Literature DB >> 31766865

Trends of Use and Outcomes Associated With Glycoprotein-IIb/IIIa Inhibitors in Patients With Acute Coronary Syndromes Undergoing Percutaneous Coronary Intervention.

Rochelle M Gellatly1, Cia Connell1, Christianne Tan1, Nick Andrianopoulos2, Andrew E Ajani2,3,4, David J Clark5, Shane Nanayakkara1, Martin Sebastian6, Angela Brennan2, Melanie Freeman7, Jessica O'Brien1, Laura A Selkrig1, Christopher M Reid2, Stephen J Duffy1,2.   

Abstract

Background: Glycoprotein IIb/IIIa inhibitors (GPIs) are a treatment option in the management of acute coronary syndromes (ACSs). Evidence supporting the use of GPIs predates trials establishing the benefits of P2Y12 inhibitors, routine early invasive therapy, and thrombectomy devices in patients with ACS. Objective: The aim of this study was to determine trends in GPI use and their associated outcomes in contemporary practice.
Methods: We assessed GPI use in patients with ACS undergoing percutaneous coronary intervention (PCI) from the Melbourne Interventional Group registry (2005-2013). The primary endpoint was the 30-day incidence of major adverse cardiovascular events (MACE). The safety endpoint was in-hospital major bleeding.
Results: GPIs were used in 40.5% of 12 357 patients with ACS undergoing PCI. GPI use decreased over the study period (P for trend <0.0001). Patients were more likely to receive GPIs if they were younger, presented with a ST-elevation myocardial infarction (STEMI), had more complex (B2/C-type) lesions, and when thrombectomy devices were used (all P < 0.0001). MACE were higher in patients receiving GPI (4.9% vs 4.1%, P = 0.03). Propensity score matching revealed no difference in 30-day mortality and 30-day MACE (odds ratio [OR] = 1.00; 95% CI = 0.99-1.004 and OR = 1.01; 95% CI = 0.99-1.02, respectively). GPI use was associated with more bleeding complications (3.6% vs 1.8%, P < 0.0001). Conclusion and Relevance: GPI use in ACS patients undergoing PCI has declined, and use appears to be dictated by ACS type and lesion complexity, as opposed to high-risk comorbidities. GPI use was associated with a doubling in bleeding complications.

Entities:  

Keywords:  acute coronary syndrome; bleeding; drugs; glycoprotein-IIb/IIIa inhibitors; percutaneous coronary intervention

Mesh:

Substances:

Year:  2019        PMID: 31766865     DOI: 10.1177/1060028019889550

Source DB:  PubMed          Journal:  Ann Pharmacother        ISSN: 1060-0280            Impact factor:   3.154


  4 in total

1.  Incidence and risk factors for major bleeding among patients undergoing percutaneous coronary intervention: Findings from the Norwegian Coronary Stent Trial (NORSTENT).

Authors:  Per-Jostein Samuelsen; Anne Elise Eggen; Terje Steigen; Tom Wilsgaard; Andreas Kristensen; Anne Skogsholm; Elizabeth Holme; Christian van den Heuvel; Jan Erik Nordrehaug; Bjørn Bendz; Dennis W T Nilsen; Kaare Harald Bønaa
Journal:  PLoS One       Date:  2021-03-04       Impact factor: 3.240

2.  Rescue PCI in the management of STEMI: Contemporary results from the Melbourne Interventional Group registry.

Authors:  Himawan Fernando; Diem Dinh; Stephen J Duffy; Angela Brennan; Anand Sharma; David Clark; Andrew Ajani; Melanie Freeman; Karlheinz Peter; Dion Stub; Chin Hiew; Christopher M Reid; Ernesto Oqueli
Journal:  Int J Cardiol Heart Vasc       Date:  2021-03-15

3.  Primary Percutaneous Coronary Intervention with High-Bolus Dose Tirofiban: The FASTER (Favorite Approach to Safe and Effective Treatment for Early Reperfusion) Multicenter Registry.

Authors:  Stefano Rigattieri; Corrado Lettieri; Gianluca Tiberti; Michele Romano; Marco Ferlini; Luca Testa; Simona Pierini; Federica Ettori; Enrico Passamonti; Alfredo Marchese; Giuseppe Musumeci; Giovanni Esposito; Giuseppe Tarantini
Journal:  J Interv Cardiol       Date:  2022-03-29       Impact factor: 2.279

4.  Glycoprotein IIb/IIIa Inhibitors May Modulate the Clinical Benefit of Radial Access as Compared to Femoral Access in Primary Percutaneous Coronary Intervention: A Meta-Regression and Meta-Analysis of Randomized Trials.

Authors:  Stefano Rigattieri; Ernesto Cristiano; Francesca Giovannelli; Antonella Tommasino; Francesco Cava; Barbara Citoni; Domenico Maria Zardi; Andrea Berni; Massimo Volpe
Journal:  J Interv Cardiol       Date:  2021-06-15       Impact factor: 2.279

  4 in total

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