Shortening antibiotic duration in the treatment of acute cholangitis: rationale and study protocol for an open-label randomized controlled trial

被引:2
|
作者
Iwata, Kentaro [1 ]
Doi, Asako [2 ]
Oba, Yuichiro [3 ]
Matsuo, Hiroo [4 ]
Ebisawa, Kei [1 ]
Nagata, Manabu [1 ]
Nishimura, Sho [1 ]
Yoshimura, Kenichi [5 ]
Masuda, Atsuhiro [6 ]
Shiomi, Hideyuki [6 ]
Kodama, Yuzo [6 ]
机构
[1] Kobe Univ, Grad Sch Med, Div Infect Dis, Chuo Ku, Kusunokicho 7-5-2, Kobe, Hyogo 6500017, Japan
[2] Kobe City Med Ctr Gen Hosp, Dept Infect Dis, Chuo Ku, Kobe, Hyogo 6500047, Japan
[3] Osaka Gen Med Ctr, Dept Gen Med, Bandaihigashi 3-1-56, Sumiyoshi, Osaka 5588558, Japan
[4] Hyogo Prefectural Amagasaki Gen Med Ctr, Dept Infect Dis, Higashinanbacho 2-17-77, Amagasaki, Hyogo 6608550, Japan
[5] Kanazawa Univ Hosp, Innovat Clin Res Ctr iCREK, 13-1 Takara Machi, Kanazawa, Ishikawa 9208641, Japan
[6] Kobe Univ, Grad Sch Med, Dept Gastroenterol, Kusunokicho 7-5-2, Kobe, Hyogo 6500017, Japan
关键词
Acute cholangitis; Antimicrobial therapy; Short-course therapy; RCT; PROGNOSTIC DETERMINANTS; EPIDEMIOLOGY; NONINFERIORITY; THERAPY;
D O I
10.1186/s13063-020-4046-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Antimicrobial therapy with appropriate biliary drainage is considered the standard of care for acute cholangitis, but the optimal duration of antimicrobial therapy remains unknown. Seven to 10 days of antimicrobial therapy are common for the treatment of acute cholangitis, but a recent retrospective cohort study suggested a shorter duration might be effective. A shorter duration of antimicrobial therapy can be beneficial in decreasing the length of hospital stay, improving patients' quality of life, decreasing adverse effects, and even contributing to a decrease in the occurrence of antimicrobial resistance. Methods/design We will conduct a multi-centre, open-label, randomized, non-inferiority trial to compare short-course therapy (SCT) with conventional long-course therapy (LCT) in treating patients with acute cholangitis. SCT consists of 5-day intravenous antimicrobial therapy if the patients had clinical improvement, while at least 7 days of intravenous antibiotics will be provided to the LCT group. The primary outcome is clinical cure at 30 days after onset. Patients will be randomly assigned in an open-label fashion. A total sample size of 150 was estimated to provide a power of 80% with a one-sided alpha level of 2.5% and a non-inferiority margin of 10%. Discussion This trial is expected to reveal whether SCT is non-inferior to conventional LCT or not, and may provide evidence that one can shorten the treatment duration for acute cholangitis for the benefit of patients.
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页数:6
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