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Low Molecular Weight Heparin — VTE Prophylaxis Pregnancy: Safe in pregnancy — does not cross placenta; preferred anticoagulant in pregnancy

Dalteparin (Perioperative VTE Prophylaxis)

Brand names: Fragmin

Adult dose

Dose: 2500-5000 units SC once daily (prophylaxis); 200 units/kg SC once daily (treatment)
Route: Subcutaneous injection
Frequency: Once daily
Max: 5000 units/day (prophylaxis); 18000 units/day (treatment)
High VTE risk surgery: 5000 units SC starting 12 hours pre-op and continuing post-op. Moderate risk: 2500 units SC 1-2 hours pre-op. Duration: until ambulatory (minimum 7-10 days); extended 28 days for major abdominal/pelvic cancer surgery

Paediatric dose

Dose: 100 units/kg SC once daily (treatment); prophylaxis: seek specialist opinion units/kg
Route: SC
Frequency: Once or twice daily
Max: Seek specialist opinion
Seek specialist paediatric input for exact prophylaxis dosing

Dose adjustments

Renal

Accumulation risk in eGFR under 30 — measure anti-Xa levels; consider unfractionated heparin instead

Hepatic

Use with caution — increased bleeding risk

Paediatric weight-based calculator

Seek specialist paediatric input for exact prophylaxis dosing

Clinical pearls

  • Neuraxial anaesthesia timing (ESRA 2021): stop dalteparin 12 hours before neuraxial block (prophylactic dose); 24 hours (therapeutic dose); restart no earlier than 4 hours after catheter removal
  • NICE VTE guideline (NG89): LMWH is first-line pharmacological VTE prophylaxis for most surgical patients — rivaroxaban only for hip/knee arthroplasty
  • Anti-Xa monitoring: routine monitoring not recommended for prophylactic doses in standard patients; measure anti-Xa levels in obesity (BMI above 40), pregnancy, and renal impairment
  • Antidote: protamine partially reverses LMWH (approximately 60-70% reversal of anti-Xa activity); 1 mg protamine per 100 anti-Xa units dalteparin given in preceding 8 hours
  • Extended prophylaxis after major cancer surgery (28 days) reduces VTE by approximately 60% vs 7-day course — cost-effective and evidence-based

Contraindications

  • Active major bleeding
  • HIT
  • Severe thrombocytopenia
  • Epidural or spinal anaesthesia within timing window

Side effects

  • Bleeding
  • HIT (days 5-14 — lower risk than UFH)
  • Injection site bruising and haematoma
  • Hyperkalaemia
  • Osteoporosis (prolonged use)

Interactions

  • Antiplatelet agents (increased bleeding)
  • Warfarin / DOACs (additive anticoagulation)
  • NSAIDs (increased bleeding risk)

Monitoring

  • Signs of bleeding
  • Platelet count (day 5-14 — HIT surveillance)
  • Anti-Xa levels (high-risk patients)
  • Renal function

Reference: BNFc; BNF 90; NICE NG89 (VTE Prevention in Hospital); ESRA Guidelines 2021; Fragmin SPC. Verify against your local formulary and the latest BNF before prescribing.

Related

Curated clinical cross-links plus same-class fallbacks.