Depressive Disorder Flashcards

1
Q

What is a depressive episode

A

An ongoing or periodic episode of low mood, lack of energy and anhedonia.
10-15% of women suffer from post-natal depression within 1-2 months post-partum
10-20% lifetime prevalence for all people. Ratio is M:F of 1:2.

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2
Q

What is dysthymia?

A

Dysthymia = chronic low mood not fulfilling the criteria of depression lasting 2 years either due to severity or due to length of depressive periods.

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3
Q

What are the risk factors for depression?

A
Family History of depressive illness
Major Life changes
Chronic health problems
Substance misuse
Childhood abuse
There are certain genetic associations with Depression.
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4
Q

What are the core symptoms of depression and how many must be present?

A

2 Core symptoms must be present:

Core Symptoms: Continuous low mood for at least 2 weeks, lack of energy and anhedonia.

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5
Q

What are the somatic symptoms of depression?

A

Somatic Symptoms: Sleep changes (specifically early morning waking), appetite and weight loss or gain, diurnal variation in mood (mornings are worse), psychomotor retardation/agitation and loss of libido.

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6
Q

What are the cognitive symptoms of depression?

A

Cognitive Symptoms: Low self-esteem, guilt and self-blame, hopelessness, hypochondrial thoughts, poor attention/concentration, and suicidal thoughts – always ask.

Rumination is a key aspect involved in depression
Always ask about suicide and self-harm

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7
Q

What sort of symptoms do you get in psychotic depression?

A

Psychosis – hallucinations which are often auditory and delusions such as hypochondriacal/guilt/nihilistic and persecutory. In Post-natal depression usually, this involves worries about the baby’s health, their capability as a mother and if they can cope.

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8
Q

What questions should be asked in a detailed risk assessment of someone who has had a suicide attempt or thoughts?

A

If they have revealed suicide attempts or plans you must get a very detailed history.
Start with the day it happened, why did they feel that way, what was different to the day before, had it been planned, how were they going to do it, what did they think would happened and how do they feel about it now?

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9
Q

What are the 4 classifications of depression?

A

Mild – 2 core and 2 others
Moderate – 2 core and 3/4 others
Severe – 3 core and at least 4 others
Severe with Psychotic symptoms

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10
Q

What differentials should be considered in a patient you think has deperssion?

A
Psychiatric disorders – schizophrenia, bi-polar disorder, anorexia nervosa, anxiety 
Substance abuse
Dementia 
Sleep disorders
Physical illness 
Medication SE e.g. beta blockers
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11
Q

What questionnaire can be used by GPs to screen for depression?

A
Patient health questionnaire-9 (PHQ-9) is used by GP's as a tool to characterise severity of depression:
•	0-4 no depression identified
•	5-9 mild depression
•	10-14 moderate depression
•	15-19 moderately severe depression
•	20-27 severe depression
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12
Q

What general advice can be given to help manage/prevent depressive symptoms?

A

Self-help – exercising, eating healthy, engaging in productive activities, socialising, improving sleep relaxation and self-soothing (being kind to yourself)

Avoid – inactivity, drugs, alcohol, daytime TV and isolation.

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13
Q

How are mild, moderate and severe depression managed?

A

Mild depression – focus on holistic interventions such as low intensity psychological interventions on sleep hygiene, anxiety management (mindfulness), guided self help and computerised CBT. If symptoms persist beyond 8 weeks then can trial antidepressants.

Moderate depression – Combination of antidepressant and high intensity psychological intervention such as 8-12 sessions of CBT or interpersonal therapy

Severe depression including psychotic depression and high risk of suicide – rapid intervention with a specialist mental health assessment and consideration of inpatient treatment and ECT. If psychotic then anti-psychotics.

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14
Q

Which team should be contacted if a patient is at high risk of suicide?

A

If suicidal start with the crisis team but the patient must be willing to engage otherwise mental health act assessment would be appropriate.

