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Impact of Fluid Restriction Policy in Reducing the Use of Red Cells in Cardiac Surgery

Not Applicable
Completed
Conditions
Coronary Artery Disease
Coronary Artery Bypass
Erythrocyte Transfusion
Interventions
Procedure: Fluid Restriction Policy
Procedure: Free fluid infusion
Registration Number
NCT00600704
Lead Sponsor
Larissa University Hospital
Brief Summary

The investigators' hypothesis is that restriction of circulating fluids in comparison to a liberal fluid administration policy would lead to a reduction of allogenic red blood cells exposure in patients undergoing cardiopulmonary bypass (CPB) for primary coronary artery bypass graft supported by reinfusion of washed shed blood from thoracic cavities.

Detailed Description

192 patients operated under equal conditions were assigned prospectively and randomly either for a restrictive protocol for intravenous fluid administration (group A, 100 patients) or not (group B, 92 patients). Transfusion guidelines were common for the two groups. The volumes of intravenous fluids, priming, "extra" volume on pump and cardioplegic solution and the volume of urine were recorded. Net erythrocyte volume loss was calculated. The number of the transfused PRC was analyzed as a continuous variable. "Transfusion" was analyzed as a categorical characteristic. Analysis employed Student's two-tailed t-test, t-paired test and chitest.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
192
Inclusion Criteria
  • Ejection fraction (EF) of left ventricle (LV) > 35%
  • Preoperative serum Creatinine < 150 μmol/l
  • Preoperative Haemoglobin > 10/dl
  • Peripheral anastomosis scheduled =< 3
Exclusion Criteria
  • redo bypass-emergency operations
  • prior coronal stenting
  • active congestive heart failure
  • documented Myocardial Infraction within the previous 6 weeks
  • NYHA class > 3
  • Carotid stenosis > 50%
  • CVA
  • INR > 1.5
  • chronic obstructive pulmonary disease (COPD)
  • Steroid therapy-chronic inflammatory process
  • Use of aprotinin or tranexamic acid

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RESTRICTED FLUIDSFluid Restriction PolicyInfusion of Hes 130/0.4 up to 500 ml until the beginning of Cardiopulmonary Bypass
FREE FLUIDSFree fluid infusionFree fluid infusion unless Hb\< 6g/dl(allogenic blood use), until the beginning of Cardiopulmonary bypass
Primary Outcome Measures
NameTimeMethod
Mean Number of Packed Red Cells Units Transfused During Hospital Stay20 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Larissa University Hospital

🇬🇷

Larissa, Thesalia, Greece

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