DEPRESSION: TCAS Flashcards

1
Q

MoA

A

Inhibits the reuptake of 5-HT + NA
Also blocks a wide array of receptors (M, H1, alpha1/2 and D2)

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2
Q

Sedating TCAs

A

Amitriptyline (also used in neuropathic pain)
Clomipramine
Dosulepin (dangerous in overdose - specialist use)
Doxepin
Trimipramine
Mianserin
Trazadone

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3
Q

When would you give a sedating TCA?

A

Give in anxious, agitated patients

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4
Q

Less sedating TCAs

A

Imipramine (most antimuscarinic effects)
Lofepramine (rarely causes hepatotoxicity)
Nortriptyline (also used in neuropathic pain)

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5
Q

When would you give a less sedating TCA

A

Given in withdrawn, apathetic patients

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6
Q

How are amitriptyline SEs reduced?

A

Side-effects are reduced by titrating slowly to the minimum effective dose (every 2-3 days)

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7
Q

Amitriptylline overdose

A

o dry mouth, coma, hypotension, hypothermia hyperreflexia, extensor plantar responses, convuslions, respiratory failure, cardiac conduction defects and arrhythmias

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8
Q

Side effects

A

More sedating, epileptogenic (seizures), cardiotoxic and antimuscarinic than SSRIs.
They are also more toxic in overdose.

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9
Q

Cardiac side effects

A

QT prolongation
Arrhythmias
Heart block
Hypertension

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10
Q

Antimuscarinic side effects

A

Dry mouth
Blurred vision
Constipation
Tachycardia
Urinary retention
Pupil dilation
Raised intraocular pressure
Angle closure glaucoma

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11
Q

Other side effects

A

Hallucinations
Mania (increased 5-HT/NA)
Hypotension (alpha blockade)
Sexual dysfunction
Breast changes
Extrapyramidal SE (d blockade)

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12
Q

Interactions - increased risk of hyponatraemia

A

Diuretics (loop/thiazide)
Desmopressin
Carbamazepine

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13
Q

Interactions - increased plasma concentrations

A

Cimetidine (enzyme inhibitors)

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14
Q

Interactions - increased risk of QT prolongation (clomipramine)

A

Amiodarone
Sotalol
Antipsychotics
Citalopram/escitalopram
Loop/thiazide diuretics
B2 agonists
Corticosteroids
Theophylline

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15
Q

Interactions - increased risk of hypotension

A

Antihypertensive
- Alpha blockers
- Beta blockers
- ACEi
- CCBs
Antipsychotics
Levodopa/dopaminergic
NSAIDs
SGLT2 inhibitors (gliflozin)
Diuretics
Phosphodiesterase type-5 inhibitors (sildenafil)

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16
Q

Interactions - increased risk of hypotension

A

Antimuscarinic drugs
Antihistamines
Atropine
Antipsychotics

17
Q

Interactions - increased risk of serotonin syndrome

A

MAOIs/selegiline (MAO-B inhibitor)
Tramadol
Amphetamines, 5-HT1a agonists e.g. sumatriptan, SSRIs
5-HT3 receptor antagonists e.g. ondansetron
Lithium

18
Q

Treatment cessation

A
  • Withdrawal effects may occur within 5 days of stopping - usually mild and self-limiting.
  • Risk of increased if stopped suddenly after 8 weeks or more.
  • Preferably be reduced over 4 weeks