Comparison of Ertapenem and Ceftriaxone Therapy for Acute Pyelonephritis and Other Complicated Urinary Tract Infections in Korean Adults: A Randomized, Double-Blind, Multicenter Trial

被引:18
作者
Park, Dae Won [1 ]
Peck, Kyong Ran [2 ]
Chung, Moon Hyun [3 ]
Lee, Jin Seo [4 ]
Park, Yoon Soo [5 ]
Kim, Hyo Youl [6 ]
Lee, Mi Suk [7 ]
Kim, Jung Yeon [1 ]
Yeom, Joon Sup [8 ]
Kim, Min Ja [1 ]
机构
[1] Korea Univ, Coll Med, Dept Internal Med, Div Infect Dis, Seoul 136705, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Infect Dis, Seoul, South Korea
[3] Inha Univ, Coll Med, Dept Internal Med, Inchon, South Korea
[4] Hallym Univ, Coll Med, Kangdong Sacred Heart Hosp, Div Infect Dis,Dept Internal Med, Seoul, South Korea
[5] Gachon Univ, Gil Med Ctr, Dept Internal Med, Inchon, South Korea
[6] Yonsei Univ, Wonju Coll Med, Dept Infect Dis, Wonju, South Korea
[7] Kyung Hee Univ, Sch Med, Med Ctr, Div Infect Dis,Dept Med, Seoul, South Korea
[8] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Internal Med, Seoul, South Korea
关键词
Pyelonephritis; Urinary Tract Infections; Ertapenem; Ceftriaxone; APPROPRIATE ORAL-THERAPY; SOUTH-KOREA; ENTEROBACTERIACEAE; TOLERABILITY; PREVALENCE; GUIDELINES; RESISTANT; CYSTITIS; SAFETY;
D O I
10.3346/jkms.2012.27.5.476
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The efficacy and safety of ertapenem, 1 g once daily, were compared with that of ceftriaxone, 2 g once daily, for the treatment of adults with acute pyelonephritis (APN) and complicated urinary tract infections (cUTIs) in a prospective, multicenter, double-blinded, randomized study. After >= 3 days of parenteral study therapy, patients could be switched to an oral agent. Of 271 patients who were initially stratified by APN (n = 210) or other cUTIs (n = 61), 66 (48.9%) in the ertapenem group and 71 (52.2%) in the ceftriaxone group were microbiologically evaluable. The mean duration of parenteral and total therapy, respectively, was 5.6 and 13.8 days for ertapenem and 5.8 and 13.8 days for ceftriaxone. The most common pathogen was Escherichia coli. At the primary efficacy endpoint 5-9 days after treatment, 58 (87.9%) patients in the ertapenem group and 63 (88.7%) in the ceftriaxone had a favorable microbiological response. When compared by stratum and severity, the outcomes in the two groups were equivalent. The frequency and severity of drug-related adverse events were generally similar in both treatment groups. The results indicate that ertapenem is highly effective and safe for the treatment of APN and cUTIs.
引用
收藏
页码:476 / 483
页数:8
相关论文
共 28 条