Haemostasis
Pregnancy: Caution — desmopressin used in pregnancy for DI; hyponatraemia risk; consult haematology for vWD management in pregnancy
Desmopressin
Brand names: DDAVP, Octim, Stimate
Adult dose
Dose: 0.3 mcg/kg IV in 50 mL sodium chloride 0.9%
Route: IV (also intranasal 150–300 mcg, SC)
Frequency: Single dose; may repeat once at 12–24 hours (tachyphylaxis after 2nd dose)
Max: 20 mcg per dose
Infuse IV dose over 20–30 minutes. Intranasal: 150 mcg (1 spray) if under 50 kg, 300 mcg (2 sprays) if 50 kg and above. Restrict fluids for 24 hours after to prevent hyponatraemia
Paediatric dose
Dose: 0.3 mcg/kg mcg/kg
Route: IV or intranasal
Frequency: Single dose
Max: 20 mcg
Under 3 months: very high hyponatraemia risk — extreme caution; Central DI: 0.1–0.4 mcg/day IV in divided doses
Dose adjustments
Renal
eGFR under 30: use with extreme caution — risk of severe hyponatraemia; monitor sodium closely
Hepatic
No specific adjustment
Paediatric weight-based calculator
Under 3 months: very high hyponatraemia risk — extreme caution; Central DI: 0.1–0.4 mcg/day IV in divided doses
Clinical pearls
- Mechanism: synthetic vasopressin analogue — V2 receptor agonist (renal tubular water reabsorption) + releases vWF and factor VIII from Weibel-Palade bodies in endothelial cells; minimal V1 (vascular) activity unlike vasopressin
- Emergency haemostasis indications: mild haemophilia A (factor VIII above 5%), Type I vWD, uraemic bleeding (from platelet dysfunction), reversal of antiplatelet effect prior to urgent surgery
- TACHYPHYLAXIS: vWF/factor VIII stores in endothelial cells are depleted after 1–2 doses — subsequent doses produce diminishing responses; wait 48–72 hours between treatments; if more doses needed, switch to factor concentrates
- MHRA — HYPONATRAEMIA: fatal cases reported in children and elderly — MANDATORY fluid restriction for 24 hours after use; measure serum sodium at baseline and 4–8 hours after; avoid in patients who are polyuric or cannot restrict fluids
- Uraemic bleeding: desmopressin 0.3 mcg/kg IV is standard pre-operative treatment — shortens bleeding time within 1 hour; effect lasts 4–8 hours; conjugated oestrogens are longer-acting alternative
- Central DI: desmopressin replaces absent ADH — do NOT confuse doses: haemostasis dose (0.3 mcg/kg) vs DI dose (0.1–0.4 mcg/day) are very different
Contraindications
- Type IIB or platelet-type von Willebrand disease (causes thrombocytopenia)
- Cardiac failure
- Psychogenic polydipsia (profound hyponatraemia risk)
- Syndrome of inappropriate ADH secretion (SIADH)
- Hyponatraemia
Side effects
- Hyponatraemia — MOST IMPORTANT — can be severe and life-threatening, especially in children
- Fluid retention
- Headache
- Flushing, vasodilation, hypotension
- Tachyphylaxis after 2nd dose (factor VIII and vWF stores depleted)
- Nausea
Interactions
- NSAIDs and carbamazepine (increase antidiuretic effect — increase hyponatraemia risk)
- Chlorpropamide (enhances antidiuretic effect)
- Demeclocycline (antagonises desmopressin — used for SIADH treatment)
Monitoring
- Serum sodium at baseline and 4–8 hours post-dose (hyponatraemia monitoring — mandatory)
- Fluid intake and urine output
- Factor VIII and vWF levels (haemostasis response)
- Blood pressure (hypotension risk during IV infusion)
- Platelet count (in vWD — confirm not type IIB before giving)
Reference: BNFc; BNF 90; UKHCDO Guidelines for vWD; MHRA DSU 2017 (hyponatraemia); BSH Guidelines on haemophilia. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
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