Antidepressants Flashcards

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1
Q

What are the classes of antidepressants

A

Selective serotonin reuptake inhibitors (SSRIs)
Serotonin and Noradrenaline reuptake inhibitor (SNRI)
Tricyclic antidepressants (TCAs)
Noradrenergic and specific serotonin antidepressant (NaSSA)
Noradrenaline reuptake inhibitors (NARIs)
Monoamine Oxidase Inhibitors (MAOIs)
Reversible inhibitors of monoamine oxidase A (RIMAs)
Serotonin antagonist and reuptake inhibitor (SARI)

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2
Q

What is the MOA of SSRIs and give examples

A

Blocks the serotonin re-uptake → more serotonin in the synaptic cleft
Paroxetine, sertraline, citalopram, fluoxetine (preferred for CAMHS), escitalopram

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3
Q

How should SSRIs be taken

A

Requires 4-6 weeks to work
Continued for 6 months after remission (first episode) or 2 years (recurrence)
Then gradually stopped after 4 weeks
Should not be taken with Triptans, NSAIDs/aspirin
+ regular review

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4
Q

What are the side effects of SSRIs

A

Stomach/GI e.g. nausea, diarrhoea, constipation, GI bleeding
Sleep disturbance/insomnia with vivid dreams
Sexual dysfunction
Sodium - Hyponatraemia
Increased risk of suicide (In the first 1-2 weeks)
Serotonin syndrome
Others: Headache, dizziness, sweating, blurred vision, akathisia
Citalopram → QT prolongation

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5
Q

How should fluoxetine be swapped

A

Reduce dose over 2 weeks and wait 4-7 days after stopping before starting another

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6
Q

What is serotonin syndrome and what are the complications

A

Excessive serotonin in the synapses of the brain
From using antidepressants: side effect, in combination, overdose

Complications: DIC | rhabdomyolysis | renal failure/metabolic acidosis | seizures

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7
Q

What are the symptoms of serotonin syndrome

A

Altered mental state: agitation, confusion coma
Neuromuscular changes: myoclonus, hyperreflexia, hypertonia, tremor
Autonomic dysfunction: tachycardia, HTN, hyperthermia, diaphoresis, mydriasis (dilated pupil)

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8
Q

What is the management for serotonin syndrome

A
  1. Admit to hospital
  2. Stop offending medications
  3. Supportive measures (ABCDE) - airway management, renal care, IV fluids, temperature control
  4. Cyproheptadine (antihistamine + serotonin antagonist)
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9
Q

What is the MOA for SNRIs and give some examples

A

Blocks reuptake of serotonin > NA
(Will also block DA uptake at high doses)
Venlafaxine, duloxetine

Note: requires BP monitoring

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10
Q

What are the side effects of SNRIs

A

Headache
Stomach/GI e.g. nausea, diarrhoea, constipation, GI bleeding
Sleep disturbance/insomnia with vivid dreams
Sexual dysfunction
Sodium - Hyponatraemia
Increased risk of suicide (In the first 1-2 weeks)
Serotonin syndrome
Others: dizziness, sweating, blurred vision, akathisia

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11
Q

What is the MOA for TCAs and give some examples

A

Affects multiple transmitters (5-HT and NA re-uptake inhibition)
- High dose → all receptors
- Low dose → blocks H1 and 5-HT → good for sleep

Amitriptyline, nortiptryline, clomipramine, lofepramine

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12
Q

What are the side effects of tricyclic antidepressants

A

Anti-cholinergic/muscarinic effects (can’t see, can’t pee, can’t spit, can’t shit)
- Blurred vision
- Urinary retention
- Dry mouth
- Constipation
Cardiotoxic - QT prolongation, ST elevation, AV block
Anti-histaminergic: sedation, postural hypotension, weight gain
Thrombocytopenia
Cardiac (arrhythmia, MI, stroke, postural hypotension)

Lethal in overdose - do not give if risk of suicide

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13
Q

What is the MOA for NaSSAs and give some examples

A

Blocks presynaptic alpha-2-adrenergic receptors (Autoreceptor hence less feedback and more NA release)

Mirtazapine

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14
Q

What are the side effects of NaSSAs

A

Drowsiness (→ take in the evening)
Increased appetite
Weight gain

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15
Q

Give an example of Noradrenaline reuptake inhibitors (NARIs) and what are its side effects

A

Reboxetine

Dry mouth
Constipation
Excessive sweating
Urinary problems
Insomnia
Tachycardia

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16
Q

What is the MOA of monoamine oxidase inhibitors (MAOIs) and give examples

A

Increases the availability of 5-HT and NA in the synapses
Older = irreversible e.g. Phenelzine, tranylcypromine
Newer = reversible e.g. Moclobemide

17
Q

What are the side effects of MAOIs

A

Tyramine interaction → hypertensive crisis
- Cheese, smoked meats, yoghurt, chocolate, coffee, tea
Postural hypotension, dizziness
Headache
Drowsiness, insomnia
Blurred vision
N&V
Constipation

18
Q

What are the symptoms of stopping antidepressants suddenly

A

Discontinuation syndrome (FIRM STOP)

Flu-like symptoms
Insomnia, vivid dreams
Restlessness, irritability
Mood swings
Sweating
Tummy: pain, cramps, D&V
Off balance (ataxia), dizziness
Paraesthesia: Electric shock sensation, tingling

19
Q

What is ECT

A

Inducing a generalised tonic-clonic seizure (under GA and muscle-relaxant) for about 30 secs
Given twice a week, usually 6-12 treatments

20
Q

What are the indications for ECT

A

Severe/refractory depression: only in life-threatening situation e.g. poor oral intake, acutely suicidal, treatment resistant
Catatonia
Severe, uncontrolled mania

21
Q

What are the contraindications to ECT

A

No absolute CIs
Caution with:
- Pregnancy
- Heart disease/stroke
- Poor anaesthetic risk
- Raised ICP
- Pacemaker
- Epilepsy

22
Q

What are the side effects of ECT

A

Main risk is of the anaesthetic: MI, arrhythmia, aspiration, apnoea, malignant hyperthermia, pneumonia, death

Short-term:
- Headaches and nausea
- Muscle aches
- Confusion
- Cardiac arrhythmi
- Memory problem (retrograde > anterograde) - should recover by 6 months

Long-term: impaired memory, apathy, anhedonia

23
Q

What is the difference between bilateral and unilateral ECT

A

Bilateral ECT- shorter duration, lower dose - USUALLY RECOMMENDED
- Effective at threshold, more efficacious, quicker
- More likely to get cognitive SE, language, or visuospatial problems

Unilateral ECT- non-dominant side
- Fewer cognitive SE
- Technically difficult, not as effective, slower action