Evidence map›Paper›PMID 42888957›Full record

Observational studyCardiovascular therapeutics2026

Prasugrel Outperforms Ticagrelor in Acute Coronary Syndrome: A Real-World Analysis.

Septi Melisa, Christianus Heru Setiawan, Chun-Yao Huang, Tian-Hsing Chen, Wei-Ting Chang, Wei-Pin Chang, Min-Huei Hsu, Christine Y Lu, Jason C Hsu

Abstract readComparative StudyObservational Study
In one paragraph

Observational study in Cardiovascular therapeutics, 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

9 authors.

Septi MelisaInternational Ph.D. Program in Biotech and Healthcare Management, College of Management, Taipei Medical University, Taipei, Taiwan, tmu.edu.tw.ORCID https://orcid.org/0009-0005-6669-2390
Christianus Heru SetiawanSchool of Pharmacy, Taipei Medical University, Taipei, Taiwan, tmu.edu.tw.ORCID https://orcid.org/0000-0003-4860-1115
Chun-Yao HuangDivision of Cardiology, Taipei Medical University Hospital, Taipei, Taiwan, tmuh.org.tw.ORCID https://orcid.org/0000-0002-8978-7879
Tian-Hsing ChenDepartment of Cardiology, Chang Gung Memorial Hospital, Keelung, Taiwan, cgmh.org.tw.ORCID https://orcid.org/0000-0001-6986-9765
Wei-Ting ChangDivision of Cardiovascular Medicine, Chi Mei Hospital, Tainan, Taiwan.ORCID https://orcid.org/0000-0001-9525-2144
Wei-Pin ChangSchool of Health Care Administration, Taipei Medical University, Taipei, Taiwan, tmu.edu.tw.ORCID https://orcid.org/0000-0003-2107-612X
Min-Huei HsuGraduate Institute of Data Science, College of Management, Taipei Medical University, Taipei, Taiwan, tmu.edu.tw.ORCID https://orcid.org/0000-0003-0383-4302
Christine Y LuKolling Institute, Faculty of Medicine and Health, The University of Sydney and the Northern Sydney Local Health District, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0002-7550-6837
Jason C HsuInternational Ph.D. Program in Biotech and Healthcare Management, College of Management, Taipei Medical University, Taipei, Taiwan, tmu.edu.tw.ORCID https://orcid.org/0000-0003-2997-2404

Funding

Ministry of Education DP2-TMU-114-A-01National Science and Technology Council 114-2628-B-038-002-MY3National Science and Technology Council NSTC113-2634-F038-001
6 · The paper itself

Abstract

Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor is standard for patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI), yet real-world comparisons of ticagrelor and prasugrel remain limited. We evaluated their relative effectiveness and safety using the TriNetX Global Collaborative Network (2010-2024). Adult ACS patients receiving prasugrel or ticagrelor within 24 h post-PCI were included. The primary endpoint was a 1-year composite of all-cause mortality, myocardial infarction (MI), and cerebral infarction; secondary endpoints included individual components, major bleeding, and repeat revascularization. Propensity score matching balanced baseline characteristics, with subgroup and sensitivity analyses assessing robustness. Among 14,895 matched pairs (n = 29,790) from 126,273 patients, prasugrel was associated with lower risk of the composite endpoint (HR 0.641; 95% CI 0.613-0.671), all-cause mortality (HR 0.557; 95% CI 0.487-0.637), and MI (HR 0.648; 95% CI 0.616-0.680), without increased bleeding (HR 0.945; 95% CI 0.824-1.084). Repeat revascularization was higher with prasugrel (HR 1.791; 95% CI 1.639-1.957). Effects were consistent across subgroups. In this real-world setting, prasugrel demonstrated superior effectiveness over ticagrelor in reducing mortality and ischemic events without increasing the risk of bleeding, although higher rates of repeat revascularization warrant further study. These findings support prasugrel as a potentially preferred P2Y12 inhibitor in selected ACS patients undergoing PCI.

Indexed as

Acute Coronary SyndromePercutaneous Coronary InterventionPlatelet Aggregation InhibitorsPrasugrel HydrochloridePurinergic P2Y Receptor AntagonistsTicagrelorAgedFemaleHemorrhageHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsPlatelet Aggregation InhibitorsPrasugrel HydrochloridePurinergic P2Y Receptor AntagonistsTicagreloracute coronary syndromepercutaneous coronary interventionprasugrelticagrelor

Identifiers

PMID42888957
PMCPMC13675845

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.