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首页> 外文期刊>Intensive care medicine >Bioavailability of ciprofloxacin after multiple enteral and intravenous doses in ICU patients with severe gram-negative intra-abdominal infections.
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Bioavailability of ciprofloxacin after multiple enteral and intravenous doses in ICU patients with severe gram-negative intra-abdominal infections.

机译:在重症革兰阴性腹腔内感染的ICU患者中,多次肠内和静脉内给药后环丙沙星的生物利用度。

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摘要

BACKGROUND: Few data are available on the pharmacokinetics of multiple enteral dosing of ciprofloxacin in critically ill intensive care patients and none for those with severe gram-negative intra-abdominal infections (GNIAI). OBJECTIVE: To determine the bioavailability of enteral ciprofloxacin in tube-fed intensive care patients with severe GNIAI. DESIGN: A randomized crossover study. SETTING: University-based medical center. PATIENTS: 5 critically ill intensive care patients with GNIAI and an estimated creatinine clearance > 25 ml/ min who received continuous tube feeding. INTERVENTIONS: Multiple doses of enteral 750 mg b.i.d. versus 400 mg b.i.d.i.v. ciprofloxacin. MEASUREMENTS: The calculated 12-h area under the serum concentration versus time curve after 750 mg b.i.d. enteral dosing was equivalent to that after 400 mg b.i.d.i.v. The mean bioavailability of enteral dosing was 53.1% [95% confidence interval (CI) 43.5-62.8]. In seven additional patients, the mean serum steady-state concentration at 2 h after enteral administration was 3.9 microg/ml (95% CI 1.9-5.9), not significantly different from that found in the crossover study (p = 0.4). CONCLUSIONS: In tube-fed intensive care patients with severe GNIAI, the bioavailability of enteral ciprofloxacin is adequate.
机译:背景:在危重症重症监护患者中,关于环丙沙星多次肠内给药的药代动力学的数据很少,而对于严重的革兰氏阴性腹腔内感染(GNIAI)的患者,尚无数据。目的:确定肠饲环丙沙星在重症GNIAI管饲重症监护患者中的生物利用度。设计:一项随机交叉研究。地点:大学医疗中心。患者:5例重症重症监护病房的GNIAI患者,估计肌酐清除率> 25 ml / min,接受连续管饲。干预措施:肠内多剂量750 mg b.i.d.与400毫克b.i.d.i.v.环丙沙星。测量:750 mg b.i.d.后血清浓度与时间的关系曲线下计算的12小时面积。肠内给药等同于400 mg b.i.d.i.v.肠内给药的平均生物利用度为53.1%[95%置信区间(CI)43.5-62.8]。在另外七名患者中,肠内给药后2 h的平均血清稳态浓度为3.9 microg / ml(95%CI 1.9-5.9),与交叉研究中的值无显着差异(p = 0.4)。结论:在管饲重症GNIAI的重症监护患者中,肠环丙沙星的生物利用度足够。

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