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首页> 外文期刊>revista colombiana de reumatología (english edition) >Use of factor Xa inhibitors in antiphospholipid antibodies syndrome: A series of seven cases
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Use of factor Xa inhibitors in antiphospholipid antibodies syndrome: A series of seven cases

机译:Xa因子抑制剂在抗磷脂抗体综合征中的应用:7例病例系列

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BackgroundAntiphospholipid syndrome is an autoimmune disease with antibodies against membrane phospholipids with mainly thrombotic and/or obstetric manifestations. Its treatment is generally based on indefinite anticoagulation, usually with warfarin, and which, for various factors, is not always feasible, making it necessary to use alternative therapies. ObjectiveTo describe the experience with rivaroxaban in patients with antiphospholipid syndrome. Materials and methodsA descriptive study was conducted on subjects that met the 2006 Sydney criteria for antiphospholipid antibodies syndrome and received anticoagulation with rivaroxaban at 20mg daily dose in 2reference hospitals in Medellin, Colombia, between January 2012 and April 2015. ResultsThe study included 7 patients, with a mean age of 36±10.8 years (range 23–55). Four patients had venous thrombosis, 5arterial, 5were positive for anticardiolipin antibodies, 3reactive to lupus anticoagulant, 2anti-β2 glycoprotein positive subjects, and one patient had triple antiphospholipid antibody positivity. The median time of warfarin use was 15 months (RIQ 1–36). The reasons for starting rivaroxaban were: bleeding (n=2), sub-therapeutic coagulation ranges (n=2), toxicoderma, gastrointestinal intolerance, and re-thrombosis (n=1, each). The time of use was 17.9±13.4 months (range: 3–34). There were 2recurrent cases of thrombosis during follow-up, and no adverse events. ConclusionThe use of factor Xa inhibitors in a series of patients with antiphospholipid syndrome and unable to use warfarin showed an adequate safety profile; however, 2recurrent episodes of venous thrombosis occurred.
机译:背景抗磷脂综合征是一种自身免疫性疾病,具有针对膜磷脂的抗体,主要表现为血栓形成和/或产科表现。它的治疗通常基于无限期抗凝治疗,通常使用华法林,并且由于各种因素,这并不总是可行的,因此有必要使用替代疗法。目的探讨利伐沙班在抗磷脂综合征患者中的疗效。材料和方法2012年1月至2015年4月在哥伦比亚麦德林的2家医院对符合2006年悉尼抗磷脂抗体综合征标准并接受利伐沙班每日20mg抗凝治疗的受试者进行了描述性研究。结果该研究纳入了7例患者,平均年龄为36±10.8岁(范围23-55岁)。静脉血栓形成4例,动脉血栓5例,抗心磷脂抗体5例阳性,3例对狼疮抗凝剂反应,2例抗β2糖蛋白阳性,1例抗磷脂抗体阳性。使用华法林的中位时间为15个月(RIQ 1-36)。开始使用利伐沙班的原因有:出血(n=2)、亚治疗性凝血范围(n=2)、中毒皮肤病、胃肠道不耐受和再血栓形成(n=1)。使用时间为17.9±13.4个月(范围:3-34)。随访期间血栓复发2例,无不良事件。结论在一系列抗磷脂综合征患者中,使用Xa因子抑制剂不能使用华法林显示出足够的安全性;然而,静脉血栓形成发生了 2 次复发。

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