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Relationship between serum procalcitonin level and chronic obstructive pulmonary disease

BACKGROUND: Differentiation of the etiologies of acute exacerbations of chronic obstructive pulmonary disease (AECOPD) and differential diagnosis of other causes of respiratory attacks in chronic obstructive pulmonary disease (COPD) patients are challenging. Serum procalcitonin (PCT) which is a biom...

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Autores principales: Borsi, Hamid, Nia, Elham Pajohan, Mal-Amir, Mehrdad Dargahi, Raji, Hanieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436277/
https://www.ncbi.nlm.nih.gov/pubmed/30984705
http://dx.doi.org/10.4103/jfmpc.jfmpc_468_18
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author Borsi, Hamid
Nia, Elham Pajohan
Mal-Amir, Mehrdad Dargahi
Raji, Hanieh
author_facet Borsi, Hamid
Nia, Elham Pajohan
Mal-Amir, Mehrdad Dargahi
Raji, Hanieh
author_sort Borsi, Hamid
collection PubMed
description BACKGROUND: Differentiation of the etiologies of acute exacerbations of chronic obstructive pulmonary disease (AECOPD) and differential diagnosis of other causes of respiratory attacks in chronic obstructive pulmonary disease (COPD) patients are challenging. Serum procalcitonin (PCT) which is a biomarker of bacterial infection, but not viral infections, could possibly recognize AECOPD requiring antibiotic treatment from other etiologies of respiratory attack. METHODS: Patients aged from 40–80 years who were diagnosed with COPD according to the GOLD criteria and who referred to the Imam Khomeini Hospital of Ahvaz in 2016 were divided into two groups of exacerbated and stable COPD. Exacerbation of COPD is defined as worsening of the patient's condition from the stable state and behind normal day-to-day variations that is acute in onset and may necessitate treatment in a patient with underlying COPD. BODE Index and 6MWDT were used to assess the patients, and the severity of their disease was determined based on the GOLD criteria. Subsequently, PCT testing using electrochemiluminescence (ECL) method was carried out on patients on the same day. RESULTS: PCT level in the exacerbation group was 0.272 ± 0.586 and 0.066 ± 0.027 in the non-exacerbation group, and their difference was statistically significant with P value = 0.001. Based on the results, the cut point of differentiating between the AECOPD and the stable groups with a sensitivity of 68% and a specificity of 80% is 0.085. CONCLUSION: Overall, the findings of this study indicate that PCT levels could be regarded as a good diagnostic marker for patients with COPD, and for the differentiation of AECOPD patients from stable COPD patients.
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spelling pubmed-64362772019-04-12 Relationship between serum procalcitonin level and chronic obstructive pulmonary disease Borsi, Hamid Nia, Elham Pajohan Mal-Amir, Mehrdad Dargahi Raji, Hanieh J Family Med Prim Care Original Article BACKGROUND: Differentiation of the etiologies of acute exacerbations of chronic obstructive pulmonary disease (AECOPD) and differential diagnosis of other causes of respiratory attacks in chronic obstructive pulmonary disease (COPD) patients are challenging. Serum procalcitonin (PCT) which is a biomarker of bacterial infection, but not viral infections, could possibly recognize AECOPD requiring antibiotic treatment from other etiologies of respiratory attack. METHODS: Patients aged from 40–80 years who were diagnosed with COPD according to the GOLD criteria and who referred to the Imam Khomeini Hospital of Ahvaz in 2016 were divided into two groups of exacerbated and stable COPD. Exacerbation of COPD is defined as worsening of the patient's condition from the stable state and behind normal day-to-day variations that is acute in onset and may necessitate treatment in a patient with underlying COPD. BODE Index and 6MWDT were used to assess the patients, and the severity of their disease was determined based on the GOLD criteria. Subsequently, PCT testing using electrochemiluminescence (ECL) method was carried out on patients on the same day. RESULTS: PCT level in the exacerbation group was 0.272 ± 0.586 and 0.066 ± 0.027 in the non-exacerbation group, and their difference was statistically significant with P value = 0.001. Based on the results, the cut point of differentiating between the AECOPD and the stable groups with a sensitivity of 68% and a specificity of 80% is 0.085. CONCLUSION: Overall, the findings of this study indicate that PCT levels could be regarded as a good diagnostic marker for patients with COPD, and for the differentiation of AECOPD patients from stable COPD patients. Medknow Publications & Media Pvt Ltd 2019-02 /pmc/articles/PMC6436277/ /pubmed/30984705 http://dx.doi.org/10.4103/jfmpc.jfmpc_468_18 Text en Copyright: © 2019 Journal of Family Medicine and Primary Care http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Borsi, Hamid
Nia, Elham Pajohan
Mal-Amir, Mehrdad Dargahi
Raji, Hanieh
Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title_full Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title_fullStr Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title_full_unstemmed Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title_short Relationship between serum procalcitonin level and chronic obstructive pulmonary disease
title_sort relationship between serum procalcitonin level and chronic obstructive pulmonary disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436277/
https://www.ncbi.nlm.nih.gov/pubmed/30984705
http://dx.doi.org/10.4103/jfmpc.jfmpc_468_18
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