A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin

See also Keeling D. Thrombophilia screening or screaming. This issue, pp 1191–2. Summary.  Background:  Absolute risks of venous thromboembolism (VTE) in protein S‐, protein C‐, or antithrombin‐deficient subjects are mainly based on retrospective data. Screening asymptomatic relatives of these patie...

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Published inJournal of thrombosis and haemostasis Vol. 8; no. 6; pp. 1193 - 1200
Main Authors MAHMOODI, B. K., BROUWER, J.‐L. P., TEN KATE, M. K., LIJFERING, W. M., VEEGER, N. J. G. M., MULDER, A. B., KLUIN‐NELEMANS, H. C., VAN DER MEER, J.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2010
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ISSN1538-7933
1538-7836
1538-7836
DOI10.1111/j.1538-7836.2010.03840.x

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Summary:See also Keeling D. Thrombophilia screening or screaming. This issue, pp 1191–2. Summary.  Background:  Absolute risks of venous thromboembolism (VTE) in protein S‐, protein C‐, or antithrombin‐deficient subjects are mainly based on retrospective data. Screening asymptomatic relatives of these patients is disputed, though studies addressing this issue have yet to be conducted. Methods: We prospectively followed 382 relatives of 84 probands. Participants were assessed for other thrombophilic defects and occurrence of exogenous risk factors (i.e. surgery/trauma/immobilization, malignancies, use of systemic estrogens, and pregnancy/puerperium). After screening, deficient subjects were advised to use thromboprophylaxis during exogenous risk factors; use of oral contraceptives was discouraged. Results: Overall annual incidence of VTE was 1.53% (95% CI, 1.00–2.34) in deficient vs. 0.29% (0.13–0.64) in non‐deficient relatives; adjusted hazard ratio, 7.0 (95% CI, 2.7–18.0). Annual incidence of unprovoked VTE was 0.95% in deficient vs. 0.05% in non‐deficient subjects; age‐adjusted hazard ratio, 22.3 (P = 0.003). In contrast, annual incidence of provoked VTE was 0.58% vs. 0.24%; age‐adjusted hazard ratio, 2.8 (P = 0.08). Fifty‐five (37%) deficient and 80 (34%) non‐deficient subjects experienced 91 and 143 exogenous risk factors, respectively, during which six vs. five VTEs (6.6% vs 3.5% per risk‐period) occurred, despite the higher compliance with recommended thromboprophylaxis use in deficient (51%) vs. non‐deficient (22%) subjects. In deficient subjects all provoked VTEs occurred when thromboprophylaxis was not used. Conclusions: Protein S, protein C or antithrombin deficiencies confer high absolute risk of VTE. Screening and subsequent augmentation of thromboprophylaxis use may result in reduction of provoked VTE, whereas risk of unprovoked VTE could not be affected by screening.
Bibliography:Professor Dr Jan van der Meer recently passed away following a sudden illness.
Presented as an oral communication at the session of ‘Genetic Thrombophilia: Clinical Applications’ on 13 July 2009 at the ISTH congress in Boston, MA, USA.
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ISSN:1538-7933
1538-7836
1538-7836
DOI:10.1111/j.1538-7836.2010.03840.x