A cost-effectiveness analysis of fondaparinux sodium compared with enoxaparin sodium as prophylaxis against venous thromboembolism - Use in patients undergoing major orthopaedic surgery

被引:28
|
作者
Sullivan, SD
Davidson, BL
Kahn, SR
Muntz, JE
Oster, G
Raskob, G
机构
[1] Univ Washington, Dept Pharm & Hlth Serv, Pharmaceut Outcomes Res & Policy Program, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Seattle, WA 98195 USA
[3] Sir Mortimer B Davis Jewish Hosp, Montreal, PQ H3T 1E2, Canada
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Policy Anal Inc, Boston, MA USA
[6] Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA
关键词
D O I
10.2165/00019053-200422090-00005
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objective: To determine the cost effectiveness of fondaparinux sodium compared with enoxaparin sodium for prophylaxis against venous thromboembolism in patients undergoing major orthopaedic surgery. Methods: Using a cohort simulation model, two primary analyses were conducted from the perspective of the US healthcare payer. Probabilities for a trial-based analysis were obtained from patients participating in the fordaparinux clinical trial programme supplemented with data from published literature. Probabilities for a label-based analysis were estimated for a hypothetical cohort of US patients receiving either fondaparinux or enoxaparin as recommended by US FDA-approved labelling. Resource use and costs were obtained from large US healthcare databases. Outcome measures were rates of symptomatic thromboembolic events and healthcare costs. Costs were in 2003 values. Results: In the trial-based analysis, fordaparinux was estimated to prevent 15.1 symptomatic venous thromboembolic events (per 1000 patients) at 3 months for patients undergoing major orthopaedic surgery compared with enoxaparin. The cost savings (per patient) of using fondaparinux over enoxaparin are $US61 at 30 days, $US89 at 3 months, and $US155 at 5 years.-In the label-based analysis, fordaparinux was estimated to prevent 17.8 venous thromboembolic events (per 1000 patients) at 3 months compared with enoxaparin, producing savings per patient of $US25 at discharge, $US112 over 1 month, $US 141 over 3 months and $US:234 over 5 years. Results remain robust to clinically plausible variation in input parameters and assumptions. Conclusion: Our model suggests that fondaparinux, when compared with the current standard regimen of enoxaparin for prophylaxis of venous thromboembolism in major orthopaedic surgery, improves outcomes and is cost saving from a US healthcare-payer perspective over the broad range of assumptions evaluated.
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页码:605 / 620
页数:16
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