Application of a loading dose of colistin methanesulfonate in critically ill patients: Population pharmacokinetics, protein binding, and prediction of bacterial kill

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3061435 8 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Application of a loading dose of colistin methanesulfonate in critically ill patients: Population pharmacokinetics, protein binding, and prediction of bacterial kill
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
A previous pharmacokinetic study on dosing of colistin methanesulfonate (CMS) at 240 mg (3 million units [MU]) every 8 h indicated that colistin has a long half-life, resulting in insufficient concentrations for the first 12 to 48 h after initiation of treatment. A loading dose would therefore be beneficial. The aim of this study was to evaluate CMS and colistin pharmacokinetics following a 480-mg (6-MU) loading dose in critically ill patients and to explore the bacterial kill following the use of different dosing regimens obtained by predictions from a pharmacokinetic-pharmacodynamic model developed from an in vitro study on Pseudomonas aeruginosa. The unbound fractions of colistin A and colistin B were determined using equilibrium dialysis and considered in the predictions. Ten critically ill patients (6 males; mean age, 54 years; mean creatinine clearance, 82 ml/min) with infections caused by multidrug-resistant Gram-negative bacteria were enrolled in the study. The pharmacokinetic data collected after the first and eighth doses were analyzed simultaneously with the data from the previous study (total, 28 patients) in the NONMEM program. For CMS, a two-compartment model best described the pharmacokinetics, and the half-lives of the two phases were estimated to be 0.026 and 2.2 h, respectively. For colistin, a one-compartment model was sufficient and the estimated half-life was 18.5 h. The unbound fractions of colistin in the patients were 26 to 41% at clinical concentrations. Colistin A, but not colistin B, had a concentration-dependent binding. The predictions suggested that the time to 3-log-unit bacterial kill for a 480-mg loading dose was reduced to half of that for the dose of 240 mg. Copyright © 2012, American Society for Microbiology. All Rights Reserved.
Έτος δημοσίευσης:
2012
Συγγραφείς:
Mohamed, A.F.
Karaiskos, I.
Plachouras, D.
Karvanen, M.
Pontikis, K.
Jansson, B.
Papadomichelakis, E.
Antoniadou, A.
Giamarellou, H.
Armaganidis, A.
Cars, O.
Friberg, L.E.
Περιοδικό:
Antimicrobial Agents and Chemotherapy
Τόμος:
56
Αριθμός / τεύχος:
8
Σελίδες:
4241-4249
Λέξεις-κλειδιά:
colistimethate, adult; antibacterial activity; article; creatinine clearance; critically ill patient; dialysis; drug binding; drug half life; female; Gram negative bacterium; health program; human; in vitro study; loading drug dose; major clinical study; male; necrotizing fasciitis; prediction; priority journal; prospective study; protein binding; Pseudomonas aeruginosa; ventilator associated pneumonia, Adult; Aged; Aged, 80 and over; Anti-Bacterial Agents; Colistin; Critical Illness; Dose-Response Relationship, Drug; Female; Gram-Negative Bacterial Infections; Humans; Male; Microbial Sensitivity Tests; Middle Aged; Prospective Studies; Protein Binding; Pseudomonas aeruginosa
Επίσημο URL (Εκδότης):
DOI:
10.1128/AAC.06426-11
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