Depression QA Flashcards

1
Q

Three treatment options in depression

A
  • SSR1s (safe
  • TCA (problems with sedation and addiction)
  • MOAIs (interact with a lot of drugs)
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2
Q

Why are SSRis first line + length of treatment

A
  • They are better tolerated in overdose and have less side effects
  • TCA’s have more side effects such as sedation
  • MOAis interact with a lot of food
  • Length of treatment = 2wks
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3
Q

When do you review pt on SSRis

A

1) 1-2 start of treatment

2) After 4 wks in (6wks in elderly)

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4
Q

If SSR1s don’t work there are second line options which include

A
  • Increase SSRI dose
  • Choose another SSR1
  • Mirtazapine
  • Other TCA (consider venlafaxine in more serious depression)
  • Irreversible MOAis = only under specialist supervision
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5
Q

Third line treatment options if SSR1s don’t work

A

1) Add another antidepressant class
2) Add am augmenting agent e.g lithium / antipsychotics
3) Electroconvulsive therapy In server refractory depression

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6
Q

Side effect of antidepressant medication (4)

A
  • Hyponatremia (in SSR1s are most common)
  • Suicidal ideation (monitor)
  • Serotonin syndrome
  • Drowsiness (driving)
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7
Q

What are the three effect of Serotonin syndrome

A
o	Neuromuscular (drowsiness , confusion , convulsion
o	Altered mental state (confusion, agitation, mania) 
o	Autonomic dysfunction (liable BP, Urination , Diarrhoea , Hyperthermia
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8
Q

When switching between antidepressants how long is the waiting time + exception
MOAIs :
SSR1s:
TCAs:

A
  • MOAIs : 2 weeks before switching
  • SSR1s: One week before switching
    o 2 wks If sertraline
    o 5 wks if fluoxetine
  • TCAs: Wait 1-2 weeks before switching
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9
Q

How long should depression medication be withdrawn over

A

Reduced over 4 wks

6 months if long term use

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10
Q

Risk of withdraw increased with medication treatment over how long?

A

8 weeks

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11
Q

When do withdrawal symptoms of antidepressant occur

A

After 5 days

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12
Q

Which antidepressants have the highest risk of withdrawal

A
  • Paroxetine

- Venlafaxine

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13
Q

SSRIs MOA

A

Inhibit the reuptake of 5-HT from synaptic cleft

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14
Q

Examples of SSR1s

A

Citalopram
Esocitalopram (QT prolongation)
Fluoxetine (only one licensed in children)
Paroxetine (high risk of withdrawal)
Sertraline (safest and can be used in MI)

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15
Q

Side effects of SSRIs GASH

A
G = GI 
A = Appetite or weight disturbances 
S = Serotonin syndrome 
H = Hypersensitivity reaction 
-	Bleeding risk 
-	QT prolongation 
-	Seizure
-	Movement disorder (dyskinesia)
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16
Q

Overdose symptoms of SSRIs

A

Nausea + Vomiting , Agitation , tremor, Nystagmas , Drowsiness , Sinus tachycardia, Convulsions

17
Q

Interaction of SSRIs

A
  • Grapefruit juice
  • Increase risk of bleeding (NSAIDs/Anticoagulants/ Antiplatelet)
  • Increase risk of QT prolongation
  • Hyponatermia (Loop / thiazide diuretics / Desmopressin )
  • Serotonin syndrome (st johns wart / Sumatriptan / Tramadol / TCA / MOAis)
18
Q

Tricyclic antidepressants

- Which one is sedating

A

Amitriptyline

19
Q

Tricyclic antidepressants

- Which one is NOT sedating

A

Nortriptyline

20
Q

Side effects (TCAs)

A
T= Toxic in overdose
C= Cardiac side effects (QT prolongation / Arrhythmias / Heart Block / Hypertension) 
A = Antimuscarinic side effects 
S = Seizures 
  • Can cause hallucinations and mania
21
Q

Interaction which with drug classes of TCA

A
Increase plasma concentration 
Decrease plasma concentration 
Antimuscarinic
Serotonin syndrome 
Hyponatremia 
QT prolongation 
Hypotension
22
Q

MOAIs MOA

A

Block monoamine oxidase enzyme which leads to accumulation of monoamines.

23
Q

Examples of MOA’s

A

Irreversible MOAs

  • Phenelazine
  • Isocarboxazid
  • Tranycypromine

Reversible MOAIs
- Moclobemide (short acting / no washout period)

24
Q

Side effects of MOA’s

A

Hepatotoxic
Hypertensive crisis
Postural hypertension

25
Q

Interaction of MOA’s

A

Hypertensive crisis

26
Q

Patient counselling of MOA’s

A

Avoid tyramine rich food
Eat only fresh food
Avoid alcohol