Safety and efficacy of intranasal recombinant human interferon alfa 2b as prophylaxis for COVID-19 in patients on a hemodialysis program

A. Abdo-Cuza, R. Castellanos-Gutiérrez, Janete Treto-Ramirez, Sandra Arencibia-Larin, Thalía Gómez-Pariente, Tania González-Fernández, J. C. Hernández-Perera, Katia Arocha-Stalella, Niurka Verdecia-Gorrita, Lisy Vento-Buigues, Yanet Cordero-Vasallo, Yusmel Rivero-Yi, Odalys González-Dias, H. Nodarse-Cuní, R. Machado-Martínez, M. Blanco-González, Julio Valdivia-Arencibia, Daymiris Mendez-Felipe, Ernesto Delgado-Almora, C. Gutiérrez-Gutiérrez, J. Suárez-López, Jorge L. Leiva-Torres, Alicia Rodríguez-Sotolongo, Nilda Bejerano-Gil
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引用次数: 2

Abstract

Introduction: Patients diagnosed with end-stage chronic kidney disease on a hemodialysis program (HDP) represent a risk group for COVID-19. Scientific societies have developed guidelines for the prevention of contagion, but there is no prophylactic medicine in them. Objectives: To describe the safety and efficacy of recombinant intranasal human Interferon alfa 2b as prophylaxis for COVID-19 in patients in an HDP. Patients and Methods: Intervention description through the monitoring of 15 patients in outpatient HDP. Prior to the administration of the drug, clinical, radiological evaluation and hematology and blood chemistry studies were performed. Daily contact was made with each study patient in person or by telephone, asking about the occurrence of adverse events or symptoms of disease. Results: In 47% of the patients, there was leukopenia, lymphopenia in 67% and anemia and thrombocytopenia in 33% respectively, prior to the use of the drug. There was no clinical suspicion of COVID-19 in any of them. Adverse events occurred in 3 patients (20%), all were mild and non-severe. All patients were negative for SARS-CoV-2 real-time polymerase chain reaction (rtPCR) and antibody studies 45 days after the study started. Conclusion: the use of intranasal recombinant human interferon alfa 2b as prophylaxis of COVID-19 in patients in a HDP at a dose of 1 MIU daily for ten days, as part of a prevention protocol, has an adequate safety profile. None of the patients in the series was infected with SARS-CoV-2 during the surveillance period.
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重组人α α 2b鼻内干扰素预防血液透析患者COVID-19的安全性和有效性
在血液透析计划(HDP)中被诊断为终末期慢性肾病的患者是COVID-19的危险群体。科学团体已经制定了预防传染的指导方针,但其中没有预防性药物。目的:描述重组人α α 2b鼻内干扰素作为HDP患者预防COVID-19的安全性和有效性。患者与方法:通过对15例门诊HDP患者的监测,描述干预措施。在给药之前,进行了临床、放射学评估、血液学和血液化学研究。每天亲自或通过电话与每位研究患者进行接触,询问不良事件或疾病症状的发生情况。结果:47%的患者在用药前出现白细胞减少,67%的患者出现淋巴细胞减少,33%的患者出现贫血和血小板减少。无临床疑似病例。不良事件3例(20%),均为轻度和非重度。所有患者在研究开始后45天的SARS-CoV-2实时聚合酶链反应(rtPCR)和抗体检测均为阴性。结论:作为预防方案的一部分,在HDP患者中使用鼻内重组人干扰素α 2b作为预防COVID-19的剂量,每天1 MIU,持续10天,具有足够的安全性。该系列患者在监测期间均未感染SARS-CoV-2。
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