TY - JOUR
T1 - Ticagrelor and Aspirin or Aspirin Alone after Coronary Surgery for Acute Coronary Syndrome
AU - Jeppsson, Anders
AU - James, Stefan
AU - Moller, Christian H.
AU - Malm, Carl Johan
AU - Dalén, Magnus
AU - Vanky, Farkas
AU - Modrau, Ivy Susanne
AU - Andersen, Karl
AU - Anttila, Vesa
AU - Atroshchenko, Gennady V.
AU - Barbu, Mikael
AU - Dreifaldt, Mats
AU - El-Akkawi, Ali Imad
AU - Friberg, Örjan
AU - Gudbjartsson, Tomas
AU - Gunn, Jarmo
AU - Haaverstad, Rune
AU - Halonen, Jari
AU - Hansson, Emma C.
AU - Holm, Jonas
AU - Husso, Annastiina
AU - Juvonen, Tatu
AU - Jakobsen, Øyvind
AU - Jideus, Lena
AU - Johannesson, Emilia
AU - Jonsson Holmdahl, Anna
AU - Jonsson, Kristjan
AU - Kolseth, Solveig Moss
AU - Krasniqi, Lytfi
AU - Mäkelä, Tuomas
AU - Mennander, Ari
AU - Mohagen Krogstad, Lars-Erik
AU - Rafiq, Sulman
AU - Raivio, Peter
AU - Riber, Lars
AU - Tahir, Aminah
AU - Thorsen, Carl
AU - Tønnessen, Theis
AU - Wahba, Alexander
AU - Zindovic, Igor
AU - Pivodic, Aldina
AU - Nielsen, Susanne J.
AU - Erlinge, David
AU - Alfredsson, Joakim
AU - Sartipy, Ulrik
AU - TACSI Trial Group
N1 - Publisher Copyright:
Copyright © 2025 Massachusetts Medical Society.
PY - 2025/12/11
Y1 - 2025/12/11
N2 - BACKGROUND: Patients benefit from antiplatelet therapy after coronary-artery bypass grafting (CABG) for an acute coronary syndrome. Whether the addition of ticagrelor to aspirin, as compared with aspirin alone, further reduces the risk of adverse cardiovascular outcomes is unclear. METHODS: In this open-label, registry-based, clinical trial conducted at 22 Nordic cardiothoracic surgery centers, we randomly assigned patients in a 1:1 ratio to receive either ticagrelor plus aspirin or aspirin alone for 1 year after CABG for an acute coronary syndrome. The primary outcome was a composite of death, myocardial infarction, stroke, or repeat revascularization, evaluated at 1 year. A key secondary outcome was net adverse clinical events, defined as a primary-outcome event or major bleeding. RESULTS: A total of 2201 patients were randomly assigned to receive ticagrelor plus aspirin (1104 patients) or aspirin alone (1097 patients). The mean age of the patients was 66 years, and 14.4% were women. A primary-outcome event occurred in 53 patients (4.8%) in the ticagrelor-plus-aspirin group and 50 (4.6%) in the aspirin-alone group (hazard ratio, 1.06; 95% confidence interval [CI], 0.72 to 1.56; P = 0.77). Net adverse clinical events occurred in 9.1% of patients in the ticagrelor-plus-aspirin group and 6.4% in the aspirin-alone group (hazard ratio, 1.45; 95% CI, 1.07 to 1.97). Major bleeding occurred in 4.9% of patients in the ticagrelor-plus-aspirin group and 2.0% in the aspirin-alone group (hazard ratio, 2.50; 95% CI, 1.52 to 4.11). CONCLUSIONS: Among patients who underwent CABG for an acute coronary syndrome, ticagrelor plus aspirin did not result in a lower incidence of death, myocardial infarction, stroke, or repeat coronary revascularization than aspirin alone at 1 year. (Funded by the Swedish Research Council and others; TACSI ClinicalTrials.gov number, NCT03560310; EudraCT number, 2017-001499-43; EU Clinical Trials number, 2023-508551-40-00.).
AB - BACKGROUND: Patients benefit from antiplatelet therapy after coronary-artery bypass grafting (CABG) for an acute coronary syndrome. Whether the addition of ticagrelor to aspirin, as compared with aspirin alone, further reduces the risk of adverse cardiovascular outcomes is unclear. METHODS: In this open-label, registry-based, clinical trial conducted at 22 Nordic cardiothoracic surgery centers, we randomly assigned patients in a 1:1 ratio to receive either ticagrelor plus aspirin or aspirin alone for 1 year after CABG for an acute coronary syndrome. The primary outcome was a composite of death, myocardial infarction, stroke, or repeat revascularization, evaluated at 1 year. A key secondary outcome was net adverse clinical events, defined as a primary-outcome event or major bleeding. RESULTS: A total of 2201 patients were randomly assigned to receive ticagrelor plus aspirin (1104 patients) or aspirin alone (1097 patients). The mean age of the patients was 66 years, and 14.4% were women. A primary-outcome event occurred in 53 patients (4.8%) in the ticagrelor-plus-aspirin group and 50 (4.6%) in the aspirin-alone group (hazard ratio, 1.06; 95% confidence interval [CI], 0.72 to 1.56; P = 0.77). Net adverse clinical events occurred in 9.1% of patients in the ticagrelor-plus-aspirin group and 6.4% in the aspirin-alone group (hazard ratio, 1.45; 95% CI, 1.07 to 1.97). Major bleeding occurred in 4.9% of patients in the ticagrelor-plus-aspirin group and 2.0% in the aspirin-alone group (hazard ratio, 2.50; 95% CI, 1.52 to 4.11). CONCLUSIONS: Among patients who underwent CABG for an acute coronary syndrome, ticagrelor plus aspirin did not result in a lower incidence of death, myocardial infarction, stroke, or repeat coronary revascularization than aspirin alone at 1 year. (Funded by the Swedish Research Council and others; TACSI ClinicalTrials.gov number, NCT03560310; EudraCT number, 2017-001499-43; EU Clinical Trials number, 2023-508551-40-00.).
UR - http://www.scopus.com/inward/record.url?scp=105024732410&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2508026
DO - 10.1056/NEJMoa2508026
M3 - Journal article
C2 - 40888737
AN - SCOPUS:105024732410
SN - 0028-4793
VL - 393
SP - 2313
EP - 2323
JO - The New England journal of medicine
JF - The New England journal of medicine
IS - 23
ER -