Desmopressin (Surgical — Haemostasis/Platelet Dysfunction)
Brand names: DDAVP, Desmopressin Acetate, Octim (intranasal)
Adult dose
Paediatric dose
Dose adjustments
Useful specifically IN renal failure for uremic platelet dysfunction — DDAVP transiently improves platelet function in uraemia by releasing vWF. No dose reduction needed for effect; monitor for fluid retention (reduced urine output from V2 activation).
Use with caution in hepatic failure — fluid retention risk; monitor sodium.
Children ≥1 year: 0.3 mcg/kg IV. Fluid restriction essential in young children (hyponatraemia risk). BNFc: avoid in children <1 year or body weight <10 kg (hyponatraemia risk).
Clinical pearls
- Uremic platelet dysfunction: DDAVP 0.3 mcg/kg IV shortens bleeding time in dialysis patients with platelet dysfunction (mechanism: releases stored vWF → improves platelet adhesion); effect lasts 4–8 hours; useful bridge pre-procedure in renal failure patients with abnormal platelet function
- Tachyphylaxis after 2nd dose: endothelial Weibel-Palade bodies depleted of vWF after 2–3 doses; subsequent doses ineffective for 48–72 hours while stores replenish; plan surgery timing to avoid third dose without benefit
- MHRA hyponatraemia warning (neonates): desmopressin is CONTRAINDICATED in children <1 year and body weight <10 kg due to severe hyponatraemia risk — immature renal tubular response leads to severe water retention; adult patients should also restrict fluid intake to 500–750 mL for 8 hours post-dose
Contraindications
- vWD type 2B (paradoxical thrombocytopenia — vWF releases ultra-large multimers that consume platelets)
- Known DDAVP tachyphylaxis (after 2–3 consecutive doses)
- Hyponatraemia
- Severe cardiac failure
- Habitual or psychogenic polydipsia
Side effects
- Hyponatraemia (V2 anti-diuretic effect — serious in young children and elderly; restrict fluid intake for 8 hours post-dose)
- Fluid retention
- Facial flushing (vasodilation)
- Tachycardia
- Nausea
- Tachyphylaxis (after 2–3 doses — endothelial vWF stores exhausted)
Interactions
- NSAIDs (reduce V2-mediated antidiuretic effect — reduced haemostatic response with some NSAIDs)
- Tricyclics and SSRIs (increase antidiuretic effect — hyponatraemia risk)
Monitoring
- Serum sodium (at baseline and 4–8 hours post-dose)
- Urine output and fluid balance
- FVIII and vWF levels pre and post (haematology cases)
- Blood pressure (facial flushing / BP changes during IV infusion)
- Platelet count (exclude vWD type 2B before use)
Reference: BNFc; BNF 90; UKHCDO Guidelines on vWD Management 2014; BNFc; MHRA Drug Safety Update (desmopressin hyponatraemia); BCSH Guidelines on Perioperative Management of Anticoagulation and Antiplatelet Therapy 2016. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
- Sequential Organ Failure Assessment (SOFA) Score · Sepsis / Organ Failure
- Multiple Organ Dysfunction Score (MODS) · Organ Failure Assessment
- POSSUM Score for Surgical Morbidity and Mortality · Perioperative Risk
- SORT (Surgical Outcome Risk Tool) · Perioperative Risk
- Logistic Organ Dysfunction Score (LODS) · ICU Scoring
- ASA Physical Status Classification · Perioperative Risk
- Major Trauma — Primary Survey (ATLS) · ATLS 10th Edition; JRCALC; NICE NG39
- Major Haemorrhage / Massive Transfusion · BCSH; RCOA; RCEM; RCS — BCSH Guidelines
- Burns — TBSA Estimation & Fluid Resuscitation · British Burn Association; EMSB; RCEM 2024
- Lower Gastrointestinal Bleed · NICE; BSG; ACPGBI — Commissioning Guide
- Acute Pancreatitis · NICE; IAP/APA; ACPGBI — CG104
- Hypertrophic Pyloric Stenosis · BAPS / RCPCH