首页> 外文期刊>Current medical research and opinion >Efficacy of 750-mg, 5-day levofloxacin in the treatment of community-acquired pneumonia caused by atypical pathogens.
【24h】

Efficacy of 750-mg, 5-day levofloxacin in the treatment of community-acquired pneumonia caused by atypical pathogens.

机译:750 mg,5天左氧氟沙星治疗非典型病原体引起的社区获得性肺炎的疗效。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Current recommended durations for treatment of atypical community-acquired pneumonia (CAP) range from 10 to 21 days. However, antibiotics such as the fluoroquinolones may allow for effective, short-course regimens. OBJECTIVE: This study evaluated the efficacy of 750 mg levofloxacin for 5 days compared to a 500-mg, 10-day levofloxacin regimen for the treatment of atypical CAP. METHODS: A randomized, active-controlled, double-blind, multicenter study was conducted within the United States. Of the 528 patients enrolled in the study, 149 were diagnosed with CAP due to Legionella pneumophila, Chlamydia pneumoniae, or Mycoplasma pneumoniae. Patients' baseline symptoms were re-evaluated on Day 3 of therapy. Clinical efficacy and resolution of CAP symptoms were evaluated at the posttherapy visit (7-14 days after the last dose of active drug). RESULTS: This report represents a subgroup analysis of a previous clinical study. Among the 123 clinically evaluable patients diagnosed with atypical CAP (26 patients were unevaluable), the clinical success rates were 95.5% (63 of 66 patients) for the 750-mg group and 96.5% (55 of 57 patients) for the 500-mg group (95% CI for success rate of the 500-mg group minus that of the 750-mg group, -6.8 to 8.8). At the poststudy evaluation (31-38 days after treatment began), relapse occurred in
机译:背景:目前推荐的非典型社区获得性肺炎(CAP)治疗时间为10至21天。但是,抗生素(例如氟喹诺酮类)可能允许有效的短期治疗方案。目的:本研究评估了750 mg左氧氟沙星治疗5天的疗效,而500 mg,10天的左氧氟沙星治疗非典型CAP的疗效。方法:在美国进行了一项随机,主动控制,双盲,多中心研究。在该研究的528名患者中,有149名被诊断出患有肺炎军团菌,肺炎衣原体或肺炎支原体。在治疗的第3天重新评估患者的基线症状。在治疗后就诊(最后一次使用活性药物后7-14天)评估CAP症状的临床疗效和缓解情况。结果:本报告代表先前临床研究的亚组分析。在123例被诊断为非典型CAP的临床可评估患者中(26例是不可评估的),750毫克组的临床成功率为95.5%(66例中的63例),而500毫克组的临床成功率为96.5%(57例中的55例)。组(500毫克组的成功率减去750毫克组的成功率95%CI -6.8至8.8)。在研究后评估中(开始治疗后31-38天),任一治疗组中

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号