MIND Flashcards

1
Q

3 core symptoms of depression

A
  • persistent low mood
  • reduced energy
  • anhedonia = loss of interest/enjoyment
mild = 2 core + 2 other
moderate = 2 core + 3/4 other
severe = 3 cored + 4+ others
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2
Q

what is included in an MSE exam

A
appearance
speech
thought (+suicide/harm)
cognition
perceptions
mood and affect
insight
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3
Q

psychiatric interview components

A
  • presenting complaint
  • history of presenting complaint
  • past psychiatric history
  • past medical history
  • medication history
  • family history
  • personal history
  • social history
  • substance use
  • premorbid personality
  • forensic history
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4
Q

psychiatric interview components

A
  • presenting complaint
  • history of presenting complaint
  • past psychiatric history
  • past medical history
  • medication history
  • family history
  • personal history
  • social history
  • substance use
  • premorbid personality
  • forensic history
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5
Q

Agoraphobia

A

feel safe at home but even going outside to front garden–> anxiety
Therefore the avoid even outdoors, let alone social environments

Fear of being alone at places where escape is difficult

2x more common in women

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6
Q

3 types of stress disorders

A
  • An acute stress reaction (which occurs up to 2 days after trauma)
  • Adjustment disorder (where anxiety persists up to one month after trauma)
  • more serious = PTSD
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7
Q

anxiolytics and hypnotics

A

benzodiazepines - BOTH
(-lams/pams)

hypnotics

  • Z drugs
  • anti histamines

anxiolytics

  • 5-HT1A agonists eg. busprione (SSRIs for GAD)
  • b-adrenoceptor antagonists
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8
Q

why should you not stop benzodiazepines cold turkey

A

Benzos stimulate the GABA inhibitory

therefore body adapts and increases excitatory receptors

if you stop cold turkey

excitatory receptors > inhibitory

leads to high activation of excitatory–> seizures

so you should slowly decrease not completely withdraw

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9
Q

how do barbiturates and benzodiazpines work

A

they are positive allosteric molecules

they bind to GABA -A receptor and help binding of GABA and leave them open for longer

more Cl- into post-synaptic neurone

decreasing excitatory effects–> decreasing anxiety/insomnia

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10
Q

which drugs can lead to tolerance

A

benzodiazepines / z-drugs

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11
Q

what are z -drugs

A

act similar to Benzodiazpeines but are hypnotic (slightly different structure)

zolpiDEM

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12
Q

how to 5-HT1A agonists work

+how does SSRIs affect them

A

when activated we get less release of serotonin

(5-HT1A is auto inhibitory)

body down regulates the pre-synaptic 1a receptors (less inhibition)

leading to more serotonin in cleft

SSRIs can lead to serotonin receptor trafficking

they inhibit reuptake so there is massive activation of both pre/post receptors

body down regulated pre and post synpatic

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13
Q

B1 and B2 stimulation relating to anxiety symptoms

A

B1 - increases heart rate/renin release

B2 - increases renin release also

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14
Q

why are barbiturates not used anymore

+ but what are they still used for

A

narrow therapeutic index
(high risk of OD)
+ there is no OD antidote whereas Benzos = flumenazil (an antagonist)

capital punishment
epilepsy
euthanasia

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15
Q

drugs for depression + side effects

A

MAOis

  • only releases the NA/5-HT that was gonna be degraded (not the ones recycled in vesicles)
  • usually thymine (cheese/wine) is also broken down by MAO too
  • accumulation —-> sympathomimetic effects
  • headache/intracrainal haemorrhage/elevated BP/HT

RIMA (reversible) eg. moclobemide

  • accumulation of NA displaces RIMA
  • allows degradation of excess NA

TCAs

  • NA + 5HT reuptake inhibitor
  • increased activation on all 5-HT
  • downregulation of 5-HT1A and alpha 2 (disinhibition)
  • BUT anti-cholinergic/muscarinic activity / CVS effects

SSRI

  • 5HT reuptake inhibitor ONLY
  • no blockages of NA - less CVS effects
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16
Q

side effects of SSRIs

A

sexual dysfunction/ insonmia (5-HT2)

Nausea; GI distress; headache (5-HT3)

serotonin syndrome

  • confusion
  • hyperthemia
  • seizures