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Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study

BACKGROUND & OBJECTIVES: There is little information concerning intravenously (i.v.) administered colistin in patients with multidrug-resistant (MDR) Gram-negative infections. Thus, this pilot prospective study was undertaken to characterize efficacy and pharmacokinetics of colistin in patients...

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Autores principales: Gautam, Vikas, Shafiq, Nusrat, Mouton, Johan W., Malhotra, Sameer, Kaur, Satinder, Ray, Pallab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057249/
https://www.ncbi.nlm.nih.gov/pubmed/29998877
http://dx.doi.org/10.4103/ijmr.IJMR_1464_16
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author Gautam, Vikas
Shafiq, Nusrat
Mouton, Johan W.
Malhotra, Sameer
Kaur, Satinder
Ray, Pallab
author_facet Gautam, Vikas
Shafiq, Nusrat
Mouton, Johan W.
Malhotra, Sameer
Kaur, Satinder
Ray, Pallab
author_sort Gautam, Vikas
collection PubMed
description BACKGROUND & OBJECTIVES: There is little information concerning intravenously (i.v.) administered colistin in patients with multidrug-resistant (MDR) Gram-negative infections. Thus, this pilot prospective study was undertaken to characterize efficacy and pharmacokinetics of colistin in patients with MDR Gram-negative infections. METHODS: Nine patients with age >12 yr and MDR Gram-negative infections were included, of whom six were given colistin at the doses of 2 MU, while three patients were given 1 MU i.v. dose every 8 h. Blood samples were collected at different time intervals. Determination of colistin concentration was done by a ultra-high-performance liquid chromatography/mass spectrometry/selected reaction monitoring assay. RESULTS: The area under the plasma concentration-versus-time curve over eight hours (AUC(0-8)) for colistin after the 1(st) dose ranged from 3.3 to 16.4 mg×h/l (median, 4.59). After the 5(th) dose, AUC(0-8) for colistin ranged from 4.4 to 15.8 mg×h/l (median, 6.0). With minimal inhibitory concentration (MIC) value of 0.125 mg/l, AUC(0-8)/MIC ranged from 26.7 to 131.4 (median, 36.7) and 35.5 to 126.0 (median, 48.0) after the 1(st) and the 5(th) doses of 2 MU every 8 h, respectively. INTERPRETATION & CONCLUSIONS: As there is a paucity of information on AUC/MIC for colistin, it may not be possible to conclude whether AUC/MIC values in our patients were adequate. There is a microbiological clearance of organism, which goes in favour of the dosing schedule being adequate. Further studies need to be done to understand the pharmacokinetics of colistin in patients with infections.
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spelling pubmed-60572492018-08-08 Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study Gautam, Vikas Shafiq, Nusrat Mouton, Johan W. Malhotra, Sameer Kaur, Satinder Ray, Pallab Indian J Med Res Original Article BACKGROUND & OBJECTIVES: There is little information concerning intravenously (i.v.) administered colistin in patients with multidrug-resistant (MDR) Gram-negative infections. Thus, this pilot prospective study was undertaken to characterize efficacy and pharmacokinetics of colistin in patients with MDR Gram-negative infections. METHODS: Nine patients with age >12 yr and MDR Gram-negative infections were included, of whom six were given colistin at the doses of 2 MU, while three patients were given 1 MU i.v. dose every 8 h. Blood samples were collected at different time intervals. Determination of colistin concentration was done by a ultra-high-performance liquid chromatography/mass spectrometry/selected reaction monitoring assay. RESULTS: The area under the plasma concentration-versus-time curve over eight hours (AUC(0-8)) for colistin after the 1(st) dose ranged from 3.3 to 16.4 mg×h/l (median, 4.59). After the 5(th) dose, AUC(0-8) for colistin ranged from 4.4 to 15.8 mg×h/l (median, 6.0). With minimal inhibitory concentration (MIC) value of 0.125 mg/l, AUC(0-8)/MIC ranged from 26.7 to 131.4 (median, 36.7) and 35.5 to 126.0 (median, 48.0) after the 1(st) and the 5(th) doses of 2 MU every 8 h, respectively. INTERPRETATION & CONCLUSIONS: As there is a paucity of information on AUC/MIC for colistin, it may not be possible to conclude whether AUC/MIC values in our patients were adequate. There is a microbiological clearance of organism, which goes in favour of the dosing schedule being adequate. Further studies need to be done to understand the pharmacokinetics of colistin in patients with infections. Medknow Publications & Media Pvt Ltd 2018-04 /pmc/articles/PMC6057249/ /pubmed/29998877 http://dx.doi.org/10.4103/ijmr.IJMR_1464_16 Text en Copyright: © 2018 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Gautam, Vikas
Shafiq, Nusrat
Mouton, Johan W.
Malhotra, Sameer
Kaur, Satinder
Ray, Pallab
Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title_full Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title_fullStr Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title_full_unstemmed Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title_short Pharmacokinetics of colistin in patients with multidrug-resistant Gram-negative infections: A pilot study
title_sort pharmacokinetics of colistin in patients with multidrug-resistant gram-negative infections: a pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057249/
https://www.ncbi.nlm.nih.gov/pubmed/29998877
http://dx.doi.org/10.4103/ijmr.IJMR_1464_16
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