Fluid Chloride and AKI in Cardiopulmonary Bypass
Acute Kidney Injury
About this trial
This is an interventional prevention trial for Acute Kidney Injury
Eligibility Criteria
Inclusion Criteria:
- Planned on- or off-pump cardiac surgery including: bypass grafting, valvular procedures, congenital defect correction, and thoracic aortic procedures or a combination of these procedures
Exclusion Criteria:
- Emergency surgery
- Pregnancy
- Previous renal transplantation
- Documented moderate to severe acute kidney injury prior to enrollment (e.g. RIFLE-I or RIFLE-F/KDIGO stage 2 or 3)
- Patients already receiving dialysis (acute or chronic) or in imminent need of dialysis at time of enrollment
- Chronic kidney disease without baseline serum creatinine value obtained within 6 months of enrollment
Sites / Locations
- University of New Mexico Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Normal Saline group
Isolyte group
0.9% Normal Saline (0.9% Sodium Chloride) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients.
Isolyte S (B Braun, Irvine CA) injection intravenously as needed. The amount administered (dosage, frequency, and duration) will be left to the clinical judgment of the attending physicians, and will follow usual patterns of use in cardiac surgery patients. Isolyte S is a prepackaged solution containing sodium chloride 0.53%, sodium gluconate 0.5%, sodium acetate trihydrate 0.37%, potassium chloride 0.037%, and magnesium chloride hexahydrate 0.03% w/v.