Thromb Haemost 2002; 87(04): 580-585
DOI: 10.1055/s-0037-1613052
Review Article
Schattauer GmbH

Factor V Leiden (G1691A) and Prothrombin Gene G20210A Mutations as Potential Risk Factors for Venous Thromboembolism after Total Hip or Total Knee Replacement Surgery

K. Wåhlander
1   Department of Clinical Chemistry and Transfusion Medicine, Sahlgrenska University Hospital, Göteborg, Sweden
2   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
G. Larson
1   Department of Clinical Chemistry and Transfusion Medicine, Sahlgrenska University Hospital, Göteborg, Sweden
,
T. L. Lindahl
3   Department of Clinical Chemistry, University Hospital, Linköping, Sweden
,
C. Andersson
4   Department of Orthopaedic Surgery, University Hospital, Linköping, Sweden
,
L. Frison
2   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
D. Gustafsson
2   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
A. Bylock
2   AstraZeneca R&D Mölndal, Mölndal, Sweden
,
B. I. Eriksson
5   Department of Orthopaedic Surgery, Sahlgrenska University Hospital/Ostra, Göteborg, Sweden
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Publikationsverlauf

Received 10. September 2001

Accepted after revision 08. Januar 2002

Publikationsdatum:
08. Dezember 2017 (online)

Summary

Patients (n = 1600) from 12 European countries, scheduled for elective orthopaedic hip or knee surgery, were screened for Factor V Leiden and prothrombin gene G20210A mutations, found in 5.5% and 2.9% of the populations, respectively. All patients underwent prophylactic treatment with one of four doses of melagatran and ximelagatran or dalteparin, starting pre-operatively. Bilateral ascending venography was performed on study day 8-11. The patients were subsequently treated according to local routines and followed for 4-6 weeks postoperatively. The composite endpoint of screened deep vein thrombosis (DVT) and symptomatic pulmonary embolism (PE) during prophylaxis did not differ significantly between patients with or without these mutations. Symptomatic venous thromboembolism (VTE) during prophylaxis and follow-up (1.9%) was significantly over-represented among patients with the prothrombin gene G20210A mutation (p = 0.0002). A tendency towards increased risk of VTE was found with the Factor V Leiden mutation (p = 0.09). PE were few, but significantly over-represented in both the Factor V Leiden and prothrombin gene G20210A mutated patients (p = 0.03 and p = 0.05, respectively). However, since 90% of the patients with these genetic risk factors will not suffer a VTE event, a general pre-operative genotyping is, in our opinion, of questionable value.

 
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