Supplements Treatment Strategies for Dyslipidemia
Cost Efficiency and Formulary Considerations for Statin Therapy
Extensive epidemiologic evidence and reports issued by the National Cholesterol Education Program have repeatedly identified low-density lipoprotein cholesterol (LDL-C) as the primary target in reducing the primary and secondary risk of coronary events.
With recent evidence supporting a more aggressive approach using higher potency statins, and a lower threshold for initiating drug therapy for high-risk patients, providers and administrators in managed care are charged with finding the most effective and cost-effective means of attaining these goals. Changes in the market, such as newer high-potency statins and statin combinations available at lower cost and expiration of patents on widely accepted brand drugs, have provided practitioners with the ability to reduce LDL-C at lower costs than ever. The cost-efficiency analysis presented here finds that, for low-to-moderate reduction (<40%), generic lovastatin and simvastatin provide the lowest cost per 1% LDL-C reduction. Similarly, for reduction greater than 40%, branded rosuvastatin and ezetimibe/simvastatin have the lowest cost per 1% reduction.
(Am J Manag Care. 2006;12:S325-S331)
LDL-C Reduction Is the Basis for Cardioprotection
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in the United States. According to the American Heart Association, it accounted for or contributed to approximately 58% of the total mortality of the general population in 2003, with estimated direct and indirect cost of CVD for 2006 at $403.1 billion.1 Along with several other factors, increased low-density lipoprotein cholesterol (LDL-C) levels are associated with increased risk of CVD. A large body of epidemiologic evidence supports a direct relationship between the level of serum LDL-C and the risk of CVD. It has been documented that lower levels of LDL-C reduce risk of coronary heart disease (Figure 1).2
Along with diet and lifestyle improvement, lipid-lowering drug therapy is a primary intervention in the prevention and treatment of CVD. The Third Adult Treatment Panel (ATP III) of the National Cholesterol Education Program issued an evidence-based set of guidelines on cholesterol management in 2001.3 ATP reports have repeatedly identified LDL-C as the primary target of cholesterol-lowering therapy.2
Primary Prevention of Coronary Artery Disease
The West of Scotland Coronary Prevention Study (WOSCOPS) demonstrated the benefit and safety of lipid-lowering therapy with a statin for primary prevention of CVD in patients with hypercholesterolemia. Treatment with statin therapy reduced the risk of key end points, including death from all CVDs.4 Additional studies that have documented benefit from LDL-C reduction in primary prevention include the Air Force/ Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS)5 and the Anglo- Scandinavian Cardiac Outcomes Trial-Lipid Lowering Arm (ASCOT-LLA).6 These studies consistently demonstrated reduction of CVD risk from statin treatment in a primary setting, including in patients without CVD (Table 1).
The Atherosclerosis Risk in Communities (ARIC) study, in which more than 12 000 middle-aged subjects with no evidence of CVD were followed prospectively for 10 years, showed that the incidence of coronary heart disease (CHD)-related death, myocardial infarction (MI), silent infarction, coronary artery bypass graft, and angioplasty was lower in subjects with baseline serum LDL-C levels of less than 88 mg/dL for women and less than 95 mg/dL for men.7 The ARIC study, which can be thought of as "the Framingham of the future," confirms the wisdom of the ATP III guidelines, which identify LDL-C levels of less than 100 mg/dL as optimal and emphasize the value of aggressive, multifactorial risk reduction for primary CVD prevention.8
Regardless of baseline, patients with a history of a cardiovascular (CV) event benefit from LDL-C reduction (Table 2). The landmark Scandinavian Simvastatin Survival Study (4S) demonstrated, in a large population, a reduction in mortality secondary to LDL-C reduction. Benefit from LDL-C reduction, in terms of total risk reduction for both overall mortality and major coronary events, was documented.9
The Heart Protection Study (HPS) was noteworthy because of the large, heterogeneous patient population with a variety of comorbidities, as well as those with below-average cholesterol levels. Over 20 000 people, up to 80 years of age, were enrolled. After an average of approximately 5 years, the reduction in major vascular events from baseline was significant in patients treated with simvastatin compared with placebo, and the reduction in events was similar regardless of the baseline LDL-C concentration. Thus, all patient groups studied in the trial benefited from further reduction of their LDL-C levels.10
Intensive Therapy for Secondary Prevention
The Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis in Myocardial Infarction 22 (PROVE IT) trial,11 a randomized, double-blind study of 4162 patients with acute coronary syndromes (ACS; manifested as either acute MI or high-risk unstable angina), provides further support to the "lower is better" theory. The primary end point was a composite of death from any cause, MI, documented unstable angina requiring rehospitalization, stroke, and revascularization (performed at least 30 days after randomization). After an average follow-up time of 2 years, event reduction was compared between standard and intensive LDL-C reduction.
The key finding of this study was that patients with recent ACS benefited from LDL-C reduction that resulted in values less than 100 mg/dL. PROVE IT provided evidence that more intensive LDL-C-lowering therapy reduces major CV events in patients with ACS compared with less intensive therapy over a period of 2 years.
