antidepressants Flashcards

1
Q

Markers of severe depression?

A
Suicide plan or ideas of self-harm.
Unexplained guilt or worthlessness.
Inability to function (eg psychomotor
retardation or agitation).
Concentration impaired.
Impaired appetite.
Decreased sleep/early waking.
Energy low/unaccountable fatigue
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2
Q

Examples of SSRIs?

A

Citalopram, sertraline, fluoxetine, Fluvoxamine, paroxetine,

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3
Q

examples of tricyclics?

A

Amitriptyline, Clomipramine, dosulepin, doxepin
Imipramine and lofepramine
Trimipramine

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4
Q

Example of SNRI?

A

Venlafaxine

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5
Q

When to avoid SNRIs? Monitoring? SEs?

A

If raised BP, raised or low U+Es, heart disease
monitor BP if on >200mg/day.

SE: Constipation; nausea;
dizziness; dry mouth; BP raised ; ADH raised; Na+ reduced; T° raised; dyspnoea, hallucinations, arthralgia

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6
Q

Citalopram class? SEs?

A

SSRI

Nausea, vomiting, dyspepsia, diarrhoea, abdominal pain—also rash, sweats, agitation, headache, insomnia,
tremor,
anorgasmia/erectile dysfunction (sildenafil helps), Na+ reduced, GI bleeding

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7
Q

How to help the erectile dysfunction caused by citalopram/sertraline?

A

Sildenafil (Viagra)

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8
Q

How does the SE profile of fluoxetine differ to citalopram/sertraline?

A

Same SE profile except insomnia and agitation are commoner

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9
Q

How does the SE profile of fluvoxamine differ to citalopram/sertraline?

A

Same SE profile except nausea is commoner

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10
Q

How does the SE profile of paroxetine differ to citalopram/sertraline?

A

more antimuscarinic effects and sedation, also extrapyramidal SEs (rare)

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11
Q

Amitripytyline common and other SEs?

A

Common: sedation, dry mouth, urine retention, blurred vision, postural hypotension, tachycardia, constipation

Other: arrhythmias;
convulsions (dose-related).

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12
Q

Which tricyclics have the same SEs as amitriptyline?

A

Clomipramine, dosulepin, doxepin

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13
Q

How do the SE profiles of Imipramine and lofepramine and trimipramine differ to amitriptyline?

A

Imipramine and lofepramine less sedating

Trimipramine more sedating

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14
Q

Common side effects of tricyclics?

A
drowsiness
dry mouth
blurred vision
constipation
urinary retention
lengthening of QT interval
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15
Q

Amitriptylline coomon uses?

A

commonly used in the management of neuropathic pain and the prophylaxis of headache (both tension and migraine)

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16
Q

Most and least dangerous tricylics in OD?

A

lofepramine has a lower incidence of toxicity in overdose

amitriptyline and dosulepin (dothiepin) are considered the most dangerous in overdose

17
Q

Which tricyclics are more and less sedative?

A

More: Amitriptyline
Clomipramine
Dosulepin
Trazodone*

Less: Imipramine
Lofepramine
Nortriptyline

*trazodone is technically a ‘tricyclic-related antidepressant’

18
Q

Which SSRI to use post MI?

A

Sertraline

19
Q

Which SSRI should be used in children/adolescents?

A

fluoxetine

20
Q

When should patients be counselled on after starting SSRI?

A

to be vigilant for increased anxiety and agitation after starting a SSRI

21
Q

Which SSRIs have higher propensity for drug interactions?

A

fluoxetine and paroxetine

22
Q

Which drugs do SSRIs interact with?

A

NSAIDs - NICE guidelines advise ‘do not normally offer SSRIs’, but if given co-prescribe a proton pump inhibitor
Warfarin/heparin - avoid SSRIs and consider mertazapine
aspirin
triptans - increased risk of serotonin syndrome
Monoamine oxidase inhibitors - increased risk of serotonin syndrome

23
Q

When to review patients after starting SSRIS? How long to continue Tx?

A

patients should normally be reviewed by a doctor after 2 weeks. For patients under the age of 30 years or at increased risk of suicide they should be reviewed after 1 week.

at least 6mo

24
Q

How to stop SSRIs? Discontinuation symptoms?

A

gradually reduced over a 4 week period (this is not necessary with fluoxetine)

increased mood change
restlessness
difficulty sleeping
unsteadiness
sweating
gastrointestinal symptoms: pain, cramping, diarrhoea, vomiting
paraesthesia
25
Q

Use of SSRIs during pregnancy?

A

BNF says to weigh up benefits and risk when deciding whether to use in pregnancy.
Use during the 1st trimester gives a small increased risk of congenital heart defects
- Use during the 3rd trimester can result in persistent pulmonary hypertension of the newborn
- Paroxetine has an increased risk of congenital malformations, particularly in the first trimester

26
Q

Mirtazapine MOA? When to use? When to take?

A

blocks alpha2-adrenergic receptors, which increases the release of neurotransmitters.

In older people as fewer SEs and interactions than many other antidepressants.
Also mirtazapine can cause sedation and increased appetite - can be useful in older people.

In evening as sedative.