Impact of dual antiplatelet therapy duration on clinical outcome after coronary bifurcation stenting: results from the EuroBifurcation Club registry.


Journal

Panminerva medica
ISSN: 1827-1898
Titre abrégé: Panminerva Med
Pays: Italy
ID NLM: 0421110

Informations de publication

Date de publication:
Mar 2023
Historique:
pubmed: 14 5 2022
medline: 16 3 2023
entrez: 13 5 2022
Statut: ppublish

Résumé

Optimal duration of dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) of a bifurcation stenosis is still debated. We evaluated the impact of DAPT duration on clinical outcomes in all-comers patients undergoing bifurcation PCI included in the European Bifurcation Club (EBC) registry. We enrolled 2284 consecutive patients who completed at least 18 months follow-up. The cumulative occurrence of major adverse cardiac and cardiovascular events (MACCE), defined as a composite of overall-death, non-fatal myocardial infarction (MI), target vessel revascularization (TVR) and stroke were evaluated. Bleedings classified as Bleeding Academic Research Consortium (BARC) ≥3 were evaluated too. Patients were divided into 3 groups: short DAPT (<6-months, N.=375); standard DAPT (≥6-months but ≤12-months, N.=636); prolonged DAPT (>12-months, N.=1273). At 24 months follow-up MACCE-free survival was significantly lower in short DAPT patients (Log-Rank: 45.23, P for trend <0.001). MACCE occurred less frequently in the prolonged DAPT group (148 [11.6%]) as compared with both the short (83 [22.1%] HR: 0.48 [0.37-0.63], P<0.001) and standard DAPT groups (137 [21.5%] HR:0.51 [0.41-0.65], P<0.001). These differences remain after propensity score adjustment (respectively, HR: 0.27 [0.20-0.36] and HR: 0.44 [0.34-0.57]). Such finding was consistent in patients presenting with both acute and chronic coronary syndromes. BARC≥3 bleedings were 0.3% in the standard DAPT, 1.6% in short and 1.9% in prolonged DAPT groups. In the "real-world" EBC registry of patients undergoing PCI of coronary artery bifurcation stenosis, a prolonged DAPT duration was associated with a significantly lower risk of MACCE and a potential increased risk of major bleedings.

Sections du résumé

BACKGROUND BACKGROUND
Optimal duration of dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) of a bifurcation stenosis is still debated. We evaluated the impact of DAPT duration on clinical outcomes in all-comers patients undergoing bifurcation PCI included in the European Bifurcation Club (EBC) registry.
METHODS METHODS
We enrolled 2284 consecutive patients who completed at least 18 months follow-up. The cumulative occurrence of major adverse cardiac and cardiovascular events (MACCE), defined as a composite of overall-death, non-fatal myocardial infarction (MI), target vessel revascularization (TVR) and stroke were evaluated. Bleedings classified as Bleeding Academic Research Consortium (BARC) ≥3 were evaluated too.
RESULTS RESULTS
Patients were divided into 3 groups: short DAPT (<6-months, N.=375); standard DAPT (≥6-months but ≤12-months, N.=636); prolonged DAPT (>12-months, N.=1273). At 24 months follow-up MACCE-free survival was significantly lower in short DAPT patients (Log-Rank: 45.23, P for trend <0.001). MACCE occurred less frequently in the prolonged DAPT group (148 [11.6%]) as compared with both the short (83 [22.1%] HR: 0.48 [0.37-0.63], P<0.001) and standard DAPT groups (137 [21.5%] HR:0.51 [0.41-0.65], P<0.001). These differences remain after propensity score adjustment (respectively, HR: 0.27 [0.20-0.36] and HR: 0.44 [0.34-0.57]). Such finding was consistent in patients presenting with both acute and chronic coronary syndromes. BARC≥3 bleedings were 0.3% in the standard DAPT, 1.6% in short and 1.9% in prolonged DAPT groups.
CONCLUSIONS CONCLUSIONS
In the "real-world" EBC registry of patients undergoing PCI of coronary artery bifurcation stenosis, a prolonged DAPT duration was associated with a significantly lower risk of MACCE and a potential increased risk of major bleedings.

Identifiants

pubmed: 35546730
pii: S0031-0808.22.04604-3
doi: 10.23736/S0031-0808.22.04604-3
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-12

Auteurs

Plinio Cirillo (P)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy - pcirillo@unina.it.

Luigi DI Serafino (L)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Habib Gamra (H)

Department of Cardiology, Fattouma Bourguiba Hospital, University of Monastir, Monastir, Tunisia.

Marco Zimarino (M)

Institute of Cardiology, G. D'Annunzio University, Chieti, Italy.
Interventional Cath Lab, ASL 2 Abruzzo, Chieti, Italy.

Emanuele Barbato (E)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.
CIBERCV, University Clinical Hospital of Valladolid, Valladolid, Spain.

Carlo Briguori (C)

Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium.

Ignatio J Amat-Santos (IJ)

Unit of Interventional Cardiology, Clinica Mediterranea, Naples, Italy.

Alaide Chieffo (A)

Unit of Interventional Cardiology, IRCCS San Raffaele Hospital, Milan, Italy.

Andrejs Erglis (A)

Latvian Centre of Cardiology, Pauls Stradins Clinical University Hospital, Riga, Latvia.

Robert J Gil (RJ)

Department of Invasive Cardiology, Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland.

Sasko A Kedev (SA)

University Clinic of Cardiology Skopje, Skopje, Macedonia.

Ivo Petrov (I)

City Clinic, Sofia, Bulgaria.

Francesco Radico (F)

Institute of Cardiology, G. D'Annunzio University, Chieti, Italy.

Tullio Niglio (T)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Sunao Nakamura (S)

Department of Cardiology, New Tokyo Hospital, Chiba, Japan.

Ricardo A Costa (RA)

Instituto Dante Pazzanese de Cardiologia, Sao Paulo, Brazil.

Vojko Kanic (V)

Department of Cardiology and Angiology, University Medical Centre, Maribor, Slovenia.

Matteo Perfetti (M)

Interventional Cath Lab, ASL 2 Abruzzo, Chieti, Italy.

Mariano Pellicano (M)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.
CIBERCV, University Clinical Hospital of Valladolid, Valladolid, Spain.
Laboratory of Invasive Cardiology, Montevergine Clinic, Mercogliano, Avellino, Italy.

Kristina Maric (K)

Department of Cardiovascular Medicine, University Hospital Centre, Zagreb, Croatia.

Tullio Tesorio (T)

Laboratory of Invasive Cardiology, Montevergine Clinic, Mercogliano, Avellino, Italy.

Vladan Vukcevic (V)

Department of Cardiology, Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.

Giovanni Esposito (G)

Division of Cardiology, Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Goran Stankovic (G)

Department of Cardiology, Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH