Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.

<h4>Aim</h4>To describe the epidemiology of EOS including blood culture utilisation, across a large and geographically diverse Australian health district.<h4>Background</h4>Sepsis in the first three days of life remains a leading cause of death and morbidity. In high-income c...

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Main Authors: Kathryn Braye, Maralyn Foureur, Koert de Waal, Mark Jones, Elise Putt, John Ferguson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0214298
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spelling doaj-a1cfc111e66a48f0be598a201843d3bd2021-03-04T10:33:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01144e021429810.1371/journal.pone.0214298Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.Kathryn BrayeMaralyn FoureurKoert de WaalMark JonesElise PuttJohn Ferguson<h4>Aim</h4>To describe the epidemiology of EOS including blood culture utilisation, across a large and geographically diverse Australian health district.<h4>Background</h4>Sepsis in the first three days of life remains a leading cause of death and morbidity. In high-income countries, group B Streptococcus (GBS) and Escherichia coli (E. coli) have dominated as causes of EOS for five decades.<h4>Method</h4>An 11-year retrospective cohort study to determine the epidemiology of EOS. Incidence rates were calculated per 1000 live births. Logistic regression with linear temporal trend and covariates for potential effect modifiers were employed. Blood culture utilisation was determined by examining the rate of babies undergoing blood culture within 72 hours of birth.<h4>Results</h4>Among 93,584 live born babies, 65 had confirmed EOS (0.69/1000 live births); 22 term, 43 preterm. Across the 4 largest birth units, the proportion of babies having blood culture within 72 hours of birth varied from 1.9-5.1% for term and 21-35% for preterm babies. The annual change in the EOS rate was significant, OR 0.91 (95% CI, 0.84 to 0.99, p = 0.03). Group B Streptococcus was the most common cause of EOS in term neonates at 0.35/1000 live births (95% CI, 0.07-0.63) in 2006 and 0.1/1000 live births (95% CI, 0-0.2) in 2016. Escherichia coli was the most common cause in preterm babies at 3.4/1000 (95% CI, 0.11-6.76) in 2006 reducing significantly to 1.35/1000 live births (95% CI, -0.07-2.78) by 2016.<h4>Conclusions</h4>Escherichia coli and GBS were the most common causes of EOS in preterm and term babies respectively. Rates of all cause term and preterm EOS declined significantly as did preterm sepsis due to E. coli. While rate of sepsis due to early-onset GBS declined, this did not reach significance. Given the high proportion of preterm babies undergoing blood culture, it is unlikely that any EOS events were missed.https://doi.org/10.1371/journal.pone.0214298
collection DOAJ
language English
format Article
sources DOAJ
author Kathryn Braye
Maralyn Foureur
Koert de Waal
Mark Jones
Elise Putt
John Ferguson
spellingShingle Kathryn Braye
Maralyn Foureur
Koert de Waal
Mark Jones
Elise Putt
John Ferguson
Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
PLoS ONE
author_facet Kathryn Braye
Maralyn Foureur
Koert de Waal
Mark Jones
Elise Putt
John Ferguson
author_sort Kathryn Braye
title Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
title_short Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
title_full Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
title_fullStr Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
title_full_unstemmed Epidemiology of neonatal early-onset sepsis in a geographically diverse Australian health district 2006-2016.
title_sort epidemiology of neonatal early-onset sepsis in a geographically diverse australian health district 2006-2016.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description <h4>Aim</h4>To describe the epidemiology of EOS including blood culture utilisation, across a large and geographically diverse Australian health district.<h4>Background</h4>Sepsis in the first three days of life remains a leading cause of death and morbidity. In high-income countries, group B Streptococcus (GBS) and Escherichia coli (E. coli) have dominated as causes of EOS for five decades.<h4>Method</h4>An 11-year retrospective cohort study to determine the epidemiology of EOS. Incidence rates were calculated per 1000 live births. Logistic regression with linear temporal trend and covariates for potential effect modifiers were employed. Blood culture utilisation was determined by examining the rate of babies undergoing blood culture within 72 hours of birth.<h4>Results</h4>Among 93,584 live born babies, 65 had confirmed EOS (0.69/1000 live births); 22 term, 43 preterm. Across the 4 largest birth units, the proportion of babies having blood culture within 72 hours of birth varied from 1.9-5.1% for term and 21-35% for preterm babies. The annual change in the EOS rate was significant, OR 0.91 (95% CI, 0.84 to 0.99, p = 0.03). Group B Streptococcus was the most common cause of EOS in term neonates at 0.35/1000 live births (95% CI, 0.07-0.63) in 2006 and 0.1/1000 live births (95% CI, 0-0.2) in 2016. Escherichia coli was the most common cause in preterm babies at 3.4/1000 (95% CI, 0.11-6.76) in 2006 reducing significantly to 1.35/1000 live births (95% CI, -0.07-2.78) by 2016.<h4>Conclusions</h4>Escherichia coli and GBS were the most common causes of EOS in preterm and term babies respectively. Rates of all cause term and preterm EOS declined significantly as did preterm sepsis due to E. coli. While rate of sepsis due to early-onset GBS declined, this did not reach significance. Given the high proportion of preterm babies undergoing blood culture, it is unlikely that any EOS events were missed.
url https://doi.org/10.1371/journal.pone.0214298
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