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Late-onset neonatal sepsis: recent developments
The incidence of neonatal late-onset sepsis (LOS) is inversely related to the degree of maturity and varies geographically from 0.61% to 14.2% among hospitalised newborns. Epidemiological data on very low birth weight infants shows that the predominant pathogens of neonatal LOS are coagulase-negativ...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413803/ https://www.ncbi.nlm.nih.gov/pubmed/25425653 http://dx.doi.org/10.1136/archdischild-2014-306213 |
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author | Dong, Ying Speer, Christian P |
author_facet | Dong, Ying Speer, Christian P |
author_sort | Dong, Ying |
collection | PubMed |
description | The incidence of neonatal late-onset sepsis (LOS) is inversely related to the degree of maturity and varies geographically from 0.61% to 14.2% among hospitalised newborns. Epidemiological data on very low birth weight infants shows that the predominant pathogens of neonatal LOS are coagulase-negative staphylococci, followed by Gram-negative bacilli and fungi. Due to the difficulties in a prompt diagnosis of LOS and LOS-associated high risk of mortality and long-term neurodevelopmental sequelae, empirical antibiotic treatment is initiated on suspicion of LOS. However, empirical therapy is often inappropriately used with unnecessary broad-spectrum antibiotics and a prolonged duration of treatment. The increasing number of multidrug-resistant Gram-negative micro-organisms in neonatal intensive care units (NICU) worldwide is a serious concern, which requires thorough and efficient surveillance strategies and appropriate treatment regimens. Immunological strategies for preventing neonatal LOS are not supported by current evidence, and approaches, such as a strict hygiene protocol and the minimisation of invasive procedures in NICUs represent the cornerstone to reduce the burden of neonatal LOS. |
format | Online Article Text |
id | pubmed-4413803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44138032015-05-11 Late-onset neonatal sepsis: recent developments Dong, Ying Speer, Christian P Arch Dis Child Fetal Neonatal Ed Review The incidence of neonatal late-onset sepsis (LOS) is inversely related to the degree of maturity and varies geographically from 0.61% to 14.2% among hospitalised newborns. Epidemiological data on very low birth weight infants shows that the predominant pathogens of neonatal LOS are coagulase-negative staphylococci, followed by Gram-negative bacilli and fungi. Due to the difficulties in a prompt diagnosis of LOS and LOS-associated high risk of mortality and long-term neurodevelopmental sequelae, empirical antibiotic treatment is initiated on suspicion of LOS. However, empirical therapy is often inappropriately used with unnecessary broad-spectrum antibiotics and a prolonged duration of treatment. The increasing number of multidrug-resistant Gram-negative micro-organisms in neonatal intensive care units (NICU) worldwide is a serious concern, which requires thorough and efficient surveillance strategies and appropriate treatment regimens. Immunological strategies for preventing neonatal LOS are not supported by current evidence, and approaches, such as a strict hygiene protocol and the minimisation of invasive procedures in NICUs represent the cornerstone to reduce the burden of neonatal LOS. BMJ Publishing Group 2015-05 2014-11-25 /pmc/articles/PMC4413803/ /pubmed/25425653 http://dx.doi.org/10.1136/archdischild-2014-306213 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Review Dong, Ying Speer, Christian P Late-onset neonatal sepsis: recent developments |
title | Late-onset neonatal sepsis: recent developments |
title_full | Late-onset neonatal sepsis: recent developments |
title_fullStr | Late-onset neonatal sepsis: recent developments |
title_full_unstemmed | Late-onset neonatal sepsis: recent developments |
title_short | Late-onset neonatal sepsis: recent developments |
title_sort | late-onset neonatal sepsis: recent developments |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413803/ https://www.ncbi.nlm.nih.gov/pubmed/25425653 http://dx.doi.org/10.1136/archdischild-2014-306213 |
work_keys_str_mv | AT dongying lateonsetneonatalsepsisrecentdevelopments AT speerchristianp lateonsetneonatalsepsisrecentdevelopments |