Busse W W, Casale T B, Murray J J, Petrocella V, Cox F, Rickard K
University of Wisconsin Hospital & Clinics, Madison, WI 53792, USA.
Am J Manag Care. 1998 Nov;4(11):1579-87.
To evaluate the efficacy, safety, and impact on asthma-specific quality of life of salmeterol, a highly selective, long-acting beta 2-agonist, compared with that of placebo (i.e., "as-needed" albuterol).
Randomized, double-blind, placebo-controlled, parallel-group, multicenter study.
Five hundred thirty-eight nonsmoking symptomatic patients 12 years of age and older meeting American Thoracic Society asthma criteria were enrolled at 55 outpatient clinics; 443 patients completed the study. Patients were randomly assigned to treatment with either salmeterol aerosol 42 micrograms twice daily or placebo (as-needed albuterol) for 12 weeks. We assessed changes in quality of life using the Asthma Quality of Life Questionnaire (AQLQ). Efficacy measurements included daily peak expiratory flow (PEF) rate, daytime and nighttime asthma symptoms, results of pulmonary function tests, and supplemental albuterol use. Patients recorded their PEF rate, supplemental albuterol use, and asthma-related symptoms daily. Pulmonary function tests and AQLQ assessments were performed at baseline and after 4, 8, and 12 weeks of treatment. Safety measurements included vital signs, physical examination, and reports of clinical adverse events at baseline and after 4, 8, and 12 weeks of treatment.
Mean changes from baseline in AQLQ global and domain scores were significantly greater in the salmeterol group compared with the placebo group (P < 0.001). Patients treated with salmeterol also had significant improvements in mean PEF rates, supplemental albuterol use, asthma symptom scores, and forced expiratory volume in 1 second compared with those given placebo. Both salmeterol and placebo were well tolerated and were not associated with any clinically significant changes in vital signs or physical examination findings.
Salmeterol 42 micrograms twice daily resulted in significantly greater improvements in asthma-specific quality of life, pulmonary function, and asthma symptoms compared with placebo (as-needed albuterol) in patients with moderate persistent asthma.
评估高选择性长效β2受体激动剂沙美特罗与安慰剂(即“按需使用”的沙丁胺醇)相比,在疗效、安全性以及对哮喘特异性生活质量的影响。
随机、双盲、安慰剂对照、平行组、多中心研究。
55家门诊诊所招募了538名年龄在12岁及以上、符合美国胸科学会哮喘标准的非吸烟有症状患者;443名患者完成了研究。患者被随机分配接受每日两次42微克沙美特罗气雾剂治疗或安慰剂(按需使用沙丁胺醇)治疗12周。我们使用哮喘生活质量问卷(AQLQ)评估生活质量变化。疗效测量包括每日呼气峰值流速(PEF)率、白天和夜间哮喘症状、肺功能测试结果以及沙丁胺醇补充使用情况。患者每天记录他们的PEF率、沙丁胺醇补充使用情况以及哮喘相关症状。在基线以及治疗4、8和12周后进行肺功能测试和AQLQ评估。安全性测量包括基线以及治疗4、8和12周后的生命体征、体格检查以及临床不良事件报告。
与安慰剂组相比,沙美特罗组AQLQ总体和各领域得分相对于基线的平均变化显著更大(P < 0.001)。与接受安慰剂治疗的患者相比,接受沙美特罗治疗的患者在平均PEF率、沙丁胺醇补充使用情况、哮喘症状评分以及1秒用力呼气量方面也有显著改善。沙美特罗和安慰剂耐受性均良好,且与生命体征或体格检查结果的任何临床显著变化无关。
对于中度持续性哮喘患者,每日两次42微克沙美特罗与安慰剂(按需使用沙丁胺醇)相比,在哮喘特异性生活质量、肺功能和哮喘症状方面的改善显著更大。