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May 29, 2026Journal of Thrombosis and Thrombolysis0 citationsOpen Access

Patient-centred anti-platelet therapy following coronary artery bypass graft surgery

ELEleonora De LaurentisNSNikhil SahdevMJMarjan Jahangiri

Key Result

Patient-centered antiplatelet therapy after CABG, utilizing aspirin monotherapy and reserving dual antiplatelet therapy for high-risk patients, balances graft patency and bleeding risk.

Structured PICO

What is the optimal patient-centred anti-platelet therapy strategy following coronary artery bypass graft surgery?

P
Population
Patients following coronary artery bypass graft surgery (CABG)
I
Intervention
Patient-centred anti-platelet therapy (including dual anti-platelet therapy [DAPT] and single anti-platelet therapy [SAPT] strategies)
C
Comparator
Standard of care (lifelong aspirin mono-therapy)

Antiplatelet therapy post-CABG should be individualized based on bleeding risk, conduit type, and clinical presentation, moving away from a one-size-fits-all approach.

Limitations

  • Current guideline recommendations are largely extrapolated from PCI studies rather than dedicated CABG randomized trials.
  • Available bleeding risk scores have modest sensitivity and specificity and are not routinely used in clinical practice.
  • Differences in patient selection, adherence, and follow-up limit direct comparability between existing CABG antiplatelet studies.

Abstract

Abstract While lifelong aspirin mono-therapy remains the standard of care following coronary artery bypass graft surgery (CABG), the optimal antiplatelet strategy remains a subject of ongoing debate. The evidence argues against a ‘one-size-fits-all’ strategy and supports a patient-centred approach. Antiplatelet treatment decisions should incorporate bleeding risk which is often multifactorial and necessitates careful individualised evaluation based on patient characteristics and procedural factors. Conduit selection should also be considered as graft failure following CABG remains an important problem and varies according to conduit type, highlighting the critical role of antiplatelet therapy. Saphenous vein grafts are particularly susceptible to early thrombosis and late atherosclerotic degeneration, making optimisation of antiplatelet therapy especially relevant for preserving vein graft patency, whereas its impact on arterial grafts is less well defined. Current guideline recommendations are largely extrapolated from studies involving patients with acute or chronic coronary syndromes treated with percutaneous intervention or medical therapy. Clinical presentation is also a key determinant of antiplatelet strategy. Although current guidelines support resumption of dual antiplatelet therapy (DAPT) after CABG in patients with acute coronary syndromes (ACS), these recommendations are largely inherited from CABG subgroups of broader ACS trials rather than dedicated CABG randomised studies, and recent CABG-specific evidence has challenged the routine use of ticagrelor-based DAPT in this setting. DAPT in chronic coronary syndromes may be considered only in selected patients at low bleeding risk. Although, observational and randomised data suggest that DAPT can improve vein graft patency, but this has not consistently translated into short-term clinical benefit and is offset by increased bleeding risk. In fact, emerging evidence suggests shorter or de-escalated DAPT strategies may offer a more favourable balance between graft protection and bleeding. Graphical Abstract Patient-centred antiplatelet therapy post CABG. CABG – coronary artery bypass graft surgery; ACS – acute coronary syndrome; CCS – chronic coronary syndrome; SAPT – single anti-platelet therapy; DAPT – dual anti-platelet therapy.

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Cite This Study

Laurentis et al. (2026) conducted a review in Coronary artery disease requiring coronary artery bypass graft (CABG) surgery. Antiplatelet therapy (Single vs. Dual) was evaluated. Patient-centered antiplatelet therapy after CABG, utilizing aspirin monotherapy and reserving dual antiplatelet therapy for high-risk patients, balances graft patency and bleeding risk.

synapsesocial.com/papers/6a1aca7fca4263d615b88c54https://doi.org/10.1007/s11239-026-03331-2
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