Thromb Haemost 1996; 76(05): 682-688
DOI: 10.1055/s-0038-1650643
Original Article
Schattauer GmbH Stuttgart

Risk Factors for Bleeding during Treatment of Acute Venous Thromboembolism

Jos P J Wester
1   The Department of Internal Medicine in St. Antonius Hospital, Nieuwegein, The Netherlands
,
Harold W de Valk
2   Department of Hematology, University Hospital Utrecht, The Netherlands
,
Karel H Nieuwenhuis
2   Department of Hematology, University Hospital Utrecht, The Netherlands
,
Catherine B Brouwer
3   Eemland Hospital, Amersfoort, The Netherlands
,
Yolanda van der Graaf
4   Clinical Epidemiology, University Hospital Utrecht, The Netherlands
,
Otger J A Th Meuwissen
1   The Department of Internal Medicine in St. Antonius Hospital, Nieuwegein, The Netherlands
,
Herman C Hart
3   Eemland Hospital, Amersfoort, The Netherlands
,
Jan J Sixma
2   Department of Hematology, University Hospital Utrecht, The Netherlands
,
Jan Dirk Banga
2   Department of Hematology, University Hospital Utrecht, The Netherlands
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 07. Juni 1995

Accepted after resubmission 25. Juli 1996

Publikationsdatum:
11. Juli 2018 (online)

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Summary

Objective: Identification of risk factors for bleeding and prospective evaluation of two bleeding risk scores in the treatment of acute venous thromboembolism.

Design: Secondary analysis of a prospective, randomized, assessor-blind, multicenter clinical trial.

Setting: One university and 2 regional teaching hospitals.

Patients: 188 patients treated with heparin or danaparoid for acute venous thromboembolism.

Measurements: The presenting clinical features, the doses of the drugs, and the anticoagulant responses were analyzed using univariate and multivariate logistic regression analysis in order to evaluate prognostic factors for bleeding. In addition, the recently developed Utrecht bleeding risk score and Landefeld bleeding risk index were evaluated prospectively.

Results: Major bleeding occurred in 4 patients (2.1%) and minor bleeding in 101 patients (53.7%). For all (major and minor combined) bleeding, body surface area ≤2 m2 (odds ratio 2.3, 95% Cl 1.2-4.4; p = 0.01), and malignancy (odds ratio 2.4, 95% Cl 1.1-4.9; p = 0.02) were confirmed to be independent risk factors. An increased treatment-related risk of bleeding was observed in patients treated with high doses of heparin, independent of the concomitant activated partial thromboplastin time ratios. Both bleeding risk scores had low diagnostic value for bleeding in this sample of mainly minor bleeders.

Conclusions: A small body surface area and malignancy were associated with a higher frequency of bleeding. The bleeding risk scores merely offer the clinician a general estimation of the risk of bleeding. In patients with a small body surface area or in patients with malignancy, it may be of interest to study whether limited dose reduction of the anticoagulant drug may cause less bleeding without affecting efficacy.