Department of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, P. O. Box 80260, Jeddah, 21589, Saudi Arabia.
Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
BMC Infect Dis. 2021 Nov 1;21(1):1127. doi: 10.1186/s12879-021-06813-1.
Tocilizumab is an IgG1 class recombinant humanized monoclonal antibody that directly inhibits the IL-6 receptor. Several randomized clinical trials have evaluated its safety and efficacy in patients with coronavirus disease 2019 (COVID-19), and these studies demonstrate conflicting results. Our study aimed to determine the association between tocilizumab treatment and microbial isolation and emergence of multidrug-resistant bacteria in critically ill patients with COVID-19.
A multicenter retrospective cohort study was conducted at two tertiary government hospitals in Saudi Arabia. All critically ill patients admitted to intensive care units with a positive COVID-19 PCR test between March 1 and December 31, 2020, who met study criteria were included. Patients who received tocilizumab were compared to those who did not receive it.
A total of 738 patients who met our inclusion criteria were included in the analysis. Of these, 262 (35.5%) received tocilizumab, and 476 (64.5%) were included in the control group. Patients who received tocilizumab had higher odds for microbial isolation (OR 1.34; 95% CI 0.91-1.94, p = 0.13); however, the difference was not statistically significant. Development of resistant organisms (OR 1.00; 95% CI 0.51-1.98, p = 0.99) or detection of carbapenem-resistant Enterobacteriaceae (CRE) (OR 0.67; 95% CI 0.29-1.54, p = 0.34) was not statistically significant between the two groups.
Tocilizumab use in critically ill patients with COVID-19 is not associated with higher microbial isolation, the emergence of resistant organisms, or the detection of CRE organisms.
托珠单抗是一种 IgG1 类人源化重组单克隆抗体,可直接抑制 IL-6 受体。几项随机临床试验评估了其在 COVID-19 患者中的安全性和有效性,这些研究结果相互矛盾。我们的研究旨在确定 COVID-19 重症患者使用托珠单抗治疗与微生物分离以及多药耐药菌出现之间的关系。
这是在沙特阿拉伯的两家三级政府医院进行的一项多中心回顾性队列研究。纳入 2020 年 3 月 1 日至 12 月 31 日期间入住重症监护病房且 COVID-19 PCR 检测呈阳性且符合研究标准的所有危重症患者。将接受托珠单抗治疗的患者与未接受托珠单抗治疗的患者进行比较。
共有 738 名符合纳入标准的患者纳入分析。其中,262 名(35.5%)接受了托珠单抗治疗,476 名(64.5%)纳入对照组。接受托珠单抗治疗的患者微生物分离的可能性更高(OR 1.34;95%CI 0.91-1.94,p=0.13);然而,差异无统计学意义。耐药菌的产生(OR 1.00;95%CI 0.51-1.98,p=0.99)或产碳青霉烯类肠杆菌科细菌(CRE)的检出(OR 0.67;95%CI 0.29-1.54,p=0.34)在两组之间无统计学意义。
COVID-19 重症患者使用托珠单抗治疗与微生物分离、耐药菌出现或 CRE 菌检出无关。