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环丙沙星在患有严重革兰氏阴性腹腔内感染的重症监护病房患者中多次经肠内和静脉给药后的生物利用度。

Bioavailability of ciprofloxacin after multiple enteral and intravenous doses in ICU patients with severe gram-negative intra-abdominal infections.

作者信息

de Marie S, VandenBergh M F, Buijk S L, Bruining H A, van Vliet A, Kluytmans J A, Mouton J W

机构信息

Erasmus University Medical Center, Rotterdam/Dijkzigt Hospital, Department of Medical Microbiology and Infectious Diseases, Rotterdam, The Netherlands.

出版信息

Intensive Care Med. 1998 Apr;24(4):343-6. doi: 10.1007/s001340050577.

Abstract

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.

摘要

背景

关于环丙沙星在重症监护病房的危重症患者中多次肠内给药的药代动力学数据较少,而对于患有严重革兰氏阴性腹腔内感染(GNIAI)的患者则没有相关数据。

目的

确定肠内环丙沙星在患有严重GNIAI的鼻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

大学医学中心。

患者

5名患有GNIAI且估计肌酐清除率>25 ml/min的危重症监护患者,接受持续鼻饲。

干预措施

多次口服750 mg,每日两次,与静脉注射400 mg,每日两次的环丙沙星进行对比。

测量

750 mg每日两次肠内给药后计算得出的血清浓度-时间曲线下12小时面积与400 mg每日两次静脉注射后的相当。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7名患者中,肠内给药后2小时的平均血清稳态浓度为3.9μg/ml(95%CI 1.9-5.9),与交叉研究中的结果无显著差异(p = 0.4)。

结论

在患有严重GNIAI的鼻饲重症监护患者中,肠内环丙沙星的生物利用度足够。

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