Ide Satoshi, Saito Sho, Akazawa Tsubasa, Furuya Takahito, Masuda Junichi, Nagashima Maki, Asai Yusuke, Ogawa Tatsunori, Yamamoto Ryohei, Ishioka Haruhiko, Kanda Kohei, Okuhama Ayako, Wakimoto Yuji, Suzuki Tetsuya, Akiyama Yutaro, Miyazato Yusuke, Nakamura Keiji, Nakamoto Takato, Nomoto Hidetoshi, Moriyama Yuki, Ota Masayuki, Morioka Shinichiro, Matsuda Wataru, Uemura Tatsuki, Kobayashi Kentaro, Sasaki Ryo, Katagiri Daisuke, Kutsuna Satoshi, Hayakawa Kayoko, Ohmagari Norio
Disease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Emerging and Re-emerging Infectious Diseases, Graduate School of Medicine, Tohoku University, Sendai, Japan.
IDCases. 2021;26:e01343. doi: 10.1016/j.idcr.2021.e01343. Epub 2021 Nov 17.
Remdesivir is an antiviral drug that results in clinical improvement after five days of treatment and accelerates recovery by 31%. No studies have discussed the pharmacokinetic analysis of remdesivir in patients with severe COVID-19 requiring extracorporeal membrane oxygenation (ECMO). A 63-year-old American man who underwent mechanical ventilation and ECMO for severe COVID-19 was administered remdesivir for ten days. The loading dosage was 200 mg at 7 PM on day 12 and 100 mg daily at 0:00 PM from day 13-21, administered within 1 h. The pharmacokinetic analysis was performed. The serum creatinine concentration was within the normal range of 0.5-0.7 mg/dL during treatment. According to the pharmacokinetic analysis, the plasma concentrations of remdesivir and GS-441524 4 h after administration (C) were 662 ng/mL and 58 ng/mL, respectively, and the concentrations 18 h after administration (C) were 32 ng/mL and 44 ng/mL, respectively. Therefore, the half-life of remdesivir and GS-441524 was 3.2 and 35.1 h, respectively. Monitoring the plasma concentrations of remdesivir and GS-441524 in patients undergoing ECMO may be necessary.