Synopsis
Diagnose and treat thrombosis safely when pregnancy, postpartum physiology or active cancer changes presentation, anticoagulant choice, duration, procedures and bleeding risk.
- Pregnancy and cancer raise VTE probability but symptoms still require objective imaging; do not use D-dimer or a non-validated score alone to dismiss a clinically suspected event.
- Therapeutic LMWH is first-line treatment for most pregnancy-associated DVT or PE because it does not cross the placenta and has extensive obstetric experience.
- Continue pregnancy-associated VTE treatment for the remainder of pregnancy and at least 6 weeks postpartum, with at least 3 months total therapy.
- Warfarin and DOACs are generally avoided for treating VTE during pregnancy; warfarin is compatible with breastfeeding, whereas DOACs are not routinely recommended during breastfeeding.
- Plan delivery and neuraxial timing jointly: therapeutic LMWH is normally withheld for at least 24 hours before planned neuraxial procedures, with exact timing set by obstetric anaesthesia protocol.
- For active cancer-associated proximal DVT or PE, NICE recommends anticoagulation for 3–6 months then review; continue beyond this while cancer activity, treatment and recurrence risk justify it.
- Apixaban or rivaroxaban is an option for many adults with active cancer, but gastrointestinal or genitourinary lesions, interactions, vomiting, organ dysfunction and bleeding can favour LMWH.
- Thrombocytopenia requires specialist intensity and transfusion decisions based on clot acuity, location, platelet trend and bleeding; do not use a universal unsupervised platelet cutoff.
- A functioning, well-positioned and uninfected catheter associated with thrombosis can often remain while therapeutic anticoagulation is given; remove it if unnecessary, infected or malfunctioning.
- Incidental PE requires radiology confirmation and clot-burden-specific specialist review.