@article{138e40345b2949b7a41bd19572f5ea26,
title = "Rationale, design and baseline characteristics of the effect of ticagrelor on health outcomes in diabetes mellitus patients Intervention study",
abstract = "In the setting of prior myocardial infarction, the oral antiplatelet ticagrelor added to aspirin reduced the risk of recurrent ischemic events, especially, in those with diabetes mellitus. Patients with stable coronary disease and diabetes are also at elevated risk and might benefit from dual antiplatelet therapy. The Effect of Ticagrelor on Health Outcomes in diabEtes Mellitus patients Intervention Study (THEMIS, NCT01991795) is a Phase 3b randomized, double-blinded, placebo-controlled trial of ticagrelor vs placebo, on top of low dose aspirin. Patients ≥50 years with type 2 diabetes receiving anti-diabetic medications for at least 6 months with stable coronary artery disease as determined by a history of previous percutaneous coronary intervention, bypass grafting, or angiographic stenosis of ≥50% of at least one coronary artery were enrolled. Patients with known prior myocardial infarction (MI) or stroke were excluded. The primary efficacy endpoint is a composite of cardiovascular death, myocardial infarction, or stroke. The primary safety endpoint is Thrombolysis in Myocardial Infarction major bleeding. A total of 19 220 patients worldwide have been randomized and at least 1385 adjudicated primary efficacy endpoint events are expected to be available for analysis, with an expected average follow-up of 40 months (maximum 58 months). Most of the exposure is on a 60 mg twice daily dose, as the dose was lowered from 90 mg twice daily partway into the study. The results may revise the boundaries of efficacy for dual antiplatelet therapy and whether it has a role outside acute coronary syndromes, prior myocardial infarction, or percutaneous coronary intervention.",
keywords = "antiplatelet therapy, clinical trials, diabetes mellitus, general clinical cardiology/adult, ischemic heart disease",
author = "{the THEMIS Steering Committee} and Bhatt, {Deepak L.} and Kim Fox and Harrington, {Robert A.} and Leiter, {Lawrence A.} and Mehta, {Shamir R.} and Tabassome Simon and Marielle Andersson and Anders Himmelmann and Wilhelm Ridderstr{\aa}le and Claes Held and Steg, {Philippe Gabriel} and R. Diaz and J. Amerena and K. Huber and P. Sinnaeve and Nicolau, {J. C.} and Saraiva, {J. F.K.} and I. Petrov and R. Corbal{\'a}n and J. Ge and Q. Zhao and R. Botero and P. Widimsk{\'y} and Kristensen, {S. D.} and J. Hartikainen and N. Danchin and H. Darius and Fat, {T. H.} and Kiss, {R. G.} and P. Pais and E. Lev and Luca, {L. D.} and S. Goto and L{\'o}pez, {G. A.R.} and Cornel, {J. H.} and F. Kontny and F. Medina and N. Babilonia and G. Opolski and D. Vinereanu and D. Zateyshchikov and M. Ruda and O. Elamin and F. Kov{\'a}{\v R} and Dalby, {A. J.} and Jeong, {M. H.} and H. Bueno and S. James and Chiang, {C. E.} and D. Tresukosol",
note = "Publisher Copyright: {\textcopyright} 2019 The Authors. Clinical Cardiology published by Wiley Periodicals, Inc.",
year = "2019",
month = may,
doi = "10.1002/clc.23164",
language = "אנגלית",
volume = "42",
pages = "498--505",
journal = "Clinical Cardiology",
issn = "0160-9289",
publisher = "John Wiley and Sons Inc.",
number = "5",
}