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  • Meeting abstract
  • Open Access

2096 Phase contrast planimetry of valve area in aortic stenosis

  • 1,
  • 2,
  • 2,
  • 1 and
  • 1
Journal of Cardiovascular Magnetic Resonance200810 (Suppl 1) :A365

https://doi.org/10.1186/1532-429X-10-S1-A365

  • Published:

Keywords

  • Phase Contrast
  • Aortic Stenosis
  • Velocity Curve
  • Distinct Boundary
  • Aortic Valve Area

Introduction

Correct estimation of aortic valve area (AVA) is essential to decide when an aortic stenosis patient should undergo surgery. Traditional planimetry assumes that the AVA can be directly traced via the signal loss seen in a magnitude image. It has previously shown good correlation; however it is difficult to accurately define the signal loss boundary and is time consuming. Recently similar approaches have been explored using the phase contrast (PC). The assumption being that a clear distinct boundary for differentiating the high velocity pixels of the jet can be seen.

Purpose

To investigate the applicability of phase contrast plannimetry approaches by investigating the area vs velocity curve for distinct and consistent features that reflect AVA in a constant flow phantom and in-vivo.

Methods

A constant flow phantom has previously been constructed. It consists of a straight PVC pipe (Internal Diameter (ID) 28 mm) with a concentric circular obstruction placed in the flow to simulate a stenotic valve. Two different obstructions were used (ID = 12 mm,15 mm) and were imaged at 35 mm and at one orifice diameter downstream from the constriction at a flow rate of 400 mL/s. 15 patients with moderate-severe aortic stenois were used to acquire images at the valve plane and 1 cm downstream of the valve plane.

All experiments were conducted on a Siemens 1.5 T Avanto system. A retrospectively gated velocity encoding technique was used – for the constant flow phantom triggering was applied off an artificial ECG trace. Parameters were TE/TR of 2.79 msec/50.85 msec, typical voxel size of 1.17 × 1.17 × 6, matrix size 192 × 256 and a VENC of 500 cm/sec.

The data was analysed by contouring around the edge of the vessel and plotting (inverse) cumulative area (vessel area – cumm.area) vs velocity. If the assumption that a distinct boundary of the jet can be seen in the phase image then this should be seen as a feature in the cumm.area vs velocity curve, figure 1, as either a "elbow" indicating the rapid increase of velocity at the edge of the jet (A) or a "sudden drop off" to indicate pixels with in the jet (B). In the patients only 1–3 mid-systolic frames were chosen for analysis.
Figure 1
Figure 1

Idealised cumulative area vs velocity curve showing possible features that should be present to indicate a clear boundary for tracing pixels within a jet using phase contrast planiemetry.

Results

In the constant flow phantom the extent to which an elbow is seen depends on the size of the orifice and the location of the image plane. The more consistent elbow is seen with the smaller constriction and at 1 diameter downstream of the constriction. The larger constriction had no discernable features and instead smoothly tailed off to zero. No sudden drop-off was seen in either phantom. Similar results were seen in vivo. Some patients appeared to show a feature but it was more often that the cumm.area vs velocity curved off smoothly to zero.

Conclusion

The results show that any boundary used to trace around the jet pixels in a phase contrast image is very subjective. We found that in most cases in-vivo and experimentally that there is a smooth change in velocity from regions outside the jet to in the jet. This means that tracing around "jet pixels" to directly measure AVA would be very dependent on the user and the image display settings. Though good correlations could be found this is not an appropriate method for accurately quantifying AVA.

Authors’ Affiliations

(1)
The University of Auckland, Auckland, New Zealand
(2)
Middlemore Hospital, Auckland, New Zealand

Copyright

© O'Brien et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd.

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