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Acute bronchodilator responsiveness in subjects with and without airflow obstruction in five Latin American cities: The PLATINO study
Authors:Maria Montes de Oca  Rogelio Perez-Padilla  Carlos Tálamo  Ronald J Halbert  Dolores Moreno  Maria Victorina Lopez  Adriana Muiño  B Jardim José Roberto  Gonzalo Valdivia  Julio Pertuzé  B Menezes Ana Maria
Institution:1. Servicio de Neumonología, Hospital Universitario de Caracas, Facultad de Medicina, Los Chaguaramos, 1030, Universidad Central de Venezuela, Caracas, Venezuela;2. Institute of Respiratory Diseases, Tlalpan 4502, Mexico DF 14080, Mexico City, Mexico;3. UCLA School of Public Health, 3781 Wasatch Ave.Los Angeles, CA 90066, USA;4. Universidad de la República, Facultad de Medicina, Hospital Maciel, Washington 174 (5982) 915 3000 int. 2610, Montevideo, Uruguay;5. Federal University of São Paulo, Largo Senador Raul Cardoso, 220 apto. 4, 04021-070 Sâo Paulo Brazil;6. Departamento de Salud Publica, Facultad de Medicina, Pontifícia Universidad Católica de Chile, Santiago de Chile, Chile;7. Catedra de Neumologia, Facultad de Medicina, Pontifícia Universidad Católica de Chile, Santiago de Chile, Chile;8. Faculdade de Medicina, Universidade Federal de Pelotas, Duque de Caxias, 250 – 3 piso – 96030-002, Pelotas, RS, Brazil;1. Servicio de Neumología, Hospital Maciel, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay;2. Servicio de Neumonología, Hospital Universitario de Caracas, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela;3. Department of Community Health Sciences, UCLA School of Public Health, Los Angeles, California, Estados Unidos;4. Laboratorio de Sueño, Instituto de Enfermedades Respiratorias, Ciudad de México, México;5. Respiratory Division, Escola Paulista de Medicina, Sâo Paulo, Brasil;6. Departamento de Salud Pública, Facultad de Medicina, Pontifícia Universidad Católica de Chile, Santiago de Chile, Chile;7. Cátedra de Neumología, Facultad de Medicina, Pontifícia Universidad Católica de Chile, Santiago de Chile, Chile;8. Faculdade de Medicina, Universidade Federal de Pelotas, Pelotas, Brasil;1. Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal;2. ICVS/3B''s, PT Government Associated Laboratory, Braga/Guimarães, Portugal;3. 3B''s Research Group – Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Taipas, Guimarães, Portugal;4. Center for Neurosciences and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal;5. Cell Biology Unit, Biocant, Cantanhede, Portugal;1. Hospital Mediterráneo, Almería, España;2. Instituto Traumatológico Quirón, Barcelona, España;1. University of British Columbia James Hogg Research Centre, Vancouver, BC, Canada;2. Division of Respirology, St. Paul''s Hospital, Vancouver, BC, Canada;1. Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai, China;2. Department of Health Sciences Research, Mayo Clinic, Rochester, MN;3. Fuyuan County Hospital, Yunnan, China;4. Division of Preventive Medicine, Wenzhou Medical University, Zhejiang, China;1. Division of Tropical and Humanitarian Medicine, University Hospitals of Geneva and University of Geneva, Geneva, Switzerland;2. Department of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa;3. MRC Unit on Child and Adolescent Lung Health, University of Cape Town, Cape Town, South Africa;4. Asthma Drug Facility, International Union against Tuberculosis and Lung Disease, Paris, France;5. Faculdade de Medicina, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul, Brazil;6. National Heart and Lung Institute, Imperial College, London, UK
Abstract:BackgroundAcute bronchodilator responsiveness is an area of discussion in COPD. No information exists regarding this aspect of the disease from an unselected COPD population. We assessed acute bronchodilator responsiveness and factors influencing it in subjects with and without airway obstruction in an epidemiologic sample.MethodsCOPD was defined by GOLD criteria (post-bronchodilator FEV1/FVC < 0.70). In this analysis, subjects with pre-bronchodilator FEV1/FVC <0.70 but ≥0.70 post-bronchodilator were considered to have reversible obstruction. Bronchodilator responsiveness after albuterol 200 μg was assessed using three definitions: a) FVC and/or FEV1 increment ≥12% plus ≥200 mL over baseline; b) FEV1  15% increase over baseline; and c) FEV1 increase ≥10% of predicted value.ResultsThere were 756 healthy respiratory subjects, 481 subjects with reversible obstruction and 759 COPD subjects. Depending on the criterion used the proportion of person with acute bronchodilator responsiveness ranged between 15.0–28.2% in COPD, 11.4–21.6% in reversible obstructed and 2.7–7.2% in respiratory healthy. FEV1 changes were lower (110.6 ± 7.40 vs. 164.7 ± 11.8 mL) and FVC higher (146.5 ± 14.2 mL vs. ?131.0 ± 19.6 mL) in COPD subjects compared with reversible obstructed. Substantial overlap in FEV1 and FVC changes was observed among the groups. Acute bronchodilator responsiveness in COPD persons was associated with less obstruction and never smoking.ConclusionsOver two-thirds of persons with COPD did not demonstrate acute bronchodilator responsiveness. The overall response was small and less than that considered as significant by ATS criteria. The overlap in FEV1 and FVC changes after bronchodilator among the groups makes it difficult to determine a threshold for separating them.
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