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

Juntendo Iji Zasshi Pub Date : 2024-04-18 eCollection Date: 2024-01-01 DOI:10.14789/jmj.JMJ24-0010-P
Cheryl L Maier, Toshiaki Iba
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引用次数: 0

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.

设计针对败血症相关弥散性血管内凝血的未来临床试验。
定义临床试验的成功与否并不一定是一项简单的任务,尤其是当目标人群是危重病人时,几乎没有药物能证明其有效性。针对脓毒症相关弥散性血管内凝血(DIC)患者的抗凝试验就属于这种情况。现有研究的局限性包括抗凝剂剂量不足和延迟开始治疗。此外,28 天死亡率被作为主要终点,但它受到抗凝疗法以外的一系列因素的影响,可能不是最相关的衡量标准。未来的试验必须解决目前存在的几个局限性,以提高我们对抗凝在脓毒症相关 DIC 患者中作用的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
9 weeks
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