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灾难性抗磷脂综合征:单中心成功治疗 14 例的经验教训。叙述性报告。

Catastrophic antiphospholipid syndrome: Lessons from 14 cases successfully treated in a single center. A narrative report.

机构信息

Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy.

Apheresis Unit, Blood Transfusion Service, University-Hospital of Padua, Padua, Italy.

出版信息

J Autoimmun. 2018 Sep;93:124-130. doi: 10.1016/j.jaut.2018.07.001. Epub 2018 Jul 7.

Abstract

The study aimed to evaluate the clinical significance of laboratory findings in patients with catastrophic antiphospholipid syndrome (CAPS) and to report the effects of a well-defined treatment protocol in 14 consecutive cases. Thirteen patients (12 presenting one and one presenting two episodes of CAPS) were consecutively treated and monitored between 1986 and 2017. Antiphospholipid antibody (aPL) characteristics of the patients were compared with those of 64 matched controls (45 antiphospholipid syndrome patients and 19 aPL carriers) who did not develop CAPS during the same mean follow-up period (12 years ± 9.9 SD). Triple aPL positivity (IgG/IgM anticardiolipin + IgG/IgM anti-β2Glycoprotein I + lupus anticoagulants) significantly prevailed in the CAPS patients with respect to the controls (p = 0.003). IgG anticardiolipin and IgG anti-β2Glycoprotein I mean antibody titers of the CAPS patients were significantly higher than those of the controls (p = 0.0018 and p = 0.003, respectively). Triple therapy (anticoagulation + plasma exchange + steroids) was administered to all the CAPS cases except for one. Beginning in 2009, intravenous immunoglobulin infusion has also been included in the triple therapy protocol (six patients). All the patients recovered from CAPS; five showed renal failure and one a I-II class New York Heart Association (NYHA) dilated cardiomyopathy. Long-term outcomes of CAPS included a gradual worsening of renal failure in one patient who required hemodialysis 30 years after the acute episode. Renal function improved in the other four patients. The patient affected with dilated cardiomyopathy worsened to a II class NYHA over a five year period. Currently all the patients are alive. A specific antiphospholipid antibody profile could be considered a risk factor associated to CAPS. Early use of a defined treatment protocol based on triple therapy either or not associated with IVIG was associated with recovery in all CAPS patients.

摘要

这项研究旨在评估灾难性抗磷脂综合征(CAPS)患者实验室检查结果的临床意义,并报告 14 例连续病例采用明确治疗方案的效果。1986 年至 2017 年间,连续治疗和监测了 13 例患者(12 例出现 1 次 CAPS 发作,1 例出现 2 次 CAPS 发作)。将患者的抗磷脂抗体(aPL)特征与 64 例匹配对照(45 例抗磷脂综合征患者和 19 例 aPL 携带者)进行比较,这些对照在相同的平均随访期(12 年±9.9 标准差)内未发展为 CAPS。与对照组相比,三重 aPL 阳性(IgG/IgM 抗心磷脂+IgG/IgM 抗-β2糖蛋白 I+狼疮抗凝物)在 CAPS 患者中显著更为常见(p=0.003)。CAPS 患者的 IgG 抗心磷脂和 IgG 抗-β2 糖蛋白 I 平均抗体滴度明显高于对照组(p=0.0018 和 p=0.003)。除 1 例外,所有 CAPS 病例均接受抗凝治疗+血浆置换+皮质类固醇三联疗法。自 2009 年以来,静脉内免疫球蛋白输注也被纳入三联疗法方案(6 例患者)。所有患者均从 CAPS 中恢复;5 例发生肾衰竭,1 例出现 I-II 级纽约心脏协会(NYHA)扩张型心肌病。CAPS 的长期结局包括 1 例患者在急性发作后 30 年需要血液透析,其肾功能逐渐恶化。其他 4 例患者的肾功能有所改善。患有扩张型心肌病的患者在五年内恶化至 NYHA II 级。目前所有患者均存活。特定的抗磷脂抗体谱可能被认为是与 CAPS 相关的危险因素。尽早使用基于三联疗法的明确治疗方案,无论是否联合 IVIG,均可使所有 CAPS 患者康复。

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