B. Cosmi et al., Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study, BR MED J, 322(7293), 2001, pp. 1024-1025
Citations number
5
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Common inherited thrombophilic defects such as factor V Leiden and G20120A
mutation of the prothrombin gene inter act synergistically with oral contra
ceptives to increase the risk of venous thromboembolism.(1 2) The best appr
oach to identify women at higher risk of venous thromboembolism before taki
ng oral contraceptives is controversial. Universal screening is not cost ef
fective because 8000 women need to be screened for factor V Leiden to detec
t 400 mutations and prevent one episode of venous thromboembolism.(1) Many
authors recommend selective screening in women with a personal or family hi
story of venous thromboembolism.(1) However; the effectiveness of this appr
oach has not been proved, The aim of our study was to evaluate the sensitiv
ity and positive predictive value of a family history of venous thromboembo
lism for identifying common thrombophilic defects in women without thrombos
is before taking oral contraceptives.