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Convalescent plasma treatment of severe COVID-19: a propensity score-matched control study.
Nature Medicine ( IF 58.7 ) Pub Date : 2020-09-15 , DOI: 10.1038/s41591-020-1088-9
Sean T H Liu 1, 2 , Hung-Mo Lin 3 , Ian Baine 4 , Ania Wajnberg 5 , Jeffrey P Gumprecht 1 , Farah Rahman 1 , Denise Rodriguez 6 , Pranai Tandon 7 , Adel Bassily-Marcus 8 , Jeffrey Bander 9 , Charles Sanky 10 , Amy Dupper 1 , Allen Zheng 2 , Freddy T Nguyen 4 , Fatima Amanat 2, 11 , Daniel Stadlbauer 2 , Deena R Altman 1 , Benjamin K Chen 1 , Florian Krammer 2 , Damodara Rao Mendu 4 , Adolfo Firpo-Betancourt 4 , Matthew A Levin 12 , Emilia Bagiella 3 , Arturo Casadevall 13 , Carlos Cordon-Cardo 4 , Jeffrey S Jhang 4 , Suzanne A Arinsburg 4 , David L Reich 12 , Judith A Aberg 1 , Nicole M Bouvier 1, 2
Affiliation  

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a new human disease with few effective treatments1. Convalescent plasma, donated by persons who have recovered from COVID-19, is the acellular component of blood that contains antibodies, including those that specifically recognize SARS-CoV-2. These antibodies, when transfused into patients infected with SARS-CoV-2, are thought to exert an antiviral effect, suppressing virus replication before patients have mounted their own humoral immune responses2,3. Virus-specific antibodies from recovered persons are often the first available therapy for an emerging infectious disease, a stopgap treatment while new antivirals and vaccines are being developed1,2. This retrospective, propensity score–matched case–control study assessed the effectiveness of convalescent plasma therapy in 39 patients with severe or life-threatening COVID-19 at The Mount Sinai Hospital in New York City. Oxygen requirements on day 14 after transfusion worsened in 17.9% of plasma recipients versus 28.2% of propensity score–matched controls who were hospitalized with COVID-19 (adjusted odds ratio (OR), 0.86; 95% confidence interval (CI), 0.75–0.98; chi-square test P value = 0.025). Survival also improved in plasma recipients (adjusted hazard ratio (HR), 0.34; 95% CI, 0.13–0.89; chi-square test P = 0.027). Convalescent plasma is potentially effective against COVID-19, but adequately powered, randomized controlled trials are needed.



中文翻译:

重度COVID-19的恢复期血浆治疗:倾向评分匹配的对照研究。

由严重急性呼吸系统综合症冠状病毒2(SARS-CoV-2)引起的冠状病毒病2019(COVID-19)是一种新型人类疾病,几乎没有有效的治疗方法1。从COVID-19中恢复的人捐赠的恢复期血浆是血液中的无细胞成分,其中包含抗体,包括特异性识别SARS-CoV-2的抗体。这些抗体,当被注入感染SARS-CoV-2的患者时,被认为发挥抗病毒作用,在患者进行自身的体液免疫反应之前抑制病毒复制2,3。来自康复者的病毒特异性抗体通常是新兴传染病的首个可用疗法,是一种权宜之计,同时正在开发新的抗病毒药和疫苗1,2。这项回顾性倾向得分匹配的病例对照研究评估了纽约市西奈山医院39例严重或威胁生命的COVID-19患者的康复血浆治疗的有效性。输血后第14天的氧气需求量在17.9%的血浆接受者中较28.8%的倾向评分匹配对照者(COVID-19住院)恶化(校正比值比(OR)为0.86; 95%置信区间(CI)为0.75– 0.98;卡方检验P值= 0.025)。血浆接受者的生存率也得到了改善(调整后的危险比(HR)为0.34; 95%CI为0.13-0.89;卡方检验P  = 0.027)。恢复期血浆可能有效抵抗COVID-19,但需要有足够动力的随机对照试验。

更新日期:2020-09-15
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