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Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis

BACKGROUND: Despite the increasing prevalence of Achromobacter xylosoxidans lung infection in patients with cystic fibrosis (CF), its clinical pathogenicity remains controversial. The objective of this study was to evaluate the effects of this emerging bacterium on lung disease severity in CF childr...

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Autores principales: Marsac, Charlotte, Berdah, Laura, Thouvenin, Guillaume, Sermet-Gaudelus, Isabelle, Corvol, Harriet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165377/
https://www.ncbi.nlm.nih.gov/pubmed/34084788
http://dx.doi.org/10.1183/23120541.00076-2021
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author Marsac, Charlotte
Berdah, Laura
Thouvenin, Guillaume
Sermet-Gaudelus, Isabelle
Corvol, Harriet
author_facet Marsac, Charlotte
Berdah, Laura
Thouvenin, Guillaume
Sermet-Gaudelus, Isabelle
Corvol, Harriet
author_sort Marsac, Charlotte
collection PubMed
description BACKGROUND: Despite the increasing prevalence of Achromobacter xylosoxidans lung infection in patients with cystic fibrosis (CF), its clinical pathogenicity remains controversial. The objective of this study was to evaluate the effects of this emerging bacterium on lung disease severity in CF children. METHODS: This case–control retrospective study took place in two French paediatric CF centres. 45 cases infected by A. xylosoxidans were matched for age, sex, CFTR genotypes and pancreatic status to 45 never-infected controls. Clinical data were retrieved from clinical records over the 2 years before and after A. xylosoxidans initial infection. RESULTS: At infection onset, lung function was lower in cases compared with controls (p=0.006). Over the 2 years prior to A. xylosoxidans acquisition, compared with controls, cases had more frequent pulmonary exacerbations (p=0.02), hospitalisations (p=0.05), and intravenous (p=0.03) and oral (p=0.001) antibiotic courses. In the 2 years following A. xylosoxidans infection, cases remained more severe with more frequent pulmonary exacerbations (p=0.0001), hospitalisations (p=0.0001), and intravenous (p=0.0001) and oral antibiotic courses (p=0.0001). Lung function decline tended to be faster in cases (−5.5% per year) compared with controls (−0.5% per year). CONCLUSIONS: This case–control study demonstrates that A. xylosoxidans occurs more frequently in the patients with the worse lung disease. Further studies assessing the pathogenicity of this emerging pathogen and international treatment recommendations are warranted.
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spelling pubmed-81653772021-06-02 Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis Marsac, Charlotte Berdah, Laura Thouvenin, Guillaume Sermet-Gaudelus, Isabelle Corvol, Harriet ERJ Open Res Original Articles BACKGROUND: Despite the increasing prevalence of Achromobacter xylosoxidans lung infection in patients with cystic fibrosis (CF), its clinical pathogenicity remains controversial. The objective of this study was to evaluate the effects of this emerging bacterium on lung disease severity in CF children. METHODS: This case–control retrospective study took place in two French paediatric CF centres. 45 cases infected by A. xylosoxidans were matched for age, sex, CFTR genotypes and pancreatic status to 45 never-infected controls. Clinical data were retrieved from clinical records over the 2 years before and after A. xylosoxidans initial infection. RESULTS: At infection onset, lung function was lower in cases compared with controls (p=0.006). Over the 2 years prior to A. xylosoxidans acquisition, compared with controls, cases had more frequent pulmonary exacerbations (p=0.02), hospitalisations (p=0.05), and intravenous (p=0.03) and oral (p=0.001) antibiotic courses. In the 2 years following A. xylosoxidans infection, cases remained more severe with more frequent pulmonary exacerbations (p=0.0001), hospitalisations (p=0.0001), and intravenous (p=0.0001) and oral antibiotic courses (p=0.0001). Lung function decline tended to be faster in cases (−5.5% per year) compared with controls (−0.5% per year). CONCLUSIONS: This case–control study demonstrates that A. xylosoxidans occurs more frequently in the patients with the worse lung disease. Further studies assessing the pathogenicity of this emerging pathogen and international treatment recommendations are warranted. European Respiratory Society 2021-05-31 /pmc/articles/PMC8165377/ /pubmed/34084788 http://dx.doi.org/10.1183/23120541.00076-2021 Text en Copyright ©The authors 2021 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Articles
Marsac, Charlotte
Berdah, Laura
Thouvenin, Guillaume
Sermet-Gaudelus, Isabelle
Corvol, Harriet
Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title_full Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title_fullStr Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title_full_unstemmed Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title_short Achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
title_sort achromobacter xylosoxidans airway infection is associated with lung disease severity in children with cystic fibrosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165377/
https://www.ncbi.nlm.nih.gov/pubmed/34084788
http://dx.doi.org/10.1183/23120541.00076-2021
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