Cell salvage alters the systemic inflammatory response after off-pump coronary artery bypass grafting surgery

Stephen J Allen1, William T McBride, Terence J McMurray

  • 1Department of Clinical Anaesthesia, Royal Group of Hospitals Trust, Belfast, Ireland. stephen.allen@royalhospitals.n-i.nhs.uk

Insights

Managing shed mediastinal blood during off-pump coronary artery bypass (OPCAB) surgery alters cytokine levels. Avoiding retransfusion of unwashed cardiotomy suction blood reduces inflammatory markers but does not prevent subclinical renal injury.

Area of Science:

  • Cardiovascular Surgery
  • Immunology
  • Nephrology

Background:

  • Cardiotomy suction blood contains elevated inflammatory markers.
  • This blood is a bypass-independent source of inflammatory mediators.
  • Unwashed cardiotomy suction blood retransfusion may contribute to perioperative inflammation.

Purpose of the Study:

  • To investigate the effect of managing shed mediastinal blood on cytokine concentrations during OPCAB surgery.
  • To determine if avoiding retransfusion of unwashed cardiotomy suction blood is renoprotective.

Main Methods:

  • Thirty-seven OPCAB patients were randomized into control (unwashed blood retransfusion) and treatment (washed or discarded blood) groups.
  • Plasma and urinary cytokine concentrations (TNF-alpha, IL-8, IL-6, IL-10, TNF soluble receptor-2, IL-1 receptor antagonist) were measured over 72 hours.
  • Renal injury and dysfunction markers (NAG, alpha1-microglobulin) were assessed.

Main Results:

  • Elevated proinflammatory cytokines in cardiotomy suction blood were eliminated by cell salvage.
  • The treatment group showed reduced plasma TNF soluble receptor-2 compared to controls.
  • Significantly reduced urinary TNF soluble receptor-2 was observed in the treatment group, but no differences in renal injury markers were found.

Conclusions:

  • Management of shed mediastinal blood alters perioperative cytokine homeostasis during OPCAB surgery.
  • Altering shed blood management impacts systemic, plasma, and urinary cytokine profiles.
  • This intervention did not impact subclinical renal injury or dysfunction in this low-risk patient group.
Abstract