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首页> 外文期刊>Haematologica >The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein S | Haematologica
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The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein S | Haematologica

机译:天然抗凝剂抗凝血酶,蛋白C和蛋白S遗传性缺乏的患者再次发生静脉血栓栓塞的风险|血液学

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Few data are available on the risk of recurrent venous thromboembolism (VTE) associated with the rare inherited deficiencies of natural anticoagulants. We studied 602 patients with previous VTE: the incidence of first recurrence in the absence of anticoagulation was retrospectively estimated in 64 patients with deficiency of antithrombin (AT, n=14), protein C (PC, n=28), or protein S (PS, n=22) and 538 with no known defect, who acted as the reference group. After adjustment for sex, age, and circumstances of the first event, AT deficiency resulted an independent risk factor for recurrence (hazard ratio 1.9, 95% CI 1.0-3.9); the carriers of PC or PS deficiency had a marginal increase in risk (hazard ratio 1.4, 95% CI 0.9-2.2). In conclusion, patients with AT deficiency are potential candidates for long-term oral anticoagulation.
机译:很少有数据涉及与天然抗凝剂罕见的遗传缺陷相关的复发性静脉血栓栓塞(VTE)的风险。我们研究了602例既往接受过VTE的患者:回顾性评估了64例缺乏抗凝血酶(AT,n = 14),C蛋白(PC,n = 28)或S蛋白(A)缺乏的患者中首次复发的发生率。 PS,n = 22)和538,没有已知缺陷,充当参考组。在对首次发作的性别,年龄和情况进行调整后,AT缺乏导致了复发的独立危险因素(危险比1.9,95%CI 1.0-3.9); PC或PS缺乏症的携带者的风险略有增加(危险比1.4,95%CI 0.9-2.2)。总之,患有AT缺乏症的患者是长期口服抗凝治疗的潜在候选人。

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