Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantua, Italy.
Department of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantua, Italy.
Clin Microbiol Infect. 2024 Dec;30(12):1514-1522. doi: 10.1016/j.cmi.2024.07.020. Epub 2024 Jul 26.
Plasma collected from recovered patients with COVID-19 (COVID-19 convalescent plasma [CCP]) was the first antibody-based therapy employed to fight the COVID-19 pandemic. While the therapeutic effect of early administration of CCP in COVID-19 outpatients has been recognized, conflicting data exist regarding the efficacy of CCP administration in hospitalized patients.
To examine the effect of CCP compared to placebo or standard treatment, and to evaluate whether time from onset of symptoms to treatment initiation influenced the effect.
Electronic databases were searched for studies published from January 2020 to January 2024.
Randomized clinical trials (RCTs) investigating the effect of CCP on COVID-19 mortality in hospitalized patients with COVID-19.
Hospitalized patients with COVID-19.
CCP versus no CCP.
Cochrane risk of bias tool for RCTs.
The random-effects model was used to calculate the pooled risk ratio (RR) with 95% CI for the pooled effect estimates of CCP treatment. The Grading of Recommendations Assessment, Development and Evaluation was used to evaluate the certainty of evidence.
Twenty-seven RCTs were included, representing 18,877 hospitalized patients with COVID-19. When transfused within 7 days from symptom onset, CCP significantly reduced the risk of death compared to standard therapy or placebo (RR, 0.76; 95% CI, 0.61-0.95), while later CCP administration was not associated with a mortality benefit (RR, 0.98; 95% CI, 0.90-1.06). The certainty of the evidence was graded as moderate. Meta-regression analysis demonstrated increasing mortality effects for longer interval to transfusion or worse initial clinical severity.
In-hospital transfusion of CCP within 7 days from symptom onset conferred a mortality benefit.
从 COVID-19 康复患者中采集的血浆(COVID-19 恢复期血浆 [CCP])是用于对抗 COVID-19 大流行的第一种基于抗体的治疗方法。虽然早期使用 CCP 治疗 COVID-19 门诊患者的治疗效果已得到认可,但关于 CCP 治疗住院患者的疗效存在相互矛盾的数据。
检查 CCP 与安慰剂或标准治疗相比的效果,并评估从症状发作到开始治疗的时间是否影响效果。
从 2020 年 1 月至 2024 年 1 月,检索电子数据库以查找发表的研究。
随机临床试验(RCT),调查 COVID-19 住院患者使用 CCP 对 COVID-19 死亡率的影响。
COVID-19 住院患者。
CCP 与无 CCP。
RCT 的 Cochrane 偏倚风险工具。
使用随机效应模型计算 CCP 治疗的合并风险比(RR)及其 95%置信区间的合并效应估计值。使用推荐评估、制定和评估分级来评估证据的确定性。
纳入了 27 项 RCT,代表了 18877 名 COVID-19 住院患者。从症状发作到输血的 7 天内,CCP 与标准治疗或安慰剂相比显著降低死亡风险(RR,0.76;95%CI,0.61-0.95),而较晚的 CCP 给药与死亡率降低无关(RR,0.98;95%CI,0.90-1.06)。证据的确定性等级为中等。荟萃回归分析表明,输注时间间隔较长或初始临床严重程度恶化会增加死亡率。
从症状发作到输血的 7 天内住院患者输注 CCP 可带来死亡率降低的益处。