COVID-19住院患者抗凝治疗:系统回顾和前瞻性荟萃分析

IF 19.6 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Annals of Internal Medicine Pub Date : 2025-01-01 Epub Date: 2024-12-24 DOI:10.7326/ANNALS-24-00800
Claire L Vale, Peter J Godolphin, David J Fisher, Julian P T Higgins, Alexandra McAleenan, Francesca Spiga, Tobias Tritschler, Pedro Gabriel Melo de Barros E Silva, David D Berg, Jeffrey S Berger, Lindsay R Berry, Behnood Bikdeli, Marc Blondon, Erin A Bohula, Marco Cattaneo, Riccardo Colombo, Valeria Coluccio, Maria T DeSancho, Michael E Farkouh, Valentin Fuster, Massimo Girardis, Judith S Hochman, Thomas P Jensen, Vivekanand Jha, Peter Jüni, Ajay J Kirtane, Patrick Lawler, Grégoire Le Gal, Ramon Lecumberri, Steven R Lentz, Renato D Lopes, Elizabeth Lorenzi, Marco Marietta, Carlos Henrique Miranda, Nuccia Morici, Susan C Morpeth, David A Morrow, Zoe K McQuilten, Nuria Muñoz-Rivas, Matthew D Neal, Suman Pant, Sahil A Parikh, Usha Perepu, Parham Sadeghipour, Sanjum Sethi, Michelle Sholzberg, Alex C Spyropoulos, Gregg W Stone, Azita Hajhossein Talasaz, Steven Tong, James Totterdell, Balasubramanian Venkatesh, Maddalena Alessandra Wu, Ryan Zarychanski, Stephane Zuily, Julie Viry, Jamie Rylance, Neill K J Adhikari, Janet V Diaz, John C Marshall, Jonathan A C Sterne, Srinivas Murthy
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引用次数: 0

摘要

背景:评估COVID-19住院患者高剂量抗凝治疗的临床试验报告结果不一致。目的:评估高剂量与低剂量抗凝与临床结果的关系。数据来源:随机试验从世界卫生组织的国际临床试验注册平台和ClinicalTrials.gov中确定,不受试验状态或语言的限制。研究选择:符合条件的随机试验将因COVID-19住院的患者分配到高剂量和低剂量抗凝治疗。数据提取:20项符合条件的试验以预期商定的格式提供了数据。另外两项研究基于已发表的数据。主要终点是随机分组后28天的全因死亡率。次要结局是进展到有创机械通气或死亡、血栓栓塞事件和大出血。数据综合:与预防性剂量的肝素抗凝相比,治疗性剂量的肝素降低了28天死亡率(OR, 0.77 [95% CI, 0.64 - 0.93];I 2 = 29%;11项试验,6297例患者,其中5456例在随机分组时需要低氧或无氧。28天死亡率的or为1.21 (CI, 0.93 ~ 1.58;治疗剂量与中剂量抗凝相比(6项试验,1803例患者,843例随机化时接受无创通气)和0.95 (CI, 0.76至1.19;I 2 = 0%;10项试验,3897例患者,2935例接受无氧或低氧治疗(随机分组),用于中剂量抗凝和预防性抗凝。治疗效果在预定的患者亚组中大致一致,尽管一些分析的效力有限。与低剂量抗凝相比,高剂量抗凝与更少的血栓栓塞事件相关,但发生大出血的风险更高。结论:治疗剂量抗凝较预防剂量抗凝可降低28天死亡率。与预防剂量抗凝剂相比,中剂量抗凝剂的死亡率相似,而治疗剂量抗凝剂的死亡率高于中剂量抗凝剂,尽管这种比较没有得到精确的估计。主要资助来源:无直接资助。(普洛斯彼罗:CRD42020213461)。
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Anticoagulation Among Patients Hospitalized for COVID-19 : A Systematic Review and Prospective Meta-analysis.

Background: Reported results of clinical trials assessing higher-dose anticoagulation in patients hospitalized for COVID-19 have been inconsistent.

Purpose: To estimate the association of higher- versus lower-dose anticoagulation with clinical outcomes.

Data sources: Randomized trials were identified from the World Health Organization's International Clinical Trials Registry Platform and ClinicalTrials.gov with no restriction by trial status or language.

Study selection: Eligible randomized trials assigned patients hospitalized for COVID-19 to higher- versus lower-dose anticoagulation.

Data extraction: 20 eligible trials provided data in a prospectively agreed format. Two further studies were included based on published data. The primary outcome was all-cause mortality 28 days after randomization. Secondary outcomes were progression to invasive mechanical ventilation or death, thromboembolic events, and major bleeding.

Data synthesis: Therapeutic- compared with prophylactic-dose anticoagulation with heparins reduced 28-day mortality (OR, 0.77 [95% CI, 0.64 to 0.93]; I 2 = 29%; 11 trials, 6297 patients, of whom 5456 required low or no oxygen at randomization). The ORs for 28-day mortality were 1.21 (CI, 0.93 to 1.58; I 2 = 0%) for therapeutic-dose compared with intermediate-dose anticoagulation (6 trials, 1803 patients, 843 receiving noninvasive ventilation at randomization) and 0.95 (CI, 0.76 to 1.19; I 2 = 0%; 10 trials, 3897 patients, 2935 receiving no or low oxygen at randomization) for intermediate- versus prophylactic-dose anticoagulation. Treatment effects appeared broadly consistent across predefined patient subgroups, although some analyses were limited in power. Higher- compared with lower-dose anticoagulation was associated with fewer thromboembolic events, but a greater risk for major bleeding.

Conclusion: Therapeutic-dose compared with prophylactic-dose anticoagulation reduced 28-day mortality. Mortality was similar for intermediate-dose compared with prophylactic-dose anticoagulation and higher for therapeutic-dose compared with intermediate-dose anticoagulation, although this comparison was not estimated precisely.

Primary funding source: No direct funding. (PROSPERO: CRD42020213461).

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来源期刊
Annals of Internal Medicine
Annals of Internal Medicine 医学-医学:内科
CiteScore
23.90
自引率
1.80%
发文量
1136
审稿时长
3-8 weeks
期刊介绍: Established in 1927 by the American College of Physicians (ACP), Annals of Internal Medicine is the premier internal medicine journal. Annals of Internal Medicine’s mission is to promote excellence in medicine, enable physicians and other health care professionals to be well informed members of the medical community and society, advance standards in the conduct and reporting of medical research, and contribute to improving the health of people worldwide. To achieve this mission, the journal publishes a wide variety of original research, review articles, practice guidelines, and commentary relevant to clinical practice, health care delivery, public health, health care policy, medical education, ethics, and research methodology. In addition, the journal publishes personal narratives that convey the feeling and the art of medicine.
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