Wang Shan, Huynh Christy, Islam Shahidul, Malone Brian, Masani Naveed, Joseph D'Andrea
12297NYU Langone Hospital - Long Island, Mineola, NY.
J Intensive Care Med. 2022 Jun;37(6):764-768. doi: 10.1177/08850666211070521. Epub 2021 Dec 30.
Safety of remdesivir in patients with renal impairment is unknown. Incidence of liver injury secondary to remdesivir is also unknown. The objective of this study is to assess the incidence of acute kidney injury (AKI) and to trend the liver enzymes during remdesivir treatment and change in eGFR from baseline to end of treatment as well as 48 h post completion of remdesivir therapy.
This is a retrospective chart review study including adult patients admitted with COVID-19 receiving remdesivir with a baseline eGFR < 30 ml/min per 1.73 m^2 from December 2020 to May 2021. The primary outcome was to assess the incidence of AKI and hepatic injury. The secondary outcome was to assess the efficacy of remdesivir defined by change in oxygen requirement.
Seventy-one patients were included in the study. Patients experienced an improvement in eGFR from baseline (T0) to end of remdesivir treatment (T1), as well as 48 h after the end of the treatment (T2) ( + 30.3% and + 30.6% respectively, P < .0001). Creatinine reduced from baseline (T0) to T1 and T2 (-20.9% and -20.5% respectively, P < .0001). Creatinine clearance improved from baseline to T1 and T2 ( + 26.6% and + 26.2% respectively, p < .0001). Elevation of aminotransferase (AST) was observed at T1 ( + 2.5%, P = .727), however, AST reduction was seen at T2 (-15.8%, P = .021). Elevation in alanine transaminase (ALT) was observed at T1 and T2 ( + 25% and + 12%, P = .004 and P = .137 respectively). Both direct and total bilirubin remained stable and were not significantly changed from baseline.
Our study showed that remdesivir use in renally-impaired patients with eGFR < 30 ml/min is safe. Remdesivir may be considered as a therapeutic option in this population with COVID-19 infection.
瑞德西韦在肾功能损害患者中的安全性尚不清楚。瑞德西韦继发肝损伤的发生率也不清楚。本研究的目的是评估急性肾损伤(AKI)的发生率,并观察瑞德西韦治疗期间肝酶的变化趋势,以及从基线到治疗结束时和瑞德西韦治疗完成后48小时估算肾小球滤过率(eGFR)的变化。
这是一项回顾性病历审查研究,纳入了2020年12月至2021年5月期间因COVID-19入院且基线eGFR<30 ml/min per 1.73 m²并接受瑞德西韦治疗的成年患者。主要结局是评估AKI和肝损伤的发生率。次要结局是评估以氧需求变化定义的瑞德西韦的疗效。
71名患者纳入研究。患者的eGFR从基线(T0)到瑞德西韦治疗结束(T1)以及治疗结束后48小时(T2)均有改善(分别增加30.3%和30.6%,P<.0001)。肌酐从基线(T0)到T1和T2降低(分别降低20.9%和20.5%,P<.0001)。肌酐清除率从基线到T1和T2有所改善(分别增加26.6%和26.2%,P<.0001)。在T1时观察到转氨酶(AST)升高(增加2.5%,P = .727),然而,在T2时AST降低(降低15.8%,P = .021)。在T1和T2时观察到丙氨酸转氨酶(ALT)升高(分别增加25%和12%,P分别为.004和.137)。直接胆红素和总胆红素均保持稳定,与基线相比无显著变化。
我们的研究表明,在eGFR<30 ml/min的肾功能损害患者中使用瑞德西韦是安全的。瑞德西韦可被视为该COVID-19感染人群的一种治疗选择。