BPB Reports

Paper Details

BPB Reports
Vol. 3 No. 2 p.65-69 2020
Report
Interaction Between Piperacillin/Tazobactam and Warfarin: a Single-Center Retrospective Single-Arm Cohort Study
  • Mitsuru Sugawara (Department of Pharmacy, Hokkaido University Hospital / Laboratory of Pharmacokinetics, Faculty of Pharmaceutical Sciences, Hokkaido University / msuga@pharm.hokudai.ac.jp)
Shota Kadomura 1) 2) , Yoh Takekuma 3) , Shungo Imai 4) , Hitoshi Kashiwagi 4) , Kotaro Kawamoto 1) , Tatsuya Itoh 1) , Mitsuru Sugawara 3) 4)
1) Department of Pharmacy, Japan Community Healthcare Organization Sapporo Hokushin Hospital , 2) Graduate School of Life Science, Hokkaido University , 3) Department of Pharmacy, Hokkaido University Hospital , 4) Laboratory of Pharmacokinetics, Faculty of Pharmaceutical Sciences, Hokkaido University
Received: January 26, 2020;   Accepted: March 09, 2020;   Released: March 16, 2020
Keywords: warfarin, drug-drug interaction, antibiotics, piperacillin/tazobactam, prothrombin time international normalized ratio
Abstracts

Antibiotics influence the anticoagulation effect of warfarin and increase the bleeding risk in patients who are receiving warfarin. Piperacillin/tazobactam (PIPC/TAZ) is commonly used to treat infections such as healthcare-associated infection. However, there have been few reports about the interaction between warfarin and PIPC/TAZ. In this study, we investigated the influence of PIPC/TAZ on the anticoagulation effect of warfarin in hospitalized patients. The primary outcome was elevation of prothrombin time international normalized ratio (PT-INR) after PIPC/TAZ administration. Secondary outcomes were the proportion of patients with supratherapeutic levels of PT-INR, discontinuation of administration or reduction in the dose of warfarin, bleeding, transfusion, and vitamin-K rescue. Fifteen patients were enrolled in this study. PT-INR elevation occurred in 11 (73.3%) of the 15 patients. The median value of PT-INR after administration of PIPC/TAZ was significantly higher than the value before administration: 2.22 (interquartile range (IQR), 2.05-2.76) and 1.90 (IQR, 1.36-2.45), respectively (p = 0.024). Three (20%) of the 15 patients had PT-INR over 4, and discontinuation of administration or reduction in the dose of warfarin was needed in 6 (40%) of the 15 patients. Bleeding occurred in one patient, transfusion was performed in one patient and vitamin-K rescue was performed in one patient. This study showed that PIPC/TAZ induced elevation of PT-INR in patients receiving warfarin and that discontinuation or reduction in the dose of warfarin was needed in 40% of the patients. Therefore, we recommend to close monitoring of PT-INR in patients treated with warfarin during PIPC/TAZ administration.