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Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study
BACKGROUND: Community-acquired-pneumonia is the leading cause of child mortality worldwide. Very few studies have explored the predictive value of Proadrenomedullin and Copeptin in pediatric severe pneumonia and bacteremia. METHODS: Proadrenomedullin and Copeptin were assessed as predictors for comp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543464/ https://www.ncbi.nlm.nih.gov/pubmed/26286191 http://dx.doi.org/10.1186/s12879-015-1095-5 |
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author | Alcoba, Gabriel Manzano, Sergio Lacroix, Laurence Galetto-Lacour, Annick Gervaix, Alain |
author_facet | Alcoba, Gabriel Manzano, Sergio Lacroix, Laurence Galetto-Lacour, Annick Gervaix, Alain |
author_sort | Alcoba, Gabriel |
collection | PubMed |
description | BACKGROUND: Community-acquired-pneumonia is the leading cause of child mortality worldwide. Very few studies have explored the predictive value of Proadrenomedullin and Copeptin in pediatric severe pneumonia and bacteremia. METHODS: Proadrenomedullin and Copeptin were assessed as predictors for complicated community-acquired pneumonia (bacteremia, empyema) in 88 children aged 0 to 16 years presenting to the pediatric emergency department, using B.R.A.H.M.S. Kryptor Compact pro-ADM and Copeptin with the TRACE technology (time-resolved amplified cryptase emission). STARD standard reporting was used. RESULTS: A complicated community-acquired pneumonia was found in 11 out of 88 children (12.5 %). Proadrenomedullin median values increased more than twofold, in complicated vs. uncomplicated (0.18 vs. 0.08 nmol/L, p = 0.039), and fivefold in bacteremic vs. non-bacteremic pneumonia (0.40 vs. 0.08 nmol/L, p = 0.02). Proadrenomedullin > 0.16 nmol/L showed 100 % sensitivity (95 % CI 39.8 – 100.0) and 70 % (95 % CI 58.7 – 79.7) specificity for bacteremia. Copeptin showed no added-value. CONCLUSIONS: Proadrenomedullin seems a reliable and available predictor for complicated CAP, and could therefore help the physician with the decision to hospitalize, and choose the antibiotics administration route. Larger studies are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1095-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4543464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45434642015-08-22 Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study Alcoba, Gabriel Manzano, Sergio Lacroix, Laurence Galetto-Lacour, Annick Gervaix, Alain BMC Infect Dis Research Article BACKGROUND: Community-acquired-pneumonia is the leading cause of child mortality worldwide. Very few studies have explored the predictive value of Proadrenomedullin and Copeptin in pediatric severe pneumonia and bacteremia. METHODS: Proadrenomedullin and Copeptin were assessed as predictors for complicated community-acquired pneumonia (bacteremia, empyema) in 88 children aged 0 to 16 years presenting to the pediatric emergency department, using B.R.A.H.M.S. Kryptor Compact pro-ADM and Copeptin with the TRACE technology (time-resolved amplified cryptase emission). STARD standard reporting was used. RESULTS: A complicated community-acquired pneumonia was found in 11 out of 88 children (12.5 %). Proadrenomedullin median values increased more than twofold, in complicated vs. uncomplicated (0.18 vs. 0.08 nmol/L, p = 0.039), and fivefold in bacteremic vs. non-bacteremic pneumonia (0.40 vs. 0.08 nmol/L, p = 0.02). Proadrenomedullin > 0.16 nmol/L showed 100 % sensitivity (95 % CI 39.8 – 100.0) and 70 % (95 % CI 58.7 – 79.7) specificity for bacteremia. Copeptin showed no added-value. CONCLUSIONS: Proadrenomedullin seems a reliable and available predictor for complicated CAP, and could therefore help the physician with the decision to hospitalize, and choose the antibiotics administration route. Larger studies are needed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1095-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-19 /pmc/articles/PMC4543464/ /pubmed/26286191 http://dx.doi.org/10.1186/s12879-015-1095-5 Text en © Alcoba et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (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 Alcoba, Gabriel Manzano, Sergio Lacroix, Laurence Galetto-Lacour, Annick Gervaix, Alain Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title | Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title_full | Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title_fullStr | Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title_full_unstemmed | Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title_short | Proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
title_sort | proadrenomedullin and copeptin in pediatric pneumonia: a prospective diagnostic accuracy study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543464/ https://www.ncbi.nlm.nih.gov/pubmed/26286191 http://dx.doi.org/10.1186/s12879-015-1095-5 |
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