Vancomycin MIC creep progresses in methicillin-resistant Staphylococcus aureus despite the national antimicrobial stewardship campaign: Single facility data in Japan.


Journal

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
ISSN: 1437-7780
Titre abrégé: J Infect Chemother
Pays: Netherlands
ID NLM: 9608375

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 04 02 2022
revised: 14 03 2022
accepted: 18 03 2022
pubmed: 31 3 2022
medline: 14 5 2022
entrez: 30 3 2022
Statut: ppublish

Résumé

Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of nosocomial and community infections, and vancomycin (VCM) is widely recommended as a first-line therapeutic drug. Minimum inhibitory concentrations (MICs) of VCM ≤2 μg/mL are defined as susceptible, but increases in these levels, known as "VCM MIC creep" have been reported. The aim of this study was to investigate VCM MIC creep during the promotion of a national antimicrobial stewardship campaign. We collected data from 2013 to 2020 on S. aureus isolated at the clinical microbiology laboratory at Okayama University Hospital, Japan. We calculated the annual proportions of MRSA isolation rates by MIC levels for nosocomial and community samples and estimated annual percentage changes in the antimicrobial use density of the VCM. Of the 1,716 MRSA isolates, no strains showed intermediate or resistant ranges of VCM MIC levels. By 2020, the proportion of MRSA with an MIC of ≤0.5 μg/mL decreased to 35.4%, while that with an MIC of 1 μg/mL increased to 64.1% over time. The annual percentage changes of the VCM antimicrobial use density significantly increased without any trend change point (average 8.1%, p = 0.035). There was no clear correlation between the VCM AUD and annual proportion of nosocomial MRSA with MIC 1 μg/mL (correlation coefficient 0.48; p value = 0.24). We demonstrated a deteriorating situation of VCM MIC creep among MRSA strains isolated at our university hospital during the national antimicrobial stewardship campaign.

Sections du résumé

BACKGROUND BACKGROUND
Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of nosocomial and community infections, and vancomycin (VCM) is widely recommended as a first-line therapeutic drug. Minimum inhibitory concentrations (MICs) of VCM ≤2 μg/mL are defined as susceptible, but increases in these levels, known as "VCM MIC creep" have been reported. The aim of this study was to investigate VCM MIC creep during the promotion of a national antimicrobial stewardship campaign.
METHODS METHODS
We collected data from 2013 to 2020 on S. aureus isolated at the clinical microbiology laboratory at Okayama University Hospital, Japan. We calculated the annual proportions of MRSA isolation rates by MIC levels for nosocomial and community samples and estimated annual percentage changes in the antimicrobial use density of the VCM.
RESULTS RESULTS
Of the 1,716 MRSA isolates, no strains showed intermediate or resistant ranges of VCM MIC levels. By 2020, the proportion of MRSA with an MIC of ≤0.5 μg/mL decreased to 35.4%, while that with an MIC of 1 μg/mL increased to 64.1% over time. The annual percentage changes of the VCM antimicrobial use density significantly increased without any trend change point (average 8.1%, p = 0.035). There was no clear correlation between the VCM AUD and annual proportion of nosocomial MRSA with MIC 1 μg/mL (correlation coefficient 0.48; p value = 0.24).
CONCLUSION CONCLUSIONS
We demonstrated a deteriorating situation of VCM MIC creep among MRSA strains isolated at our university hospital during the national antimicrobial stewardship campaign.

Identifiants

pubmed: 35351391
pii: S1341-321X(22)00096-4
doi: 10.1016/j.jiac.2022.03.017
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Vancomycin 6Q205EH1VU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

918-922

Informations de copyright

Copyright © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

Takumi Fujimori (T)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Hideharu Hagiya (H)

Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, 700-8558, Japan. Electronic address: hagiya@okayama-u.ac.jp.

Koji Iio (K)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Tsukasa Higashionna (T)

Department of Pharmacy, Okayama University Hospital, Okayama, 700-8558, Japan.

Ayaka Kakehi (A)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Mami Okura (M)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Hiroshi Minabe (H)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Yukika Yokoyama (Y)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

Fumio Otsuka (F)

Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, 700-8558, Japan.

Akihito Higashikage (A)

Microbiology Division, Clinical Laboratory, Okayama University Hospital, Okayama, 700-8558, Japan.

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