Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Am J Otolaryngol. 2010 Jan-Feb;31(1):1-8. doi: 10.1016/j.amjoto.2008.08.011. Epub 2009 Mar 6.
The aim of the study was to compare early symptom resolution with a single 2-g dose of azithromycin extended release or 10 days of amoxicillin/clavulanate 875 mg/125 mg every 12 hours in patients with acute sinusitis.
This was a prospective, randomized, open-label, observational study to mimic "real-world" conditions, including patients with symptoms of acute bacterial sinusitis lasting between 7 and 30 days. Key symptoms were assessed twice daily by patient diary, and patients were interviewed by telephone at 12 and 28 days. The primary end point was symptom resolution at 5 days, defined as reporting "no problem" with at least 3 of 4 diary symptoms in 2 consecutive measures in the per-protocol population. Secondary end points included additional antibiotic use, sinusitis-related quality of life, and treatment satisfaction.
Three hundred seventy-eight patients were randomized to a single dose of azithromycin extended release and 371 to 10 days of amoxicillin/clavulanate. In the per-protocol population at day 5, 70/236 patients (29.7%) in the azithromycin extended release arm and 45/238 patients (18.9%) in the amoxicillin/clavulanate arm had resolution of symptoms (difference = 10.8%; 95% confidence interval [CI], 3.1-18.4%). By day 28, 26/236 patients (11.0%) in the azithromycin extended release arm and 27/238 patients (11.3%) in the amoxicillin/clavulanate arm had used additional antibiotics (difference = -0.4%; 95% CI: -6.1% to 5.3%). Additional physician visits, quality of life, and overall satisfaction were similar between groups.
More patients randomized to azithromycin extended release experienced symptom resolution at day 5 than those randomized to amoxicillin/clavulanate, without experiencing differences in second antibiotic use at 28 days.
本研究旨在比较急性鼻窦炎患者单次使用 2 克剂量阿奇霉素缓释片或 10 天 125 毫克/500 毫克阿莫西林/克拉维酸每 12 小时治疗的早期症状缓解情况。
这是一项前瞻性、随机、开放标签、观察性研究,旨在模拟“真实世界”的情况,包括症状持续 7 至 30 天的急性细菌性鼻窦炎患者。主要症状通过患者日记每日评估两次,在第 12 天和第 28 天通过电话对患者进行访谈。主要终点为 5 天时的症状缓解,定义为在方案人群中连续 2 次测量至少有 4 项症状日记中有 3 项报告“无问题”。次要终点包括额外使用抗生素、鼻窦炎相关生活质量和治疗满意度。
378 例患者被随机分为阿奇霉素缓释片单次剂量组,371 例患者被分为 10 天阿莫西林/克拉维酸组。在第 5 天的方案人群中,阿奇霉素缓释片组 236 例患者中有 70 例(29.7%)和阿莫西林/克拉维酸组 238 例患者中有 45 例(18.9%)症状缓解(差异=10.8%;95%置信区间[CI],3.1-18.4%)。在第 28 天,阿奇霉素缓释片组 236 例患者中有 26 例(11.0%)和阿莫西林/克拉维酸组 238 例患者中有 27 例(11.3%)使用了额外的抗生素(差异=-0.4%;95%CI:-6.1%至 5.3%)。两组之间的额外就诊次数、生活质量和总体满意度相似。
与阿莫西林/克拉维酸相比,随机接受阿奇霉素缓释片治疗的患者在第 5 天的症状缓解率更高,但在第 28 天使用第二种抗生素的情况无差异。