Clinical Pharmacy Department, Hamad General Hospital, Doha, Qatar.
Internal Medicine Department, Hamad Medical Corporation, Doha, Qatar.
J Thromb Thrombolysis. 2021 Feb;51(2):388-396. doi: 10.1007/s11239-020-02179-4.
Direct oral anticoagulant (DOAC) agents are becoming the anticoagulation strategy of choice. However, their use in the treatment of acute venous thromboembolism (VTE) in morbidly obese patients (bodyweight of > 120 kg or BMI > 40 kg/m) guarded. This is due to the scarce data supporting their use in this population. As a result, the International Society on Thrombosis and Haemostasis recommended against their use in this cohort of patients. New data emerged supporting the use of DOACs in these patients. Hence, we aimed to systematically review the literature exploring the efficacy and safety of these agents compared to warfarin in VTE treatment in morbidly obese patients. A systematic review of PubMed and EMBASE since inception until 01/04/2020. Subsequently, a non-inferiority (NI of 1.75) meta-analysis utilizing the random-effects model. Five observational studies (6585 patients) were included in our meta-analysis. DOAC analogs were non-inferior compared to warfarin in reducing the primary efficacy outcome of VTE recurrence (OR 1.07, 95% CI 0.93-1.23) and the primary safety outcome (major bleeding events) (OR 0.80, 95% CI 0.54-1.17). Our meta-analysis comprising real-world observational data concludes that the use of DOAC analogs in morbidly obese patients (bodyweight of > 120 kg or BMI > 40 kg/m) is non-inferior with regards to efficacy and safety compared to warfarin. This finding helps to resolve the uncertainty associated with the use of DOACs in this cohort. Additionally, it invites for a confirmatory non-inferiority randomized controlled trial testing DOAC vs. Warfarin in this group of patients.
直接口服抗凝剂(DOAC)正成为抗凝治疗的首选策略。然而,由于支持其在病态肥胖患者(体重>120kg 或 BMI>40kg/m)中应用的数据有限,其在治疗急性静脉血栓栓塞症(VTE)中的应用受到限制。因此,国际血栓与止血学会建议不要在该患者群体中使用这些药物。新数据表明 DOAC 在这些患者中的应用是安全有效的。因此,我们旨在系统地回顾文献,以评估与华法林相比,DOAC 在治疗病态肥胖患者 VTE 中的疗效和安全性。系统检索 PubMed 和 EMBASE 自成立至 2020 年 4 月 1 日的文献。随后采用随机效应模型进行非劣效性(NI 为 1.75)的荟萃分析。我们的荟萃分析纳入了 5 项观察性研究(共 6585 例患者)。DOAC 类似物与华法林相比,在降低 VTE 复发的主要疗效终点(OR 1.07,95%CI 0.93-1.23)和主要安全性终点(大出血事件)(OR 0.80,95%CI 0.54-1.17)方面无显著差异。本项包含真实世界观察性数据的荟萃分析表明,与华法林相比,DOAC 类似物在病态肥胖患者(体重>120kg 或 BMI>40kg/m)中的应用在疗效和安全性方面无显著差异。这一发现有助于解决在该患者群体中使用 DOAC 相关的不确定性问题。此外,还需要进行一项 DOAC 与华法林在该患者群体中的非劣效性随机对照试验,以进一步证实这一结论。