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Published on: October 20, 2012
Serum and peritoneal inflammatory mediators in children with suspected acute appendicitis
Ilan Dalal1, Eli Somekh, Avital Bilker-Reich
1Pediatric Infectious/Allergy/Immunology Unit, The E. Wolfson Medical Center, Holon, Israel.
Insights
Inflammatory markers in peritoneal fluid, but not serum, can help diagnose appendicitis in children. However, systemic markers are not yet practical for differentiating appendicitis from other abdominal pain causes.
Area of Science:
- Pediatric Surgery
- Biochemistry
- Immunology
Background:
- Appendicitis is a common surgical emergency in children.
- Accurate and timely diagnosis is crucial to prevent complications.
- Systemic and local inflammatory markers are potential diagnostic tools.
Purpose of the Study:
- To investigate differences in inflammatory markers between children with and without appendicitis.
- To compare inflammatory marker levels in serum versus peritoneal fluid.
- To assess the utility of these markers in identifying appendicitis and perforation.
Main Methods:
- A cross-sectional study involving 24 children undergoing appendectomy.
- Measured serum and peritoneal fluid levels of various cytokines and enzymes (IL-8, IL-10, G-CSF, etc.) using ELISA.
- Compared marker concentrations between appendicitis patients (Group A) and controls (Group N), and between perforated and non-perforated cases.
Main Results:
- Peritoneal fluid concentrations of IL-8, IL-10, MMP-9, and TIMP-1 were significantly higher in children with appendicitis compared to controls.
- Peritoneal G-CSF was elevated in perforated appendicitis cases.
- Serum TIMP-1 was also significantly higher in perforated appendicitis compared to controls, but not in appendicitis overall.
Conclusions:
- Peritoneal inflammatory markers show promise in differentiating appendicitis in children.
- Systemic inflammatory markers are currently insufficient for reliably diagnosing appendicitis in pediatric patients.
- Further research may refine the use of specific markers for improved diagnostic accuracy.
Hypothesis:
Inflammatory markers differ between subjects with appendicitis and controls. Markers of inflammation differ in serum compared with intraperitoneal fluid. Among subjects with appendicitis, inflammatory markers differ between subjects with and without perforation.
Design:
Cross-sectional.
Setting:
Hospitalized care.
Patients:
Twenty-four children who underwent an appendectomy. Group A (n = 19) consisted of patients with appendicitis and group N (n = 5) of patients with normal appendixes.
Main Outcome Measures:
Serum and peritoneal levels of interleukin (IL)8, IL-10, granulocyte colony-stimulating factor, interferon gamma soluble intercellular adhesion molecule-1, matrix metalloproteinase-9, and tissue inhibitor of metalloproteinases-1 were measured by enzyme-linked immunosorbent assay.
Results:
Age, sex, complete blood count, C-reactive protein level, and serum cytokines did not significantly differ by group. Peritoneal concentrations of interleukin-8 (mean +/- SD, 1416.8 +/- 1436 pg/mL vs 48 +/- 74.4 pg/mL, P = .001), IL-10 (mean +/- SD, 3085 +/- 5893 pg/mL vs 84 +/- 46 pg/mL, P = .02), matrix metalloproteinase-9 (mean +/- SD, 1784 +/- 1225.1 ng/mL vs 435 +/- 563 ng/mL, P = .03), and tissue inhibitor of metalloproteinases-1 (mean +/- SD, 8939.2 +/- 7312.2 ng/mL vs 602.1 +/- 345.6 ng/mL, P<.001) were significantly different in group A compared with group N. When compared by perforation (n = 8 with perforation vs n = 11 without perforation), peritoneal granulocyte colony-stimulating factor levels were elevated in subjects with perforation (mean +/- SD, 4.3 +/- 14.4 pg/mL vs 62.7 +/- 79.2 pg/mL, P = .02). Although serum tissue inhibitor of metalloproteinases-1 was not different between groups N and A, it was significantly different between group N and patients with a perforated appendicitis (mean +/- SD, 205.9 +/- 43.8 ng/mL vs 3068.9 +/- 5122.4 ng/mL, P = .04).
Conclusion:
Presently, it is not practical to differentiate appendicitis in a pediatric population from other causes of abdominal pain based on the detection of systemic inflammatory response markers.
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