P2Y12 inhibitor monotherapy versus dual antiplatelet therapy after complex percutaneous coronary intervention in patients with acute coronary syndromes: a NEO-MINDSET trial substudy

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Authors: Guy F A Prado, Pedro Beraldo de, Stefano Garzon Dias, Marcelo Franken, Patrícia O. Guimarães, Caio de Assis, Fábio Grunspun Pitta, Felipe Mateus Teixeira, Willterson Carlos Bandeira, Maria Sanali, Silvia Regina Lamas, Frederico Monfardini
+19 more Lailah Cristina de, Rosana Coura Rocha, Fernanda Mangione, Vitor Arantes Pazolini, Adriadne Justi Bertolin, M O Antunes, Fabio Serra Silveira, Bruno Ramos Nascimento, L N Ohe, Esmeralci Ferreira, Fernanda Barbosa de Almeida Sampaio, Rogério Sarmento‐ Leite, Marco Vugman Wainstein, Cristiano Guedes Bezerra, Jose Airton Arruda, Breno Oliveira Almeida, Valeria Paradies, Jose Mariani Junior, Pedro Alves Lemos
Cited by: 1
References: 15

Abstract

BACKGROUND: Whether the anatomical complexity of percutaneous coronary intervention (PCI) in patients with acute coronary syndromes (ACS) influences the effects of antiplatelet therapy remains unknown. AIMS: inhibitor monotherapy or dual antiplatelet therapy (DAPT). METHODS: In the NEO-MINDSET trial, patients with ACS were randomised after successful PCI to 12-month ticagrelor- or prasugrel-based monotherapy or DAPT, initiated within the first 4 days of hospitalisation. The co-primary endpoints were (i) a composite of death, myocardial infarction, urgent target vessel revascularisation, or stroke; and (ii) Bleeding Academic Research Consortium (BARC) Type 2, 3, or 5 bleeding. Complex PCI was defined by one or more of the following criteria: three-vessel PCI, ≥3 treated lesions, ≥3 stents implanted, total stent length >60 mm, two-stent bifurcation, or stenting in the left main coronary artery, in a bypass graft, or in a chronic total occlusion lesion. RESULTS: Of the 3,408 randomised patients with available procedural data, 791 (23.2%) underwent complex PCI. Compared with the non-complex PCI group, patients in the complex PCI group were older (mean age 60.63±10.52 years vs 59.33±10.83 years; p=0.005) and had a higher prevalence of hypertension (67.9% vs 62.9%; p=0.010). Among patients undergoing complex PCI, 1, 2, or ≥3 complexity criteria were present in 45.5% (n=360), 22.5% (n=178), and 32.0% (n=253), respectively. PCI complexity did not significantly modify the treatment effects of monotherapy versus DAPT on the ischaemic co-primary endpoint (p-interaction=0.68). Likewise, PCI complexity did not have an effect on the comparative risk of BARC Type 2, 3, or 5 bleeding between monotherapy versus DAPT. CONCLUSIONS: inhibitor monotherapy versus DAPT on the co-primary ischaemic or bleeding outcomes. CLINICALTRIALS: gov: NCT04360720.

Fields of Study & Subjects

Antiplatelet Therapy and Cardiovascular Diseases Coronary Interventions and Diagnostics Acute Myocardial Infarction Research

Publication details

Journal / source
EuroIntervention
Publisher
Europa Digital & Publishing
Volume
22
Issue
14
Pages
e765–e772
Publication date
1 July 2026
Language
EN