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动脉血栓栓塞中的高凝状态。

Hypercoagulable states in arterial thromboembolism.

作者信息

Eason J D, Mills J L, Beckett W C

机构信息

Vascular Surgery Section, Wilford Hall USAF Medical Center, Lackland, AFB.

出版信息

Surg Gynecol Obstet. 1992 Mar;174(3):211-5.

PMID:1542837
Abstract

Hypercoagulable states are disorders of blood coagulation, which include deficiencies of natural anticoagulants, disorders of the fibrinolytic system, presence of antiphospholipid antibody and abnormalities of platelet function. These disorders are well known causes of venous thromboembolic disease and are being recognized in association with arterial thromboembolic occurrences with increasing frequency. The performance of standard prosthetic vascular reconstructions may result in disastrous outcomes in patients with unrecognized and untreated hypercoagulable states. From 1986 to 1990, we identified 12 patients with hypercoagulable states, six of whom presented with evidence of arterial thromboembolism. All of the patients were men who smoked and were somewhat younger than the usual patient with atherosclerosis. Their ages ranged from 41 to 62 years. Four patients presented with ischemic rest pain, one patient with blue toe syndrome and one with rapidly progressive claudication. Four patients had undergone prior vascular reconstruction and two had previous pulmonary emboli. Evaluation of these patients to identify hypercoagulability included determinations of prothrombin time (PT) and partial thromboplastin time (PTT), platelet count, antithrombin III, protein C, free protein S and total protein S levels, along with platelet aggregometry. Two patients had protein S deficiency, one had protein C deficiency, one patient had protein C and S deficiency and two patients had hyperaggregable platelets. Four patients had prosthetic reconstructions and two had autogenous reconstructions. Three of the four patients undergoing prosthetic reconstructions had subsequent loss of limb and one patient died. Only one patient with prosthetic reconstruction had a patent graft on long term anticoagulation. Both patients undergoing autogenous procedures had successful revascularization with limb salvage.

摘要

高凝状态是血液凝固紊乱,包括天然抗凝剂缺乏、纤维蛋白溶解系统紊乱、抗磷脂抗体的存在以及血小板功能异常。这些紊乱是静脉血栓栓塞性疾病的常见病因,并且与动脉血栓栓塞事件的关联正日益受到关注。对于未被识别和未治疗的高凝状态患者,进行标准的人工血管重建可能会导致灾难性后果。1986年至1990年期间,我们识别出12例高凝状态患者,其中6例有动脉血栓栓塞证据。所有患者均为男性,有吸烟习惯,且比一般的动脉粥样硬化患者略年轻。他们的年龄在41岁至62岁之间。4例患者出现静息性缺血性疼痛,1例患者出现蓝趾综合征,1例患者出现快速进展性跛行。4例患者曾接受过血管重建,2例曾有过肺栓塞。对这些患者进行高凝状态评估包括测定凝血酶原时间(PT)和部分凝血活酶时间(PTT)、血小板计数、抗凝血酶III、蛋白C、游离蛋白S和总蛋白S水平,以及血小板聚集试验。2例患者存在蛋白S缺乏,1例患者存在蛋白C缺乏,1例患者同时存在蛋白C和S缺乏,2例患者血小板高聚集。4例患者进行了人工血管重建,2例进行了自体血管重建。接受人工血管重建的4例患者中有3例随后肢体丧失,1例患者死亡。只有1例接受人工血管重建的患者在长期抗凝治疗下移植血管保持通畅。接受自体血管重建的2例患者均成功实现血管再通并挽救了肢体。

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