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Author
Bando, Takashi Department of Pharmacy, Tokushima University Hospital
Chuma, Masayuki Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital
Hamano, Hirofumi Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences
Niimura, Takahiro Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital
Okada, Naoto Department of Pharmacy, Tokushima University Hospital
Kondo, Masateru Department of Pharmacy, Tokushima University Hospital
Izumi, Yuki Department of Pharmacy, Tokushima University Hospital
Ishida, Shunsuke Department of Pharmacy, Tokushima University Hospital
Yoshioka, Toshihiko Department of Pharmacy, Tokushima University Hospital
Asada, Mizuho Department of Medical Molecular Informatics, Meiji Pharmaceutical University
Zamami, Yoshito Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences ORCID Kaken ID publons researchmap
Takechi, Kenshi Department of Drug Information Analysis, College of Pharmaceutical Sciences, Matsuyama University
Goda, Mitsuhiro Department of Pharmacy, Tokushima University Hospital
Miyata, Koji Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences
Yagi, Kenta Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital
Izawa-Ishizawa, Yuki Department of Pharmacology, Tokushima University Graduate School of Biomedical Sciences
Azuma, Momoyo Department of Infection Control and Prevention, Tokushima University Hospital
Yanagawa, Hiroaki Department of Nursing, Faculty of Health and Welfare, Tokushima Bunri University
Tasaki, Yoshikazu Department of Hospital Pharmacy and Pharmacology, Asahikawa Medical University
Ishizawa, Keisuke Department of Pharmacy, Tokushima University Hospital
Abstract
There is a growing concern about the relationship between vancomycin-associated nephrotoxicity (VAN) and concomitant use of nephrotoxins. We examined this relationship by combined retrospective analyses of two real-world databases. Initially, the FDA Adverse Event Reporting System (FAERS) was analyzed for the effects of concomitant use of one or more nephrotoxins on VAN and the types of combinations of nephrotoxins that exacerbate VAN. Next, electronic medical records (EMRs) of patients who received vancomycin (VCM) at Tokushima University Hospital between January 2006 and March 2019 were examined to confirm the FAERS analysis. An elevated reporting odds ratio (ROR) was observed with increases in the number of nephrotoxins administered (VCM + one nephrotoxin, adjusted ROR (95% confidence interval [CI]) 1.67 [1.51-1.85]; VCM + ≥2 nephrotoxins, adjusted ROR [95% CI] 1.54 [1.37-1.73]) in FAERS. EMRs analysis showed that the number of nephrotoxins was associated with higher incidences of VAN [odds ratio: 1.99; 95% CI: 1.42-2.78]. Overall, concomitant use of nephrotoxins was associated with an increased incidence of VAN, especially when at least one of those nephrotoxins was a renal hypoperfusion medication (furosemide, non-steroidal anti-inflammatory drugs, and vasopressors). The concomitant use of multiple nephrotoxins, especially including renal hypoperfusion medication, should be avoided to prevent VAN.
Keywords
vancomycin-associated nephrotoxicity
polypharmacy
nephrotoxin
spontaneous adverse event reporting database
electronic medical records
Amo Type
Original Article
Publication Title
Acta Medica Okayama
Published Date
2023-12
Volume
volume77
Issue
issue6
Publisher
Okayama University Medical School
Start Page
595
End Page
605
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
Copyright Ⓒ 2023 by Okayama University Medical School
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publisher
Refereed
True
PubMed ID
Web of Science KeyUT