論文

査読有り 国際誌
2021年10月18日

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

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
  • Shota Kadomura
  • ,
  • Shungo Imai
  • ,
  • Kenji Momo
  • ,
  • Yuki Sato
  • ,
  • Hitoshi Kashiwagi
  • ,
  • Tatsuya Itoh
  • ,
  • Mitsuru Sugawara
  • ,
  • Yoh Takekuma

28
7
開始ページ
10781552211034703
終了ページ
10781552211034703
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1177/10781552211034703

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.

リンク情報
DOI
https://doi.org/10.1177/10781552211034703
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34661469
ID情報
  • DOI : 10.1177/10781552211034703
  • PubMed ID : 34661469

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