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每日一次,使用缓释环丙沙星治疗复杂性尿路感染和急性单纯性肾盂肾炎。

Once daily, extended release ciprofloxacin for complicated urinary tract infections and acute uncomplicated pyelonephritis.

作者信息

Talan David A, Klimberg Ira W, Nicolle Lindsay E, Song James, Kowalsky Steven F, Church Deborah A

机构信息

University of California-Los Angeles Medical Center-Olive View, Sylmar, 91342, USA.

出版信息

J Urol. 2004 Feb;171(2 Pt 1):734-9. doi: 10.1097/01.ju.0000106191.11936.64.

Abstract

PURPOSE

We assessed the efficacy and safety of 1,000 mg extended release ciprofloxacin orally once daily vs conventional 500 mg ciprofloxacin orally twice daily, each for 7 to 14 days, in patients with a complicated urinary tract infection (cUTI) or acute uncomplicated pyelonephritis (AUP).

MATERIALS AND METHODS

In this prospective, randomized, double-blind, North American multicenter clinical trial adults were stratified based on clinical presentation of cUTI or AUP and randomized to extended release ciprofloxacin or ciprofloxacin twice daily. Efficacy valid patients had positive pretherapy urine cultures (105 or greater cFU/ml) and pyuria within 48 hours of study entry. Bacteriological and clinical outcomes were assessed at the test of cure visit (5 to 11 days after therapy) and the late followup visit (28 to 42 days after therapy).

RESULTS

The intent to treat population comprised 1,035 patients (extended release ciprofloxacin in 517 and twice daily in 518), of whom 435 were efficacy valid (cUTI in 343 and AUP in 92). For efficacy valid patients (cUTI and AUP combined) bacteriological eradication rates at test of cure were 89% (183 of 206) vs 85% (195 of 229) (95% CI -2.4%, 10.3%) and clinical cure rates were 97% (198 of 205) vs 94% (211 of 225) (95% CI -1.2%, 6.9%) for extended release vs twice daily ciprofloxacin. Late followup outcomes were consistent with test of cure findings. Eradication rates for Escherichia coli, which accounted for 58% of pathogens, were 97% or greater per group. Drug related adverse event rates were similar for extended release and twice daily ciprofloxacin (13% and 14%, respectively).

CONCLUSIONS

Extended release ciprofloxacin at a dose of 1,000 mg once daily was as safe and effective as conventional treatment with 500 mg ciprofloxacin twice daily, each given orally for 7 to 14 days in adults with cUTI or AUP. It provides a convenient, once daily, empirical treatment option.

摘要

目的

我们评估了每日口服一次1000mg缓释环丙沙星与每日口服两次常规500mg环丙沙星,各治疗7至14天,对复杂性尿路感染(cUTI)或急性非复杂性肾盂肾炎(AUP)患者的疗效和安全性。

材料与方法

在这项前瞻性、随机、双盲、北美多中心临床试验中,成人患者根据cUTI或AUP的临床表现进行分层,并随机分为缓释环丙沙星组或每日两次环丙沙星组。疗效有效患者在研究入组后48小时内尿培养前呈阳性(菌落形成单位/毫升≥10⁵)且有脓尿。在治疗结束访视(治疗后5至11天)和后期随访访视(治疗后28至42天)评估细菌学和临床结局。

结果

意向性治疗人群包括1035例患者(517例接受缓释环丙沙星治疗,518例接受每日两次环丙沙星治疗),其中435例疗效有效(343例为cUTI,92例为AUP)。对于疗效有效患者(cUTI和AUP合并),治疗结束时缓释环丙沙星组与每日两次环丙沙星组的细菌清除率分别为89%(206例中的183例)和85%(229例中的195例)(95%CI -2.4%,10.3%),临床治愈率分别为97%(205例中的198例)和94%(225例中的211例)(95%CI -1.2%,6.9%)。后期随访结果与治疗结束时的结果一致。占病原体58%的大肠杆菌清除率每组均≥97%。缓释环丙沙星组和每日两次环丙沙星组的药物相关不良事件发生率相似(分别为13%和14%)。

结论

对于cUTI或AUP成人患者,每日口服一次1000mg缓释环丙沙星与每日口服两次500mg常规环丙沙星各治疗7至14天一样安全有效。它提供了一种方便的每日一次经验性治疗选择。

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