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首页> 外文期刊>Clinical therapeutics >A multicenter, randomized, investigator-blinded study of 5- and 10-day gatifloxacin versus 10-day amoxicillin/clavulanate in patients with acute bacterial sinusitis.
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A multicenter, randomized, investigator-blinded study of 5- and 10-day gatifloxacin versus 10-day amoxicillin/clavulanate in patients with acute bacterial sinusitis.

机译:研究者对急性细菌性鼻窦炎患者的5天和10天加替沙星与10天阿莫西林/克拉维酸进行了一项多中心,随机,研究者盲的研究。

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BACKGROUND: Treatment guidelines for acute bacterial sinusitis recommend 10 to 14 days of therapy with amoxicillin/clavulanate, high-dose amoxicillin, cefpodoxime, cefuroxime, or a newer fluoroquinolone. Objective: This study compared the clinical efficacy of short-course (5-day) gatifloxacin with standard 10-day regimens of amoxicillin/clavulanate or gatifloxacin in patients with a diagnosis of acute, uncomplicated maxillary sinusitis. METHODS: This was a multicenter, investigator-blinded study in adult patients (age >18 years) with physical findings, signs and symptoms (for at least 7 days), and radiographic findings indicating acute, uncomplicated maxillary sinusitis. Patients were randomized to receive gatifloxacin 400 mg once daily for 5 days, gatifloxacin 400 mg once daily for 10 days, or amoxicillin/clavulanate 875 mg twice daily for 10 days. Clinical response was assessed once between days 3 and 5 of treatment, once I to 3 days after the completion of study treatment, once 7 to 14 days posttreatment (test-of-cure visit), and once 21 to 28 days posttreatment. Safety was assessed throughout the study. RESULTS: The study enrolled 445 patients. The treatment groups were similar in terms of history of sinusitis, presenting signs and symptoms, and radiographic findings. The most common presenting symptoms were nasal congestion, sinus tenderness, and purulent nasal discharge (>90% of patients); 99% of patients had abnormal radiographic findings. At the test-of-cure visit, clinical cure rates for clinically evaluable patients in the 3 treatment groups were 74% (102/137) for 5-day gatifloxacin, 80% (101/127) for 10-day gatifloxacin, and 72% (101/ 141) for 10-day amoxicillin/clavulanate (95% CI for the difference in cure rates: 5-day gatifloxacin vs amoxicillin/clavulanate, -7.6 to 13.2; 5- vs 10-day gatifloxacin, -15.2 to 5.1; 10-day gatifloxacin vs amoxicillin/clavulanate, -2.3 to 18.1). The distribution and incidence of drug-related adverse events (AEs) were comparable between treatment groups, and the majority (>95%) were mild or moderate in severity. The most common drug-related AEs included vaginitis, diarrhea, and nausea. CONCLUSION: In this population of patients with acute, uncomplicated sinusitis of presumed bacterial origin, a short course (5 days) of gatifloxacin therapy was associated with comparable clinical cure rates and tolerability to those of standard 10-day therapy with gatifloxacin or amoxicillin/clavulanate.
机译:背景:急性细菌性鼻窦炎的治疗指南建议使用阿莫西林/克拉维酸盐,大剂量阿莫西林,头孢泊肟,头孢呋辛或更新的氟喹诺酮治疗10到14天。目的:本研究将短疗程(5天)加替沙星与标准的10天阿莫西林/克拉维酸或加替沙星方案在诊断为急性单纯性上颌窦炎的患者中的临床疗效进行了比较。方法:这是一项多中心,研究者盲的研究,研究对象是体征,体征和症状(至少7天)且成年患者(年龄> 18岁),且影像学发现表明急性,简单的上颌窦炎。患者被随机分配接受加替沙星400 mg,每天5天,加替沙星400 mg,每天10天,或阿莫西林/克拉维酸875 mg,每天两次,共10天。在治疗的第3至5天之间评估一次临床反应,在完成研究治疗后1至3天评估一次,在治疗后7至14天(治愈测试就诊)评估一次,在治疗后21至28天评估一次临床反应。在整个研究中评估安全性。结果:该研究招募了445例患者。就鼻窦炎的病史,体征和症状以及影像学表现而言,治疗组相似。最常见的症状是鼻充血,鼻窦压痛和脓性鼻涕(> 90%的患者)。 99%的患者影像学检查结果异常。在就诊测试中,这3个治疗组的5天加替沙星临床可评估患者的临床治愈率分别为74%(102/137),10天加替沙星80%(101/127)和72 10天的阿莫西林/克拉维酸盐的%(101/141)(治愈率差异的95%CI:5天的加替沙星与阿莫西林/克拉维酸盐的-7.6至13.2; 5天和10天的加替沙星,-15.2至5.1 ;加替沙星与阿莫西林/克拉维酸盐治疗10天,-2.3至18.1)。在各治疗组之间,与药物相关的不良事件(AE)的分布和发生率相当,并且大多数(> 95%)的严重程度为轻度或中度。最常见的药物相关不良事件包括阴道炎,腹泻和恶心。结论:在这一人群中,假定的细菌源性急性,简单并发鼻窦炎患者,加替沙星治疗的短疗程(5天)与标准加替沙星或阿莫西林/克拉维酸治疗10天的可治愈率和可耐受性相关。

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