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Publication
Featured researches published by Antonia Fuster.
European Respiratory Journal | 2017
Ciro Casanova; Bartolome R. Celli; Juan P. de-Torres; Cristina Martinez-Gonzalez; Borja G. Cosío; Victor Pinto-Plata; Pilar de Lucas-Ramos; Miguel Divo; Antonia Fuster; Germán Peces-Barba; Myriam Calle-Rubio; Ingrid Solanes; Ramón Agüero; Nuria Feu-Collado; Inmaculada Alfageme; Alfredo De Diego; Amparo Romero; Eva Balcells; Antonia Llunell; Juan B. Gáldiz; Margarita Marín; A. Moreno; Carlos Cabrera; Rafael Golpe; Celia Lacarcel; Joan B. Soriano; José Luis López-Campos; Juan José Soler-Cataluña; Jose M. Marin
The impact of blood eosinophilia in chronic obstructive pulmonary disease (COPD) remains controversial. To evaluate the prevalence and stability of a high level of blood eosinophils (≥300 cells·μL–1) and its relationship to outcomes, we determined blood eosinophils at baseline and over 2 years in 424 COPD patients (forced expiratory volume in 1 s (FEV1) 60% predicted) and 67 smokers without COPD from the CHAIN cohort, and in 308 COPD patients (FEV1 60% predicted) in the BODE cohort. We related eosinophil levels to exacerbations and survival using Cox hazard analysis. In COPD patients, 15.8% in the CHAIN cohort and 12.3% in the BODE cohort had persistently elevated blood eosinophils at all three visits. A significant proportion (43.8%) of patients had counts that oscillated above and below the cut-off points, while the rest had persistent eosinophil levels <300 cells·μL–1. A similar eosinophil blood pattern was observed in controls. Exacerbation rates did not differ in patients with and without eosinophilia. All-cause mortality was lower in patients with high eosinophils compared with those with values <300 cells·μL–1 (15.8% versus 33.7%; p=0.026). In patients with COPD, blood eosinophils ≥300 cells·μL–1 persisting over 2 years was not a risk factor for COPD exacerbations. High eosinophil count was associated with better survival. The stability of blood eosinophils ≥300 cells per μL is low in COPD patients and it does not confer a poor prognosis http://ow.ly/TwGX30etVIy
Chest | 2018
Cristina Esteban Martínez; Ciro Casanova; Juan P. de-Torres; Jose M. Marin; Pilar de Lucas; Antonia Fuster; Borja G. Cosío; Myriam Calle; Germán Peces-Barba; Ingrid Solanes; Ramón Agüero; Nuria Feu-Collado; Inmaculada Alfageme; Amparo Romero Plaza; Eva Balcells; Alfredo De Diego; Margarita Marín Royo; Amalia Moreno; Antonia Llunel Casanova; Juan B. Gáldiz; Rafael Golpe; Celia Lacárcel Bautista; Carlos Cabrera; Alicia Marin; Joan B. Soriano; José Luis López-Campos
Background Despite the existing evidence‐based smoking cessation interventions, chances of achieving that goal in real life are still low among patients with COPD. We sought to evaluate the clinical consequences of changes in smoking habits in a large cohort of patients with COPD. Methods CHAIN (COPD History Assessment in Spain) is a Spanish multicenter study carried out at pulmonary clinics including active and former smokers with COPD. Smoking status was certified by clinical history and co‐oximetry. Clinical presentation and disease impact were recorded via validated questionnaires, including the London Chest Activity of Daily Living (LCADL) and the Hospital Anxiety and Depression Scale (HADS). No specific smoking cessation intervention was carried out. Factors associated with and clinical consequences of smoking cessation were analyzed by multivariate regression and decision tree analyses. Results One thousand and eighty‐one patients with COPD were included (male, 80.8%; age, 65.2 [SD 8.9] years; FEV1, 60.2 [20.5]%). During the 2‐year follow‐up time (visit 2, 906 patients; visit 3, 791 patients), the majority of patients maintained the same smoking habit. Decision tree analysis detected chronic expectoration as the most relevant variable to identify persistent quitters in the future, followed by an LCADL questionnaire (cutoff 9 points). Total anxiety HADS score was the most relevant clinical impact associated with giving up tobacco, followed by the LCADL questionnaire with a cutoff value of 10 points. Conclusions In this real‐life prospective COPD cohort with no specific antismoking intervention, the majority of patients did not change their smoking status. Our study also identifies baseline expectoration, anxiety, and dyspnea with daily activities as the major determinants of smoking status in COPD. Trial Registry ClinicalTrials.gov; No. NCT01122758; URL: www.clinicaltrials.gov.
