4.8 Article

Polypill Strategy in Secondary Cardiovascular Prevention

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 387, Issue 11, Pages 967-977

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa2208275

Keywords

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Funding

  1. European Union Horizon 2020 research and innovation program [633765]
  2. Instituto de Salud Carlos III [PTC20/00018, PT17/0017]
  3. Ministerio de Ciencia e Innovacion
  4. Pro CNIC Foundation
  5. MICIN/AEI [633765]
  6. State Plan for Research, Development, and Innovation [CEX2020-001041-S]
  7. State Plan for Scientific and Technical Research and Innovation [201316]
  8. Subdirectorate Gen-eral for Evaluation and Promotion of Research
  9. European Regional Development Fund
  10. [201720]
  11. H2020 Societal Challenges Programme [633765] Funding Source: H2020 Societal Challenges Programme

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The study showed that taking a polypill containing aspirin, ramipril, and atorvastatin within 6 months after myocardial infarction significantly reduced the risk of major adverse cardiovascular events compared to usual care.
BACKGROUND A polypill that includes key medications associated with improved outcomes (aspirin, angiotensin-converting-enzyme [ACE] inhibitor, and statin) has been proposed as a simple approach to the secondary prevention of cardiovascular death and complications after myocardial infarction. METHODS In this phase 3, randomized, controlled clinical trial, we assigned patients with myocardial infarction within the previous 6 months to a polypill-based strategy or usual care. The polypill treatment consisted of aspirin (100 mg), ramipril (2.5, 5, or 10 mg), and atorvastatin (20 or 40 mg). The primary composite outcome was cardiovascular death, nonfatal type 1 myocardial infarction, nonfatal ischemic stroke, or urgent revascularization. The key secondary end point was a composite of cardiovascular death, nonfatal type 1 myocardial infarction, or nonfatal ischemic stroke. RESULTS A total of 2499 patients underwent randomization and were followed for a median of 36 months. A primary-outcome event occurred in 118 of 1237 patients (9.5%) in the polypill group and in 156 of 1229 (12.7%) in the usual-care group (hazard ratio, 0.76; 95% confidence interval [CI], 0.60 to 0.96; P=0.02). A key secondary-outcome event occurred in 101 patients (8.2%) in the polypill group and in 144 (11.7%) in the usual-care group (hazard ratio, 0.70; 95% CI, 0.54 to 0.90; P=0.005). The results were consistent across prespecified subgroups. Medication adherence as reported by the patients was higher in the polypill group than in the usual-care group. Adverse events were similar between groups. CONCLUSIONS Treatment with a polypill containing aspirin, ramipril, and atorvastatin within 6 months after myocardial infarction resulted in a significantly lower risk of major adverse cardiovascular events than usual care.

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