Three-year analysis of microbial aetiology and antimicrobial susceptibilities of PD peritonitis

Heidi Leppänen1, Kaj P Metsärinne, Jukka Nikoskelainen

  • 1Department of Internal Medicine, Turku University Central Hospital, Turku, Finland.

Insights

Empirical antibiotic treatment for peritoneal dialysis (PD) peritonitis should target common pathogens. A cephalosporin-aminoglycoside combination showed superior antimicrobial activity against PD peritonitis pathogens compared to other common regimens.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Microbiology

Background:

  • Peritoneal dialysis (PD) peritonitis requires effective first-line antibiotic therapy targeting common causative microorganisms.
  • Antimicrobial resistance patterns necessitate ongoing evaluation of empirical treatment protocols.

Purpose of the Study:

  • To analyze the antimicrobial sensitivities of various empirical antibiotic protocols used for the initial treatment of PD peritonitis.
  • To identify the most effective antibiotic strategy based on local microbial patterns.

Main Methods:

  • Retrospective analysis of 86 PD peritonitis cases over 36 months.
  • Identification of etiological microorganisms and assessment of their in vitro antimicrobial sensitivities.
  • Comparison of the efficacy of different empirical antibiotic protocols.

Main Results:

  • Staphylococcus aureus was the most frequent pathogen, often associated with severe illness.
  • The combination of a first-generation cephalosporin and an aminoglycoside demonstrated superior in vitro efficacy compared to other tested regimens, except vancomycin-ceftazidime.
  • Culture-negative peritonitis was over-represented in icodextrin PD fluid users.

Conclusions:

  • The combination of a first-generation cephalosporin and an aminoglycoside remains a highly effective empirical treatment for PD peritonitis.
  • Continued use of aminoglycosides in empirical treatment is supported by current antimicrobial sensitivity data.
  • Icodextrin use may be associated with an increased risk of culture-negative peritonitis.

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