Dosing Regimen for Cefotaxime Should Be Adapted to the Stage of Renal Dysfunction in Critically Ill Adult Patients-A Retrospective Study

Cefotaxime administration is recommended in doses of 3-12 g/day in adults with a Glomerular Filtration Rate (GFR) > 5 mL/min. This study aimed to assess the impact of renal function and obesity on cefotaxime concentrations in intensive care unit (ICU) patients. A retrospective cohort study was co...

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Main Authors: Théo Dillies (Author), Sophie Perinel-Ragey (Author), Patricia Correia (Author), Jérôme Morel (Author), Guillaume Thiery (Author), Manon Launay (Author)
Format: Book
Published: MDPI AG, 2024-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Théo Dillies  |e author 
700 1 0 |a Sophie Perinel-Ragey  |e author 
700 1 0 |a Patricia Correia  |e author 
700 1 0 |a Jérôme Morel  |e author 
700 1 0 |a Guillaume Thiery  |e author 
700 1 0 |a Manon Launay  |e author 
245 0 0 |a Dosing Regimen for Cefotaxime Should Be Adapted to the Stage of Renal Dysfunction in Critically Ill Adult Patients-A Retrospective Study 
260 |b MDPI AG,   |c 2024-03-01T00:00:00Z. 
500 |a 10.3390/antibiotics13040313 
500 |a 2079-6382 
520 |a Cefotaxime administration is recommended in doses of 3-12 g/day in adults with a Glomerular Filtration Rate (GFR) > 5 mL/min. This study aimed to assess the impact of renal function and obesity on cefotaxime concentrations in intensive care unit (ICU) patients. A retrospective cohort study was conducted on consecutive ICU patients receiving continuous cefotaxime infusion between 2020 and 2022 [IRBN992021/CHUSTE]. Doses were not constant; consequently, a concentration-to-dose ratio (C/D) was considered. Statistical analysis was performed to assess the relationship between cefotaxime concentrations, renal function, and obesity. A total of 70 patients, median age 61 years, were included, with no significant difference in cefotaxime concentrations between obese and non-obese patients. However, concentrations varied significantly by GFR, with underdosing prevalent in patients with normal to increased renal function and overdosing in those with severely impaired renal function. Adjustment of cefotaxime dosing according to GFR was associated with improved target attainment. Cefotaxime dosing in critically ill patients should consider renal function, with higher initial doses required in patients with normal to increased GFR and lower doses in those with severely impaired renal function. Therapeutic drug monitoring may aid in optimising dosing regimens. Prospective studies are warranted to validate these findings and inform clinical practice. 
546 |a EN 
690 |a cefotaxime 
690 |a renal function 
690 |a therapeutic drug monitoring 
690 |a augmented renal clearance 
690 |a personalised medicine 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antibiotics, Vol 13, Iss 4, p 313 (2024) 
787 0 |n https://www.mdpi.com/2079-6382/13/4/313 
787 0 |n https://doaj.org/toc/2079-6382 
856 4 1 |u https://doaj.org/article/675da4c25e7b47e9879dc6ccc0f4946c  |z Connect to this object online.