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Journal of Antimicrobial Chemotherapy (1994) 33, 341-348
© 1994 The British Society for Antimicrobial Chemotherapy


other

Monitoring serum concentrations for once-daily netilmicin dosing regimens

Jürg Blasera,, Christiane Königa, Hans-Peter Simmenb and Ueli Thurnheerc

a Departments of Medicine, Anna-Seiler-Haus, Inselspital Berne Berne, Switzerland b Surgery, University Hospital, Anna-Seiler-Haus, Inselspital Berne Zürich, Berne, Switzerland c Department of Medicine, Anna-Seiler-Haus, Inselspital Berne Berne, Switzerland

Received 23 June 1993; accepted 7 September 1993


Dr Jürg Blaser, Department of Medicine, University Hospital, Ramistrasse 100, CH-8091 Zürich, Switzerland.

A once-daily dosing regimen for aminoglycosides is less expensive, at least as effective and possibly less toxic than multiple-daily dosing regimens. Once-daily dosing might also allow the frequency of measuring the serum concentrations of these antibiotics to be reduced since two of the major objectives of monitoring, high peak and low trough concentrations, are more likely to be achieved with this regimen. A novel strategy for monitoring serum concentrations which relies on a single sample obtained 8 h after a dose, as opposed to both trough and peak samples, is evaluated here. Serum kinetics of netilmicin were studied prospectively in 51 adult patients with initial serum creatinine concentrations of < 130 µmol/L who were treated with a median daily dosage of 400 mg. Concentrations measured 8 h after administration were within the target range of 1.5–6 mg/L in 113 of 134 dosing intervals studied. Concentrations above and below this range correlated significantly with higher and lower 24-h trough concentrations and areas under the curve respectively. There was also a significant correlation between 8-h netilmicin concentrations and nephrotoxicity (P < 0.05); a relative increase of greater double equals 25% in the serum creatinine concentration or an absolute increase of > 25 µmol/L was detected in 0 of 7 patients with an 8-h concentration of < 1.5 mg/L, in 3 of 33 patients (9.1%) with an 8-h concentration of 1.5–6 mg/L and in 4 of 11 patients (36%) with an 8-h concentration of > 6 mg/L. The results of this study suggest that adequate information about serum netilmicin concentrations in patients receiving a once-daily dose may be derived from a sample obtained 8 h after administration.


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