Etomidate
Etomidate
CLINICAL USE
Induction of anaesthesia
DOSE IN NORMAL RENAL FUNCTION
150–300 mcg/kg
PHARMACOKINETICS
Molecular weight                           :244.3 %Protein binding                           :76 %Excreted unchanged in urine     : 2 Volume of distribution (L/kg)       :2–4.5half-life – normal/ESRD (hrs)      :4–5/Unchanged DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
20 to 50     : Dose as in normal renal function 10 to 20     : Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Unknown dialysability. Dose as in normal renal function HD                     :Unknown dialysability. Dose as in normal renal functionHDF/high flux   :Unknown dialysability. Dose as in normal renal functionCAV/VVHD      :Unknown dialysability. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsAdrenergic neurone blockers: enhanced hypotensive effectAntihypertensives: enhanced hypotensive effectAntidepressants: avoid MAOIs for 2 weeks before surgery; increased risk of arrhythmias and hypotension with tricyclicsAntipsychotics: enhanced hypotensive effect ADMINISTRATION
Reconstition
Route
Intravenous injection only Rate of Administration
–Comments
– OTHER INFORMATION
In cases of adrenocortical gland dysfunction and during very long surgical procedures, a prophylactic cortisol supplement may be required (e.g. 50–100 mg hydrocortisone)
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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