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15
Q

How is recurrent depression managed?

A

Recurrent depression – very likely after one episode of depression to develop further episodes so maintenance therapy should be started. If a drug worked before use this as maintenance. CBT and psychoeducation can also help.

First line – Fluoxetine, sertraline, or citalopram
Second line – alternative SSRI
Third line – TeCAs, SNRI’s
Fourth line – TCA and lithium can sometimes be helpful as an adjunct

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16
Q

What is the psychotherapy of choice for depression in <18s?

A

Psychoanalysis (treatment of choice in <18s)

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17
Q

What information should be offered to patient before starting antidepressants?

A

Warn that symptoms may get worse in the first few weeks and important to monitor closely for suicidal ideation. Assess formerly after 4 weeks and if effective continue for at least 6 months. Can titrate dose up if only minor response. Discuss discontinuation problems and advice not to stop without consulting a doctor.

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18
Q

What are SSRIs?

A

Inhibit the reuptake of serotonin at the synapse

Fluoxetine
Paroxetine
Sertraline
Citalopram + Escitalopram

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19
Q

What are the side effects of SSRIs?

A

Nausea and diarrhoea, restlessness, agitation, headache, (all of which usually go after a few weeks)
Long term - sexual dysfunction, weight changes (usually loss), bleeding and suicidal ideation (especially young men).

Can precipitate mania in Bi-polar

Associated with hyponatraemia especially in the elderly

1st trimester: congenital heart defects
3rd trimester: pulmonary HTN of new-born

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20
Q

Which specific side effect must you be careful of in citalopram and what precautions should you take as a result?

A

Citalopram lengthens QT interval and can cause torsade’s de pointes so check ECG before.

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21
Q

Are SSRIs safe in overdose?

A

Safe in overdose other than citalopram – only used in lower doses in elderly due to QT risk

22
Q

Which SSRI is safest in heart disease?

A

Sertraline safest in heart disease

23
Q

Which SSRI is the only licensed anti depressant in <18s?

A

Fluoxetine only licensed drug in under 18s but watch out for serotonin syndrome as it lasts a long time in the body.

24
Q

What drugs should be avoided when taking SSRIs?

A

Avoid NSAIDs (consider PPI), warfarin + heparin (use mirtazapine), triptans

25
Q

Can SSRIs be stopped suddenly?

A

Gradually reduce dose over 4 weeks to avoid discontinuation syndrome.

Paroxetine often causes discontinuation syndrome

26
Q

What are TCAs?

A

Serotonin and noradrenaline reuptake inhibitors with muscarinic and alpha 1 adrenoreceptor inhibition

Amitriptyline Imipramine Clomipramine Lofepramine

27
Q

What are the side effects of TCAs?

A

CNS: Sedation, reduced psychomotor performance, lowering of seizure threshold

CVS: tachycardia, postural hypotension, lengthening of QT interval and impaired myocardial contractility

Constipation, urinary retention, reduced secretions (dry mouth) and blurred vision,

28
Q

Are TCAs safe in overdose?

A

More dangerous in overdose due to QTC prolongation and neuropath arrhythmias.

29
Q

What is special about the TCA clomipramine and separately lofepramine ?

A

Clomipramine – predominantly serotonergic activity whilst other TCAs are predominantly noradrenaline.

Lofepramine good in elderly as it has a low level of side effects and is unlike other TCAs

30
Q

What are SNRIs?

A

Serotonin and Nor-adrenaline reuptake inhibitors

Venlafaxine Duloxetine

31
Q

What side effects do SNRIs have?

A

Same as SSRIs but more potential for sedation, nausea and sexual dysfunction.

Also sleep disturbance, increased BP, dry mouth, and hyponatraemia

Caution in heart disease and BP problems if at higher doses.

32
Q

How does the action of SNRIs change at different doses?

A

Lower doses have serotonin action and higher doses noradrenaline action.

33
Q

What are TeCAs?

