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August 15, 2025КАРДИОЛОГИЯ УЗБЕКИСТАНА23 citationsOpen Access

Aspirin or P2Y12 Inhibitor Monotherapy After Percutaneous Coronary Intervention for Acute Coronary Syndromes

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CLClaudio LaudaniDGDaniele GiacoppoGOG. Occhipinti

Key Points

  • P2Y12 inhibitor monotherapy reduces net adverse clinical events (NACE) significantly compared to aspirin monotherapy, highlighting its potential benefits.
  • Among 45,394 patients, P2Y12 inhibitor monotherapy notably lowers any bleeding and major bleeding incidents compared to aspirin monotherapy during short DAPT.
  • Network meta-analyses indicate significant differences in outcomes between aspirin and P2Y12 inhibitor monotherapy for patients with acute coronary syndrome after PCI.
  • Short DAPT duration benefits varied based on the type of monotherapy, emphasizing the need for personalized treatment approaches in ACS management.

Abstract

In patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI), shortening dual antiplatelet therapy (DAPT) duration reduces bleeding, but the relative benefit of maintaining aspirin or P2Y12 inhibitor monotherapy is debated. The authors sought to compare the net benefits of aspirin vs P2Y12 inhibitor monotherapy after short DAPT. Randomized trials of short DAPT in ACS patients undergoing PCI were identified. The primary outcome was trial-defined net adverse clinical events (NACE), a composite of ischemic and bleeding events. Secondary outcomes included single components of the primary endpoint. Pairwise and network meta-analyses were conducted. Heterogeneity sources were explored through sensitivity analyses. Twenty-three studies (N = 45,394) were included. Median DAPT duration was 4.8 (3.0-6.0) months and 2.2 (1.0-3.0) months in trials of aspirin and P2Y12 inhibitor monotherapy, respectively. Significant interaction between the 2 monotherapies was detected for NACE (Pint = 0.026) and any bleeding (Pint = 0.008), as being reduced by P2Y12 inhibitor (incidence rate ratio IRR: 0.78; 95% CI: 0.64-0.95 for NACE; IRR: 0.56; 95% CI: 0.46-0.67 for any bleeding), but not aspirin monotherapy. At indirect comparison, P2Y12 inhibitor monotherapy reduced NACE (IRR: 0.77; 95% CI: 0.62-0.95) and any bleeding (IRR: 0.68; 95% CI: 0.48-0.95) compared with aspirin monotherapy. Differences for bleeding endpoints, but not NACE, were mitigated when accounting for DAPT duration. In patients with ACS undergoing PCI, the benefits of short DAPT varied according to the subsequent monotherapy administered, with P2Y12 inhibitor monotherapy significantly reducing NACE, any bleeding, and major bleeding, whereas aspirin monotherapy had neutral results. (Dual Antiplatelet Therapy De-Escalation Followed By Aspirin or P2Y12 Inhibitor Monotherapy after Percutaneous Coronary Intervention for Acute Coronary Syndrome: a Systematic Review and Meta-analysis; CRD42025645844).

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Cite This Study

Laudani et al. (2025) studied this question.

synapsesocial.com/papers/68a365560a429f797332b0e1https://doi.org/10.1016/j.jcin.2025.05.044
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