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Susceptibility testing of bacteria recovered from patients with peritonitis complicating continuous ambulatory

H Ludlam1, L Johnston, P Hopkins

  • 1Department of Medical Microbiology, St. Bartholmew's Hospital, West Smithfield, London, United Kingdom.

Insights

Peritoneal dialysis fluid reduces antibiotic effectiveness, but this study found no evidence it causes treatment failure in peritonitis. Standard laboratory testing for antibiotic susceptibility remains reliable for continuous ambulatory peritoneal dialysis patients.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Clinical Microbiology

Background:

  • Peritonitis is a serious complication of continuous ambulatory peritoneal dialysis (CAPD).
  • Reduced antibiotic activity in peritoneal dialysate has been suspected as a cause of treatment failure in CAPD peritonitis.
  • Ciprofloxacin is a common monotherapy for CAPD peritonitis.

Purpose of the Study:

  • To investigate if antagonism of ciprofloxacin activity by peritoneal dialysate contributes to treatment failure in CAPD peritonitis.
  • To determine if standard laboratory susceptibility testing methods are adequate for CAPD peritonitis.

Main Methods:

  • A case-control study was conducted on bacteria from 34 CAPD peritonitis episodes treated with ciprofloxacin.
  • Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of ciprofloxacin were determined in Iso-Sensitest broth (IB), fresh dialysate (FD), and pooled dialysis effluent (PDE).
  • Antibiotic activity was compared between patients with treatment failure (relapse) and those who resolved without sequelae.

Main Results:

  • Ciprofloxacin exhibited significantly reduced activity in FD and PDE compared to IB (P < 0.05).
  • Median MIC increased from 0.5 µg/ml in IB to 2.0 µg/ml in FD and PDE.
  • Median MBC increased from 8.0 µg/ml in IB to 64.0-128.0 µg/ml in FD and PDE.
  • No significant differences in ciprofloxacin MIC or MBC were observed between relapsers and non-relapsers in any tested medium.

Conclusions:

  • Dialysate antagonizes ciprofloxacin activity, but this antagonism does not appear to be a cause of treatment failure in CAPD peritonitis.
  • Conventional laboratory susceptibility testing methods are likely sufficient and do not need to be replaced with testing in dialysate-containing media.
  • Further research may explore other factors contributing to treatment failure in CAPD peritonitis.

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