Treatment With Icosapent Ethyl to Reduce Ischemic Events in Patients With Prior Percutaneous Coronary Intervention: Insights From REDUCE-IT PCI

  • Benjamin E. Peterson
  • , Deepak L. Bhatt
  • , Ph Gabriel Steg
  • , Michael Miller
  • , Eliot A. Brinton
  • , Terry A. Jacobson
  • , Steven B. Ketchum
  • , Rebecca A. Juliano
  • , Lixia Jiao
  • , Ralph T. Doyle
  • , Craig Granowitz
  • , C. Michael Gibson
  • , Duane Pinto
  • , Robert P. Giugliano
  • , Matthew J. Budoff
  • , Jean Claude Tardif
  • , Subodh Verma
  • , Christie M. Ballantyne

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

BACKGROUND: Patients who undergo percutaneous coronary intervention (PCI) are at increased risk for recurrent cardiovascular events despite aggressive medical therapy. METHODS AND RESULTS: This post hoc analysis focused on the subset of patients with prior PCI enrolled in REDUCE-IT (Reduction of Cardiovascular Events With Icosapent Ethyl–Intervention Trial), a multicenter, randomized, double-blind, placebo-controlled trial of icosapent ethyl versus placebo. Icosapent ethyl was added to statins in patients with low-density lipoprotein cholesterol <100 mg/dL and fasting triglycerides 135–499 mg/dL. The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina requiring hospitalization. There were 8179 patients randomized in REDUCE-IT followed for a median of 4.9 years, and 3408 (41.7%) of them had a prior PCI with a median follow-up of 4.8 years. These patients were randomized a median of 2.9 years (11 days to 30.7 years) after PCI. Among patients treated with icosapent ethyl versus placebo, there was a 34% reduction in the primary composite end point (hazard ratio [HR], 0.66; 95% CI, 0.58–0.76; P<0.001; number needed to treat4.8 years=12) and a 34% reduction in the key secondary composite end point of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke (HR, 0.66; 95% CI, 0.56–0.79; P<0.001; NNT4.8 years=19) versus placebo. Similarly, large reductions occurred in total coronary revascularizations and revascularization subtypes. There was also a 39% reduction in total events (rate ratio, 0.61; 95% CI, 0.52–0.72; P<0.001). CONCLUSIONS: Among patients treated with statins with elevated triglycerides and a history of prior PCI, icosapent ethyl substantially reduced the risk of recurrent events during an average of ~5 years of follow-up with a number needed to treat of only 12. REGISTRATION: URL: https://www.clini​caltr​ials.gov; Unique identifier: NCT01492361.

Original languageEnglish
Article numbere022937
JournalJournal of the American Heart Association
Volume11
Issue number6
DOIs
StatePublished - 15 Mar 2022
Externally publishedYes

Keywords

  • eicosapentaenoic acid
  • icosapent ethyl
  • prevention
  • revascularization

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