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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Treatment of complicated urinary tract infection in adults: combined analysis of two randomized, double-blind, multicentre trials comparing ertapenem and ceftriaxone followed by appropriate oral therapy.
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Treatment of complicated urinary tract infection in adults: combined analysis of two randomized, double-blind, multicentre trials comparing ertapenem and ceftriaxone followed by appropriate oral therapy.

机译:成人复杂性尿路感染的治疗:两项比较,比较厄他培南和头孢曲松钠的随机,双盲,多中心试验,然后进行适当的口服治疗的综合分析。

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摘要

The efficacy and safety of parenteral ertapenem, a Group 1 carbapenem, 1 g once a day, for the treatment of complicated urinary tract infections (UTIs; i.e. acute pyelonephritis, UTI in men, or UTI associated with obstruction, foreign body or a urological abnormality interfering with normal voiding) in adults, were compared with those of parenteral ceftriaxone, 1 g once a day, in two similarly designed prospective, double-blind, randomized studies. In both studies, patients could be switched to an oral agent after >/=3 days of parenteral study therapy. At entry, 850 patients were stratified according to whether they had acute pyelonephritis or other complicated UTI without acute pyelonephritis. Two hundred and fifty-six patients in the ertapenem group and 224 in the ceftriaxone group were microbiologically evaluable. Ninety-six per cent of these patients were switched to oral therapy, usually ciprofloxacin; the median (range) duration of parenteral and total therapy, respectively, was 4 (2-14) days and13 (14-18) days for ertapenem and 4 (2-14) days and 13 (3-17) days for ceftriaxone. The most common pathogens were Escherichia coli and Klebsiella pneumoniae, which accounted for 64.7% and 9.8% of isolates, respectively. At the primary efficacy endpoint 5-9 days after treatment, 229 (89.5%) patients who received ertapenem and 204 (91.1%) patients who received ceftriaxone had a favourable microbiological response (95% confidence interval, -7.4 to 4.0), indicating that outcomes in the two treatment groups were equivalent. Success rates in both treatment groups were similar when compared by stratum and severity of infection. The frequency and severity of drug-related adverse events were generally similar in both treatment groups. In this combined analysis, ertapenem was highly effective therapy for the treatment of complicated UTIs in adults with moderate-to-severe disease.
机译:胃肠外ertapenem(1碳青霉烯类,每天1 g)用于治疗复杂的尿路感染(UTI;即急性肾盂肾炎,男性UTI或与梗阻,异物或泌尿系统异常相关的UTI)的功效和安全性在两项类似设计的前瞻性,双盲,随机研究中,将成人的正常排尿与胃肠外头孢曲松钠(每天1 g)进行了比较。在两项研究中,肠胃外研究治疗> / = 3天后都可以改用口服药物。入院时,根据是否患有急性肾盂肾炎或其他无急性肾盂肾炎的复杂UTI分为850例患者。依他培南组的256例患者和头孢曲松组的224例具有微生物学评价。这些患者中有96%改用口服治疗,通常是环丙沙星。 ertapenem的肠胃外和总疗法的中位(范围)持续时间分别为4(2-14)天和13(14-18)天,而头孢曲松钠为4(2-14)天和13(3-17)天。最常见的病原体是大肠杆菌和肺炎克雷伯菌,分别占分离株的64.7%和9.8%。在治疗后5-9天的主要疗效终点,接受厄他培南治疗的229名患者(89.5%)和接受头孢曲松治疗的204名患者(91.1%)的微生物学应答良好(95%置信区间为-7.4至4.0)。两个治疗组的预后相同。当按感染的程度和严重程度进行比较时,两个治疗组的成功率相似。在两个治疗组中,与药物相关的不良事件的发生频率和严重程度通常相似。在这项综合分析中,厄他培南是治疗中重度成年人复杂UTI的高效疗法。

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