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Desmopressin
From WikEM
Contents
Administration
- Type: synthetic replacement for vasopressin
- Dosage Forms:
- injectable solution: 4 mcg/mL
- tablet: 0.1mg, 0.2mg
- nasal spray: 0.1mg/ mL (5mL); Delivers 10 mcg/spray, 1.5mg/mL (2.5mL); Delivers 150 mcg/spray
- Routes of Administration: IV, IM, SC, intranasal, oral
- Common Trade Names: DDAVP, Stimate
Adult Dosing
Diabetes Insipidus
- Intranasal: 10-40 mcg/day qday or divided q8-12 hr
- PO:
- Initial: 0.05mg q 12 hr
- Effective range: 0.1-1.2mg divided q 8-12 hr
- IV/SC: 2-4 mcg/day divided q12 hr or 1/10th the maintenance of intranasal dose
Hemophilia A & Von Willebrand Disease
- IV: 0.3 mcg/kg IV over 15-30 minutes IV (for pre-op 30 min before procedure)
- intranasal:
- <50 kg: 150 mcg; for pre-op, give 2 hr before procedure
- >50 kg: 300 mcg; for pre-op, give 2 hr before procedure
Nocturnal Enuresis
- 0.2mgPO qHS (up to 0.6mg/day)
Uremic Bleeding in Acute or Chronic Renal Failure
- 0.4 mcg/kg IV over 10 minutes
Pediatric Dosing
Diabetes Insipidus
3 months to 12 years (intranasal)
- 5-30 mcg/day qday or divided q12 hr (using 100 mcg/mL solution)
>12 years (intranasal)
- 10-40mcg/day qday or divided q12 hr (using 100 mcg/mL solution)
3 months to 12 years (oral)
- Initial: 0.05mg q 12 hr
- Effective range: 0.1-1.2mg
>12 years (oral)
- Initial 0.05mg PO q 12 hr
- Effective range: 0.1-1.2mg divided q8-12 hr
3 months to 12 years (IV/SC)
- 0.1-1 mcg qday or divded q12 hr
>12 years (IV/SC)
- 2-4 mcg/day divided q 12 hr or one tenth the maintenance of intranasal dose
Nocturnal Enuresis
- >6 years: 0.2mg PO qHS; up to 0.6mg/day
Hemophilia A & Von Willebrand Disease
- 0.3 mcg/kg IV over 15-30 minutes; for pre-op, give 30 minutes before procedure
- 1 spray (150 mcg) per nostril (300 mcg total dose) if >12 years of age or >50 kg body weight
- administer single spray (150 mcg) if patient >12 years of age but <50 kg body weight
- (Fluid intake should be limited 1 hr prior to dose until the next morning or at least 8 hr after administration)
Special Populations
- Pregnancy Rating:Pregnancy Category B
- Lactation risk: minimally excreted in breast milk, acceptable to use
Renal Dosing
- CrCl <50 mL/min: Contraindicated; has been used unlabeled in acute and chronic renal failure patients experiencing uremic bleeding or prevention of surgical bleeding, limit to 1 dose
- CrCl ≥50 mL/min: No adjustments necessary
Hepatic Dosing
- not defined
Contraindications
- Allergy to class/drug
- patients <3 months (hemophilia A or von Willebrand disease patients)
- CrCl <50
- von Willebrand disease, type IIB
- hyponatremia
Caution to use
- renal impairment
- fluid and electrolyte imbalance
- polydipsia
- elderly patients
- young children
- cystic fibrosis
- coronary artery disease
- hypertension
- Congestive Heart Failure
- thrombosis risk
Adverse Reactions
Serious
- anaphylaxis
- respiratory arrest
- hyponatremia
- water intoxication
- seizures
- thrombosis
Common
- flushing
- headache
- rhinitis
- nausea
- abdominal pain
- dizziness
- cough
- epistaxis
- rigors
- conjunctivitis
- hypertension
- hypotension
Pharmacology
- Half-life: 1.5 -2.5 hr (oral); 3 hr (IV)
- Metabolism: kidney; CYP 450
- Excretion: urine primarily
Mechanism of Action
- synthetic arginine vasopressin (antidiuretic hormone) analogue; exerts antidiuretic effects and increases plasma factor VIII and von Willebrand factor levels
Comments
See Also
References
epocrates, medscape