Abstract

BackgroundQuantification of myocardial perfusion from first-pass cardiovascular magnetic resonance (CMR) images at high contrast agent (CA) dose requires separate acquisition of blood pool and myocardial tissue enhancement. In this study, a dual-sequence approach interleaving 2D imaging of the arterial input function with high-resolution 3D imaging for myocardial perfusion assessment is presented and validated for low and high CA dose.MethodsA dual-sequence approach interleaving 2D imaging of the aortic root and 3D imaging of the whole left ventricle using highly accelerated k-t PCA was implemented. Rest perfusion imaging was performed in ten healthy volunteers after administration of a Gadolinium-based CA at low (0.025 mmol/kg b.w.) and high dose (0.1 mmol/kg b.w.). Arterial input functions extracted from the 2D and 3D images were analysed for both doses. Myocardial contrast-to-noise ratios (CNR) were compared across volunteers and doses. Variations of myocardial perfusion estimates between volunteers and across myocardial territories were studied.ResultsHigh CA dose imaging resulted in strong non-linearity of the arterial input function in the 3D images at peak CA concentration, which was avoided when the input function was derived from the 2D images. Myocardial CNR was significantly increased at high dose compared to low dose, with a 2.6-fold mean CNR gain. Most robust myocardial blood flow estimation was achieved using the arterial input function extracted from the 2D image at high CA dose. In this case, myocardial blood flow estimates varied by 24 % between volunteers and by 20 % between myocardial territories when analysed on a per-volunteer basis.ConclusionInterleaving 2D imaging for arterial input function assessment enables robust quantitative 3D myocardial perfusion imaging at high CA dose.

Highlights

  • Quantification of myocardial perfusion from first-pass cardiovascular magnetic resonance (CMR) images at high contrast agent (CA) dose requires separate acquisition of blood pool and myocardial tissue enhancement

  • Knowledge of both the arterial input function (AIF) and the myocardial signal intensity-time curves is needed to calculate estimates of myocardial blood flow (MBF) per unit muscle mass [5]. Both the AIF and the myocardial signal intensity-time curves are extracted from the same CMR image [5]

  • The present study introduces a dual-sequence approach interleaving 3D high-resolution myocardial perfusion imaging and 2D low-resolution AIF acquisition for high dose first-pass perfusion imaging with wholeheart coverage

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Summary

Introduction

Quantification of myocardial perfusion from first-pass cardiovascular magnetic resonance (CMR) images at high contrast agent (CA) dose requires separate acquisition of blood pool and myocardial tissue enhancement. Qualitative assessment and quantitative evaluation of conventional first-pass perfusion cardiovascular magnetic resonance (CMR) is subject to a trade-off pertaining to contrast agent (CA) dosage. MBF estimation from first-pass contrast-enhanced CMR data is based on a linear time-invariant impulse response model [9]. Knowledge of both the AIF and the myocardial signal intensity-time curves is needed to calculate estimates of MBF per unit muscle mass [5]. For a quantitative estimation of MBF, the AIF may be acquired separately using a low resolution image in conjunction with highresolution image data to obtain myocardial signals [6]

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