Ticagrelor-Based antiplatelet therapy versus aspirin alone after coronary artery bypass grafting: A systematic review

Zaryab Bacha1, Aizaz Anwar Khalid2, Munazza Sikandar3

  • 1Department of Medicine, Khyber Medical College, Peshawar, Pakistan. zaryab03443578390@gmail.com.

Insights

Ticagrelor therapy after coronary artery bypass grafting (CABG) did not improve major clinical outcomes compared to aspirin. However, ticagrelor significantly reduced saphenous vein graft (SVG) failure, suggesting potential benefits in graft patency.

Area of Science:

  • Cardiology
  • Vascular Surgery
  • Pharmacology

Background:

  • Coronary artery bypass grafting (CABG) success is limited by saphenous vein graft (SVG) occlusion.
  • Aspirin is standard antiplatelet therapy, but graft failure and adverse events persist.
  • Ticagrelor offers more potent antiplatelet effects but carries bleeding concerns.

Purpose of the Study:

  • To systematically review and meta-analyze randomized controlled trials (RCTs) comparing ticagrelor-based therapy with aspirin monotherapy in CABG patients.
  • To evaluate the impact of ticagrelor on major bleeding, major adverse cardiovascular events (MACE), and graft patency.

Main Methods:

  • Systematic review and meta-analysis of five RCTs involving 4,208 patients.
  • Comparison of ticagrelor-based therapy versus aspirin monotherapy post-CABG.
  • Primary endpoints: major bleeding, MACE, all-cause mortality. Secondary endpoints: SVG failure, stroke, myocardial infarction, repeat revascularization.

Main Results:

  • Ticagrelor-based therapy showed no significant difference in MACE, all-cause mortality, or major bleeding compared to aspirin.
  • No significant differences were observed for stroke, myocardial infarction, or repeat revascularization.
  • Ticagrelor significantly reduced saphenous vein graft (SVG) failure (RR 0.62, 95% CI 0.50-0.78).

Conclusions:

  • Ticagrelor-based therapy does not improve major clinical outcomes but enhances SVG patency after CABG.
  • Routine use of ticagrelor is not recommended; consider for selected high-risk patients.
  • Further trials are needed to confirm if SVG patency benefits translate to improved clinical outcomes.
Abstract

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