Rd. Hull et al., TREATMENT OF PROXIMAL VEIN-THROMBOSIS WITH SUBCUTANEOUS LOW-MOLECULAR-WEIGHT HEPARIN VS INTRAVENOUS HEPARIN - AN ECONOMIC-PERSPECTIVE, Archives of internal medicine, 157(3), 1997, pp. 289-294
Background: Subcutaneous low-molecular-weight heparin is at least as e
ffective and safe as classic intravenous heparin therapy for the treat
ment of proximal vein thrombosis. Anticoagulant monitoring is not requ
ired with low-molecular-weight heparin. Objective: To perform an econo
mic evaluation of these therapeutic approaches by comparing cost and e
ffectiveness. Patients and Methods: A randomized trial in 432 patients
with proximal vein thrombosis that compared intravenous heparin and l
ow-molecular-weight heparin with objective documentation of clinical o
utcomes provided the opportunity to perform an analysis of cost-effect
iveness to rank these alternative therapies in terms of both their cos
t and effectiveness. The economic viewpoint of this analysis was that
of a third-party payer (ie, a ministry of health in Canada or an insur
ance company in the United States). Results: In the intravenous hepari
n-treated group, the cost incurred for 100 patients was $414 655 (Cana
dian dollars) or $375 836 (US dollars), with a frequency of objectivel
y documented venous thromboembolism of 6.9%. Tn the low-molecular-weig
ht heparin-treated group, the cost incurred for 100 patients was $399
403 (Canadian dollars) or $335 687 (US dollars), with a frequency of o
bjectively documented venous thromboembolism of 2.8%, thus providing a
cost saving of $15 252 (Canadian dollars) or $40 149 (US dollars). Mu
ltiple sensitivity analyses were performed, and these procedures did n
ot alter the findings of the study. Conclusions: The findings indicate
that low-molecular-weight heparin therapy is at least as effective an
d safe but less costly than intravenous heparin treatment. The potenti
al for outpatient therapy in up to 37% of patients who are receiving l
ow-molecular-weight heparin would substantially augment the cost savin
g.