Cargando…
A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance
BACKGROUND: Using standard vancomycin dosage in critically ill patients might lead to therapy failure and worse patient outcomes, augmented renal clearance (ARC) may be the leading risk factor. In this study, we comprehensively investigated the pharmacokinetics-pharmacodynamics (PK-PD) of vancomycin...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658164/ https://www.ncbi.nlm.nih.gov/pubmed/33209680 http://dx.doi.org/10.21037/tau-20-1048 |
_version_ | 1783608608978632704 |
---|---|
author | He, Juan Yang, Zhi-Tao Qian, Xian Zhao, Bing Mao, En-Qiang Chen, Er-Zhen Bian, Xiao-Lan |
author_facet | He, Juan Yang, Zhi-Tao Qian, Xian Zhao, Bing Mao, En-Qiang Chen, Er-Zhen Bian, Xiao-Lan |
author_sort | He, Juan |
collection | PubMed |
description | BACKGROUND: Using standard vancomycin dosage in critically ill patients might lead to therapy failure and worse patient outcomes, augmented renal clearance (ARC) may be the leading risk factor. In this study, we comprehensively investigated the pharmacokinetics-pharmacodynamics (PK-PD) of vancomycin in critically ill patients with ARC, hoping to explore the precise and accurate dose adjustment method for vancomycin. METHODS: All critically ill patients tested for steady-state trough vancomycin serum concentrations during the recent 6 years in a tertiary level hospital were collected retrospectively and divided into ARC and non-ARC groups, respectively, according to creatinine clearance (CLcr). Serum vancomycin concentrations were measured by the fluorescence polarization immunoassay method. PK-PD parameters of vancomycin were recorded or calculated. The desired daily dose successful in achieving the lower target trough levels (10 mg/L) of vancomycin were investigated correspondingly. RESULTS: A total of 280 vancomycin concentrations were eligible for analysis. The ARC group (n=139) contained more male patients (64.7%) with average age and CLcr of 40 years old (P<0.05) and 180.8 mL/min (P<0.001), respectively. Those patients exhibited higher clearance (CL) and lower trough serum concentrations than the non-ARC patients under comparable daily doses of vancomycin. All the ICU patients demonstrated lower AUC(24h) values than the target level of 400 µg·h/mL, and this value showed a lower trend in the ARC group than the non-ARC group (232.9 vs. 316.2 µg·h/mL). Subtherapeutic trough concentrations of vancomycin (<10.0 mg/L) were observed in 77.7% and 68.8% of the ARC and non-ARC patients (P<0.05). The proportion of patients with a trough concentration of 10–15 and 15–20 mg/L was 17.9% and 4.3%, respectively, in the ARC group and 24.8% and 2.8%, respectively, in the non-ARC group., a daily dose of 46.0 and 35.5 mg/kg of vancomycin is needed, respectively, in the ARC and non-ARC group to achieve a target trough concentration of 10 mg/L. CONCLUSIONS: A higher dose of vancomycin is needed in critically ill patients, especially those with ARC, and appropriate TDM-guided dose adjustment should be considered to achieve the targeted therapeutic range and to provide dosing guidance for this: patient population. |
format | Online Article Text |
id | pubmed-7658164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-76581642020-11-17 A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance He, Juan Yang, Zhi-Tao Qian, Xian Zhao, Bing Mao, En-Qiang Chen, Er-Zhen Bian, Xiao-Lan Transl Androl Urol Original Article BACKGROUND: Using standard vancomycin dosage in critically ill patients might lead to therapy failure and worse patient outcomes, augmented renal clearance (ARC) may be the leading risk factor. In this study, we comprehensively investigated the pharmacokinetics-pharmacodynamics (PK-PD) of vancomycin in critically ill patients with ARC, hoping to explore the precise and accurate dose adjustment method for vancomycin. METHODS: All critically ill patients tested for steady-state trough vancomycin serum concentrations during the recent 6 years in a tertiary level hospital were collected retrospectively and divided into ARC and non-ARC groups, respectively, according to creatinine clearance (CLcr). Serum vancomycin concentrations were measured by the fluorescence polarization immunoassay method. PK-PD parameters of vancomycin were recorded or calculated. The desired daily dose successful in achieving the lower target trough levels (10 mg/L) of vancomycin were investigated correspondingly. RESULTS: A total of 280 vancomycin concentrations were eligible for analysis. The ARC group (n=139) contained more male patients (64.7%) with average age and CLcr of 40 years old (P<0.05) and 180.8 mL/min (P<0.001), respectively. Those patients exhibited higher clearance (CL) and lower trough serum concentrations than the non-ARC patients under comparable daily doses of vancomycin. All the ICU patients demonstrated lower AUC(24h) values than the target level of 400 µg·h/mL, and this value showed a lower trend in the ARC group than the non-ARC group (232.9 vs. 316.2 µg·h/mL). Subtherapeutic trough concentrations of vancomycin (<10.0 mg/L) were observed in 77.7% and 68.8% of the ARC and non-ARC patients (P<0.05). The proportion of patients with a trough concentration of 10–15 and 15–20 mg/L was 17.9% and 4.3%, respectively, in the ARC group and 24.8% and 2.8%, respectively, in the non-ARC group., a daily dose of 46.0 and 35.5 mg/kg of vancomycin is needed, respectively, in the ARC and non-ARC group to achieve a target trough concentration of 10 mg/L. CONCLUSIONS: A higher dose of vancomycin is needed in critically ill patients, especially those with ARC, and appropriate TDM-guided dose adjustment should be considered to achieve the targeted therapeutic range and to provide dosing guidance for this: patient population. AME Publishing Company 2020-10 /pmc/articles/PMC7658164/ /pubmed/33209680 http://dx.doi.org/10.21037/tau-20-1048 Text en 2020 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article He, Juan Yang, Zhi-Tao Qian, Xian Zhao, Bing Mao, En-Qiang Chen, Er-Zhen Bian, Xiao-Lan A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title | A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title_full | A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title_fullStr | A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title_full_unstemmed | A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title_short | A higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
title_sort | higher dose of vancomycin is needed in critically ill patients with augmented renal clearance |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658164/ https://www.ncbi.nlm.nih.gov/pubmed/33209680 http://dx.doi.org/10.21037/tau-20-1048 |
work_keys_str_mv | AT hejuan ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT yangzhitao ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT qianxian ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT zhaobing ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT maoenqiang ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT chenerzhen ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT bianxiaolan ahigherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT hejuan higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT yangzhitao higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT qianxian higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT zhaobing higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT maoenqiang higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT chenerzhen higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance AT bianxiaolan higherdoseofvancomycinisneededincriticallyillpatientswithaugmentedrenalclearance |