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The unique challenges of enrolling patients into multiple clinical trials.

机译:将患者纳入多项临床试验的独特挑战。

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摘要

Multiple interventions are implemented to save the lives of a critically ill patients. The therapeutic value of most of these interventions remains untested. Enrollment of patients in the intensive care unit into multiple studies could improve the efficiency of testing interventions in the intensive care unit. Unfortunately, enrollment of intensive care unit patients into multiple studies is often discouraged. If the same patient is enrolled into more than one study, there is a risk that interactions between interventions could lead to false conclusions. In addition, there is a belief that the families of critically ill patients might feel overly stressed if they are repeatedly approached for consent. This article provides a rationale for enrolling intensive care unit patients into multiple clinical trials. Factorial designs are efficient, but their inherent limitations must be noted. The little evidence that is available shows that most patients would enroll in multiple studies and do not feel overly stressed by participating in more than one study. Modifications to subject consent, data collection, and data analysis for coenrollment could facilitate it. In conclusion, more vigorous promotion of thoughtful coenrollment policies could increase the efficiency of critical care research.
机译:为了挽救重症患者的生命,实施了多种干预措施。这些干预措施中大多数的治疗价值尚未得到检验。将重症监护室的患者纳入多项研究可以提高重症监护室中测试干预措施的效率。不幸的是,通常不鼓励重症监护病房的患者参加多项研究。如果同一位患者参加了一项以上的研究,则干预措施之间的相互作用可能会导致错误的结论。此外,人们认为,如果反复征求他们的同意,危重病人的家属可能会感到压力过大。本文提供了将重症监护病房患者纳入多个临床试验的依据。析因设计是有效的,但必须注意其固有的局限性。现有的少量证据表明,大多数患者会参加多项研究,并且不会因参加一项以上研究而感到压力过大。修改受试者同意书,数据收集和数据分析以共同注册可能会促进这种情况。总之,大力推广有思想的共同注册政策可以提高重症监护研究的效率。

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