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

BMJ 2001; 322 doi: http://dx.doi.org/10.1136/bmj.322.7293.1024 (Published 28 April 2001) Cite this as: BMJ 2001;322:1024
  1. Benilde Cosmi, lecturera (bcosmi{at}med.unibo.it),
  2. Cristina Legnani, researchera,
  3. Francesco Bernardi, professor of biochemistryb,
  4. Sergio Coccheri, professor of cardiovascular medicinea,
  5. Gualtiero Palareti, consultant in thrombosis and haemostasisa
  1. a Cardiovascular Department, Division of Angiology, Unità Ricerca Clinica sulla Trombofilia “M Golinelli”, University Hospital, S Orsola-Malpighi, 40138, Bologna, Italy
  2. b Centro di Studi Biochimici del Genoma Umano, Department of Biochemistry and Molecular Biology, University of Ferrara, Italy
  1. Correspondence to: B Cosmi

    Common inherited thrombophilic defects such as factor V Leiden and G20120A mutation of the prothrombin gene interact 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.

    Sensitivity and positive predictive values of family history as a predictor of thrombophilic defects in 324 women with no personal history of venous thromboembolism

    View this table:

    Participants, methods, and results

    We prospectively evaluated a cohort of women (age range 15–49 years) consecutively referred to our thrombophilia unit by gynaecologists at family planning clinics in Bologna, Italy, between 1998 and 2000. The gynaecologists had established that the women were eligible to take oral contraceptives and had no history of venous thromboembolism. Before the women were screened, experienced investigators administered a modified structured questionnaire3 that was designed and validated to evaluate both personal and family history (first degree=parents and siblings, second degree=grandparents, aunts, uncles, and cousins) of venous thromboembolism (see BMJ's website for details). We considered family history positive if a thromboembolism was reported in any first or second degree relatives.

    Thrombophilia screening was conducted as previously described.4 Prothrombin activity was measured by chromogenic assay5 and lupus anticoagulant by LA-test and LA-check assays (Organon Teknika, Rome, Italy). If prothrombin activity was confirmed to be above 1.10 U/ml, we analysed the DNA for the G20120A mutation according to the method of Poort et al.5 The tests were performed by staff blind to the results of the questionnaire.

    We calculated sensitivity and positive predictive values according to standard methods. The 95% confidence intervals for proportions were calculated by an approximate method, and we used the χ2 test when appropriate. A two sided probability value <0.05 was considered significant. All data were analysed with the statistical package SOLO (BMDP, Los Angeles).

    We evaluated 324 women (mean age 34 years) who had a negative personal history for venous thromboembolism confirmed by our questionnaire. Thirty four women reported a positive family history (10%, 95% confidence interval 7% to 14%), of whom two were heterozygous for factor V Leiden and one had protein S deficiency. Thrombophilic defects were identified in 19 women (6%, 3% to 8%), only three of whom had a positive family history. Among the 290 women with a negative family history, thrombophilic defects were detected in 16 (6%, 3% to 8%); eight were heterozygous for factor V Leiden and eight were heterozygous for the G20120A mutation.

    The table shows the sensitivity and positive predictive value of family history for identifying thrombophilic defects. The proportion of women with thrombophilia was similar among those with a positive history and those with a negative history of venous thromboembolism when first and second degree family history was considered (9% (3/34) v 5% (16/290), P=0.44) and when only first degree family history was considered (8% (2/26) v 6% (17/298), P=0.68).

    Comment

    Family history of venous thromboembolism has unsatisfactory sensitivity and positive predictive value for identifying carriers of common thrombophilic defects before taking oral contraceptives. A policy of selective screening may therefore miss a substantial number of women at increased risk of thromboembolism when taking oral contraceptives.

    Acknowledgments

    We thank the gynaecologists at Bologna family planning clinics who referred women for screening.

    Contributors: BC was involved in the conception and design of the study and drafting the article. GP was involved in the conception and design of the study and critical revision of the article and is the paper's guarantor. CL and SG analysed and interpreted the data and helped revise the article. All authors approved the final draft.

    Footnotes

    • Funding This project was supported by a grant from the University of Bologna.

    • Competing interests None declared.

    • Graphic The questionnaire is available on the BMJ's website

    References

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