Comparison of inflammatory response during on-pump and off-pump coronary artery bypass surgery

Thomas Rimmelé1, Ramesh Venkataraman, Nicholas J Madden

  • 1The CRISMA (Clinical Research, Investigation, and Systems Modeling of Acute Illness) Laboratory, Department of Critical Care Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 1526, USA.

Insights

Modern extracorporeal circuits minimize inflammatory differences between on-pump and off-pump coronary artery bypass graft (CABG) surgery. The surgical procedure itself is the primary driver of the inflammatory response, not the bypass circuit.

Area of Science:

  • Cardiovascular Surgery
  • Immunology
  • Biomaterials Science

Background:

  • On-pump coronary artery bypass graft (CABG) surgery traditionally elicits a greater inflammatory response than off-pump CABG.
  • Advancements in polymer-coated biocompatible extracorporeal circuits may alter this inflammatory profile.

Purpose of the Study:

  • To investigate whether cardiopulmonary bypass, using modern extracorporeal circuits, still significantly contributes to the inflammatory response in CABG surgery.
  • To compare the inflammatory response between on-pump and off-pump CABG procedures with advanced circuit technology.

Main Methods:

  • Prospective observational study of 33 patients undergoing CABG (25 on-pump, 8 off-pump).
  • Serial measurement of plasma cytokines (TNF, IL-6, IL-10) and procalcitonin.
  • Collection of demographic, clinical, intra-operative, and post-operative data.

Main Results:

  • Plasma levels of all measured inflammatory mediators (cytokines and procalcitonin) increased during surgery and normalized postoperatively.
  • No significant differences in mediator levels were observed between the on-pump and off-pump CABG groups at any time point.

Conclusions:

  • Modern polymer-coated biocompatible extracorporeal circuits result in an inflammatory response magnitude and pattern similar to off-pump CABG.
  • The surgical procedure itself is the main contributor to the inflammatory response, with minimal impact from the extracorporeal circuit.
Abstract