Optimal Timing of P2Y12 Inhibitor Loading in Patients Undergoing PCI: A Meta-Analysis.


Journal

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

Informations de publication

Date de publication:
Jun 2019
Historique:
pubmed: 29 3 2019
medline: 18 12 2019
entrez: 29 3 2019
Statut: ppublish

Résumé

 The timing of P2Y12 inhibitor loading in patients undergoing percutaneous coronary intervention (PCI) is a matter of debate. The aim of our study was to compare the efficacy and safety of oral P2Y12 inhibitors: clopidogrel, ticagrelor and prasugrel administered at two different time points in relation to PCI: early (> 2 hours pre-PCI) versus late (< 2 hours pre-PCI or post-PCI).  This is a systematic review and meta-analysis. Randomized controlled trials and non-randomized studies were included. Outcomes evaluated were combined major adverse cardiovascular events (MACEs), myocardial infarction (MI), target vessel revascularization, death and bleeding complications. Summary estimates of the relative risks with therapy were calculated.  Twenty-three studies met the selection criteria and included 60,907 patients. Early P2Y12 inhibitor loading was associated with a 22% relative risk reduction (RRR) of MACE (95% confidence interval [CI] = 0.68-0.89;  Early clopidogrel loading is associated with a better efficacy and similar safety, whereas timing of ticagrelor or prasugrel loading had no effects on ischaemic events.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
 The timing of P2Y12 inhibitor loading in patients undergoing percutaneous coronary intervention (PCI) is a matter of debate. The aim of our study was to compare the efficacy and safety of oral P2Y12 inhibitors: clopidogrel, ticagrelor and prasugrel administered at two different time points in relation to PCI: early (> 2 hours pre-PCI) versus late (< 2 hours pre-PCI or post-PCI).
METHODS METHODS
 This is a systematic review and meta-analysis. Randomized controlled trials and non-randomized studies were included. Outcomes evaluated were combined major adverse cardiovascular events (MACEs), myocardial infarction (MI), target vessel revascularization, death and bleeding complications. Summary estimates of the relative risks with therapy were calculated.
RESULTS RESULTS
 Twenty-three studies met the selection criteria and included 60,907 patients. Early P2Y12 inhibitor loading was associated with a 22% relative risk reduction (RRR) of MACE (95% confidence interval [CI] = 0.68-0.89;
CONCLUSION CONCLUSIONS
 Early clopidogrel loading is associated with a better efficacy and similar safety, whereas timing of ticagrelor or prasugrel loading had no effects on ischaemic events.

Identifiants

pubmed: 30919382
doi: 10.1055/s-0039-1683421
doi:

Substances chimiques

Purinergic P2Y Receptor Antagonists 0
Clopidogrel A74586SNO7
Prasugrel Hydrochloride G89JQ59I13
Ticagrelor GLH0314RVC

Types de publication

Comparative Study Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1000-1020

Informations de copyright

Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

None declared.

Auteurs

Anna Komosa (A)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Maciej Lesiak (M)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Zbigniew Krasiński (Z)

Department of General and Vascular Surgery, Poznan University of Medical Sciences, Poznan, Poland.

Marek Grygier (M)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Andrzej Siniawski (A)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Włodzimierz Skorupski (W)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Anna Olasińska-Wiśniewska (A)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Małgorzata Pyda (M)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Aleksander Araszkiewicz (A)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Przemysław Mitkowski (P)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Stefan Grajek (S)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Tatiana Mularek-Kubzdela (T)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Christian Hengstenberg (C)

Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Jolanta M Siller-Matula (JM)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.
Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

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Classifications MeSH