Efficacy and safety of long-term use of low molecular weight heparins in patients with systemic lupus erythematosus and antiphospholipid syndrome

N. V. Seredavkina, F. A. Cheldieva, A. A. Shumilova, T. M. Reshetnyak
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Abstract

To date, the management of patients with antiphospholipid syndrome (APS) with ineffectiveness and/or intolerance to vitamin K antagonists and direct oral anticoagulants remains controversial. One of the treatment strategies is the administration of low molecular weight heparins (LMWH) over a long period of time. Objective: to evaluate the efefficacy and safety of long-term treatment with LMWH in patients with APS. Material and methods. The study included 15 patients (13 women and 2 men) with APS. In 2 of them APS was isolated, in 12 it was combined with systemic lupus erythematosus (SLE), and in 1 – with SLE and psoriatic arthritis. The mean age of patients was 44 ± 12 years, and the mean duration of disease was 12 [6; 18] years. All patients were repeatedly examined in the V. A. Nasonova Research Institute of Rheumatology during hospitalizations and continued outpatient care in the clinical diagnostic center of the Institute. Results and discussion. Ten (67 %) patients received nadroparin, 5 (33 %) patients received enoxaparin. The median duration of therapy was 4 [1; 10] years. Indications for the use of LMWH were inefficacy and intolerance of oral anticoagulants (n = 12, 100 %) and vascular involvement such as thromboangiitis obliterans with the development of chronic arterial insufficiency, ulcers and necrosis of the toes (n = 6, 40 %). During therapy, 13 (86 %) of 15 patients showed clinical improvement: healing of ulcers and necrosis, reduction in the stage of arterial insufficiency, recanalization of venous blood clots. During the entire treatment period with LMWH, one patient experienced a relapse of thrombosis due to an insufficient dose of the drug. No hemorrhagic complications occurred in any case. Other adverse events, including elevated liver aminotransferases, osteoporosis, and thrombocytopenia, were also not observed. Conclusion. The results obtained suggest that long-term therapy with LMWH may be safe and effective in patients with APS.
长期使用低分子肝素治疗系统性红斑狼疮合并抗磷脂综合征的疗效和安全性
迄今为止,对维生素K拮抗剂和直接口服抗凝剂无效和/或不耐受的抗磷脂综合征(APS)患者的管理仍存在争议。治疗策略之一是长期使用低分子肝素(LMWH)。目的:评价低分子肝素长期治疗APS患者的疗效和安全性。材料和方法。该研究包括15例APS患者(13名女性和2名男性)。其中2例单独存在APS, 12例合并系统性红斑狼疮(SLE), 1例合并系统性红斑狼疮合并银屑病关节炎。患者平均年龄44±12岁,平均病程12 [6];18年。所有患者在V. A. Nasonova风湿病研究所住院期间和在该研究所临床诊断中心继续门诊治疗期间反复检查。结果和讨论。10例(67%)患者接受nadroparin治疗,5例(33%)患者接受依诺肝素治疗。治疗中位持续时间为4 [1];10)年。使用低分子肝素的适应症是口服抗凝剂无效和不耐受(n = 12,100%),以及血管受累,如血栓闭塞性脉管炎伴慢性动脉功能不全、溃疡和脚趾坏死(n = 6.40%)。在治疗期间,15例患者中有13例(86%)表现出临床改善:溃疡和坏死愈合,动脉功能不全阶段缩短,静脉血凝块再通。在整个低分子肝素治疗期间,有1例患者由于药物剂量不足而出现血栓复发。无出血性并发症发生。其他不良事件,包括肝转氨酶升高、骨质疏松和血小板减少症,也未观察到。结论。结果表明,低分子肝素长期治疗APS患者可能是安全有效的。
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