Olanzapine is a second generation antipsychotic agent that acts on multiple receptors (incl. serotonin and dopamine receptors), resulting in sedation
Onset of effect usually ~ 10 mins.
Indications
Disturbed and Abnormal Behaviour (RASS 1 ~ 2) where risk to safety is evident and the patient is able to tolerate or self-administer an oral wafer
Preferred first line sedation agent in frail patients and those with Dementia
Contraindications
Known Allergy
Known Parkinsons Disease
< 6 years of age
Precautions / Notes
Sedation of any patient < 16 years of age –should prompt a prior ASMA consult wherever practicable.
Organic causes such as suspected sepsis, traumatic brain injury or spontaneous intra-cranial event must be considered unlikely
‘Agitated or Excited Delirium’, ‘Acute Behavioural Disturbance’ and ‘Drug Induced Psychosis’ are some alternative terms that may be used by other agencies
Effects may be amplified in patients with alcohol intoxication
Oral dispersible tablet may be dissolved in water (may slightly delay onset of action but still preferable in non-emergent cases)
Early monitoring as soon as practicable is required when administering Olanzapine; including SpO2, respiratory rate, pulse and blood pressure
SpO2 and etCO2 monitoring must be applied whenever level of consciousness drops (~RASS < 0)
Management
Adults < 70 years old:
10mg
Repeat once only after 15 mins if indicated to total maximum cumulative dose via all routes 20mg/24hrs.
Adults > 70 years old or frail:
5mg
Repeat once only after 15 mins if indicated to total maximum cumulative dose via all routes 10mg/24hrs.
Paediatric 6 - 15 years old, > 40kg:
5 - 10mg
Repeat once after 15mins if indicated to a total maximum cumulative dose via all routes 20mg/24hrs.
Paediatric < 40kg
ASMA consult required
Special Considerations
Extrapyramidal effects / Dyskinesia
Increased falls risk
Hypotension – Apply monitoring as soon as practicable