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An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study
BACKGROUND: To refine the bacterial meningitis (BM) score by improving its predictability of neonatal BM. METHODS: A multicenter, ambispective cohort study was conducted in China, comprising 9 hospitals (retrospective cohort: January 2001 to December 2017; prospective cohort: January 2018 to August...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882280/ https://www.ncbi.nlm.nih.gov/pubmed/33633938 http://dx.doi.org/10.21037/tp-20-255 |
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author | Wang, Yiwen Lei, Xiaoping Zhao, Youyan Tan, Jintong Li, Jing Gong, Xiaohui Shan, Liqin Zhang, Qian Zhou, Qin Zhang, Yongjun |
author_facet | Wang, Yiwen Lei, Xiaoping Zhao, Youyan Tan, Jintong Li, Jing Gong, Xiaohui Shan, Liqin Zhang, Qian Zhou, Qin Zhang, Yongjun |
author_sort | Wang, Yiwen |
collection | PubMed |
description | BACKGROUND: To refine the bacterial meningitis (BM) score by improving its predictability of neonatal BM. METHODS: A multicenter, ambispective cohort study was conducted in China, comprising 9 hospitals (retrospective cohort: January 2001 to December 2017; prospective cohort: January 2018 to August 2019). Of 3,504 eligible full-term neonates, 475 neonates with cerebrospinal fluid (CSF) pleocytosis were included. Based on the receiver operating characteristic (ROC) curve and logistic regression analyses, the BM score was refined by changing the thresholds of CSF protein level and the CSF absolute neutrophil count (ANC), and removing some variables (the peripheral blood ANC and a history of seizure before or at the time of presentation). RESULTS: Of 475 neonates, 94 (19.8%) had BM. Based on the refined BM score, neonates with none of the following high-risk predictors were classified as being at very low risk for BM: CSF protein level ≥1,650 mg/L, CSF ANC ≥84×10(6) cells/L, and positive CSF Gram stain result. The refined score showed 100% sensitivity in identifying BM and much higher specificity compared to that for the BM score (70.9% vs. 19.4%). CONCLUSIONS: The refined BM score effectively identifies neonatal BM, and further studies are required to confirm our findings in prospective studies. |
format | Online Article Text |
id | pubmed-7882280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-78822802021-02-24 An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study Wang, Yiwen Lei, Xiaoping Zhao, Youyan Tan, Jintong Li, Jing Gong, Xiaohui Shan, Liqin Zhang, Qian Zhou, Qin Zhang, Yongjun Transl Pediatr Original Article BACKGROUND: To refine the bacterial meningitis (BM) score by improving its predictability of neonatal BM. METHODS: A multicenter, ambispective cohort study was conducted in China, comprising 9 hospitals (retrospective cohort: January 2001 to December 2017; prospective cohort: January 2018 to August 2019). Of 3,504 eligible full-term neonates, 475 neonates with cerebrospinal fluid (CSF) pleocytosis were included. Based on the receiver operating characteristic (ROC) curve and logistic regression analyses, the BM score was refined by changing the thresholds of CSF protein level and the CSF absolute neutrophil count (ANC), and removing some variables (the peripheral blood ANC and a history of seizure before or at the time of presentation). RESULTS: Of 475 neonates, 94 (19.8%) had BM. Based on the refined BM score, neonates with none of the following high-risk predictors were classified as being at very low risk for BM: CSF protein level ≥1,650 mg/L, CSF ANC ≥84×10(6) cells/L, and positive CSF Gram stain result. The refined score showed 100% sensitivity in identifying BM and much higher specificity compared to that for the BM score (70.9% vs. 19.4%). CONCLUSIONS: The refined BM score effectively identifies neonatal BM, and further studies are required to confirm our findings in prospective studies. AME Publishing Company 2021-01 /pmc/articles/PMC7882280/ /pubmed/33633938 http://dx.doi.org/10.21037/tp-20-255 Text en 2021 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Wang, Yiwen Lei, Xiaoping Zhao, Youyan Tan, Jintong Li, Jing Gong, Xiaohui Shan, Liqin Zhang, Qian Zhou, Qin Zhang, Yongjun An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title | An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title_full | An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title_fullStr | An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title_full_unstemmed | An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title_short | An improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
title_sort | improved clinical prediction rule for identifying neonatal bacterial meningitis: a multicenter cohort study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882280/ https://www.ncbi.nlm.nih.gov/pubmed/33633938 http://dx.doi.org/10.21037/tp-20-255 |
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