Prevention of Renal Failure by Nitric Oxide in Prolonged Cardiopulmonary Bypass.
Heart Valve Diseases, Heart; Complications, Valve, Prosthesis, Cardiac Valve Replacement Complication
About this trial
This is an interventional prevention trial for Heart Valve Diseases
Eligibility Criteria
Inclusion Criteria:
- Provide written informed consent
- Are > 18 years of age
- Elective cardiac or aortic surgery with CPB, when the surgeon plans double valve replacement.
- Stable pre-operative renal function, without dialysis.
Exclusion Criteria:
- Emergent cardiac surgery
- Life expectancy < 1 year
- Hemodynamic instability as defined by a systolic blood pressure <90 mmHg
- Administration of ≥1 Packed Red Blood Cell transfusion in the week before surgery
- X-ray contrast infusion less than 1 week before surgery
- Anticipate administration of nephrotoxic agents, such as hydroxyethyl starch
- Evidence of intravascular or extravascular hemolysis
Sites / Locations
- Xijing Hospital
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
inhaled nitrogen
inhaled nitric oxide
Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, pure nitrogen (placebo) is mixed with pure O2 or air. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the NO is delivered through the inspiratory limb of the anesthetic or ventilator circuit.
Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, 800 ppm NO gas is mixed with pure O2 or air to obtain a final concentration of 80 ppm NO. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the gas is delivered through the inspiratory limb of the anesthetic or ventilator circuit. NO, NO2 and O2 and methemoglobin levels are monitored by an unblinded observer.