Abstract | BACKGROUND: OBJECTIVE: DESIGN: A randomized crossover study. SETTING: University-based medical center. PATIENTS: 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:
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Authors | S de Marie, M F VandenBergh, S L Buijk, H A Bruining, A van Vliet, J A Kluytmans, J W Mouton |
Journal | Intensive care medicine
(Intensive Care Med)
Vol. 24
Issue 4
Pg. 343-6
(Apr 1998)
ISSN: 0342-4642 [Print] United States |
PMID | 9609412
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Infective Agents
- Ciprofloxacin
- Creatinine
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Topics |
- Adult
- Aged
- Anti-Infective Agents
(administration & dosage, pharmacokinetics)
- Biological Availability
- Ciprofloxacin
(administration & dosage, pharmacokinetics)
- Creatinine
(blood)
- Critical Care
- Critical Illness
- Cross-Over Studies
- Drug Monitoring
- Enteral Nutrition
- Gram-Negative Bacterial Infections
(drug therapy, metabolism)
- Humans
- Infusions, Intravenous
- Middle Aged
- Peritonitis
(drug therapy, metabolism)
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