Journal article
Authors list: Stolz, E; Kemkes-Matthes, B; Pötzsch, B; Hahn, M; Kraus, J; Wirbartz, A; Kaps, M
Publication year: 2000
Pages: 31-36
Journal: Acta Neurologica Scandinavica
Volume number: 102
Issue number: 1
ISSN: 0001-6314
Open access status: Gold
DOI Link: https://doi.org/10.1034/j.1600-0404.2000.102001031.x
Publisher: Wiley
Abstract:
Objectives - In this study the frequency of inherited thrombophilic risk factors in a population of German CVT patients and their influence on clinical outcome were evaluated. Material and methods - Twenty-five patients (age 37.1 +/- 16.3 years) with CVT were screened for inherited coagulation disorders. All participants received a full clinical follow-up (mean follow-up period 4.8 +/- 6.4 years). Results - Inherited thrombophilic risk factors were identified in 9 (36%) of the 25 patients studied. Four were found positive for the heterozygous factor V Leiden mutation, 2 were heterozygous carriers of the prothrombin-G20210A-polymorphism. APC resistance proved to be a reliable screening method for factor V Leiden mutation, whereas genetic evaluation for protein S and C deficiencies failed to demonstrate any mutations despite the identification of 1 patient with a protein C and protein S deficiency each. One patient suffered from a familial plasminogen deficiency. These 9 patients had a less favorable outcome (P < 0.05). Conclusion - Our results demonstrate that screening for inherited thrombophilia should be an integral part in the diagnostic work up of CVT patients. Patients with inherited coagulopathies tended to have a less favorable outcome, corroborating recommendations for a longer period of oral anticoagulation.
Citation Styles
Harvard Citation style: Stolz, E., Kemkes-Matthes, B., Pötzsch, B., Hahn, M., Kraus, J., Wirbartz, A., et al. (2000) Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis, Acta Neurologica Scandinavica, 102(1), pp. 31-36. https://doi.org/10.1034/j.1600-0404.2000.102001031.x
APA Citation style: Stolz, E., Kemkes-Matthes, B., Pötzsch, B., Hahn, M., Kraus, J., Wirbartz, A., & Kaps, M. (2000). Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis. Acta Neurologica Scandinavica. 102(1), 31-36. https://doi.org/10.1034/j.1600-0404.2000.102001031.x
Keywords
3'-UNTRANSLATED REGION; Cerebral venous thrombosis; dural sinuses; FACTOR-V-LEIDEN; INHERITED THROMBOPHILIA; intracranial veins; Leiden-mutation; ORAL ANTICOAGULANT-THERAPY; protein C deficiency; PROTEIN-C DEFICIENCY; protein S deficiency; PROTHROMBIN-GENE; pro-thrombin polymorphism; THROMBOEMBOLISM; VEIN THROMBOSIS