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托珠单抗治疗重症和危重症 COVID-19 的最佳应用:系统评价和荟萃分析。

Optimal use of tocilizumab for severe and critical COVID-19: a systematic review and meta-analysis.

机构信息

Department of Internal Medicine, Faculty of Medicine, Airlangga University, Surabaya, East Java, 60132, Indonesia.

Universitas Airlangga Hospital, Surabaya, East Java, 60115, Indonesia.

出版信息

F1000Res. 2021 Feb 4;10:73. doi: 10.12688/f1000research.45046.1. eCollection 2021.

Abstract

Several studies have revealed the potential use of tocilizumab in treating COVID-19 since no therapy has yet been approved for COVID-19 pneumonia. Tocilizumab may provide clinical benefits for cytokine release syndrome in COVID-19 patients. We searched for relevant studies in PubMed, Embase, Medline, and Cochrane published from March to October 2020 to evaluate optimal use and baseline criteria for administration of tocilizumab in severe and critically ill COVID-19 patients. Research involving patients with confirmed SARS-CoV-2 infection, treated with tocilizumab and compared with the standard of care (SOC) was included in this study. We conducted a systematic review to find data about the risks and benefits of tocilizumab and outcomes from different baseline criteria for administration of tocilizumab as a treatment for severe and critically ill COVID-19 patients. A total of 26 studies, consisting of 23 retrospective studies, one prospective study, and two randomised controlled trials with 2112 patients enrolled in the tocilizumab group and 6160 patients in the SOC group, were included in this meta-analysis. Compared to the SOC, tocilizumab showed benefits for all-cause mortality events and a shorter time until death after first intervention but showed no difference in hospital length of stay. Upon subgroup analysis, tocilizumab showed fewer all-cause mortality events when CRP level ≥100 mg/L, P/F ratio 200-300 mmHg, and P/F ratio <200 mmHg. However, tocilizumab showed a longer length of stay when CRP <100 mg/L than the SOC. This meta-analysis demonstrated that tocilizumab has a positive effect on all-cause mortality. It should be cautiously administrated for optimal results and tailored to the patient's eligibility criteria.

摘要

几项研究表明,在尚未批准针对 COVID-19 肺炎的疗法的情况下,托珠单抗在治疗 COVID-19 方面可能具有潜在用途。托珠单抗可能为 COVID-19 患者的细胞因子释放综合征提供临床益处。我们在 PubMed、Embase、Medline 和 Cochrane 上搜索了 2020 年 3 月至 10 月发表的相关研究,以评估在重症和危重症 COVID-19 患者中使用托珠单抗的最佳方法和给药的基线标准。本研究纳入了涉及已确诊 SARS-CoV-2 感染患者的研究,这些患者接受了托珠单抗治疗,并与标准治疗(SOC)进行了比较。我们进行了系统评价,以查找关于托珠单抗的风险和益处的数据,并根据不同的基线标准评估托珠单抗作为治疗重症和危重症 COVID-19 患者的治疗效果。共有 26 项研究,包括 23 项回顾性研究、1 项前瞻性研究和 2 项随机对照试验,共纳入了 2112 例接受托珠单抗治疗的患者和 6160 例接受 SOC 治疗的患者。与 SOC 相比,托珠单抗在全因死亡率事件方面显示出益处,并且在首次干预后死亡的时间更短,但在住院时间方面没有差异。亚组分析显示,当 CRP 水平≥100mg/L、P/F 比值为 200-300mmHg 和 P/F 比值<200mmHg 时,托珠单抗的全因死亡率事件更少。然而,与 SOC 相比,CRP<100mg/L 时托珠单抗的住院时间更长。这项荟萃分析表明,托珠单抗对全因死亡率有积极影响。为了获得最佳效果,应谨慎使用,并根据患者的资格标准进行调整。

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