4.0 Article

Bloodstream Infections in Children With Cancer: Pathogen Distribution and Antimicrobial Susceptibility Patterns Over a 10-Year Period

期刊

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
卷 44, 期 1, 页码 E160-E167

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MPH.0000000000002258

关键词

bloodstream infection; febrile neutropenia; pathogen distribution; antimicrobial susceptibility; antimicrobial therapy

资金

  1. Danish Childhood Cancer Foundation [2017-2003]
  2. National Institutes of Health (NIH)
  3. Wellcome Trust

向作者/读者索取更多资源

This study retrospectively examined the distribution of pathogens in bloodstream infections (BSIs) and the antibiotic susceptibility in children with cancer over a 10-year period. The study found an increase in Gram-positive BSIs and stable, low-resistance rates against commonly used antibiotics. Piperacillin-tazobactam and meropenem showed consistent efficacy, while some resistance was observed in certain bacteria.
Bloodstream infections (BSIs) adversely affect clinical outcome in children with cancer. Over 1 decade, this retrospective cohort study describes pathogen distribution in BSIs and antimicrobial susceptibility against empirical antibiotics frequently prescribed in children with cancer. The antibiotic efficacy was evaluated through the determination of minimal inhibitory concentrations for piperacillin-tazobactam and meropenem and by disk diffusion for remaining antibiotics. From 2004 to 2013, 398 BSIs occurred in 196 children with cancer (median age: 5.4 y), resulting in 457 bacteria. Overall, 266 (58.2%) were Gram-positive, and 191 (41.8%) were Gram-negative with a significant Gram-positive increase over time (P=0.032). Coagulase-negative staphylococci (74, 16.2%), viridans group streptococci (67, 14.7%), Escherichia coli (52, 11.4%), and Staphylococcus aureus (39, 8.5%) were the most common pathogens. Susceptibility to piperacillin-tazobactam (95.9%, P=0.419) and meropenem (98.9%, P=0.752) was stable over time, and resistance was observed among viridans group streptococci against piperacillin-tazobactam (18%) and meropenem (7%) and among Enterobacterales against piperacillin-tazobactam (3%). Vancomycin showed 98% Gram-positive activity, gentamicin 82% Gram-negative activity and ampicillin, cefotaxime, and cefuroxime were active in 50%, 72%, and 69% of pathogens, respectively, and BSI-related mortality was 0%. In conclusion, over 1 decade, we report an increase in Gram-positive BSIs, and stable, low-resistance rates against currently recommended empirical antibiotics, piperacillin-tazobactam and meropenem.

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