Respiratory Medicine | 2018
Joan B. Soriano; Michael Hahsler; Cecilia Soriano; Cristina Martinez; Juan P. de-Torres; Jose M. Marin; Pilar de Lucas; Borja G. Cosío; Antonia Fuster; Ciro Casanova
BACKGROUND The stability of the new GOLD 2017 COPD staging is unknown, as well as the frequency of individual transitions in COPD stages beyond one year. METHODS All COPD participants in the CHAIN cohort were re-analysed according to GOLD 2017 up to five years of follow-up. Their individual changes within COPD stages were aggregated into cohort-wide Markov chains; group stability was evaluated using joinpoint regression. RESULTS At baseline, 959 COPD patients were distributed according to GOLD 2017 stages as 37.7% in A, 38.3% B, 8.2% C, and 15.7% D. The group proportion of patients in each stage was maintained from years one to five. However, we found significant changes between stages at the individual patient level, especially in the more severe stages. The probability of a patient remaining in the same GOLD 2017 COPD stage for two consecutive years ranged during the five years of follow-up for stage C from 16% to 31% per year, while for D from 23% to 43% per year, indicating substantial variation either increasing or decreasing severity for the vast majority of patients. CONCLUSIONS We conclude that group stability observed in COPD staging according to GOLD 2017 recommendations is paired with a large variability at the individual patient level.
Respiratory Medicine | 2014
Luis Puente-Maestu; Myriam Calle; Ángel Ortega-González; Antonia Fuster; Cruz González; Eduardo Márquez-Martín; Pedro Jorge Marcos-Rodriguez; Carmen Calero; Juan Luis Rodríguez-Hermosa; Rosa Malo de Molina; Myriam Aburto; Patricia Sobradillo; Bernardino Alcázar; Gema Tirado-Conde
Archivos De Bronconeumologia | 2016
Luis Puente-Maestu; Jorge Chancafe-Morgan; Myriam Calle; Juan Luis Rodríguez-Hermosa; Rosa Malo de Molina; Ángel Ortega-González; Antonia Fuster; Eduardo Márquez-Martín; Pedro J. Marcos; Laura Ramírez; Shaunta' M. Ray; Andrea S. Franks
European Respiratory Journal | 2013
Patricia Sobradillo; Antonia Fuster; Pedro J. Marcos; Ángel Ortega; Cruz González; Myriam Aburto; Juan Luis Rodríguez; Bernardino Alcázar; Myriam Calle; Luis Puente
Archive | 2016
Luis Puente-Maestu; Jorge Chancafe-Morgan; Myriam Calle; Juan Luis Rodríguez-Hermosa; Rosa Malo de Molina; Ángel Ortega-González; Antonia Fuster; Eduardo Márquez-Martín
BMC Pulmonary Medicine | 2016
Bernardino Alcazar; Pilar de Lucas; Joan B. Soriano; Alonso Fernández-Nistal; Antonia Fuster; José Miguel Rodríguez González-Moro; Aurelio Arnedillo; Patricia García Sidro; María José Espinosa de los Monteros
European Respiratory Journal | 2015
Bernardino Alcázar Navarrete; Pilar de Lucas; Joan B. Soriano; Alonso Fernández-Nistal; Antonia Fuster; José Miguel Rodríguez González-Moro; Aurelio Arnedillo; Patricia García Sidro; María José Espinosa de los Monteros
European Respiratory Journal | 2013
Rosa Malo de Molina; Antonia Fuster; Pedro J. Marcos; Eduardo Márquez; Carmen Calero; Gema Tirado; Bernardino Alcázar; Myriam Calle; Luis Puente
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University of Texas Health Science Center at San Antonio
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