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设计脓毒症相关弥散性血管内凝血的未来临床试验。

Designing Future Clinical Trials for Sepsis-associated Disseminated Intravascular Coagulation.

作者信息

Maier Cheryl L, Iba Toshiaki

出版信息

Juntendo Iji Zasshi. 2024 Apr 18;70(2):125-128. doi: 10.14789/jmj.JMJ24-0010-P. eCollection 2024.

Abstract

Defining success in a clinical trial is not necessarily a straightforward task, especially when the target population is critically ill patients where few agents have demonstrated effectiveness. This has been the case for trials of anticoagulation in patients with sepsis-associated disseminated intravascular coagulation (DIC), which have generally examined patients with severe sepsis but not specifically DIC. Limitations of existing studies include inadequate anticoagulant doses and delayed initiation of treatment. Furthermore, 28-day mortality has been adopted as the primary endpoint but is affected by a panoply of factors other than anticoagulant therapies and may not be the most relevant measure. Future trials must address several current limitations in order to improve our understanding of the role of anticoagulation in patients with sepsis-associated DIC.

摘要

在临床试验中定义成功并非一定是一项简单的任务,尤其是当目标人群为重症患者时,因为很少有药物显示出有效性。脓毒症相关弥散性血管内凝血(DIC)患者的抗凝试验就是这种情况,这些试验通常研究的是严重脓毒症患者,而非专门的DIC患者。现有研究的局限性包括抗凝剂量不足和治疗开始延迟。此外,28天死亡率已被用作主要终点,但它受抗凝治疗以外的一系列因素影响,可能不是最相关的衡量指标。未来的试验必须解决当前的几个局限性,以增进我们对抗凝在脓毒症相关DIC患者中作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bed/11487357/6863cde9a2f5/2188-2126-70-2-0125-g001.jpg

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