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Journal article

Treatment of Proximal Vein Thrombosis With Subcutaneous Low-Molecular-Weight Heparin vs Intravenous Heparin: An Economic Perspective

Abstract

Background: Subcutaneous low-molecular-weight heparin is at least as effective and safe as classic intravenous heparin therapy for the treatment of proximal vein thrombosis. Anticoagulant monitoring is not required with low-molecular-weight heparin.Objective: To perform an economic evaluation of these therapeutic approaches by comparing cost and effectiveness.Patients and Methods: A randomized trial in 432 patients with proximal vein thrombosis that compared intravenous heparin and low-molecular-weight heparin with objective documentation of clinical outcomes provided the opportunity to perform an analysis of cost-effectiveness to rank these alternative therapies in terms of both their cost and effectiveness. The economic viewpoint of this analysis was that of a third-party payer (ie, a ministry of health in Canada or an insurance company in the United States).Results: In the intravenous heparin-treated group, the cost incurred for 100 patients was $414 655 (Canadian dollars) or $375 836 (US dollars), with a frequency of objectively documented venous thromboembolism of 6.9%. In the low-molecular-weight heparin—treated group, the cost incurred for 100 patients was $399 403 (Canadian dollars) or $335 687 (US dollars), with a frequency of objectively documented venous thromboembolism of 2.8%, thus providing a cost saving of $15 252 (Canadian dollars) or $40 149 (US dollars). Multiple sensitivity analyses were performed, and these procedures did not alter the findings of the study.Conclusions:The findings indicate that low-molecular-weight heparin therapy is at least as effective and safe but less costly than intravenous heparin treatment. The potential for outpatient therapy in up to 37% of patients who are receiving low-molecular-weight heparin would substantially augment the cost saving.Arch Intern Med. 1997;157:289-294

Authors

Hull RD; Raskob GE; Rosenbloom D; Pineo GF; Lerner RG; Gafni A; Trowbridge AA; Elliott CG; Green D; Feinglass J

Journal

JAMA Internal Medicine, Vol. 157, No. 3, pp. 289–294

Publisher

American Medical Association (AMA)

Publication Date

February 10, 1997

DOI

10.1001/archinte.1997.00440240051008

ISSN

2168-6106

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