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COVID-19感染中治疗性与非治疗性剂量抗凝治疗:随机对照试验的系统评价和荟萃分析

Therapeutic Versus Non-Therapeutic Dose Anticoagulation in COVID-19 Infection: A Systematic Review and Meta-analysis of Randomised Controlled Trials.

作者信息

Selvarajan Sushil, John Jisha Sara, Tharyan Prathap, Kirubakaran Richard, Singh Bhagteshwar, George Biju, Mathew Joseph L, Rupali Priscilla

机构信息

Department of Clinical Haematology Christian Medical College Vellore India.

Department of Infectious Diseases Christian Medical College Vellore India.

出版信息

EJHaem. 2025 Feb 10;6(1):e1100. doi: 10.1002/jha2.1100. eCollection 2025 Feb.

Abstract

BACKGROUND

Abnormal coagulation and thrombotic complications prompted many guidelines to recommend thromboprophylaxis for patients hospitalised with COVID-19, but the dose required for prophylaxis remains unclear. This systematic review (SR) analyses the safety and efficacy of therapeutic dose anticoagulation (TDA) versus non-therapeutic dose anticoagulation (NDA) in COVID-19 patients.

METHODS

According to the , we performed an SR. The protocol is registered in Prospero (CRD42021269197, date 12 August 2021).

RESULTS

In this SR of 18 studies, TDA was shown to reduce all-cause mortality (risk ratio [RR] 0.83; 95% confidence interval [95% CI] 0.70, 0.99) in COVID-19 infection. TDA also reduced thrombosis (RR 0.55; 95% CI 0.48, 0.72) but increased major bleeding (RR 1.87; 95% CI 1.29, 2.69). A stratified analysis according to severity revealed that, in non-critical patients, TDA resulted in mortality benefit (RR 0.79; 95% CI 0.67, 0.94). In critical patients, TDA did not affect all-cause mortality (RR 1.03; 95% CI 0.89, 1.18) but reduced thrombosis (RR 0.65; 95% CI 0.48, 0.86) and increased major bleeding (RR 1.85; 95% CI 1.06, 3.23).

CONCLUSION

TDA significantly reduced all-cause mortality and thrombosis in non-critical COVID-19 patients at the expense of increased major bleeding. In critical COVID-19, this mortality benefit was not observed.

摘要

背景

异常凝血和血栓形成并发症促使许多指南建议对COVID-19住院患者进行血栓预防,但预防所需剂量仍不明确。本系统评价(SR)分析了治疗剂量抗凝(TDA)与非治疗剂量抗凝(NDA)在COVID-19患者中的安全性和有效性。

方法

根据 ,我们进行了一项系统评价。该方案已在国际前瞻性系统评价注册库(Prospero,注册号CRD42021269197,日期为2021年8月12日)注册。

结果

在这项对18项研究的系统评价中,TDA被证明可降低COVID-19感染患者的全因死亡率(风险比[RR]0.83;95%置信区间[95%CI]0.70,0.99)。TDA还可降低血栓形成(RR 0.55;95%CI 0.48,0.72),但会增加大出血(RR 1.87;95%CI 1.29,2.69)。根据严重程度进行的分层分析显示,在非重症患者中,TDA可带来死亡率获益(RR 0.79;95%CI 0.67,0.94)。在重症患者中,TDA不影响全因死亡率(RR 1.03;95%CI 0.89,1.18),但可降低血栓形成(RR 0.65;95%CI 0.48,0.86)并增加大出血(RR 1.85;95%CI 1.06,3.23)。

结论

TDA可显著降低非重症COVID-19患者的全因死亡率和血栓形成,但代价是大出血增加。在重症COVID-19患者中,未观察到这种死亡率获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a32/11811394/a4be054ccbf3/JHA2-6-e1100-g006.jpg

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