Zeiger Robert S, Baker James W, Kaplan Michael S, Pearlman David S, Schatz Michael, Bird Steven, Hustad Carolyn, Edelman Jonathan
Department of Allergy-Immunology, Kaiser Permanente Medical Center, 7060 Clairemont Mesa Boulevard, San Diego, CA 92111, USA.
Respir Med. 2004 Sep;98(9):898-905. doi: 10.1016/j.rmed.2004.02.016.
To describe the variability of the asthma phenotype in patients with mild persistent asthma enrolled in the Mild Asthma Montelukast versus Inhaled Corticosteroid (MIAMI) study.
The variability of asthma rescue-free days, asthma symptoms, albuterol use, medical resource use, and exercise Limitations among patients with documented mild persistent asthma was compared between the month before study enrollment and the last 2 weeks of the run-in period.
Patients eligible for randomization (n = 400), aged 15-85 years, exhibited symptoms (mean +/- SD) 3.6 +/- 1.3 days/week, beta-agonist use 3.5 +/- 1.3 days/week, and normal FEV1 (94.0 +/- 9.9% predicted) during the last 2 weeks of the run-in period. In the year before enrollment, medical intervention for asthma flares was common: 38.5% made office visits, 15.8% had oral corticosteroids, and 8.3% required emergency room or hospitalized care. In the month before enrollment, 11.8% experienced daily symptoms, and 28.3% had limitations of normal activity. Patients with daily symptoms in the month before study enrollment, compared with those having less-than-daily symptoms, experienced fewer rescue-free days (P = 0.024) and had more days per week with symptoms (P = 0.008) and requiring albuterol (P = 0.048) during the run-in; FEV1 was similar for both groups (93.1% vs. 94.2% predicted, respectively).
Patients with mild persistent asthma reported a substantial disease burden in the year before enrollment. The asthma burden experienced by these patients both before and during the run-in period was of sufficient severity to support the recommendation that mild persistent asthma should be managed with daily controller therapy.
描述参与轻度哮喘孟鲁司特与吸入性糖皮质激素对比研究(MIAMI研究)的轻度持续性哮喘患者的哮喘表型变异性。
对有记录的轻度持续性哮喘患者在研究入组前一个月和导入期最后2周的无哮喘急救天数、哮喘症状、沙丁胺醇使用情况、医疗资源使用情况及运动受限情况的变异性进行比较。
符合随机分组条件的患者(n = 400),年龄在15 - 85岁之间,在导入期最后2周表现出症状(均值±标准差)为每周3.6±1.3天,β受体激动剂使用为每周3.5±1.3天,FEV1正常(预测值为94.0±9.9%)。在入组前一年,哮喘发作的医疗干预很常见:38.5%进行了门诊就诊,15.8%使用了口服糖皮质激素,8.3%需要急诊室治疗或住院治疗。在入组前一个月,11.8%的患者有每日症状,28.3%的患者日常活动受限。与入组前一个月症状少于每日发作的患者相比,每日有症状的患者在导入期无急救天数更少(P = 0.024),每周有症状的天数更多(P = 0.008)且需要使用沙丁胺醇的天数更多(P = 0.048);两组的FEV1相似(分别为预测值的93.1%和94.2%)。
轻度持续性哮喘患者在入组前一年报告了相当大的疾病负担。这些患者在导入期之前和期间所经历的哮喘负担严重程度足以支持推荐对轻度持续性哮喘采用每日控制治疗。