Platelet P2Y12 Inhibitor Monotherapy after Percutaneous Coronary Intervention: An Emerging Option for Antiplatelet Therapy De-escalation.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
Feb 2023
Historique:
pubmed: 31 12 2022
medline: 10 2 2023
entrez: 30 12 2022
Statut: ppublish

Résumé

Antiplatelet therapy is considered essential for secondary prevention of ischemic heart disease. After percutaneous coronary intervention (PCI), temporary dual antiplatelet therapy (DAPT), a combination consisting of aspirin and an oral P2Y12 receptor blocker, is recommended. In the long term, this strategy results in more bleeding than antiplatelet therapy with aspirin alone. Therefore, to reduce bleeding, an increasing trend has been to keep DAPT as short as clinically acceptable, after which aspirin monotherapy is continued. Another option to diminish bleeding is to discontinue aspirin at the moment of DAPT cessation after PCI, and to continue on P2Y12 blocker monotherapy. This survey reviews the evidence on P2Y12 blocker monotherapy. Some clinical guidance will be provided on when and in whom P2Y12 inhibitor monotherapy may be applied after DAPT cessation following PCI.

Identifiants

pubmed: 36584699
doi: 10.1055/s-0042-1755330
doi:

Substances chimiques

Aspirin R16CO5Y76E
Platelet Aggregation Inhibitors 0
Purinergic P2Y Receptor Antagonists 0
P2RY12 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-165

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

F.W.A.V. has received honoraria for consulting and presentations from AstraZeneca, Bayer Healthcare, and Daiichi-Sankyo. K.H. has received honoraria for consulting and lectures from AstraZeneca, Chiesi, Daiichi Sankyo, and Sanofi-Aventis. P.C. has received lecture fees, performed consulting, or been involved in research contracts outside the context of the present work: Abbott, AstraZeneca, Aventis, Bayer, Boehringer Ingelheim, Boston Scientific, Bristol Myers Squibb, Daiichi Sankyo, Eli-Lilly, Evolva, Fiberx, Janssen, Merck, Myogen, Medtronic, Mitsubishi Pharma, The Medicines Company, Nycomed, Organon, Pfizer, Pharmacia, Regado, Sanofi, Searle, Servier, ViFor Pharma. J.-P.C. does not report any conflict of interest. T.C. has received consulting and lectures fees from Abbott, Boston Scientific, Edwards, and Medtronic. F.A. reports honoraria for consulting or lectures from Amgen, AstraZeneca, Bayer, BMS/Pfizer, and Daiichi Sankyo.

Auteurs

Freek W A Verheugt (FWA)

Department of Cardiology, Onze Lieve Vrouwe Gasthuis (OLVG), Amsterdam, The Netherlands.

Kurt Huber (K)

3rd Department of Medicine, Cardiology and Intensive Care Medicine, Wilhelminen Hospital, Vienna, Austria.
Medical Faculty, Sigmund Freud University, Vienna, Austria.

Peter Clemmensen (P)

Department of Cardiology, University Heart and Vascular Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Medicine, Nykøbing F Hospital, Nykøbing Falster, Denmark.

Jean-Philippe Collet (JP)

Sorbonne Université, ACTION Group, INSERM UMRS 1166, HÔpital Pitié-Salpêtrière (AP-HP), Institut de Cardiologie, Paris, France.

Thomas Cuisset (T)

Department of Cardiology, La Timone Hospital, Marseille, France.

Felicita Andreotti (F)

Department of Cardiovascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

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