Volume 84, Issue 3 pp. 351-358
Coronary Artery Disease

A prospective intravascular ultrasound investigation of the necessity for and efficacy of postdilation beyond nominal diameter of 3 current generation DES platforms for the percutaneous treatment of the left main coronary artery

James A. Shand MD, MRCP

James A. Shand MD, MRCP

St James's Hospital, Dublin, Ireland

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

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Divyesh Sharma MBBS, MRCP

Divyesh Sharma MBBS, MRCP

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

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Colm Hanratty MD, FRCP

Colm Hanratty MD, FRCP

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

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Anthony McClelland MD, MRCP

Anthony McClelland MD, MRCP

Department of Cardiology, Craigavon Area Hospital, Portadown, Northern Ireland, United Kingdom

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Ian B.A. Menown MD, FRCP

Ian B.A. Menown MD, FRCP

Department of Cardiology, Craigavon Area Hospital, Portadown, Northern Ireland, United Kingdom

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Mark S. Spence MD, FRCP

Mark S. Spence MD, FRCP

Department of Cardiology, Royal Victoria Hospital, Belfast, Northern Ireland, United Kingdom

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Geoffrey Richardson MD, FRCP

Geoffrey Richardson MD, FRCP

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

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Niall A. Herity MD, FRCP

Niall A. Herity MD, FRCP

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

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Simon J. Walsh MD, FRCP

Corresponding Author

Simon J. Walsh MD, FRCP

Department of Cardiology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom

Correspondence to: Dr Simon J. Walsh, Consultant Cardiologist, Belfast City Hospital, 51 Lisburn Road, Belfast BT9 7AB, Northern Ireland, United Kingdom. E-mail: [email protected]Search for more papers by this author
First published: 25 October 2013
Citations: 17

Conflict of interest: Nothing to report.

Abstract

Objectives

To define the size of the left mainstem coronary artery (LMS) in the Northern Irish population and investigate the clinical feasibility, safety, and efficacy of post dilation beyond nominal diameter of current generation Drug eluting stent (DES) when treating the LMS.

Background

There is no prospective data examining the need, feasibility, and safety of over-expansion of current generation DES beyond nominal diameter.

Methods

Patients with flow-limiting coronary atheroma requiring IVUS assessment of the LMS were recruited. Standardized measurements of the distal LMS were made. Subsequently, patients requiring post dilation of current generation DES within the LMS were entered into a PCI registry.

Results

Overall, 125 patients were recruited into the initial study. Mean cross-sectional area (CSA) of the distal LMS was 22.6 mm2 (SD ± 5.4 mm2). Mean maximal vessel diameter was 5.7 mm (SD ± 0.7 mm). Increasing plaque burden was associated with reduced CSA (P < 0.001). In 31 consecutive patients undergoing IVUS guided PCI of the LMS with 5.5 and 6.0 mm balloon catheters, mean maximal stent diameters were >5.0 mm with the Biomatrix Flex 9 crown and Promus Element Large vessel platforms. No intraprocedural complications occurred. Mean follow up was 13.4 months. Clinical restenosis rate was 3.2%, with 2 deaths unrelated to index procedure.

Conclusions

The majority of patients with angiographic coronary atheroma have a mean LMS diameter of >4 mm indicating the requirement for post dilation beyond nominal diameter all of current generation DES in almost all patients when treating the LMS. This is achievable with current DES platforms with no intraprocedural complication. Clinical follow up indicates excellent short-term efficacy. © 2013 Wiley Periodicals, Inc.

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