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Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study

OBJECTIVES: To describe critically ill children with respiratory infections, classify them by infection syndrome type and determine the prevalence of Mycoplasma pneumoniae detection. STUDY DESIGN: A retrospective, single-centre cohort study. All children aged 2 months–18 years with presumed respirat...

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Autores principales: Alfaraidi, Haifa, Luinstra, Kathy, Eshaghi, Alireza, Smieja, Marek, Gubbay, Jonathan B, Pernica, Jeffrey M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213883/
https://www.ncbi.nlm.nih.gov/pubmed/32411832
http://dx.doi.org/10.1136/bmjpo-2020-000640
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author Alfaraidi, Haifa
Luinstra, Kathy
Eshaghi, Alireza
Smieja, Marek
Gubbay, Jonathan B
Pernica, Jeffrey M
author_facet Alfaraidi, Haifa
Luinstra, Kathy
Eshaghi, Alireza
Smieja, Marek
Gubbay, Jonathan B
Pernica, Jeffrey M
author_sort Alfaraidi, Haifa
collection PubMed
description OBJECTIVES: To describe critically ill children with respiratory infections, classify them by infection syndrome type and determine the prevalence of Mycoplasma pneumoniae detection. STUDY DESIGN: A retrospective, single-centre cohort study. All children aged 2 months–18 years with presumed respiratory infection who were admitted to a tertiary hospital paediatric intensive care unit (PICU) between September 2015 and October 2016 were eligible. Subjects were grouped by clinical syndrome (viral respiratory infection, asthma exacerbation, undifferentiated/uncomplicated pneumonia, pneumonia complicated by effusion/empyema and ‘other’). All subjects had nasopharyngeal swabs tested for respiratory viruses, M. pneumoniae and Chlamydia pneumoniae. RESULTS: There were 221 subjects; the median age was 3.1 years; 44% were female; and 78% had medical comorbidities. The majority (75%) was treated with antibiotics, most often ceftriaxone (90% of treated children). Those with any pneumonia were significantly less likely to have a respiratory virus identified in their nasopharynges and had significantly higher C reactive protein (CRP) values than those in the viral infection and asthma groups. There were 10 subjects in whom M. pneumoniae was detected (4.5%, 95% CI 2.2% to 8.2%). Mycoplasma-positive children were older (difference 3.5 years, 95% CI 0.66 to 6.4 years) and had fewer viral coinfections (30% compared with 69%, p=0.02). The prevalence of Mycoplasma infection in children aged >5 years with any pneumonia was 13.2% (95%CI 4.4% to 28%). CONCLUSIONS: The majority of participants had respiratory viruses detected and were treated with broad-spectrum antibiotics. Differences in CRP and viral prevalence were observed between children with different infection syndrome types. M. pneumoniae infection was not rare in school-aged children with pneumonia admitted to the PICU. Attention to antibiotic treatment and rapid diagnostic testing for Mycoplasma in older, critically ill children should be considered to optimise management and avert morbidity and mortality from respiratory infection.
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spelling pubmed-72138832020-05-14 Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study Alfaraidi, Haifa Luinstra, Kathy Eshaghi, Alireza Smieja, Marek Gubbay, Jonathan B Pernica, Jeffrey M BMJ Paediatr Open Infectious Diseases OBJECTIVES: To describe critically ill children with respiratory infections, classify them by infection syndrome type and determine the prevalence of Mycoplasma pneumoniae detection. STUDY DESIGN: A retrospective, single-centre cohort study. All children aged 2 months–18 years with presumed respiratory infection who were admitted to a tertiary hospital paediatric intensive care unit (PICU) between September 2015 and October 2016 were eligible. Subjects were grouped by clinical syndrome (viral respiratory infection, asthma exacerbation, undifferentiated/uncomplicated pneumonia, pneumonia complicated by effusion/empyema and ‘other’). All subjects had nasopharyngeal swabs tested for respiratory viruses, M. pneumoniae and Chlamydia pneumoniae. RESULTS: There were 221 subjects; the median age was 3.1 years; 44% were female; and 78% had medical comorbidities. The majority (75%) was treated with antibiotics, most often ceftriaxone (90% of treated children). Those with any pneumonia were significantly less likely to have a respiratory virus identified in their nasopharynges and had significantly higher C reactive protein (CRP) values than those in the viral infection and asthma groups. There were 10 subjects in whom M. pneumoniae was detected (4.5%, 95% CI 2.2% to 8.2%). Mycoplasma-positive children were older (difference 3.5 years, 95% CI 0.66 to 6.4 years) and had fewer viral coinfections (30% compared with 69%, p=0.02). The prevalence of Mycoplasma infection in children aged >5 years with any pneumonia was 13.2% (95%CI 4.4% to 28%). CONCLUSIONS: The majority of participants had respiratory viruses detected and were treated with broad-spectrum antibiotics. Differences in CRP and viral prevalence were observed between children with different infection syndrome types. M. pneumoniae infection was not rare in school-aged children with pneumonia admitted to the PICU. Attention to antibiotic treatment and rapid diagnostic testing for Mycoplasma in older, critically ill children should be considered to optimise management and avert morbidity and mortality from respiratory infection. BMJ Publishing Group 2020-04-27 /pmc/articles/PMC7213883/ /pubmed/32411832 http://dx.doi.org/10.1136/bmjpo-2020-000640 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Infectious Diseases
Alfaraidi, Haifa
Luinstra, Kathy
Eshaghi, Alireza
Smieja, Marek
Gubbay, Jonathan B
Pernica, Jeffrey M
Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title_full Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title_fullStr Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title_full_unstemmed Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title_short Paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
title_sort paediatric critical illness associated with respiratory infection: a single-centre, retrospective cohort study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213883/
https://www.ncbi.nlm.nih.gov/pubmed/32411832
http://dx.doi.org/10.1136/bmjpo-2020-000640
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