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Individualised aminoglycoside dosage based on pharmacokinetic analysis is superior to dosage based on physician intuition at achieving target plasma drug concentrations [see comments]
Author(s) -
Begg EJ,
Atkinson HC,
Jeffery GM,
Taylor NW
Publication year - 1989
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/j.1365-2125.1989.tb05405.x
Subject(s) - pharmacokinetics , aminoglycoside , medicine , trough concentration , pharmacology , chemistry , antibiotics , biochemistry
1. A prospective randomised trial was conducted to compare aminoglycoside dose prediction based on individually measured pharmacokinetic data, with dosage based on physician intuition. 2. After 2 days of therapy more patients in the pharmacokinetic group had achieved both peak (6‐10 mg 1(‐1] and trough (1‐2 mg 1(‐1] target plasma concentrations (P = 0.007), peaks alone (P = 0.01) and troughs alone (P = 0.01). Their mean (s.e. mean) peak concentration was 6.49 +/‐ 0.39 mg 1(‐1) compared with 4.27 +/‐ 0.52 mg 1(‐1) in the control group (P = 0.001), with trough concentrations of 1.44 +/‐ 0.22 mg 1(‐1) and 0.94 +/‐ 0.21 mg 1(‐1) respectively (P = 0.054). 3. After 5 days of therapy, peak and trough concentrations were still significantly higher in the pharmacokinetic group despite empirical dose adjustment (P = 0.01 and P = 0.013 respectively). 4. The mean (s.e. mean) daily dose of aminoglycoside was higher in the computer group (312 +/‐ 17 mg vs 203 +/‐ 13 mg, P = 0.001). 5. These findings suggest that dose estimation based on measured pharmacokinetic parameters is superior at achieving target plasma drug concentrations.