Anticoagulant in percutaneous coronary intervention
Adult: Initially, 0.75 mg/kg inj followed by an infusion of 1.75 mg/kg/hr during procedure and up to 4 hours postprocedure. If needed, may continue infusion at 0.25 mg/kg/hr for 4-12 hours.
Indications and Dosage
Intravenous
Anticoagulant in percutaneous coronary intervention Adult: Initially, 0.75 mg/kg inj followed by an infusion of 1.75 mg/kg/hr during procedure and up to 4 hours postprocedure. If needed, may continue infusion at 0.25 mg/kg/hr for 4-12 hours.
|
||||||
Special Patient Group
Patients w/ ACS: Initially, 0.1 mg/kg IV bolus followed by 0.25 mg/kg/hr IV infusion. Medically managed patients may continue infusion for up to 72 hr. If will proceed to PCI: Additional IV inj of 0.5 mg/kg before the procedure then increased to 1.75 mg/kg/hr for the duration of the procedure. After PCI: Infusion may continue at 0.25 mg/kg/hr for a further 4-12 hr if necessary. If will proceed to CABG: Stop infusion 1 hr pre-op and patient should be treated w/ unfractionated heparin.
|
||||||
Renal Impairment
Dialysis patients: Contraindicated.
|
||||||
Hepatic Impairment
No dosage adjustment needed.
|
||||||
Reconstitution
Dilute a 250 mg vial w/ 5 mL of sterile water for inj. Further dilute the reconstituted soln w/ 50 mL of dextrose 5% or NaCl 0.9% inj to produce a final concentration of 5 mg/mL.
|
||||||
Incompatibility
Amiodarone, alteplase, diazepam, prochlorperazine, amphotericin B, vancomycin, chlorpromazine, reteplase, streptokinase. Concentration-dependent incompatibility w/ dobutamine, famotidine, haloperidol, labetalol, lorazepam and promethazine.
|
||||||
Contraindications
Active major bleeding. CrCl <30 mL/min and dialysis-dependent patients. Severe uncontrolled HTN; subacute bacterial endocarditis.
|
||||||
Special Precautions
Increased risk of potentially fatal thrombosis during brachytherapy procedure. Patients at high risk of serious bleeding; recent major surgery or puncture of large vessels or organ biopsy. Renal impairment. Pregnancy, lactation, elderly.
|
||||||
Adverse Reactions
Acute stent thrombosis, bleeding, ecchymosis, hypotension, HTN, headache, nausea, dyspepsia, insomnia, nervousness, anxiety, pelvic and abdominal pain, urinary retention, anaemia, thrombocytopaenia, inj site pain; rarely, thrombosis, tachycardia, bradycardia, vomiting, back pain, dyspnoea, fever.
Potentially Fatal: Anaphylaxis including anaphylactic shock. |
||||||
Overdosage
Symptoms: Bleeding. Management: Discontinue treatment w/ bivalirudin. Bivalirudin is haemodialysable.
|
||||||
Drug Interactions
May increase risk of bleeding when used w/ thrombolytics, oral anticoagulants or drugs that affect platelet function.
|
||||||
Food Interaction
Avoid alfalfa, anise, bilberry as it may enhance the adverse/toxic effect of anticoagulants.
|
||||||
Action
Description:
Mechanism of Action: Bivalirudin is a synthetic 20-amino acid analogue of the naturally occurring hirudin. It is a specific and reversible direct thrombin inhibitor thats works by binding to the catalytic and anionic exosite of circulating and clot-bound thrombin. It is used as an anticoagulant in percutaneous coronary intervention. Pharmacokinetics: Distribution: Does not bind to plasma proteins. Volume of distribution: 200 mL/kg. Metabolism: Partly metabolised by the kidneys. Excretion: Via urine (approx 20%) and proteolytic cleavage. Elimination half-life (normal renal function): Approx 25 min. |
||||||
Storage
Unopened vial: Store between 15-30°C. Reconstituted soln: Store between 2-8°C for up to 24 hr.
|
||||||