Alfehaid Lama, Alsuhebany Nada, Albahlal Hussah, Alomran Albatoul, Alshehri Abdulmajeed M, AlSheef Mohammed, Almutairi Abdulaali
Department of Pharmacy Practice, College of Pharmacy, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Clin Appl Thromb Hemost. 2025 Jan-Dec;31:10760296251364269. doi: 10.1177/10760296251364269. Epub 2025 Aug 1.
BackgroundAntiphospholipid Syndrome (APS) is an autoimmune condition that increases thrombosis risk. Although Vitamin K antagonists (VKA) are standard treatment, interest in direct oral anticoagulants (DOAC) has grown. Recent studies evaluated DOAC across all APS subgroups. This review updates our understanding of DOAC's efficacy and safety compared to VKA in preventing thrombotic complications, integrating new findings into the literature.MethodsA systematic review across PubMed/Medline, Embase, and Cochrane was conducted in accordance with PRISMA guidelines. The quality of randomized controlled trials (RCTs) and cohort studies was assessed using the Cochrane Risk of Bias tool and the Newcastle-Ottawa Scale, respectively. Meta-analysis calculated odds ratios (OR) using the random effect model for arterial and venous thrombotic and bleeding outcomesResultsOf a total of 2385 records identified, the meta-analysis included 11 studies, comprising 5 RCTs and 7 observational studies, with a combined total of 1813 participants. The analysis revealed no significant difference in the odds of venous thromboembolism (VTE) between DOAC and VKA (OR = 0.80; 95% CI 0.41-1.56). However, a significant increase in thromboembolism recurrence was noted in triple-positive APS patients using DOAC compared to VKA (OR = 3.62; 95% CI 1.10-11.98). The risk of major bleeding was similar between DOAC and VKA (OR = 1.02; 95% CI 0.62-1.68). Additionally, the pooled analysis indicated a higher risk of arterial thrombosis with DOAC (OR = 6.21; 95% CI 2.06-18.76).ConclusionOverall, findings suggest DOAC are comparably safe but increase the risk of arterial thrombosis and VTE in triple-positive APS, favoring warfarin for prophylaxis.
背景
抗磷脂综合征(APS)是一种增加血栓形成风险的自身免疫性疾病。尽管维生素K拮抗剂(VKA)是标准治疗方法,但人们对直接口服抗凝剂(DOAC)的兴趣与日俱增。最近的研究评估了DOAC在所有APS亚组中的应用情况。本综述更新了我们对DOAC与VKA相比在预防血栓形成并发症方面的疗效和安全性的认识,并将新发现纳入文献。
方法
根据PRISMA指南,对PubMed/Medline、Embase和Cochrane进行了系统综述。分别使用Cochrane偏倚风险工具和纽卡斯尔-渥太华量表评估随机对照试验(RCT)和队列研究的质量。荟萃分析使用随机效应模型计算动脉和静脉血栓形成及出血结局的比值比(OR)。
结果
在总共识别出的2385条记录中,荟萃分析纳入了11项研究,包括5项RCT和7项观察性研究,共有1813名参与者。分析显示,DOAC和VKA之间静脉血栓栓塞(VTE)的比值比无显著差异(OR = 0.80;95% CI 0.41 - 1.56)。然而,与VKA相比,使用DOAC的三阳性APS患者血栓栓塞复发显著增加(OR = 3.62;95% CI 1.10 - 11.98)。DOAC和VKA之间大出血风险相似(OR = 1.02;95% CI 0.62 - 1.68)。此外,汇总分析表明DOAC导致动脉血栓形成的风险更高(OR = 6.21;95% CI 2.06 - 18.76)。
结论
总体而言,研究结果表明DOAC安全性相当,但会增加三阳性APS患者动脉血栓形成和VTE的风险,因此华法林更适合用于预防。