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1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital
BACKGROUND: From January 2012 PCV13 was introduced into immunization program in Argentina, 2 + 1 schedule for <2 years. The aims of this study were to describe epidemiological-clinical pattern of community-acquired bacteremic pneumonia (CABP) in the post-vaccination period and the risks factors o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252622/ http://dx.doi.org/10.1093/ofid/ofy210.1290 |
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author | Gentile, Angela Bakir, Julia Lucion, Maria Florencia Juarez, Maria Del Valle Rapaport, Solana Areso, Maria Soledad |
author_facet | Gentile, Angela Bakir, Julia Lucion, Maria Florencia Juarez, Maria Del Valle Rapaport, Solana Areso, Maria Soledad |
author_sort | Gentile, Angela |
collection | PubMed |
description | BACKGROUND: From January 2012 PCV13 was introduced into immunization program in Argentina, 2 + 1 schedule for <2 years. The aims of this study were to describe epidemiological-clinical pattern of community-acquired bacteremic pneumonia (CABP) in the post-vaccination period and the risks factors of CABP occurrence, complications and lethality. METHODS: Cross-sectional study was performed in children with CABP diagnosis, hospitalized in Ricardo Gutierrez Children’s Hospital from January 2012 to December 2017. RESULTS: A total of 135 CABP cases were included; 63% male; 31.1% <2 years; 75% of <5 years received PCV13; 30.4% had underlying diseases. The pathogens isolated were (n = 136): Streptococcus pneumoniae (Sp) 44.9% (all susceptible to Penicillin), Staphylococcus aureus (Sa) 37.5% (Methicillin-Resistant 90.2%), Haemophilus influenzae (Hi) 15.4% (33.3% nontypable Hi), Β-hemolytic Streptococci Group A 1.5% and Neisseria meningitidis 0.7%. Seventy-one percent of cases had complications (pleural effusion 63%, necrotizing pneumonia 11.1%, pneumothorax 8.1%, lung abscess 3.7%, atelectasis 0.7%). Other clinical manifestations combined with CABP were: sepsis 20%, cellulitis/abscess 9.6%, arthritis 6.7%, meningitis 5.9% and osteomyelitis 3.7%. Condensation was the predominant radiological pattern for all agents in 88.1%. Lethality rate was 3%. Sp was more associated with age ≥24 months [OR 2.78 (1.18–6.64)] and Hi was more associated with age <24 months [OR 4.76 (1.62–14.31)]. Complications were significantly higher among Sa pneumonia cases. Children with CABP and sepsis or arthritis had higher lethality [OR 13.38 (1.14–355.45) and OR 17.71 (1.46–223.73)], respectively. CONCLUSION: After PCV13 introduction Sp was still the most common organism causing CABP, mainly in ≥24 months of age. Sa followed in frequency with high morbility. CABP combined with other clinical manifestations were more associated with lethality. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6252622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62526222018-11-28 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital Gentile, Angela Bakir, Julia Lucion, Maria Florencia Juarez, Maria Del Valle Rapaport, Solana Areso, Maria Soledad Open Forum Infect Dis Abstracts BACKGROUND: From January 2012 PCV13 was introduced into immunization program in Argentina, 2 + 1 schedule for <2 years. The aims of this study were to describe epidemiological-clinical pattern of community-acquired bacteremic pneumonia (CABP) in the post-vaccination period and the risks factors of CABP occurrence, complications and lethality. METHODS: Cross-sectional study was performed in children with CABP diagnosis, hospitalized in Ricardo Gutierrez Children’s Hospital from January 2012 to December 2017. RESULTS: A total of 135 CABP cases were included; 63% male; 31.1% <2 years; 75% of <5 years received PCV13; 30.4% had underlying diseases. The pathogens isolated were (n = 136): Streptococcus pneumoniae (Sp) 44.9% (all susceptible to Penicillin), Staphylococcus aureus (Sa) 37.5% (Methicillin-Resistant 90.2%), Haemophilus influenzae (Hi) 15.4% (33.3% nontypable Hi), Β-hemolytic Streptococci Group A 1.5% and Neisseria meningitidis 0.7%. Seventy-one percent of cases had complications (pleural effusion 63%, necrotizing pneumonia 11.1%, pneumothorax 8.1%, lung abscess 3.7%, atelectasis 0.7%). Other clinical manifestations combined with CABP were: sepsis 20%, cellulitis/abscess 9.6%, arthritis 6.7%, meningitis 5.9% and osteomyelitis 3.7%. Condensation was the predominant radiological pattern for all agents in 88.1%. Lethality rate was 3%. Sp was more associated with age ≥24 months [OR 2.78 (1.18–6.64)] and Hi was more associated with age <24 months [OR 4.76 (1.62–14.31)]. Complications were significantly higher among Sa pneumonia cases. Children with CABP and sepsis or arthritis had higher lethality [OR 13.38 (1.14–355.45) and OR 17.71 (1.46–223.73)], respectively. CONCLUSION: After PCV13 introduction Sp was still the most common organism causing CABP, mainly in ≥24 months of age. Sa followed in frequency with high morbility. CABP combined with other clinical manifestations were more associated with lethality. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6252622/ http://dx.doi.org/10.1093/ofid/ofy210.1290 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Gentile, Angela Bakir, Julia Lucion, Maria Florencia Juarez, Maria Del Valle Rapaport, Solana Areso, Maria Soledad 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title | 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title_full | 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title_fullStr | 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title_full_unstemmed | 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title_short | 1460. Community-Acquired Bacteremic Pneumonia in Post-pneumococcal Vaccination Era in a Pediatric Hospital |
title_sort | 1460. community-acquired bacteremic pneumonia in post-pneumococcal vaccination era in a pediatric hospital |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252622/ http://dx.doi.org/10.1093/ofid/ofy210.1290 |
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