Robert R Edelman1,2, Emily A Aherne1, Amit Pursnani3,4, Jianing Pang5, and Ioannis Koktzoglou1,6
1Radiology, NorthShore University HealthSystem, Evanston, IL, United States, 2Feinberg School of Medicine, Northwestern University, Chicago, IL, United States, 3Medicine, NorthShore University HealthSystem, Evanston, IL, United States, 4Medicine, University of Chicago Pritzker School of Medicine, Chicago, IL, United States, 5Siemens Medical Solutions USA Inc, Chicago, IL, United States, 6Radiology, University of Chicago Pritzker School of Medicine, Chicago, IL, United States
Synopsis
Evaluation of hemodynamic patterns is often an essential
component of the cardiac MRI exam. We
hypothesized that cine fast interrupted steady-state (FISS) ASL could prove
advantageous for demonstrating flow patterns in the heart and great vessels and
tested this technique in 19 patients undergoing cardiac MRI for standard
indications. We found that cine FISS ASL
is a robust, efficient imaging technique that is easily incorporated into
cardiac MRI protocols and shows promise for depicting abnormal blood flow
patterns in patients with a variety of cardiovascular disorders, including
aortic stenosis, hypertrophic cardiomyopathy, and congenital shunts.
INTRODUCTION
Evaluation of hemodynamic patterns is often an essential
component of the cardiac MRI exam. Cine
balanced steady-state free precession (bSSFP) can demonstrate flow jets but is
otherwise of limited utility for hemodynamic evaluation. Two-dimensional cine phase contrast (2DPC) is
a key part of most cardiac MRI protocols but has several technical limitations. 4D flow overcomes many of these limitations but
at present is too time-consuming for routine clinical use.
Cine arterial spin labeling (ASL) using a fast interrupted
steady-state (FISS) readout was recently described as a novel alternative to
phase contrast for the dynamic evaluation of hemodynamic patterns.1 Rather
than depict the evolution of flow-dependent phase shifts that are the basis for
phase contrast imaging, cine FISS ASL demonstrates the bulk transport of
labeled intravascular spins with enough temporal resolution to enable
quantification of in-plane flow velocity.
We performed a feasibility study to determine whether cine FISS ASL provides
additional value for hemodynamic evaluation of the heart and great vessels in
comparison with standard cine imaging and 2DPC.METHODS
This IRB-approved retrospective study was conducted in 19
adult patients who underwent cardiac MRI on a 1.5 Tesla scanner (MAGNETOM Avanto,
Siemens Healthcare, Erlangen, Germany) for a variety of clinical indications
including cardiomyopathy; aortic stenosis, aneurysm and dissection; and
congenital heart disease. The protocol
included cine bSSFP and 2DPC. In
addition, one or more breath-hold scans were acquired using a prototype cine FISS ASL pulse sequence (slice thickness
from 5 to 18-mm, temporal resolution ~20 msec).
For imaging of the LVOT and aortic root in patients with hypertrophic
cardiomyopathy (HCM) or aortic stenosis, the adiabatic inversion RF pulse used
for spin labeling was applied over the left ventricular cavity prior to the
onset of systole. For imaging of mitral
insufficiency and atrial septal defect, the RF labeling pulse was applied to
the left atrium, whereas for imaging of aortic insufficiency it was applied to
the aortic root.RESULTS
Diagnostic image quality was obtained in all patients using
cine FISS ASL. Use of thick slices permitted
the efficient hemodynamic evaluation of extensive lengths of the cardiac
chambers and great vessels and facilitated measurement of the severity of
aortic stenosis and LVOT obstruction. In
patients with aortic stenosis, cross-sectional thin-slice cine FISS ASL improved the
delineation of the valve leaflets compared with cine bSSFP by enhancing
contrast and suppressing flow artifacts (Figure 1). Cine FISS ASL was superior to both cine bSSFP
and 2DPC in demonstrating left-to-right shunting across a large atrial septal
defect (Figure 2). DISCUSSION
In this clinical feasibility study, we found that cine FISS
ASL robustly depicted in-plane flow patterns within the heart and great vessels. The capability for creating semi-projective
images with excellent lumen-to-background contrast was particularly helpful for
the evaluation of LVOT obstruction and aortic stenosis. Thin-slice cross-sectional imaging with cine FISS ASL better demonstrated the aortic valve leaflets and lumen than cine bSSFP. The technique also proved capable of
depicting regurgitant jets and left-to-right shunting.
A potential limitation of 2DPC was the need for the technologist
to select a single VENC and direction of the flow-encoding gradient for a given
acquisition. For instance, in our patient
with a large atrial septal defect, the left-to-right shunt likely varied in both direction
and velocity over the cardiac cycle. The
fact that only a single flow direction and VENC could be used may partly explain
the suboptimal visualization of the shunt in 2DPC images. However, cine FISS ASL has no such limitation
- flow contrast is preserved over a wide range of flow directions and
velocities. Consequently, this technique
was better able to demonstrate the shunt than 2DPC.
While not suffering from the same limitations as 2DPC, care is
required with cine FISS ASL to apply the RF label in an optimal location and
cardiac phase for a given indication, which can be challenging given the
complex geometry of the heart. For
instance, imaging of a regurgitant jet in a patient with aortic insufficiency
requires that the RF label be applied to the aortic root after closure of the
aortic valve to avoid having the labeled spins prematurely washed away by
inflow of unlabeled spins from the left ventricle.CONCLUSION
We found that cine FISS ASL is a robust, efficient imaging
technique that is easily incorporated into cardiac MRI protocols and shows
promise for depicting abnormal blood flow patterns in patients with a variety
of cardiovascular disorders, including aortic stenosis, HCM, and congenital
shunts. Acknowledgements
FUNDING SOURCES:
NIH grants R01 HL137920 and R01 HL130093References
1. Edelman
et al. J
Cardiovasc Magn Reson. 2018; 20(1): 12.