Psychopharmacology: anxiety + mood disorders Flashcards

(36 cards)

1
Q

What is the predominant biochemical theory for depression?

A

monoamine hypothesis of depression - lack of serotonergic and noradrenergic activity in the brain can cause symptoms of depression

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2
Q

What are the 5 grades of depression set by NICE?

A

sub-threshold
mild
moderate
severe
complex

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3
Q

Depression key presenting symptoms

A

poor sleep
anxiety
mood varying throughout the day
altered appetite
tiredness, slowness, loss of energy
feeling depressed or agitated
loss of interest in previously enjoyed activities
feelings of worthlessness/guilt
poor memory
recurrent thoughts of death or suicide

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4
Q

Non-pharmacological treatments for depression

A

social support
guided self-help
being active
counselling
psychological therapies (CBT, relaxation therapy, mindfulness)
general support and advice eg. on financial matters, to reduce stress

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5
Q

4 main stages of drug treatment for depression

A

1) symptom control - moderate/severe = antidepressant trial for 6 weeks, continue for 12 weeks if some response

2) continuation - for at least 6 months to prevent relapse

3) relapse prevention - for those with risk factors keep on antidepressant longer (2nd episode = 1-2 years, 3rd episode = 5 years +)

4) discontinuation - slow reduction

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6
Q

Name some classes of antidepressants

A

tricyclic antidepressants (TCAs)
selective serotonin reuptake inhibitors (SSRIs)
serotonin noradrenaline reuptake inhibitors (SNRIs)
noradrenaline and specific serotoninergic antidepressant (NaSSA)
monoamine oxidase inhibitors (MAOIs)

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7
Q

Name some tricyclic antidepressants

A

amitriptyline
imipramine
dosulepin
clomipramine
lofepramine
trimipramine

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8
Q

Tricyclic antidepressants MOA

A

block reuptake of noradrenaline and serotonin

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9
Q

Tricyclic antidepressants side effects

A

GI upsets, dry mouth, blurred vision, constipation, urinary retention, postural hypotension, cardiac arrhythmias, sedation, confusion, memory problems

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10
Q

Name some SSRIs

A

citalopram
sertraline
fluoxetine
paroxetine
fluvoxamine
escitalopram

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11
Q

SSRIs MOA

A

increases the level of serotonin in the synapse by blocking the reuptake pump

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12
Q

SSRIs common side effects

A

GI upset
anxiety symptoms (initially)

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13
Q

Name some SNRIs

A

venlafaxine
duloxetine

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14
Q

Who can’t take SNRIs?

A

contraindicated in people with cardiovascular risk factors

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15
Q

SNRIs common side effects

A

nausea
headache
dry mouth
sweating

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16
Q

Name a NaSSA?

17
Q

NaSSA (mirtazapine) MOA

A

enhances the action of noradrenaline and serotonin in the synapse

18
Q

Mirtazapine side effects

A

sedation
increase in appetite
dizziness
dry mouth

19
Q

Name some MAOIs

A

phenelzine
isocarboxazid
tranylcypromine
moclobemide

20
Q

MOAIs MOA

A

inhibit (either reversibly or irreversibly) monoamine oxidase enzymes to prevent the breakdown of monoamine neurotransmitters

21
Q

What dietary restrictions are in place for patients on MAOIs and why is this?

A

avoid food or drinks that contain tyramine (including alcohol) because this can cause a very large sudden increase in blood pressure (hypertensive crisis)

22
Q

What foods contain tyramine?

A

cheese
liver
yoghurt
marmite
oxo
bovril
yeast
dried sausage eg. pepperoni
beer, lager, wine

23
Q

How should antidepressants be dosed?

A

most antidepressants are more tolerable if started at lower initial dose (half the standard) and increased to target dose over days or weeks

exception is mirtazapine - start at 30mg/day as it is less sedating at this dose than at lower doses

24
Q

Signs and symptoms of serotonin syndrome

A

restlessness
sweating
tremor
shivering
muscular rigidity
confusion
convulsions
death

25
Name some anxiety disorders
generalised anxiety disorder obsessive compulsive disorder post-traumatic stress disorder panic disorder phobic anxiety disorders
26
Anxiety disorders pathophysiology
in the CNS, the major mediators of the symptoms of anxiety disorders appear to be noradrenaline, serotonin, dopamine and GABA
27
Short term pharmacological treatment of anxiety disorder
benzodiazepines beta blockers eg. propranolol antihistamines eg. hydroxyzine antipsychotics
28
Long term pharmacological treatment of anxiety disorder
antidepressants (eg. SSRIs, TCAs, MAOIs, venlafaxine, mirtazapine) buspirone pregabalin
29
When are benzodiazepines useful in anxiety?
up to 4 weeks when symptoms are severe (disabling) long term use risks tolerance and dependence
30
Symptoms of benzodiazepine withdrawal
mild - restlessness, tremor, agitation severe - depression, convulsions, psychosis
31
When are antipsychotics used in anxiety disorder?
frequently used for tranquilising effects used in acute inpatient environment if a patient is extremely anxious and agitated and is causing harm to themselves or others
32
When are beta blockers (propranolol) used in anxiety disorder?
primarily for specific physical symptoms and reducing the vicious cycle of feeling more anxious, become tremulous and tachycardic, fuelling the anxiety
33
First line pharmacological treatment for GAD
SSRI (eg. paroxetine)
34
First line pharmacological treatment for PTSD
SSRI eg. sertraline needs long term treatment as relapse is common avoid benzodiazepines as can be counter-productive
35
OCD pharmacological treatment principles
only central serotonin enhancers are effective - SSRIs/clomipramine daily dose usually needs to be very high should see improvements on maximum tolerated dose by 3 months stay on drug for minimum 1-2 years as relapse is common in discontinuation gradual discontinuation over several months
36