Therapeutic drug monitoring of commonly used anti-infective agents: A nationwide cross-sectional survey of Australian hospital practices.


Journal

International journal of antimicrobial agents
ISSN: 1872-7913
Titre abrégé: Int J Antimicrob Agents
Pays: Netherlands
ID NLM: 9111860

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 13 06 2020
revised: 01 09 2020
accepted: 19 09 2020
pubmed: 29 9 2020
medline: 16 7 2021
entrez: 28 9 2020
Statut: ppublish

Résumé

When performed according to best-practice principles, therapeutic drug monitoring (TDM) can optimise anti-infective treatment and directly benefit clinical outcomes. We evaluated TDM performance and clinical decision-making for established anti-infective agents amongst Australian hospitals. A nationwide cross-sectional survey was conducted between August and September 2019. The survey consisted of multiple-choice questions regarding TDM of anti-infective agents in general as well as clinical vignettes specific to vancomycin, gentamicin and voriconazole. We sought to survey all Australian hospitals operating both in the public and private health sectors. Responses were captured from 85 unique institutions, from all Australian states and territories. Regarding guidelines, 26% of hospitals did not have endorsed guidelines to advise on the ordering, sampling and interpretation of TDM for any anti-infective agent. Admitting teams were predominantly responsible for ordering TDM (85%) and interpreting results (76%). Only 51% of hospitals had access to dose prediction software, with access generally better amongst principal referral (69%) (P = 0.01) and children's hospitals (100%) (P = 0.04). Whenever a laboratory-derived minimum inhibitory concentration (MIC) was not available to guide dosing decisions, a surrogate target MIC was assumed in 77% of hospitals. This was based on a 'worst-case' scenario infection in 11% of hospitals. The rates of clinical practice consistent with current guideline recommendations across all aspects of TDM were demonstrated to be 0% for vancomycin, 4% for gentamicin and 35% for voriconazole. At present, there is significant institutional variability in the clinical practice of TDM for anti-infective agents in Australia for established TDM drugs.

Identifiants

pubmed: 32987102
pii: S0924-8579(20)30386-1
doi: 10.1016/j.ijantimicag.2020.106180
pii:
doi:

Substances chimiques

Anti-Infective Agents 0
Gentamicins 0
Vancomycin 6Q205EH1VU
Voriconazole JFU09I87TR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106180

Informations de copyright

Copyright © 2020.

Auteurs

Sahand Imani (S)

School of Medicine, The University of Notre Dame Australia, Sydney, NSW, Australia; Hornsby Ku-ring-gai Hospital, Northern Sydney Local Health District, Sydney, NSW, Australia.

Jan-Willem Alffenaar (JW)

School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Westmead Hospital, Western Sydney Local Health District, Sydney, NSW, Australia; Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney, NSW, Australia.

Menino O Cotta (MO)

University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia; Centre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, QLD, Australia.

Kathryn Daveson (K)

Department of Infectious Diseases, Canberra Hospital, Canberra, ACT, Australia; Queensland Statewide Antimicrobial Stewardship Program, Metro North Hospital and Health Services, Brisbane, QLD, Australia.

Sebastiaan van Hal (S)

Department of Infectious Diseases and Microbiology, New South Wales Health Pathology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Cindy Lau (C)

School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Department of Pharmacy, St Vincent's Hospital, Sydney, NSW, Australia.

Debbie Marriott (D)

Department of Clinical Microbiology, SydPath, St Vincent's Hospital, Sydney, NSW, Australia; St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Sydney, NSW, Australia.

Jonathan Penm (J)

School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.

Jason A Roberts (JA)

University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia; Centre for Translational Anti-infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, QLD, Australia; Departments of Pharmacy and Intensive Care, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.

Alexis Tabah (A)

Intensive Care Unit, Redcliffe and Caboolture Hospitals, Brisbane, QLD, Australia; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.

Nicholas Trethewy (N)

School of Pharmacy, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.

Paul Williams (P)

University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia; Department of Pharmacy, Sunshine Coast University Hospital, Sunshine Coast, QLD, Australia.

Indy Sandaradura (I)

Westmead Hospital, Western Sydney Local Health District, Sydney, NSW, Australia; St Vincent's Clinical School, Faculty of Medicine, The University of New South Wales, Sydney, NSW, Australia; Westmead Clinical School, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia; Institute of Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead Hospital, Sydney, NSW, Australia. Electronic address: Indy.Sandaradura@health.nsw.gov.au.

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Classifications MeSH