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Enterococcal peritonitis in children receiving chronic peritoneal dialysis
Scott M Sutherland1, Steven R Alexander, Reinhard Feneberg
1Stanford University Medical Center, Department of Pediatrics, Division of Nephrology, 300 Pasteur Drive, Room G-306, Stanford, CA 94035, USA. suthersm@stanford.edu
Insights
Enterococcus causes about 6% of peritonitis in children on chronic peritoneal dialysis (CPD). Treatment outcomes are good despite antibiotic resistance, with cephalosporin regimens showing effectiveness.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Dialysis
Background:
- Peritonitis is a frequent complication of chronic peritoneal dialysis (CPD), often leading to technique failure.
- Enterococcus is an infrequent cause of peritonitis in pediatric CPD patients, posing treatment challenges due to antibiotic resistance.
Purpose of the Study:
- To evaluate the incidence, clinical presentation, and outcomes of enterococcal peritonitis in children undergoing CPD.
- To assess the impact of antibiotic resistance patterns on treatment efficacy.
Main Methods:
- Data from 392 children with CPD experiencing 340 culture-positive peritonitis episodes (2001-2004) were analyzed from the International Pediatric Peritonitis Registry.
- Clinical characteristics, in vitro antibiotic resistance, and treatment responses were assessed.
Main Results:
- Enterococcus species accounted for 5.9% of culture-positive peritonitis episodes.
- No unique clinical features distinguished enterococcal peritonitis at presentation.
- Despite in vitro resistance to cephalosporins and 21% resistance to glycopeptides, all patients achieved full functional recovery, irrespective of empiric antibiotic choice.
Conclusions:
- Enterococci are a significant cause of peritonitis in pediatric CPD patients, requiring careful management.
- Clinical outcomes are favorable and not influenced by in vitro resistance patterns or initial antibiotic regimens, suggesting prompt recovery even with cephalosporin-based empiric therapy.
Background:
Peritonitis is a common complication of chronic peritoneal dialysis (CPD) and can be associated with technique failure. Enterococcus is an uncommon peritoneal pathogen in children receiving CPD but represents a potential therapeutic challenge due to its innate resistance to cephalosporins and emerging resistance to glycopeptides.
Methods:
The International Pediatric Peritonitis Registry is a global consortium of 47 paediatric dialysis centres designed to address validation of the International Society for Peritoneal Dialysis paediatric peritonitis treatment guidelines. Between 2001 and 2004, peritonitis episodes were assessed in 392 participating children receiving CPD.
Results:
Among the 392 patients, 340 episodes of culture-positive peritonitis were evaluated. Twenty of these episodes were due to Enterococcus species (5.9%). There were no clinical characteristics uniquely associated with enterococcal peritonitis at presentation. After 3 days of therapy, 75% of patients were pain free, 95% had decreased effluent cloudiness and 90% were afebrile. Only one patient required a catheter exchange, and all patients experienced full functional recovery. Despite broad in vitro resistance to cephalosporins and 21% resistance to glycopeptides, neither in vitro resistance pattern nor choice of empiric antibiotic regimen affected short- or long-term outcomes.
Conclusions:
Enterococci are likely responsible for ∼6% of culture-positive peritonitis episodes in children receiving CPD. Although it was not possible to identify patients with enterococcal peritonitis based on presentation, clinical response was not associated with in vitro resistance patterns, and patients who initially received a cephalosporin-based empiric regimen until culture results are available are likely to respond quickly and have full functional recovery.
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