Department of Transfusion Medicine, AIIMS Rishikesh, Rishikesh, India.
Department of Internal Medicine, AIIMS Rishikesh, Rishikesh, India.
Recent Adv Antiinfect Drug Discov. 2023;18(3):188-196. doi: 10.2174/2772434417666220622140416.
Convalescent plasma has been used to provide passive immunotherapy to patients with COVID-19 with a high level of safety. Very few efficacy studies were available, and due to COVID being a relatively new disease, its exact therapeutic role was unclear. This observational study on the impact of COVID convalescent plasma (CCP) on clinical outcomes attempts to evaluate the effectiveness of convalescent COVID-19 plasma therapy in the treatment of COVID-19 patients at the tertiary care center in the Uttarakhand state of India.
CCP was collected by plasmapheresis/whole blood from willing COVIDrecovered donors who underwent pre-donation testing including ABO and RhD grouping, mandatory blood screening tests for HIV, HBV, HCV, syphilis and Malaria, Haemoglobin estimation and COVID IgG assay. Hospitalized patients with severe COVID-19 pneumonia who received these CCP units were followed up and the outcome (Recovery/death) was observed.
A total of 63 patients who received CCP were included in the study. Out of the total, 13 (20.7%) were females and 50 (79.3%) were males and their ages ranged from 24 to 80 years with a median age of 53 years. The period between the start of symptoms and hospitalization ranged from 1 to 14 days with an average duration of 4.7 days. Symptoms on presentation included Fever 53/63 (84.1%), Tachypnoea 60/63 (95.2%) and Cough 42/63 (66.7%). Among these patients, 22/63 (34.9%) were on non-invasive ventilation (NIV), 6/63 (9.5%) on non-rebreather mask (NRBM) and 32/63 (50.8%) were on Ventilator support. The infused convalescent plasma had a Mean IgG value of 57.3 AU with a range of (10-142 AU). A total of 37 (58.7%) patients were lost to COVID-19 infection and 26 (41.3%) were discharged from the hospital in a healthy state.
The use of convalescent plasma in addition to standard treatment in our study on patients with severe pneumonia due to COVID-19 did not demonstrate reduced mortality of COVID-19 patients amidst numerous variables. The results showed that the use of convalescent plasma as a treatment option in the present conditions needs a serious re-evaluation. Studies on a strictly defined recipient group and transfusion of CCP units, with adequate antibody titer and/or neutralization activity, must be analyzed for future works.
恢复期血浆已被用于为 COVID-19 患者提供被动免疫治疗,且安全性较高。关于其疗效的研究非常少,且由于 COVID-19 是一种相对较新的疾病,其确切的治疗作用尚不清楚。本研究旨在评估三级保健中心在印度北阿坎德邦治疗 COVID-19 患者时,COVID 恢复期血浆(CCP)对临床结局的影响,观察 COVID 恢复期血浆对 COVID-19 的治疗效果。
通过血浆置换/全血从愿意捐献的 COVID 康复供体中采集 CCP,这些供体在捐献前进行了 ABO 和 RhD 分组、HIV、HBV、HCV、梅毒和疟疾的强制性血液筛查检测、血红蛋白估计和 COVID IgG 检测。接受这些 CCP 单位治疗的严重 COVID-19 肺炎住院患者进行了随访,并观察其结局(康复/死亡)。
共有 63 名接受 CCP 的患者纳入本研究。其中,女性 13 例(20.7%),男性 50 例(79.3%),年龄 24-80 岁,中位年龄 53 岁。从症状开始到住院的时间为 1-14 天,平均为 4.7 天。就诊时的症状包括发热 53/63(84.1%)、呼吸急促 60/63(95.2%)和咳嗽 42/63(66.7%)。这些患者中,22/63(34.9%)接受无创通气(NIV),6/63(9.5%)接受非重复呼吸面罩(NRBM),32/63(50.8%)接受呼吸机支持。输注的恢复期血浆平均 IgG 值为 57.3 AU,范围为(10-142 AU)。共有 37 例(58.7%)患者死于 COVID-19 感染,26 例(41.3%)患者在健康状态下出院。
在我们对 COVID-19 严重肺炎患者的研究中,除了标准治疗外,使用恢复期血浆并不能降低 COVID-19 患者的死亡率,尽管存在众多变量。结果表明,在目前的情况下,将恢复期血浆作为一种治疗选择需要重新进行认真评估。必须对严格定义的受者群体进行研究,并对 CCP 单位进行输血,以确保抗体滴度和/或中和活性充足,为未来的研究提供参考。