Effect of coronary artery bypass grafting with gastroepiploic artery on gastric intramucosal pH and systemic inflammation

J Cardiovasc Surg (Torino). 2001 Dec;42(6):723-9.

Abstract

Background: The purpose of this study was to investigate the effect of coronary arterial bypass grafting (CABG) with gastroepiploic artery (GEA) on gastric intramucosal pH and systemic inflammation.

Design: retrospective study.

Setting: University hospital.

Participants: 22 patients underwent CABG.

Investigations: the GEA group (n=13) received CABG with the GEA graft. The non-GEA group (n=9) received conventional CABG without the GEA graft.

Measurements: gastric intramucosal pH (pHi) and carbon dioxide tension (PrCO(2)) were assessed by capnometric air tonometry. The difference between PrCO(2) and PaCO(2), PCO(2)-gap, was also determined. Systemic inflammatory responses were evaluated by serum interleukin-6 (IL-6) and leucocyte counts. Hemodynamics, oxygen delivery index (DO(2)I) and uptake index (VO(2)I) were monitored with catheters in the radial and pulmonary arteries (thermodilution).

Results: The duration of aortic cross-clamping and cardiopulmonary bypass was similar in both groups. Both groups did not show any significant difference in gastric pHi, PCO(2)-gap, systemic inflammation and hemodynamics.

Conclusions: Our findings suggest that CABG using the GEA graft does not disturb gastric mucosal perfusion, and that laparotomy for the GEA graft does not aggravate systemic oxygen demand-supply imbalance or systemic inflammatory responses induced by hypothermic CPB. CABG with the GEA graft does not seem to pose an additional risk and is a safe technique compared with conventional CABG with regard to pHi and systemic inflammation.

MeSH terms

  • Aged
  • Carbon Dioxide / physiology*
  • Coronary Artery Bypass*
  • Epigastric Arteries / transplantation*
  • Female
  • Gastric Acidity Determination
  • Gastric Mucosa / physiopathology*
  • Graft Survival*
  • Hemodynamics
  • Humans
  • Hydrogen-Ion Concentration
  • Inflammation / blood
  • Inflammation / physiopathology*
  • Interleukin-6 / blood
  • Leukocyte Count
  • Male
  • Middle Aged
  • Oxygen Consumption

Substances

  • Interleukin-6
  • Carbon Dioxide