Evidence map›Paper›PMID 42622795›Full record

ArticleDrugs - real world outcomes2026

Association Between Follow-Up Therapeutic Drug Monitoring and Vancomycin-Induced Nephrotoxicity: A Claims Database Study.

Tomoyuki Yamada, Shungo Imai, Kenta Minami, Taku Ogawa, Akira Ukimura, Masami Nishihara, Masashi Neo

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Article in Drugs - real world outcomes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tomoyuki YamadaDepartment of Pharmacy, Osaka Medical and Pharmaceutical University Hospital, 2-7, Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan. tomoyuki.yamada.cd@ompu.ac.jp.ORCID http://orcid.org/0000-0001-8993-4333
Shungo ImaiKeio University Faculty of Pharmacy, 1-5-30, Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.ORCID http://orcid.org/0000-0001-5706-613X
Kenta MinamiDepartment of Clinical Laboratory, Osaka Police Hospital, 10-31, Kitayama-cho, Tennouji-ku, Osaka, 543-0035, Japan.
Taku OgawaInfection Control Center, Osaka Medical and Pharmaceutical University Hospital, 2-7, Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan.ORCID http://orcid.org/0000-0003-1569-4642
Akira UkimuraInfection Control Center, Osaka Medical and Pharmaceutical University Hospital, 2-7, Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan.
Masami NishiharaDepartment of Pharmacy, Osaka Medical and Pharmaceutical University Hospital, 2-7, Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan.
Masashi NeoDepartment of Pharmacy, Osaka Medical and Pharmaceutical University Hospital, 2-7, Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn vancomycin treatment, follow-up therapeutic drug monitoring (TDM) within 1 week after the initial TDM is recommended in patients with dose change after the initial TDM or high risk of vancomycin-induced nephrotoxicity (VIN); however, the effectiveness of follow-up TDM implementation remains unclear. This study aimed to delineate outcomes of follow-up TDM after the initial assessment under real-world conditions in Japan and clarify its association with VIN.

methodsRetrospective data analysis was conducted using a Japanese health insurance claims database. Approval was granted by the Ethics Committee of Osaka Medical and Pharmaceutical University (protocol number: 2022-105). Adult patients who received intravenous vancomycin, excluding those without a dose change after the initial TDM and without risk of VIN between January 2020 and December 2021, were included. Follow-up TDM was defined as conducting TDM within 1 week after the initial assessment. The association between performing follow-up TDM and the occurrence of VIN was assessed in patients with dose change after the initial TDM or high risk of VIN.

resultsAmong 492 patients who underwent the initial TDM, 403 (81.9%) had follow-up TDM performed. Cox proportional hazards model analysis revealed that follow-up TDM was associated with a lower occurrence of VIN after adjustment for estimated glomerular filtration rate <30 mL/min/1.73 m

conclusionThis study found that follow-up TDM was associated with a lower occurrence of VIN, supporting guidelines recommending follow-up TDM in vancomycin therapy. Health providers should consider conducting follow-up TDM to potentially lower the occurrence of VIN, although further prospective studies are warranted to clarify its independent effect.

Identifiers

PMID42622795
PMCPMC13570862

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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.