Mood disorders Flashcards

1
Q

Name some examples of mood disorders

A
  • manic episode
  • bipolar affective disorder (BPAD)
  • depressive episode
  • recurrent depressive disorder
  • other mood disorders: cyclothymia and dysthymia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

3 main domains of treatment options for mood disorders (in general)

A

Biological: Medications such as antidepressants and mood

stabilisers, but can include ECT as a last line treatment

Psychological: Talking therapies, CBT, Mindfulness, Counselling, keeping Mood Diaries, Family Work

Social: All manner of social support depending on what social problems the mood disorder has contributed to – financial support, housing support, family work, employment, re-housing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Mnemonic for clinical features of depression

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Management of depression

A
  • Bio: SSRIs are first line, but other anti-depressive medication is used – SNRIs/TCAs/NaSSA – very rarely MAOIs
  • Psycho: CBT, Mindfulness, Counselling, Psychotherapy can all help
  • Social: depends on the individual but help with financial problems, housing issues, employment, family problems etc
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Aetiology for maniac phase of bipolar disorder

A

Trigger factors for inducing a manic phase can be a mixture of events:

  • stress
  • over excitement
  • using ‘stimulant’ substances such as amphetamines, cocaine and caffeine
  • while using anti-depressants for depressive episode
  • It can occur idiopathically in people who are predisposed to changes in mood
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What to be aware of/careful about while treating a depressive episode in a person with the bipolar affective disorder?

A
  • if someone with BPAD is recovering from a depressive episode using antidepressant medication → monitor this closely
  • the mood-elevating properties of the medication → potential to trigger a manic episode
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Mnemonic for features of mania

A

People who would DIG FAST

DDistracted (unable to concentrate)

I Irritable and Increased energy

G Grandiose ideas (if deluded a common delusion)

F Flight of Ideas (thoughts jump from topic to topic)

A Accelerated behaviour

S Spending and Sex (spending sprees and increased libido common)

T Talkative (Pressure of speech and logorrhea = “talkativeness”)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Are talking therapies effective for a person in a maniac phase?

A
  • highly likely → no insight and in high risk → hospitalization, often under the MHA is common
  • it’s difficult to rationally converse with someone who is manic → talking therapies are usually ineffective at this stage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Management of Manic phase

A
  • usually hospitalisation under MHA (due to lack of insight during manic episode)
  • Bio: Antipsychotic medication and benzodiazepines are first-line (known as rapid tranquillisation), a mixture of Haloperidol (AP) and Lorazepam (BZD) are given, usually as IM injection until the person is calmer and less agitated/energized
  • Psycho/Social: Risk Assessment and risk management is essential. Family support and ensuring the person doesn’t have access to credit cards/car keys etc in a manic state
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Types of Bipolar Affective Disorder

A

DSM (The American Psychiatric Association classification system):

  • Type I → Classic ‘manic-depression’ episodes of mania and depression
  • Type II → More frequent episodes of depression are reported and elevated mood is hypomania (so not full manic phases)
  • Rapid Cycling → 4 or more episodes of mania or depression are experienced in a 12 month period

*ICD just have Bipolar as a classification, with specific current types i.e. mania/depressed/in remission etc

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Biological management of Bipolar Affective Disorder

A

Mood Stabilisers → first line

There are 3 different classes of medication that have mood-stabilizing properties.

  • Lithium: sedating and mood stabilising effects. Lithium Carbonate is the most commonly used type
  • Anticonvulsants: Sodium Valproate, Carbamazepine and Lamotrigine all have mood stabilising properties
  • Atypical Antipsychotics: Olanzapine, Quetiapine and other Atypicals are used for mood stabilising effects as well as being used as antipsychotics
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Psycho-social management of Bipolar Affective Disorder

A
  • Psycho: CBT; Keeping mood diaries is very helpful as it can help people and their family record mood changes so hopefully detect the future onset of depression/mania, so hopefully receive help quickly before the change in mood escalates/deteriorates into a major problem
  • Social: Would depend on the individual but highly likely to include help with financial problems, housing issues, employment and the social fallout of behaviours undertaken when depressed or manic.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What’s cyclothymia?

