Zeiger Robert S, Bird Steven R, Kaplan Michael S, Schatz Michael, Pearlman David S, Orav E John, Hustad Carolyn M, Edelman Jonathan M
Department of Allergy-Immunology, Kaiser Permanente Medical Center, Los Angeles, California, USA.
Am J Med. 2005 Jun;118(6):649-57. doi: 10.1016/j.amjmed.2005.03.003.
To determine whether montelukast is as effective as fluticasone in controlling mild persistent asthma as determined by rescue-free days.
Participants aged 15 to 85 years with mild persistent asthma (n = 400) were randomized to oral montelukast (10 mg once nightly) or inhaled fluticasone (88 mug twice daily) in a year-long, parallel-group, multicenter study with a 12-week, double-blind period, followed by a 36-week, open-label period.
The mean percentage of rescue-free days was similar between treatments after 12 weeks (fluticasone: 74.9%, montelukast: 73.1%; difference = 1.8%, 95% confidence interval [CI]: -3.2% to 6.8%) but not during the open-label period (fluticasone: 77.3%, montelukast: 71.1%; difference = 6.2%, 95% CI: 0.8% to 11.7%). Although both fluticasone and montelukast significantly improved symptoms, quality of life, and symptom-free days during both treatment periods, greater improvements occurred with fluticasone in lung function during both periods and in asthma control during open-label treatment. Post hoc analyses revealed a difference in rescue-free days favoring fluticasone in participants in the quartiles for lowest lung function and greatest albuterol use at baseline.
In patients with mild persistent asthma, rescue-free days and most asthma control measures improved similarly with fluticasone or montelukast over the short term, but with prolonged open-label treatment, asthma control improved more with fluticasone. Improved asthma control with fluticasone appeared to occur in those with decreased lung function and greater albuterol use at baseline. In the remaining patients, the two treatments appeared to be comparable. These results suggest that classification criteria for mild persistent asthma may need to be re-evaluated.
通过无急救天数来确定孟鲁司特在控制轻度持续性哮喘方面是否与氟替卡松一样有效。
在一项为期一年的平行组多中心研究中,将400名年龄在15至85岁的轻度持续性哮喘患者随机分为口服孟鲁司特组(每晚一次,每次10毫克)或吸入氟替卡松组(每日两次,每次88微克),研究包括一个为期12周的双盲期,随后是一个为期36周的开放标签期。
12周后,两种治疗方法的无急救天数平均百分比相似(氟替卡松:74.9%,孟鲁司特:73.1%;差异=1.8%,95%置信区间[CI]:-3.2%至6.8%),但在开放标签期则不同(氟替卡松:77.3%,孟鲁司特:71.1%;差异=6.2%,95%CI:0.8%至11.7%)。虽然氟替卡松和孟鲁司特在两个治疗期均显著改善了症状、生活质量和无症状天数,但在两个时期中,氟替卡松在肺功能方面以及开放标签治疗期间在哮喘控制方面的改善更大。事后分析显示,在基线时肺功能最低和沙丁胺醇使用量最大的四分位数参与者中,无急救天数方面氟替卡松更具优势。
在轻度持续性哮喘患者中,短期内氟替卡松和孟鲁司特在无急救天数和大多数哮喘控制指标方面的改善相似,但随着开放标签治疗时间延长,氟替卡松对哮喘控制的改善更明显。氟替卡松在基线时肺功能下降且沙丁胺醇使用量较大的患者中似乎能更好地控制哮喘。在其余患者中,两种治疗方法似乎相当。这些结果表明,轻度持续性哮喘的分类标准可能需要重新评估。