Severe exacerbation and pneumonia in COPD patients treated with fixed combinations of inhaled corticosteroid and long-acting beta2 agonist

被引:18
|
作者
Yang, Hsi-Hsing [1 ,2 ]
Lai, Chih-Cheng [1 ]
Wang, Ya-Hui [3 ,4 ]
Yang, Wei-Chih [5 ]
Wang, Cheng-Yi [3 ,4 ]
Wang, Hao-Chien [6 ,7 ]
Chen, Likwang [5 ]
Yu, Chong-Jen [6 ,7 ]
机构
[1] Chi Mei Med Ctr, Dept Intens Care Med, Tainan, Taiwan
[2] Southern Taiwan Univ Sci & Technol, Dept Biotechnol, Tainan, Taiwan
[3] Fu Jen Catholic Univ, Cardinal Tien Hosp, Dept Internal Med, 510,Zhongzheng Rd, New Taipei, Taiwan
[4] Fu Jen Catholic Univ, Sch Med, Coll Med, 510,Zhongzheng Rd, New Taipei, Taiwan
[5] Natl Hlth Res Inst, Inst Populat Hlth Sci, Zhunan, Miaoli County, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Internal Med, 7 Chung Shan South Rd, Taipei 100, Taiwan
[7] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
关键词
COPD; ICS/LABA; exacerbation; pneumonia; OBSTRUCTIVE PULMONARY-DISEASE; METERED-DOSE INHALER; CLINICAL-TRIAL; FLUTICASONE; BUDESONIDE; BUDESONIDE/FORMOTEROL; EFFICACY; SALMETEROL; FORMOTEROL; SAFETY;
D O I
10.2147/COPD.S139035
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: It remains unclear whether severe exacerbation and pneumonia of COPD differs between patients treated with budesonide/formoterol and those treated with fluticasone/salmeterol. Therefore, we conducted a comparative study of those who used budesonide/formoterol and those treated with fluticasone/salmeterol for COPD. Methods: Subjects in this population-based cohort study comprised patients with COPD who were treated with a fixed combination of budesonide/formoterol or fluticasone/salmeterol. All patients were recruited from the Taiwan National Health Insurance database. The outcomes including severe exacerbations, pneumonia, and pneumonia requiring mechanical ventilation (MV) were measured. Results: During the study period, 11,519 COPD patients receiving fluticasone/salmeterol and 7,437 patients receiving budesonide/formoterol were enrolled in the study. Pairwise matching (1: 1) of fluticasone/salmeterol and budesonide/formoterol populations resulted in to two similar subgroups comprising each 7,295 patients. Patients receiving fluticasone/salmeterol had higher annual rate and higher risk of severe exacerbation than patients receiving budesonide/formoterol (1.2219/year vs 1.1237/year, adjusted rate ratio, 1.08; 95% CI, 1.07-1.10). In addition, patients receiving fluticasone/salmeterol had higher incidence rate and higher risk of pneumonia than patients receiving budesonide/formoterol (12.11 per 100 person-years vs 10.65 per 100 person-years, adjusted hazard ratio [aHR], 1.13; 95% CI, 1.08-1.20). Finally, patients receiving fluticasone/salmeterol had higher incidence rate and higher risk of pneumonia requiring MV than patients receiving budesonide/formoterol (3.94 per 100 person-years vs 3.47 per 100 person-years, aHR, 1.14; 95% CI, 1.05-1.24). A similar trend was seen before and after propensity score matching analysis, intention-to-treat, and as-treated analysis with and without competing risk. Conclusions: Based on this retrospective observational study, long-term treatment with fixed combination budesonide/formoterol was associated with fewer severe exacerbations, pneumonia, and pneumonia requiring MV than fluticasone/salmeterol in COPD patients.
引用
收藏
页码:2477 / 2484
页数:8
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