Park Somi, Kim A Reum, Lee Jiyoung, Kang Sung-Woon, Sung Heungsup, Kim Mi-Na, Chang Euijin, Bae Seongman, Jung Jiwon, Kim Min Jae, Kim Sung-Han, Lee Sang-Oh, Choi Sang-Ho, Kim Yang Soo, Song Eun Hee, Chong Yong Pil
Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Department of Laboratory Meidicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
J Infect Chemother. 2024 Apr;30(4):366-370. doi: 10.1016/j.jiac.2023.10.026. Epub 2023 Nov 5.
Though remdesivir benefits COVID-19 patients, its use in those with renal dysfunction is currently limited due to concerns about possible toxic effects of accumulated sulfobutylether-β-cyclodextrin (SBECD) on liver and kidney. We examined renal and hepatic function for a month in renally-impaired COVID-19 patients who were treated or not treated with remdesivir to assess the safety of the drug. A retrospective study was performed in adult COVID-19 patients with glomerular filtration rates of <30 ml/min/1.73 m at admission to a tertiary care hospital between November 2020 and March 2022. Data on serum creatinine and liver chemistry were collected serially. A total of 101 patients with impaired renal function were analyzed, comprising 64 remdesivir-treated patients and 37 who did not receive any antiviral agent. Although remdesivir-treated patients were more likely to be infected with the Omicron variant (79.7% vs. 48.6%), baseline characteristics did not differ significantly between the two groups. Among patients who initially did not require dialysis, 18.4% (7/38) of remdesivir-treated patients developed acute kidney injury (AKI) at days 4-6, compared with 51.7% (15/29) of non-remdesivir-treated patients. Liver injury severity worsened in 3.1% (2/64) of remdesivir-treated patients and 5.4% (2/37) of non-remdesivir-treated patients at days 4-6. In addition, there was no significant increase in AKI and liver injury over time in remdesivir-treated patients, and there were no cases of discontinuation of remdesivir due to adverse reactions. Concerns regarding the safety of SBECD should not lead to hasty withholding of remdesivir treatment in renally-impaired COVID-19 patients.
尽管瑞德西韦对新冠肺炎患者有益,但由于担心磺丁基醚-β-环糊精(SBECD)蓄积对肝脏和肾脏可能产生的毒性作用,目前其在肾功能不全患者中的应用受到限制。我们对接受或未接受瑞德西韦治疗的肾功能受损新冠肺炎患者的肾功能和肝功能进行了为期一个月的检查,以评估该药物的安全性。对2020年11月至2022年3月期间入住三级医院时肾小球滤过率<30 ml/min/1.73 m² 的成年新冠肺炎患者进行了一项回顾性研究。连续收集血清肌酐和肝功能数据。共分析了101例肾功能受损患者,其中64例接受瑞德西韦治疗,37例未接受任何抗病毒药物治疗。尽管接受瑞德西韦治疗的患者感染奥密克戎变异株的可能性更高(79.7%对48.6%),但两组的基线特征无显著差异。在最初不需要透析的患者中,接受瑞德西韦治疗的患者中有18.4%(7/38)在第4至6天发生急性肾损伤(AKI),而未接受瑞德西韦治疗的患者中这一比例为51.7%(15/29)。在第4至6天,接受瑞德西韦治疗的患者中有3.1%(2/64)的肝损伤严重程度加重,未接受瑞德西韦治疗的患者中有5.4%(2/37)的肝损伤严重程度加重。此外,接受瑞德西韦治疗的患者中,AKI和肝损伤并未随时间显著增加,也没有因不良反应而停用瑞德西韦的病例。对于SBECD安全性的担忧不应导致匆忙停止对肾功能受损的新冠肺炎患者使用瑞德西韦治疗。