The inflammatory response in transgastric surgery: gastric content leak leads to localized inflammatory response and higher adhesive disease

Surg Endosc. 2010 Mar;24(3):531-5. doi: 10.1007/s00464-009-0636-7. Epub 2009 Aug 18.

Abstract

Background: Risk of gastric spillage during transgastric surgery is a potential complication of NOTES procedures. The aim of this study was to determine risk outcomes from gastric spillage in a rat survival model by measuring local and systemic inflammatory markers, adhesive disease, and morbidity.

Methods: We performed a minilaparotomy with needle aspiration of 2 ml of gastric contents mixed with 2 ml of sterile saline (study group, SG) or 4 ml of sterile saline (control group, CG) injected into the peritoneal cavity of 60 male rats. Inflammatory markers (TNFalpha, IL-6, and IL-10) were analyzed at 1, 3, 6, and 24 h postoperatively by obtaining plasma levels and peritoneal washings. At necropsy, the peritoneal cavity was examined grossly for adhesions.

Results: Adhesions were seen more frequently in the SG versus the CG (100% vs. 33.3%, p < 0.014). There was a significant difference in the peritoneal TNFalpha levels in the SG compared with the CG, which peaked 1 h after surgery (p < 0.02). Both peritoneal IL-6 and IL-10 levels were higher in the SG versus the CG, which peaked 3 h after surgery (p < 0.005 and p < 0.001, respectively). All peritoneal inflammatory markers returned to undetectable levels at 24 h for both groups. Plasma cytokines were undetectable at all time intervals.

Conclusion: The inflammatory response was found to be a localized and not systemic event, with plasma cytokine levels remaining normal while peritoneal washings revealed a brisk, short-lived localized inflammatory response. There was a significantly higher rate of adhesive disease in the SG compared with the CG; this, however did not translate into a difference in apparent clinical outcome. We conclude that gastric leakage in this NOTES rodent model induces a localized inflammatory response, followed by mild to moderate adhesive disease. This may be important in human NOTES.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chi-Square Distribution
  • Enzyme-Linked Immunosorbent Assay
  • Gastrointestinal Contents / chemistry*
  • Inflammation Mediators / analysis*
  • Interleukin-10 / analysis*
  • Interleukin-6 / analysis*
  • Laparotomy
  • Models, Animal
  • Postoperative Complications / etiology*
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Risk Factors
  • Stomach / surgery*
  • Tissue Adhesions / etiology*
  • Tumor Necrosis Factor-alpha / analysis*

Substances

  • Inflammation Mediators
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Interleukin-10