Psychopharmacology Flashcards

1
Q

What basis is selection of antidepressants based upon?

A

Generally no difference in efficacy so based on: -Any past history of response -Side effect profile -Coexisting medical conditions

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

How long does it take for symptoms to improve when an antidepressant is diagnosed? What should be done if symptoms do not improve?

A

Delay of 3-6 weeks after a therapeutic dose is reached before symptoms improve. If no improvement is seen after prescription of an adequate dose for at least two months then the treatment should be switched to another agent or augmented with one

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

What are the classes of antidepressant?

A

Tricyclics (TCAs) Monoamine Oxidase Inhibitors (MAOIs) Selective Serotonin Reuptake Inhibitors (SSRIs) Serotonin/Noradrenaline Reuptake Inhibitors (SNRIs) Novel antidepressants

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

What is the mechanism behind tertiary TCAs?

A

Act on serotonin receptors

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

What are the side effects of tertiary TCAs?

A

Antihistaminic Anticholinergic Antiadrenergic QT lengthening

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are some examples of tertiary TCAs?

A

Amitriptyline Clomipramine Imipramine Doxepin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

When should tertiary TCAs be avoided and why?

A

In high risk suicide patients as they can be taken in overdose

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

What is the mechanism behind secondary TCAs?

A

Block noradrenaline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the side effects of secondary TCAs?

A

Similar to tertiary TCAs but less severe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are some examples of secondary TCAs?

A

Desipramine Nortriptyline

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

What is the mechanism behind monoamine oxidase inhibtors?

A

Binds irreversibly to monoamine oxidase, preventing inactivation of amines (norepinephrine, dopamine, serotonin) and so increases synaptic levels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the side effects of monoamine oxidase inhibitors?

A

Antiadrenergic side effects Antihistaminic side effects Dry mouth Sleep disturbance Hypertensive crisis if eating tyramine rich foods (cheese, red wine, processed meats, beans) Serotonin syndrome (more info below) can develop if also taking meds that increase serotonin/have sympathomimetic actions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are some examples of monoamine oxidase inhibitors?

A

Phenelzine Tranylcypromine Selegiline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

In what situation is a monoamine oxidase inhibitor most effective?

A

Treatment resistant depression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What mechanism is behind selective serotonin reuptake inhibitors?

A

Blocks presynaptic serotonin uptake

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the side effects of selective serotonin reuptake inhibitors?

A

GI upset (most often nausea) Sexual dysfunction (most common reason for discontinuation by patient) Anxiety Restlessness Nervousness Insomnia Fatigue/sedation Dizziness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What are some examples of selective serotonin reuptake inhibitors?

A

Paroxetine Sertraline Fluoxetine Citalopram Escitalopram Fluvoxamine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What are the symptoms of SSRI discontinuation syndrome?

A

Agitation Nausea Disequilibrium Dysphoria Usually lasts 7-10 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is the mechanism behind serotonin/norepinephrine reuptake inhibitors (SNRIs)?

A

Inhibits both serotonin and noradrenergic reuptake like TCAs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What are some examples of SNRIs?

A

Venlafaxine Duloxetine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What are the possible uses of SNRIs?

A

Depression Anxiety Neuropathic pain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What is the mechanism behind mirtazapine?

A

Different mechanism of action may provide good augmentation for SSRIs Can be used as hypnotic at lower doses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What are the side effects of mirtazapine?

A

Increases serum cholesterol Sedative at low doses Weight gain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What are the side effects of buproprion?

A

Seizure risk at high doses Anxiety Agitation Insomnia Psychotic side effects at high doses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What are the contraindications of buproprion?

A

Traumatic brain injury Bulimia Anorexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What are the symptoms of serotonin syndrome?

A

Abdominal pain Diarrhoea Sweats Tachycardia Hypertension Myoclonus Irritability Delirium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

What are the potential complications of serotonin syndrome?

A

Hyperpyrexia Cardiovascular shock Death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

How is serotonin syndrome prevented?

