20 to 50     : Dose as in normal renal function
10 to 20     : Dose as in normal renal function for prophylaxis only.
<10           : Dose as in normal renal function for prophylaxis only.
DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Not dialysed. Dose as in GFR <10 mL/min
HD                     :Not dialysed. Dose as in GFR <10 mL/min
HDF/high flux   :Dialysed. Dose as in GFR
<10           : mL/min
CAV/VVHD      :Not dialysed. Dose as in GFR=10–20 mL/min
IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugs
Analgesics: increased risk of bleeding with NSAIDs – avoid concomitant use with IV diclofenac; increased risk of haemorrhage with ketorolac – avoid concomitant usedrotrecogin alfa: manufacturer advises to avoid use of high doses of heparin with drotrecogin alfa
Nitrates: GTN infusions increase the excretion of bemiparin; anticoagulant effect reduced
Use with care in patients receiving oral anticoagulants, platelet aggregation inhibitors, aspirin or dextran
ADMINISTRATION
Reconstition
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Route
SC
Rate of Administration
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Comments
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OTHER INFORMATION
In extracorporeal circulation during a 4-hour or less haemodialysis session, for patients 60 kg, 3500 units bemiparin is used
Additional doses may be required if using LMWHs for anticoagulation in HDF
1.4 mg of protamine should neutralise the effect of 100 units of bemiparin
Low molecular weight heparins are renally excreted and hence accumulate in severe renal impairment. While the doses recommended for prophylaxis against DVT and prevention of thrombus formation in extracorporeal circuits are well tolerated in patients with ESRF, the doses recommended for treatment of DVT and PE have been associated with severe, sometimes fatal, bleeding episodes in such patients. Hence the use of unfractionated heparin would be preferable in these instances