Psychopharmacology Flashcards

1
Q

What are the principles of psychiatric treatment?

A

Bio Psycho Social model
Combinations more effective
Social interventions important

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2
Q

Name some antipsychotic drugs

A
First gen (typical)
- chlorpromazine, haloperidol, sulpride
Second gen (atypical)
- clozapine, lurasidone, olanzapine, risperidole
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3
Q

What are the main effects of antipsychotics?

A

Sedation, anti-cholinergic, extrapyramidal, hypotensive

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4
Q

What is the MOA of antipsychotics?

A

Block dopamine receptors - D2 receptors (+ histamine, ACh, 5-HT)

  • blockade of mesolimbic + mesocortical pathways gives anti-psychotic effects
  • blockade of nigrostriatal gives motor side effects
  • Takes a few weeks to become effective
  • Control positive symptoms (e.g. delusions, hallucinations), but not the negative symptoms (e.g. social isolation, low mood)
  • Atypicals could help with negative symptoms
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5
Q

What are the clinical effects of antipsychotics?

A

Depression of emotional responses - delusions, thought disorders, perception problems
Sedation - confusion + restlessness
Antiemetic - vomiting
Antihistamine - allergies

Atypical better compliance due to less side effects

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6
Q

What are the clinical indications for use of antipsychotics?

A

Mainly schizophrenia + acute behavioural disturbances

Can be used as adjuvants in other psychiatric conditions e.g. mania, psychotic depression

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7
Q

What are the pharmacokinetics?

A

Extensive first pass metabolism
Eliminated by liver metabolism
Given orally or IM injection

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8
Q

What are the adverse effects of antipsychotics?

A

Mediated by nigrostriatal pathway

  • motor symptoms
  • acute dystonia, Parkinsonism, akathisia, tardive dyskinesia (after months/years of use)

These effects are less prominent with atypical antipsychotics + do not occur with clozapine

Mediated by tuberoinfundibular system

  • prolactin elevation
  • galactorrhoea, gynaecomastia, amenorrhoea, impotence
  • less common with atypical

Mediated by other receptors

  • metabolic side effects
  • more common with atypical
  • weight gain, dyslipidaemia, T2D, increased risk of seizures
  • rarely neuroleptic malignant syndrome which can cause death
    (signs: fever, rigidity, hypertension, sweating, urinary incontinence, altered concsiousness)
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9
Q

What are the types of antidepressants?

A

SSRIS, SNRIs, NASSAs, MAOIs, TCAs

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10
Q

What is the MOA of SSRIs?

A

Reduce neuronal reuptake of serotonin

  • initial increase in serotonin conc, and onset of action delayed for a couple weeks
  • increase BDNF + stimulates neurogenesis, moderates limbic system to reduce negative cognitive bias, increases serotinergic transmission
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11
Q

What are the pharmacokinetic properties of SSRIs?

A
  • Well absorbed from gut
  • Should be taken in morning to avoid sleep disturbance
  • Paroxetine + fluoxetine should not be used in conjunction with TCAs due to toxicity
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12
Q

What are the adverse effects of SSRIs?

A

Increased anxiousness, emotional numbness, headache, nausea, weight loss/weight gain, vomiting, insomnia
- small increased risk of suicidal thoughts esp. in children

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13
Q

What is the MOA of benzodiazepines?

A

Type of anxiolytics to treat anxiety

  • agonist at GABA-A receptor on separate site from GABA binding site
  • increase affinity for GABA - enhance inhibitory effect
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14
Q

Give examples of benzodiazepines.

A

Lorazepam, diazepam, alprazolam, clonazepam

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15
Q

What are the clinical uses of benzodiazepines?

A

Anxiolytics, hypnotic, muscle relaxant, anti-convulsant, amnestic

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16
Q

What are the side effects of benzodiazepines?

A

Headaches, confusion, ataxia, dysarthria, blurred vision

  • paradoxical reaction (at risk: children, learning disability, CNS disorder)
  • overdose dangerous in comb. with alcohol
17
Q

What other drugs act on the GABA receptor?

A

Z-drugs
Barbiturates (amobarbital, phenobarbital)
Flumazenil (antagonist)
Alcohol

18
Q

What are barbiturates used for?

A

Rarely used now

  • only in severe insomnia, epilepsy, anaesthesia
  • highly addictive, dangerous in od
19
Q

What is flumazenil used for?

A

Competitive antagonist in benzodiazepine binding site

  • can treat overdose
  • rapid onset of action but short half-life so needs repeated doses
  • no effect on barbiturates as they bind to different site
  • should not be used in epilepsy as abrupt withdrawal of benzos can cause seizure