Skip to content

Advertisement

  • Walking poster presentation
  • Open Access

High-temporal velocity-encoded MRI for the assessment of left ventricular inflow propagation velocity: head-to-head comparison with Color M-mode echocardiography

  • 1,
  • 2,
  • 2,
  • 3,
  • 1,
  • 3 and
  • 3
Journal of Cardiovascular Magnetic Resonance201517 (Suppl 1) :Q38

https://doi.org/10.1186/1532-429X-17-S1-Q38

  • Published:

Keywords

  • Left Ventricular Diastolic Function
  • Free Breathing
  • Inflow Velocity
  • Difference Quotient
  • Ischemic Heart Failure

Background

Left ventricular (LV) inflow propagation velocity (Vp) is a useful parameter used in the complex assessment of LV diastolic function and is measured by Color M-mode echocardiography. The aim of current study was to develop an alternative method for Vp-assessment using high-temporal single-directional velocity-encoded Magnetic Resonance Imaging (VE-MRI).

Methods

43 patients with ischemic heart failure (61±11years) and 22 healthy volunteers (29±13years) were included. Vp by Color M-mode echocardiography (Vp-echo), was measured according to current recommendations (Figure 1). VE-MRI was performed on a 1.5 or 3.0 Tesla MRI system during free breathing, with single-direction in-plane velocity-encoding in phase-encoding direction, angulated parallel to the LV inflow direction. Velocity sensitivity Venc was set to 30cm/s and scan parameters were: spatial resolution 2.5×2.5×8.0 mm3, flip angle 10°, echo-time 3.4-3.8ms and repetition-time 5.4-5.9ms. Local LV inflow velocity was sampled along a 4cm scan line starting from the tip of the mitral valve and directed into the LV, similarly to the Color M-mode echocardiography; for 11 consecutive sample points equidistantly positioned along the scan line, the point-in-time was assessed when local velocity exceeded 30cm/s (Figure 1). From the position-time relation, Vp was calculated by 2 methods: 1) from the difference quotient between the first and the last sample point (Vp-MRI-DQ) and 2) from linear regression from all sample points (Vp-MRI-LR).
Figure 1
Figure 1

Vp assessment with Color M-mode echocardiography (panel A) and velocity-encoded MRI (panel B). The position-time graph (panel C) with Vp-MRI-Difference-Quotient (dotted line) and Vp-MRI-Lineair-Regression (solid line).

Results

Good correlation was found between Vp-echo and both Vp-MRI-DQ (r=0.83 p<0.001) and Vp-MRI-LR (r=0.84 p<0.001). For both Vp-MRI-DQ and Vp-MRI-LR, a significant but small underestimation was observed as compared to Vp measured by Color M-mode echocardiography (Vp-MRI-DQ: -7.3±19.7 cm/s, p=0.004; Vp-MRI-LR: -9.9±15.2cm/s, p<0.001), with increasing bias for higher Vp values. Applying age-related cut-off values for Vp to identify elevated LV filling pressures (Table 1), we observed a Kappa-agreement with echocardiography of 0.72, (p<0.001) for Vp-MRI-DQ and 0.69 (p<0.001) for Vp-MRI-LR.
Table 1

Weighted-kappa agreement between Vp-echo and MRI Vp-MRI-DQ and Vp-MRI-LR.

 

Vp-MRI-DQ

Vp-MRI-LR

 

< 45/55 cm/s

≥ 45/55 cm/s

< 45/55 cm/s

≥ 45/55 cm/s

Vp-echo

< 45/55 cm/s

23

6

23

7

 

≥ 45/55 cm/s

3

33

3

32

Age-related cut-off values were used to classify elevated LV filling pressures (Vp<45 cm/s for subjects older than 30 years and Vp<55 cm/s for subjects younger than 30 years old).

Conclusions

High-temporal VE-MRI represents a novel approach to assess Vp showing good correlation with Color M-mode echocardiography. In healthy subjects and patients with heart failure, this new method demonstrated good agreement with echocardiography to identify elevated LV filling pressures.

Funding

E.E. Calkoen is financially supported by a grant from the Willem-Alexander Kinder- en Jeugdfonds, J.J.M. Westenberg is financially supported by a grant from the Dutch Technology Foundation (STW), project number 11626

Authors’ Affiliations

(1)
Pediatric cardiology, Leiden University Medical Center, Leiden, Netherlands
(2)
Cardiology, Leiden University Medical Center, Leiden, Netherlands
(3)
Radiology, Leiden University Medical Center, Leiden, Netherlands

Copyright

© Calkoen et al; licensee BioMed Central Ltd. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement