MedPath

Intraoperative Cell Salvage and Postoperative Acidosis

Completed
Conditions
Metabolic Acidosis
Interventions
Procedure: routine administration of 0.9% sodium chloride
Registration Number
NCT02800343
Lead Sponsor
University of Edinburgh
Brief Summary

Metabolic acidosis is a common complication that patients experience in the early postoperative period following cardiac surgery. Increasingly, the composition and volume of intravenous fluids administered during surgery have been implicated in the development of postoperative acidosis. Intraoperative Cell Salvage (ICS), an autologous blood transfusion technique employed by Cardiac/Perfusion Units to minimize blood loss during surgery, involves the infusion of of one such fluid, 0.9% sodium chloride. The rapid infusion of large volumes of 0.9% sodium chloride has previously been linked with the development of hyperchloraemic acidosis. It was therefore hypothesized that the volume of mechanically salvaged of red blood cells re-infused into patients undergoing heart surgery contributes to the acidosis that occurs in the early postoperative period.

To test this, the investigators have designed an observational cohort study to check for correlation between the volume of cell salvaged blood infused during surgery and the severity of postoperative acidosis (which will be assessed using data from routine arterial blood gas samples).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
37
Inclusion Criteria
  • Age ≥ 18 years
  • Patients scheduled for cardiac surgery including both on- and off-pump coronary artery bypass grafting surgery, heart valve surgery, septal surgery, and aortic surgery)
  • Patients must have consented to participate
Exclusion Criteria
  • Patients under 18 years of age
  • Patients who are unable or unwilling to provide informed consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Cardiovascular surgeryroutine administration of 0.9% sodium chlorideAll adult patients undergoing elective or emergency cardiovascular surgery at the study site
Primary Outcome Measures
NameTimeMethod
plasma hydrogen ion concentrationat the start of surgery (before fluid infusion) and immediately after surgery (after fluid infusion)

Plasma hydrogen ion concentration is measured by the arterial blood gas analyzer machine, and serves as a direct indicator of plasma acidity at a given time point.

Data from two routine blood gas samples are of interest:

T1 - baseline measurement taken on insertion of an arterial line immediately after the induction of anaesthesia (i.e. before any fluid infusion has commenced); T2 - postoperative measurement made immediately after patient arrives in ICU (i.e. once all the cell salvaged blood has been transfused)

Secondary Outcome Measures
NameTimeMethod
plasma chloride concentrationat the start of surgery (before fluid infusion) and immediately after surgery (after fluid infusion)

Plasma chloride concentration is measured by the arterial blood gas analyzer machine.

Data from two routine blood gas samples are of interest:

T1 - baseline measurement taken on insertion of an arterial line immediately after the induction of anaesthesia (i.e. before any fluid infusion has commenced); T2 - postoperative measurement made immediately after patient arrives in ICU (i.e. once all the cell salvaged blood has been transfused)

plasma strong ion differenceat the start of surgery (before fluid infusion) and immediately after surgery (after fluid infusion)

Plasma strong ion difference can be computed from routine arterial blood gas electrolyte measurements (chloride, lactate, sodium, potassium) using a formula.

Strong ion difference serves as an indirect measure of plasma acidity.

Data from two routine blood gas samples are of interest:

T1 - baseline measurement taken on insertion of an arterial line immediately after the induction of anaesthesia (i.e. before any fluid infusion has commenced); T2 - postoperative measurement made immediately after patient arrives in ICU (i.e. once all the cell salvaged blood has been transfused)

Trial Locations

Locations (1)

Royal Infirmary of Edinburgh

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Edinburgh, Midlothian, United Kingdom

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