Cost-Effectiveness of Duloxetine in Chronic Low Back Pain A Quebec Societal Perspective

被引:8
|
作者
Wielage, Ronald [1 ]
Bansal, Megha [1 ]
Wilson, Kinsley [2 ]
Klein, Robert [1 ]
Happich, Michael [3 ]
机构
[1] Med Decis Modeling Inc, Indianapolis, IN 46268 USA
[2] Eli Lilly Canada, Toronto, ON, Canada
[3] Lilly Deutschland GmbH, Bad Homburg, Germany
关键词
duloxetine; chronic low back pain; cost-effectiveness; pharmacoeconomic model; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PROTON-PUMP INHIBITORS; TRAMADOL/ACETAMINOPHEN COMBINATION TABLETS; DIABETIC PERIPHERAL NEUROPATHY; THERAPEUTIC ARTHRITIS RESEARCH; DAILY OROS(R) HYDROMORPHONE; ACUTE-RENAL-FAILURE; EVENT TRIAL TARGET; DOUBLE-BLIND; EXTENDED-RELEASE;
D O I
10.1097/BRS.0b013e31828264f9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. Cost-effectiveness model from a Quebec societal perspective using meta-analyses of clinical trials. Objective. To evaluate the cost-effectiveness of duloxetine in chronic low back pain (CLBP) compared with other post-first-line oral medications. Summary of Background Data. Duloxetine has recently received a CLBP indication in Canada. The cost-effectiveness of duloxetine and other oral medications has not previously been evaluated for CLBP. Methods. A Markov model was created on the basis of the economic model documented in the 2008 osteoarthritis clinical guidelines of the National Institute for Health and Clinical Excellence. Treatment-specific utilities were estimated via a meta-analysis of CLBP clinical trials and a transfer-to-utility regression estimated from duloxetine CLBP trial data. Adverse event rates of comparator treatments were taken from the National Institute for Health and Clinical Excellence model or estimated by a meta-analysis of clinical trials in osteoarthritis using a maximum-likelihood simulation technique. Costs were developed primarily from Quebec and Ontario public sources as well as the published literature and expert opinion. The 6 comparators were celecoxib, naproxen, amitriptyline, pregabalin, hydromorphone, and oxycodone. Subgroup analyses and 1-way and probabilistic sensitivity analyses were performed. Results. In the base case, naproxen, celecoxib, and duloxetine were on the cost-effectiveness frontier, with naproxen the least expensive medication, celecoxib with an incremental cost-effectiveness ratio of $19,881, and duloxetine with an incremental cost-effectiveness ratio of $43,437. Other comparators were dominated. Key drivers included the rates of cardiovascular and gastrointestinal adverse events and proton pump inhibitor usage. In subgroup analysis, the incremental cost-effectiveness ratio for duloxetine fell to $21,567 for a population 65 years or older and to $18,726 for a population at higher risk of cardiovascular and gastrointestinal adverse events. Conclusion. The model estimates that duloxetine is a moderately cost-effective treatment for CLBP, becoming more cost-effective for populations older than 65 years or at greater risk of cardiovascular and gastrointestinal events.
引用
收藏
页码:936 / 946
页数:11
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