A Risk Prediction Flowchart of Vancomycin-Induced Acute Kidney Injury to Use When Starting Vancomycin Administration: A Multicenter Retrospective Study
Takayuki Miyai,
Shungo Imai,
Hitoshi Kashiwagi,
Yuki Sato,
Shota Kadomura,
Kenji Yoshida,
Eri Yoshimura,
Toshiaki Teraya,
Takashi Tsujimoto,
Yukari Kawamoto,
Tatsuya Itoh,
Hidefumi Ueno,
Yoshikazu Goto,
Yoh Takekuma,
Mitsuru Sugawara
Affiliations
Takayuki Miyai
Graduate School of Life Science, Hokkaido University, Sapporo 060-0810, Japan
Shungo Imai
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
Hitoshi Kashiwagi
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
Yuki Sato
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
Shota Kadomura
Department of Pharmacy, Japan Community Healthcare Organization Sapporo Hokushin Hospital, Sapporo 004-8618, Japan
Kenji Yoshida
Department of Pharmacy, Sunagawa City Medical Center, Sunagawa 073-0196, Japan
Eri Yoshimura
Department of Pharmacy, Sunagawa City Medical Center, Sunagawa 073-0196, Japan
Toshiaki Teraya
Department of Pharmacy, Sapporo City General Hospital, Sapporo 060-8604, Japan
Takashi Tsujimoto
Department of Pharmacy, Sapporo City General Hospital, Sapporo 060-8604, Japan
Yukari Kawamoto
Department of Pharmacy, Sapporo City General Hospital, Sapporo 060-8604, Japan
Tatsuya Itoh
Department of Pharmacy, Japan Community Healthcare Organization Sapporo Hokushin Hospital, Sapporo 004-8618, Japan
Hidefumi Ueno
Department of Pharmacy, Sunagawa City Medical Center, Sunagawa 073-0196, Japan
Yoshikazu Goto
Department of Pharmacy, Sapporo City General Hospital, Sapporo 060-8604, Japan
Yoh Takekuma
Department of Pharmacy, Hokkaido University Hospital, Sapporo 060-8648, Japan
Mitsuru Sugawara
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
We previously constructed a risk prediction model of vancomycin (VCM)-associated nephrotoxicity for use when performing initial therapeutic drug monitoring (TDM), using decision tree analysis. However, we could not build a model to be used at the time of initial administration due to insufficient sample size. Therefore, we performed a multicenter study at four hospitals in Japan. We investigated patients who received VCM intravenously at a standard dose from the first day until the initial TDM from November 2011 to March 2019. Acute kidney injury (AKI) was defined according to the criteria established by the “Kidney disease: Improving global outcomes” group. We extracted potential risk factors that could be evaluated on the day of initial administration and constructed a flowchart using a chi-squared automatic interaction detection algorithm. Among 843 patients, 115 (13.6%) developed AKI. The flowchart comprised three splitting variables (concomitant drugs (vasopressor drugs and tazobactam/piperacillin) and body mass index ≥ 30) and four subgroups. The incidence rates of AKI ranged from 9.34 to 36.8%, and they were classified as low-, intermediate-, and high-risk groups. The accuracy of flowchart was judged appropriate (86.4%). We successfully constructed a simple flowchart predicting VCM-induced AKI to be used when starting VCM administration.