Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa, 41110 Larissa, Greece.
Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa, 41110 Larissa, Greece.
Eur J Intern Med. 2021 Jun;88:52-62. doi: 10.1016/j.ejim.2021.03.026. Epub 2021 Mar 26.
Aims Infection by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) may lead to the development of severe respiratory failure. In hospitalized-patients, prompt interruption of the virus-driven inflammatory process by using combination treatments seems theoretically of outmost importance. Our aim was to investigate the hypothesis of multifaceted management of these patients. Methods A treatment algorithm based on ferritin was applied in 311 patients (67.2% males; median age 63-years; moderate disease, n=101; severe, n=210). Patients with ferritin <500ng/ml received anakinra 2-4mg/kg/day ± corticosteroids (Arm A, n=142) while those with ≥500ng/ml received anakinra 5-8mg/kg/day with corticosteroids and γ-globulins (Arm B, n=169). In case of no improvement a single dose of tocilizumab (8mg/kg; maximum 800mg) was administered with the potential of additional second and/or third pulses. Treatment endpoints were the rate of the development of respiratory failure necessitating intubation and the SARS-CoV-2-related mortality. The proposed algorithm was also validated in matched hospitalized-patients treated with standard-of-care during the same period. Results In overall, intubation and mortality rates were 5.8% and 5.1% (0% in moderate; 8.6% and 7.6% in severe). Low baseline pO/FiO and older age were independent risk factors. Comparators had significantly higher intubation (HR=7.4; 95%CI: 4.1-13.4; p<0.001) and death rates (HR=4.5, 95%CI: 2.1-9.4, p<0.001). Significant adverse events were rare, including severe secondary infections in only 7/311 (2.3%). Conclusions Early administration of personalized combinations of immunomodulatory agents may be life-saving in hospitalized-patients with COVID-19. An immediate intervention (the sooner the better) could be helpful to avoid development of full-blown acute respiratory distress syndrome and improve survival.
严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)感染可能导致严重呼吸衰竭。在住院患者中,通过联合治疗迅速中断病毒驱动的炎症过程似乎在理论上至关重要。我们的目的是研究对这些患者进行多方面管理的假设。
根据铁蛋白,对 311 例患者(67.2%为男性;中位年龄 63 岁;中度疾病 101 例;严重疾病 210 例)应用治疗算法。铁蛋白<500ng/ml 的患者接受 2-4mg/kg/天的阿那白滞素+/-皮质类固醇(A 组,n=142),而铁蛋白≥500ng/ml 的患者接受 5-8mg/kg/天的阿那白滞素+皮质类固醇+γ球蛋白(B 组,n=169)。如果没有改善,则给予单次托珠单抗(8mg/kg;最大 800mg),并可能给予额外的第二剂和/或第三剂。治疗终点是需要插管的呼吸衰竭发生率和 SARS-CoV-2 相关死亡率。在同一时期接受标准护理治疗的匹配住院患者中也验证了该方案。
总体而言,插管和死亡率分别为 5.8%和 5.1%(中度为 0%;严重为 8.6%和 7.6%)。低基线 pO/FiO 和年龄较大是独立的危险因素。对照组的插管(HR=7.4;95%CI:4.1-13.4;p<0.001)和死亡率(HR=4.5,95%CI:2.1-9.4,p<0.001)显著更高。严重不良事件罕见,仅 7/311(2.3%)例发生严重继发感染。
早期给予个体化免疫调节剂联合治疗可能对 COVID-19 住院患者有救命作用。尽早干预(越早越好)可能有助于避免发生急性呼吸窘迫综合征,并提高生存率。