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首页> 外文期刊>Current medical research and opinion >Clinical implications of 750 mg, 5-day levofloxacin for the treatment of community-acquired pneumonia.
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Clinical implications of 750 mg, 5-day levofloxacin for the treatment of community-acquired pneumonia.

机译:750 mg,5天左氧氟沙星治疗社区获得性肺炎的临床意义。

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OBJECTIVE: To evaluate the time to symptom resolution and IV-to-PO transition in community-acquired pneumonia (CAP) patients treated with 750 mg or 500 mg levofloxacin. Research Design: A retrospective, subset analysis of a multicenter, randomized, double-blind, controlled trial comparing 750 mg levofloxacin for 5 days to 500 mg levofloxacin for 10 days for the treatment of CAP. PATIENTS AND METHODS: A total of 528 CAP patients were included. Baseline symptoms were re-evaluated on Day 3 of therapy, and time to IV-to-PO transition was recorded for inpatients. RESULTS: For the overall population, 67.4% of patients receiving 750 mg levofloxacin had resolution of fever by Day 3 of therapy, compared to 54.6% of 500 mg treated patients (P = 0.006). Patients who started on 750 mg levofloxacin IV (N = 108) transitioned to PO in an average of 2.68 days while those starting on 500 mg IV (N = 124) transitioned in 2.95 days (P = 0.144). The median time for IV-to-PO switch was 2.35 days and 2.75 days for patients receiving 750 mg and 500 mg levofloxacin, respectively (P = 0.098, log rank test). By Day 3 of therapy, 68% of patients receiving the 750 mg dose had transitioned from IV to PO levofloxacin, compared with 61% of the 500 mg group (P = 0.280). The safety profiles were comparable for the two regimens. CONCLUSIONS: The 750 mg levofloxacin dose resulted in a greater proportion of patients with resolution of CAP symptoms by Day 3 when compared with 500 mg therapy. Consequently, the 750 mg regimen trended toward more rapid transition to PO, potentially resulting in lower overall drug costs. Time to switch from IV to PO was determined by the investigators' discretion rather than a set protocol. Additionally, length of stay data was not collected in this study, which can significantly impact overall healthcare costs. Further research is required to fully understand the economic impact of the 750 mg, 5-day levofloxacin regimen.
机译:目的:评估接受750 mg或500 mg左氧氟沙星治疗的社区获得性肺炎(CAP)患者症状缓解和IV-PO转变的时间。研究设计:一项多中心,随机,双盲,对照试验的回顾性亚组分析,比较了750 mg左氧氟沙星治疗5天与500 mg左氧氟沙星治疗10天的疗效。患者与方法:总共包括528例CAP患者。在治疗的第3天重新评估基线症状,并记录住院患者从IV到PO过渡的时间。结果:在总体人群中,接受750 mg左氧氟沙星治疗的患者中有67.4%的患者在治疗的第3天发烧了,而接受500 mg左氧氟沙星治疗的患者中这一比例为54.6%(P = 0.006)。开始使用750 mg左氧氟沙星静脉注射(N = 108)的患者平均需要2.68天才能转变为PO,而开始使用500 mg静脉注射左氧氟沙星(N = 124)的患者可以在2.95天之内转变为PO(P = 0.144)。对于接受750 mg和500 mg左氧氟沙星治疗的患者,IV至PO转换的中位时间分别为2.35天和2.75天(P = 0.098,对数秩检验)。到治疗的第3天,接受750 mg剂量的患者中有68%从左氧氟沙星转为静脉使用左氧氟沙星,而500 mg组则为61%(P = 0.280)。两种方案的安全性均相当。结论:与500 mg治疗相比,左氧氟沙星750 mg剂量在第3天导致CAP症状缓解的患者比例更高。因此,750 mg方案倾向于向PO过渡更快,从而可能降低总体药物成本。从IV切换到PO的时间取决于研究者的判断力,而不是确定的规程。此外,该研究未收集住院时间数据,这可能会严重影响总体医疗保健成本。需要进一步研究以充分了解750 mg,5天左氧氟沙星治疗方案的经济影响。

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