Desmopressin (DDAVP) Dosing for Bleeding ESRD Patients
For bleeding ESRD patients, the recommended dose of DDAVP (desmopressin) is 0.3 μg/kg intravenously, diluted in 50 ml saline and infused over 30 minutes. 1
Mechanism of Action and Indications
- DDAVP enhances platelet adherence and platelet aggregate growth on human artery subendothelium, making it particularly useful for patients with impaired platelet function 1
- DDAVP is especially indicated for ESRD patients who have uremic platelet dysfunction, which contributes significantly to their bleeding risk 2
- In uremic patients, DDAVP has been shown to shorten bleeding time and increase platelet retention, improving hemostasis 3
Dosing Protocol
- The standard intravenous dose is 0.3 μg/kg diluted in 50 ml saline and infused over 30 minutes 1
- For subcutaneous administration, the dose is also 0.3 μg/kg 4
- DDAVP can be administered as a single dose prior to invasive procedures in uremic patients to reduce bleeding risk 2
Clinical Efficacy in ESRD
- Studies have demonstrated that DDAVP significantly shortens collagen/epinephrine-closure time from 252.7 ± 40.7 to 144.6 ± 51.0 seconds in uremic patients on antiplatelet therapy 2
- DDAVP infusion leads to increased plasma levels of factor VIII coagulant (FVIII:C) and von Willebrand factor (vWF) activities in uremic patients 3
- A single infusion before invasive procedures in uremic patients taking antiplatelet drugs has been shown to improve platelet dysfunction and reduce bleeding complications 2
Important Monitoring and Precautions
- Monitor for potential adverse effects including water retention with consecutive hyponatremia and convulsions, particularly in elderly patients 1
- After DDAVP administration, slight decreases in hematocrit and platelet count may occur without significant changes in prothrombin time or activated partial thrombin time 2
- Fluid restriction should be observed to prevent water intoxication 5
- Polydipsia is a contraindication to desmopressin treatment 5
Alternative Approaches
- For patients with severe bleeding who don't respond adequately to DDAVP, consider:
Clinical Decision Algorithm
- Confirm ESRD patient has active bleeding or requires an invasive procedure
- Assess for contraindications (polydipsia, severe hyponatremia)
- Calculate dose: 0.3 μg/kg IV diluted in 50 ml saline
- Administer over 30 minutes
- Monitor for clinical response and adverse effects
- Consider additional hemostatic measures if bleeding persists