Cargando…
Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens
BACKGROUND AND OBJECTIVE: COPD exacerbation is characterized by worsening of symptoms, warranting change in treatment. Systemic and airway inflammation play roles in the pathogenesis of COPD exacerbation. We hypothesized whether increased serum inflammatory biomarkers are associated with the clinica...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459973/ https://www.ncbi.nlm.nih.gov/pubmed/28615935 http://dx.doi.org/10.2147/COPD.S132132 |
_version_ | 1783242067621707776 |
---|---|
author | Kawamatawong, Theerasuk Apiwattanaporn, Apitch Siricharoonwong, Warisara |
author_facet | Kawamatawong, Theerasuk Apiwattanaporn, Apitch Siricharoonwong, Warisara |
author_sort | Kawamatawong, Theerasuk |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: COPD exacerbation is characterized by worsening of symptoms, warranting change in treatment. Systemic and airway inflammation play roles in the pathogenesis of COPD exacerbation. We hypothesized whether increased serum inflammatory biomarkers are associated with the clinical outcomes of COPD exacerbation caused by different infectious pathogens. METHODS: COPD patients with exacerbation were recruited from a hospital emergency department during 2014–2015. Serum procalcitonin (PCT) and C-reactive protein (CRP) were measured. Dyspnea, eosinopenia, consolidation, acidemia, and atrial fibrillation (DECAF) score was calculated for predicting mortality. Multiplex polymerase chain reaction was carried out for respiratory viral assay from nasopharyngeal swabs, and sputum bacterial culture was also performed. Hospital mortality, invasive mechanical ventilation requirement, and length of hospital stay (LOS) were evaluated, and their associations with clinical characteristics, DECAF score, and serum biomarkers were examined. RESULTS: A total of 62 COPD patients were enrolled. These patients were classified as Global Initiative for Obstructive Lung Disease (GOLD) stage 2, 3, and 4 in 12.9%, 6.4%, and 80.7% of cases, respectively. Isolated bacterial exacerbation was recovered in 30.6% of exacerbation episodes: Klebsiella pneumoniae was the most commonly identified bacteria. Viral pathogens and coinfections were noted in 9.6% and 16.1% of exacerbated patients, respectively. Influenza was the most commonly detected viral pathogen. Serum biomarkers and DECAF score for viruses, bacteria, coinfection, and noninfectious causes of exacerbations were similar. Neither DECAF score nor serum biomarkers were able to differentiate patients with and without mortality or requiring mechanical ventilation. Increased serum PCT was noted in patients with LOS ≥7 days when compared with those with LOS <7 days (0.38 ng/mL vs 0.1 ng/mL; P=0.035). CONCLUSION: Increased serum PCT is associated with longer LOS in COPD exacerbation. However, CRP and DECAF score play limited roles in predicting clinical outcome and lack an association with causes of exacerbation. |
format | Online Article Text |
id | pubmed-5459973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54599732017-06-14 Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens Kawamatawong, Theerasuk Apiwattanaporn, Apitch Siricharoonwong, Warisara Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND AND OBJECTIVE: COPD exacerbation is characterized by worsening of symptoms, warranting change in treatment. Systemic and airway inflammation play roles in the pathogenesis of COPD exacerbation. We hypothesized whether increased serum inflammatory biomarkers are associated with the clinical outcomes of COPD exacerbation caused by different infectious pathogens. METHODS: COPD patients with exacerbation were recruited from a hospital emergency department during 2014–2015. Serum procalcitonin (PCT) and C-reactive protein (CRP) were measured. Dyspnea, eosinopenia, consolidation, acidemia, and atrial fibrillation (DECAF) score was calculated for predicting mortality. Multiplex polymerase chain reaction was carried out for respiratory viral assay from nasopharyngeal swabs, and sputum bacterial culture was also performed. Hospital mortality, invasive mechanical ventilation requirement, and length of hospital stay (LOS) were evaluated, and their associations with clinical characteristics, DECAF score, and serum biomarkers were examined. RESULTS: A total of 62 COPD patients were enrolled. These patients were classified as Global Initiative for Obstructive Lung Disease (GOLD) stage 2, 3, and 4 in 12.9%, 6.4%, and 80.7% of cases, respectively. Isolated bacterial exacerbation was recovered in 30.6% of exacerbation episodes: Klebsiella pneumoniae was the most commonly identified bacteria. Viral pathogens and coinfections were noted in 9.6% and 16.1% of exacerbated patients, respectively. Influenza was the most commonly detected viral pathogen. Serum biomarkers and DECAF score for viruses, bacteria, coinfection, and noninfectious causes of exacerbations were similar. Neither DECAF score nor serum biomarkers were able to differentiate patients with and without mortality or requiring mechanical ventilation. Increased serum PCT was noted in patients with LOS ≥7 days when compared with those with LOS <7 days (0.38 ng/mL vs 0.1 ng/mL; P=0.035). CONCLUSION: Increased serum PCT is associated with longer LOS in COPD exacerbation. However, CRP and DECAF score play limited roles in predicting clinical outcome and lack an association with causes of exacerbation. Dove Medical Press 2017-05-31 /pmc/articles/PMC5459973/ /pubmed/28615935 http://dx.doi.org/10.2147/COPD.S132132 Text en © 2017 Kawamatawong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kawamatawong, Theerasuk Apiwattanaporn, Apitch Siricharoonwong, Warisara Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title | Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title_full | Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title_fullStr | Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title_full_unstemmed | Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title_short | Serum inflammatory biomarkers and clinical outcomes of COPD exacerbation caused by different pathogens |
title_sort | serum inflammatory biomarkers and clinical outcomes of copd exacerbation caused by different pathogens |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459973/ https://www.ncbi.nlm.nih.gov/pubmed/28615935 http://dx.doi.org/10.2147/COPD.S132132 |
work_keys_str_mv | AT kawamatawongtheerasuk seruminflammatorybiomarkersandclinicaloutcomesofcopdexacerbationcausedbydifferentpathogens AT apiwattanapornapitch seruminflammatorybiomarkersandclinicaloutcomesofcopdexacerbationcausedbydifferentpathogens AT siricharoonwongwarisara seruminflammatorybiomarkersandclinicaloutcomesofcopdexacerbationcausedbydifferentpathogens |