disturbances

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8
Q

aetiology of bipolar disorder

A

strong genetic component - inheritability

usually diagnosed in late teens

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9
Q

use of lithium in bipolar disorder

A
  • used to calm manic patients and prophylactically as a mood stabiliser
  • results observed relatively quick and are considered safe (no overdose risk)
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10
Q

lithium potential moa

A
  • modulation of glutamate, GABA and DA neurotransmission
  • inhibition of inositol triphosphate formation
  • interference of cAMP formation
  • accumulation of Li+ in cell leading to sustained depolarisation
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11
Q

side effects of lithium

A

long half-life leads to common side effects such as nausea, thirst, tremor and mental confusion

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12
Q

key symptoms for major depressive disorder (MDD)

A
  • persistent sadness or low mood
  • loss of interests or pleasure
  • fatigue or low energy
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13
Q

associated symptoms of major depressive disorder (MDD)

A
  • disturbed sleep
  • poor concentration or indecisiveness
  • low self-confidence
  • poor or increased appetite
  • suicidal thoughts or acts
  • agitation or slowing of movements
  • guilt or self-blame
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14
Q

degrees of depression

A

not depressed - <4
mild depression - 4 symptoms
moderate depression - 5 or 6
severe depression - >7 symptoms with or without psychotic symptoms

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15
Q

monoamine hypothesis

A
  • suggests that depression results from deficient monoamine transmission
  • monoamine oxidase inhibitor developed for TB, elevated the mood of the treated patients
  • thus the Amine hypothesis proposes that depression occurs due to decreased levels of amines (NA, 5-HT and DA) in the CNS
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16
Q

problems with the monoamine hypothesis

A
  • drug action is relatively fast (hours) but relief of symptoms takes longer (weeks)
  • antidepressants have differing mode of action but work similarly on symptoms
17
Q

noradrenergic system neuromodulation in the brain

A

locus coeruleus

18
Q

serotenergic system neuromodulation in the brain

A

raphe nucleus

19
Q

dopaminergic system neuromodulation in the brain

A

ventral tegmental area (VTA) and substantial nigra (SN)

20
Q

antidepressant groups

A

selective serotonin reuptake inhibitors (SSRIs)
serotonin noradrenaline reuptake inhibitors (SNRIs)
monoamine oxidase inhibitors (MAOIs)
tricyclic antidepressants (TCAs)

21
Q

psychotherapies for depression

A
  • behavioural therapy
  • interpersonal therapy
  • group therapy
  • cognitive behavioural therapy (CBT)
  • mindfulness based cognitive therapy (MBCT)
22
Q

brain stimulation methods in depression

A
  • electroconvulsive therapy (ECT)
  • vagus nerve stimulation (VNS)
  • transcranial magnetic stimulation (TMS)
  • deep brain stimulation (DBS)
23
Q

benefits and risks of SSRIs

A
  • better tolerated and reduced risk of overdose
  • increased risk of bleeding esp. in older pts/those taking anticoagulants
  • less sedating and fewer antimuscarinic and cardiotoxic effect than TCAs
  • sertraline safe with cardio issues (do not use citalopram)
  • fluoxetine, fluvoxamine and paroxetine have higher drug interactions than other SSRIs
24
Q

benefits and risks of TCAs

A
  • similar to SSRIs but adverse effects
  • antimuscarinic side effects - dry mouth, urinary retention, blurred vision etc.
  • cardiotoxicity
  • sedation
  • weight gain
  • risk of overdose
  • increased risk of coma/seizure, and potentially fatal cardiac arrhythmia/arrest
25
Q

benefits and risks of MAOIs

A
  • should only be prescribed by specialists
  • hepatotoxicity (isocarboxazid and phenelzine)
  • dangerous interactions with some food and drugs > hypertensive crisis - ‘cheese reaction’
26
Q

use of electroconvulsive shock treatment (ECT)

A
  • even most severe bouts of depression are usually responsive to ECT
  • still used to day in cases of very severe depression with a high risk of suicide, where there has been no response to drug treatments
27
Q

first line for depression

A

sertraline + CBT/IPT

28
Q

how long do you continue on an antidepressant before switching to a different kind

A

6-9 months (assess efficacy after 1-4 weeks)

29
Q

novel treatments: ketamine and esketamine

A
  • single dose of NMDA inhibitors can cause a rapid (next day) antidepressant effect in pts with MDD
  • primarily used in treatment resistant depression (resistant to 2 or more antidepressants)
30
Q

SSRI drugs

A

fluoxetine
citalopram
escitalopram
paroxetine
sertraline

31
Q

SNRI drugs

A

duloxetine
venlafaxine

32
Q

TCA drugs

A

amitriptyline
clomipramine
dosulepin
imipramine
lofepramine
nortitriptyline

33
Q

MAOI drugs

A

tranylcypromine
phenelzine
isocarboxazid