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Treatment of complicated urinary tract infection and acute pyelonephritis by short-course intravenous levofloxacin (750 mg/day) or conventional intravenous/oral levofloxacin (500 mg/day): prospective, open-label, randomized, controlled, multicenter, non-inferiority clinical trial  期刊论文  

  • 编号:
    74240ccf-dbd8-4498-a888-1002e9e858ef
  • 作者:
    Ren, Hong[1] Li, Xiao[1] Ni, ZhaoHui[2] Niu, JianYing[3] Cao, Bin[4] Xu, Jie[5] Cheng, Hong[6] Tu, XiaoWen[7] Ren, AiMin[8] Hu, Ying[9] Xing, ChangYing[10] Liu, YingHong[11] Li, YanFeng[12] Cen, Jun[13] Zhou, Rong[14] Xu, XuDong[15] Qiu, XiaoHui[16] Chen, Nan[1]
  • 语种:
    English
  • 期刊:
    INTERNATIONAL UROLOGY AND NEPHROLOGY ISSN:0301-1623 2017 年 49 卷 3 期 (499 - 507) ; MAR
  • 收录:
  • 关键词:
  • 摘要:

    To compare the efficacy and safety of short-course intravenous levofloxacin (LVFX) 750 mg with a conventional intravenous/oral regimen of LVFX 500 mg in patients from China with complicated urinary tract infections (cUTIs) and acute pyelonephritis (APN). This was a prospective, open-label, randomized, controlled, multicenter, non-inferiority clinical trial. Patients with cUTI and APN were randomly assigned to a short-course therapy group (intravenous LVFX at750 mg/day for 5 days) or a conventional therapy group (intravenous/oral regimen of LVFX at 500 mg/day for 7-14 days). The clinical, laboratory, and microbiological results were evaluated for efficacy and safety. The median dose of LVFX was 3555.4 mg in the short-course therapy group and 4874.2 mg in the conventional therapy group. Intention-to-treat analysis indicated the clinical effectiveness in the short-course therapy group (89.87%, 142/158) was non-inferior to that in the conventional therapy group (89.31%, 142/159). The microbiological effectiveness rates were also similar (short-course therapy: 89.55%, 60/67; conventional therapy: 86.30%, 63/73; p > 0.05). There were no significant differences in other parameters, including clinical and microbiological recurrence rates. The incidence of adverse effects and drug-related adverse effects were also similar for the short-course therapy group (21.95%, 36/164; 18.90%, 31/164) and the conventional therapy group (23.03%, 38/165; 15.76%, 26/165). Patients with cUTIs and APN who were given short-course LVFX therapy and conventional LVFX therapy had similar outcomes in clinical and microbiological efficacy, tolerance, and safety. The short-course therapy described here is a more convenient alternative to the conventional regimen with potential implication in anti-resistance and cost saving.

  • 推荐引用方式
    GB/T 7714:
    Ren Hong,Li Xiao,Ni Zhao-Hui, et al. Treatment of complicated urinary tract infection and acute pyelonephritis by short-course intravenous levofloxacin (750 mg/day) or conventional intravenous/oral levofloxacin (500 mg/day): prospective, open-label, randomized, controlled, multicenter, non-inferiority clinical trial [J].INTERNATIONAL UROLOGY AND NEPHROLOGY,2017,49(3):499-507.
  • APA:
    Ren Hong,Li Xiao,Ni Zhao-Hui,Niu Jian-Ying,&Chen Nan.(2017).Treatment of complicated urinary tract infection and acute pyelonephritis by short-course intravenous levofloxacin (750 mg/day) or conventional intravenous/oral levofloxacin (500 mg/day): prospective, open-label, randomized, controlled, multicenter, non-inferiority clinical trial .INTERNATIONAL UROLOGY AND NEPHROLOGY,49(3):499-507.
  • MLA:
    Ren Hong, et al. "Treatment of complicated urinary tract infection and acute pyelonephritis by short-course intravenous levofloxacin (750 mg/day) or conventional intravenous/oral levofloxacin (500 mg/day): prospective, open-label, randomized, controlled, multicenter, non-inferiority clinical trial" .INTERNATIONAL UROLOGY AND NEPHROLOGY 49,3(2017):499-507.
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