Microbiology and Immunology Postgraduate Program, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.
Clinical Pharmacy Department, Faculty of Pharmacy, October 6 University, Giza 12585, Egypt.
Medicina (Kaunas). 2024 Oct 11;60(10):1670. doi: 10.3390/medicina60101670.
Elevated levels of pro-inflammatory cytokines have been linked to increased mortality in COVID-19 patients. Infliximab, a tumor necrosis factor inhibitor, has been reported to improve outcomes in COVID-19 patients by targeting the hyperinflammatory response. Our objective was to evaluate the effectiveness of incorporating Infliximab into standard care guidelines for the management of COVID-19. : A retrospective analysis was conducted on 111 participants who were moderate to severe COVID-19 patients admitted to the hospital. Among them, 74 individuals received solely standard treatment, while 37 received standard therapy plus Infliximab. The primary outcomes of the study centered around the changes in laboratory test parameters. The secondary clinical findings included clinical recovery defined as improvement in patient oxygenation, time till recovery, and assessing necessity for ICU admission, and mortality rates. There was no statistical difference observed in the inflammatory markers including, LDH, Ferritin, CRP, neutrophil to lymphocyte ratio (NLR), and P/F ratio between both groups and in the clinical outcomes including clinical recovery ( = 1.0), time to improvement ( = 0.436), and mortality rate ( = 0.601). However, there was a significant increase in secondary infection (45.9%, 20.3%; = 0.005), and in liver enzymes, ALT (79.5, 50.0 IU/L; = 0.02) and AST (57.5, 38.0 IU/L; = 0.019) in the Infliximab group and the standard care group, respectively. Infliximab therapy did not demonstrate significant benefits compared to standard of care in moderate to severe hospitalized COVID-19 patients.
炎症细胞因子水平升高与 COVID-19 患者死亡率增加有关。肿瘤坏死因子抑制剂英夫利昔单抗通过靶向过度炎症反应,据报道可改善 COVID-19 患者的预后。我们的目的是评估将英夫利昔单抗纳入 COVID-19 管理标准治疗指南的有效性。
对 111 名中度至重度 COVID-19 住院患者进行回顾性分析。其中 74 例仅接受标准治疗,37 例接受标准治疗加英夫利昔单抗。研究的主要结局是实验室检测参数的变化。次要临床发现包括临床恢复,定义为患者氧合改善、恢复时间和评估是否需要 ICU 入院以及死亡率。两组之间的炎症标志物(包括 LDH、铁蛋白、CRP、中性粒细胞与淋巴细胞比值 (NLR) 和 P/F 比值)和临床结局(临床恢复=1.0)、改善时间(=0.436)和死亡率(=0.601)均无统计学差异。然而,继发性感染(45.9%,20.3%;=0.005)和肝酶 ALT(英夫利昔单抗组 79.5,50.0 IU/L;=0.02)和 AST(英夫利昔单抗组 57.5,38.0 IU/L;=0.019)在英夫利昔单抗组和标准治疗组中均显著增加。与标准治疗相比,英夫利昔单抗治疗在中度至重度住院 COVID-19 患者中并未显示出显著益处。