American Journal of Cardiology
Volume 108, Issue 5 , Pages 691-697, 1 September 2011

Estimating Health and Economic Benefits from Using Prescription Omega-3 Fatty Acids in Patients With Severe Hypertriglyceridemia

  • Stuart Samuel, PhD

      Affiliations

    • Archimedes, Inc., San Francisco, California
    • Corresponding Author InformationCorresponding author: Tel: 510-420-1015; fax: 415-490-0399
  • ,
  • Barbara Peskin, PhD

      Affiliations

    • Archimedes, Inc., San Francisco, California
  • ,
  • Bhakti Arondekar, PhD

      Affiliations

    • GlaxoSmithKline, Philadelphia, Pennsylvania
  • ,
  • Peter Alperin, MD

      Affiliations

    • Archimedes, Inc., San Francisco, California
  • ,
  • Susan Johnson, MD

      Affiliations

    • GlaxoSmithKline, Philadelphia, Pennsylvania
  • ,
  • Ian Blumenfeld, PhD

      Affiliations

    • Archimedes, Inc., San Francisco, California
  • ,
  • Glenda Stone, PhD

      Affiliations

    • GlaxoSmithKline, Philadelphia, Pennsylvania
  • ,
  • Terry A. Jacobson, MD

      Affiliations

    • Department of Medicine, Emory University, Atlanta, Georgia

Received 19 January 2011; received in revised form 10 April 2011; accepted 10 April 2011.

Patients with increased triglyceride levels compared to those with normal levels are at higher risk for coronary heart disease. In patients with severe (≥500 mg/dl) hypertriglyceridemia (SHTG), clinical trials have demonstrated that prescription ω-3 fatty acids (P-OM3s) 4 g/day can decrease triglyceride levels by 45%. However, the precise health and economic benefits of decreasing SHTG with P-OM3 are unknown. We used the previously validated Archimedes model to simulate a 20-year trial involving subjects 45 to 75 years old with SHTG. The trial consisted of an intervention arm (P-OM3 4 g/day) and a control arm. Simulation results for the control arm indicated that subjects with SHTG are at about 2 times higher risk for myocardial infarction than those with normal triglyceride levels. Using estimates from previous epidemiologic studies and meta-analyses with OM3s, the model predicted 29% to 36% decreases in various measurements of adverse cardiac events for the intervention arm. The model also predicted a decrease in ischemic stroke of 24% (95% confidence interval 15 to 33). For the 20-year simulated trial, the cost per quality-adjusted life-year gained for the currently available P-OM3 approved by the Food and Drug Administration was $47,000. Results remained robust under different clinical assumptions. In our model P-OM3 was effective in decreasing triglyceride levels and cardiovascular disease risk in patients with SHTG. In conclusion, P-OM3 medication is cost effective in our simulated trial and comparable to other cost-effective cardiovascular interventions.

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 Funding for this study was provided by GlaxoSmithKline, Inc., Philadelphia, Pennsylvania.

PII: S0002-9149(11)01603-1

doi:10.1016/j.amjcard.2011.04.019

American Journal of Cardiology
Volume 108, Issue 5 , Pages 691-697, 1 September 2011