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KMID : 0311120090500050672
Yonsei Medical Journal
2009 Volume.50 No. 5 p.672 ~ p.676
Severity Staging of Chronic Obstructive Pulmonary Disease: Differences in Pre- and Post-Bronchodilator Spirometry
Lin Sheng-Hsiang

Kuo Ping-Hung
Kuo Sow-Hsong
Yang Pan-Chyr
Abstract
Purpose:The Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines for chronic obstructive pulmonary disease (COPD) uses the post-bronchodilator spirometry for diagnosis and severity staging. We evaluated differences in the severity classification of COPD, based on pre- and post-bronchodilator spirometry.

Materials and Methods:From 2000 to 2004, 207 COPD patients who underwent spirometry before and after inhalation of 400 ¥ìg of fenoterol were analyzed. A responder to the bronchodilator test (BDT) was defined by the American Thoracic Society (ATS) as an increase in forced expiratory volume in one second (FEV1) or forced vital capacity ¡Ã 12% and ¡Ã 200 mL, and by the European Respiratory Society (ERS) as an increase in FEV1 ¡Ã 10% of the predicted value. COPD severity was classified according to the 2008 GOLD guidelines.

Results;For the entire study population, the FEV1 increased by 11.8 ¡¾ 12.5% of baseline after BDT and 41.1% and 27.1% of subjects were classified as responders using the ATS and ERS criteria, respectively. Based on pre-BDT spirometry, 55, 85, 58, and 9 patients were classified as Stage I-IV COPD, respectively. Sixty-seven (32.4%) patients changed severity staging after BDT, including 20.0%, 28.2%, 44.8%, and 66.7% of pre-BDT patients Stages I through IV, respectively. More ATS or ERS BDT-responders had a change in severity staging than non-responders (52.9% vs. 18.9% and 62.5% vs. 21.2%, both p < 0.001).

Conclusion;Our data suggest that the severity staging of COPD using pre-BDT spirometry might lead to significant differences as compared to staging, based on post-BDT spirometry, as recommended by the current GOLD guidelines.
KEYWORD
Bronchodilator test, chronic obstructive pulmonary disease, severity staging
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