Cm. Schambeck et al., SELECTIVE SCREENING FOR THE FACTOR-V-LEIDEN MUTATION - IS IT ADVISABLE PRIOR TO THE PRESCRIPTION OF ORAL-CONTRACEPTIVES, Thrombosis and haemostasis, 78(6), 1997, pp. 1480-1483
The cumulative thrombotic risk of Factor V (FV) Leiden and oral contra
ceptives (OC) recommends screening for the mutation. Assuming that a f
amily history of thrombosis increases the patient's likelihood of bear
ing FV Leiden, a selective rather than universal screening would be pe
rformed. We studied the utility of a family history of thrombosis for
screening of FV Leiden before prescription of OC and, furthermore, the
utility of screening even if oral contraception is favoured. 101 pati
ents who had their first and single thromboembolic event while using O
C were interviewed. 609 women without any history of thromboembolism r
ecruited by gynecologists completed a standard questionnaire. 101 of t
hese women, age-matched and currently using OC, were selected for a ca
se-control study. Regarding patients with previous thromboembolism, a
family history in a first-degree relative had a positive predictive va
lue (PPV) of only 14% for FV Leiden. A PPV of 12% was calculated by in
vestigating the 609 thrombosis-free women. Inherited FV Leiden (odds r
atio = 4.9) and acquired risk factors (odds ratio = 10.1) were both fo
und to be the most prominent, but independent additional risks. Nevert
heless, FV Leiden carriers, both heterozygotes and homozygotes, did no
t suffer earlier from thromboembolism than patients without the mutati
on. In conclusion, family history is an unreliable criterion to detect
FV Leiden carriers. Screening for factor V Leiden can be worthwhile e
ven if the advantages of oral contraception are higher assessed than t
he thrombotic risk. Affected women knowing about their additional risk
could contribute to the prevention of thrombosis in risk situations.