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Infection with and Carriage of Mycoplasma pneumoniae in Children

“Atypical” pneumonia was described as a distinct and mild form of community-acquired pneumonia (CAP) already before Mycoplasma pneumoniae had been discovered and recognized as its cause. M. pneumoniae is detected in CAP patients most frequently among school-aged children from 5 to 15 years of age, w...

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Autores principales: Meyer Sauteur, Patrick M., Unger, Wendy W. J., Nadal, David, Berger, Christoph, Vink, Cornelis, van Rossum, Annemarie M. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803743/
https://www.ncbi.nlm.nih.gov/pubmed/27047456
http://dx.doi.org/10.3389/fmicb.2016.00329
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author Meyer Sauteur, Patrick M.
Unger, Wendy W. J.
Nadal, David
Berger, Christoph
Vink, Cornelis
van Rossum, Annemarie M. C.
author_facet Meyer Sauteur, Patrick M.
Unger, Wendy W. J.
Nadal, David
Berger, Christoph
Vink, Cornelis
van Rossum, Annemarie M. C.
author_sort Meyer Sauteur, Patrick M.
collection PubMed
description “Atypical” pneumonia was described as a distinct and mild form of community-acquired pneumonia (CAP) already before Mycoplasma pneumoniae had been discovered and recognized as its cause. M. pneumoniae is detected in CAP patients most frequently among school-aged children from 5 to 15 years of age, with a decline after adolescence and tapering off in adulthood. Detection rates by polymerase chain reaction (PCR) or serology in children with CAP admitted to the hospital amount 4–39%. Although the infection is generally mild and self-limiting, patients of every age can develop severe or extrapulmonary disease. Recent studies indicate that high rates of healthy children carry M. pneumoniae in the upper respiratory tract and that current diagnostic PCR or serology cannot discriminate between M. pneumoniae infection and carriage. Further, symptoms and radiologic features are not specific for M. pneumoniae infection. Thus, patients may be unnecessarily treated with antimicrobials against M. pneumoniae. Macrolides are the first-line antibiotics for this entity in children younger than 8 years of age. Overall macrolides are extensively used worldwide, and this has led to the emergence of macrolide-resistant M. pneumoniae, which may be associated with severe clinical features and more extrapulmonary complications. This review focuses on the characteristics of M. pneumoniae infections in children, and exemplifies that simple clinical decision rules may help identifying children at high risk for CAP due to M. pneumoniae. This may aid physicians in prescribing appropriate first-line antibiotics, since current diagnostic tests for M. pneumoniae infection are not reliably predictive.
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spelling pubmed-48037432016-04-04 Infection with and Carriage of Mycoplasma pneumoniae in Children Meyer Sauteur, Patrick M. Unger, Wendy W. J. Nadal, David Berger, Christoph Vink, Cornelis van Rossum, Annemarie M. C. Front Microbiol Microbiology “Atypical” pneumonia was described as a distinct and mild form of community-acquired pneumonia (CAP) already before Mycoplasma pneumoniae had been discovered and recognized as its cause. M. pneumoniae is detected in CAP patients most frequently among school-aged children from 5 to 15 years of age, with a decline after adolescence and tapering off in adulthood. Detection rates by polymerase chain reaction (PCR) or serology in children with CAP admitted to the hospital amount 4–39%. Although the infection is generally mild and self-limiting, patients of every age can develop severe or extrapulmonary disease. Recent studies indicate that high rates of healthy children carry M. pneumoniae in the upper respiratory tract and that current diagnostic PCR or serology cannot discriminate between M. pneumoniae infection and carriage. Further, symptoms and radiologic features are not specific for M. pneumoniae infection. Thus, patients may be unnecessarily treated with antimicrobials against M. pneumoniae. Macrolides are the first-line antibiotics for this entity in children younger than 8 years of age. Overall macrolides are extensively used worldwide, and this has led to the emergence of macrolide-resistant M. pneumoniae, which may be associated with severe clinical features and more extrapulmonary complications. This review focuses on the characteristics of M. pneumoniae infections in children, and exemplifies that simple clinical decision rules may help identifying children at high risk for CAP due to M. pneumoniae. This may aid physicians in prescribing appropriate first-line antibiotics, since current diagnostic tests for M. pneumoniae infection are not reliably predictive. Frontiers Media S.A. 2016-03-23 /pmc/articles/PMC4803743/ /pubmed/27047456 http://dx.doi.org/10.3389/fmicb.2016.00329 Text en Copyright © 2016 Meyer Sauteur, Unger, Nadal, Berger, Vink and van Rossum. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Meyer Sauteur, Patrick M.
Unger, Wendy W. J.
Nadal, David
Berger, Christoph
Vink, Cornelis
van Rossum, Annemarie M. C.
Infection with and Carriage of Mycoplasma pneumoniae in Children
title Infection with and Carriage of Mycoplasma pneumoniae in Children
title_full Infection with and Carriage of Mycoplasma pneumoniae in Children
title_fullStr Infection with and Carriage of Mycoplasma pneumoniae in Children
title_full_unstemmed Infection with and Carriage of Mycoplasma pneumoniae in Children
title_short Infection with and Carriage of Mycoplasma pneumoniae in Children
title_sort infection with and carriage of mycoplasma pneumoniae in children
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803743/
https://www.ncbi.nlm.nih.gov/pubmed/27047456
http://dx.doi.org/10.3389/fmicb.2016.00329
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