American Heart Journal
Volume 156, Issue 1 , Pages 31-36, July 2008

Rationale and design of the Post-MI FREEE trial: A randomized evaluation of first-dollar drug coverage for post–myocardial infarction secondary preventive therapies

  • Niteesh K. Choudhry, MD, PhD

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
    • Corresponding Author InformationReprint requests: Niteesh K. Choudhry, MD, PhD, Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, 1620 Tremont Street, Suite 3030, Boston, MA 02120.
  • ,
  • Troyen Brennan, MD, JD, MPH

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Michele Toscano, MS

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Claire Spettell, PhD

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Robert J. Glynn, ScD, PhD

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
    • Division of Preventive Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
  • ,
  • Mark Rubino, MHA, RPh

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Sebastian Schneeweiss, MD, ScD

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
  • ,
  • Alan M. Brookhart, PhD

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
  • ,
  • Joaquim Fernandes, MS

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Susan Mathew, MPH

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Blake Christiansen, MS, RPh

      Affiliations

    • Aetna Inc Hartford, CT
  • ,
  • Elliott M. Antman, MD

      Affiliations

    • Division of Cardiology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
  • ,
  • Jerry Avorn, MD

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA
  • ,
  • William H. Shrank, MD, MSHS

      Affiliations

    • Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA

Received 26 November 2007; accepted 12 March 2008. published online 09 June 2008.

Background

Medication nonadherence is a major public health problem, especially for patients with coronary artery disease. The cost of prescription drugs is a central reason for nonadherence, even for patients with drug insurance. Removing patient out-of-pocket drug costs may increase adherence, improve clinical outcomes, and even reduce overall health costs for high-risk patients. The existing data are inadequate to assess whether this strategy is effective.

Trial Design

The Post-Myocardial Infarction Free Rx and Economic Evaluation (Post-MI FREEE) trial aims to evaluate the effect of providing full prescription drug coverage (ie, no copays, coinsurance, or deductibles) for statins, β-blockers, angiotensin-converting enzyme inhibitors, and angiotensin II receptor blockers to patients after being recently discharged from the hospital. Potentially eligible patients will be those individuals who receive their health and pharmacy benefits through Aetna, Inc. Patients enrolled in a Health Savings Account plan, who are ≥65 years of age, whose plan sponsor (ie, the employer, union, government, or association that sponsors the particular benefits package) has opted out of participating in the study, and who do not receive both medical services and pharmacy coverage through Aetna will be excluded. The plan sponsor of each eligible patient will be block randomized to either full drug coverage or current levels of pharmacy benefit, and all subsequently eligible patients of that same plan sponsor will be assigned to the same benefits group. The primary outcome of the trial is a composite clinical outcome of readmission for acute MI, unstable angina, stroke, congestive heart failure, revascularization, or inhospital cardiovascular death. Secondary outcomes include medication adherence and health care costs. All patients will be followed up for a minimum of 1 year.

Conclusion

The Post-MI FREEE trial will be the first randomized study to evaluate the impact of reducing cost-sharing for essential cardiac medications in high-risk patients on clinical and economic outcomes.

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 Trial Registration Number: NCT00566774.

 Funding information: This work was supported by a research grant from Aetna Inc to Brigham and Women's Hospital.

PII: S0002-8703(08)00231-7

doi:10.1016/j.ahj.2008.03.021

American Heart Journal
Volume 156, Issue 1 , Pages 31-36, July 2008