在COVID-19严重缺血性呼吸衰竭中使用alteplase:TRISTARDS多中心随机试验
Giovanni Landoni1,2, Pratima Chowdary3, Ferhat Meziani4
1Department of Anesthesia and Intensive Care, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Annals of intensive care
|November 10, 2024
概括
阿尔特普拉斯在严重的COVID-19呼吸衰竭中没有加速临床康复. 虽然表现出改善生存和氧化率的趋势,但高高治疗也增加了出血风险.
科学领域:
- 肺部病理学 肺部病理学
- 临界护理医学 临界护理医学
- 药理学 药理学是指药理学的学科.
背景情况:
- 肺血管内血栓形成在呼吸衰竭中很常见,包括COVID-19.
- 在COVID-19中,严重的缺血性呼吸衰竭带来了重大的临床挑战.
研究的目的:
- 评估阿尔特等血栓溶解在COVID-19导致严重低血量呼吸衰竭的患者中的疗效和安全性.
- 为了比较Alteplase加标准护理 (SOC) 与单独的SOC.
主要方法:
- 多中心,开放标签研究,随机分配患者接受高高 (低剂量或高剂量) 加SOC,或单独使用SOC.
- 主要终点:临床改善的时间 (WHO尺度或医院出院) 至28日.
- 二级终点:全因死亡率,治疗失败,以及PaO2/FiO2比率的变化.
主要成果:
- 临床改善的中位时间在各组之间没有显著差异 (25天与>28天).
- 阿尔特普拉斯显示出降低全因死亡率的趋势 (12% vs. 29%) 和改善PaO2/FiO2比率,特别是在非侵入性通风患者中.
- 在阿尔特剂组中观察到主要出血事件的增加 (9 vs 0);26.1%的患者因不良事件而停止治疗.
结论:
- 在严重的COVID-19缺血性呼吸衰竭中,阿尔特普拉斯没有显示出加速的临床恢复.
- 探索性分析表明,在特定亚组中,潜在的生存和氧化益处,需要进一步调查.
- 该研究因患者招募不足而提前结束,限制了最终的结论.
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