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Centrifugation vs. Multiple-pass Hemofiltration of the Residual Cardiopulmonary Bypass Volume

Outcomes & Biochemical Parameters Following Cardiac Surgery: Effects of Transfusion of Residual Blood Using Centrifugation and Multiple-Pass Hemofiltration

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01416792
Enrollment
61
Registered
2011-08-15
Start date
2011-03-31
Completion date
2012-10-31
Last updated
2013-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Heart Valve Diseases

Brief summary

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.

Detailed description

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).

Interventions

PROCEDUREMultiple-pass hemofiltration

The residual volume from the CPB circuit is pumped though a hemofilter for multiple passes removing the crystalloid component thereby concentrating the plasma.

Sponsors

Saskatoon Health Region
CollaboratorOTHER
University of Saskatchewan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* all males and females that will be receiving open heart surgery (Coronary Artery Bypass Grafts and / or Valve repair/replacement) during the study period.

Exclusion criteria

* history of bleeding disorders * history inflammatory diseases rheumatoid arthritis

Design outcomes

Primary

MeasureTime frameDescription
HemoglobinBaseline, Hemodilution and 12-hours post-operatively in ICUSerum hemoglobin will be measured from the patient at baseline, after hemodilution, and at 12-hours post-operatively in the ICU.
Albuminbaseline, hemodilution and 12-hours post-operatively in ICUSerum albumin in g/L will be measured at baseline, hemodilution and 12-hours post-operatively in ICU.
Total ProteinBaseline, hemodilution, and-12 hours post-operatively in ICUSerum total protein will be measured in g/L at the specified time intervals.

Secondary

MeasureTime frameDescription
Vasoactive Inotrope score12-hours post-operatively in ICUWe will calculate the vasoactive inotrope score to determine if there is an increased risk of adverse outcomes.
Length of stay in ICUWithin 24 hoursThe average time of discharged from ICU.
Allogeneic blood products12-hours post-operatively in ICUThe volume of allogeneic blood products will be recorded.
Indicators of Kidney Function12-hours ICUSerum creatinine, creatinine clearance, volume of IV fluid intake, volume of urine output, fluid balance
Markers of inflammationAt 12-hours ICUInflammatory mediators: tumor necrosis factor alpha (TNF-alpha), soluble receptors for advanced glycation end products (sRAGE), and high sensitivity C-reactive protein (hs CRP).
Ventilation time12-hours post-operatively in ICUThe time between intubation in OR and extubation in the ICU.
Chest tube drainage12-hours post-operatively in ICUThe total volume of chest tube drainage in ICU.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026