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Grose, William E.; Bodey, Gerald P.; Stewart, Dorothy
Clinical pharmacology and therapeutics, November 1976, Letnik: 20, Številka: 5Journal Article
Comparative studies of cefamandole and cephalothin were carried out in 32 cancer patients. After rapid intravenous injection of 1 gm cefamandole or cephalothin, the peak mean serum concentrations in 11 patients achieved at 0.25 hr were 103.4 mcg/ml and 56.7 mcg/ml, respectively. Except at 6 hr, the serum concentration of cefamandole was higher (p < 0.05) at alt times. The terminal half‐lives (t½) were similar, being 1.2 hr for cefamandole and 1.0 hr for cephalothin. Cefamandole, 1 gm intramuscularly, induced a peak mean serum concentration of 26.6 mcg/ml at 1 hr, with a slow decay. Intermittent cefamandole (2 gm intravenously every 6 hr) induced very high mean serum concentrations (7 patients), but at 4 hr the concentrations were similar to those after 1 gm intravenously. Per cent of urinary excretion was simi lar for both drugs regardless of dose and mode of administration. Continuous‐infusion cefamandole or cephalothin (2 gm loading followed by 2 gm every 6 hr) in 14 patients showed consistently higher serum concentrations for cefamandole (p < 0.05) over a 5‐day period. There was no evidence of drug accumulation in the multiple‐dose studies. Both the single‐ and multiple‐dose schedules were well tolerated.
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