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Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network

BACKGROUND: The identification of sepsis in children varies depending on the definition used. Our purpose was to compare clinical data and outcome of atypical sepsis, manifested as having sepsis but not fulfilling the criteria of systemic inflammatory response syndrome (SIRS-negative sepsis, SNS), i...

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Autores principales: Wang, Yuanyuan, Lin, Xiaofei, Yue, Hongni, Kissoon, Niranjan, Sun, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325779/
https://www.ncbi.nlm.nih.gov/pubmed/30621637
http://dx.doi.org/10.1186/s12887-018-1364-8
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author Wang, Yuanyuan
Lin, Xiaofei
Yue, Hongni
Kissoon, Niranjan
Sun, Bo
author_facet Wang, Yuanyuan
Lin, Xiaofei
Yue, Hongni
Kissoon, Niranjan
Sun, Bo
author_sort Wang, Yuanyuan
collection PubMed
description BACKGROUND: The identification of sepsis in children varies depending on the definition used. Our purpose was to compare clinical data and outcome of atypical sepsis, manifested as having sepsis but not fulfilling the criteria of systemic inflammatory response syndrome (SIRS-negative sepsis, SNS), in children based on the modified Angus criteria with those of sepsis (S) and severe sepsis (SS) based on the international consensus criteria. METHODS: Pediatric departments in 11 regional city and county referral hospitals with emergency and intensive care settings in Huai’an serving for 843,000 children participated in a parallel multicenter prospective survey. Clinical data registry was used to recruit those who fulfilled the diagnostic criteria for pediatric sepsis from all admissions (n = 27,836) from 28 days to 15 years old, from September 1, 2010 to August 31, 2011. RESULTS: A total of 1606 children met the criteria for pediatric sepsis and were divided into three groups: S, (n = 1377), SS (n = 153, including 32 septic shock), based on the consensus definition criteria, and SNS (n = 76) based on the modified Angus criteria. Most deaths (38/54, 70.3%) occurred within three days of admission. The SNS mainly occurred in infants and was associated with cardiopulmonary and neurologic dysfunction without satisfying the SIRS criteria. CONCLUSIONS: SNS differed from SS in that it predominantly affected infants and manifested with cardiopulmonary and neurologic dysfunction. There were no laboratory variables which were useful in identification of SNS, or predicting response to therapy or outcome.
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spelling pubmed-63257792019-01-11 Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network Wang, Yuanyuan Lin, Xiaofei Yue, Hongni Kissoon, Niranjan Sun, Bo BMC Pediatr Research Article BACKGROUND: The identification of sepsis in children varies depending on the definition used. Our purpose was to compare clinical data and outcome of atypical sepsis, manifested as having sepsis but not fulfilling the criteria of systemic inflammatory response syndrome (SIRS-negative sepsis, SNS), in children based on the modified Angus criteria with those of sepsis (S) and severe sepsis (SS) based on the international consensus criteria. METHODS: Pediatric departments in 11 regional city and county referral hospitals with emergency and intensive care settings in Huai’an serving for 843,000 children participated in a parallel multicenter prospective survey. Clinical data registry was used to recruit those who fulfilled the diagnostic criteria for pediatric sepsis from all admissions (n = 27,836) from 28 days to 15 years old, from September 1, 2010 to August 31, 2011. RESULTS: A total of 1606 children met the criteria for pediatric sepsis and were divided into three groups: S, (n = 1377), SS (n = 153, including 32 septic shock), based on the consensus definition criteria, and SNS (n = 76) based on the modified Angus criteria. Most deaths (38/54, 70.3%) occurred within three days of admission. The SNS mainly occurred in infants and was associated with cardiopulmonary and neurologic dysfunction without satisfying the SIRS criteria. CONCLUSIONS: SNS differed from SS in that it predominantly affected infants and manifested with cardiopulmonary and neurologic dysfunction. There were no laboratory variables which were useful in identification of SNS, or predicting response to therapy or outcome. BioMed Central 2019-01-08 /pmc/articles/PMC6325779/ /pubmed/30621637 http://dx.doi.org/10.1186/s12887-018-1364-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Yuanyuan
Lin, Xiaofei
Yue, Hongni
Kissoon, Niranjan
Sun, Bo
Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title_full Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title_fullStr Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title_full_unstemmed Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title_short Evaluation of systemic inflammatory response syndrome-negative sepsis from a Chinese regional pediatric network
title_sort evaluation of systemic inflammatory response syndrome-negative sepsis from a chinese regional pediatric network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325779/
https://www.ncbi.nlm.nih.gov/pubmed/30621637
http://dx.doi.org/10.1186/s12887-018-1364-8
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