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Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study
OBJECTIVES: To describe children hospitalized with community-acquired pneumonia complicated by effusion (cCAP). DESIGN: Retrospective cohort study. SETTING: A Canadian children’s hospital. PARTICIPANTS: Children without significant medical comorbidities aged < 18 years admitted from January 2015-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113124/ https://www.ncbi.nlm.nih.gov/pubmed/37072740 http://dx.doi.org/10.1186/s12887-023-04004-2 |
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author | Alemayheu, Gelila Lee, Claire S. J. Erdman, Laura K. Wong, Jacqueline Rutherford, Candy Smieja, Marek Khan, Sarah Pernica, Jeffrey M. |
author_facet | Alemayheu, Gelila Lee, Claire S. J. Erdman, Laura K. Wong, Jacqueline Rutherford, Candy Smieja, Marek Khan, Sarah Pernica, Jeffrey M. |
author_sort | Alemayheu, Gelila |
collection | PubMed |
description | OBJECTIVES: To describe children hospitalized with community-acquired pneumonia complicated by effusion (cCAP). DESIGN: Retrospective cohort study. SETTING: A Canadian children’s hospital. PARTICIPANTS: Children without significant medical comorbidities aged < 18 years admitted from January 2015-December 2019 to either the Paediatric Medicine or Paediatric General Surgery services with any pneumonia discharge code who were documented to have an effusion/empyaema using ultrasound. OUTCOME MEASURES: Length of stay; admission to the paediatric intensive care unit; microbiologic diagnosis; antibiotic use. RESULTS: There were 109 children without significant medical comorbidities hospitalized for confirmed cCAP during the study period. Their median length of stay was 9 days (Q1-Q3 6–11 days) and 35/109 (32%) were admitted to the paediatric intensive care unit. Most (89/109, 74%) underwent procedural drainage. Length of stay was not associated with effusion size but was associated with time to drainage (0.60 days longer stay per day delay in drainage, 95%CI 0.19-1.0 days). Microbiologic diagnosis was more often made via molecular testing of pleural fluids (43/59, 73%) than via blood culture (12/109, 11%); the main aetiologic pathogens were S. pneumoniae (40/109, 37%), S. pyogenes (15/109, 14%), and S. aureus (7/109, 6%). Discharge on a narrow spectrum antibiotic (i.e. amoxicillin) was much more common when the cCAP pathogen was identified as compared to when it was not (68% vs. 24%, p < 0.001). CONCLUSIONS: Children with cCAP were commonly hospitalized for prolonged periods. Prompt procedural drainage was associated with shorter hospital stays. Pleural fluid testing often facilitated microbiologic diagnosis, which itself was associated with more appropriate antibiotic therapy. |
format | Online Article Text |
id | pubmed-10113124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101131242023-04-20 Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study Alemayheu, Gelila Lee, Claire S. J. Erdman, Laura K. Wong, Jacqueline Rutherford, Candy Smieja, Marek Khan, Sarah Pernica, Jeffrey M. BMC Pediatr Research OBJECTIVES: To describe children hospitalized with community-acquired pneumonia complicated by effusion (cCAP). DESIGN: Retrospective cohort study. SETTING: A Canadian children’s hospital. PARTICIPANTS: Children without significant medical comorbidities aged < 18 years admitted from January 2015-December 2019 to either the Paediatric Medicine or Paediatric General Surgery services with any pneumonia discharge code who were documented to have an effusion/empyaema using ultrasound. OUTCOME MEASURES: Length of stay; admission to the paediatric intensive care unit; microbiologic diagnosis; antibiotic use. RESULTS: There were 109 children without significant medical comorbidities hospitalized for confirmed cCAP during the study period. Their median length of stay was 9 days (Q1-Q3 6–11 days) and 35/109 (32%) were admitted to the paediatric intensive care unit. Most (89/109, 74%) underwent procedural drainage. Length of stay was not associated with effusion size but was associated with time to drainage (0.60 days longer stay per day delay in drainage, 95%CI 0.19-1.0 days). Microbiologic diagnosis was more often made via molecular testing of pleural fluids (43/59, 73%) than via blood culture (12/109, 11%); the main aetiologic pathogens were S. pneumoniae (40/109, 37%), S. pyogenes (15/109, 14%), and S. aureus (7/109, 6%). Discharge on a narrow spectrum antibiotic (i.e. amoxicillin) was much more common when the cCAP pathogen was identified as compared to when it was not (68% vs. 24%, p < 0.001). CONCLUSIONS: Children with cCAP were commonly hospitalized for prolonged periods. Prompt procedural drainage was associated with shorter hospital stays. Pleural fluid testing often facilitated microbiologic diagnosis, which itself was associated with more appropriate antibiotic therapy. BioMed Central 2023-04-19 /pmc/articles/PMC10113124/ /pubmed/37072740 http://dx.doi.org/10.1186/s12887-023-04004-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Alemayheu, Gelila Lee, Claire S. J. Erdman, Laura K. Wong, Jacqueline Rutherford, Candy Smieja, Marek Khan, Sarah Pernica, Jeffrey M. Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title | Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title_full | Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title_fullStr | Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title_full_unstemmed | Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title_short | Children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
title_sort | children hospitalized with community-acquired pneumonia complicated by effusion: a single-centre retrospective cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113124/ https://www.ncbi.nlm.nih.gov/pubmed/37072740 http://dx.doi.org/10.1186/s12887-023-04004-2 |
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