We determined the blood concentrations after administration of cefuroxime (CXM) in patients on hemodialysis (HD) and conducted a pharmacokinetic study. This paper is a report of our findings.
The subjects are 24 HD patients. CXM 1.5g (dissolved in 50m
l of saline solution) was administered by intravenous drip infusion taking 30 minutes during the period of non-HD and blood was collected over the time in 18 HD patients [HD (-) group]. In 6 other patients, the same test was performed during HD [HD (+) group].
The blood level in the HD (-) group was as follows. 0.5h after the start of drip infusion (immediately after the end of drip infusion): 112.9±32.2, 1.5h: 97.1±27.6, 35h: 81.4±24.2, 6.5h: 77.1±19.8, 8.5h: 70.9±15.8, 24.5h (24 hours after the end of drip infusion): 27.5±8.4μg/m
lThe blood level in the HD (+) group was as follows. 0.5h after the start of drip infusion: 76.9±24.9, 1.5h: 39.6±3.6, 3.5h: 23.8±6.5, 4.0h: 19.7±5.3μg/m
lAccording to the results of pharmacokinetic analysis, the HD (-) group showed the T1/2: 12.2h, Cmax: 106.2μg/m
l AUC (0→4h): 363.8, AUC (0→24h): 1, 405.4μg·h/m
l, against T1/2: α phase 0.07, β phase 2.58h, Cmax: 76.9μg/m
l, AUC (0→4h): 143.6μg·h/m
l in the HD (+) group.
CXM is excreted from the kidney. In our studies, it was confirmed that excretion of CXM from blood was delayed in HD patients and that the CXM was eliminated by HD.
According to a simulation based on a 7-day consecutive administration, results of analysis showing that intravenous drip infusion of CXM in a dose of 1.5g/day is effective and safe were obtained in patients with renal failure who are in such a condition as to undergo HD once every two days.
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