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Severe bacterial infection in young infants with pyrexia admitted to the emergency department

The objectives of this study were to understand the clinical presentations of febrile young infants with severe bacterial infection (SBI), and to investigate the pathogen variations throughout the vaccine era and after antenatal group B Streptococcus (GBS) screening. All infants < 90 days old wit...

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Autores principales: Chen, Yin-Ting, Chang, Yu-Jun, Liu, Bang-Yan, Lee, En-Pei, Wu, Han-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270585/
https://www.ncbi.nlm.nih.gov/pubmed/34232210
http://dx.doi.org/10.1097/MD.0000000000026596
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author Chen, Yin-Ting
Chang, Yu-Jun
Liu, Bang-Yan
Lee, En-Pei
Wu, Han-Ping
author_facet Chen, Yin-Ting
Chang, Yu-Jun
Liu, Bang-Yan
Lee, En-Pei
Wu, Han-Ping
author_sort Chen, Yin-Ting
collection PubMed
description The objectives of this study were to understand the clinical presentations of febrile young infants with severe bacterial infection (SBI), and to investigate the pathogen variations throughout the vaccine era and after antenatal group B Streptococcus (GBS) screening. All infants < 90 days old with a body temperature of ≥38.0°C and admitted to the emergency department were retrospectively enrolled in our study. SBI was defined as a positive culture of urine, blood, or cerebrospinal fluid. All clinical variables were analyzed and compared between the SBI group and the non-SBI group, to identify the relevant risk factors for SBI in infants with pyrexia. A total of 498 infants were studied, 279 of whom (56%) had SBI. The body temperature at triage was higher in the SBI group, and the difference was highly obvious in the neonatal group. White blood cell count and C-reactive protein levels were both significantly higher in the SBI group (P < .05), whereas neutrophil percentage and band percentage demonstrated no significant differences. Escherichia coli was the most common pathogen and plasmid-mediated extended-spectrum lactamases were detected in up to 9.1%. GBS was detected in 16 cases of bacteremia (6 cases with concurrent meningitis). The body temperature at triage may provide a clue for differentiating sick babies, especially in the neonatal group. Complete serum analysis is required for infection survey, especially white blood cell and C-reactive protein. Escherichia coli is the most common pathogen, and clinician should raise awareness of drug resistance in some patients. The prevalence of GBS infection in the young infant group remains high after routine antenatal GBS screening
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spelling pubmed-82705852021-07-12 Severe bacterial infection in young infants with pyrexia admitted to the emergency department Chen, Yin-Ting Chang, Yu-Jun Liu, Bang-Yan Lee, En-Pei Wu, Han-Ping Medicine (Baltimore) 3900 The objectives of this study were to understand the clinical presentations of febrile young infants with severe bacterial infection (SBI), and to investigate the pathogen variations throughout the vaccine era and after antenatal group B Streptococcus (GBS) screening. All infants < 90 days old with a body temperature of ≥38.0°C and admitted to the emergency department were retrospectively enrolled in our study. SBI was defined as a positive culture of urine, blood, or cerebrospinal fluid. All clinical variables were analyzed and compared between the SBI group and the non-SBI group, to identify the relevant risk factors for SBI in infants with pyrexia. A total of 498 infants were studied, 279 of whom (56%) had SBI. The body temperature at triage was higher in the SBI group, and the difference was highly obvious in the neonatal group. White blood cell count and C-reactive protein levels were both significantly higher in the SBI group (P < .05), whereas neutrophil percentage and band percentage demonstrated no significant differences. Escherichia coli was the most common pathogen and plasmid-mediated extended-spectrum lactamases were detected in up to 9.1%. GBS was detected in 16 cases of bacteremia (6 cases with concurrent meningitis). The body temperature at triage may provide a clue for differentiating sick babies, especially in the neonatal group. Complete serum analysis is required for infection survey, especially white blood cell and C-reactive protein. Escherichia coli is the most common pathogen, and clinician should raise awareness of drug resistance in some patients. The prevalence of GBS infection in the young infant group remains high after routine antenatal GBS screening Lippincott Williams & Wilkins 2021-07-09 /pmc/articles/PMC8270585/ /pubmed/34232210 http://dx.doi.org/10.1097/MD.0000000000026596 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 3900
Chen, Yin-Ting
Chang, Yu-Jun
Liu, Bang-Yan
Lee, En-Pei
Wu, Han-Ping
Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title_full Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title_fullStr Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title_full_unstemmed Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title_short Severe bacterial infection in young infants with pyrexia admitted to the emergency department
title_sort severe bacterial infection in young infants with pyrexia admitted to the emergency department
topic 3900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270585/
https://www.ncbi.nlm.nih.gov/pubmed/34232210
http://dx.doi.org/10.1097/MD.0000000000026596
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