A

Wait for two weeks when switching from an SSRI to an MAOI, with the exception of fluoxetine where you need to wait for five weeks due to the long half-life

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

What is activation syndrome and when does it occur?

A

Activation syndrome occurs when serotonin increases in the brain and can cause nausea and increased levels of anxiety. Usually goes away after a few days of prescription but can be prolonged.

30
Q

How is antidepressant prophylaxis given?

A

Following first episode- 6 months prophylaxis Following second episode- 2 years prophylaxis Following third episode- lifelong prophylaxis

31
Q

How is treatment resistant depression managed?

A

Generally- change SSRI to SNRI then add to SNRI Combination of antidepressants Adjunctive treatment with lithium Adjunctive treatment with atypical antipsychotic (Quetipaine, olanzapine, aripiprazole) Electroconvulsive therapy

32
Q

What are the possible indications for mood stabilisers?

A

Bipolar disorder Cyclothymia Schizoaffective disorder

33
Q

What are the classes of mood stabilisers?

A

Lithium Anticonvulsants Antipsychotics

34
Q

In what situations is lithium helpful?

A

Only medication to reduce suicide rate Effective in long term prophylaxis of depressive and manic episodes

35
Q

What factors predict a good response to lithium?

A

Prior long-term response or family member with good response Classic pure mania Mania is followed by depression

36
Q

What monitoring should be done with a lithium prescription?

A

Before lithium is started a baseline Us&Es and TSH should be done, as well as a pregnancy test in women of child bearing age. Lithium can cause Ebstein’s anomaly is prescribed during the first trimester and is nephrotoxic and can cause hypothyroidism. The goal blood level is 0.6-1.2, which can be achieved after five days and should be checked 12 hours after the last dose at this point. Levels should be checked at 3 months and creatinine and TSH checked at 6 months.

37
Q

What are the side effects of lithium?

A

GI distress- reduced appetite, N&V, diarrhea Thyroid abnormalities Nonsignificant leukocytosis Polyuria/polydipsia secondary to ADH antagonism (can cause interstitial renal fibrosis, hair loss and acne in small number of patients) Reduces seizure threshold Cognitive slowing Intention tremor

38
Q

What blood levels define each type of lithium toxicity?

A

Mild = 1.5-2.0 Moderate = 2.0-2.5 Severe = >2.5

39
Q

What are the symptoms of mild lithium toxicity?

A

Vomiting Diarrhea Ataxia Dizziness Slurred speech Nystagmus

40
Q

What are the symptoms of moderate lithium toxicity?

A

Nausea Vomiting Anorexia Blurred vision Clonic limb movements Convulsions Delirium Syncope

41
Q

What are the symptoms of severe lithium toxicity?

A

Generalised convulsions Oliguria Renal failure

42
Q

What factors predict a good response to valproic acid?

A

Rapid cycling patients (female>male) Comorbid substance issues Mixed patients Patients with comorbid anxiety disorders Good in mania prophylaxis but not so good in depressive prophylaxis

43
Q

What monitoring should be done with a valproic acid prescription?

A

Before the medication is started baseline LFTs, FBC and a pregnancy test are done. The drug is generally not started in anyone of child bearing age, but a folic acid supplement should be given if it is started in women. A steady state is achieved after 4-5 days and levels should be checked 12 hours after this dose. LFTs should also be repeated at this point. The target level is 50-125

44
Q

What are the side effects of valproic acid?

A

Thrombocytopenia and platelet dysfunction N&V Weight gain Sedation Tremor Hair loss Risk of neural tube defect in pregnancy

45
Q

What are the uses of carbamazepine?

A

First line medication for patients with acute mania and mania prophylaxis. It is indicated in rapid cyclers and mixed patients

46
Q

What monitoring is required with a carbamazepine prescription?

A

Baseline LFTs, FBC and an ECG Check levels after reaching therapeutic doses- five days later and then again at a month

47
Q

What are the side effects of carbamazepine?

A

Rash (most common side effect) N&V Diarrhoea Sedation, dizziness, ataxia and confusion AV conduction delays Aplastic anemia and agranulocytosis Water retention Drug-drug interactions (many contraindications)

48
Q

What are the side effects of lamotrigine?

