Is delayed introduction of inhaled corticosteroids harmful in patients with obstructive airways disease (asthma and COPD)?

被引:70
作者
Overbeek, SE
Kerstjens, HAM
Bogaard, JM
Mulder, PGH
Postma, DS
Kerrebijn, KF
Quanjer, PH
Sluiter, HJ
Pouw, EM
Schoonbrood, DFME
Roos, CH
Jansen, HM
Brand, PLP
deGooijer, A
vanderMark, TW
Koeter, GH
deJong, PM
Sterk, PJ
Wever, AMJ
Dijkman, JH
Dekhuijzen, PNR
Folgering, H
vanHerwaarden, CLA
Hilvering, C
Mengelers, SJ
Gans, SJ
vanderBruggen, B
Kreukniet, J
vanEssenZandvliet, EEM
Duiverman, EJ
Kouwenberg, JM
Prinsen, JE
Waalkens, HJ
Gerritsen, J
Knol, K
deMonchy, JGR
Kaptein, AA
Dekker, FW
Merkus, PJFM
Hughes, MD
Robinson, NJ
Pocock, SJ
Bleecker, ER
Meyers, DA
机构
[1] UNIV HOSP DIJKZIGT,DEPT EPIDEMIOL & BIOSTAT,NL-3015 GD ROTTERDAM,NETHERLANDS
[2] UNIV HOSP,DEPT PULM DIS,GRONINGEN,NETHERLANDS
[3] UNIV HOSP AMSTERDAM,DEPT PULMONOL,AMSTERDAM,NETHERLANDS
[4] UNIV GRONINGEN HOSP,DEPT PULMONOL,GRONINGEN,NETHERLANDS
[5] LEIDEN UNIV HOSP,DEPT PULMONOL,LEIDEN,NETHERLANDS
[6] UNIV NIJMEGEN HOSP,DEPT PULMONOL,NL-6500 HB NIJMEGEN,NETHERLANDS
[7] UNIV ROTTERDAM HOSP,DEPT PULMONOL,ROTTERDAM,NETHERLANDS
[8] UNIV UTRECHT HOSP,DEPT PULMONOL,UTRECHT,NETHERLANDS
[9] SOPHIA CHILDRENS UNIV HOSP,DEPT PEDIAT PULMONOL,ROTTERDAM,NETHERLANDS
[10] JULIANA CHILDRENS HOSP,DEPT PEDIAT PULMONOL,THE HAGUE,NETHERLANDS
[11] UNIV GRONINGEN HOSP,DEPT PEDIAT PULMONOL,GRONINGEN,NETHERLANDS
[12] UNIV GRONINGEN HOSP,DEPT ALLERGY,GRONINGEN,NETHERLANDS
[13] LEIDEN UNIV,DEPT GEN PRACTICE,LEIDEN,NETHERLANDS
[14] LEIDEN UNIV,DEPT PSYCHOL,LEIDEN,NETHERLANDS
关键词
airway hyperresponsiveness; asthma; COPD; inhaled corticosteroids; lung function;
D O I
10.1378/chest.110.1.35
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: The institution of inhaled corticosteroids is generally advocated for effective treatment of patients with asthma. It is yet unknown what is the best time to start inhaled corticosteroid therapy and especially whether delayed introduction is harmful. Phase 1: In a previous study in patients with asthma and COPD, we found that 2.5 years of treatment with a beta(2)-agonist plus inhaled corticosteroid (BA+CS) was more effective in improving the FEV(1) and the provocative concentration of histamine causing a 20% reduction in FEV(1) (PC20) than treatment with a beta(2)-agonist plus anticholinergic (BA+AC) or placebo (BA+PL). Phase 2: We extended this study with 6 months to investigate whether delayed introduction of inhaled CS therapy (800 mu g beclomethasone dipropionate) in the groups previously not treated with inhaled CS (BA+/-AC) could also improve FEV(1) and PC20 to the same degree, A distinction was made between patients with predominantly asthma (high baseline reversibility, Delta FEV(1) greater than or equal to 9% of predicted), and predominantly COPD (low baseline reversibility, Delta FEV(1) <9% of predicted), Results: Improvement of FEV(1) percent predicted by inhaled CS was comparable both in the asthmatics between phase 1 (13.8% predicted) and phase 2 (8.5% predicted; p=0.13) as well as in the patients with COPD (2.5% and 1.5% predicted, respectively), PC20, however, increased significantly more in the asthmatics in phase 1 (1.77 doubling concentration [DC]) than in phase 2 (0.79 DC; p=0.03). Improvement of PC20 in the patients with COPD was not significantly higher in phase 1 (0.74 DC) than in phase 2 (0.00 DC; p=0.19). Conclusions: Our study indicates that although delayed introduction of inhaled CS in asthmatics leads to similar improvements in FEV(1), improvements in PC20 are significantly less. These findings in patients with longer-existing asthma concur with other findings in newly detected asthma. We suggest that institution of inhaled CS therapy should not be postponed in asthmatics with documented airways obstruction and reversibility.
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页码:35 / 41
页数:7
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