Evidence map›Paper›PMID 42892998›Full record

ArticleAmerican heart journal plus : cardiology research and practice2026

Ticagrelor versus prasugrel following PCI in acute coronary syndromes and high-risk coronary artery disease: A meta-analysis of one-year randomized trial outcomes.

Mohamed Ibrahim Gbreel, Ahmed Samy Badran, Daniel Robinson, Islam Ebeid, Marwa Hassan, Abdelhakim A Abdelrahman, Jonas Bodanowitz, Stephan Valenta, Christin Valenta, Plamen Kochev and 3 more

Abstract read
In one paragraph

Article in American heart journal plus : cardiology research and practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Mohamed Ibrahim GbreelDepartment of Cardiology, General Organization for Teaching Hospitals and Institutions (GOTHI), Cairo, Egypt.
Ahmed Samy BadranFaculty of Medicine, Ain Shams University, Cairo, Egypt.
Daniel RobinsonDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Islam EbeidDepartment of Cardiology, National Institute of Diabetes and Endocrinology, Cairo, Egypt.
Marwa HassanTheodor Bilharz Research Institute, Giza, Egypt.
Abdelhakim A AbdelrahmanKing's College Hospital, Denmark Hill, London, United Kingdom.
Jonas BodanowitzDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Stephan ValentaDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Christin ValentaDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Plamen KochevDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Jasmin OrtakDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Hüseyin InceDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.
Mahmoud BalataDepartment of Cardiology, University Hospital of Rostock, Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Guidelines recommend potent P2Y12 inhibitors over clopidogrel following percutaneous coronary intervention. Whether ticagrelor- or prasugrel-based dual antiplatelet therapy (DAPT) provides superior clinical outcomes following percutaneous coronary intervention (PCI) remains uncertain, particularly across acute coronary syndromes (ACS) and high-risk coronary artery disease (CAD) populations. Methods: We searched databases for randomized controlled trials comparing ticagrelor- and prasugrel-based DAPT in patients with CAD undergoing PCI with 1-year follow-up. The primary outcomes were major adverse cardiovascular events (MACE) and all-cause mortality. Secondary outcomes included cardiovascular death, myocardial infarction, stroke, stent thrombosis, and major bleeding. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled using random-effects models. Sensitivity analyses were performed in ACS populations. Results: Three trials randomized a total of 7048 patients. In the primary analysis, prasugrel-based therapy was not associated with a statistically significant reduction in MACE compared with ticagrelor-based therapy (HR = 0.83; 95% CI: 0.67-1.03; Conclusions: Among patients with ACS and high-risk CAD undergoing PCI, current randomized evidence does not establish conclusive superiority between ticagrelor- and prasugrel-based DAPT for 1-year ischemic or bleeding endpoints.

Indexed as

Acute coronary syndromeCoronary artery diseaseDual antiplatelet therapyMeta-analysisP2Y12 inhibitorsPercutaneous coronary interventionPrasugrelTicagrelor

Identifiers

PMID42892998
PMCPMC13676095

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.