A

Noradrenergic and specific serotonergic antidepressant which increases release of neurotransmitters by blocking alpha2 adrenoreceptors

Unwanted anti-histamine activity hence side effects of sedation.

Mirtazapine

34
Q

What are the side effects of mirtazepine?

A

Doesn’t cause as many sexual function problems, has anxiolytic properties, stimulates appetite and causes drowsiness.

35
Q

What are MOAIs?

A

Monoamine oxidase inhibitors

MAOIs
Phenelzine, Isocarboxazid, Moclobamide and Tranylycypromine

36
Q

What is the most important side effects of MOAIs to consider?

A

Potential for significant and dangerous interaction with other drugs. Potential for tyramine reaction leading to hypertensive crisis.

Should avoid pickled meats, wine and cheese.

37
Q

Can you change from an MOAI to another antidepressant easily?

A

If changing to another antidepressant need a washout period up to 6 weeks.

38
Q

If an antidepressant has absolutely no benefit at a typical dose should you increase or trial a new one?

A

It is not worth increasing the dose (unless you’re treating anxiety), just switch, if partial benefit then increase the dose.

39
Q

When should patients be reviewed after starting antidepressants?

A

Patients should be reviewed after 2 weeks or after 1 week if under 30yrs or at high risk of suicide.

40
Q

How long should antidepressants be used for?

A

Antidepressants should be used for at least 6 months even after remission as this prevents relapse – they are not addictive, and this is important to stress.

41
Q

How do you change from one antidepressant to another?

A

When changing antidepressant must cross tapper to avoid withdrawal and should consult guidelines for how to do this with different drugs. However, some are contraindicated with each other and may induce serotonin syndrome.

42
Q

What are the symptoms of serotonin syndrome?

A

Cognitive – headaches, agitation, hypomania, confusions, and coma
Autonomic – shivering, sweating, hyperthermia, tachycardia, nausea, and vomiting
Somatic – myoclonus, hyperreflexia, and tremor

43
Q

How is serotonin syndrome managed?

A

Management – stop serotonergic drugs and give supportive with fluids and monitoring

44
Q

What is a discontinuation syndrome?

A

Note discontinuation syndrome is different from withdrawal symptoms as this implies addiction. Discontinuation occurs as a result of the drug not doing what it was previously doing in your body i.e. if a drug has an anticholinergic effect you may expect diarrhoea on withdrawal.

45
Q

What discontinuation syndrome do you get with antidepressants?

A

For most antidepressants there will be a discontinuation syndrome even when tapered.

Increased mood change
Restlessness
Difficulty sleeping
Unsteadiness
Sweating
Gastrointestinal symptoms: pain, cramping, diarrhoea, vomiting
Paraesthesia

Paroxetine and Venlafaxine are the most difficult to stop, sometimes worth switching to fluoxetine.

46
Q

When is ECT useful?

A

Electroconvulsive therapy is a useful treatment option for patients with
• Severe, treatment resistant depression
• Life threatening catatonia
• Moderate depression shown to improve with ECT previously
• Manic episodes
Do not stop current anti-depressant medication but do reduce to the minimum dose

47
Q

When is ECT contraindicated?

A

Contraindications = raised intracranial pressure secondary to SOL, recent MI within the last 3 months, severe hypertension, narcotic intolerance, acute glaucoma, aneurysms and angiomas. Note pregnancy and pacemakers are not contraindications.

48
Q

What are the short and long term side effects of ECT?

A
Short-term side-effects
•	Headache
•	Nausea/Vomiting
•	Short term memory impairment
•	Cardiac arrhythmia
•	Muscle aches from seizures

Long-term side-effects
• Some patients report impaired memory

49
Q

What is seasonal affective disorder?

A

Seasonal affective disorder (SAD) describes depression which occurs predominately around the winter months. SAD should be treated the same way as depression.

50
Q

What is atypical depression?

A

Atypical depression – hypersomnia (lots of poor quality sleep) and increased appetite.