Evidence map›Paper›PMID 36137672›Full record

Trial reportJournal of the American College of Cardiology2022

Abbreviated Antiplatelet Therapy After Coronary Stenting in Patients With Myocardial Infarction at High Bleeding Risk.

Pieter C Smits, Enrico Frigoli, Pascal Vranckx, Yukio Ozaki, Marie-Claude Morice, Bernard Chevalier, Yoshinobu Onuma, Stephan Windecker, Pim A L Tonino, Marco Roffi and 20 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of the American College of Cardiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03023020 (Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen), which is not on this map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% of its field
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.

NCT03023020 nacompletednot on this map

Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen

TypeinterventionalSponsorECRI bvRan2017 to 2021Enrolled4,579ConditionsHigh Bleeding Risk, Coronary Artery Disease, PCIArmsAspirin, P2Y12 inhibitor
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Insights on DAPT Abbreviation and De-escalation from ULTIMATE-DAPT and Related Trials: Are we Heading Toward an Aspirin-Free Strategy?American journal of cardiovascular drugs : drugs, devices, and other interventions · 2025
    Article
  6. Observational
  7. Can DAPT be discontinued at one month after PCI in high bleeding risk patients presenting with ACS?EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2024
    Article
  8. One- versus three-month dual antiplatelet therapy in high bleeding risk patients undergoing percutaneous coronary intervention for non-ST-segment elevation acute coronary syndromes.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2024
    Article
  9. Article
  10. Review
  11. P2yFrontiers in cardiovascular medicine · 2023
    Review
  12. Post-PCI Antithrombotic Treatment With High Bleeding Risk.Journal of the American College of Cardiology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 20 institutions in 19 countries.

Pieter C SmitsDepartment of Cardiology, Maasstad Hospital, Rotterdam, the Netherlands. Electronic address: SmitsP@maasstadziekenhuis.nl.
Enrico FrigoliClinical Trial Unit, University of Bern, Bern, Switzerland.
Pascal VranckxDepartment of Cardiology and Critical Care Medicine, Hartcentrum Hasselt, Jessa Ziekenhuis, Hasselt, Belgium; Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium.
Yukio OzakiDepartment of Cardiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Marie-Claude MoriceCardiovascular European Research Center (CERC), Massy, France.
Bernard ChevalierRamsay Générale de Santé, Interventional Cardiology Department, Institut Cardiovasculaire Paris Sud, Massy, France.
Yoshinobu OnumaNational University of Ireland, Galway, Ireland.
Stephan WindeckerDepartment of Cardiology, Bern University Hospital, Bern, Switzerland.
Pim A L ToninoDepartment of Cardiology, Catharina Hospital, Eindhoven, the Netherlands.
Marco RoffiDivision of Cardiology, Geneva University Hospitals, Geneva, Switzerland.
Maciej Lesiak1st Department of Cardiology, University of Medical Sciences, Poznan, Poland.
Felix MahfoudDepartment of Cardiology, Angiology, Intensive Care Medicine, Saarland University, Homburg, Germany.
Jozef BartunekCardiovascular Center, OLV Hospital, Aalst, Belgium.
David Hildick-SmithBrighton and Sussex University Hospitals NHS Trust, Brighton, United Kingdom.
Antonio ColomboDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele-Milan and Humanitas Clinical and Research Center IRCCS, Rozzano-Milan, Italy.
Goran StankovicDepartment of Cardiology, Clinical Center of Serbia, and Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Andrés IñiguezHospital Alvaro Cunqueiro, Vigo, Spain.
Carl SchultzDepartment of Cardiology, Royal Perth Hospital Campus, University of Western Australia, Perth, Western Australia, Australia.
Ran KornowskiRabin Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Paul J L OngTan Tock Seng Hospital, Singapore.
Mirvat AlasnagCardiac Center, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
Alfredo E RodriguezCardiac Unit Otamendi Hospital, Buenos Aires School of Medicine Cardiovascular Research Center (CECI), Buenos Aires, Argentina.
Valeria ParadiesDepartment of Cardiology, Maasstad Hospital, Rotterdam, the Netherlands.
Petr KalaUniversity Hospital Brno, Brno, Czech Republic.
Sasko KedevUniversity Clinic of Cardiology, Ss Cyril and Methodius University, Skopje, Macedonia.
Amar Al MafragiDepartment of Cardiology, Zorgsaam Hospital, Terneuzen, the Netherlands.
Willem DewildeDepartment of Cardiology, Imelda Hospital Bonheiden, Bonheiden, Belgium.
Dik HegClinical Trial Unit, University of Bern, Bern, Switzerland.
Marco ValgimigliCardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Università della Svizzera Italiana (USI), CH-6900 Lugano, Switzerland.
MASTER DAPT Investigators
Maasstad Ziekenhuis · NLPoznan University of Medical Sciences · PLUniversity of Bern · CHCardiovascular European Research Center · FREnte Ospedaliero Cantonale · CHFujita Health University · JPHumanitas University · ITInstitut Cardiovasculaire Paris Sud · FRJessa Hospital · BEKing Fahd Armed Forces Hospital · SAOllscoil na Gaillimhe – University of Galway · IEOnze Lieve Vrouwziekenhuis Hospital · BERadboud University Nijmegen · NLSaarland University · DESanatorio Otamendi y Miroli · ARSs. Cyril and Methodius University in Skopje · MKTan Tock Seng Hospital · SGTel Aviv University · ILThe University of Western Australia · AUUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe optimal duration of antiplatelet therapy (APT) after coronary stenting in patients at high bleeding risk (HBR) presenting with an acute coronary syndrome remains unclear.

objectivesThe objective of this study was to investigate the safety and efficacy of an abbreviated APT regimen after coronary stenting in an HBR population presenting with acute or recent myocardial infarction.

methodsIn the MASTER DAPT trial, 4,579 patients at HBR were randomized after 1 month of dual APT (DAPT) to abbreviated (DAPT stopped and 11 months single APT or 5 months in patients with oral anticoagulants) or nonabbreviated APT (DAPT for minimum 3 months) strategies. Randomization was stratified by acute or recent myocardial infarction at index procedure. Coprimary outcomes at 335 days after randomization were net adverse clinical outcomes events (NACE); major adverse cardiac and cerebral events (MACCE); and type 2, 3, or 5 Bleeding Academic Research Consortium bleeding.

resultsNACE and MACCE did not differ with abbreviated vs nonabbreviated APT regimens in patients with an acute or recent myocardial infarction (n = 1,780; HR: 0.83; 95% CI: 0.61-1.12 and HR: 0.86; 95% CI: 0.62-1.19, respectively) or without an acute or recent myocardial infarction (n = 2,799; HR: 1.03; 95% CI: 0.77-1.38 and HR: 1.13; 95% CI: 0.80-1.59; P

conclusionsA 1-month DAPT strategy in patients with HBR presenting with an acute or recent myocardial infarction results in similar NACE and MACCE rates and reduces bleedings compared with a nonabbreviated DAPT strategy. (Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen [MASTER DAPT]; NCT03023020).

Indexed as

Myocardial InfarctionPercutaneous Coronary InterventionAnticoagulantsDimapritDrug Therapy, CombinationHemorrhageHumansPlatelet Aggregation InhibitorsPolymersStentsTreatment OutcomeAnticoagulantsAPTDimapritPlatelet Aggregation InhibitorsPolymersacute coronary syndromeantiplatelet therapydual antiplatelet therapypercutaneous coronary intervention

Identifiers

PMID36137672
OpenAlexW4296301595

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Registered trials

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.