Safety and Efficacy of the Use of Regional Anticoagulation With Citrate in Continuous Venovenous Hemofiltration
Kidney Failure, Acute
About this trial
This is an interventional treatment trial for Kidney Failure, Acute focused on measuring kidney failure, acute, venovenous hemofiltration, hemorrhage, heparin, low-molecular-weight, nadroparin, citrates
Eligibility Criteria
Inclusion Criteria: Intensive care patients scheduled for continuous venovenous hemofiltration Exclusion Criteria: Severe pre-existent liver failure (cirrhosis Child C), acute liver dysfunction as occurring with septic shock is not a reason for exclusion Active bleeding or bleeding necessitating the infusion of two red blood cell units within 24 hours before starting hemofiltration or a fall in hemoglobin of > 0.5 mmol/l. A fall in hemoglobin/hematocrit as a result of fluid loading is not regarded as bleeding. Surgery within 24 h prior to CVVH. Patients needing full systemic anticoagulation (unfractionated heparin in a dose of > 10000 IU/day, or nadroparin > 3800 IU/day) for other reasons Expectation to die within 24 hours Chronic dialysis Proven or suspected heparin-induced thrombocytopenia
Sites / Locations
- Onze Lieve Vrouwe Gasthuis
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
citrate
nadroparin
regional anticoagulation with citrate
nadroparin is a low molecular weight heparin