antidepressants Flashcards
Markers of severe depression?
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
Examples of SSRIs?
Citalopram, sertraline, fluoxetine, Fluvoxamine, paroxetine,
examples of tricyclics?
Amitriptyline, Clomipramine, dosulepin, doxepin
Imipramine and lofepramine
Trimipramine
Example of SNRI?
Venlafaxine
When to avoid SNRIs? Monitoring? SEs?
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
Citalopram class? SEs?
SSRI
Nausea, vomiting, dyspepsia, diarrhoea, abdominal pain—also rash, sweats, agitation, headache, insomnia,
tremor,
anorgasmia/erectile dysfunction (sildenafil helps), Na+ reduced, GI bleeding
How to help the erectile dysfunction caused by citalopram/sertraline?
Sildenafil (Viagra)
How does the SE profile of fluoxetine differ to citalopram/sertraline?
Same SE profile except insomnia and agitation are commoner
How does the SE profile of fluvoxamine differ to citalopram/sertraline?
Same SE profile except nausea is commoner
How does the SE profile of paroxetine differ to citalopram/sertraline?
more antimuscarinic effects and sedation, also extrapyramidal SEs (rare)
Amitripytyline common and other SEs?
Common: sedation, dry mouth, urine retention, blurred vision, postural hypotension, tachycardia, constipation
Other: arrhythmias;
convulsions (dose-related).
Which tricyclics have the same SEs as amitriptyline?
Clomipramine, dosulepin, doxepin
How do the SE profiles of Imipramine and lofepramine and trimipramine differ to amitriptyline?
Imipramine and lofepramine less sedating
Trimipramine more sedating
Common side effects of tricyclics?
drowsiness dry mouth blurred vision constipation urinary retention lengthening of QT interval
Amitriptylline coomon uses?
commonly used in the management of neuropathic pain and the prophylaxis of headache (both tension and migraine)
Most and least dangerous tricylics in OD?
lofepramine has a lower incidence of toxicity in overdose
amitriptyline and dosulepin (dothiepin) are considered the most dangerous in overdose
Which tricyclics are more and less sedative?
More: Amitriptyline
Clomipramine
Dosulepin
Trazodone*
Less: Imipramine
Lofepramine
Nortriptyline
*trazodone is technically a ‘tricyclic-related antidepressant’
Which SSRI to use post MI?
Sertraline
Which SSRI should be used in children/adolescents?
fluoxetine
When should patients be counselled on after starting SSRI?
to be vigilant for increased anxiety and agitation after starting a SSRI
Which SSRIs have higher propensity for drug interactions?
fluoxetine and paroxetine
Which drugs do SSRIs interact with?
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
When to review patients after starting SSRIS? How long to continue Tx?
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
How to stop SSRIs? Discontinuation symptoms?
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
Use of SSRIs during pregnancy?
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
Mirtazapine MOA? When to use? When to take?
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.