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Desmopressin
Aka: Desmopressin, dDAVP
- Indications
- Diabetes Insipidus
- Control of Hemophilia A related bleeding
- Von Willebrand's Disease
- Primary Nocturnal Enuresis
- Mechanism
- Synthetic ADH replacement hormone (anologue of Vasopressin)
- Potent antidiuretic
- No vasopressor activity
- Urine volume decreases by resorbing water at distal renal tubules
- Pharmacokinetics
- Duration of action: 12 hours
- Dosing: Nocturnal Enuresis
- General
- If effective, may continue for 3-6 months
- Maintain dose for 4-6 weeks and then slowly taper off over 6 months
- Discontinue slowly (e.g. 10 mcg/month)
- Reduces risk of relapse
- Consider in combination with Bed-Wetting Alarm or Oxybutynin
- Desmopressin Intranasal
- Not recommended due to risk of water intoxication
- Initial: 5 mcg spray each nostril qhs
- Increase as needed up to 20 mcg each nostril qhs
- Desmopressin Oral
- Initial: 0.2 mg PO qhs
- Use lowest effective dose
- Increase as needed to 0.6 mg at bedtime
- Dosing: General
- Nasal Spray: 5-20 mcg daily to twice daily
- Intranasal 5 mcg equivalent to 0.1 mg PO
- Oral Tablet: 0.1 mg PO daily to twice daily
- Adverse Effects
- Nasal irritation or Epistaxis with nasal spray
- Behavior changes
- Aggressive behavior
- Nightmares
- Nocturia
- Administer at night to reduce nocturia
- Water retention and Hypernatremia (water intoxication)
- Efficacy: Nocturnal Enuresis
- Most effective in over age 8-9 years (60-70% respond)
- Also more effective if only a few wet nights and normal Bladder capacity
- High relapse rate (>80%); Reduced if slowly tapered - see doing above
- Disadvantages
- Very Expensive
- References
- Tullus (1999) Acta Paediatr 88:1274-8
- Kruse (2001) BJU Int 88:572-6
- Robson (2007) J Urol 178: 24-30