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Viremia as a predictor of absence of serious bacterial infection in children with fever without source
Most children with fever without source (FWS) require diagnostic laboratory tests to exclude a serious bacterial infection (SBI), often followed by admission and empirical antibiotics. As febrile children with a viral infection are less likely to have a SBI, identifying patients with systemic viral...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672567/ https://www.ncbi.nlm.nih.gov/pubmed/36399200 http://dx.doi.org/10.1007/s00431-022-04690-7 |
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author | Galetto-Lacour, Annick Cordey, Samuel Papis, Sebastien Mardegan, Chiara Luterbacher, Fanny Combescure, Christophe Lacroix, Laurence Gervaix, Alain Kaiser, Laurent Posfay-Barbe, Klara M. L’Huillier, Arnaud G. |
author_facet | Galetto-Lacour, Annick Cordey, Samuel Papis, Sebastien Mardegan, Chiara Luterbacher, Fanny Combescure, Christophe Lacroix, Laurence Gervaix, Alain Kaiser, Laurent Posfay-Barbe, Klara M. L’Huillier, Arnaud G. |
author_sort | Galetto-Lacour, Annick |
collection | PubMed |
description | Most children with fever without source (FWS) require diagnostic laboratory tests to exclude a serious bacterial infection (SBI), often followed by admission and empirical antibiotics. As febrile children with a viral infection are less likely to have a SBI, identifying patients with systemic viral infection could contribute to exclude SBI. We evaluated whether the presence of virus in the blood could be used as a biomarker to rule out SBI. Children < 3 years old with FWS were prospectively enrolled and had real-time (reverse-transcription) PCR performed on the blood for adenovirus, enterovirus, parechovirus, and HHV6. 20/135 patients had SBI, and in 47/135, at least one virus was detected in the blood. Viremia had a higher sensitivity and negative predictive value (90% and 96%) to rule out SBI compared to CRP (65% and 93%) and PCT (55% and 90%). The odds ratio (OR) for the presence of SBI among non-viremic patients was 5.8 (p = 0.0225), compared to 5.5 for CRP ≥ 40 mg/l (p = 0.0009) and 3.7 for PCT ≥ 0.5 ng/mL (0.0093). This remained significant after adjusting for CRP and PCT (OR 5.6 and 5.9, respectively; p = 0.03 for both). Area under the ROC curve for CRP and PCT were 0.754 and 0.779, respectively, but increased to 0.803 and 0.832, respectively, when combined with viremia. Conclusion: The presence of viremia had a better performance than commonly used biomarkers to rule-out SBI and could potentially be used in conjunction with CRP and/or PCT in the evaluation of children with FWS. Larger studies should evaluate the role of point-of-care testing of viruses by (revere-transcription) PCR in the plasma in management algorithms of children with FWS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-022-04690-7. |
format | Online Article Text |
id | pubmed-9672567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-96725672022-11-18 Viremia as a predictor of absence of serious bacterial infection in children with fever without source Galetto-Lacour, Annick Cordey, Samuel Papis, Sebastien Mardegan, Chiara Luterbacher, Fanny Combescure, Christophe Lacroix, Laurence Gervaix, Alain Kaiser, Laurent Posfay-Barbe, Klara M. L’Huillier, Arnaud G. Eur J Pediatr Study Protocol Most children with fever without source (FWS) require diagnostic laboratory tests to exclude a serious bacterial infection (SBI), often followed by admission and empirical antibiotics. As febrile children with a viral infection are less likely to have a SBI, identifying patients with systemic viral infection could contribute to exclude SBI. We evaluated whether the presence of virus in the blood could be used as a biomarker to rule out SBI. Children < 3 years old with FWS were prospectively enrolled and had real-time (reverse-transcription) PCR performed on the blood for adenovirus, enterovirus, parechovirus, and HHV6. 20/135 patients had SBI, and in 47/135, at least one virus was detected in the blood. Viremia had a higher sensitivity and negative predictive value (90% and 96%) to rule out SBI compared to CRP (65% and 93%) and PCT (55% and 90%). The odds ratio (OR) for the presence of SBI among non-viremic patients was 5.8 (p = 0.0225), compared to 5.5 for CRP ≥ 40 mg/l (p = 0.0009) and 3.7 for PCT ≥ 0.5 ng/mL (0.0093). This remained significant after adjusting for CRP and PCT (OR 5.6 and 5.9, respectively; p = 0.03 for both). Area under the ROC curve for CRP and PCT were 0.754 and 0.779, respectively, but increased to 0.803 and 0.832, respectively, when combined with viremia. Conclusion: The presence of viremia had a better performance than commonly used biomarkers to rule-out SBI and could potentially be used in conjunction with CRP and/or PCT in the evaluation of children with FWS. Larger studies should evaluate the role of point-of-care testing of viruses by (revere-transcription) PCR in the plasma in management algorithms of children with FWS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00431-022-04690-7. Springer Berlin Heidelberg 2022-11-18 2023 /pmc/articles/PMC9672567/ /pubmed/36399200 http://dx.doi.org/10.1007/s00431-022-04690-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Study Protocol Galetto-Lacour, Annick Cordey, Samuel Papis, Sebastien Mardegan, Chiara Luterbacher, Fanny Combescure, Christophe Lacroix, Laurence Gervaix, Alain Kaiser, Laurent Posfay-Barbe, Klara M. L’Huillier, Arnaud G. Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title | Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title_full | Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title_fullStr | Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title_full_unstemmed | Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title_short | Viremia as a predictor of absence of serious bacterial infection in children with fever without source |
title_sort | viremia as a predictor of absence of serious bacterial infection in children with fever without source |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672567/ https://www.ncbi.nlm.nih.gov/pubmed/36399200 http://dx.doi.org/10.1007/s00431-022-04690-7 |
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