Biological Therapy Flashcards

1
Q

Typical Vs Atypical APs

A

TAP
= around since 1950s
E.g. chlorpromazine

AAP
= around since 1970s, aim of development was to maintain/improve effectiveness but minimise side effects
E.g. clozapine, risperidone

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2
Q

Administration & dosage of chlorpromazine

A

Tablets, syrup, injection
400-800mg
Orally = max. dose of 1000mg

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3
Q

How do TAPs work

A

Dopamine antagonists
- block DA receptors in brain synapses = reduce DA action
Initial taking of TAP = increase DA levels, but then decrease
= normalises neurotransmission in key brain areas
= reduce symptoms like hallucinations

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4
Q

Sedation effect of chlorpromazine

A

Believed to be due to effect on histamine receptors
- often used to calm individuals, not only SZPNics
- e.g. done when patients first admitted to hospitals & very anxious

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5
Q

How does Clozapine work

A
  • same as TAPs, DA antagonist
    + act on serotonin and glutamate receptors
    = believed this helps improve mood, & reduce depression/anxiety, may also improve cognitive functioning
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6
Q

When may clozapine be prescribed

A

Mood-enhancing effects = sometimes prescribed when individual considered high suicide risk
- 30-50% of SZPNics attempt suicide

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7
Q

Why was risperidone developed, how does it work

A

Attempt to produce drug as effective as clozapine but without serious side effect (agranulacytosis)
- same as clozapine, but bind more strongly to DA = effective in much smaller doses

Evidence to suggests leads to fewer side effects then other APs

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8
Q

Administration and Dosage of clozapine vs risperidone

A

Clozapine
not available as injection
daily dosage = 300-450 mg

Risperidone
all options
daily dosage = 4-8 mg, max 12 mg

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9
Q

Strength of APs for treating SZPN

A

Evidence for effectiveness
= large bodies of evidence supporting T/AAPS being atleast moderatively effective in tackling symptoms
- Thornley at al = data from 13 trails, over 1100 pps, comparing effects of chlorpromazine to control = chlorpromazine associated with better overall functioning and reduced symptom severity compared to placebo

= shows APs work

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10
Q

Weakness of APs for treating SZPN

A

Serious side effects
TAPs = associated with dizziness, agitation, sleepiness, stiff jaw, weight gain, itchy skin
most serious = neuroleptic malignant syndrome
- NMS results in high temp, delirium, coma, can be fatal

AAPs = potential fatal side effects of blood condition ‘agranulacytosis’ (severe lowered white blood cell count)
(clozapine)

= can do harm as well as good, avoidance of them if side effects experienced = makes treatment ineffective

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11
Q

Further weakness of APs for treating SZPN

A

Mechanism Unclear
= do not know how some of them work
- understanding strongly tied up with OG DA hypothesis, which is not complete as it does not include cortical hypodominergia
- if this is true, most APs should not work

= this along with already questioning effectiveness due to side effects = adds to argument of being ineffective

= atleast some APs may not be best opting treatment, other factors may be involved in apparent success

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12
Q

Why can biological therapy be seen as more appropriate than psychological therapy

A

Easy to administer
= simply remember to take required daily dosage
- less physical time and cognitive effort required
- symptoms such as speech poverty = unlikely to work well with CBT
+ no waiting list for therapist
= quicker symptom relief

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13
Q

link between APs and severe side effect of NMS

A

= believed to be caused by drug blocking DA action in hypothalamus (which regulates homeostasis/internal body temp.)

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