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Can fast wall shear stress computation predict adverse cardiac events in patients with intermediate non-flow limiting stenoses?

  • Vincenzo Tufaro
  • , Ryo Torii
  • , Jean Paul Aben
  • , Ramya Parasa
  • , Bon Kwon Koo
  • , Roby Rakhit
  • , Grigoris V. Karamasis
  • , Ibrahim H. Tanboga
  • , Ameer Hamid A Khan
  • , Michael McKenna
  • , Murat Cap
  • , Mazen A. Gamrah
  • , Patrick W. Serruys
  • , Yoshinobu Onuma
  • , Giulio G. Stefanini
  • , Daniel A. Jones
  • , Krishna Rathod
  • , Anthony Mathur
  • , Andreas Baumbach
  • , Christos V. Bourantas
  • St Bartholomew's Hospital
  • Barts and The London School of Medicine and Dentistry
  • Humanitas University
  • University College London
  • Pie Medical Imaging
  • Seoul National University Hospital
  • Royal Free NHS Trust
  • Essex Cardiothoracic Centre
  • Nisantasi University Medical School
  • The Adelaide Hospital
  • University of Health Sciences
  • Humanitas Research Hospital

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

3 Citations (Scopus)

Abstract

Background and aims: Coronary angiography-derived wall shear stress (WSS) may enable identification of vulnerable plaques and patients. A new recently introduced software allows seamless three-dimensional quantitative coronary angiography (3D-QCA) reconstruction and WSS computation within a single user-friendly platform carrying promise for clinical applications. This study examines for the first time the efficacy of this software in detecting vulnerable lesions in patients with intermediate non-flow limiting stenoses. Methods: This multicentre retrospective study included patients who had coronary angiography showing at least one lesion with borderline negative fractional flow reserve (FFR: 0.81–0.85). In these lesions, 3D-QCA reconstruction and blood flow simulation were performed using the CAAS Workstation WSS prototype (Pie Medical Imaging, Maastricht, Netherlands). Time averaged and multidirectional WSS were extracted across the lesion at every 3 mm segments. The primary endpoint of the study was lesion-oriented clinical events (LOCE), defined as the composite of cardiac death, target lesion related myocardial infarction (MI) or clinically indicated target lesion revascularization. Results: 352 patients (355 lesions) were included in the analysis. Over a median follow-up of 4.1 years, 57 LOCE were recorded. Lesions causing events had a larger area stenosis (AS) [59.4 (54.6–67.7)% vs 52.8 (43.8–60.1)%, p < 0.001], maximum time averaged WSS (TAWSS) [11.56 (8.25–13.64)Pa vs 7.73 (5.41–11.51)Pa, p < 0.001], mean TAWSS at the minimum lumen area (MLA) [9.30 (5.44–11.94)Pa vs 6.19 (3.96–9.00)Pa, p < 0.001] and maximum transverse WSS [0.30 (0.21–0.45)Pa vs 0.23 (0.17–0.32)Pa, p=0.002] than those remaining quiescent. In multivariable models, AS was the only independent predictor of LOCE. Kaplan-Meier curves demonstrated that lesions with elevated maximum TAWSS and AS had a higher rate of LOCE than those with low TAWSS and AS values (26 % vs 7 %, p < 0.001). Conclusions: For non-flow limiting lesions with borderline negative FFR, fast WSS computation using a dedicated software is feasible and holds potential for cardiovascular risk stratification.

Original languageEnglish
Article number119099
JournalAtherosclerosis
Volume401
DOIs
Publication statusPublished - Feb 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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