Evidence map›Paper›PMID 37532840›Full record

ArticleInternational journal of clinical pharmacy2023

Feasibility of individualised patient modelling for continuous vancomycin infusions in outpatient antimicrobial therapy, a retrospective study.

J Nolan, K McCarthy, A Farkas, M L Avent

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Article in International journal of clinical pharmacy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing 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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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

J NolanThe Royal Brisbane and Women's Hospital, Herston, Australia. j.nolan@uq.edu.au.ORCID http://orcid.org/0009-0009-0092-8216
K McCarthyThe Royal Brisbane and Women's Hospital, Herston, Australia.
A FarkasMount Sinai West Hospital, New York, USA.
M L AventThe Royal Brisbane and Women's Hospital, Herston, Australia.ORCID http://orcid.org/0000-0001-7228-2834

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe area under the curve (AUC) to minimum inhibitory concentration (MIC) ratio is proposed as a therapeutic drug-monitoring parameter for dosing vancomycin continuous infusion in methicillin-resistant Staphylococcus aureus (MRSA) infection. Individualised pharmacokinetic-pharmacodynamic (PK/PD) calculation of AUC

aimTo compare real world TDM practice to theoretical, individualised, PK/PD target parameters utilising Bayesian predictions to steady state concentrations (Css) for outpatients on continuous vancomycin infusions.

methodA retrospective single centre study was conducted at a tertiary hospital on adult patients, enrolled in an outpatient parenteral antimicrobial therapy (OPAT) program, receiving vancomycin infusions for MRSA infection. Retrospective Bayesian dosing was modelled to target PK/PD parameters and compared to real world data.

resultsFifteen patients were evaluated with 53% (8/15) achieved target C

conclusionBayesian modelling could assist in obtaining more timely target parameters at lower doses for patients receiving continuous vancomycin infusion as part of an OPAT program, which may beget fewer adverse effects. Utilisation of personalised predictive modelling may optimise vancomycin prescribing, achieving earlier target concentrations as compared to empiric dosing regimens.

Indexed as

Anti-Infective AgentsMethicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsAdultAnti-Bacterial AgentsBayes TheoremFeasibility StudiesHumansOutpatientsRetrospective StudiesVancomycinAnti-Bacterial AgentsAnti-Infective AgentsVancomycinBayesian modellingInfusionOutpatient Parenteral Antimicrobial TherapyPDPKVancomycin

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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.