Therapeutic drug monitoring of commonly used anti-infective agents: A nationwide cross-sectional survey of Australian hospital practices.
Anti-Infective Agents
/ therapeutic use
Australia
Bacteria
/ drug effects
Bacterial Infections
/ drug therapy
Clinical Decision-Making
Cross-Sectional Studies
Drug Monitoring
/ methods
Fungi
/ drug effects
Gentamicins
/ therapeutic use
Health Personnel
/ psychology
Humans
Microbial Sensitivity Tests
Mycoses
/ drug therapy
Surveys and Questionnaires
Vancomycin
/ therapeutic use
Voriconazole
/ therapeutic use
Clinical practice
Gentamicin
Questionnaire
Therapeutic drug monitoring
Vancomycin
Voriconazole
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
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
106180Informations de copyright
Copyright © 2020.