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World J Crit Care Med. Dec 9, 2025; 14(4): 108370
Published online Dec 9, 2025. doi: 10.5492/wjccm.v14.i4.108370
Table 3 Dosing and monitoring of desmopressin in intensive care unit indications
Clinical Indication
Desmopressin dose and route
Frequency/duration
Monitoring/notes
Uremic bleeding (end-stage renal disease)0.3 µg/kg IV (approximately 20-30 µg)Single dose; may repeat in 24 hours with cautionCheck bleeding time or PFA-100 if available; effect begins in approximately 1 hour, lasts 6-8 hours. Implement fluid restriction for 12-24 hours post-dose
Antiplatelet-associated intracerebral hemorrhage0.4 µg/kg IV (max approximately 30 µg)One-time dose at presentationAdminister promptly upon confirmation of hemorrhage. Monitor blood pressure during infusion (risk of hypotension). Reassess hematoma size on imaging. No routine repeat dosing
Trauma-induced coagulopathy (suspected platelet dysfunction/vWD)0.3 µg/kg IVSingle dose early during resuscitationIndicated for patients on antiplatelet agents or with known vWD. Incorporate into massive transfusion protocols. Monitor bleeding parameters (e.g., TEG/ROTEM). Not for empirical use
Inherited von Willebrand disease (type 1 and select type 2)0.3 µg/kg IV/SC or 300 µg intranasal (150 µg/nostril)Single dose; repeat in 12-24 hours if needed (max 2-3 doses)Verify normal serum sodium before administration. Trial dose recommended to confirm responsiveness. Ineffective in Type 3 vWD—use vWF concentrate instead. Monitor vWF: FVIII levels if possible
Qualitative platelet dysfunction (e.g., CPB, liver disease)0.3 µg/kg IVOne-time dose as needed for diffuse bleedingUse in microvascular bleeding when platelet count is adequate but function impaired. Observe bleeding control (e.g., chest drain output). Consider adjunctive use of TXA
Central diabetes insipidus1-2 µg IV/SC (fixed dose)q8-12h; titrate based on clinical responseMonitor urine output hourly, urine specific gravity, and serum sodium every 4-6 hours. Adjust dose to maintain balanced output and stable sodium. Reduce or pause if sodium drops rapidly. Transition to oral/intranasal forms when stable


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