Based on the results of 5 major recent clinical trials, in 2004 the ATP III authors issued an interim report that updated recommendations to the 2001 guidelines on cholesterol management, the second time the guidelines have been updated since their inception in 1993.2 Therapeutic lifestyle changes (eating a diet low in saturated fat and cholesterol, getting regular physical exercise, achieving overall weight management, and smoking cessation) remain essential modalities in clinical management. However, a more aggressive approach with a lower threshold for initiating drug therapy (from <130 mg/dL to <100 mg/dL) is now recommended for high-risk patients. An LDL-C goal of less than 70 mg/dL is an optional target for consideration based on recommendations from 2004 in patients at very high risk; established atherosclerotic CVD combined with either: (1) diabetes mellitus, (2) cigarette smoking, (3) metabolic syndrome, or (4) ACS.2
Since the 2004 interim report on ATP III, several trials have set out to strengthen the direct relationship between LDL-C levels and relative risk of CVD. Included in these trials are the Cholesterol and Recurrent Events (CARE) trial12 and the Long-Term Intervention with Pravastatin in Ischemic Disease (LIPID) study.13 These clinical studies, along with the findings of the Lescol Intervention Prevention Study (LIPS) published in 2002,14 laid a stable foundation for institution of therapy with these agents even when LDL-C levels are not markedly elevated.
Treating to Target
Although reduction of LDL-C contributing to lower incidence of CVD had been documented, the actual relationship between incidence of CVD and lower LDL-C attributed to statin therapy remained unexamined until publication of the results of the Greek Atorvastatin and Coronary-Heart-Disease Evaluation (GREACE) study in 2004. This study demonstrated a linear relationship between lower LDL-C levels obtained with statin therapy and lower incidence of adverse cardiology outcomes. It also showed that patients with the highest baseline LDL-C levels benefited the most from reduction to less than 100 mg/dL.15
Two additional studies have validated that aggressive LDL-C reduction provides enhanced avoidance of CVD events in patients with CHD. Both the A to Z trial and the Treating to New Targets (TNT) trial support a dosing strategy tailored to achieve lower LDL-C levels. When early initiation of aggressive statin therapy was compared with delayed, less intensive therapy in the A to Z trial in patients with recent ACS events, there was a favorable trend toward reduced CV events (hazard ratio at study's end, 0.75; P = .02).16 In TNT, reduction of LDL-C to a level below 80 mg/dL reduced the occurrence of events significantly greater than reduction to approximately 100 mg/dL.17
With the widely accepted idea that aggressive LDL-C reduction reduces risk of CVD in both a primary and a secondary setting, the challenge arises for practitioners to achieve the desired reduction, with safety, at the lowest possible cost. Current guidelines promote the concept of a target-based strategy as opposed to a specific initial dosing strategy. Recent changes in the statin marketplace reduce the cost of achieving these goals.
Extent of LDL-C reduction appears to be a critical factor in the success of statin treatment. The extent of reduction required is determined by the LDL-C level existing in the patient and the LDL-C level that is desired (target LDL-C). The percent reduction required for the treatment of a specific patient is a critical assessment in each situation where a statin is to be used. Selection of a statin that offers maximum cost-efficiency (in terms of greatest reduction per dollar cost) while providing the desired LDL-C reduction needed to reach a particular treatment goal will minimize unnecessary treatment costs.
In a recent pooled data study of 3 active-comparator trials, 76% of patients receiving rosuvastatin 10 mg for 12 weeks achieved ATP III LDL-C targets, whereas 53% of those receiving atorvastatin 10 mg achieved goal (P <.001).18 The highest CHD risk category goal of LDL-C less than 100 mg/dL was attained by 60% of rosuvastatin patients compared with only 19% of those receiving atorvastatin (P <.001). Pooled data from 2 trials comparing rosuvastatin with simvastatin and pravastatin also showed that 86% of patients who received rosuvastatin 10 mg for 12 weeks met their ATP III LDL-C goals, but only 64% of patients receiving simvastatin 20 mg and 49% of those receiving pravastatin 20 mg met their lipoprotein targets (P <.001).18 These analyses provide further credence to the recommendations derived from the comparison presented in Figure 2.
Cost per LDL-C Reduction
Cost-effective care can be defined as the point at which the minimum amount of input (of which cost is one measurement) is used to achieve a given output or result. Thus, in the search for cost-effective statin therapy, achieving a given level of LDL-C reduction at the lowest pharmacy and medical cost (attained via efficacy and safety) achieves high cost efficiency. Therefore, one would seek to achieve optimal utilization of resources by minimizing the cost to achieve the defined goal (LDL-C reduction). In the area of statin therapy, this analysis would be performed if it can be stated that the adverse event occurrence rates for the various statins were similar. In spite of some concerns on the introduction of some new products, postmarketing analysis has determined that the occurrence of serious side effects from various statins is similar.19
Concomitant with the introduction of new high-potency LDL-C-reduction drugs (with lower wholesale cost than previous high-potency drugs) in 2004 and 2005, widely accepted brand drugs were nearing patent expiration. Newly available generic medications, previously only available as a brand, have been introduced in mid-2006. These changes have provided practitioners the ability to reduce LDL-C at costs lower than ever.