A
  • milder, less severe form of bipolar disorder
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Aetiology of cyclothymia

A
  • Unknown
  • It is probably part of a spectrum of mood disorders such as bipolar and depression – so the factors that contribute to those conditions will also contribute to cyclothymia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Clinical features of cyclothymia

A
  • may start in early life
  • the key diagnostic criteria: the mood variations are not severe or prolonged enough to warrant a diagnosis of BPAD or recurrent depressive disorders
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What’s dysthymia?

A
  • a chronic depression of mood which
  • does not currently fulfil the criteria for recurrent depressive disorder, mild, moderate or severe
  • usually have periods of days or weeks when they describe themselves as well, but most of the time (often for months or years) they feel tired and depressed
  • can normally cope with the basic demands of life (which is why this isn’t classed as mild depression) but describe feeling mostly unhappy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Aetiology and treatment of dysthymia

A
  • the same as for depression
  • combination of medication and talking therapy → SSRI/CBT probably the most effective
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Citalopram

  • monitoring
  • the worst SEs
A

Citalopram → SSRI

  • ECG needed
  • the worst in terms of QT prolongation
19
Q

Escitalopram

  • use
  • advantages
A

Escitalopram → SSRI

  • best in pure anxiety
  • least drug interactions
  • lower doses needed than others

*but expensive

20
Q

Fluoxetine

  • use
  • advantages
A

Fluoxetine → SSRI

  • long half-life
  • good for adolescents
  • good for OCD/Bulimia

*bad for interactions

21
Q

Paroxetine

SEs

A

Paroxetine → SSRI

  • Enters + leaves system fast – so side effects and withdrawals
  • bad for teratogenic effects
22
Q

Sertraline

  • use
  • advantages
  • main SE
A

Sertraline → SSRI

  • good for anxiety
  • well-tolerated
  • OK for breastfeeding

SE: diarrhoea

23
Q

Duloxetine

  • class
  • use
A

Duloxetine

Class: dual action (5-HT+NA) → SNRI

  • depression
  • anxiety
  • neuropathic painkiller (DM, fibromyalgia)
  • used in stress incontinence
24
Q

Venlafaxine

  • class
  • what group of patients not to use in
A

Venlafaxine

  • worst for CVS
  • don’t use in patients with HTN or bad cardio problems

Class: SNRI → at low doses = mostly 5-HT (like SSRI), higher doses = 5-HT + NA

25
Q

Class of Mirtazapine

A

Mirtazapine - tetracyclic

  • Noradrenergic and specific serotonergic antidepressant (NASSA), a2 on post synaptic that causes increase in: 5-HT, NA
26
Q

Trazodone

  • class
  • SEs
A

Trazodone

Class: tetracyclic → serotonin antagonist and reuptake inhibitor

SEs: drowsiness, priapism

27
Q

Tricyclic anti-depressants

  • names
  • use
  • SEs
A

Names: Amitriptyline, Clomipramine, Imipramine, Doxepin

Use: neuropathic pain, depression, migraine prophylaxis

Bad SEs: arrhythmias, overdose is easy, wide QRS

alpha receptors→ postural hypotension

dopamine → breasts

ACh → dry, constipation, confusion, urine retention

Histamine → drowsy

28
Q

Examples of MAOis

A

Mono Amine Oxidase inhibitors

  • Phenelzine
  • Isocarboxazid
  • Tranylcypromine
  • Selegiline
29
Q

MoA and use of Mono Amine Oxidase inhibitors (MAOi)

A
  • Prevent monoamines (5-HT, NA, dopamine) from being put back into vesicles = keeps them active!
  • MOA - A = Mood. MOAi used in psych act on MOA-A, as its acts on 5-HT & NA mainly (not dopamine).
  • MOA – B = for Mx of Parkinson’s (mostly increase dopamine (e.g. Selegiline)
30
Q

