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Lack of Association between Inhaled Corticosteroid Use Based on the Exhaled Nitric Oxide and Acute Exacerbation of Chronic Obstructive Pulmonary Diseaseopen accessLack of Association between Inhaled Corticosteroid Use Based on the Exhaled Nitric Oxide and Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Other Titles
Lack of Association between Inhaled Corticosteroid Use Based on the Exhaled Nitric Oxide and Acute Exacerbation of Chronic Obstructive Pulmonary Disease
Authors
Bo-Guen KimSun Hye ShinJung-Wan YooYong Suk JoHye Yun Park
Issue Date
Jul-2024
Publisher
대한결핵및호흡기학회
Keywords
Chronic Obstructive Pulmonary Disease; Fractional Exhaled Nitric Oxide; Inhaled Corticosteroid; Exacerbation
Citation
Tuberculosis and Respiratory Diseases, v.87, no.3, pp 329 - 337
Pages
9
Indexed
SCOPUS
ESCI
KCI
Journal Title
Tuberculosis and Respiratory Diseases
Volume
87
Number
3
Start Page
329
End Page
337
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/70921
DOI
10.4046/trd.2023.0175
ISSN
1738-3536
2005-6184
Abstract
Background: Fractional exhaled nitric oxide (FeNO) is known to useful biomarker fordetecting eosinophilic airway inflammation. However, there is a lack of evidence regardingthe role of FeNO in chronic obstructive pulmonary disease (COPD). We aimedto assess whether elevated FeNO and its impact on treatment change into an inhaledcorticosteroid (ICS)-containing regimen and association with acute exacerbation (AE)in patients with COPD. Methods: We retrospectively analyzed 107 COPD patients without a history of asthmafrom March 2016 to December 2019. The patients whose FeNO value was more than50 parts per billion (ppb) were defined into the high FeNO group. Multivariable analysiswith logistic regression was used to identify factors associated with AE in COPD. Results: The median FeNO value was 32 ppb (interquartile range, 19 to 45) and 34(20.0%) patients were classified as high FeNO group (median 74 ppb). In the high FeNOgroup, changes in inhaler treatment into an ICS-containing regimen occurred in 23 of34 patients after the measurement of FeNO. In multivariate analysis, high FeNO was nota contributing factor for AE, but only the high blood eosinophil count (≥300 cells/μL)was associated with AE (adjusted odds ratio, 2.63; 95% confidence interval, 1.01 to 6.91;p=0.049). Conclusion: High FeNO value had a significant impact on the prescription of ICSs inCOPD patients, but it did not show a significant association with AE either on its own orwith changes in treatment.
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