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Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection

PURPOSE: Despite the availability of molecular methods, identification of the causative virus in children with acute respiratory infections (ARIs) has proven difficult as the same viruses are often detected in asymptomatic children. METHODS: Multiplex reverse transcription polymerase chain reaction...

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Autores principales: Choi, Eunjin, Ha, Kee-Soo, Song, Dae Jin, Lee, Jung Hwa, Lee, Kwang Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021362/
https://www.ncbi.nlm.nih.gov/pubmed/29963101
http://dx.doi.org/10.3345/kjp.2018.61.6.180
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author Choi, Eunjin
Ha, Kee-Soo
Song, Dae Jin
Lee, Jung Hwa
Lee, Kwang Chul
author_facet Choi, Eunjin
Ha, Kee-Soo
Song, Dae Jin
Lee, Jung Hwa
Lee, Kwang Chul
author_sort Choi, Eunjin
collection PubMed
description PURPOSE: Despite the availability of molecular methods, identification of the causative virus in children with acute respiratory infections (ARIs) has proven difficult as the same viruses are often detected in asymptomatic children. METHODS: Multiplex reverse transcription polymerase chain reaction assays were performed to detect 15 common respiratory viruses in children under 15 years of age who were hospitalized with ARI between January 2013 and December 2015. Viral epidemiology and clinical profiles of single virus infections were evaluated. RESULTS: Of 3,505 patients, viruses were identified in 2,424 (69.1%), with the assay revealing a single virus in 1,747 cases (49.8%). While major pathogens in single virus-positive cases differed according to age, human rhinovirus (hRV) was common in patients of all ages. Respiratory syncytial virus (RSV), influenza virus (IF), and human metapneumovirus (hMPV) were found to be seasonal pathogens, appearing from fall through winter and spring, whereas hRV and adenovirus (AdV) were detected in every season. Patients with ARIs caused by RSV and hRV were frequently afebrile and more commonly had wheezing compared with patients with other viral ARIs. Neutrophil-dominant inflammation was observed in ARIs caused by IF, AdV, and hRV, whereas lymphocyte-dominant inflammation was observed with RSV A, parainfluenza virus, and hMPV. Monocytosis was common with RSV and AdV, whereas eosinophilia was observed with hRV. CONCLUSION: In combination with viral identification, recognition of virus-specific clinical and laboratory patterns will expand our understanding of the epidemiology of viral ARIs and help us to establish more efficient therapeutic and preventive strategies.
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spelling pubmed-60213622018-06-29 Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection Choi, Eunjin Ha, Kee-Soo Song, Dae Jin Lee, Jung Hwa Lee, Kwang Chul Korean J Pediatr Original Article PURPOSE: Despite the availability of molecular methods, identification of the causative virus in children with acute respiratory infections (ARIs) has proven difficult as the same viruses are often detected in asymptomatic children. METHODS: Multiplex reverse transcription polymerase chain reaction assays were performed to detect 15 common respiratory viruses in children under 15 years of age who were hospitalized with ARI between January 2013 and December 2015. Viral epidemiology and clinical profiles of single virus infections were evaluated. RESULTS: Of 3,505 patients, viruses were identified in 2,424 (69.1%), with the assay revealing a single virus in 1,747 cases (49.8%). While major pathogens in single virus-positive cases differed according to age, human rhinovirus (hRV) was common in patients of all ages. Respiratory syncytial virus (RSV), influenza virus (IF), and human metapneumovirus (hMPV) were found to be seasonal pathogens, appearing from fall through winter and spring, whereas hRV and adenovirus (AdV) were detected in every season. Patients with ARIs caused by RSV and hRV were frequently afebrile and more commonly had wheezing compared with patients with other viral ARIs. Neutrophil-dominant inflammation was observed in ARIs caused by IF, AdV, and hRV, whereas lymphocyte-dominant inflammation was observed with RSV A, parainfluenza virus, and hMPV. Monocytosis was common with RSV and AdV, whereas eosinophilia was observed with hRV. CONCLUSION: In combination with viral identification, recognition of virus-specific clinical and laboratory patterns will expand our understanding of the epidemiology of viral ARIs and help us to establish more efficient therapeutic and preventive strategies. The Korean Pediatric Society 2018-06 2018-06-25 /pmc/articles/PMC6021362/ /pubmed/29963101 http://dx.doi.org/10.3345/kjp.2018.61.6.180 Text en Copyright © 2018 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Eunjin
Ha, Kee-Soo
Song, Dae Jin
Lee, Jung Hwa
Lee, Kwang Chul
Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title_full Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title_fullStr Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title_full_unstemmed Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title_short Clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
title_sort clinical and laboratory profiles of hospitalized children with acute respiratory virus infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021362/
https://www.ncbi.nlm.nih.gov/pubmed/29963101
http://dx.doi.org/10.3345/kjp.2018.61.6.180
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