External Validation of Obese/Critically Ill Vancomycin Population Pharmacokinetic Models in Critically Ill Patients Who Are Obese

医学 病危 体质指数 加药 人口 重症监护医学 万古霉素 回顾性队列研究 内科学 环境卫生 生物 细菌 遗传学 金黄色葡萄球菌
作者
Abdullah Alsultan,Shereen A. Dasuqi,Abdullah Almohaizeie,Abdullah Aljutayli,Fadi Aljamaan,Rasha A. Omran,Abdulaziz Alolayan,Mohammed A. Hamad,Haifa Alotaibi,Sarah Altamimi,Sarah S. Alghanem
出处
期刊:The Journal of Clinical Pharmacology [Wiley]
卷期号:64 (3): 353-361
标识
DOI:10.1002/jcph.2375
摘要

Abstract Obesity combined with critical illness might increase the risk of acquiring infections and hence mortality. In this patient population the pharmacokinetics of antimicrobials vary significantly, making antimicrobial dosing challenging. The objective of this study was to assess the predictive performance of published population pharmacokinetic models of vancomycin in patients who are critically ill or obese for a cohort of critically ill patients who are obese. This was a multi‐center retrospective study conducted at 2 hospitals. Adult patients with a body mass index of ≥30 kg/m 2 were included. PubMed was searched for published population pharmacokinetic studies in patients who were critically ill or obese. External validation was performed using Monolix software. A total of 4 models were identified in patients who were obese and 5 models were identified in patients who were critically ill. In total, 138 patients who were critically ill and obese were included, and the most accurate models for these patients were the Goti and Roberts models. In our analysis, models in patients who were critically ill outperformed models in patients who were obese. When looking at the most accurate models, both the Goti and the Roberts models had patient characteristics similar to ours in terms of age and creatinine clearance. This indicates that when selecting the proper model to apply in practice, it is important to account for all relevant variables, besides obesity.
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