Intravenous Anaesthetic Agents Flashcards
What do IV induction agents do?
They induce loss of consciousness when injected at the start of general anaesthetic.
Do IV induction agents allow rapid recovery?
Yes. They allow rapid recovery from unconsciousness as they are rapidly redistributed. Some could be given intermittently or by infusion for maintenance of anaesthesia.
General pharmacology of Intravenous anaesthetic agents. What are there general classification?
Either rapid loss of consciousness in one arm-brain circulation time +- 30 seconds and those with a slower onset.
Which drugs are true induction agents?
The rapidly acting agents: Propofol, Thiopentone, Ethomidate, Ketamine.
Acronym for rapidly acting induction agents?
KEPT: Patients are KEPT induced faster. Ketamine, Ethomiidate, Propofol, Thiopentone.
Acronym for slower acting agents?
Benzo-pams
Neuro-dols
Opioids-morphine-nyl/nil
What are the advantages of intravenous induction?
- Rapid onset
- Smooth muscle induction
- More pleasant for pt
- Pollution free
(fast, smooth m, pleasant, no smoke.. how sex should be)
What isn’t so nice about IV induction?
- Venepuncture required
- Overdose is easy
- No removal of drugs (compared to inhalation drugs via the lungs) Once its in its in > recovery requires metabolism, redistribution and excretion.
- Sudden loss of normal protective mechanisms and often apnoea.
(the negative of sex: you need to insert something.. may be sore, you could get too much of it, once you get pregnant there’s no way of stopping it have to wait for metabolism and retrisbution and when you climax your protective mechanisms are gone and you can stop breathing.)
Sooo how does IV induction agents work?
Not completely understood but just remember GABA GABA. GABA = inhibitory neurotransmitter.
However> Ketamine is an opioid receptor antagonist (NMDA receptor)
What are the pharmacokinetics of IV agents?
induction starts to end as the agent is resdistributed from the brain to less perfused tissues. i.e rapid awakening is NOT due to metabolism or excretion of the drug.
Why is it not okay to drive after IV induction?
Because subclinical levels of the drug still persists in the brain. so wait 24-48 hours before operating heavy machinery/ making decisions.
Metabolism and excretion of IV agents?
Lipid-soluble drugs are metabolised in the liver to inactive water-soluble metabolites then excreted in the urine.
What is TIVA?
Total Intravenous Anaesthesia. No inhalation agents are used during induction or maintenance.
What is TCI?
Target controlled Infusion. A microprocessor-controlled syringe pump automatically and variably controls the rate of infusion of a drug to attain the anaesthetic-defined target level in the plasma or an effect site.
Propofol = most common IV induction
Describe Propofol. (Physical properties, PK, PD, Organ effects, recommendations)
Key words: 10mg/ml; fatty, rapid emergence, younger pts require more, older patients require less.
Physical properties: insoluble in water, fatty (use within 6hrs of opening otherwise culture medium eew), Ampoule sizes 20ml, 50ml, 100ml (each contain 10mg/ml Propofol)
PK: Unique therefore: good for induction, maintenance and sedation. highly fat soluble.
PD: Induction: children: 2.5-3mg/kg. adults: 1,5 - 2.5 mg/kg. old: 1-1.5mg/kg
Maintenance: TIVA: 6-12mg/kg/hr. Used wiyh N20 and opiods> reduce.
TCI: inductio 4-8ug/ml & maintenance 3-6ug/ml
Sedation: 1.5 mg/kg/hr
Organ effects: CNS:
Recommendations: