Modeling the cost effectiveness and budgetary impact of Polypills for secondary prevention of cardiovascular disease in the United States

Am Heart J. 2019 Aug:214:77-87. doi: 10.1016/j.ahj.2019.04.020. Epub 2019 May 7.

Abstract

Background: There is underutilization of appropriate medications for secondary prevention of cardiovascular disease (CVD).

Methods: Usual care (UC) was compared to polypill-based care with 3 versions using a validated micro-simulation model in the NHANES population with prior CVD. UC included individual prescription of up to 4 drug classes (antiplatelet agents, beta-blockers, renin-angiotensin-aldosterone inhibitors and statins). The polypills modeled were aspirin 81 mg, atenolol 50 mg, ramipril 5 mg, and either simvastatin 40 mg (Polypill I), atorvastatin 80 mg (Polypill II), or rosuvastatin 40 mg (Polypill III). Baseline medication use and adherence came from United Healthcare claims data.

Results: When compared to UC, there were annual reductions of 130,000 to 178,000 myocardial infarctions and 54,000 to 74,000 strokes using Polypill I and II, respectively. From a health sector perspective, in incremental analysis the ICERs for Polypill I and II were $20,073/QALY and $21,818/QALY respectively; Polypill III was dominated but had a similar cost-effectiveness ratio to Polypill II when compared directly to usual care. From a societal perspective, Polypill II was cost-saving and dominated all strategies. Over a 5-year period, those taking Polypill I and II compared to UC saved approximately $12 and $6 per-patient-per-year alive, respectively. Polypill II was the preferred strategy in 98% of runs at a willingness to pay of $50,000 in the probability sensitivity analysis.

Conclusions: Use of a polypill has a favorable cost profile for secondary CVD prevention in the United States. Reductions in CVD-related healthcare costs outweighed medication cost increases on a per-patient-per-year basis, suggesting that a polypill would be economically advantageous to both patients and payers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / economics
  • Aspirin / economics
  • Atenolol / economics
  • Budgets*
  • Cardiovascular Diseases / economics
  • Cardiovascular Diseases / mortality
  • Cardiovascular Diseases / prevention & control*
  • Cost Savings
  • Cost-Benefit Analysis
  • Drug Combinations*
  • Drug Costs
  • Female
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / economics
  • Life Expectancy
  • Male
  • Medication Adherence
  • Middle Aged
  • Nutrition Surveys
  • Platelet Aggregation Inhibitors / economics
  • Ramipril / economics
  • Renin-Angiotensin System
  • Secondary Prevention / economics*
  • Secondary Prevention / methods
  • Secondary Prevention / statistics & numerical data
  • Stroke / economics
  • Stroke / mortality
  • Stroke / prevention & control*
  • United States

Substances

  • Adrenergic beta-Antagonists
  • Drug Combinations
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Platelet Aggregation Inhibitors
  • Atenolol
  • Ramipril
  • Aspirin