droperidol Flashcards
what type of medication is it
class 1 antipsychotic
droperidol is low potency meaning
it dose not attach as tightly to the dopamine 2 (D2) receptor as high potency ones, leading to a-adrenergic, cholinergic and histamine effects as well as dopamine receptors begin impacted
impact of droperidol in Alpha receptors
blocks A receptors leading to postural hypotension,
cholinergic effects of dreperidol
blocks muscarinic receptors causing dry mouth, blurred vision and difficulty with urination and constipation
block of histamine receptors caused by droperidol leads too
sedative effect
patients at risk of developing a prolonged QT interval from droperidol include…..
CHF, bradycardia, use of diuretics, use of other sedative
antiemetic effect of droperidol occurs due too
blockage of dopamine receptor stimulation in the chemoreceptor trigger zone of the brain
guideline mechanism of action
Droperidol blocks dopamine and alpha receptors centrally, resulting in sedation, reduced agitation and a state of mental detachment, and antiemetic action.
Indications
Patients aged greater than or equal to 12 years with acute behavioural disturbance causing a mild to moderate risk to safety, when olanzapine has not been administered or is ineffective.
Moderate to severe pain associated with one of the following, despite opiate analgesia, and ketamine is not appropriate:
Chronic or complex pain.
Chronic use of opiates.
Severe headache.
Severe pain associated with agitation.
Pain associated with severe nausea and/or vomiting.
Management of agitation or pain that does not respond to an opiate during end of life care.
Nausea and/or vomiting that persists despite ondansetron, or where motion sickness is a component of the patient’s nausea and/or vomiting
contraindications
Known severe allergy.
Aged less than 12 years.
Pregnancy (analgesia and nausea and/or vomiting only).
cautions
Altered level of consciousness. This will increase and prolong the effects.
Parkinson’s disease. There is a risk of worsening the movement disorder associated with Parkinson’s disease.
Concurrent administration of ketamine or midazolam. This will increase and prolong the effects.
Aged greater than or equal to 75 years, particularly if frail. The effects of droperidol will be increased and prolonged in this cohort.
Signs of shock. Droperidol may make shock worse.
use in pregnancy?
The likelihood of a pregnant or breastfeeding patient requiring droperidol for acute behavioural disturbance is very low, however the balance of risk is such that it should be administered if indicated in this context.
In the context of analgesia and nausea and/or vomiting, the balance of risk is not in favour of administration of droperidol and therefore is contraindicated.
dosage for analgesia
1.25 mg IV for an adult, once only. Consider reducing the dose to 0.625 mg IV if a caution is present.
dosage for acute behavioral disturbance
10 mg IV or IM.
Consider reducing the dose to 5 mg if a caution is present.
The dose may be repeated once after 20 minutes.
dose for end of life care
2.5 mg IV/IM/SC.
The dose may be repeated as required.