奥伦堡系统性红斑狼疮患者的存活率和致死率

N. V. Lazareva, O. V. Bugrova, N. E. Artemova, K. Nagornova
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摘要

目前,系统性红斑狼疮(SLE)的预后已明显改善,但这些患者的相对死亡风险仍高于普通人群。血栓并发症是系统性红斑狼疮的主要死因之一。 目的:分析奥伦堡系统性红斑狼疮患者的存活率和致命结果的结构,包括血栓并发症导致的死亡。 材料与方法从 2007 年至 2022 年,对系统性红斑狼疮的病情发展和患者存活率进行了两个阶段的研究。对所有基线患者(68 人)和 15 年后存活患者(50 人)的临床症状进行了分析。参加研究时的中位年龄为 35 [29; 45]岁,病程为 7.5 [3; 13.5]年。在第二阶段,确定了存活患者的病程特征和 15 年死亡患者的死亡原因。 结果与讨论在奥伦堡的系统性红斑狼疮患者中,10年、15年和20年的存活率分别达到98.5%、95.5%和86.3%。在此期间,有18人(26.5%)死亡,死者的中位年龄为48.5 [39; 57]岁,病程为22 [16; 30]年。最常见的死因是抗磷脂综合征、狼疮肾炎和动脉高血压引起的血栓并发症(14 例,78%)。感染并发症是较少见的死亡原因(4 人,22%)。血栓并发症患者的20年存活率为80.2%,明显低于无血栓形成的系统性红斑狼疮患者。 结论研究结果表明,在奥伦堡的系统性红斑狼疮患者中,血栓并发症是一个不利的预后因素。
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Survival and lethal outcomes in Orenburg population of patients with systemic lupus erythematosus
   Currently, the prognosis for systemic lupus erythematosus (SLE) has improved significantly, but the relative risk of death in these patients is stillhigher than in the general population. Thrombotic complications are one of the leading causes of death in SLE.   Objective: to analyze the survival rate and structure of lethal outcomes in Orenburg population of patients with SLE, including deaths due to thrombotic complications.   Material and methods. A two-stage study of SLE progression and patient survival was conducted from 2007 to 2022. Clinical signs of the diseasewere analyzed in all patients at baseline (n = 68) and in survivors (n = 50) after 15 years. The median age at the time of enrolment in the study was 35 [29; 45] years, the disease duration – 7.5 [3; 13.5] years. During the second stage, the characteristics of the course of the disease in the survived patients and the causes of death in those who died over 15-year period were determined.   Results and discussion. The 10-, 15- and 20-year survival rates in Orenburg population of patients with SLE reached 98.5, 95.5 and 86.3%, respectively. During this period, 18 (26.5 %) deaths were registered, the median age of the deceased was 48.5 [39; 57] years, and the duration of the disease was 22 [16; 30] years. The most common causes of death were thrombotic complications (n = 14, 78 %) due to antiphospholipid syndrome, lupus nephritis, and arterial hypertension. Less frequently, infectious complications were the cause of death (n = 4, 22 %). Patients with thrombotic complications had a 20-year survival rate of 80.2% that was significantly lower than in the SLE group without thrombosis.   Conclusion. The results obtained allow to consider the presence of thrombotic complications in patients with SLE in Orenburg population as an unfavorable prognostic factor.
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