SEs of Mono Amine Oxidase inhibitors

A

Hypertensive crisis →can happen due to a buildup of Tyramine, if Tyramine rich foods are consumed (cheeses, wine, yeast based food, chocolate, oily fish) → therefore patients have to follow a strict diet – so last line of treatment normally

31
Q

Lamotrigine

  • class
  • use
  • SEs (important one to look for)
A

Lamotrigine

Class: anti-epileptic; mood stabiliser

Use: good for bipolar that is mainly depressive (because no GABA action – which is inhibit = for mania). Na+ (not GABA)

SEs: Steven Johnson syndrome (mucosa). Look out for rash early in Tx (<8wks)

Start very low, titrate up

32
Q

Carbamazepine

  • use
  • MoA
  • SEs to be aware of
A

Carbamazepine

Use: trigeminal neuralgia, bipolar affective disorder, seizures

MoA: Na+ channel blocker

SEs:

  • Aplastic anaemia
  • Agranulocytosis!! Enzyme inducer – loads of drug interactions
  • Teratogenic
33
Q

Sodium valproate

MoA

SEs

monitoring

A

Sodium Valproate

Increase of GABA ­(PIP3 pathway) & blockage of Na+

channels

SEs:

  • uses up folate → neural tube defects if taken

during pregnancy (Don’t give in childbearing age)

  • Hepatotoxicity
  • Weight gain
  • Interaction with aspirin and warfarin

Monitoring: Baseline LFT needed

34
Q

Risperidone

  • Class
  • MoA
  • SEs
A

Risperidone

Class: atypical antipsychotic

MOA: D2 – dopamine antagonist and 5HT antagonist

SEs:

  • metabolic syndrome
  • weight gain
  • Prolactin ­ → sexual dysfunction, galactorrhoea, gynecomastia (worst antipysch for this)

*Not as sedating as other antipsychotics.

35
Q

Aripiprazole

  • class
  • MoA
  • SE
  • extra info (2)
A

Aripiprazole

Class: atypical antipsychotic

MoA: Partial D2 and 5HT2A antagonist

SE: Hypersalivation

  • Slow to start working!
  • Only one that has partial D2 action → so it doesn’t cause metabolic syndrome
36
Q

What antipsychotics (2) are frequently used as adjunctive treatment?

A

Olanzapine and Quetiapine used frequently either alone or as adjunctive treatments

  • Both are atypical antipsychotics
  • Quetiapine → sedating
  • Olanzapine → bad for weight gain
37
Q

Examples of Lithium Salts (2)

A
  • Lithium carbonate
  • Lithium Citrate
38
Q

SEs of Lithium salts

A
  • tremor
  • nephrotoxicity– causes dehydration (damages kidney which reduces filtration, pee more). When dehydrated = increased levels → toxicity
  • Polyuria
  • Polydipsia
  • hypOthryoid → features of hypothyroid are depression, so consider this in low mood in people taking lithium
  • Epstein anomaly and tricuspid valve anomaly (congenital if pregnant on lithium)
  • QT prolongation – careful with SSRI
  • Metallic taste
39
Q

Therapeutic index of lithium

A

Narrow therapeutic index

0.4-1.0 mm/l

40
Q

What meds to avoid when taking lithium as they may contribute to lithium toxicity?

A
  • NSAID
  • ACEi
  • Diuretic (thiazide worst)
  • SSRI
41
Q

Lithium toxicity

  • levels of lithium
  • clinical features/presentaiton
A

Toxicity when levels >1.5

  • GI features (N+V)
  • CNS (ataxia, weakness, slurred speech, seizures, death)
42
Q

What affects lithium levels?

A

Levels affected by:

Na+ + hydration (renal function) keep hydrated

43
Q

Monitoring of lithium

A
  • Measure serum Lithium levels 12 hrs after dose (trough levels)
  • Weekly at the start until steady levels

3/12 → serum Li

6/12 → TFT, U&E