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Value of Exhaled Nitric Oxide (FeNO) And Eosinophilia During the Exacerbations of Chronic Obstructive Pulmonary Disease Requiring Hospital Admission

Authors :
Virginia Álvarez Rodríguez
María Antonia Juretschke Moragues
Elena Aznar Andrés
Juan Pedro Zabaleta Camino
Rodolfo Romero Pareja
Andrés Esteban de la Torre
Rocío Fernández González
María Teresa Río Ramírez
Source :
COPD. 15(4)
Publication Year :
2018

Abstract

The aim of this study was to analyze whether FeNO levels in acute exacerbation of COPD (AECOPD) with hospital admission have better diagnostic value than eosinophilia in blood, and to evaluate its usefulness in predicting a better clinical response. An observational prospective study of patients with AECOPD was carried out. FeNO determinations were made on arrival at the emergency room (ER), at discharge and during stability 3-6 months after discharge. Co-morbidities, bronchodilators, inhaled (IGC) and systemic (SGC) glucocorticoids, eosinophils, systemic inflammation markers (procalcitonin, C-reactive protein), eosinophil cationic protein, and total IgE were collected. Fifty consecutive patients (92% men, mean age 75 ± 6 years) were included in this study. Phenotypes were 26% Asthma-COPD Overlap Syndrome (ACOS), 42% chronic bronchitis (CB) and 32% emphysema. ACOS patients showed significantly higher levels of FeNO (73 ppb) and eosinophils (508 cells/mm3) than the rest (CB: 23 ppb, 184 cells/mm3, emphysema: 27 ppb, 159 cells/mm3; p < 0.05). A significant correlation between FeNO levels measured in ER and eosinophils was observed (r = 0.7; p < 0.001), but not at discharge or in stable phase. No significant association was found with parameters of systemic inflammation and mean stay. In conclusion, the determination of FeNO in AECOPD does not offer advantages over the evaluation of eosinophilia. These parameters rise at arrival in ER, descend at discharge, and remain unchanged in the stable phase. Both present similar diagnostic utility and are able to better identify the ACOS phenotype, which helps select a population that could benefit from a glucocorticoids therapy. Sin financiación 2.503 JCR (2018) Q3, 37/63 Respiratory System 1.034 SJR (2018) Q1, 526/2488 Medicine (miscellaneous) No data IDR 2018 UEM

Details

ISSN :
15412563
Volume :
15
Issue :
4
Database :
OpenAIRE
Journal :
COPD
Accession number :
edsair.doi.dedup.....b7f1f6a900185143566fd7585f5e9d33