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大剂量恢复期血浆治疗严重 COVID-19。

High-Dose Convalescent Plasma for Treatment of Severe COVID-19.

出版信息

Emerg Infect Dis. 2022 Mar;28(3):548-555. doi: 10.3201/eid2803.212299. Epub 2022 Jan 26.

DOI:10.3201/eid2803.212299
PMID:35081022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8888205/
Abstract

To assess whether high-dose coronavirus disease (COVID-19) convalescent plasma (CCP) transfusion may benefit patients with severe COVID-19, we conducted a multicenter randomized trial in Brazil. Patients with severe COVID-19 who were within 10 days of initial symptom onset were eligible. Patients in the CCP group received 3 daily doses of CCP (600 mL/d) in addition to standard treatment; control patients received standard treatment only. Primary outcomes were death rates at days 30 and 60 of study randomization. Secondary outcomes were ventilator-free days and hospital-free days. We enrolled 107 patients: 36 CCP and 71 control. At day 30, death rates were 22% for CCP and 25% for the control group; at day 60, rates were 31% for CCP and 35% for control. Needs for invasive mechanical ventilation and durations of hospital stay were similar between groups. We conclude that high-dose CCP transfused within 10 days of symptom onset provided no benefit for patients with severe COVID-19.

摘要

为评估大剂量新型冠状病毒疾病(COVID-19)恢复期血浆(CCP)输注是否对重症 COVID-19 患者有益,我们在巴西进行了一项多中心随机试验。符合条件的患者为症状发作后 10 天内的重症 COVID-19 患者。CCP 组患者在标准治疗的基础上额外接受 3 天的 CCP(600mL/d)输注;对照组患者仅接受标准治疗。主要结局为研究随机分组后第 30 天和第 60 天的死亡率。次要结局为无呼吸机天数和无住院天数。我们共纳入 107 例患者:CCP 组 36 例,对照组 71 例。第 30 天,CCP 组死亡率为 22%,对照组为 25%;第 60 天,CCP 组死亡率为 31%,对照组为 35%。两组患者需要有创机械通气和住院时间相似。我们的结论是,在症状发作后 10 天内输注大剂量 CCP 对重症 COVID-19 患者没有益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/d4d6bf6507d4/21-2299-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/c151a3d3dc89/21-2299-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/01cd4c131c19/21-2299-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/d4d6bf6507d4/21-2299-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/c151a3d3dc89/21-2299-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/01cd4c131c19/21-2299-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c4/8888205/d4d6bf6507d4/21-2299-F3.jpg

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本文引用的文献

1
An oral SARS-CoV-2 M inhibitor clinical candidate for the treatment of COVID-19.一种用于治疗 COVID-19 的口服 SARS-CoV-2 M 抑制剂临床候选药物。
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2
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Nat Med. 2021 Nov;27(11):2012-2024. doi: 10.1038/s41591-021-01488-2. Epub 2021 Sep 9.
3
A multicenter randomized open-label clinical trial for convalescent plasma in patients hospitalized with COVID-19 pneumonia.
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Life (Basel). 2024 Feb 1;14(2):214. doi: 10.3390/life14020214.
4
Defining Parameters That Modulate Susceptibility and Protection to Respiratory Murine Coronavirus MHV1 Infection.定义调节呼吸道鼠冠状病毒 MHV1 感染易感性和保护作用的参数。
J Immunol. 2024 Feb 15;212(4):563-575. doi: 10.4049/jimmunol.2300434.
5
Rates Among Hospitalized Patients With COVID-19 Treated With Convalescent Plasma: A Systematic Review and Meta-Analysis.接受恢复期血浆治疗的新冠肺炎住院患者的发生率:一项系统评价和荟萃分析。
Mayo Clin Proc Innov Qual Outcomes. 2023 Oct 10;7(5):499-513. doi: 10.1016/j.mayocpiqo.2023.09.001. eCollection 2023 Oct.
6
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Virol J. 2023 Mar 27;20(1):53. doi: 10.1186/s12985-023-02007-0.
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5
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6
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7
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8
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