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

医学 呼出气一氧化氮 慢性阻塞性肺病 内科学 恶化 嗜酸性粒细胞增多症 降钙素原 哮喘 嗜酸性粒细胞 胃肠病学 嗜酸性阳离子蛋白 人口 全身炎症 炎症 免疫学 败血症 环境卫生
作者
María Teresa Río Ramírez,M.A. Juretschke Moragues,Rocío Fernández González,Virginia Álvarez Rodríguez,Elena Aznar Andrés,Juan Pedro Zabaleta Camino,Rodolfo Romero Pareja,A. Esteban de la Torre
出处
期刊:COPD: Journal of Chronic Obstructive Pulmonary Disease [Informa]
卷期号:15 (4): 369-376 被引量:18
标识
DOI:10.1080/15412555.2018.1482532
摘要

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.
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