Convalescent plasma in hospitalized patients with COVID-19 pneumonia: a case-control prospective study

G. Roveroni, L. Moro, Michela Pivetta, M. Orfano, M. Siviero, Alessia Bagatin, Raffaella Berti, Federico Manente, G. Gessoni
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Abstract

Background: This case-control prospective study aimed to describe the effects of COVID convalescent plasma (CCP) therapy in patients diagnosed with coronavirus disease 2019 (COVID-19) pneumonia due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, during the fourth trimester of 2020 in Venice Prefecture (North East Italy). Methods: Overall, 214 consecutive patients admitted to COVID-19 Hospitals of our district were enrolled. The confirmation of SARS-CoV-2 infection was made through the reverse transcription-polymerase chain reaction test in nasopharyngeal swabs. The severity of each patient’s clinical condition was determined following the Berlin score. The clinical data, laboratory test reports and imaging diagnosis of all patients were analyzed at hospitalization. All subjects were showing symptoms of severe COVID-19 pneumonia and were treated with conventional therapy;108 patients received standard therapy and 106 received standard therapy in combination with CCP. The endpoint was mortality at 30 days. Results: The two patient series were comparable for gender, age, risk factors, Berlin score, PaO2/FiO2. Both groups received standard therapy: NSAIDs, ventilator support, LMWH, steroids, antibiotics and antivirals;106 subjects were additionally administered CCP. The mortality rate at 30 days was 30.6% among subjects treated with standard therapy versus 30.2% among subjects treated with standard therapy plus CCP. Considering the radiological findings and ventilatory support data, it would appear that the disease was more severe in patients treated with ST plus CCP. Conclusions: This case-control prospective study showed that in a cohort of hospitalized patients suffering from severe COVID-19 pneumonia, the addition of CCP to the standard therapy did not impact the mortality rate at 30 days. However, we believe that further studies are needed to evaluate the effectiveness of convalescent plasma therapy.
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COVID-19肺炎住院患者恢复期血浆的病例对照前瞻性研究
背景:本病例对照前瞻性研究旨在描述2020年第四个月意大利威尼斯县(东北部)因严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染而被诊断为冠状病毒病2019 (COVID-19)肺炎的患者的COVID恢复期血浆(CCP)治疗的效果。方法:选取我院新冠肺炎住院患者214例。通过鼻咽拭子逆转录聚合酶链反应试验确认SARS-CoV-2感染。根据柏林评分确定每位患者临床状况的严重程度。对所有患者住院时的临床资料、实验室检查报告及影像学诊断进行分析。所有患者均出现COVID-19重症肺炎症状,均采用常规治疗,108例患者采用标准治疗,106例患者采用标准治疗联合CCP治疗。终点是30天的死亡率。结果:两组患者在性别、年龄、危险因素、柏林评分、PaO2/FiO2方面具有可比性。两组均接受标准治疗:非甾体抗炎药、呼吸机支持、低分子肝素、类固醇、抗生素和抗病毒药物;106例患者另外给予CCP治疗。接受标准治疗的患者30天死亡率为30.6%,而接受标准治疗加CCP治疗的患者为30.2%。考虑到影像学表现和通气支持资料,似乎ST + CCP治疗的患者病情更严重。结论:本病例对照前瞻性研究显示,在一组重症COVID-19肺炎住院患者中,在标准治疗中加入CCP对30天死亡率没有影响。然而,我们认为需要进一步的研究来评估恢复期血浆治疗的有效性。
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