抗凝作为新冠肺炎住院患者的治疗策略

Q4 Medicine Thrombosis Update Pub Date : 2022-03-01 DOI:10.1016/j.tru.2022.100097
S. Cullivan , M. Sholzberg , F.Ní Áinle , B. Kevane
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引用次数: 1

摘要

2019冠状病毒病大流行给国际社会造成了严重破坏,并继续在世界范围内造成严重的发病率和死亡率。研制有效疫苗是朝着减少传播和疾病严重程度迈出的重要一步,但仍然存在重大挑战,特别是在疫苗获取有限的地区。COVID-19与高凝性和血栓形成风险增加有关,危重患者的风险最大。有趣的是,早期观察数据表明,抗凝治疗可能会改善COVID-19患者的临床结果,除了血栓事件。在本综述中,我们总结了三项已发表的随机临床试验的数据,这些试验旨在确定治疗性肝素抗凝对COVID-19住院患者疗效和安全性结局的影响:多平台REMAP-CAP、ACTIV-4a和ATTACC随机对照试验和RAPID试验。在多平台REMAP-CAP、ACTIV-4a和ATTACC随机对照试验中,与常规护理相比,治疗性肝素与COVID-19危重患者的获益无关(器官支持免费天数增加至第21天的调整比例优势比(OR): 0.83;95%可信区间为0.67-1.03,后验概率为99.9%)。相反,在没有危重疾病的住院患者中,治疗性肝素与无器官支持存活天数增加的可能性相关(调整OR, 1.27;95%可信区间1.03-1.58)。RAPID试验还评估了治疗性肝素与预防性肝素在非危重患者中的效果。在这项研究中,治疗性肝素并没有显著降低主要复合结局(死亡、机械通气或重症监护病房入院)的几率(or 0.69;95%置信区间[CI], 0.43 ~ 1.10;p = 0.12),但与全因死亡率的显著降低相关[OR, 0.22 (95% ci, 0.07 ~ 0.65)]。总的来说,这些研究表明,肝素治疗性抗凝可能会降低COVID-19住院的非危重患者的疾病严重程度,甚至可能带来生存益处。在COVID-19危重患者中,肝素治疗性抗凝治疗无明显效果。因此,尽管这一不断发展的领域的其他研究结果尚未公布,但重要的是要以有分寸和个性化的方式对COVID-19中度住院患者进行治疗性肝素的决策。
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Anticoagulation as a therapeutic strategy for hospitalised patients with COVID-19

The COVID-19 pandemic has devastated the global community and continues to cause significant morbidity and mortality worldwide. The development of effective vaccines has represented a major step towards reducing transmission and illness severity but significant challenges remain, particularly in regions where vaccine access has been limited. COVID-19 is associated with hypercoagulability and increased risk of thrombosis, with greatest risk among the critically ill. Interestingly, early observational data suggested that anticoagulant therapy might improve clinical outcomes, aside from thrombotic events, in patients with COVID-19. In this review we summarise data generated from three published randomised clinical trials which have sought to determine the effect of therapeutic heparin anticoagulation on efficacy and safety outcomes in hospitalised patients with COVID-19: the multiplatform REMAP-CAP, ACTIV-4a and ATTACC randomised controlled trials and the RAPID trial. In the multiplatform REMAP-CAP, ACTIV-4a and ATTACC randomised controlled trials, therapeutic heparin was not associated with benefit in critically ill patients with COVID-19 compared with usual care (adjusted proportional odds ratio (OR) for increased organ-support free days up to day 21: 0.83; 95% credible interval, 0.67–1.03, posterior probability of futility 99.9%). Conversely, among hospitalised patients without critical illness, therapeutic heparin was associated with an increased probability of organ support-free days alive (adjusted OR, 1.27; 95% credible interval, 1.03–1.58). The RAPID trial also evaluated the effect of therapeutic heparin compared with prophylactic heparin in non-critically ill patients. In this study, therapeutic heparin did not significantly reduce the odds of the primary composite outcome (death, mechanical ventilation or intensive care unit admission) (OR 0.69; 95% confidence interval [CI], 0.43 to 1.10; p = 0.12) but was associated with a significant reduction in all-cause mortality [OR, 0.22 (95%-CI, 0.07 to 0.65)]. Collectively these studies suggest that therapeutic anticoagulation with heparin may reduce the severity of illness and potentially even confer a survival benefit in hospitalised, non-critically ill patients with COVID-19. No benefit for therapeutic anticoagulation with heparin was evident in critically ill patients with COVID-19. Therefore, while the results of additional studies in this evolving field are pending, it is important to approach decisions regarding therapeutic heparin in moderately ill hospitalised patients with COVID-19 in a measured and individualised manner.

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来源期刊
Thrombosis Update
Thrombosis Update Medicine-Hematology
CiteScore
1.90
自引率
0.00%
发文量
33
审稿时长
86 days
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