J Korean Med Sci.  2015 Jan;30(1):54-59. 10.3346/jkms.2015.30.1.54.

Three-month Treatment Response and Exacerbation in Chronic Obstructive Pulmonary Disease

Affiliations
  • 1Department of Pulmonary and Critical Care Medicine, and Clinical Research Center for Chronic Obstructive Airway Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. ymoh55@amc.seoul.kr
  • 2Department of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Korea.
  • 3Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea.
  • 4Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.
  • 5Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
  • 6Division of Pulmonology, Department of Internal Medicine, Hanyang University Guri Hospital, Hanyang University College of Medicine, Guri, Korea.
  • 7Department of Internal Medicine and Environmental Health Center, Kangwon National University Hospital, School of Medicine, Kangwon National University, Chuncheon, Korea.
  • 8Department of Internal Medicine, Ewha Womans University Mokdong Hospital, College of Medicine, Ewha Womans University, Seoul, Korea.
  • 9Division of Pulmonary and Critical Care Medicine, Department of Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.

Abstract

The aim of this study was to investigate relationships between acute exacerbation and Forced Expiratory Volume 1 second (FEV1) improvement after treatment with combined long-acting beta-agonist (LABA) and inhaled corticosteroid (ICS) in patients with chronic obstructive pulmonary disease (COPD). A total of 137 COPD patients were classified as responders or nonresponders according to FEV1 improvement after 3 months of LABA/ICS treatment in fourteen referral hospitals in Korea. Exacerbation occurrence in these two subgroups was compared over a period of 1 yr. Eighty of the 137 COPD patients (58.4%) were classified as responders and 57 (41.6%) as nonresponders. Acute exacerbations occurred in 25 patients (31.3%) in the responder group and in 26 patients (45.6%) in the nonresponder group (P=0.086). FEV1 improvement after LABA/ICS treatment was a significant prognostic factor for fewer acute exacerbations in a multivariate Cox proportional hazard model adjusted for age, sex, FEV1, smoking history, 6 min walk distance, body mass index, exacerbation history in the previous year, and dyspnea scale.Three-month treatment response to LABA/ICS might be a prognostic factor for the occurrence of acute exacerbation in COPD patients.

Keyword

Pulmonary Disease, Chronic Obstructive; Forced Expiratory Volume; Disease Progression

MeSH Terms

Adrenal Cortex Hormones/*therapeutic use
Adrenergic beta-2 Receptor Agonists/*therapeutic use
Bronchodilator Agents/*therapeutic use
Budesonide/therapeutic use
Drug Therapy, Combination
Female
Fluticasone/therapeutic use
Forced Expiratory Volume/drug effects/*physiology
Formoterol Fumarate/therapeutic use
Humans
Male
Pulmonary Disease, Chronic Obstructive/*drug therapy/physiopathology
Recurrence
Republic of Korea
Salmeterol Xinafoate/therapeutic use
Smoking
Spirometry
Treatment Outcome
Adrenal Cortex Hormones
Adrenergic beta-2 Receptor Agonists
Bronchodilator Agents
Budesonide
Fluticasone
Formoterol Fumarate
Salmeterol Xinafoate

Figure

  • Fig. 1 Exacerbation rates according to 3-month treatment response (3MTR). (A) The 3MTR was evaluated with the change of FEV1 in mL after 3-month treatment (P=0.035). A cut-off value of 120 mL was defined by the minimal clinically important difference (MCID)(3, 17).The other cut-off of 300 mL was defined as it was near the upper tertile value. Exacerbation occurrence represents % of COPD patients who experienced exacerbation during the one year of follow-up. (B) The 3MTR was evaluated with the change of FEV1 in % of the predicted reference value after 3-month treatment (P=0.039). According to MCID (3, 17), the responder group was defined when FEV1 improvement was 4% or more of the predicted value after 3-month treatment. We further classified the responder group arbitrarily into two categories based on the change in FEV1, with a cut-off of 8% predicted value.

  • Fig. 2 Exacerbation occurrence according to baseline characteristics.


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