Comparison of Routine Versus Selective Glycoprotein IIb/IIIa Inhibitors Usage in Primary Percutaneous Coronary Intervention (from the British Cardiovascular Interventional Society).


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 08 2019
Historique:
received: 27 01 2019
revised: 24 04 2019
accepted: 06 05 2019
pubmed: 31 5 2019
medline: 25 2 2020
entrez: 1 6 2019
Statut: ppublish

Résumé

The role of glycoprotein IIb/IIIa inhibitors (GPI) in primary percutaneous coronary intervention (PPCI) remains uncertain. Previous analyses compare PPCI outcomes with clopidogrel plus GPI, versus without GPI. This does not reflect modern contemporary PPCI practice with ticagrelor or prasugrel. Nor does it answer the important question faced daily by PPCI operators: should GPI be used routinely or selectively? We aim to determine whether a strategy of routine use of GPI in contemporary PPCI practice is superior to selective GPI use. A total of 110,327 consecutive PPCIs performed in England were prospectively recorded in the British Cardiovascular Intervention Society Database (2009 to 2015). The cohort was divided into routine and selective GPI usage groups based on the PPCI operator's strategy, defined as GPI used in >75% and <25% PPCIs, respectively. Overall, GPI use declined from 73.1% to 43.3% of PPCIs. Routine compared with selective GPI usage was associated with lower all-cause 1-year mortality: 9.7% versus 11.0%, p < 0.001. There was a consistent survival benefit for routine GPI usage as compared with selective GPI usage: univariable analysis (hazard ratio = 0.88 [95% confidence interval 0.83 to 0.93], p < 0.001), multivariable analysis (hazard ratio = 0.82 [0.77 to 0.88], p < 0.001). For survival, there was no interaction between GPI usage and the type of P2Y12-inhibitor used. In conclusion, a strategy of routine GPI usage in patients who underwent PPCI was associated with lower all-cause mortality as compared with selective GPI usage. This benefit was maintained despite 44.3% of patients receiving prasugrel or ticagrelor.

Identifiants

pubmed: 31146891
pii: S0002-9149(19)30519-3
doi: 10.1016/j.amjcard.2019.05.010
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Platelet Glycoprotein GPIIb-IIIa Complex 0
Clopidogrel A74586SNO7
Prasugrel Hydrochloride G89JQ59I13
Ticagrelor GLH0314RVC
Eptifibatide NA8320J834
Abciximab X85G7936GV

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

373-380

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Mateusz Orzalkiewicz (M)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK; Institute of Translational Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

James Hodson (J)

Institute of Translational Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Chun Shing Kwok (CS)

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, Keele, UK.

Peter F Ludman (PF)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Joel P Giblett (JP)

Department of Cardiology, Royal Papworth Hospital NHS Foundation Trust, Cambridge, UK; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.

Sudhakar George (S)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Sagar N Doshi (SN)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Sohail Q Khan (SQ)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Timothy Kinnaird (T)

Department of Cardiology, University Hospital Wales, Cardiff, UK.

David Hildick-Smith (D)

Sussex Cardiac Centre, Brighton and Sussex University Hospital NHS Trust, Brighton, UK.

Jonathan N Townend (JN)

Department of Cardiology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK; Institute of Translational Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.

Mamas A Mamas (MA)

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, Keele, UK.

Patrick A Calvert (PA)

Department of Cardiology, Royal Papworth Hospital NHS Foundation Trust, Cambridge, UK; Division of Cardiovascular Medicine, University of Cambridge, Cambridge, UK. Electronic address: patrick.calvert1@nhs.net.

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Classifications MeSH