Nelson Harold S, Wolfe James D, Gross Gary, Greos Leon S, Baitinger Leslie, Scott Catherine, Dorinsky Paul
National Jewish Medical and Research Center, Denver, Colorado 80206, USA.
Ann Allergy Asthma Immunol. 2003 Sep;91(3):263-9. doi: 10.1016/s1081-1206(10)63528-4.
We wanted to evaluate whether treatment with an inhaled corticosteroid and an inhaled long-acting beta2-agonist is more effective than an inhaled corticosteroid alone for patients using as-needed albuterol who are initiating maintenance treatment.
To compare the efficacy and safety of twice-daily fluticasone propionate (FP) 88 microg and salmeterol 42 microg combined in a chlorofluorocarbon (CFC)-free (hydrofluoroalkane 134a) metered-dose inhaler (MDI) with the individual agents alone, each delivered through an MDI containing CFC propellants, in patient with persistent asthma previously uncontrolled with as-needed short-acting beta2-agonists alone.
Patients with asthma (n = 283) were randomized to twice-daily treatment for 12 weeks with FP 88 microg combined with salmeterol 42 microg (FSC) in a CFC-free MDI or the individual components alone from CFC-containing MDIs.
At endpoint, mean change from baseline in morning predose forced expiratory volume in 1 second was significantly (P < or = 0.016) greater with FSC (0.69 L) compared with FP (0.51 L) or salmeterol (0.47 L). Fewer patients treated with FSC withdrew due to worsening asthma (1%) compared with FP (3%) or salmeterol (8%; P = 0.024). FSC significantly increased (P < or = 0.002) morning and evening peak expiratory flow rate at endpoint (66.5 and 51.5 L/min, respectively) compared with FP (43.0 and 29.9 L/min, respectively) and salmeterol (29.2 and 21.6 L/min, respectively). In addition, asthma symptom scores were reduced, and percentages of days with no asthma symptoms increased in all treatment groups.
Treatment with FSC in a CFC-free MDI is more effective than FP or salmeterol alone in asthma patients who are symptomatic taking short-acting beta2-agonists alone.
我们想要评估对于开始维持治疗且按需使用沙丁胺醇的患者,吸入性糖皮质激素与吸入性长效β2受体激动剂联合治疗是否比单独使用吸入性糖皮质激素更有效。
比较每日两次使用88微克丙酸氟替卡松(FP)和42微克沙美特罗联合于不含氯氟烃(CFC,氢氟烷烃134a)的定量吸入器(MDI)中,与单独使用各药物(均通过含CFC抛射剂的MDI给药)相比,在既往仅按需使用短效β2受体激动剂无法控制的持续性哮喘患者中的疗效和安全性。
哮喘患者(n = 283)被随机分为每日两次接受为期12周的治疗,一组使用不含CFC的MDI中88微克FP与42微克沙美特罗联合制剂(FSC),另一组使用含CFC的MDI中的单独药物成分。
在研究终点,与单独使用FP(0.51升)或沙美特罗(0.47升)相比,FSC组早晨给药前1秒用力呼气容积自基线的平均变化显著更大(P≤0.016)(0.69升)。与单独使用FP(3%)或沙美特罗(8%;P = 0.024)相比,因哮喘恶化而退出FSC治疗的患者更少(1%)。与单独使用FP(分别为43.0和29.9升/分钟)和沙美特罗(分别为29.2和21.6升/分钟)相比,FSC在研究终点显著提高了早晨和晚上的呼气峰值流速(分别为66.5和51.5升/分钟)(P≤0.002)。此外,所有治疗组的哮喘症状评分均降低,无哮喘症状天数的百分比增加。
在仅按需使用短效β2受体激动剂时有症状的哮喘患者中,使用不含CFC的MDI中的FSC治疗比单独使用FP或沙美特罗更有效。