Abstract | AIM: METHOD: Literature was primarily identified using Pharmline, Embase and Medline databases using the search terms " imipenem," "haemofiltration," "haemodialysis" and "pharmacokinetics." Papers that discussed only intermittent haemodialysis were excluded. RESULTS: Seven papers were identified which described the pharmacokinetics of imipenem in patients receiving CRRT. Four different modes of CRRT were used. The methods of sampling, dosages used and assumptions made during pharmacokinetic calculations varied widely between the studies. Total body clearance of imipenem during CRRT in patients suffering from acute renal failure was found to range between 89 and 149 ml/min. Total body clearance of cilastatin ranged between 9 and 32 ml/min. Total body clearance of both imipenem and cilastatin was reduced in patients with chronic renal failure. Total body clearance of cilastatin was also reduced by impaired liver function. Dose recommendations made ranged between 500 mg 6-hourly and 500 mg 12-hourly. CONCLUSIONS: The heterogeneity of the studies identified prevents them being analysed as a single group. For meaningful dosage recommendations to be made, further studies are required using larger populations and with more detail regarding liver dysfunction and duration of renal failure.
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Authors | Alison Cotton, Bryony Dean Franklin, Stephen Brett, Alison Holmes |
Journal | Pharmacy world & science : PWS
(Pharm World Sci)
Vol. 27
Issue 5
Pg. 371-5
(Oct 2005)
ISSN: 0928-1231 [Print] Germany |
PMID | 16341743
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Bacterial Agents
- Protease Inhibitors
- Cilastatin
- Imipenem
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Topics |
- Acute Kidney Injury
(metabolism, therapy)
- Anti-Bacterial Agents
(administration & dosage, pharmacokinetics)
- Cilastatin
(administration & dosage, pharmacokinetics)
- Drug Administration Schedule
- Drug Therapy, Combination
- Female
- Hemofiltration
(methods)
- Humans
- Imipenem
(administration & dosage, pharmacokinetics)
- Male
- Middle Aged
- Protease Inhibitors
(administration & dosage, pharmacokinetics)
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