Surgery
Volume 148, Issue 3 , Pages 567-572, September 2010

The antiendotoxin agent taurolidine potentially reduces ischemia/reperfusion injury through its metabolite taurine

  • Kishore K. Doddakula, Mch

      Affiliations

    • Department of Cardiac Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • Peter M. Neary, MB

      Affiliations

    • Academic Department of Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • Jiang H. Wang, PhD

      Affiliations

    • Academic Department of Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • Shastri Sookhai, MD, FRCSI

      Affiliations

    • Academic Department of Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • Aongus O'Donnell, MD, FRCSI(CTh)

      Affiliations

    • Department of Cardiac Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • Tom Aherne, MB, FRCSI

      Affiliations

    • Department of Cardiac Surgery, University College Cork, Cork University Hospital, Cork, Ireland
  • ,
  • David J. Bouchier-Hayes, MD, FRCS

      Affiliations

    • Department of Surgery, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland
  • ,
  • Henry P. Redmond, Mch, FRCSI

      Affiliations

    • Academic Department of Surgery, University College Cork, Cork University Hospital, Cork, Ireland
    • Corresponding Author InformationReprint requests: Henry P. Redmond, Mch, FRCSI, Department of Academic Surgery, Cork University Hospital, Wilton, Cork, Ireland.

Accepted 14 January 2010. published online 12 March 2010.

Background

Cardiopulmonary bypass results in ischemia/reperfusion (I/R)-induced endotoxemia. We conducted a prospective randomized trial to investigate the effect of taurolidine, an antiendotoxin agent with antioxidant and membrane-stabilizing properties, on patients undergoing coronary artery bypass grafting (CABG).

Methods

A total of 60 patients undergoing CABG were randomized into 4 groups. St Thomas' Hospital cold crystalloid cardioplegia was used in groups A and B, and cold blood cardioplegia in groups C and D. Groups A and C received a placebo infusion of normal saline, whereas groups B and D were administered intravenous taurolidine. Arrhythmias induced by pro- and anti-inflammatory cytokines (interleukin [IL]-6 and IL-10), and I/R were assessed perioperatively.

Results

Administration of taurolidine in crystalloid cardioplegia patients resulted in a significant decrease in serum IL-6 and an increase in serum IL-10 at 24 hours postaortic unclamping compared to placebo (P < .0001). Although not statistically significant, this trend in serum IL-6 decrease was mirrored in the blood cardioplegia patients (P = .068). Taurolidine treatment also significantly decreased I/R-induced arrhythmias compared to placebo in the crystalloid cardioplegia patients (P < .003). There were fewer I/R-induced arrhythmias compared to placebo in the blood cardioplegia patients; the difference, however, was marginal and not statistically significant (P = .583).

Conclusion

This study demonstrates that administration of taurolidine in CABG patients induces a potent anti-inflammatory response that is associated with a significant decrease in arrhythmias.

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 Conflict of interest: The authors are currently engaged in an unrelated, sponsored clinical trial using taurolidine.

PII: S0039-6060(10)00022-X

doi:10.1016/j.surg.2010.01.006

Surgery
Volume 148, Issue 3 , Pages 567-572, September 2010