Bivalirudin
Bivalirudin.JPG

Bivalirudin

CLINICAL USE

Anticoagulant:
  • Percutaneous coronary intervention

    DOSE IN NORMAL RENAL FUNCTION

    Initially bolus of 750 mcg/kg then an infusion of 1.75 mg/kg/hour

    PHARMACOKINETICS

  • Molecular weight                           :2180.3
  • %Protein binding                           :0
  • %Excreted unchanged in urine     : 20
  • Volume of distribution (L/kg)       :0.1
  • half-life – normal/ESRD (hrs)      :13–37 minutes/ 57 minutes (310 minutes in dialysis patients on non-
  • HD days)

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

    30–50 Dose as in normal renal function10–30 Normal bolus dose. Reduce infusion dose by 20% (1.4 mg/kg/hour). See ‘Other Information’
  • <10           : Normal bolus dose. Reduce infusion dose by 80% and monitor ACT. See ‘Other Information’

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Unknown dialysability. Dose as for GFR <10 mL/min
  • HD                     :Dialysed. Dose as for GFR
  • <10           : mL/min
  • HDF/high flux   :Dialysed. Dose as for GFR
  • <10           : mL/min
  • CAV/VVHD      :Unknown dialysability. Dose as for GFR=10–29 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Antiplatelets and anticoagulants: increased risk of bleeding
  • Thrombolytics: may increase risk of bleeding complications; enhance effect of bivalirudin

    ADMINISTRATION

    Reconstition

    Reconstitute each 250 mg vial with 5 mL water for injection

    Route

    IV

    Rate of Administration

    1.75 mg/kg/hour

    Comments

    Further dilute with 50 mL sodium chloride 0.9% or glucose 5% if for infusion
  • Stable for 24 hours at room temperature

    OTHER INFORMATION

  • Monitor ACT in renal impairment
  • Can start bivalirudin 30 minutes after stopping unfractionated heparin and 8 hours after stopping LMWHNo known antidote Dose recommendations vary from country to country; doses above are from New Zealand
  • UK doses: GFR=30–59 mL/min: reduce dose by —20%GFR<30 mL/min: contraindicated —USA doses: Normal dose: 1 mg/kg bolus then —2.5 mg/kg infusionGFR=30–59 mL/min: reduce dose by —20%GFR=10–29 mL/min: reduce dose by —60%Dialysis dependent: reduce dose by —90%
  • Lobo BL. Use of newer anticoagulants in patients with chronic kidney disease. Am J Health-Syst Pharm. 2007, Oct 1; 64: 2017–26:
  • GFR=30–50 mL/min: 1.75 mg/kg/hour —
  • GFR<30 mL/min: 1 mg/kg/hour —
  • On haemodialysis: 0.25 mg/kg/hour



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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