Prescribing high-dose lipid-lowering therapy early to avoid subsequent cardiovascular events: is this a cost-effective strategy?

Eur J Prev Cardiol. 2012 Jun;19(3):474-83. doi: 10.1177/1741826711406616. Epub 2011 Apr 1.

Abstract

Background: While evidence shows high-dose statins reduce cardiovascular events compared with moderate doses in individuals with acute coronary syndrome (ACS), many primary care trusts (PCT) advocate the use of generic simvastatin 40 mg/day for these patients.

Methods and results: Data from 28 RCTs were synthesized using a mixed treatment comparison model. A Markov model was used to evaluate the cost-effectiveness of treatments taking into account adherence and the likely reduction in cost for atorvastatin when the patent expires. There is a clear dose-response: rosuvastatin 40 mg/day produces the greatest reduction in low-density lipoprotein cholesterol (56%) followed by atorvastatin 80 mg/day (52%), and simvastatin 40 mg/day (37%). Using a threshold of £20,000 per QALY, if adherence levels in general practice are similar to those observed in RCTs, all three higher dose statins would be considered cost-effective compared to simvastatin 40 mg/day. Using the net benefits of the treatments, rosuvastatin 40 mg/day is estimated to be the most cost-effective alternative. If the cost of atorvastatin reduces in line with that observed for simvastatin, atorvastatin 80 mg/day is estimated to be the most cost-effective alternative.

Conclusion: Our analyses show that current PCT policies intended to minimize primary care drug acquisition costs result in suboptimal care.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Atorvastatin
  • Bayes Theorem
  • Cardiovascular Diseases / drug therapy*
  • Cardiovascular Diseases / economics*
  • Cardiovascular Diseases / prevention & control
  • Clinical Trials, Phase III as Topic
  • Cost-Benefit Analysis
  • Drug Costs*
  • Drug Prescriptions / economics
  • Drugs, Generic / administration & dosage*
  • Drugs, Generic / economics*
  • Fluorobenzenes / administration & dosage
  • Fluorobenzenes / economics
  • Heptanoic Acids / administration & dosage
  • Heptanoic Acids / economics
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage*
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / economics*
  • Markov Chains
  • Medication Adherence
  • Models, Economic
  • Pyrimidines / administration & dosage
  • Pyrimidines / economics
  • Pyrroles / administration & dosage
  • Pyrroles / economics
  • Quality Indicators, Health Care / economics
  • Quality-Adjusted Life Years
  • Randomized Controlled Trials as Topic
  • Rosuvastatin Calcium
  • Secondary Prevention / economics*
  • Simvastatin / administration & dosage
  • Simvastatin / economics
  • Sulfonamides / administration & dosage
  • Sulfonamides / economics
  • Time Factors
  • Treatment Outcome

Substances

  • Drugs, Generic
  • Fluorobenzenes
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrimidines
  • Pyrroles
  • Sulfonamides
  • Rosuvastatin Calcium
  • Atorvastatin
  • Simvastatin