Antiphospholipid-thrombosis syndromes.

Haemostasis Pub Date : 1999-01-01 DOI:10.1159/000022492
R L Bick, B Arun, E P Frenkel
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引用次数: 86

Abstract

Antiphospholipid antibodies are strongly associated with thrombosis and appear to be the most common of the acquired blood protein defects causing thrombosis. Based upon our experience, approximately 25% of patients with unexplained venous thrombosis, approximately 60% of patients with cerebrovascular thrombosis, approximately 37% of patients with transient ischemic attacks, approximately 18% with premature coronary artery thrombosis and approximately 60% of patients with recurrent fetal loss (recurrent miscarriage syndrome) harbor antiphospholipid antibodies. Although the precise mechanism(s) whereby antiphospholipid antibodies alter hemostasis to induce a hypercoagulable state remain unclear, several theories have been advanced. Since the aPTT is unreliable in patients with lupus anticoagulant and is not usually prolonged in patients with anticardiolipin antibodies, definitive tests, ELISA for IgG, IgA and IgM anticardiolipin antibodies and the dilute Russel's viper venom time (followed by cephalin correction for confirmation) for lupus anticoagulant should be immediately ordered when suspecting the antiphospholipid syndrome in individuals with otherwise unexplained thrombotic or thromboembolic events or recurrent fetal loss. However, if one strongly suspects antiphospholipid thrombosis syndrome clinically and assays for lupus anticoagulants and anticardiolipin antibodies are negative, specific assays for all three idiotypes of phosphatidylserine, phosphatidylethanolamine, phosphatidylcholine, phosphatidylinositol and phosphatidylglycerol are available and should be considered. These may clearly be indicated for difficult diagnostic cases of fetal wastage syndrome, and cerebrovascular events, but their significance in other types of thrombosis, particularly venous, remains unclear at present. Since about 65% of patients with antiphospholipid antibodies will fail warfarin therapy (rethrombose), it is important to define this common defect and institute appropriate antithrombotic therapy for appropriate time periods.

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Antiphospholipid-thrombosis综合症。
抗磷脂抗体与血栓形成密切相关,似乎是最常见的获得性血蛋白缺陷引起血栓形成。根据我们的经验,大约25%的不明原因静脉血栓患者、大约60%的脑血管血栓患者、大约37%的短暂性脑缺血发作患者、大约18%的过早冠状动脉血栓患者和大约60%的复发性胎儿丢失(复发性流产综合征)患者携带抗磷脂抗体。虽然抗磷脂抗体改变止血诱导高凝状态的确切机制尚不清楚,但已经提出了几种理论。由于aPTT在狼疮抗凝患者中是不可靠的,并且在抗心磷脂抗体患者中通常不会延长,因此确定试验,ELISA检测IgG,当怀疑患有其他原因不明的血栓形成或血栓栓塞事件或复发性胎儿丢失的个体存在抗磷脂综合征时,应立即安排IgA和IgM抗心磷脂抗体和稀释的罗素毒蛇毒液时间(随后进行头蛋白校正以确认)。然而,如果临床强烈怀疑抗磷脂血栓形成综合征,并且狼疮抗凝血剂和抗心磷脂抗体的检测结果为阴性,则应考虑对所有三种独特型的磷脂酰丝氨酸、磷脂酰乙醇胺、磷脂酰胆碱、磷脂酰肌醇和磷脂酰甘油进行特异性检测。这些可能明确适用于胎儿浪费综合征和脑血管事件的难诊断病例,但它们在其他类型血栓,特别是静脉血栓中的意义目前尚不清楚。由于约65%的抗磷脂抗体患者华法林治疗失败(rethrombose),因此确定这种常见缺陷并在适当的时间内进行适当的抗血栓治疗是很重要的。
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