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Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine

We describe the aetiology of community-acquired pneumonia in children before and after the introduction of the pneumococcal conjugate vaccination (PCV) programme in 2006. Prospective studies were conducted in 2001–2002 (pre-vaccine) and 2009–2011 (post-vaccine) of children aged 0–16 years with radio...

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Autores principales: Elemraid, Mohamed A., Sails, Andrew D., Eltringham, Gary J.A., Perry, John D., Rushton, Stephen P., Spencer, David A., Thomas, Matthew F., Eastham, Katherine M., Hampton, Fiona, Gennery, Andrew R., Clark, Julia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844138/
https://www.ncbi.nlm.nih.gov/pubmed/23598951
http://dx.doi.org/10.1183/09031936.00199112
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author Elemraid, Mohamed A.
Sails, Andrew D.
Eltringham, Gary J.A.
Perry, John D.
Rushton, Stephen P.
Spencer, David A.
Thomas, Matthew F.
Eastham, Katherine M.
Hampton, Fiona
Gennery, Andrew R.
Clark, Julia E.
author_facet Elemraid, Mohamed A.
Sails, Andrew D.
Eltringham, Gary J.A.
Perry, John D.
Rushton, Stephen P.
Spencer, David A.
Thomas, Matthew F.
Eastham, Katherine M.
Hampton, Fiona
Gennery, Andrew R.
Clark, Julia E.
author_sort Elemraid, Mohamed A.
collection PubMed
description We describe the aetiology of community-acquired pneumonia in children before and after the introduction of the pneumococcal conjugate vaccination (PCV) programme in 2006. Prospective studies were conducted in 2001–2002 (pre-vaccine) and 2009–2011 (post-vaccine) of children aged 0–16 years with radiologically confirmed pneumonia seen in hospital. Investigations included culture, serology, immunofluorescence antibody and urine antigen testing, with an increased use of PCR assays and expanded panels of pathogens in the post-vaccine study. 241 and 160 children were enrolled in the pre- and post-vaccine studies, respectively (73% aged <5 years). Identification of a causative pathogen was higher post-vaccination (61%) than pre-vaccination (48.5%) (p=0.019). Rates of bacterial infections were not different between post- and pre-vaccine studies (17.5% versus 24%, p=0.258). Viral (31%) and mixed (12.5%) infections were found more often post-vaccination (19.5%, p=0.021) than pre-vaccination (5%, p=0.015). Rates of identified pneumococcal infections were comparable between pre- and post-vaccine studies (14.7% versus 17.4%, p=0.557). Diagnosis of pneumococcal infection post-vaccination improved when PCR was used compared to culture (21.6% versus 6%, p=0.0004). Serotypes included in PCV13 but not PCV7 were identified in 75% (18 out of 24) post-vaccination. Infection with nonvaccine pneumococcal serotypes continues to be a significant cause of pneumonia in children in the UK.
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spelling pubmed-38441382013-12-05 Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine Elemraid, Mohamed A. Sails, Andrew D. Eltringham, Gary J.A. Perry, John D. Rushton, Stephen P. Spencer, David A. Thomas, Matthew F. Eastham, Katherine M. Hampton, Fiona Gennery, Andrew R. Clark, Julia E. Eur Respir J Original Article We describe the aetiology of community-acquired pneumonia in children before and after the introduction of the pneumococcal conjugate vaccination (PCV) programme in 2006. Prospective studies were conducted in 2001–2002 (pre-vaccine) and 2009–2011 (post-vaccine) of children aged 0–16 years with radiologically confirmed pneumonia seen in hospital. Investigations included culture, serology, immunofluorescence antibody and urine antigen testing, with an increased use of PCR assays and expanded panels of pathogens in the post-vaccine study. 241 and 160 children were enrolled in the pre- and post-vaccine studies, respectively (73% aged <5 years). Identification of a causative pathogen was higher post-vaccination (61%) than pre-vaccination (48.5%) (p=0.019). Rates of bacterial infections were not different between post- and pre-vaccine studies (17.5% versus 24%, p=0.258). Viral (31%) and mixed (12.5%) infections were found more often post-vaccination (19.5%, p=0.021) than pre-vaccination (5%, p=0.015). Rates of identified pneumococcal infections were comparable between pre- and post-vaccine studies (14.7% versus 17.4%, p=0.557). Diagnosis of pneumococcal infection post-vaccination improved when PCR was used compared to culture (21.6% versus 6%, p=0.0004). Serotypes included in PCV13 but not PCV7 were identified in 75% (18 out of 24) post-vaccination. Infection with nonvaccine pneumococcal serotypes continues to be a significant cause of pneumonia in children in the UK. European Respiratory Society 2013-12 2013-04-18 /pmc/articles/PMC3844138/ /pubmed/23598951 http://dx.doi.org/10.1183/09031936.00199112 Text en ©ERS 2013 http://creativecommons.org/licenses/by-nc/3.0/ ERJ Open articles are open access and distributed under the terms of the (Creative Commons Attribution Licence 3.0> (http://creativecommons.org/licenses/by-nc/3.0/) )
spellingShingle Original Article
Elemraid, Mohamed A.
Sails, Andrew D.
Eltringham, Gary J.A.
Perry, John D.
Rushton, Stephen P.
Spencer, David A.
Thomas, Matthew F.
Eastham, Katherine M.
Hampton, Fiona
Gennery, Andrew R.
Clark, Julia E.
Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title_full Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title_fullStr Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title_full_unstemmed Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title_short Aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
title_sort aetiology of paediatric pneumonia after the introduction of pneumococcal conjugate vaccine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844138/
https://www.ncbi.nlm.nih.gov/pubmed/23598951
http://dx.doi.org/10.1183/09031936.00199112
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