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SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward

BACKGROUND: Respiratory syncytial virus (RSV) is responsible for severe respiratory infections and higher costs in medical care. The two aims of this work were to assess the performances of SOFIA(®)RSV tests in “real-life-laboratory” conditions (study 1) and implemented at point-of-care testing in a...

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Autores principales: Tran, Léa C., Tournus, Céline, Dina, Julia, Morello, Rémy, Brouard, Jacques, Vabret, Astrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485495/
https://www.ncbi.nlm.nih.gov/pubmed/28651525
http://dx.doi.org/10.1186/s12879-017-2557-8
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author Tran, Léa C.
Tournus, Céline
Dina, Julia
Morello, Rémy
Brouard, Jacques
Vabret, Astrid
author_facet Tran, Léa C.
Tournus, Céline
Dina, Julia
Morello, Rémy
Brouard, Jacques
Vabret, Astrid
author_sort Tran, Léa C.
collection PubMed
description BACKGROUND: Respiratory syncytial virus (RSV) is responsible for severe respiratory infections and higher costs in medical care. The two aims of this work were to assess the performances of SOFIA(®)RSV tests in “real-life-laboratory” conditions (study 1) and implemented at point-of-care testing in a pediatric emergency department (ED, study 2), during two consecutive winter seasons. METHODS: In study 1, fresh nasopharyngeal swabs from patients of all ages were sampled in 1.5 ml of Universal virological Transport Medium (UTM) and prospectively tested using SOFIA(®)RSV tests. In study 2, conducted in a pediatric ED, nasopharyngeal swabs were placed in 3 ml of UTM. All SOFIA(®)RSV tests were confirmed by molecular testing, considered as reference method. The epidemiological and clinical features of tested patients, as well as the care of these patients after obtaining quick results were evaluated. RESULTS: The sensitivities of SOFIA(®)RSV in infants (aged under 24 months) performed in the laboratory and in the pediatric ED were respectively 95% (95% CI: 86.8–98.1) and 74.8% (95% CI: 68.0–80.9) compared to PCR. In study 1, the sensitivity among children (from 2 to 15 years old) and adults (above 15 years old) dropped to 45% (95% CI: 23.1–68.5) and 59% (95% CI: 32.9–81.6), respectively. In study 2, there were some differences in bed-management of SOFIA(®)RSV positive compared to SOFIA(®)RSV negative infants. CONCLUSIONS: SOFIA(®)RSV tests performed in the laboratory and in the pediatric ED show high and satisfactory sensitivities among young children under 24 months, which supports its robustness and reliability. However, the impact of these tests on patient care at point-of-care cannot be clearly assessed when considering the limits of the study 2 design. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2557-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-54854952017-06-30 SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward Tran, Léa C. Tournus, Céline Dina, Julia Morello, Rémy Brouard, Jacques Vabret, Astrid BMC Infect Dis Research Article BACKGROUND: Respiratory syncytial virus (RSV) is responsible for severe respiratory infections and higher costs in medical care. The two aims of this work were to assess the performances of SOFIA(®)RSV tests in “real-life-laboratory” conditions (study 1) and implemented at point-of-care testing in a pediatric emergency department (ED, study 2), during two consecutive winter seasons. METHODS: In study 1, fresh nasopharyngeal swabs from patients of all ages were sampled in 1.5 ml of Universal virological Transport Medium (UTM) and prospectively tested using SOFIA(®)RSV tests. In study 2, conducted in a pediatric ED, nasopharyngeal swabs were placed in 3 ml of UTM. All SOFIA(®)RSV tests were confirmed by molecular testing, considered as reference method. The epidemiological and clinical features of tested patients, as well as the care of these patients after obtaining quick results were evaluated. RESULTS: The sensitivities of SOFIA(®)RSV in infants (aged under 24 months) performed in the laboratory and in the pediatric ED were respectively 95% (95% CI: 86.8–98.1) and 74.8% (95% CI: 68.0–80.9) compared to PCR. In study 1, the sensitivity among children (from 2 to 15 years old) and adults (above 15 years old) dropped to 45% (95% CI: 23.1–68.5) and 59% (95% CI: 32.9–81.6), respectively. In study 2, there were some differences in bed-management of SOFIA(®)RSV positive compared to SOFIA(®)RSV negative infants. CONCLUSIONS: SOFIA(®)RSV tests performed in the laboratory and in the pediatric ED show high and satisfactory sensitivities among young children under 24 months, which supports its robustness and reliability. However, the impact of these tests on patient care at point-of-care cannot be clearly assessed when considering the limits of the study 2 design. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-017-2557-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-26 /pmc/articles/PMC5485495/ /pubmed/28651525 http://dx.doi.org/10.1186/s12879-017-2557-8 Text en © The Author(s). 2017 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
Tran, Léa C.
Tournus, Céline
Dina, Julia
Morello, Rémy
Brouard, Jacques
Vabret, Astrid
SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title_full SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title_fullStr SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title_full_unstemmed SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title_short SOFIA(®)RSV: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
title_sort sofia(®)rsv: prospective laboratory evaluation and implementation of a rapid diagnostic test in a pediatric emergency ward
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485495/
https://www.ncbi.nlm.nih.gov/pubmed/28651525
http://dx.doi.org/10.1186/s12879-017-2557-8
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