Epoprostenol
Epoprostenol.JPG

Epoprostenol

CLINICAL USE

Vasodilation and inhibition of platelet aggregation without prolonging bleeding timeAlternative to heparin in haemodialysis Treatment of peripheral vascular disease and pulmonary hypertension

DOSE IN NORMAL RENAL FUNCTION

2–50 ng/kg/minute, adjusted according to responseDialysis anticoagulation: 4 ng/kg/minute starting 10–15 minutes before and continuing during dialysis via the arterial line, adjusted according to response (range: 0.5–12 ng/kg/minute)

PHARMACOKINETICS

  • Molecular weight                           :352.5
  • %Protein binding                           :No data
  • %Excreted unchanged in urine     : 40–90 (as drug + metabolites)
  • Volume of distribution (L/kg)       :0.357–1.015
  • half-life – normal/ESRD (hrs)      :2–6 minutes/–

    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 function
  • HDF/high flux   :Unknown dialysability. Dose as in normal renal function
  • CAV/VVHD      :Unknown dialysability. Dose as in normal renal function

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugsIncreased hypotensive effect with ‘acetate’ dialysis

    ADMINISTRATION

    Reconstition

    500 microgram vial with diluent provided gives solution of 10 micrograms/mL. Can be diluted further

    Route

    IV or into blood supplying dialyser

    Rate of Administration

    Via CRIP

    Comments

    Complicated dosing schedule – check calculations carefullyInfusion rate may be calculated by the following formula:Dose rate (mL/hr) Dosage (ng/kg/min) × body wt (kg) × 60 Concentration of infusion (ng/mL) (usually 10 000 ng/mL)

    OTHER INFORMATION

    Monitor BP and heart rate. Reduce dose if patient becomes hypotensive. Cardiovascular effects cease 30 minutes after stopping the infusionSome patients may exhibit allergic reaction to buffer solution used to reconstitute epoprostenolSolution retains 90% potency for 12 hours after dilutionThe concentrated solution should be filtered using the filter provided in the pack



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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