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Timing of follow-up blood cultures for community-onset bacteremia
Bacteremia is associated with high morbidity and mortality, but the utility and optimal timing of follow-up blood cultures (FUBCs) remain undefined. To assess the optimal timing of FUBCs related to appropriate antibiotic therapy (AAT), adults with community-onset bacteremia and FUBCs after bacteremi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787025/ https://www.ncbi.nlm.nih.gov/pubmed/31601858 http://dx.doi.org/10.1038/s41598-019-51032-z |
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author | Lee, Ching-Chi Yang, Chao-Yung Hsieh, Chih-Chia Hong, Ming-Yuan Lee, Chung-Hsun Tang, Hung-Jen Ko, Wen-Chien |
author_facet | Lee, Ching-Chi Yang, Chao-Yung Hsieh, Chih-Chia Hong, Ming-Yuan Lee, Chung-Hsun Tang, Hung-Jen Ko, Wen-Chien |
author_sort | Lee, Ching-Chi |
collection | PubMed |
description | Bacteremia is associated with high morbidity and mortality, but the utility and optimal timing of follow-up blood cultures (FUBCs) remain undefined. To assess the optimal timing of FUBCs related to appropriate antibiotic therapy (AAT), adults with community-onset bacteremia and FUBCs after bacteremia onset were retrospectively studied during the 6-year period in two hospitals. Based on the time gap between the initiation of AAT and FUBC sampling, 1,247 eligible patients were categorized as FUBCs prior to AAT (65 patients, 5.2%), 0–3 days (202, 16.2%), 3.1–6 days (470, 37.7%), 6.1–9 days (299, 24.0%), and ≥9 days (211, 16.9%) after AAT. The prognostic impact of the growth of the same bacteria in FUBCs on 30-day mortality was evidenced only in patients with FUBCs at 3.1–6 days after AAT (adjusted odds ratio [AOR], 3.75; P < 0.001), not in those with FUBCs prior to AAT (AOR, 2.86; P = 0.25), 0–3 days (AOR, 0.39; P = 0.08), 6.1–9 days (AOR, 2.19; P = 0.32), and ≥9 days (AOR, 0.41; P = 0.41) of AAT, after adjusting independent factors of 30-day mortality recognized by the multivariable regression in each category. Conclusively, persistent bacteremia in FUBCs added prognostic significance in the management of adults with community-onset bacteremia after 3.1–6 days of AAT. |
format | Online Article Text |
id | pubmed-6787025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67870252019-10-17 Timing of follow-up blood cultures for community-onset bacteremia Lee, Ching-Chi Yang, Chao-Yung Hsieh, Chih-Chia Hong, Ming-Yuan Lee, Chung-Hsun Tang, Hung-Jen Ko, Wen-Chien Sci Rep Article Bacteremia is associated with high morbidity and mortality, but the utility and optimal timing of follow-up blood cultures (FUBCs) remain undefined. To assess the optimal timing of FUBCs related to appropriate antibiotic therapy (AAT), adults with community-onset bacteremia and FUBCs after bacteremia onset were retrospectively studied during the 6-year period in two hospitals. Based on the time gap between the initiation of AAT and FUBC sampling, 1,247 eligible patients were categorized as FUBCs prior to AAT (65 patients, 5.2%), 0–3 days (202, 16.2%), 3.1–6 days (470, 37.7%), 6.1–9 days (299, 24.0%), and ≥9 days (211, 16.9%) after AAT. The prognostic impact of the growth of the same bacteria in FUBCs on 30-day mortality was evidenced only in patients with FUBCs at 3.1–6 days after AAT (adjusted odds ratio [AOR], 3.75; P < 0.001), not in those with FUBCs prior to AAT (AOR, 2.86; P = 0.25), 0–3 days (AOR, 0.39; P = 0.08), 6.1–9 days (AOR, 2.19; P = 0.32), and ≥9 days (AOR, 0.41; P = 0.41) of AAT, after adjusting independent factors of 30-day mortality recognized by the multivariable regression in each category. Conclusively, persistent bacteremia in FUBCs added prognostic significance in the management of adults with community-onset bacteremia after 3.1–6 days of AAT. Nature Publishing Group UK 2019-10-10 /pmc/articles/PMC6787025/ /pubmed/31601858 http://dx.doi.org/10.1038/s41598-019-51032-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Ching-Chi Yang, Chao-Yung Hsieh, Chih-Chia Hong, Ming-Yuan Lee, Chung-Hsun Tang, Hung-Jen Ko, Wen-Chien Timing of follow-up blood cultures for community-onset bacteremia |
title | Timing of follow-up blood cultures for community-onset bacteremia |
title_full | Timing of follow-up blood cultures for community-onset bacteremia |
title_fullStr | Timing of follow-up blood cultures for community-onset bacteremia |
title_full_unstemmed | Timing of follow-up blood cultures for community-onset bacteremia |
title_short | Timing of follow-up blood cultures for community-onset bacteremia |
title_sort | timing of follow-up blood cultures for community-onset bacteremia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787025/ https://www.ncbi.nlm.nih.gov/pubmed/31601858 http://dx.doi.org/10.1038/s41598-019-51032-z |
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