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dc.contributor.authorRomero Linares, Alejandro
dc.contributor.authorAlvarez Muro, Lucía
dc.contributor.authorHammadi, A
dc.contributor.authorHoyas-Sánchez, Clara
dc.contributor.authorJiménez Antón, A
dc.contributor.authorAlmansa López, Angel
dc.contributor.authorCasares Martín Moreno, Laura
dc.contributor.authorSánchez Álvarez, Esther
dc.contributor.authorMurillo Rodriguez, A
dc.contributor.authorGómez Mora, M
dc.contributor.authorGómez-Pontes Cabrera, T
dc.contributor.authorRomero Palacios, Pedro José 
dc.contributor.authorAlcázar Navarrete, Bernardino
dc.date.accessioned2025-05-20T10:24:18Z
dc.date.available2025-05-20T10:24:18Z
dc.date.issued2025-04-29
dc.identifier.citationRespiratory Medicine 243 (2025) 108134es_ES
dc.identifier.urihttps://hdl.handle.net/10481/104159
dc.description.abstractIntroduction: Exacerbations of chronic obstructive pulmonary disease (COPD) significantly impact morbidity and healthcare utilization. Identifying biomarkers predictive of exacerbation risk can optimize management strategies. We evaluated the role of baseline fractional exhaled nitric oxide (FENO) as a predictor of moderate and severe exacerbations over 90 days. Methods: A prospective cohort study included COPD patients attending pulmonology clinics. Patients were stratified based on baseline FENO levels: FENO <20 ppb and FENO ≥20 ppb. The primary outcome was time-tofirst exacerbation, analysed using Kaplan-Meier survival curves and Cox proportional hazards models. Secondary outcomes included differences in baseline characteristics and hazard ratios (HR) for severe exacerbations. Results: A total of 322 patients were included (220 with FENO <20 ppb, 102 with FENO ≥20 ppb). Kaplan-Meier analysis showed significantly shorter survival time without moderate/severe exacerbations in those with high FENO. Cox regression demonstrated a 3.01-fold increased risk of moderate/severe exacerbations in high FENO (HR: 3.01, 95 % CI: 1.83–4.93; p < 0.001). For severe exacerbations, those patients exhibited a non-significant trend toward increased risk (HR: 2.49, 95 % CI: 0.91–6.86; p = 0.058). Conclusion: Elevated FENO (≥20 ppb) is associated with increased short-term risk of moderate and severe COPD exacerbations. These findings highlight FENO as a potential biomarker for early risk stratification and tailored interventions in COPD patientses_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleShort term exacerbation risk and exhaled nitric oxide in COPDes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.rmed.2025.108134
dc.type.hasVersionAMes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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