Dohar Joseph, Giles William, Roland Peter, Bikhazi Nadim, Carroll Sean, Moe Roderick, Reese Bradley, Dupre Sheryl, Wall Michael, Stroman David, McLean Celeste, Crenshaw Krista
Department of Otolaryngology, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Pediatrics. 2006 Sep;118(3):e561-9. doi: 10.1542/peds.2005-2033. Epub 2006 Jul 31.
This study was a comparison of topical ciprofloxacin/dexamethasone otic suspension to oral amoxicillin/clavulanic acid suspension in children with acute otitis media with otorrhea through tympanostomy tubes.
This was a randomized, observer-masked, parallel-group, multicenter trial of topical ciprofloxacin/dexamethasone otic suspension versus amoxicillin/clavulanic acid suspension in 80 children aged 6 months to 12 years with acute otitis media with otorrhea through tympanostomy tubes of < or = 3 weeks' duration and visible otorrhea. Patients were randomly assigned to receive either 4 drops of topical ciprofloxacin 0.3%/dexamethasone 0.1% (Ciprodex Sterile Otic Suspension) into the affected ear(s) twice daily for 7 days or 600 mg of amoxicillin/42.9 mg of clavulanic acid oral suspension (Augmentin ES-600 Oral Suspension) every 12 hours for 10 days. Clinical signs and symptoms of acute otitis media with otorrhea through tympanostomy tubes were evaluated on days 1 (baseline), 3, 11 (end-of-therapy), and 18 (test-of-cure), and twice-daily assessments of otorrhea were recorded in patient diaries.
The median time to cessation of otorrhea was significantly shorter with ciprofloxacin/dexamethasone otic suspension than with amoxicillin/clavulanic acid suspension (4.0 vs 7.0 days; n = 79). This resulted in significantly more clinical cures at the test-of-cure visit (85% vs 59%, respectively). Frequent adverse events (> 3%) related to ciprofloxacin/dexamethasone otic suspension included ear pain (5.1%) and related to amoxicillin/clavulanic acid suspension included diarrhea (19.5%), dermatitis (7.3%), and gastroenteritis (4.9%).
Topical otic treatment with ciprofloxacin/dexamethasone otic suspension is superior to treatment with oral amoxicillin/clavulanic acid suspension and results in more clinical cures and earlier cessation of otorrhea with fewer adverse effects in children with acute otitis media with otorrhea through tympanostomy tubes.
本研究旨在比较局部使用环丙沙星/地塞米松耳用混悬液与口服阿莫西林/克拉维酸混悬液治疗经鼓膜置管出现耳漏的急性中耳炎患儿的疗效。
这是一项随机、观察者盲法、平行组、多中心试验,比较局部使用环丙沙星/地塞米松耳用混悬液与阿莫西林/克拉维酸混悬液治疗80例年龄在6个月至12岁、经鼓膜置管出现耳漏且病程小于或等于3周、有明显耳漏的急性中耳炎患儿的疗效。患者被随机分配,每日两次向患耳滴入4滴0.3%环丙沙星/0.1%地塞米松(西普洛德无菌耳用混悬液),共7天;或每12小时口服600mg阿莫西林/42.9mg克拉维酸口服混悬液(奥格门汀ES-600口服混悬液),共10天。在第1天(基线)、第3天、第11天(治疗结束)和第18天(治愈检测)评估经鼓膜置管出现耳漏的急性中耳炎的临床体征和症状,并在患者日记中记录每日两次的耳漏评估情况。
环丙沙星/地塞米松耳用混悬液组耳漏停止的中位时间显著短于阿莫西林/克拉维酸混悬液组(4.0天对7.0天;n = 79)。这导致在治愈检测访视时临床治愈率显著更高(分别为85%对59%)。与环丙沙星/地塞米松耳用混悬液相关的常见不良事件(> 3%)包括耳痛(5.1%),与阿莫西林/克拉维酸混悬液相关的包括腹泻(19.5%)、皮炎(7.3%)和肠胃炎(4.9%)。
对于经鼓膜置管出现耳漏的急性中耳炎患儿,局部使用环丙沙星/地塞米松耳用混悬液治疗优于口服阿莫西林/克拉维酸混悬液治疗,可实现更多临床治愈,更早停止耳漏,且不良反应更少。