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Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018

Background: The epidemiology of early-onset sepsis (EOS) may change over time. Longitudinal surveillance of causative pathogens, antibiotic susceptibility patterns and antibiotic therapy is important for optimal therapy strategies. Objectives: To describe the incidence of culture-confirmed EOS, caus...

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Autores principales: Vatne, Anlaug, Klingenberg, Claus, Rettedal, Siren, Øymar, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010672/
https://www.ncbi.nlm.nih.gov/pubmed/33816402
http://dx.doi.org/10.3389/fped.2021.634798
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author Vatne, Anlaug
Klingenberg, Claus
Rettedal, Siren
Øymar, Knut
author_facet Vatne, Anlaug
Klingenberg, Claus
Rettedal, Siren
Øymar, Knut
author_sort Vatne, Anlaug
collection PubMed
description Background: The epidemiology of early-onset sepsis (EOS) may change over time. Longitudinal surveillance of causative pathogens, antibiotic susceptibility patterns and antibiotic therapy is important for optimal therapy strategies. Objectives: To describe the incidence of culture-confirmed EOS, causative pathogens, antibiotic susceptibility patterns and antibiotic therapy over a 23-year period. Methods: Retrospective population-based study from a single-center neonatal intensive care unit at Stavanger University Hospital, Norway, covering a population in South-West Norway, during the 23-year period 1996–2018. Results: Of 104,377 live born infants, 101 infants (0.97/1,000) had culture-confirmed EOS; 89 with Gram positive and 12 with Gram-negative bacteria. The EOS-attributable mortality was 6/101 (5.8%). For the three most prevalent pathogens the incidences were; Group B streptococcus (GBS) 0.57/1,000, Escherichia coli 0.11/1,000 and viridans group streptococci (VGS) 0.10/1,000. GBS was the most common pathogen (59/93; 63%) in infants with gestational age (GA) ≥ 28 weeks. In contrast, among extremely preterm infants (GA <28 weeks) the incidence of E. coli infection was higher than for GBS infection. The second most common bacterial pathogens causing EOS among term infants were VGS. There was no change in the incidence of EOS for the entire study period, but from 2000 to 2018 there was a mean decline in EOS by 6% per year (95% CI 1%−10%) (p = 0.019). The incidences of GBS and E. coli did not change during the study period. The initial empirical antibiotic regimen for EOS was in all cases a combination of benzylpenicillin or ampicillin and an aminoglycoside, but in 21/101 (21%) of cases a broad-spectrum antibiotic was either added or substituted this regimen. In 2/101 (2%) EOS cases, the pathogens were nonsusceptible to the empirical antibiotic regimen. All E. coli isolates were susceptible to aminoglycosides. Conclusion: GBS was the most common causative pathogens in EOS, but E. coli dominated in infants with GA <28 weeks. There was no change in the incidence of EOS during the entire study period. The current empiric regimen with benzylpenicillin and gentamicin provides a very high coverage for EOS in our setting.
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spelling pubmed-80106722021-04-01 Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018 Vatne, Anlaug Klingenberg, Claus Rettedal, Siren Øymar, Knut Front Pediatr Pediatrics Background: The epidemiology of early-onset sepsis (EOS) may change over time. Longitudinal surveillance of causative pathogens, antibiotic susceptibility patterns and antibiotic therapy is important for optimal therapy strategies. Objectives: To describe the incidence of culture-confirmed EOS, causative pathogens, antibiotic susceptibility patterns and antibiotic therapy over a 23-year period. Methods: Retrospective population-based study from a single-center neonatal intensive care unit at Stavanger University Hospital, Norway, covering a population in South-West Norway, during the 23-year period 1996–2018. Results: Of 104,377 live born infants, 101 infants (0.97/1,000) had culture-confirmed EOS; 89 with Gram positive and 12 with Gram-negative bacteria. The EOS-attributable mortality was 6/101 (5.8%). For the three most prevalent pathogens the incidences were; Group B streptococcus (GBS) 0.57/1,000, Escherichia coli 0.11/1,000 and viridans group streptococci (VGS) 0.10/1,000. GBS was the most common pathogen (59/93; 63%) in infants with gestational age (GA) ≥ 28 weeks. In contrast, among extremely preterm infants (GA <28 weeks) the incidence of E. coli infection was higher than for GBS infection. The second most common bacterial pathogens causing EOS among term infants were VGS. There was no change in the incidence of EOS for the entire study period, but from 2000 to 2018 there was a mean decline in EOS by 6% per year (95% CI 1%−10%) (p = 0.019). The incidences of GBS and E. coli did not change during the study period. The initial empirical antibiotic regimen for EOS was in all cases a combination of benzylpenicillin or ampicillin and an aminoglycoside, but in 21/101 (21%) of cases a broad-spectrum antibiotic was either added or substituted this regimen. In 2/101 (2%) EOS cases, the pathogens were nonsusceptible to the empirical antibiotic regimen. All E. coli isolates were susceptible to aminoglycosides. Conclusion: GBS was the most common causative pathogens in EOS, but E. coli dominated in infants with GA <28 weeks. There was no change in the incidence of EOS during the entire study period. The current empiric regimen with benzylpenicillin and gentamicin provides a very high coverage for EOS in our setting. Frontiers Media S.A. 2021-03-17 /pmc/articles/PMC8010672/ /pubmed/33816402 http://dx.doi.org/10.3389/fped.2021.634798 Text en Copyright © 2021 Vatne, Klingenberg, Rettedal and Øymar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Vatne, Anlaug
Klingenberg, Claus
Rettedal, Siren
Øymar, Knut
Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title_full Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title_fullStr Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title_full_unstemmed Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title_short Early-Onset Sepsis in Neonates - A Population-Based Study in South-West Norway From 1996 to 2018
title_sort early-onset sepsis in neonates - a population-based study in south-west norway from 1996 to 2018
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010672/
https://www.ncbi.nlm.nih.gov/pubmed/33816402
http://dx.doi.org/10.3389/fped.2021.634798
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