Cargando…
Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017)
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 strategie...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652097/ https://www.ncbi.nlm.nih.gov/pubmed/33209953 http://dx.doi.org/10.1093/ofid/ofaa465 |
_version_ | 1783607635525763072 |
---|---|
author | Heston, Sarah M Young, Rebecca R Hong, Hwanhee Akinboyo, Ibukunoluwa C Tanaka, John S Martin, Paul L Vinesett, Richard Jenkins, Kirsten McGill, Lauren E Hazen, Kevin C Seed, Patrick C Kelly, Matthew S |
author_facet | Heston, Sarah M Young, Rebecca R Hong, Hwanhee Akinboyo, Ibukunoluwa C Tanaka, John S Martin, Paul L Vinesett, Richard Jenkins, Kirsten McGill, Lauren E Hazen, Kevin C Seed, Patrick C Kelly, Matthew S |
author_sort | Heston, Sarah M |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7652097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76520972020-11-17 Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) Heston, Sarah M Young, Rebecca R Hong, Hwanhee Akinboyo, Ibukunoluwa C Tanaka, John S Martin, Paul L Vinesett, Richard Jenkins, Kirsten McGill, Lauren E Hazen, Kevin C Seed, Patrick C Kelly, Matthew S Open Forum Infect Dis Major Articles 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. Oxford University Press 2020-09-30 /pmc/articles/PMC7652097/ /pubmed/33209953 http://dx.doi.org/10.1093/ofid/ofaa465 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Articles Heston, Sarah M Young, Rebecca R Hong, Hwanhee Akinboyo, Ibukunoluwa C Tanaka, John S Martin, Paul L Vinesett, Richard Jenkins, Kirsten McGill, Lauren E Hazen, Kevin C Seed, Patrick C Kelly, Matthew S Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title | Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title_full | Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title_fullStr | Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title_full_unstemmed | Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title_short | Microbiology of Bloodstream Infections in Children After Hematopoietic Stem Cell Transplantation: A Single-Center Experience Over Two Decades (1997–2017) |
title_sort | microbiology of bloodstream infections in children after hematopoietic stem cell transplantation: a single-center experience over two decades (1997–2017) |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652097/ https://www.ncbi.nlm.nih.gov/pubmed/33209953 http://dx.doi.org/10.1093/ofid/ofaa465 |
work_keys_str_mv | AT hestonsarahm microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT youngrebeccar microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT honghwanhee microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT akinboyoibukunoluwac microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT tanakajohns microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT martinpaull microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT vinesettrichard microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT jenkinskirsten microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT mcgilllaurene microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT hazenkevinc microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT seedpatrickc microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 AT kellymatthews microbiologyofbloodstreaminfectionsinchildrenafterhematopoieticstemcelltransplantationasinglecenterexperienceovertwodecades19972017 |