Anticoagulant — ACS / PE / Thrombus
Pregnancy: Safe in pregnancy — does not cross placenta; preferred anticoagulant in pregnancy
Unfractionated Heparin (IV)
Brand names: Heparin Sodium
Adult dose
Dose: 5000 units IV bolus, then 1000-2000 units/hr IV infusion titrated to APTT ratio 1.5-2.5
Route: Intravenous bolus + continuous infusion
Frequency: Continuous infusion
Max: Titrated to APTT; use weight-based nomogram
STEMI (not undergoing PCI): 60 units/kg bolus (max 4000 units), then 12 units/kg/hr. Massive PE: 80 units/kg bolus then 18 units/kg/hr. Use heparin nomogram for titration. Protamine antidote available
Paediatric dose
Dose: 75 units/kg IV bolus over 10 min; then 28 units/kg/hr (under 1 year); 20 units/kg/hr (over 1 year) units/kg
Route: IV
Frequency: Continuous infusion
Max: Titrated to anti-Xa or APTT
Seek specialist haematology input for paediatric anticoagulation
Dose adjustments
Renal
No dose adjustment; however renal impairment increases bleeding risk — monitor more closely
Hepatic
Use with caution — impaired synthesis of coagulation factors increases bleeding risk
Paediatric weight-based calculator
Seek specialist haematology input for paediatric anticoagulation
Clinical pearls
- Antidote: protamine sulfate — 1 mg neutralises approximately 100 units heparin; give slowly IV (max 50 mg over 10 min); risk of anaphylaxis (especially in fish-allergy or prior protamine exposure)
- HIT: suspect if platelets fall by more than 50% between days 5-14 — use 4Ts score; stop heparin immediately and switch to argatroban or fondaparinux; NEVER give warfarin until platelets recover above 150
- IV heparin preferred over LMWH in acute settings requiring rapid reversal (PCI, surgery, bleeding risk) — shorter half-life and protamine reversal are key advantages
- APTT monitoring: therapeutic range is APTT ratio 1.5-2.5; check 6 hours after bolus, then 6 hours after each dose change, then daily when stable
- Anti-Xa monitoring preferred in obesity (BMI above 40), pregnancy, or renal impairment — APTT unreliable in these groups
Contraindications
- Active major bleeding
- HIT (heparin-induced thrombocytopenia)
- Haemorrhagic stroke
- Severe thrombocytopenia (platelets under 80)
Side effects
- Bleeding (most common)
- HIT (immune-mediated — platelet fall day 5-14; paradoxical thrombosis)
- Hyperkalaemia (aldosterone suppression)
- Osteoporosis (prolonged use)
- Transaminase elevation
Interactions
- Antiplatelet agents (increased bleeding risk)
- NSAIDs (increased bleeding)
- Other anticoagulants (additive)
Monitoring
- APTT ratio (or anti-Xa) every 6 hours until stable, then daily
- Platelet count (daily from day 4-14 — HIT surveillance)
- Signs of bleeding
- Potassium (aldosterone suppression)
Reference: BNFc; BNF 90; NICE NG185 (ACS); NICE NG158 (VTE); BSH HIT Guidelines 2012; Anticoagulation UK. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- DOAC Score for Selecting Direct Oral Anticoagulant in Non-Valvular AF · Anticoagulation
- Corrected Sodium (Hyperglycaemia) · Electrolytes
- Hyponatraemia Cause Algorithm · Electrolyte Disorders
- MELD-Na Score · Liver Disease
- MELD-Na Score for Liver Cirrhosis · Hepatology
- 4Ts Score for Heparin-Induced Thrombocytopenia · Thrombocytopenia
Pathways
- Paracetamol overdose · TOXBASE/NPIS; MHRA DSU 2012/2024; SNAP regimen (Lancet 2014); BNF
- TCA overdose · TOXBASE/NPIS; AACT/EAPCCT position statements; Resuscitation Council UK ALS
- Opioid overdose · TOXBASE/NPIS; Resuscitation Council UK; BNF
- Anticholinergic toxidrome · TOXBASE/NPIS; AACT/EAPCCT; BNF
- Benzodiazepine overdose · TOXBASE/NPIS; AACT/EAPCCT; BNF
- β-blocker overdose · TOXBASE/NPIS; AACT/EAPCCT; ESC; BNF