Diagnostic value of effluent endotoxin level in gram-negative peritonitis in CAPD patients

Objective:To evaluate the diagnostic usefulness of effluent endotoxin by Li mulus amoebocyte lysate (LAL) assay in gram-negative peritonitis patients o n continuous ambulatory peritoneal dialysis (CAPD) therapy. Design: Prospective study with patients serving as their own controls. Stan dard microbiologic work up and endotoxin analysis of effluents (night dwell ) were done during the pre- and posttreatment phases. Setting: Specimens from three teaching hospitals were processed and tested at a common center. Patients were left for treatment at their respective ce nters without intervention. Patients: 32 clinical peritonitis and 40 infection-free CAPD patients were studied. Results: 75% (n = 24) of cultures were positive: 41.6% (n = 10) gram-negati ve and 58.4% (n = 14) grampositive bacteria. Effluents of pre- and posttrea ted gram-negative cultures had endotoxin levels of 1.53 +/- 0.169 and 0.214 +/- 0.085 endotoxin units (EU)/mL, respectively (p < 0.0001); pre- and pos ttreated gram-positive levels of 0.102 +/- 0.06 and 0.122 =/- 0.052 EU/mL, respectively (p > 0.05); pre- and posttreated culture-negative peritonitis levels of 0.110 +/- 0.025 and 0.087 +/- 0.031 EU/mL, respectively (p > 0.05 ); peritonitis-free effluents contained 0.117 +/- 0.079 EU/mL. The diagnost ic specificity and the sensitivity of LAL assay were 100% and 98.2% respect ively. Conclusion: Where initial microbiological work-up cannot demonstrate a path ogen, effluent endotoxin determined by quantitative LAL assay is a useful m arker for diagnosis and management, within safe time limits, of gram-negati ve peritonitis in CAPD patients.