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Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae

To identify differences in the clinical characteristics of early- and late-onset sepsis (EOS and LOS) caused by Klebsiella pneumoniae (K. pneumoniae) and to describe the risk factors for multidrug-resistant K. pneumoniae (MDR-KP) infection. Infants with K. pneumoniae-induced sepsis who were admitted...

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Autores principales: You, Ting, Zhang, Han, Guo, Lu, Ling, Ke-Ran, Hu, Xiao-Yu, Li, Lu-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444108/
https://www.ncbi.nlm.nih.gov/pubmed/32816593
http://dx.doi.org/10.1177/2058738420950586
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author You, Ting
Zhang, Han
Guo, Lu
Ling, Ke-Ran
Hu, Xiao-Yu
Li, Lu-Quan
author_facet You, Ting
Zhang, Han
Guo, Lu
Ling, Ke-Ran
Hu, Xiao-Yu
Li, Lu-Quan
author_sort You, Ting
collection PubMed
description To identify differences in the clinical characteristics of early- and late-onset sepsis (EOS and LOS) caused by Klebsiella pneumoniae (K. pneumoniae) and to describe the risk factors for multidrug-resistant K. pneumoniae (MDR-KP) infection. Infants with K. pneumoniae-induced sepsis who were admitted to a children’s Hospital between Jan 2000 and Dec 2019 were included. All infants were divided into EOS and LOS groups, as well as MDR-KP and non-MDR-KP groups. Demographics, clinical characteristics, and risk factors were compared between the two groups. One hundred eighty infants (66 with EOS and 114 with LOS) were further analyzed, accounting for 36.8% of sepsis cases caused by MDR-KP. The frequency of respiratory failure, bronchopulmonary dysplasia, and intraventricular hemorrhage were more common in the LOS group and a higher rate of acute respiratory distress syndrome was more common in infants in the EOS group (P < 0.05). K. pneumoniae showed a low sensitivity to penicillin, beta-lactams and cephalosporins, and it showed a high sensitivity to levofloxacin, ciprofloxacin, and amikacin. Prematurity, low birth weight, longer antibiotic exposure time, long duration of peripheral catheter insertion, long mechanical ventilation time, and long parenteral nutrition time were associated with an increased rate of MDR-KP infection by univariate analysis (P < 0.05). The regression analysis identified a long antibiotic exposure time (OR = 1.37, 95% CI: 1.01–1.89) and long parenteral nutrition time (OR = 1.39, 95% CI: 1.01–1.89) as independent risk factors for a MDR-KP infection, and a greater gestational age and birth weight were associated with a lower risk of MDR-KP infection (OR = 0.57, 95% CI: 0.40–0.79). LOS caused by K. pneumoniae may lead to a higher frequency of complications. The risk factors for MDR-KP infection were longer duration of antibiotic exposure and parenteral nutrition. A greater gestational age and larger birth weight may decrease the risk of MDR-KP infection.
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spelling pubmed-74441082020-09-09 Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae You, Ting Zhang, Han Guo, Lu Ling, Ke-Ran Hu, Xiao-Yu Li, Lu-Quan Int J Immunopathol Pharmacol Original Research Article To identify differences in the clinical characteristics of early- and late-onset sepsis (EOS and LOS) caused by Klebsiella pneumoniae (K. pneumoniae) and to describe the risk factors for multidrug-resistant K. pneumoniae (MDR-KP) infection. Infants with K. pneumoniae-induced sepsis who were admitted to a children’s Hospital between Jan 2000 and Dec 2019 were included. All infants were divided into EOS and LOS groups, as well as MDR-KP and non-MDR-KP groups. Demographics, clinical characteristics, and risk factors were compared between the two groups. One hundred eighty infants (66 with EOS and 114 with LOS) were further analyzed, accounting for 36.8% of sepsis cases caused by MDR-KP. The frequency of respiratory failure, bronchopulmonary dysplasia, and intraventricular hemorrhage were more common in the LOS group and a higher rate of acute respiratory distress syndrome was more common in infants in the EOS group (P < 0.05). K. pneumoniae showed a low sensitivity to penicillin, beta-lactams and cephalosporins, and it showed a high sensitivity to levofloxacin, ciprofloxacin, and amikacin. Prematurity, low birth weight, longer antibiotic exposure time, long duration of peripheral catheter insertion, long mechanical ventilation time, and long parenteral nutrition time were associated with an increased rate of MDR-KP infection by univariate analysis (P < 0.05). The regression analysis identified a long antibiotic exposure time (OR = 1.37, 95% CI: 1.01–1.89) and long parenteral nutrition time (OR = 1.39, 95% CI: 1.01–1.89) as independent risk factors for a MDR-KP infection, and a greater gestational age and birth weight were associated with a lower risk of MDR-KP infection (OR = 0.57, 95% CI: 0.40–0.79). LOS caused by K. pneumoniae may lead to a higher frequency of complications. The risk factors for MDR-KP infection were longer duration of antibiotic exposure and parenteral nutrition. A greater gestational age and larger birth weight may decrease the risk of MDR-KP infection. SAGE Publications 2020-08-20 /pmc/articles/PMC7444108/ /pubmed/32816593 http://dx.doi.org/10.1177/2058738420950586 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
You, Ting
Zhang, Han
Guo, Lu
Ling, Ke-Ran
Hu, Xiao-Yu
Li, Lu-Quan
Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title_full Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title_fullStr Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title_full_unstemmed Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title_short Differences in clinical characteristics of early- and late-onset neonatal sepsis caused by Klebsiella pneumoniae
title_sort differences in clinical characteristics of early- and late-onset neonatal sepsis caused by klebsiella pneumoniae
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444108/
https://www.ncbi.nlm.nih.gov/pubmed/32816593
http://dx.doi.org/10.1177/2058738420950586
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