Traditional cardiac surgery requires patient connection to the Cardiopulmonary Bypass (CPB) apparatus which takes over the function of the heart and lungs while the surgeon performs the necessary surgery. The residual blood left in the CPB equipment (1.5-2.0 L) is centrifuged and washed leaving only red blood cells (RBCs) suspended in a saline solution. The RBCs are reinfused into the patient as needed by the anesthesiologist. The main problem with this technique is that many of the important components of the blood such as plasma proteins and clotting factors are discarded through cell washing. This study will explore a novel method (multiple-pass hemofiltration) of processing the residual pump blood which will allow the patient to receive their own whole blood with minimum waste of important components. The newer method of processing the residual pump volume has also been termed off-line modified ultrafiltration (off-line MUF) and is similar to the process that the kidneys use to filter the blood. It is hypothesized that multiple-pass hemofiltration of the residual CPB volume will reduce the occurrence of inflammatory responses, preserve plasma proteins, and decrease allogenic blood exposure and improve clinical outcomes as compared to centrifugation.
This study is being performed because the traditional method of recovery of the residual volume of blood from the cardiopulmonary bypass circuit involves centrifugation and washing of whole blood with a saline solution. This process is sufficient for the recovery of red blood cells however; it results in the discarding of other important components of the blood. The removal of white blood cells, plasma proteins and clotting factors may result in an increased risk of a adverse outcomes during the post-operative period. The new technique our team wants to investigate returns a greater proportion of the patients' whole blood for reinfusion. Our study objectives are to compare the two techniques and determine which technique produces the safest most reliable method of blood processing to help the patient have a smooth, short, transfusion free post-operative period in the intensive care unit (ICU).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
61
The residual volume from the CPB circuit is pumped though a hemofilter for multiple passes removing the crystalloid component thereby concentrating the plasma.
Royal University Hospital
Saskatoon, Saskatchewan, Canada
Hemoglobin
Serum hemoglobin will be measured from the patient at baseline, after hemodilution, and at 12-hours post-operatively in the ICU.
Time frame: Baseline, Hemodilution and 12-hours post-operatively in ICU
Albumin
Serum albumin in g/L will be measured at baseline, hemodilution and 12-hours post-operatively in ICU.
Time frame: baseline, hemodilution and 12-hours post-operatively in ICU
Total Protein
Serum total protein will be measured in g/L at the specified time intervals.
Time frame: Baseline, hemodilution, and-12 hours post-operatively in ICU
Allogeneic blood products
The volume of allogeneic blood products will be recorded.
Time frame: 12-hours post-operatively in ICU
Ventilation time
The time between intubation in OR and extubation in the ICU.
Time frame: 12-hours post-operatively in ICU
Chest tube drainage
The total volume of chest tube drainage in ICU.
Time frame: 12-hours post-operatively in ICU
Vasoactive Inotrope score
We will calculate the vasoactive inotrope score to determine if there is an increased risk of adverse outcomes.
Time frame: 12-hours post-operatively in ICU
Length of stay in ICU
The average time of discharged from ICU.
Time frame: Within 24 hours
Markers of inflammation
Inflammatory mediators: tumor necrosis factor alpha (TNF-alpha), soluble receptors for advanced glycation end products (sRAGE), and high sensitivity C-reactive protein (hs CRP).
Time frame: At 12-hours ICU
Indicators of Kidney Function
Serum creatinine, creatinine clearance, volume of IV fluid intake, volume of urine output, fluid balance
Time frame: 12-hours ICU
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