Department of Anaesthesiology and Intensive Care, 1st Faculty of Medicine, Charles University and General University Hospital in Prague, U Nemocnice 2, Prague 2, Prague, 12800, Czech Republic.
Department of Anaesthesiology and Intensive Care, 3rd Faculty of Medicine, Charles University and Kralovske Vinohrady University Hospital in Prague, Prague, Czech Republic.
Sci Rep. 2024 Sep 6;14(1):20825. doi: 10.1038/s41598-024-71588-9.
Remdesivir therapy has been declared as efficient in the early stages of Covid-19. Of the 339 patients (males 55.8%, age 71(59;77) years) with a detectable viral load, 140 were treated with remdesivir (of those 103 in the ICU and 57 immunosuppressed) and retrospectively compared with 199 patients (of those 82 in the ICU and 28 immunosuppressed) who were denied therapy due to advanced Covid-19. The viral load was estimated by detecting nucleocapsid antigen in serum (n = 155, median 217(28;1524)pg/ml), antigen in sputum (n = 18, COI 18(4.6;32)), nasopharyngeal antigen (n = 44, COI 17(8;35)) and the real-time PCR (n = 122, Ct 21(18;27)). After adjustment for confounders, patients on remdesivir had better 12-month survival (HR 0.66 (0.44;0.98), p = 0.039), particularly when admitted to the ICU (HR 0.49 (0.29;0.81), p = 0.006). For the immunocompromised patients, the difference did not reach statistical significance (HR 0.55 (0.18;1.69), p = 0.3). The other most significant confounders were age, ICU admission, mechanical ventilation, leukocyte/lymphocyte ratio, admission creatinine and immunosuppression. The impact of monoclonal antibodies or previous vaccinations was not significant. Despite frequent immune suppression including haemato-oncology diseases, lymphopenia, and higher inflammatory markers in the remdesivir group, the results support remdesivir administration with respect to widely available estimates of viral load in patients with high illness severity.
瑞德西韦治疗在新冠病毒感染的早期阶段已被证实有效。在 339 例可检测到病毒载量的患者(男性 55.8%,年龄 71(59;77) 岁)中,有 140 例接受了瑞德西韦治疗(其中 103 例在 ICU,57 例免疫抑制),并与因新冠病毒感染进展而拒绝治疗的 199 例患者(其中 82 例在 ICU,28 例免疫抑制)进行了回顾性比较。病毒载量通过检测血清中的核衣壳抗原(n=155,中位数 217(28;1524)pg/ml)、痰中的抗原(n=18,COI 18(4.6;32))、鼻咽部抗原(n=44,COI 17(8;35))和实时 PCR(n=122,Ct 21(18;27))来估计。调整混杂因素后,接受瑞德西韦治疗的患者 12 个月生存率更好(HR 0.66(0.44;0.98),p=0.039),尤其是在 ICU 住院的患者(HR 0.49(0.29;0.81),p=0.006)。对于免疫抑制患者,差异无统计学意义(HR 0.55(0.18;1.69),p=0.3)。其他最重要的混杂因素是年龄、入住 ICU、机械通气、白细胞/淋巴细胞比值、入院时肌酐和免疫抑制。单克隆抗体或既往疫苗接种的影响不显著。尽管瑞德西韦组经常发生免疫抑制,包括血液肿瘤疾病、淋巴细胞减少和更高的炎症标志物,但结果支持在病情严重的患者中根据广泛存在的病毒载量估计值给予瑞德西韦治疗。