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Conventional Wisdom versus Actual Outcomes: Challenges in the Conduct of an Ebola Vaccine Trial in Liberia during the International Public Health Emergency

机译:传统智慧与实际结果:在国际公共卫生紧急情况下,利比里亚埃博拉疫苗审判进行挑战

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摘要

Clinical trials are challenging endeavors. Planning and implementing an investigational vaccine trial in Liberia, in the midst of an Ebola virus disease (EVD) epidemic that World Health Organization classified a public health emergency of international concern, presented extraordinary challenges. Normally, years of preparation and a litany of tasks lay the groundwork for a successful, randomized, blinded, placebo-controlled trial focused on safety and efficacy. Difficult research settings, unpredictable events, and other unique circumstances can add complexity. The setting in Liberia was especially problematic due to an infrastructure still badly damaged following a lengthy civil war and a very fragile health-care system that was further devastated by the EVD outbreak. The Partnership for Research on Vaccines in Liberia I EVD vaccine trial was planned and implemented in less than 3 months by a Liberian and U. S. research partnership, and its Phase II substudy was fully enrolled 3 months later. Contrasting conventional wisdom with trial outcomes offers an opportunity to compare early assumptions, barriers encountered, and adaptive strategies used, with end results. Understanding what was learned can inform future trial responses when disease outbreaks, especially in resource-poor locations with minimal infrastructure, pose a significant threat to public health.
机译:临床试验致力于努力。在埃博拉病毒疾病(EVD)疫情中,世界卫生组织归类了国际问题的公共卫生紧急情况,规划和实施了对利比里亚的调查疫苗试验,提出了非凡的挑战。通常,多年的准备和一连串的任务奠定了成功,随机,盲,安慰剂对照试验的基础,其专注于安全性和有效性。困难的研究设置,不可预测的事件和其他独特的情况可以增加复杂性。利比里亚的环境由于基础设施仍然在漫长的内战之后仍然严重损坏,并且通过EVD爆发进一步摧毁了一个非常脆弱的医疗保健系统。利比里亚IEVD疫苗审判的研究伙伴关系在利比里亚和美国研究伙伴关系不到3个月内计划和实施,并在3个月内完成了3个月后全部注册。与审判结果对比传统智慧提供了比较早期假设,遇到的障碍和使用的适应策略的机会,最终结果。了解所学的内容可以在疾病爆发中,特别是在基础设施最小的资源差的地方,对公共卫生构成重大威胁时,将来试验反应。

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