Messina Emanuela, Danise Anna, Ferrari Giulio, Andolina Andrea, Chiurlo Matteo, Razanakolona Marie, Barakat Maxime, Israel Robert J, Castagna Antonella
Infectious Diseases Unit, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Cornea and Ocular Surface Unit, San Raffaele Scientific Institute, Milan, Italy.
Infect Dis Ther. 2021 Dec;10(4):2791-2804. doi: 10.1007/s40121-021-00493-9. Epub 2021 Jul 23.
Ribavirin is an inosine monophosphate dehydrogenase inhibitor with demonstrated activity against coronaviruses, including SARS-CoV-2. Five hospitalized patients with COVID-19 (confirmed by positive tests for SARS-CoV-2) received treatment with ribavirin for inhalation solution (ribavirin aerosol) as part of a compassionate use program. Patients included four men and one woman, with an age range of 29-72 years. Patients were managed according to international and Italian treatment guidelines for COVID-19. In addition, therapy with ribavirin aerosol 100 mg/mL was administered for 30 min twice daily for 6 days (i.e., 12 doses) in all patients. In order to address concerns about a possible increase in viral dispersal with the use of a nebulizer, healthcare providers remained outside the patient room during ribavirin aerosol administration. Pretreatment chest computed tomography (CT) scans showed pseudonodular areas of parenchymal thickening in the upper right lobe with associated ground glass opacities, multiple areas of parenchymal consolidation in both lower lobes with associated ground glass opacities, bilateral parenchymal thickening and multiple associated ground glass areas, or focal ground glass areas in the upper lobes bilaterally, which were almost completely resolved (three patients) or moderately cleared (one patient) on imaging at the end of ribavirin treatment. For a fifth patient, CT scans showed a stable pulmonary picture at the end of ribavirin treatment. No adverse reactions to ribavirin treatment were observed in any of the five patients. All patients recovered fully, and nasopharyngeal swabs obtained after hospital discharge tested negative for SARS-CoV-2. Ribavirin aerosol appears to be efficacious in the treatment of patients with COVID-19. A controlled trial of ribavirin aerosol is ongoing and will provide additional data across a broader patient population.
利巴韦林是一种肌苷单磷酸脱氢酶抑制剂,已证明对包括严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在内的冠状病毒具有活性。5名住院的冠状病毒病(COVID-19,通过SARS-CoV-2检测呈阳性确诊)患者作为一项同情用药计划的一部分,接受了吸入用利巴韦林溶液(利巴韦林气雾剂)治疗。患者包括4名男性和1名女性,年龄在29至72岁之间。患者按照国际和意大利的COVID-19治疗指南进行管理。此外,所有患者均接受了浓度为100 mg/mL的利巴韦林气雾剂治疗,每天两次,每次30分钟,共6天(即12剂)。为了解决使用雾化器可能增加病毒传播的担忧,医护人员在利巴韦林气雾剂给药期间留在病房外。治疗前的胸部计算机断层扫描(CT)显示,右上叶有实性增厚的假结节区域并伴有磨玻璃影,两下叶有多个实性实变区域并伴有磨玻璃影,双侧实性增厚及多个相关磨玻璃区域,或双侧上叶有局灶性磨玻璃区域,在利巴韦林治疗结束时的影像学检查中,这些病变几乎完全消退(3例患者)或中度吸收(1例患者)。对于第5例患者,CT扫描显示在利巴韦林治疗结束时肺部情况稳定。5例患者中均未观察到对利巴韦林治疗的不良反应。所有患者均完全康复,出院后采集的鼻咽拭子SARS-CoV-2检测呈阴性。利巴韦林气雾剂似乎对COVID-19患者的治疗有效。一项关于利巴韦林气雾剂的对照试验正在进行,将在更广泛的患者群体中提供更多数据。