Levy D M, Massicotte M P, Harvey E, Hebert D, Silverman E D
Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Lupus. 2003;12(10):741-6. doi: 10.1191/0961203303lu458oa.
Paediatric patients with systemic lupus erythematosus (SLE) and antiphospholipid antibodies (aPL), specifically lupus anticoagulants (LAC) are at high risk of developing thromboembolic events (TE). Our objectives were to determine the prevalence of TE in paediatric SLE patients with LAC and to determine if anticoagulation was effective to decrease morbidity, and prevent recurrent TE. We reviewed data on 149 paediatric SLE patients treated over 10 years. In all, 24 patients (16%) were LAC positive, and 21 TE occurred in 13 of these LAC positive patients (54% incidence of TE in LAC positive patients). The events were cerebral venous thrombosis (9), arterial stroke (3), deep venous thrombosis (4), pulmonary embolism (2), other venous event (1) and other arterial events (2). The median duration between SLE diagnosis and first TE was 15.2 months (range 0-62), and the median age at first TE was 15.1 years (range 11.4-18.4). Long-term anticoagulation was prescribed, and eight patients (62%) were transferred to adult care on lifelong oral warfarin; four (31%) remain under our care on lifelong warfarin, and one patient died of causes unrelated to her TE. No patient has been identified with deficiencies of protein C, protein S or antithrombin III. One patient is heterozygous for Factor V Leiden, and one is heterozygous for both the Prothrombin 20210A mutation and the MTHFR (methylene tetrahydrofolate reductase) mutation. Four patients had recurrent TE (31%), and three were not anticoagulated at the time of their second event. One patient had two recurrences on therapeutic anticoagulation. Thromboembolic events are prevalent in the LAC positive paediatric SLE population, and consideration for lifelong anticoagulation must occur after an initial TE.
患有系统性红斑狼疮(SLE)和抗磷脂抗体(aPL),尤其是狼疮抗凝物(LAC)的儿科患者发生血栓栓塞事件(TE)的风险很高。我们的目标是确定患有LAC的儿科SLE患者中TE的患病率,并确定抗凝治疗是否能有效降低发病率并预防TE复发。我们回顾了10年间接受治疗的149例儿科SLE患者的数据。总共有24例患者(16%)LAC呈阳性,其中13例LAC阳性患者发生了21次TE(LAC阳性患者中TE的发生率为54%)。这些事件包括脑静脉血栓形成(9例)、动脉性中风(3例)、深静脉血栓形成(4例)、肺栓塞(2例)、其他静脉事件(1例)和其他动脉事件(2例)。SLE诊断至首次TE的中位时间为15.2个月(范围0 - 62个月),首次TE时的中位年龄为15.1岁(范围11.4 - 18.4岁)。患者接受了长期抗凝治疗,8例患者(62%)转至成人科室接受终身口服华法林治疗;4例患者(31%)仍在我们的治疗下接受终身华法林治疗,1例患者死于与TE无关的原因。未发现患者存在蛋白C、蛋白S或抗凝血酶III缺乏。1例患者为因子V莱顿杂合子,1例患者同时为凝血酶原20210A突变和亚甲基四氢叶酸还原酶(MTHFR)突变的杂合子。4例患者发生了TE复发(31%),其中3例在第二次事件发生时未接受抗凝治疗。1例患者在接受治疗性抗凝时复发了两次。血栓栓塞事件在LAC阳性的儿科SLE人群中很普遍,首次TE后必须考虑进行终身抗凝治疗。