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Updated: Dec 26, 2025

Intramyocardial Cell Delivery: Observations in Murine Hearts
Published on: January 24, 2014
Does Intraoperative Cell Salvage Reduce Postoperative Infection Rates in Cardiac Surgery?
Jan van Klarenbosch1, Edwin R van den Heuvel2, Willem van Oeveren3
1Department of Anesthesiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Objective:
Primary outcome was the risk for infections after cell salvage in cardiac surgery.
Design:
Data of a randomized controlled trial on cell salvage and filter use (ISRCTN58333401).
Setting:
Six cardiac surgery centers in the Netherlands.
Participants:
All 716 patients undergoing elective coronary artery bypass grafting, valve surgery, or combined procedures over a 4-year period who completed the trial.
Interventions:
Postoperative infection data were assessed according to Centre of Disease Control and Prevention/National Healthcare Safety Network surveillance definitions.
Measurements And Main Results:
Fifty-eight (15.9%) patients with cell salvage had infections, compared with 46 (13.1%) control patients. Mediation analysis was performed to estimate the direct effect of cell salvage on infections (OR 2.291 [1.177;4.460], p = 0.015) and the indirect effects of allogeneic transfusion and processed cell salvage blood on infections. Correction for confounders, including age, seks and body mass index was performed. Allogeneic transfusion had a direct effect on infections (OR = 2.082 [1.133;3.828], p = 0.018), but processed cell salvage blood did not (OR = 0.999 [0.999; 1.001], p = 0.089). There was a positive direct effect of cell salvage on allogeneic transfusion (OR = 0.275 [0.176;0.432], p < 0.001), but a negative direct effect of processed cell salvage blood (1.001 [1.001;1.002], p < 0.001) on allogeneic transfusion. Finally, there was a positive direct effect of cell salvage on the amount of processed blood.
Conclusions:
Cell salvage was directly associated with higher infection rates, but this direct effect was almost completely eliminated by its indirect protective effect through reduced allogeneic blood transfusion.
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