Evaluation of switching low-dose inhaled corticosteroid to pranlukast for step-down therapy in well-controlled patients with mild persistent asthma

被引:7
|
作者
Harada, Sonoko [1 ,2 ,3 ]
Harada, Norihiro [1 ,2 ,3 ,4 ]
Itoigawa, Yukinari [1 ,2 ]
Katsura, Yoko [1 ,2 ]
Kasuga, Fumiko [1 ,2 ]
Ishimori, Ayako [1 ,2 ]
Makino, Fumihiko [1 ,2 ]
Ito, Jun [1 ,2 ]
Atsuta, Ryo [1 ,2 ,3 ]
Takahashi, Kazuhisa [1 ,2 ,3 ]
机构
[1] Juntendo Univ, Fac Med, Dept Resp Med, Tokyo 1138421, Japan
[2] Grad Sch Med, Tokyo, Japan
[3] Juntendo Univ, Fac Med, Res Inst Dis Old Ages, Tokyo 1138421, Japan
[4] Juntendo Univ, Fac Med, Atopy Allergy Res Ctr, Tokyo 1138421, Japan
基金
日本学术振兴会;
关键词
inhaled corticosteroid; Antagonist; pranlukast hydrate; step-down therapy; asthma; leukotriene receptor; EXHALED NITRIC-OXIDE; LEUKOTRIENE RECEPTOR ANTAGONIST; RANDOMIZED CONTROLLED-TRIAL; FLUTICASONE PROPIONATE; CONVENTIONAL TESTS; MONTELUKAST; CHILDREN; AIR; COMBINATION; BECLOMETHASONE;
D O I
10.3109/02770903.2015.1087556
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Objective: Treatment guidelines for asthma recommend step-down therapy for well-controlled asthma patients. However, the precise strategy for step-down therapy has not been well defined. We investigated whether well-controlled patients with mild persistent asthma can tolerate a step-down therapy of either a reduced dose of inhaled corticosteroid (ICS) or a switch to a leukotriene receptor antagonist (LTRA), pranlukast hydrate. Methods: We recruited 40 adult patients with mild persistent asthma who were well-controlled for at least 3 months with a low-dose ICS therapy. The patients were randomly assigned to either an ICS dose reduction or a switch to pranlukast for 6 months. Results: FeNO levels in the pranlukast group were significantly increased over that in the ICS group. There were no significant differences between the two groups for lung function, FOT, at the endpoint. The percentage of patients with controlled asthma was 72.2% in the pranlukast group and 90% in the ICS group. No statistically significant difference between the two groups in the percentages of patients with treatment failure was observed. Conclusions: Patients with mild persistent asthma that is well-controlled by a low dose of ICS can be switched to pranlukast safely for at least 6 months. However, 27.8% of the pranlukast group failed to maintain well-control, and FeNO levels increased with the switch to pranlukast at 6 months. This study was been limited by the small sample size and should therefore be considered preliminary. Further studies are needed to investigate the therapeutic efficacy of LTRA monotherapy as a step-down therapy.
引用
收藏
页码:207 / 212
页数:6
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