Cargando…
237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts
BACKGROUND: Elizabethkingia species are environmental opportunistic pathogens that are a rare but potentially severe cause of bloodstream infection (BSI). The objective of this study was to determine the incidence, risk factors, and outcomes of Elizabethkingia species BSI in a large Australian popul...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678878/ http://dx.doi.org/10.1093/ofid/ofad500.310 |
_version_ | 1785150462276665344 |
---|---|
author | Stewart, Adam Laupland, Kevin Edwards, Felicity Paterson, David Harris, Patrick N A |
author_facet | Stewart, Adam Laupland, Kevin Edwards, Felicity Paterson, David Harris, Patrick N A |
author_sort | Stewart, Adam |
collection | PubMed |
description | BACKGROUND: Elizabethkingia species are environmental opportunistic pathogens that are a rare but potentially severe cause of bloodstream infection (BSI). The objective of this study was to determine the incidence, risk factors, and outcomes of Elizabethkingia species BSI in a large Australian population. METHODS: Retrospective, laboratory-based surveillance was conducted among residents of Queensland, Australia (population approximately 5 million) over a twenty-year study period. All microbiological data was collected from a government-funded, centralised laboratory service. Clinical and outcome information was obtained from statewide databases. RESULTS: During 86 million person-years of surveillance, 112 incident Elizabethkingia species BSI occurred for an annualized age and sex-standardized incidence of 1.4 per million residents. Elizabethkingia species isolates were identified as E. meningoseptica in 104 (93%) and were not speciated in 8 (7%). Fifty-three percent were male, and the median age was 69 years (IQR, 55-80). Almost 80% were hospital onset or healthcare-associated BSI, and the median length of hospital stay being 10 days (IQR, 5-30). Comorbidity was common with a median Charlson Co-morbidity Index of 3 (IQR, 1-4), with 25% having active malignancy. Almost 80% were monomicrobial infections, with the majority having no focus identified. Ninety-day overall case-fatality rate was 23%. In vitro susceptibility to ciprofloxacin, sulfamethoxazole, piperacillin-tazobactam was 75%, 71%, 18%, respectively; all isolates were resistant to vancomycin. CONCLUSION: Elizabethkingia species BSI is an important cause of opportunistic infection, particularly among vulnerable hosts. Although uncommon, it is associated with a high case-fatality rate and limited antibiotic treatment options due to intrinsic resistance mechanisms. DISCLOSURES: David Paterson, AMR Action Fund: Board Member|Entasis: Board Member|Merck: Board Member|Pfizer: Board Member|QPex: Board Member|Venatorx: Board Member Patrick N A Harris, PhD, DTMH, MRCP, FRACP, FRCPA, Merck: Advisor/Consultant|Opgen: Advisor/Consultant|Sandoz: Advisor/Consultant |
format | Online Article Text |
id | pubmed-10678878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106788782023-11-27 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts Stewart, Adam Laupland, Kevin Edwards, Felicity Paterson, David Harris, Patrick N A Open Forum Infect Dis Abstract BACKGROUND: Elizabethkingia species are environmental opportunistic pathogens that are a rare but potentially severe cause of bloodstream infection (BSI). The objective of this study was to determine the incidence, risk factors, and outcomes of Elizabethkingia species BSI in a large Australian population. METHODS: Retrospective, laboratory-based surveillance was conducted among residents of Queensland, Australia (population approximately 5 million) over a twenty-year study period. All microbiological data was collected from a government-funded, centralised laboratory service. Clinical and outcome information was obtained from statewide databases. RESULTS: During 86 million person-years of surveillance, 112 incident Elizabethkingia species BSI occurred for an annualized age and sex-standardized incidence of 1.4 per million residents. Elizabethkingia species isolates were identified as E. meningoseptica in 104 (93%) and were not speciated in 8 (7%). Fifty-three percent were male, and the median age was 69 years (IQR, 55-80). Almost 80% were hospital onset or healthcare-associated BSI, and the median length of hospital stay being 10 days (IQR, 5-30). Comorbidity was common with a median Charlson Co-morbidity Index of 3 (IQR, 1-4), with 25% having active malignancy. Almost 80% were monomicrobial infections, with the majority having no focus identified. Ninety-day overall case-fatality rate was 23%. In vitro susceptibility to ciprofloxacin, sulfamethoxazole, piperacillin-tazobactam was 75%, 71%, 18%, respectively; all isolates were resistant to vancomycin. CONCLUSION: Elizabethkingia species BSI is an important cause of opportunistic infection, particularly among vulnerable hosts. Although uncommon, it is associated with a high case-fatality rate and limited antibiotic treatment options due to intrinsic resistance mechanisms. DISCLOSURES: David Paterson, AMR Action Fund: Board Member|Entasis: Board Member|Merck: Board Member|Pfizer: Board Member|QPex: Board Member|Venatorx: Board Member Patrick N A Harris, PhD, DTMH, MRCP, FRACP, FRCPA, Merck: Advisor/Consultant|Opgen: Advisor/Consultant|Sandoz: Advisor/Consultant Oxford University Press 2023-11-27 /pmc/articles/PMC10678878/ http://dx.doi.org/10.1093/ofid/ofad500.310 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Stewart, Adam Laupland, Kevin Edwards, Felicity Paterson, David Harris, Patrick N A 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title | 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title_full | 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title_fullStr | 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title_full_unstemmed | 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title_short | 237. Elizabethkingia species: An Emerging Cause of Healthcare-Associated Bloodstream Infection Among Immunocompromised Hosts |
title_sort | 237. elizabethkingia species: an emerging cause of healthcare-associated bloodstream infection among immunocompromised hosts |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678878/ http://dx.doi.org/10.1093/ofid/ofad500.310 |
work_keys_str_mv | AT stewartadam 237elizabethkingiaspeciesanemergingcauseofhealthcareassociatedbloodstreaminfectionamongimmunocompromisedhosts AT lauplandkevin 237elizabethkingiaspeciesanemergingcauseofhealthcareassociatedbloodstreaminfectionamongimmunocompromisedhosts AT edwardsfelicity 237elizabethkingiaspeciesanemergingcauseofhealthcareassociatedbloodstreaminfectionamongimmunocompromisedhosts AT patersondavid 237elizabethkingiaspeciesanemergingcauseofhealthcareassociatedbloodstreaminfectionamongimmunocompromisedhosts AT harrispatrickna 237elizabethkingiaspeciesanemergingcauseofhealthcareassociatedbloodstreaminfectionamongimmunocompromisedhosts |