Using Imipenem and Cilastatin During Continuous Renal Replacement Therapy
- 238 Downloads
Aim: To identify and review studies which have sought to define the pharmacokinetics of imipenem and cilastatin in patients receiving continuous renal replacement therapy (CRRT).
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.
KeywordsAcute kidney failure Cilastatin Clearance CRRT Haemodialysis Haemofiltration Imipenem Pharmacokinetics
Unable to display preview. Download preview PDF.
- 1.Norrby, SR, Alestig, K, Ferber, F, Huber, JL, Jones, KH, Kahan, FM, et al. 1983aPharmacokinetics and tolerance of N-formimidoyl thienamycin (MK0787) in humansAntimicrob Agents Chemother232939Google Scholar
- 2.Norrby, SR, Alestig, K, Björnegård, B, Burman, LA, Ferber, F, Huber, JL, et al. 1983bUrinary recovery of N-formimidoyl thienamycin (MK0787) as affected by co-administration of of N-formimidoyl thienamycin dihydropeptidase inhibitorAntimicrob Agents Chemother233007Google Scholar
- 3.AHFS Drug Information. Bethesda: American Society of Health-System Pharmacists Inc., 2003. ISBN 1-58528-039-9Google Scholar
- 4.Rogers, JD, Meisinger, MAL, Ferber, F, Calendra, GB, Demetriades, JL, Bland, JA 1985Pharmacokinetics of imipenem/ cilastatin in volunteersRev Infec Dis7S43546Google Scholar
- 5.Drussano, GL, Standiford, HC 1985Pharmacokinetic profile of imipenem/cilastatin in normal volunteersAm J Med784753Google Scholar
- 6.British National Formulary 46. London: British Medical Association & Royal Pharmaceutical Society Great Britain, Sept 2003. ISBN 0-85369-556-3Google Scholar
- 10.Hashimoto S, Honda M, Yamaguchi M, Sekimoto M, Tanaka Y. Pharmacokinetics of imipenem and cilastatin during continuous venovenous hemodialysis in patients who are critically iII. ASAIO J 1997; 84–8.Google Scholar
- 16.Reeves DS. Human pharmacokinetics of N-formimidoylthienamycin alone and in combination with a dehydropeptidase inhibitor (MK-701) and probenecid. Proc 13th Int Congress Chemother 30–33Google Scholar