Benzos Flashcards
Flumazenil DOA? Metabolism?
30-60 min, meaning you may need to redose
Hepatic metabolism, renal excretion
Why is there a ceiling effect with benzos?
Because all it can do is assist GABA to open the Cl- channels. After that, it can’t do anything else to achieve any effects.
Midazolam CV effects?
Cardio stable;
CO unchanged
Dec SVR at induction dosage
Dec BP from anxiolysis
Doesn’t attenuate laryngoscopy HR/BP changes
Benzodiazepine MOA
- Facilitate action of GABA and GABA-A receptor, enhance affinity of GABA to the receptor (but DOES NOT activate GABA-A receptor)
- This leads to Cl channels open, inc conductance, hyperpolarization of post-synaptic membrane, increased resistance of post-synaptic membrane to excitation
Diazepam E1/2t?
Diazepam is ≈ day (20-50h)
Desmethyldiazepam is 2-4 days!
Lorazepam solvent?
Propylene glycol
Flumazenil (romazicon) dose?
reversal
(what about infusion?)
- 2 mg IV, wait 2 min,
- 1 mg IV subsequent doses at 60 sec intervals to
max total 3 mg
Infusion: 0.1-0.4 mg/h
Which benzodiazepine is most potent?
Lorazepam (ativan) It is 5-10x more potent than diazepam
Structure of midazolam (versed)?
Water soluble preparation
Imidazole ring
(same compound that etomidate has)
Midazolam metabolism?
Extensive hepatic metabolism
ACTIVE METABOLITE: 1-hydroxy-midazolam
Conjugated and excreted in the urine
Renal failure doesn’t effect VD, E1/2t, or clearance
Diazepam metabolism?
Oxidation, n-demethylation to desmethyldiazepam (ACTIVE METABOLITE)
which is oxidized, conjugated, and excreted in the urine
Dosage of midazolam for…
Premedication peds, IV sedation adults, Induction
Premed peds: 0.25-0.5 mg/kg po (not on drug cards)
Peds po dose max 20mg IV
sedation adults (premedication): 0.5-5 mg IV or 0.04-0.08 mg/kg
Induction: 0.05-0.35 mg/kg over 30-60 sec
*Per drug cards, not powerpoint
Benzos are highly _____ (water/lipid) soluble and _____ (high/low) protein binding
Lipid soluble
High PB
Flumazenil antagonizes what effects of benzos?
Antagonizes depression of ventilation and sedation
What does it mean if a drug has a short effect site equilibration time?
It means that the effects on the brain occur promptly after IV administration