恢复期血浆治疗对COVID-19患者疗效的回顾性研究

Mahboobeh Shojaei, S. Shahrabi, Nastaran Khodakarim, Mehran Amrovani, A. Salah, Zohre Saleh Nassaj, M. Esmaeili
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After complete recovery from COVID-19, patients were recalled for apheresis and plasma isolation for convalescent plasma (CP) preparation; they were referred to the blood donation centers of Shiraz. According to the hospital request, compatible and related plasma was sent for COVID-19-hospitalized patients. At the same time, hospitals were asked to send the clinical condition documents of the patients based on the medical records and the outcomes after CPT. The Iranian Blood Transfusion Organization evaluated the results. Results: The median antibody titer was 1300. Titers higher and lower than 1300 were considered high and low, respectively. Blood group O had 54 times higher antibody titers above 1300 than other blood groups (odds ratio (OR) = 54, confidence interval (CI): 19.5 - 205.3, P < 0.001). Additionally, most deceased cases received plasma with antibody titers less than 1300 (OR = 0.08, CI: 0.009 - 0.36, P < 0.001). 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摘要

背景:2019冠状病毒病(COVID-19)于2019年12月在中国武汉首次发现。人们使用了不同的治疗方法来对抗这种病毒;然而,最有效和最容易获得的是恢复期血浆治疗(CPT)。目的:探讨CPT对改善COVID-19患者临床状况的作用。方法:本研究于2020年5月至2021年2月在伊朗法尔斯省设拉子采用随机抽样方法,对440名个体进行了研究,其中包括220名covid -19康复个体作为血浆供体和220名血浆受体。COVID-19完全康复后,召回患者进行采血和血浆分离,制备恢复期血浆(CP);他们被转到设拉子的献血中心。根据医院要求,为新冠肺炎住院患者发送了兼容的相关血浆。同时,要求医院根据患者的医疗记录和CPT后的结果发送患者的临床状况文件。伊朗输血组织对结果进行了评估。结果:抗体效价中位数为1300。高于和低于1300分别被认为是高和低滴度。O型血在1300以上抗体滴度比其他血型高54倍(优势比(OR) = 54,置信区间(CI): 19.5 ~ 205.3, P < 0.001)。此外,大多数死亡患者的血浆抗体滴度低于1300 (OR = 0.08, CI: 0.009 ~ 0.36, P < 0.001)。但出院患者血浆抗体滴度大多高于1300 (OR = 1.5, CI: 1.06 ~ 2.3, P = 0.01)。此外,当供体抗体滴度高于1300时,生存机会增加50%。此外,本研究结果显示,接受血浆容量小于387 mL的患者死亡率更高(OR = 0.3, CI: 0.10 - 0.91, P = 0.018)。然而,接受超过387 mL CP的患者更有可能出院(OR = 5.7, CI: 3.7 - 8.8, P < 0.001)。结论:使用最小容量为387 mL的O型血浆可非常有效地改善COVID-19患者的临床症状,提高患者的生存机会。
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Effect of Convalescent Plasma Therapy on COVID-19 Patients: A Retrospective Study
Background: Coronavirus disease 2019 (COVID-19) was first detected in December 2019 in Wuhan, China. Different treatments have been used to fight against the virus; however, one of the most effective and accessible is convalescent plasma therapy (CPT). Objectives: The present study investigated the effect of CPT on improving the clinical conditions of COVID-19 patients. Methods: This study was conducted on 440 individuals, including 220 COVID-19-recovered individuals as plasma donors and 220 plasma recipients, in Shiraz, Fars province, Iran, from May 2020 to February 2021 using random sampling. After complete recovery from COVID-19, patients were recalled for apheresis and plasma isolation for convalescent plasma (CP) preparation; they were referred to the blood donation centers of Shiraz. According to the hospital request, compatible and related plasma was sent for COVID-19-hospitalized patients. At the same time, hospitals were asked to send the clinical condition documents of the patients based on the medical records and the outcomes after CPT. The Iranian Blood Transfusion Organization evaluated the results. Results: The median antibody titer was 1300. Titers higher and lower than 1300 were considered high and low, respectively. Blood group O had 54 times higher antibody titers above 1300 than other blood groups (odds ratio (OR) = 54, confidence interval (CI): 19.5 - 205.3, P < 0.001). Additionally, most deceased cases received plasma with antibody titers less than 1300 (OR = 0.08, CI: 0.009 - 0.36, P < 0.001). Nevertheless, most discharged patients received plasma with antibody titers higher than 1300 (OR = 1.5, CI: 1.06 - 2.3, P = 0.01). Moreover, when donors’ antibody titer was higher than 1300, the chance of survival increased by 50%. In addition, the results of this study showed higher mortality in patients whose volume of received plasma was less than 387 mL (OR = 0.3, CI: 0.10 - 0.91, P = 0.018). However, patients who received more than 387 mL CP were more likely to discharge (OR = 5.7, CI: 3.7 - 8.8, P < 0.001). Conclusions: Using blood group O plasma with a minimum volume of 387 mL can be very effective in improving the clinical symptoms of patients with COVID-19 and increasing the chances of survival for these patients.
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