A

N&V Sedation, dizziness, ataxia and confusion Toxic epidermal necrolysis/steven johnsons syndrome (if ANY rash develops- stop drug) Blood dyscrasias (rare) Valproate doubles concentration

49
Q

What antipsychotics can be used in manic patients?

A

Aripiprazole Risperdone Quetiapine Quetiapine XR Olanzapine

50
Q

What antipsychotics can be used in mixed patients?

A

Aripiprazole Risperdone Olanzapine

51
Q

What antipsychotics can be used in maintenance situations?

A

Aripiprazole Quetiapine Quetiapine XR Olanzapine

52
Q

What antipsychotics can be used in depressed patients?

A

Quetiapine XR

53
Q

What are the possible indications for antipsychotics?

A

Schizophrenia Schizoaffective disorder Bipolar disorder Psychotic depression Augmenting agent in treatment resistant anxiety

54
Q

What are the characteristics of typical antipsychotics?

A

D2 dopamine receptor antagonists Extrapyramidal side effects common Can be split into low potency and high affinity Low potency: Interact with nondopaminergic receptors, causing cardiotoxic and anticholinergic side effects High potency: Higher risk of extrapyramidal side effects due to high affinity for D2 receptors

55
Q

What are some examples of low and high potency typical antipsychotics?

A

Low potency- chlorpromazine, thioridazine High potency- fluphenazine, haloperidol, pimozide

56
Q

What are the characteristics of atypical antipsychotics?

A

Serotonin-dopamine 2 antagonists Don’t get extrapyramidal side effects but do cause weight gain

57
Q

What are some examples of atypical antipsychotics?

A

Risperidone Olanzapine Quetiapine Aripiprazole Clozapine

58
Q

What treatments can be given in antipsychotic resistant patients?

A

Clozapine If clozapine fails: -Add another antipsychotic -Add lithium/anticonvulsant -ECT

59
Q

What additional measures are required with a clozapine prescription?

A

Due to the risk of agranulocytosis it is required that patients on clozapine have weekly blood tests for the first six months of prescription followed by fortnightly blood tests for the next six months

60
Q

How long should prophylaxis be given after a schizophrenic episode?

A

Lifelong prophylaxis required

61
Q

What are the potential serious adverse events that are associated with antipsychotics?

A

Tardive dyskinesia Neuroleptic malignant syndrome Extrapyramidal side effects- acute dystonia, parkinsonism syndrome, akathisia

62
Q

What drugs can be given to reduce extrapyramidal side effects?

A

Anticholinergics (benztropine etc) Dopamine facilitators (Amantadine) Beta-blockers (propranolol)

63
Q

What is akathisia?

A

Characterised by a feeling of inner restlessness and inability to stay still and is associated with an increased risk of suicide

64
Q

What are the indications for anxiolytics?

A

Panic disorder Generalised anxiety disorder Substance-related disorders Insomnias and parasomnias Often used in conjunction with SSRIs/SNRIs in anxiety disorders

65
Q

What are the key anxiolytics?

A

Buspirone and benzodiazapines

66
Q

What are the pros and cons of buspirone?

A

Pros- no sedation and it works independent of exogenous serotonin Cons- it takes around two weeks to work and it will not work if patients are used to benzodiazapines

67
Q

What can benzodiazapines be used to treat?

A

Insomnias Parasomnias Anxiety disorders CNS withdrawal states

68
Q

What are the side effects of benzodiazapines?

A

Somnolence Cognitive deficits Amnesia Disinhibition Tolerance Dependence

69
Q

What are some examples of benzodiazapines?

A

Diazepam Temazepam Alprazolam (Xanax) Lorazepam

70
Q

What are the antihistaminic side effects?

A

Sedation Weight gain

71
Q

What are the anticholinergic side effects?

A

Dry mouth Dry eyes Constipation Memory deficits Delirium

72
Q

What are the antiadrenergic side effects?

A

Orthostatic hypertension Sexual dysfunction Sedation