Abstract

A comprehensive review is undertaken of the methods available for 3D whole-heart first-pass perfusion (FPP) and their application to date, with particular focus on possible acceleration techniques. Following a summary of the parameters typically desired of 3D FPP methods, the review explains the mechanisms of key acceleration techniques and their potential use in FPP for attaining 3D acquisitions. The mechanisms include rapid sequences, non-Cartesian k-space trajectories, reduced k-space acquisitions, parallel imaging reconstructions and compressed sensing. An attempt is made to explain, rather than simply state, the varying methods with the hope that it will give an appreciation of the different components making up a 3D FPP protocol. Basic estimates demonstrating the required total acceleration factors in typical 3D FPP cases are included, providing context for the extent that each acceleration method can contribute to the required imaging speed, as well as potential limitations in present 3D FPP literature. Although many 3D FPP methods are too early in development for the type of clinical trials required to show any clear benefit over current 2D FPP methods, the review includes the small but growing quantity of clinical research work already using 3D FPP, alongside the more technical work. Broader challenges concerning FPP such as quantitative analysis are not covered, but challenges with particular impact on 3D FPP methods, particularly with regards to motion effects, are discussed along with anticipated future work in the field.

Highlights

  • Detection of coronary artery disease (CAD) through examination of dynamically contrast-enhanced myocardial perfusion cardiovascular magnetic resonance (CMR) is well established clinically [1, 2], following its first demonstrations in 1990 [3]

  • Alongside the implementation of the compartmental-based adaptation to k-t principal component analysis (PCA) and comparison with conventional k-t PCA using time intensity curves, this paper examined performance due to number of k-t PCA training profiles and principal components, and various respiratory motion types

  • While its clinical utility in comparison to multi-slice 2D remains hypothetical, advances in acceleration methods have opened up the feasibility of achieving 3D whole-heart coverage in first-pass perfusion (FPP)

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Summary

Introduction

Detection of coronary artery disease (CAD) through examination of dynamically contrast-enhanced myocardial perfusion cardiovascular magnetic resonance (CMR) is well established clinically [1, 2], following its first demonstrations in 1990 [3]. Dynamic contrast enhancement (DCE), here called first-pass perfusion (FPP), has shown high diagnostic accuracy [4] and compares favourably with other modalities as a “gate-keeper” to invasive coronary x-ray angiography [5]. The characteristics of ideal FPP methods are reviewed first, with some reflection on the issues governing typical multi-slice 2D FPP.

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