External validation of the GRACE risk score 2.0 in the contemporary all-comers GLOBAL LEADERS trial.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
10 2021
Historique:
revised: 28 04 2021
received: 23 02 2021
accepted: 03 05 2021
pubmed: 18 5 2021
medline: 21 10 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

This study aimed to assess the predictive ability of the Global Registry of Acute Coronary Events (GRACE) risk score 2.0 in contemporary acute coronary syndrome (ACS) patients, and its relation to antiplatelet strategies. The predictive value of the GRACE risk score in the contemporary ACS cohort and the appropriate antiplatelet regimen according to the risk remain unclear. This is a subgroup analysis of the all-comers, randomized GLOBAL LEADERS trial, comparing ticagrelor monotherapy versus conventional dual-antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI). The GRACE risk score 2.0 with 1-year mortality prediction was implemented. The randomized antiplatelet effect was assessed in predefined three GRACE risk-groups; low-risk (GRACE <109), moderate-risk (GRACE 109-140), and high-risk (GRACE >140). The GRACE risk score was available in 6,594 out of 7,487 ACS patients among whom 1,743, 2,823, and 2,028 patients were classified as low-risk, moderate-risk, and high-risk, respectively. At 1 year, all-cause mortality occurred in 120 patients (1.8%). The discrimination ability of the GRACE model was moderate (C-statistic = 0.742), whereas 1-year mortality risk was overestimated (mean predicted mortality rate: 3.9%; the Hosmer-Lemeshow chi-square: 21.47; p = 0.006). There were no significant interactions between the GRACE risk strata and effects of the ticagrelor monotherapy on ischemic or bleeding outcomes at 1 year compared to the reference strategy. The GRACE risk score 2.0 is valuable in discriminating high risk ACS patients, however, the recalibration of the score is recommended for better risk stratification. There is no significant differences in efficacy and safety of ticagrelor monotherapy across the three GRACE risk strata.

Sections du résumé

OBJECTIVES
This study aimed to assess the predictive ability of the Global Registry of Acute Coronary Events (GRACE) risk score 2.0 in contemporary acute coronary syndrome (ACS) patients, and its relation to antiplatelet strategies.
BACKGROUND
The predictive value of the GRACE risk score in the contemporary ACS cohort and the appropriate antiplatelet regimen according to the risk remain unclear.
METHODS
This is a subgroup analysis of the all-comers, randomized GLOBAL LEADERS trial, comparing ticagrelor monotherapy versus conventional dual-antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI). The GRACE risk score 2.0 with 1-year mortality prediction was implemented. The randomized antiplatelet effect was assessed in predefined three GRACE risk-groups; low-risk (GRACE <109), moderate-risk (GRACE 109-140), and high-risk (GRACE >140).
RESULTS
The GRACE risk score was available in 6,594 out of 7,487 ACS patients among whom 1,743, 2,823, and 2,028 patients were classified as low-risk, moderate-risk, and high-risk, respectively. At 1 year, all-cause mortality occurred in 120 patients (1.8%). The discrimination ability of the GRACE model was moderate (C-statistic = 0.742), whereas 1-year mortality risk was overestimated (mean predicted mortality rate: 3.9%; the Hosmer-Lemeshow chi-square: 21.47; p = 0.006). There were no significant interactions between the GRACE risk strata and effects of the ticagrelor monotherapy on ischemic or bleeding outcomes at 1 year compared to the reference strategy.
CONCLUSION
The GRACE risk score 2.0 is valuable in discriminating high risk ACS patients, however, the recalibration of the score is recommended for better risk stratification. There is no significant differences in efficacy and safety of ticagrelor monotherapy across the three GRACE risk strata.

Identifiants

pubmed: 34000088
doi: 10.1002/ccd.29772
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

E513-E522

Subventions

Organisme : WOA Institution: National University of Ireland Galway Blended DEAL: IReL

Informations de copyright

© 2021 The Authors. Catheterization and Cardiovascular Interventions published by Wiley Periodicals LLC.

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Auteurs

Masafumi Ono (M)

Department of Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
Department of Cardiology, National University of Ireland, Galway, Ireland.

Hideyuki Kawashima (H)

Department of Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
Department of Cardiology, National University of Ireland, Galway, Ireland.

Hironori Hara (H)

Department of Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
Department of Cardiology, National University of Ireland, Galway, Ireland.

Amr Gamal (A)

Department of Cardiology, National University of Ireland, Galway, Ireland.
Department of Cardiology, North Cumbria University Hospitals NHS Trust, Carlisle, UK.

Rutao Wang (R)

Department of Cardiology, National University of Ireland, Galway, Ireland.
Department of Cardiology, Radboud University Medical Center, Nijmegen, Netherlands.

Chao Gao (C)

Department of Cardiology, National University of Ireland, Galway, Ireland.
Department of Cardiology, Radboud University Medical Center, Nijmegen, Netherlands.

Neil O'Leary (N)

Department of Cardiology, National University of Ireland, Galway, Ireland.

Osama Soliman (O)

Department of Cardiology, National University of Ireland, Galway, Ireland.

Jan J Piek (JJ)

Department of Cardiology, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.

Robert-Jan van Geuns (RJ)

Department of Cardiology, Radboud University Medical Center, Nijmegen, Netherlands.

Peter Jüni (P)

Applied Health Research Centre, Li Ka Shing Knowledge Institute, St Michael's Hospital, University of Toronto, Toronto, Canada.

Christian W Hamm (CW)

Kerckhoff Heart Center, Campus University of Giessen, Bad Nauheim, Germany.

Marco Valgimigli (M)

Department of Cardiology, Bern University Hospital, Bern, Switzerland.

Pascal Vranckx (P)

Department of Cardiology and Critical Care Medicine, Hartcentrum Hasselt, Jessa Ziekenhuis, Hasselt; and Faculty of Medicine and Life Sciences, University of Hasselt, Hasselt, Belgium.

Stephan Windecker (S)

Department of Cardiology, Bern University Hospital, Bern, Switzerland.

Philippe Gabriel Steg (PG)

Université de Paris, FACT, French Alliance for Cardiovascular Trials; Hôpital Bichat, AP-HP and INSERM U-1148, Paris, France.

Keith Aa Fox (KA)

Centre For cardiovascular Science, University of Edinburgh, Edinburgh, UK.

Yoshinobu Onuma (Y)

Department of Cardiology, National University of Ireland, Galway, Ireland.

Patrick W Serruys (PW)

Department of Cardiology, National University of Ireland, Galway, Ireland.
NHLI, National Heart and Lung Institute, Imperial College, London, UK.

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