Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China.
Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China; Institute of Clinical Pharmacy, Central South University, Changsha, Hunan 410011, China.
Int Immunopharmacol. 2021 Jul;96:107732. doi: 10.1016/j.intimp.2021.107732. Epub 2021 Apr 30.
The benefit of IVIG (Intravenous Immunoglobulin) therapy for COVID-19 remains controversial. We performed a meta-analysis to investigate the efficacy of IVIG treatment in patients with COVID-19.
We searched articles from Web of Science, PubMed, Embase, the Cochrane Library, MedRxiv between 1 January 2020 and February 17, 2021. We selected randomized clinical trials and observational studies with a control group to assess the efficiency of IVIG in treating patients with COVID-19. Subjects were divided into 'non-severe', 'severe' and 'critical' three subgroups based on the information of the study and the World Health Organization (WHO) definition of severity. We pooled the data of mortality and other outcomes using either a fixed-effect model or a random-effects model.
Our meta-analysis retrieved 4 clinical trials and 3 cohort studies including 825 hospitalized patients. The severity of COVID-19 is associated with the efficiency of IVIG. In critical subgroup, IVIG could reduce the mortality compared with the control group [RR = 0.57 (0.42-0.79, I = 025%). But there was no significant difference in the severe or non-severe subgroups.
IVIG has demonstrated clinical efficacy on critical ill patients with COVID-19. There may be a relationship between the efficacy of IVIG and the COVID-19 disease severity. Well-designed clinical trials to identify the clinical and biochemical characteristics in COVID-19 patients' population that could benefit from IVIG are warranted in the future.
静脉注射免疫球蛋白(IVIG)治疗 COVID-19 的益处仍存在争议。我们进行了一项荟萃分析,以研究 IVIG 治疗 COVID-19 患者的疗效。
我们检索了 2020 年 1 月 1 日至 2021 年 2 月 17 日期间来自 Web of Science、PubMed、Embase、Cochrane Library 和 MedRxiv 的文章。我们选择了随机临床试验和对照研究,以评估 IVIG 治疗 COVID-19 患者的效率。根据研究信息和世界卫生组织(WHO)对严重程度的定义,将患者分为“非重症”、“重症”和“危重症”三个亚组。我们使用固定效应模型或随机效应模型汇总死亡率和其他结局的数据。
我们的荟萃分析检索到 4 项临床试验和 3 项队列研究,共纳入 825 名住院患者。COVID-19 的严重程度与 IVIG 的疗效相关。在危重症亚组中,IVIG 可降低死亡率,与对照组相比 [RR=0.57(0.42-0.79,I=25%)]。但在重症或非重症亚组中,差异无统计学意义。
IVIG 对 COVID-19 危重症患者显示出临床疗效。IVIG 的疗效与 COVID-19 疾病严重程度之间可能存在关联。未来需要设计良好的临床试验,以确定 COVID-19 患者人群中可能从 IVIG 中获益的临床和生化特征。