Department of Nephrology, Topiwala Nair Medical College and BYL Nair Hospital, Mumbai, Maharashtra, India.
Saudi J Kidney Dis Transpl. 2021 Jul-Aug;32(4):1034-1042. doi: 10.4103/1319-2442.338277.
We aimed to study the effect of remdesivir therapy on renal and hepatic function in coronavirus disease-2019 (COVID-19) patients with renal dysfunction at baseline or after starting therapy and identify the factors, if any, related to the efficacy of remdesivir therapy on patient outcome. Patients included in the study were those who met all the following criteria irrespective of baseline glomerular filtration rate [including those already on maintenance hemodialysis (HD)] or baseline deranged liver function test. (1) Age >18 years, (2) COVID-19 reverse transcriptase-polymerase chain reaction positive, (3) Meeting criteria for administration of remdesivir - [any one of the following: (a) COVID-19 pneumonia with respiratory rate >30/min or SPO<94% on room air, (b) Acute respiratory distress syndrome (ARDS)]. (4) Renal dysfunction at baseline, during or within 48 h of completion of therapy. Thirty-four patients had renal dysfunction at baseline or developed it after remdesivir therapy - 16 were acute kidney injury (AKI), 10 chronic kidney diseases (CKD), four CKD stage 5D, and four were postrenal transplant. The overall mortality was 18/34 (52.9%). Eight out of 30 (26.66%) needed HD during or after therapy and of these, 15 died and among 15 survivors, 14 returned to their baseline renal function after cessation of therapy, one patient is still dialysis dependent. In the dialysis-dependent CKD (n = 4) subgroup, three died and one was discharged. In the postrenal transplant (n = 4) group, all developed AKI during or after the completion of therapy. None required HD, two returned to their baseline renal function, and two died. Only five had alanine aminotransferase elevation (×1 upper limit of normal) during or within 48 h of completion of therapy - three died and two returned to baseline. Lower PaO/FiO (severe ARDS) (P = 0.0001), higher C-reactive protein (P = 0.022), higher serum lactate dehydrogenase (P = 0.038), and duration of symptoms before starting therapy (P = 0.05) were statistically significant variables at baseline associated with higher mortality. Remdesivir can be tried in moderate-to-severe COVID-19 cases with renal dysfunction as a complete recovery of renal function was noted in survivors. However, larger and well-controlled studies evaluating its safety and efficacy in patients with AKI and CKD are needed.
我们旨在研究瑞德西韦治疗对基线或开始治疗后肾功能障碍的 2019 冠状病毒病(COVID-19)患者的肾脏和肝脏功能的影响,并确定与瑞德西韦治疗患者结局相关的任何因素。本研究纳入的患者符合以下所有标准,无论基线肾小球滤过率如何(包括已接受维持性血液透析(HD)的患者)或基线肝功能检查异常。(1)年龄>18 岁,(2)COVID-19 逆转录酶-聚合酶链反应阳性,(3)符合使用瑞德西韦的标准-以下任何一种:(a)呼吸频率>30/min 或在空气室内血氧饱和度<94%的 COVID-19 肺炎,(b)急性呼吸窘迫综合征(ARDS))。(4)基线、治疗期间或治疗完成后 48 小时内出现肾功能障碍。34 例患者基线时存在肾功能障碍或在接受瑞德西韦治疗后出现肾功能障碍-16 例为急性肾损伤(AKI),10 例为慢性肾脏病(CKD),4 例为 CKD 5D 期,4 例为肾移植后。总死亡率为 18/34(52.9%)。8/30(26.66%)例在治疗期间或治疗后需要进行 HD,其中 15 例死亡,在 15 例幸存者中,14 例在停止治疗后恢复到基线肾功能,1 例仍依赖透析。在依赖透析的 CKD(n=4)亚组中,3 例死亡,1 例出院。在肾移植后(n=4)组中,所有患者在完成治疗期间或之后均出现 AKI。无一例需要 HD,2 例恢复到基线肾功能,2 例死亡。仅有 5 例在完成治疗后 48 小时内出现丙氨酸氨基转移酶升高(×1 正常值上限)-3 例死亡,2 例恢复到基线。较低的 PaO/FiO(严重 ARDS)(P=0.0001)、较高的 C 反应蛋白(P=0.022)、较高的血清乳酸脱氢酶(P=0.038)和开始治疗前的症状持续时间(P=0.05)是与较高死亡率相关的基线统计学显著变量。瑞德西韦可用于中度至重度 COVID-19 合并肾功能障碍的患者,因为幸存者的肾功能完全恢复。然而,需要更大规模和对照良好的研究来评估其在 AKI 和 CKD 患者中的安全性和疗效。