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Efficacy and safety with ticagrelor in patients with prior myocardial infarction in the approved European label: insights from PEGASUS-TIMI 54

Editorial by Stefan Agewall published on the October Issue of European Heart Journal – Cardiovascular Pharmacotherapy

Antiplatelet Drugs
Cardiovascular Pharmacotherapy

In PEGASUS-TIMI 54, ticagrelor significantly reduced the risk of the composite of major adverse cardiovascular events by 15–16% in stable patients with a prior myocardial infarction (MI) 1–3 years earlier.(1) In the October issue of European Heart Journal – Cardiovascular Pharmacotherapy, Dr Dellborg and co-workers report the efficacy and safety in the subpopulation recommended for treatment in the European label, i.e. treatment with 60 mg b.i.d. initiated up to 2 years from the MI, or within 1 year after stopping previous ADP receptor inhibitor treatment.(2) In this subgroup of patients, the composite of cardiovascular death, MI, or stroke occurred less frequently in the ticagrelor group. Ticagrelor also significantly reduced the risk of all-cause mortality; however, TIMI major bleeding was more frequent in the ticagrelor group.

References


  1. Bonaca MP, Bhatt DL, Cohen M, Steg PG, Storey RF, Jensen EC, Magnani G, Bansilal S, Fish MP, Im K, Bengtsson O, Oude Ophuis T, Budaj A, Theroux P, Ruda M, Hamm C, Goto S, Spinar J, Nicolau JC, Kiss RG, Murphy SA, Wiviott SD, Held P, Braunwald E, Sabatine MS, PEGASUS-TIMI 54 Steering Committee and Investigators. Long-term use of ticagrelor in patients with prior myocardial infarction. N Engl J Med 2015;372:1791–1800.
  2. http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Assessment_Report_-_Variation/human/001241/WC500203874.pdf (17 December 2015), EMA/CHMP/18297/2016
The content of this article reflects the personal opinion of the author/s and is not necessarily the official position of the European Society of Cardiology.