In the absence of any special circumstances detailed below, patients should be started on apixaban 10mg bd for 7 days, then reduce dose to 5mg bd.
- If direct oral anticoagulant (DOAC) use is contra-indicated, dalteparin 200units/kg od is a suitable alternative for most patients. Dalteparin dose should be reduced to 150 units/kg after 1 month.
- Patients should initially be anticoagulated for 6 months.
- If cancer incurable, or systemic anti-cancer therapy (SACT) ongoing at 6 months, consider extended anticoagulation with:
- apixaban 2.5mg bd OR
- dalteparin 150units/kg od.
Special circumstances:
Patients with primary brain tumours or brain metastases
- In the absence of a recent CNS haemorrhage, benefits of anticoagulation are usually likely to outweigh risks.
- Risk of haemorrhage is increased in patients with glioblastoma multiforme (GBM), melanoma or renal cancer metastases but anticoagulation is still likely to be beneficial.
- Anticoagulation decisions should be discussed with patient's consultant or consultant on call and patient documented in the notes.
Patients with renal impairment
- DOAC - if CrCl>30, treat with apixaban at standard dose.
- Low molecular weight heparin (LMWH) - if CrCl>30, treat with dalteparin at standard dose.
- If CrCl<30, dalteparin with dose modifications or alternative anticoagulation - refer to LUHD antithrombotic guidelines (adults) (only accessible when connected to intranet)
Patients with hepatic impairment
- Severe hepatic impairment (Child-Pugh C; bilirubin >1.5xULN, ALT/AST >2xULN)
- The risks and benefits of anticoagulation should be discussed.
- If anticoagulation required treat with dalteparin.
- Coagulopathy (PT ratio or APTT ratio >1.5)
- Not for anticoagulation.
Patients at risk of significant thrombocytopenia (platelets <50)
- Consider treatment with dalteparin due to the greater flexibility of dosing.