Department of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Department of Pharmacotherapy and Outcome Sciences, Virginia Commonwealth University, Richmond, Virginia, United States.
Thromb Haemost. 2023 Feb;123(2):186-191. doi: 10.1055/a-1956-9641. Epub 2022 Oct 7.
Data suggest that coronavirus disease 2019 (COVID-19) results in a prothrombotic state leading to arterial and venous thromboses. Vaccination, novel antiviral drugs, and emerging variants have changed the course of the disease in many ways; however, their effects on the incidence of thrombotic events and the efficacy of preventative antithrombotic agents have not been yet evaluated. A systematic search was conducted to identify studies reported on the incidence of thrombotic events based on vaccination status, use of novel antiviral drugs, and emerging viral variants. Similarly, we screened the ongoing/published randomized trials of preventative antithrombotic therapy in any COVID-19 population to assess whether subgroup-specific results were reported based on any of these variants. Upon searching a total of 3,451 records, only one entry fulfilled the inclusion criteria of our systematic review, which was a self-controlled case series on 29,121,633 vaccinated individuals, the incidence rate ratio of thrombotic complication after breakthrough infection was 13.86 (95% confidence interval [CI]: 12.76-15.05) compared with 1.10 (95% CI: 1.02-1.18) during the 28-day postvaccination. In conclusion, although the mortality benefit of mass vaccination and the early promising results of the new antiviral therapies are well known, we were unable to find clinical evidence on whether vaccination, the use of novel antiviral agents, and emerging viral variants have affected the incidence rate of thrombotic events or impacted the efficacy of prophylactic antithrombotic therapy in patients with COVID-19. Analyses from existing trials and large-scale registries can provide interim knowledge and any findings of relevance should be incorporated in the design of future trials.
数据表明,2019 年冠状病毒病(COVID-19)导致促血栓状态,从而引发动脉和静脉血栓形成。疫苗接种、新型抗病毒药物和新出现的变异株在许多方面改变了疾病的进程;然而,它们对血栓事件发生率和预防性抗血栓药物疗效的影响尚未得到评估。我们进行了系统检索,以确定基于疫苗接种状况、新型抗病毒药物使用和新出现的病毒变异株报告的血栓事件发生率的研究。同样,我们筛选了正在进行/发表的 COVID-19 人群中预防性抗血栓治疗的随机试验,以评估是否根据任何这些变异株报告了亚组特异性结果。总共搜索了 3451 条记录,只有一项符合我们系统评价的纳入标准,这是一项针对 29121633 名接种者的自我对照病例系列研究,突破性感染后的血栓并发症发生率为 13.86(95%置信区间[CI]:12.76-15.05),而接种后 28 天内为 1.10(95%CI:1.02-1.18)。总之,尽管大规模疫苗接种的死亡率获益和新型抗病毒疗法的早期有希望的结果是众所周知的,但我们无法找到关于疫苗接种、新型抗病毒药物的使用以及新出现的病毒变异株是否影响 COVID-19 患者血栓事件发生率或影响预防性抗血栓治疗疗效的临床证据。现有试验和大规模登记处的分析可以提供中期知识,任何相关发现都应纳入未来试验的设计中。