A simulation of loading doses for vancomycin continuous infusion regimens in intensive care
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F17%3A10364155" target="_blank" >RIV/00216208:11110/17:10364155 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1080/23744235.2017.1328741" target="_blank" >http://dx.doi.org/10.1080/23744235.2017.1328741</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/23744235.2017.1328741" target="_blank" >10.1080/23744235.2017.1328741</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
A simulation of loading doses for vancomycin continuous infusion regimens in intensive care
Popis výsledku v původním jazyce
Background: Delayed achievement of target vancomycin serum concentrations may adversely affect clinical outcomes. The objective of this retrospective study was to compare the prediction accuracy of different body weight descriptors for volume of distribution and to propose an optimal loading dose (LD) for continuous infusion regimens in adults.Methods: Pharmacokinetic variables were computed using one-compartmental analysis. Simulated LDs of vancomycin were evaluated for each patient.Results: Volume of distribution, clearance, and half-life median values (interquartile range) for vancomycin in the study population (n = 30) were 0.45 (0.39-0.61) L.kg(-1), 0.026 (0.015-0.040) L.h(-1).kg(-1), and 10.3 (7.7-21.3) h, respectively. The observed volume of distribution was better predicted by total body weight (TBW) than by the ideal body weight or the adjusted body weight.Conclusions: An LD of 10.7 mg per kg TBW was optimal in our study population. Using this LD, 17.9% of simulated vancomycin serum levels were just below the therapeutic range, only 10.7% concentrations exceeded the target range and no concentration was toxic. The use of a LD would lead to reduced median time to reach target concentrations from 17 to 1h.
Název v anglickém jazyce
A simulation of loading doses for vancomycin continuous infusion regimens in intensive care
Popis výsledku anglicky
Background: Delayed achievement of target vancomycin serum concentrations may adversely affect clinical outcomes. The objective of this retrospective study was to compare the prediction accuracy of different body weight descriptors for volume of distribution and to propose an optimal loading dose (LD) for continuous infusion regimens in adults.Methods: Pharmacokinetic variables were computed using one-compartmental analysis. Simulated LDs of vancomycin were evaluated for each patient.Results: Volume of distribution, clearance, and half-life median values (interquartile range) for vancomycin in the study population (n = 30) were 0.45 (0.39-0.61) L.kg(-1), 0.026 (0.015-0.040) L.h(-1).kg(-1), and 10.3 (7.7-21.3) h, respectively. The observed volume of distribution was better predicted by total body weight (TBW) than by the ideal body weight or the adjusted body weight.Conclusions: An LD of 10.7 mg per kg TBW was optimal in our study population. Using this LD, 17.9% of simulated vancomycin serum levels were just below the therapeutic range, only 10.7% concentrations exceeded the target range and no concentration was toxic. The use of a LD would lead to reduced median time to reach target concentrations from 17 to 1h.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30104 - Pharmacology and pharmacy
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Infectious Diseases
ISSN
2374-4235
e-ISSN
—
Svazek periodika
49
Číslo periodika v rámci svazku
9
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
6
Strana od-do
674-679
Kód UT WoS článku
000403158500005
EID výsledku v databázi Scopus
2-s2.0-85019210992