Unit of Infectious Diseases, Virgen de las Nieves University Hospital/Instituto de Investigación Biosanitario (IBS)-Granada, Spain.
Medicine (Baltimore). 2021 Sep 17;100(37):e27228. doi: 10.1097/MD.0000000000027228.
Remdesivir is the only antiviral approved for lower respiratory tract infection produced by SARS-CoV-2. The main objective of this study was to determine the mortality rate, readmissions, mean hospital stay, need for higher levels of oxygen support, and adverse effect-induced abandonment rate in hospitalized patients diagnosed with COVID-19 and treated with remdesivir (RDSV). The secondary objective was to determine mortality-related risk factors in these patients.The study included a prospective cohort of patients admitted to a third level Spanish hospital between July 5, 2020 and February 3, 2021 for COVID-19 diagnosed by SARS-CoV-2 polymerase chain reaction and/or antigen test and treated with RDSV.Remdesivir was received by 185 patients (69.7% males) with a mean age of 62.5 years, median Charlson index of 3 (interquartile range [IQR]: 1-4), and median ambient air oxygen saturation of 91% (IQR: 90-93); 61.6% of patients had hyper-inflammatory syndrome at admission. Median time with symptoms before RDSV treatment was 5 days (IQR: 3-6) and the median hospital stay was 10 days (IQR: 7-15); 19 patients (10.3%) died after a median stay of 13.5 days (IQR: 9.7-24 days), 58 patients (12.9%) were admitted to ICU, 58 (31.4%) needed higher levels of oxygen support, 0.5% abandoned the treatment due to adverse effects, and there were no readmissions. The only mortality-related factor was the need for higher levels of oxygen support (odds ratio 12.02; 95% confidence interval 2.25-64.2).All studied patients were admitted to hospital with a diagnosis of COVID-19 and in respiratory failure, needing initial low-flow oxygen support, and all received RDSV within 1 week of symptom onset. The percent mortality was lower in these patients than was observed in all patients with severe COVID-19 admitted to our center (10.3% vs 20.3%, respectively). Despite receiving RDSV, 1 in 3 patients needed higher levels of oxygen support, the sole mortality-related factor.
瑞德西韦是唯一批准用于治疗由 SARS-CoV-2 引起的下呼吸道感染的抗病毒药物。本研究的主要目的是确定住院的 COVID-19 患者接受瑞德西韦(RDSV)治疗后的死亡率、再入院率、平均住院时间、需要更高水平的氧气支持以及因不良事件而停药的比例,并确定这些患者的死亡相关危险因素。本研究纳入了 2020 年 7 月 5 日至 2021 年 2 月 3 日期间因 COVID-19 住院的西班牙三级医院的患者前瞻性队列,这些患者的 SARS-CoV-2 聚合酶链反应和/或抗原检测阳性,并接受了 RDSV 治疗。
共纳入 185 名患者(69.7%为男性),平均年龄 62.5 岁,Charlson 合并症指数中位数为 3(四分位距 [IQR]:1-4),环境空气血氧饱和度中位数为 91%(IQR:90-93%);入院时 61.6%的患者存在高炎症综合征。在接受 RDSV 治疗前,中位症状持续时间为 5 天(IQR:3-6),中位住院时间为 10 天(IQR:7-15);19 名患者(10.3%)在中位住院时间 13.5 天后死亡(IQR:9.7-24 天),58 名患者(12.9%)转入 ICU,58 名患者(31.4%)需要更高水平的氧气支持,0.5%的患者因不良事件停药,无再入院患者。唯一与死亡相关的因素是需要更高水平的氧气支持(比值比 12.02;95%置信区间 2.25-64.2)。
所有研究患者均因 COVID-19 住院,呼吸衰竭,需要初始低流量氧气支持,所有患者均在症状出现后 1 周内接受了 RDSV 治疗。与本中心收治的所有重症 COVID-19 患者(10.3% vs 20.3%)相比,这些患者的死亡率较低。尽管接受了 RDSV 治疗,仍有 1/3 的患者需要更高水平的氧气支持,这是唯一与死亡相关的因素。