Antimicrobial Agents and Chemotherapy · 1993 · 89 citations · 7 references
PharmacyPharmacokineticsPharmacologyDrug ClearanceHemodialysisRenal PharmacokineticsPharmacokinetics In Renal ImpairmentRenal ClearanceRenal DiseaseRenal Drug ClearanceRenal PharmacologyCumulative Urinary ExcretionDrug Clearance During HemodialysisDrug Elimination Half-lifeEnd-stage Renal Disease PharmacokineticsEstimated Creatinine ClearanceHemodialysis PharmacokineticsPharmacokinetics In Kidney DiseaseRenal Half-life
The pharmacokinetics of meropenem were studied after intravenous infusion in 13 patients grouped according to the impairment of their renal function. Creatinine clearance (CLCR) was greater than 50, 50 to 30, and less than 30 ml/min in groups I, II, and III, respectively. Two other groups, groups IV and V, each comprising four patients with end-stage renal disease (CLCR, < 5 ml/min), were also studied, the former on days off of hemodialysis and the latter on days of hemodialysis. The elimination half-lives of meropenem were 1.54 +/- 0.70 h in group I patients, 3.36 +/- 1.02 h in group II patients, and 5.00 +/- 1.05 h in group III patients. Cumulative urinary excretion accounted for 48.5% of the dose in group I patients and decreased progressively with a decline in renal function. Hemodialysis shortened the elimination half-life of meropenem from 7.0 h to 2.9 h. H-4295, the main metabolite of meropenem, had a peak level in plasma of 0.5 to 1.0 h in patients with renal failure. The level of H-4295 decreased with hemodialysis. The dosing interval of meropenem should be prolonged in a regular proportion to the decline in CLCR (12 h in group II patients and 24 h in group III patients). In patients receiving hemodialysis, dosing after each hemodialysis session is recommended.
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A pharmacokinetic analysis program (multi) for microcomputer.
Kiyoshi Yamaoka, Yusuke Tanigawara, Terumichi Nakagawa et al. · Journal of Pharmacobio-Dynamics · 1981 · 2.5K citations · Full text
The pharmacokinetics of meropenem in volunteers
Richard Bax, W Bastain, A. Featherstone et al. · Journal of Antimicrobial Chemotherapy · 1989 · 160 citations
GA Verpooten, L. Verbist, AP Buntinx et al. · British Journal of Clinical Pharmacology · 1984 · 64 citations · Full text