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患有遗传性抗凝血酶III、蛋白C和蛋白S缺乏症的女性服用口服避孕药的血栓形成风险。GTH天然抑制剂研究小组。

Thrombotic risk of women with hereditary antithrombin III-, protein C- and protein S-deficiency taking oral contraceptive medication. The GTH Study Group on Natural Inhibitors.

作者信息

Pabinger I, Schneider B

机构信息

First Department of Medicine, University of Vienna, Austria.

出版信息

Thromb Haemost. 1994 May;71(5):548-52.

PMID:8091378
Abstract

The thrombotic risk of women with a heterozygous natural clotting inhibitor deficiency taking oral contraceptives (OC) has not been evaluated. Therefore, a retrospective collaborative controlled cohort-study was carried out in 8 coagulation laboratories and thrombosis units in Austria, Germany and Switzerland. The incidence of thromboembolism in 48 females heterozygous for hereditary type I deficiency of antithrombin III (n = 15), protein C (n = 16) or protein S (n = 17), who had taken OC at least once in their life were compared with that of 48 deficient women, who had never taken OC (controls). Diagnosis of the deficiency state was made in the participating centers. Data on the onset and duration of OC intake and the date and site of thrombotic events were obtained from a questionnaire filled in by the patient or a physician during a visit at a participating center. The observation period in the OC patients was started with onset of OC intake and was terminated when a thromboembolic event had occurred or when OC medication were discontinued. In the patients without OC, the observation period began at an age matched to that of the OC patient and ended when a thromboembolic event had occurred or was continued as long as the corresponding OC patient was on treatment. In AT III-deficient females the probability for thrombosis was significantly higher for patients taking OC compared to the non-OC-patients (Wilcoxon test p = 0.004, Log Rank test p = 0.005).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

携带杂合子天然凝血抑制剂缺乏症的女性服用口服避孕药(OC)的血栓形成风险尚未得到评估。因此,在奥地利、德国和瑞士的8个凝血实验室和血栓形成治疗中心开展了一项回顾性协作对照队列研究。对48名抗凝血酶III遗传性I型缺乏症(n = 15)、蛋白C缺乏症(n = 16)或蛋白S缺乏症(n = 17)的杂合子女性进行研究,这些女性一生中至少服用过一次OC,将她们的血栓栓塞发生率与48名从未服用过OC的缺陷女性(对照组)进行比较。缺陷状态的诊断在参与研究的中心进行。通过患者或医生在参与研究中心就诊时填写的问卷,获取OC摄入的起始时间和持续时间以及血栓形成事件的日期和部位等数据。OC患者的观察期从开始服用OC时开始,当发生血栓栓塞事件或停止OC用药时结束。在未服用OC的患者中,观察期从与OC患者年龄匹配时开始,当发生血栓栓塞事件时结束,或者只要相应的OC患者仍在接受治疗,观察期就持续。在抗凝血酶III缺乏的女性中,服用OC的患者发生血栓形成的概率显著高于未服用OC的患者(Wilcoxon检验p = 0.004,对数秩检验p = 0.005)。(摘要截短至250字)

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