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有静脉血栓栓塞病史患者中遗传性抗凝血酶III缺乏症的患病率。

The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism.

作者信息

Vikydal R, Korninger C, Kyrle P A, Niessner H, Pabinger I, Thaler E, Lechner K

出版信息

Thromb Haemost. 1985 Dec 17;54(4):744-5.

PMID:4089808
Abstract

Antithrombin-III activity was determined in 752 patients with a history of venous thrombosis and/or pulmonary embolism. 54 patients (7.18%) had an antithrombin-III activity below the normal range. Among these were 13 patients (1.73%) with proven hereditary deficiency. 14 patients were judged to have probable hereditary antithrombin-III deficiency, because they had a positive family history, but antithrombin-III deficiency could not be verified in other members of the family. In the 27 remaining patients (most of them with only slight deficiency) hereditary antithrombin-III deficiency was unlikely. The prevalence of hereditary antithrombin-III deficiency was higher in patients with recurrent venous thrombosis.

摘要

对752例有静脉血栓形成和/或肺栓塞病史的患者测定了抗凝血酶III活性。54例患者(7.18%)的抗凝血酶III活性低于正常范围。其中13例患者(1.73%)经证实存在遗传性缺陷。14例患者被判定可能存在遗传性抗凝血酶III缺乏,因为他们有阳性家族史,但家族其他成员的抗凝血酶III缺乏无法得到证实。在其余27例患者中(大多数仅有轻度缺乏),遗传性抗凝血酶III缺乏的可能性不大。复发性静脉血栓形成患者中遗传性抗凝血酶III缺乏的患病率更高。

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