Abstract
Purpose: HMG-CoA reductase inhibitors have become the drugs of choice for hypercholesterolemia, demonstrating a favorable side effect profile, ease of administration, and reduction of cardiovascular mortality in both primary and secondary prevention trials. Use of these agents has been suboptimal, however, possibly due to their cost. The objective of this study was to evaluate the cost-effectiveness of the five commercially available HMG-CoA reductase inhibitors in a large population of hypercholesterolemic patients using a population-based treat-to-target analysis. Methods: Cardiac risk factors (CRFs) and lipid panels were collected for drug-naïve patients from five different regions of the United States. Risk stratification using CRFs was performed, and LDLcholesterol (LDL-C) was based on national guidelines. Using meta-analysis to derive LDL-C lowering efficacy, each agent was modeled to achieve NCEP goals. Costing methodology was done using a third-party payer perspective. Drug costs were extracted from Medi-span, and clinic costs were based on CPT codes for office visits and lipid panels. Results: Data were obtained for 5436 patients: high-risk (coronary artery disease [CAD]; n=1773), moderate-risk (no CAD and more than 2 CRFs; n=1318), and low-risk patients (no CAD and fewer than 2 CRFs; n=2345). High-risk, moderate-risk, and low-risk patients achieving LDL-C target with the primary agent, respectively, were: atorvastatin 100%, 100%, 100%; fluvastatin 4%, 74%, 100%; lovastatin 25%, 100%, 100%; pravastatin 25%, 95%, 100%; and simvastatin 89%, 100%, 100%. Yearly US dollar cost per patient to treat to goal LDL-C are shown in the table below: Conclusions: The most cost-effective approach to treating a population with varying degrees of coronary heart disease risk is to individualize statin selection based on the expected LDL-C percentage required to achieve NCEP target. This approach would indicate that low-risk patients can be treated with fluvastatin and moderate-risk and high-risk patients with atorvastatin or fluvastatin. Notably, atorvastatin was the only agent achieving NCEP goals in patients in all risk groups.
| Original language | English |
|---|---|
| Journal | Journal of Applied Research |
| Volume | 2 |
| Issue number | 2 |
| State | Published - 2002 |
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All Science Journal Classification (ASJC) codes
- Medicine(all)
- Pharmacology
Cite this
Multicenter treat-to-target cost-effectiveness evaluation of HMG-CoA reductase inhibitor monotherapy. / Lucas, B. Daniel; Sanoski, Cynthia A.; Ito, Matthew K.; Aldrige, Martha A.; Cheng, Judy W M; Hilleman, Daniel E.
In: Journal of Applied Research, Vol. 2, No. 2, 2002.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Multicenter treat-to-target cost-effectiveness evaluation of HMG-CoA reductase inhibitor monotherapy
AU - Lucas, B. Daniel
AU - Sanoski, Cynthia A.
AU - Ito, Matthew K.
AU - Aldrige, Martha A.
AU - Cheng, Judy W M
AU - Hilleman, Daniel E.
PY - 2002
Y1 - 2002
N2 - Purpose: HMG-CoA reductase inhibitors have become the drugs of choice for hypercholesterolemia, demonstrating a favorable side effect profile, ease of administration, and reduction of cardiovascular mortality in both primary and secondary prevention trials. Use of these agents has been suboptimal, however, possibly due to their cost. The objective of this study was to evaluate the cost-effectiveness of the five commercially available HMG-CoA reductase inhibitors in a large population of hypercholesterolemic patients using a population-based treat-to-target analysis. Methods: Cardiac risk factors (CRFs) and lipid panels were collected for drug-naïve patients from five different regions of the United States. Risk stratification using CRFs was performed, and LDLcholesterol (LDL-C) was based on national guidelines. Using meta-analysis to derive LDL-C lowering efficacy, each agent was modeled to achieve NCEP goals. Costing methodology was done using a third-party payer perspective. Drug costs were extracted from Medi-span, and clinic costs were based on CPT codes for office visits and lipid panels. Results: Data were obtained for 5436 patients: high-risk (coronary artery disease [CAD]; n=1773), moderate-risk (no CAD and more than 2 CRFs; n=1318), and low-risk patients (no CAD and fewer than 2 CRFs; n=2345). High-risk, moderate-risk, and low-risk patients achieving LDL-C target with the primary agent, respectively, were: atorvastatin 100%, 100%, 100%; fluvastatin 4%, 74%, 100%; lovastatin 25%, 100%, 100%; pravastatin 25%, 95%, 100%; and simvastatin 89%, 100%, 100%. Yearly US dollar cost per patient to treat to goal LDL-C are shown in the table below: Conclusions: The most cost-effective approach to treating a population with varying degrees of coronary heart disease risk is to individualize statin selection based on the expected LDL-C percentage required to achieve NCEP target. This approach would indicate that low-risk patients can be treated with fluvastatin and moderate-risk and high-risk patients with atorvastatin or fluvastatin. Notably, atorvastatin was the only agent achieving NCEP goals in patients in all risk groups.
AB - Purpose: HMG-CoA reductase inhibitors have become the drugs of choice for hypercholesterolemia, demonstrating a favorable side effect profile, ease of administration, and reduction of cardiovascular mortality in both primary and secondary prevention trials. Use of these agents has been suboptimal, however, possibly due to their cost. The objective of this study was to evaluate the cost-effectiveness of the five commercially available HMG-CoA reductase inhibitors in a large population of hypercholesterolemic patients using a population-based treat-to-target analysis. Methods: Cardiac risk factors (CRFs) and lipid panels were collected for drug-naïve patients from five different regions of the United States. Risk stratification using CRFs was performed, and LDLcholesterol (LDL-C) was based on national guidelines. Using meta-analysis to derive LDL-C lowering efficacy, each agent was modeled to achieve NCEP goals. Costing methodology was done using a third-party payer perspective. Drug costs were extracted from Medi-span, and clinic costs were based on CPT codes for office visits and lipid panels. Results: Data were obtained for 5436 patients: high-risk (coronary artery disease [CAD]; n=1773), moderate-risk (no CAD and more than 2 CRFs; n=1318), and low-risk patients (no CAD and fewer than 2 CRFs; n=2345). High-risk, moderate-risk, and low-risk patients achieving LDL-C target with the primary agent, respectively, were: atorvastatin 100%, 100%, 100%; fluvastatin 4%, 74%, 100%; lovastatin 25%, 100%, 100%; pravastatin 25%, 95%, 100%; and simvastatin 89%, 100%, 100%. Yearly US dollar cost per patient to treat to goal LDL-C are shown in the table below: Conclusions: The most cost-effective approach to treating a population with varying degrees of coronary heart disease risk is to individualize statin selection based on the expected LDL-C percentage required to achieve NCEP target. This approach would indicate that low-risk patients can be treated with fluvastatin and moderate-risk and high-risk patients with atorvastatin or fluvastatin. Notably, atorvastatin was the only agent achieving NCEP goals in patients in all risk groups.
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M3 - Article
VL - 2
JO - Journal of Applied Research
JF - Journal of Applied Research
SN - 1537-064X
IS - 2
ER -