Microbiology of Bloodstream Infections in Children after Hematopoietic Stem Cell Transplantation: A Single-Center Experience over Two Decades (1997–2017)

Sarah M. Heston*, Rebecca R. Young, Hwanhee Hong, Ibukunoluwa C. Akinboyo, John S. Tanaka, Paul L. Martin, Richard Vinesett, Kirsten Jenkins, Lauren E. McGill, Kevin C. Hazen, Patrick C. Seed, Matthew S. Kelly

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

9 Scopus citations

Abstract

Background. Bloodstream infections (BSIs) occur frequently after hematopoietic stem cell transplantation (HSCT). We examined the microbiology of BSI in pediatric HSCT recipients over a 2-decade period at our institution to inform empirical antimicrobial prescribing and infection prevention strategies. Methods. We conducted a retrospective cohort study of children (<18 years) who underwent HSCT at Duke University between 1997 and 2015. We used recurrent-event gap-time Cox proportional hazards models to determine the hazards of all-cause and cause-specific BSI according to HSCT year. We compared the median time to BSI by causative organism type and evaluated for temporal trends in the prevalence of antibiotic resistance among causative organisms. Results. A total of 865 BSI occurred in 1311 children, including 412 (48%) Gram-positive bacterial, 196 (23%) Gram-negative bacterial, 56 (6%) fungal, 23 (3%) mycobacterial, and 178 (21%) polymicrobial BSI. The hazard of all BSIs did not change substantially over time during the study period, but the hazard of fungal BSIs declined over time during the study period (P = .04). Most fungal BSIs (82%) occurred in the first 100 days after HSCT, whereas mycobacterial BSIs occurred later after HSCT than BSIs caused by other organisms (P < .0001). The prevalence of vancomycin resistance among BSIs caused by Enterococcus faecium increased during the study period (P = .0007). The risk of 2-year mortality in children was increased with BSI (P = .02), Gram-negative bacterial BSI (P = .02), and fungal BSI (P < .0001). Conclusions. Despite expanded practices for BSI prevention over the past several decades, the incidence of BSI remains high in pediatric HSCT recipients at our institution. Additional strategies are urgently needed to effectively prevent BSIs in this high-risk population.

Original languageEnglish (US)
Article numberofaa465
JournalOpen Forum Infectious Diseases
Volume7
Issue number11
DOIs
StatePublished - Nov 1 2020

Funding

This work was funded by National Institute of Child Health and Human Development of the National Institutes of Health under award number T32HD094671 (to S. M. H.). and M. S. K. was supported by a National Institutes of Health Career Development Award (K23-AI135090).

Keywords

  • Antibiotic resistance
  • Bloodstream infections
  • Hematopoietic stem cell transplantation
  • Immunocompromised host
  • Pediatrics

ASJC Scopus subject areas

  • Oncology
  • Infectious Diseases

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