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
相关论文
共 41 条
  • [31] Efficacy of budesonide/formoterol maintenance and reliever therapy compared with higher-dose budesonide as step-up from low-dose inhaled corticosteroid treatment
    Christine R. Jenkins
    Göran Eriksson
    Eric D. Bateman
    Helen K. Reddel
    Malcolm R. Sears
    Magnus Lindberg
    Paul M. O’Byrne
    BMC Pulmonary Medicine, 17
  • [32] Efficacy of budesonide/formoterol maintenance and reliever therapy compared with higher-dose budesonide as step-up from low-dose inhaled corticosteroid treatment
    Jenkins, Christine R.
    Eriksson, Goran
    Bateman, Eric D.
    Reddel, Helen K.
    Sears, Malcolm R.
    Lindberg, Magnus
    O'Byrne, Paul M.
    BMC PULMONARY MEDICINE, 2017, 17
  • [33] Omalizumab versus Mepolizumab as add-on therapy in asthma patients not well controlled on at least an inhaled corticosteroid: A network meta-analysis
    Nachef, Zahi
    Krishnan, Amita
    Mashtare, Terry
    Zhuang, Tingting
    Mador, M. Jeffery
    JOURNAL OF ASTHMA, 2018, 55 (01) : 89 - 100
  • [34] Efficacy and safety comparison: Fluticasone furoate and fluticasone propionate, after step down from fluticasone furoate/vilanterol in Japanese patients with well-controlled asthma, a randomized trial
    Adachi, Mitsuru
    Goldfrad, Caroline
    Jacques, Loretta
    Nishimura, Yoshie
    RESPIRATORY MEDICINE, 2016, 120 : 78 - 86
  • [35] Efficacy and safety evaluation of once-daily fluticasone furoate/vilanterol in Asian patients with asthma uncontrolled on a low- to mid-strength inhaled corticosteroid or low-dose inhaled corticosteroid/long-acting beta2-agonist
    Lin, Jiangtao
    Tang, Huaping
    Chen, Ping
    Wang, Haoyan
    Kim, Mi-Kyeong
    Crawford, Jodie
    Jacques, Loretta
    Stone, Sally
    ALLERGY AND ASTHMA PROCEEDINGS, 2016, 37 (04) : 302 - 310
  • [36] Efficacy and safety of inhaled once-daily low-dose indacaterol acetate/mometasone furoate in patients with inadequately controlled asthma: Phase III randomised QUARTZ study findings
    Kornmann, Oliver
    Mucsi, Janos
    Kolosa, Nadezda
    Bandelli, Lorraine
    Sen, Biswajit
    Satlin, Lisa C.
    D'Andrea, Peter
    RESPIRATORY MEDICINE, 2020, 161
  • [37] The Effect of Low-Dose Inhaled Budesonide on Pc20 Amp Levels in Patients with Mild Asthma: A 3-Month Follow-Up Study
    Kokturk, Nurdan
    Mullaoglu, Sema
    Ozyilmaz, Ezgi
    Turktas, Haluk
    JOURNAL OF ASTHMA, 2009, 46 (03) : 259 - 264
  • [38] Comparison of mometasone furoate dry powder inhaler and fluticasone propionate dry powder inhaler in patients with moderate to severe persistent asthma requiring high-dose inhaled corticosteroid therapy: Findings from a noninferiority trial
    Harnest, Ulf
    Price, David
    Howes, Tim
    Sussman, Gordon
    JOURNAL OF ASTHMA, 2008, 45 (03) : 215 - 220
  • [39] Late Breaking Abstract - Cost effectiveness of as-needed budesonide/formoterol vs low-dose ICS maintenance therapy in mild asthma patients: A UK perspective
    FitzGerald, J. Mark
    Arnetorp, Sofie
    Smare, Caitlin
    Gibson, Danny
    Coulton, Karen
    Hounsell, Kirsty
    Sadatsafavi, Mohsen
    EUROPEAN RESPIRATORY JOURNAL, 2019, 54
  • [40] A prospective study of switching asthma patients from a Fixed-Dose Combination (FDC) Inhaled Corticosteroid [ICS]/Long-Acting Beta Agonist [LABA] therapy delivered by Dry Powder Inhaler (DPI) to ICS/LABA delivered by pressurised Metered Dose Inhaler (pMDI)
    Al-Ahmad, Mona
    Webb, David
    RESPIRATORY MEDICINE, 2022, 194