Effects of piperacillin/tazobactam or cefepime on folinate dose in patients receiving high-dose methotrexate: A retrospective cohort study using Japanese administrative claims data

Author:

Kadomura Shota12ORCID,Imai Shungo3ORCID,Momo Kenji4ORCID,Sato Yuki3ORCID,Kashiwagi Hitoshi3ORCID,Itoh Tatsuya1,Sugawara Mitsuru356ORCID,Takekuma Yoh5ORCID

Affiliation:

1. Department of Pharmacy, Japan Community Healthcare Organization Sapporo Hokushin Hospital, Sapporo, Japan

2. Graduate School of Life Science, Hokkaido University, Sapporo, Japan

3. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan

4. Department of Hospital Pharmaceutics, School of Pharmacy, Showa University, Tokyo, Japan

5. Department of Pharmacy, Hokkaido University Hospital, Sapporo, Japan

6. Global Station for Biosurfaces and Drug Discovery, Hokkaido University, Sapporo, Japan

Abstract

Introduction Delayed methotrexate (MTX) clearance with the co-administration of piperacillin/tazobactam (PIPC/TAZ) has been reported. Penicillins have been associated with reduced MTX clearance but the evidence is limited. There are no cases described with cefepime but penicillins are listed as interacting with MTX. We aimed to reveal whether the co-administration of PIPC/TAZ or CFPM affects MTX clearance using data from an administrative database. Methods We used data from the JMDC database, a large insurance claims database constructed in Japan. We included patients who were prescribed PIPC/TAZ or CFPM between days 1 and 3 in high-dose MTX (HD-MTX). We compared one co-administration episode (with PIPC/TAZ or CFPM) to one control episode (without), as a match-control study of two different episodes in the same patient. The primary outcomes were the duration and cumulative dose of leucovorin (LV) as a surrogate indicator of delayed MTX clearance. Results Three patients who were co-administered PIPC/TAZ and 16 patients who were co-administered CFPM with HD-MTX were included. In the PIPC/TAZ group, the duration and the cumulative doses of LV were similar in co-administration and control episode (median 3.0 vs. 3.0 days and 288.0 vs. 219.0 mg). In the CFPM group, the duration and the cumulative doses of LV were not significantly different in co-administration and control episode (3.0 vs. 4.0 days and 169.5 vs. 258.0 mg). Conclusions Our findings revealed that PIPC/TAZ did not necessarily cause a delay in MTX clearance during HD-MTX therapy. Moreover, the co-administration of CFPM with HD-MTX did not affect MTX clearance.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Oncology

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