PT SAFETY IN MENTAL HEALTH Flashcards

1
Q

switching/cross titration

A

occurs when no response seen or intolerable side effects

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2
Q

discontinuation (withdrawal) effects

A

electric shocks
flu like symptoms
disturbed sleep
GI issues
ataxia/sensory vasomotor

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3
Q

serotonin syndrome

A

caused by too much serotonin in the synapses of the brain
likely during augmentation, or when treating resistant depression

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4
Q

3 main symptoms of serotonin syndrome

A

neuromuscular hyperactivity/abnormality (tremor, clonus, rigidity)

autonomic dysfunction/instability (tachycardia, hyperthermia, cold sweats)

altered mental state (agitation, confusion)

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5
Q

drugs that increase likeliness of developing serotonin syndrome

A

triptans
synthetic cannabinoids
tramadol
hallucinogens

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6
Q

safety issues with lithium

A
  • lithium has a narrow therapeutic index, with a high potential for toxicity and therefore careful monitoring is required
  • can interchange with sodium and potassium levels in the body, if dehydrated then lithium ions can get reabsorbed instead of the sodium (toxicity)
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7
Q

NSAIDs and lithium

A

NSAIDs reduce the renal excretion of lithium via their action on renal prostaglandins, resulting in increased plasma lithium levels

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8
Q

safety issues with antipsychotics

A
  • metabolic syndrome
  • thromboemoblism
  • myocarditis/cardiomyopathy
  • QTC elongation (arrhythmias, sudden death)
  • higher risk of seizures
  • neuroleptic malignant syndrome
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9
Q

high dose antipsychotic therapy (HDAT)

A

defined as either a total daily dose of a single antipsychotic which exceeds the max limit stated in the BNF or a total daily dose of two ore more antipsychotics which exceed the BNF max

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10
Q

when/why does HDAT happen?

A
  1. acute psychotic episode (switching)
  2. relapse prevention/poor concordance
  3. acute disturbance/emergency tranquillisation
  4. treatment resistance/refractory
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11
Q

why are some patients on both the depot and oral

A

poor concordance
ensures some of the drug is taken

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12
Q

monitoring parameters in antipsychotics

A

baseline tests and every 3 months
- ECG
- pulse/HR
- BP
- Temp.
- FBC
- LFTs/U and Es
- electrolytes associated with homeostasis (Ca, Mg etc.)

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13
Q

dangerous side effects of clozapine

A

agranulocytosis
neutropenia

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14
Q

when to prescribe clozapine

A

trial of 2 other antipsychotics for 6-8 weeks before clozapine

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15
Q

clozapine dispensing arrangements

A
  • pt must have valid blood test before supply
  • NO BLOOD = NO DRUG
  • regular monitoring of WBCs, esp. neutrophils
  • neutrophil count coded red, amber and green
  • medication supplied when green, discontinue on red
  • more likely to be neutropenic at the beginning of treatment
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16
Q

clozapine blood testing intervals

A

0-18 weeks = weekly bloods
next 18 weeks = fortnightly
thereafter = monthly

17
Q

titrating clozapine

A

gradual titration of dose starting from 25mg daily up to 900mg (max), however break in treatment >48 hours, must re-titrate from starting dose (25mg)

18
Q

clozapine specific safety issues

A
  • red/amber result (no supply)
  • management of leukopenia/agranulocytosis
  • missed doses (>48 hrs)
  • CYP induction/inhibition
  • co-prescribing (esp. other neutropenic drugs)
  • other medicines via GP10 Rx or depot (diff. supply routes)
19
Q

how to withdraw or stop BZs

A

need to convert BZ dose to ‘diazepam dose equivalents’

gradual reduction by 1/8th or 1/6th of total daily dose every fortnight - over 6 months (depending on symptoms)

20
Q

inappropriate use of psychotropic drugs

A
  1. incorrect diagnosis/co-morbidity of personality disorder
  2. to provide relief or sedation in heightened state
  3. high doses/combination therapy (adverse effects)
  4. patient group/status (elderly, pregnant/breast feeding)