国际,前性的COSMOS (CytOSorb® 治疗重症患者) 注册表:来自前300名患者的结果
Ricard Ferrer1, Matthias Thielmann2, Moritz Unglaube3
1Intensive Care Department, Vall d'Hebron University Hospital, Shock, Organ Dysfunction and Resuscitation Research Group (SODIR), Barcelona, Spain. ricard.ferrer@vallhebron.cat.
Journal of anesthesia, analgesia and critical care
|February 24, 2026
概括
这项研究表明,CytoSorb® (CS) 治疗重症患者的临床标志物得到改善,与历史估计相比,死亡率降低. 由于观测设计,需要进一步研究.
科学领域:
- 关键护理医学 关键护理医学
- 身体外疗法 身体外疗法
- 炎症管理 炎症管理
背景情况:
- 血液净化在危急病患者中被探索,以控制炎症并消除在狂犬病溶解中的肌球蛋白等毒素.
- 目前关于临床益处的证据有限,需要进一步调查.
研究的目的:
- 为了跟踪CytoSorb® (CS) 使用模式和重症监护机构的患者结果.
- 在现实环境中评估CS治疗的安全性和有效性.
主要方法:
- 国际前性COSMOS注册表在22个地点注册了300名成年患者.
- 数据包括在CS治疗之前,期间和之后的临床评估,以及90天的随访.
- 统计分析涉及描述性统计数据和配对测试,以比较治疗前和治疗后的值.
主要成果:
- 常见的适应症包括败血性休克 (48.3%),狂肠分裂 (12.8%) 和心脏性休克 (11.5%).
- 脑神经系统治疗改善了液体平衡,减少了对北上腺素的需求,并增加了P/F比率 (p < 0.0001).
- 集中治疗室死亡率为33.1%,低于严重性得分预测的水平;没有报告与设备相关的严重不良影响.
结论:
- 在重症监护中使用真实世界的CS显示了临床和实验室参数的改善.
- 结果表明潜在的好处,但由于观察设计,应谨慎解释.
- 观察到的死亡率低于具有类似严重性得分的患者的历史估计.
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