Drugs: doses, MOA, etc Flashcards
fentanyl dosing
1-2mcg/kg low dose; awake patients
2-20mcg/kg
fentanyl MOA
binds to opioid receptors of the presynaptic and postsynaptic sites in the CNS and peripherally
major advantages of fentanyl
- no direct myocardial depression
- no histamine release
- suppresses stress response to surgery
fentanyl side effects
- respiratory depression
- increased ICP
- reflex coughing
- decreases HR
Propofol dosing
2-2.5mg/kg
propofol MOA
GABA receptor agonist (enhances inhibition), hyperpolarizes cell membranes
propofol common side effects
- decreases HR, BP, RR, CMRO2, CBF, and ICP
- injection site pain
- inhibits platelet aggregation
advantages of propofol
- fast on/off with minimal residual effects
- antiemetic
- antipruritic
- anticonvulsant
Ketamine dosing
1-2mg/kg
ketamine MOA
NMDA receptor antagonist; inhibits glutamate; inhibits catecholamine uptake in postganglionic nerves
ketamine side effects
“increases everything”: ICP, BP, HR, O2 demands
-emergence delirium
advantages of using ketamine
- bronchodilating properties
- maintains spontaneous ventilation
what 2 drugs are often administered with ketamine
glycopyrrolate and benzo for secretions and emergence delirium
Etomidate dose
0.3mg/kg
Etomidate MOA
mimics inhibitory effects of GABA by increasing the receptors affinity to GABA; depresses the reticular activating system; opens Cl channels
avoid etomidate with what patients
seizure
major disadvantages of etomidate
- emetic
- adrenocortical suppression
advantage of etomidate
good hemodynamic profile
Dexmedetomidine dosing
loading dose: 0.5-1mcg/kg over 10min
infusion: 0.2-1.4mcg/kg/hr
Dexmedetomidine MOA
alpha 2 agonist: hyperpolarizes cell w/ efflux of K, reduced NE release, decreased cAMP by inhibiting adenylyl cyclase
Side effects of precedex bolus
bradycardia and HTN
Midazolam dosing
1-2mg IV
0.3-0.5mg/kg PO
midazolam MOA
causes increased binding of GABA to its receptor-> opening of Cl channel-> hyperpolarization
cardioprotectant feature of versed
prolongs adenosine