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  5. Pharmacokinetic‐pharmacodynamic evaluation of ceftazidime continuous infusion <i>vs</i> intermittent bolus injection in septicaemic melioidosis

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Article
English
2000

Pharmacokinetic‐pharmacodynamic evaluation of ceftazidime continuous infusion <i>vs</i> intermittent bolus injection in septicaemic melioidosis

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English
2000
British Journal of Clinical Pharmacology
Vol 50 (2)
DOI: 10.1111/j.1365-2125.2000.00179.x

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Sir Nicholas White
Sir Nicholas White

University Of Cambridge

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Brian Angus
Michelle Smith
Yupin Suputtamongkol
+5 more

Abstract

Aims Experimental studies have suggested that constant intravenous infusion would be preferable to conventional intermittent bolus administration of beta‐lactam antibiotics for serious Gram‐negative infections. Severe melioidosis ( Burkholderia pseudomallei infection) carries a mortality over 40% despite treatment with high dose ceftazidime. The aim of this study was to measure the pharmacokinetic and pharmacodynamic effects of continuous infusion of ceftazidime vs intermittent bolus dosing in septicaemic melioidosis. Methods Patients with suspected septicaemic melioidosis were randomised to receive ceftazidime 40 mg kg −1 8 hourly by bolus injection or 4 mg kg −1 h −1 by constant infusion following a 12 mg kg −1 priming dose and pharmacokinetic and pharmacodynamic parameters were compared. Results Of the 34 patients studied 16 (59%) died. Twenty patients had cultures positive for B. pseudomallei of whom 12 (60%) died. The median MIC 90 of B. pseudomallei was 2 mg l −1 , giving a minimum target concentration (4*MIC) of 8 mg l −1 . The median (range) estimated total apparent volume of distribution, systemic clearance and terminal elimination half‐lives of ceftazidime were 0.468 (0.241–0.573) l kg −1 , 0.058 (0.005–0.159) l kg −1 h −1 and 7.74 (1.95–44.71) h, respectively. Clearance of ceftazidime and creatinine clearance were correlated closely ( r = 0.71; P &lt; 0.001) and there was no evidence of significant nonrenal clearance. Conclusions Simulations based on these data and the ceftazidime sensitivity of the B. pseudomallei isolates indicated that administration by constant infusion would allow significant dose reduction and cost saving. With conventional 8 h intermittent dosing to patients with normal renal function, plasma ceftazidime concentrations could fall below the target concentration but this would be unlikely with a constant infusion. Correction for renal failure, which is common in patients with meliodosis is Clearance = k * creatinine clearance where k = 0.72. Calculation of a loading dose gives median (range) values of loading dose, D L of 18.7 mg kg −1 (9.5–23) and infusion rate I = 3.5 mg kg −1 h −1 (0.4–13) (which equals 84 mg kg −1 day −1 ). A nomogram for adjustment in renal failure is given.

How to cite this publication

Brian Angus, Michelle Smith, Yupin Suputtamongkol, H. Mattie, Amanda L. Walsh, Vanaporn Wuthiekanun, Wipada Chaowagul, Sir Nicholas White (2000). Pharmacokinetic‐pharmacodynamic evaluation of ceftazidime continuous infusion <i>vs</i> intermittent bolus injection in septicaemic melioidosis. British Journal of Clinical Pharmacology, 50(2), pp. 184-191, DOI: 10.1111/j.1365-2125.2000.00179.x.

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Publication Details

Type

Article

Year

2000

Authors

8

Datasets

0

Total Files

0

Language

English

Journal

British Journal of Clinical Pharmacology

DOI

10.1111/j.1365-2125.2000.00179.x

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