Evidence map›Paper›PMID 39964202›Full record

ArticleTherapeutic drug monitoring2025

Predictive Performance of Bayesian Dosing Software for Vancomycin in Intensive Care Unit Patients.

Gali Bai, Hui Qi, Yaqun Huang, Jiao Zhang, Huiying Zhao, Ruiting Wen, Xiaohong Zhang

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Article in Therapeutic drug monitoring, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Gali BaiDepartment of Pharmacy, Peking University People's Hospital, Beijing, China.
Hui QiBeijing Key Laboratory of Pediatric Respiratory Infection Diseases, Key Laboratory of Major Diseases in Children, Ministry of Education, National Clinical Research Center for Respiratory Diseases, Laboratory of Respiratory Diseases, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; and.
Yaqun HuangDepartment of Pharmacy, Peking University People's Hospital, Beijing, China.
Jiao ZhangDepartment of Pharmacy, Peking University People's Hospital, Beijing, China.
Huiying ZhaoDepartment of Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Ruiting WenDepartment of Pharmacy, Peking University People's Hospital, Beijing, China.ORCID 0000-0003-1551-0268
Xiaohong ZhangDepartment of Pharmacy, Peking University People's Hospital, Beijing, China.

Funding

Beijing Pharmaceutical Association clinical pharmacy research program LCYX-2022-12Peking University People's Hospital scientific research development funds RDL2022-42
6 · The paper itself

Abstract

backgroundAccording to the updated guidelines, Bayesian-derived area under the curve estimation is recommended to guide vancomycin dosing. However, the Bayesian dosing software that facilitates this procedure has not been adequately assessed in intensive care unit (ICU) patients. This study evaluated the performance of 3 commonly used Bayesian software programs in predicting vancomycin concentrations in ICU patients before they could be utilized for personalized dosing in this population.

methodsRetrospective data from adult ICU patients who were administered vancomycin intravenously were obtained to predict serum concentrations a priori (based solely on patient characteristics) or a posteriori (Bayesian forecasting using measured concentrations). The predictive performance was evaluated via bias and precision using relative bias (rBias) and relative root mean squared error, respectively.

resultsData from 139 patients with 284 vancomycin concentrations were evaluated using 3 software programs: SmartDose (He model), Pharmado (Yasuhara model), and PrecisePK (Rodvald and Goti model). All 3 programs showed clinically acceptable bias with the exception of the Goti model of PrecisePK in an a priori estimation (rBias, 27.44%). A relatively low level of precision in terms of relative root mean squared error was observed in all these programs, but with a marked improvement in the a posteriori estimation (27.69%-37.64%) compared with the a priori situation (45.12%-68.59%).

conclusionsBayesian dosing software is a potential tool for vancomycin dose optimization in ICU patients. Patients with different physiological and pathological features may be referred to specific Bayesian programs.

Indexed as

Anti-Bacterial AgentsSoftwareVancomycinAdultAgedArea Under CurveBayes TheoremDose-Response Relationship, DrugDrug MonitoringFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesAnti-Bacterial AgentsVancomycinBayesian dosing softwareintensive care unitpredictive performancetherapeutic drug monitoringvancomycin

Identifiers

PMID39964202
PMCPMC12422620

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.