Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study

被引:42
作者
Cosmi, B [1 ]
Legnani, C
Bernardi, F
Coccheri, S
Palareti, G
机构
[1] Univ Hosp S Orsola Malpighi, Unita Ric Clin Trombofilia M Golinelli, Div Angiol, Cardiovasc Dept, I-40138 Bologna, Italy
[2] Univ Ferrara, Dept Biochem & Mol Biol, Ctr Biochim Genoma Umano, I-44100 Ferrara, Italy
来源
BRITISH MEDICAL JOURNAL | 2001年 / 322卷 / 7293期
关键词
D O I
10.1136/bmj.322.7293.1024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Common inherited thrombophilic defects such as factor V Leiden and G20120A mutation of the prothrombin gene inter act synergistically with oral contraceptives to increase the risk of venous thromboembolism.(1 2) The best approach to identify women at higher risk of venous thromboembolism before taking oral contraceptives is controversial. Universal screening is not cost effective because 8000 women need to be screened for factor V Leiden to detect 400 mutations and prevent one episode of venous thromboembolism.(1) Many authors recommend selective screening in women with a personal or family history of venous thromboembolism.(1) However; the effectiveness of this approach has not been proved, The aim of our study was to evaluate the sensitivity and positive predictive value of a family history of venous thromboembolism for identifying common thrombophilic defects in women without thrombosis before taking oral contraceptives.
引用
收藏
页码:1024 / 1025
页数:2
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