使用替考韦瑞治疗严重的人类 mpox 病毒感染:病例系列。

Koray K Demir, Michaël Desjardins, Claude Fortin, Simon Grandjean-Lapierre, Arpita Chakravarti, François Coutlée, Gerasimos Zaharatos, Jean Morin, Cécile Tremblay, Jean Longtin
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引用次数: 0

摘要

背景:特考韦利马特(Tecovirimat,TCV,TPOXX®)是一种天花特异性抗病毒药物,用于治疗天花。它在天花感染中的应用也有一定的机理基础。然而,该药物的批准是基于动物实验,其对人类患者的疗效和副作用尚不清楚:方法:在 2022 年国际水痘疫情期间,加拿大的临床医生从加拿大公共卫生署的国家紧急战略储备中获得了 TCV,用于治疗严重的水痘病例。我们描述了加拿大蒙特利尔市九名严重感染天花病毒的成人使用 TCV 的情况:结果:五名患者因出现严重且可能危及生命的头颈部症状而接受治疗,四名患者因泌尿生殖系统或肛门直肠疾病而接受治疗。三分之二的患者还接受了疑似细菌超级感染的治疗。所有患者均已康复(缓解严重症状的中位时间:9 天),没有复发或再次入院。没有患者报告TCV引起的不良反应,也没有患者提前停止治疗:我们的经验表明,TCV 的耐受性良好,可加速重症患者的康复。这些初步的观察数据也可能是由于同时接受了超级感染治疗所致,并且由于没有对照组而受到限制。应开展对照临床试验,以明确 TCV 对严重水痘感染的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of severe human mpox virus infection with tecovirimat: A case series.

Background: Tecovirimat (TCV, TPOXX®) is an orthopox-specific antiviral drug indicated for the treatment of smallpox. There is also a mechanistic basis for its use in mpox infection. However, its approval was based on animal studies, and its efficacy and side-effect profile in human patients with disease is unknown.

Methods: During the 2022 international mpox epidemic, clinicians in Canada accessed TCV from the Public Health Agency of Canada's National Emergency Strategic Stockpile for severe cases of mpox disease. We describe the use of TCV in nine adults with severe mpox virus infection in Montréal, Canada.

Results: Five patients were treated for severe and potentially life-threatening head and neck symptoms, while four were treated for genitourinary or anorectal disease. Two-thirds of patients were also treated for suspected bacterial superinfection. All patients recovered (median time to resolution of severe symptoms: nine days) without relapse or hospital readmission. No patients reported adverse events attributable to TCV and no patients stopped their treatment early.

Conclusion: Our experience suggests that TCV is well tolerated and may accelerate recovery in severe cases. These preliminary, observational data may also be explained by concomitant treatment for superinfection and are limited by the absence of a control group. Controlled, clinical trials should be conducted to clarify the attributable benefit of TCV in severe mpox infection.

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