INDICATIONS
- Anticoagulation in patients with Heparin Induced Thrombocytopenia (HIT)
- see HIT guideline
- Argatroban is preferred alternative anticoagulant in patients with HIT
- For advice, contact consultant haematologist
ARGATROBAN
- Preferred alternative anticoagulant in patients with HIT
- Direct thrombin inhibitor with a half-life of 50 min
- Eliminated by hepato-biliary route
Administration
- Check baseline platelet count and APTT
- No dose modification in patients with renal impairment
- Specific dosage protocol for patients on haemodialysis, contact haematologist
- Use with caution in patients in critical care and hepatic impairment
- Contraindicated in patients with severe hepatic impairment
- If patient bleeds, contact consultant haematologist
IV infusion by syringe pump
- Preparation: 50mg/50ml (1mg/mL) solution for infusion – ready to use
- Administer via a syringe driver
Dosage
- Maximum dose 10 microgram/kg/min
Critically ill/hepatic impairment
- In severe hepatic impairment, argatroban is contraindicated, contact haematologist
- Otherwise, start with 0.5 microgram/kg/min
- 2 hr after initiation of infusion, check APTT
Change due to APTT result
- If APTT <1.5, increase infusion rate by 0.1 microgram/kg/min
- repeat APTT in 4 hrs
- If APTT 1.5-3.0, no change in infusion rate
- repeat APTT in 4 hrs
- after 2 consecutive APTTs within target range, check at least once daily
- If APTT >3.0, stop infusion
- repeat APTT 4hrly until APTT between 1.5–3.0
- resume at half previous infusion rate and monitor
Standard schedule
- Start with 2 microgram/kg/min
- 2 hr after initiation of infusion, check APTT
Change due to APTT result
- If APTT <1.5, increase infusion rate by 0.5 microgram/kg/min
- repeat APTT in 2 hrs
- If APTT 1.5-3.0, no change in infusion rate
- repeat APTT in 2 hrs
- after 2 consecutive APTTs within target range, check at least once daily
- If APTT >3.0, stop infusion
- repeat APTT 2hrly until APTT between 1.5–3.0
- resume at half previous infusion rate and monitor
Pump rate for selected dose
Weight (kg) Dose selected (mcg/kg/min, between 0.0 - 10):DANAPAROID
- Danaparoid is a low-molecular-weight heparinoid, chemically distinct from heparin
- Use to treat suspected or proven HIT (with or without thrombosis)
- Use to prevent venous thrombosis in patients with a history of HIT
- If patient bleeds, contact consultant haematologist
Administration
- For patients undergoing dialysis, discuss with haematology
- Check baseline platelet count and APTT
Bolus preparation
- Take 4500 units (3.6 mL of 1250 units/mL) danaparoid sodium injection
- make up to 45 mL in a syringe with sodium chloride 0.9% or glucose 5% = 100 units/mL
- The diluted solution is stable for 24 hr
Treatment of HIT (suspected or proven)
Weight (kg)Prevention of venous thrombosis in patients with history of HIT
- Give 750 units (0.6 mL of 1250 units/mL solution) SC every 12 hr
FONDAPARINUX
- Use in HIT is unlicensed. Seek haematology advice before prescribing
- Fondaparinux is an indirect anti-Xa inhibitor and has a half-life of 17–20 hr
- Avoid in patients with renal impairment, use argatroban instead
- Before starting, check baseline platelet count and APTT, renal function
- If patient bleeds, contact consultant haematologist
Fondaparinux dosing for adult patients with HIT
- If body weight <50 kg, give 5 mg SC once daily
- If body weight 50 – 100 kg, give 7.5 mg SC once daily
- If body weight >100 kg, give 10 mg SC once daily
- If use in patients with renal impairment unavoidable, reduce dose and monitor anti-Xa levels
BIVALIRUDIN
- Use in HIT is unlicensed. Seek haematology advice before prescribing
- Bivalirudin is a direct thrombin inhibitor licensed for use in coronary interventions
- it has a short half-life of 30–40 min which can be prolonged to 3 hr in patients with severe renal impairment
- for patients with renal impairment, use argatroban
- elimination of bivalirudin is by enzymic metabolism and renal excretion. No dose adjustment is required for hepatic impairment
- there is no known antidote
- rare cases of anaphylactic reaction have been associated with IV bolus or infusion
- Before starting infusion, obtain baseline platelet count and APTT
- If patient bleeds, contact consultant haematologist
Preparation
- 250mg powder for reconstitution for injection or infusion
Administration for HIT
- Check baseline platelet count and APTT, renal function
- Reconstitute each 250mg vial with 5ml water for injection
- swirl gently until completely dissolved and the solution is clear
- Withdraw 5ml from the vial, and further dilute to a total volume of 50ml with glucose 5% or sodium chloride 0.9%
- gives a final concentration of 5mg/ml
- For HIT, given by intravenous infusion via infusion pump
Dosage for HIT
Normal renal function
- Start with 0.2mg/kg/hr continuous infusion
- 2 hr after initiation of infusion, check APTT
Change due to APTT result
- If APTT <1.5, increase infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT 1.5-2.5, no change in infusion rate
- repeat APTT in 2 hrs
- after 2 consecutive APTTs within target range, check once daily
- If APTT 2.5-4.0 (no bleeding), reduce infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT >4.0, stop infusion
- repeat APTT in 30 min and then 2 hrly
- when APTT<2.5, restart infusion at 50% reduced infusion rate
- repeat APTT in 2 hours
Creatinine Clearance 30-60mL/min
- Start with 0.1mg/kg/hr continuous infusion
- 2 hr after initiation of infusion, check APTT
Change due to APTT result
- If APTT <1.5, increase infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT 1.5-2.5, no change in infusion rate
- repeat APTT in 2 hrs
- after 2 consecutive APTTs within target range, check once daily
- If APTT 2.5-4.0 (no bleeding), reduce infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT >4.0, stop infusion
- repeat APTT in 30 min and then 2 hrly
- when APTT<2.5, restart infusion at 50% reduced infusion rate
- repeat APTT in 2 hours
Creatinine Clearance <30 mL/min
- Start with 0.05 mg/kg/hr continuous infusion
- 2 hr after initiation of infusion, check APTT
Change due to APTT result
- If APTT <1.5, increase infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT 1.5-2.5, no change in infusion rate
- repeat APTT in 2 hrs
- after 2 consecutive APTTs within target range, check once daily
- If APTT 2.5-4.0 (no bleeding), reduce infusion rate by 20%
- repeat APTT in 2 hrs
- If APTT >4.0, stop infusion
- repeat APTT in 30 min and then 2 hrly
- when APTT<2.5, restart infusion at 50% reduced infusion rate
- repeat APTT in 2 hours
Pump rate for selected dose
Weight (kg) Dose selected (mg/kg/min):© 2022 The Bedside Clinical Guidelines Partnership.
Created by University Hospital North Midlands and Keele University School of Computing and Mathematics.
Research and development team: James Mitchell, Ed de Quincey, Charles Pantin, Naveed Mustfa