Outcomes in Pediatric Central Line-associated Bloodstream Infections Treated With Antimicrobial Locks: A 14-Year

Lorne W Walker1,2, Shyam Visweswaran3,4, Andrew J Nowalk5

  • 1From the Division of Pediatric Infectious Disease.

Insights

Antimicrobial lock therapy (ALT) effectively treats pediatric central line-associated bloodstream infections (CLABSI), with 85% initial clearance. Recurrence was 20%, influenced by infection history and resistant pathogens.

Area of Science:

  • Pediatric Infectious Diseases
  • Healthcare Epidemiology
  • Antimicrobial Stewardship

Background:

  • Central line-associated bloodstream infections (CLABSI) are the most common healthcare-associated infections in children.
  • Antimicrobial lock therapy (ALT) is recommended for CLABSI treatment, but pediatric data are limited.

Purpose of the Study:

  • To characterize pediatric CLABSI treated with ALT.
  • To identify factors associated with treatment outcomes and pathogen patterns.

Main Methods:

  • Retrospective chart review of 1188 pediatric CLABSI cases treated with ALT (2004-2018).
  • Data extraction included demographics, clinical, microbiological, and pharmacy information.
  • Outcomes assessed: CLABSI clearance, central venous catheter (CVC) removal, and infection recurrence.

Main Results:

  • 85% of CLABSI cases achieved initial clearance, with CVCs retained a median of 63 days.
  • 20% of initially cleared infections recurred.
  • Skin-colonizing microbes (e.g., Staphylococcus aureus) caused monomicrobial infections, while bowel microbes (e.g., E. coli) were linked to polymicrobial infections.
  • Infection history, resistant pathogens, and CVC type predicted recurrence; transplant status and neutrophil count influenced CVC removal.

Conclusions:

  • ALT is an effective component of pediatric CLABSI therapy, with varying efficacy across patient populations.
  • Findings provide guidance for optimizing ALT use in pediatric CLABSI management.
  • Further research is needed to refine therapeutic strategies for pediatric CLABSI.
Abstract

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