Volume 92, Issue 4 pp. 659-665
Coronary Artery Disease

Antiplatelet drug selection in PCI to vein grafts in patients with acute coronary syndrome and adverse clinical outcomes: Insights from the British Cardiovascular Intervention Society database

Alex Sirker MB BChir, PhD

Alex Sirker MB BChir, PhD

Department of Cardiology, University College London Hospitals and St Bartholomew's Hospital, London, United Kingdom

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Chun Shing Kwok MBBS MSc BSc

Chun Shing Kwok MBBS MSc BSc

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, Stoke-on-Trent, United Kingdom

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Evangelos Kontopantelis PhD

Evangelos Kontopantelis PhD

The Farr Institute for Health Informatics Research, University of Manchester, Manchester, United Kingdom

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Tom Johnson MD

Tom Johnson MD

University of Bristol, Bristol, United Kingdom

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Philip Freeman MBBS

Philip Freeman MBBS

Aalborg University Hospital, Aalborg, Denmark

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Mark A de Belder MD

Mark A de Belder MD

Department of Cardiology, James Cook University Hospital, Middlesbrough, United Kingdom

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Peter Ludman MD

Peter Ludman MD

Department of Cardiology, Queen Elizabeth Hospital, Birmingham, United Kingdom

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Azfar Zaman MD

Azfar Zaman MD

Department of Cardiology, Freeman Hospital, Newcastle, United Kingdom and Institute of Cellular Medicine, Newcastle University, United Kingdom

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Mamas A Mamas BM BCh DPhil

Corresponding Author

Mamas A Mamas BM BCh DPhil

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, Stoke-on-Trent, United Kingdom

Correspondence Mamas A. Mamas, Professor of Cardiology/Honorary Consultant Cardiologist, Keele Cardiovascular Research Group, Centre for Prognosis Research, Institute for Primary care and Health Sciences, Keele University, Stoke-on-Trent, United Kingdom. Email: [email protected]Search for more papers by this author
First published: 22 January 2018
Citations: 5

Abstract

Objective

This study aims to evaluate outcomes associated with different P2Y12 agents in Saphenous Vein graft (SVG) percutaneous coronary intervention (PCI).

Background

SVG PCI is associated with greater risks of ischemic complications, compared with native coronary PCI. Outcomes associated with the use of potent P2Y12 blocking drugs, Prasugrel and Ticagrelor, in SVG PCI are unknown.

Methods

Patients included in the study underwent SVG PCI in the United Kingdom between 2007 and 2014 for acute coronary syndrome and were grouped by P2Y12 antiplatelet use. In-hospital major adverse cardiac events, major bleeding and 30-day and 1-year mortality were examined. Multiple imputations with chained equations to impute missing data were used. Adjustment for baseline imbalances was performed using (1) multiple logistic regression (MLR) and (separately) (2) propensity score matching (PSM).

Results

Data weres analyzed from 8,119 patients and most cases were treated with Clopidogrel (n = 7,401), followed by Ticagrelor (n = 497) and Prasugrel (n = 221). In both MLR and PSM models, there was no significant evidence to suggest that either Prasugrel or Ticagrelor was associated with significantly lower 30-day mortality compared with Clopidogrel. The odds ratios reported from the multivariable analysis were 1.22 (95% CI: 0.60–2.51) for Prasugrel vs. Clopidogrel and 0.48 (95% CI: 0.20–1.16) for Ticagrelor vs. Clopidogrel. No significant differences were seen for in-hospital ischemic or bleeding events.

Conclusions

Our real world national study provides no clear evidence to indicate that use of potent P2Y12 blockers in SVG PCI is associated with improved clinical outcomes.

CONFLICT OF INTEREST DISCLOSURE

Nothing to report.

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