| Title: | Impact of concomitant metamizole treatment on the exposure of mould-active triazoles |
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| Authors: | ID Vanneste, Dorian (Author)
ID De Booser, Ine (Author)
ID Nadrah, Kristina (Author)
ID Somrak, Matej (Author)
ID Gijsen, Matthias (Author)
ID Matos, Aleš (Author)
ID Kalan, Katja (Author)
ID Morlion, Bart (Author)
ID Rex, Steffen (Author)
ID Battelino, Saba (Author), et al. |
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| Files: |  PDF - Presentation file, download (257,71 KB)
MD5: CFAC9AF987509D913500E3D0895DBC7F
 URL - Source URL, visit https://onlinelibrary.wiley.com/doi/10.1111/myc.70173
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| Language: | English |
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| Typology: | 1.01 - Original Scientific Article |
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| Organization: |  UKC LJ - Ljubljana University Medical Centre
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| Abstract: | Aim: Metamizole is an analgesic drug with moderate cytochrome P450 (CYP) inductive properties. The antifungal triazoles aremetabolized by several CYP enzymes, but the interaction with metamizole remains poorly described. We investigated the influ-ence of metamizole on the exposure of voriconazole, isavuconazole, and posaconazole.Methods: Patients from UZ Leuven (Belgium) and Ljubljana University Medical Centre (Slovenia) receiving voriconazole, is-avuconazole, or posaconazole concomitantly with metamizole were included in the study. Routine therapeutic drug monitoring(TDM) measurements collected between January 2019 and December 2024 were retrieved retrospectively. TDM concentrationsoutside of concomitant therapy were collected as controls. The influence of metamizole and other clinically relevant covariateswas analysed using generalized estimating equations (GEE).Results: A total of 126 distinct treatments with a triazole from 115 patients, accounting for 392 measurements, were includedin the study. GEE analysis revealed a significant negative association between the 7-day cumulative metamizole dose and lowervoriconazole and posaconazole concentrations. Additionally, C-reactive protein had a positive association with voriconazole con-centrations. Only ICU admission and patient characteristics, that is, sex and weight, had a significant influence on isavuconazoleconcentrations.Conclusion: Concomitant therapy with metamizole led to lower voriconazole and posaconazole concentrations, presumablythrough induction of CYP enzymes and possibly UDP-glucuronyltransferase. We recommend avoiding concomitant use of meta-mizole with the antifungal triazoles to prevent underexposure and treatment failure or frequent TDM if the combination cannotbe avoided. Further studies are needed to confirm our findings and investigate the influence of metamizole on other triazoles |
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| Keywords: | drug interactions, metamizole, mould-active triazoles |
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| Publication status: | Published |
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| Publication version: | Version of Record |
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| Year of publishing: | 2026 |
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| Number of pages: | str. 1-7 |
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| Numbering: | Vol. 69, no. 5, no. 5, [article no.] e70173 |
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| PID: | 20.500.12556/DiRROS-31270  |
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| UDC: | 61 |
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| ISSN on article: | 1439-0507 |
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| DOI: | 10.1111/myc.70173 |
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| COBISS.SI-ID: | 279285763 |
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| Note: | Nasl. z nasl. zaslona;
Opis vira z dne 25. 5. 2026;
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| Publication date in DiRROS: | 23.07.2026 |
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| Views: | 96 |
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| Downloads: | 60 |
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