Erin K Englund1, Lorna P Browne1, Takashi Fujiwara1, Richard Friesen2, Mehdi H Moghari1, and Alex J Barker1
1Radiology, University of Colorado, Anschutz Medical Campus, Aurora, CO, United States, 2Pediatric Cardiology, University of Colorado, Anschutz Medical Campus, Aurora, CO, United States
Synopsis
Fetal
CMR is difficult due to the lack of an ECG signal, fetal motion, small anatomic
sizes and high fetal heart rates. Initial results are presented which use a
doppler ultrasound gating device to capture fetal cardiac motion in standard cardiac
views and blood flow was quantified with 4D flow MRI. bSSFP cine images were
scored for image quality by two radiologists and flow in the umbilical vein,
ascending aorta and main pulmonary artery were quantified and agreed well with
reported values. Unique insight was provided with dynamic imaging regarding the
fetal circulation and the impact of congenital disease.
Introduction
High resolution imaging of
fetal cardiac function and flow by MRI remains difficult due to fetal motion,
small anatomic sizes, and high fetal heart rates (>130bpm). The use of doppler
ultrasound-gating (DUS) for cine and 4D flow [1] MRI hold promise for overcoming
these challenges. In particular, the fetal cardiovascular system has several
distinctive features that are difficult to visualize or quantify, including
blood flow in the umbilical vein, ductus venosus, ductus arteriosus, and
foramen ovale. Additionally, it is imperative that normal anatomic variance is
understood to detect abnormalities in the setting of congenital disease. The purpose
of this abstract is therefore to demonstrate our experience using DUS-gated
cine MRI to capture fetal cardiac motion and the preliminary utility of 4D flow
MRI to visualize and quantify the unique features of the fetal circulation in volunteers
and patients.Methods
In this IRB-approved study
with ongoing recruitment, ten healthy pregnant volunteers (gestational age = 34.6±1.4 weeks) were scanned at 1.5T (n=6) or 3T (n=4) (Philips
Ingenia MRI). Two patients, one with congenital
diaphragmatic hernia (CDH, GA=35 weeks), and one with craniosynostosis
(GA=30 weeks) were scanned at 1.5T. Images
were obtained using a torso coil with the volunteers lying supine/decubitus
according to comfort. Scout images were acquired to determine the location of
the fetal heart. Once verified, a DUS gating device (Northh Medical) [2,3] was
positioned superficially over the fetal heart and secured tightly with an
elastic band. Localizers were repeated to ensure proper placement of the
doppler probe and to plan fetal cardiac acquisitions. Cine balanced steady-state
free precession (bSSFP) images of the fetal heart were acquired in the axial
plane. If possible (dictated by amount of fetal motion) a combination of images
were also acquired in standard cardiac planes (Figure 1). When achievable, anatomical
images were acquired during maternal breath-hold. Following cine acquisitions,
and provided that a consistent fetal cardiac gating signal persisted, 4D flow
data were acquired. Pulse sequence parameters are summarized in Figure 2. Flow
in the umbilical vein, ascending aorta, and main pulmonary artery were
quantified using EnSight (Ansys, Inc.). Two
radiologists scored short-axis (SA) bSSFP cines for sharpness, SNR, and lack of
artifact on a 5-point Likert scale (5:excellent, 4:good, 3:satisfactory,
2:marginal 1:unusable).Results
Fetal
CMR was not achieved in one volunteer due to lack of a reliable gating signal. In
an additional 3 volunteers, fetal motion and/or time prevented the ability to
acquire 4D flow data. Therefore, cine bSSFP images of the fetal heart were
obtained in 9 volunteers, with 4D flow data in 6. Two of the volunteer 4D flow
datasets were not of sufficient quality for quantitative analysis (due to fetal
motion or ineffective gating). Across
all 9 healthy volunteers, the average fetal heart rate was 139±7 bpm. Example short-axis views acquired at 1.5T
and 3T are shown in Figure 1. Likert scoring for image quality was not
different for the SA views at 1.5T and 3T (average scores of 4.2±0.8 and
4.2±0.8, respectively). Figure 3 and 4 show a 4D
flow pathline visualization of the fetal circulation in a healthy volunteer. Across
the four volunteer subjects, average flow in the ascending aorta was 1.5±0.7 mL/beat, main pulmonary artery was 2.3±0.7 mL/beat, and umbilical vein was 1.5±1.0 mL/beat. In the two patients, a limit of 15 minutes for research ‘add-ons’
prevented the acquisition of 4D flow data; however, both patients had diagnostic
quality cine bSSFP images. Example fetal CMR images for the CDH patient are
shown in Figure 5 showing
the stomach and liver compressing the left atrium and an underdeveloped
left ventricle.Discussion
Use
of DUS gating allowed acquisition of both cine images of the fetal heart as
well as 4D flow MR data. Success rates and gating signal stability increased in
later volunteers due to experience, careful doppler probe placement, and
training of staff. A transition to 3T imaging in later volunteers allowed for
fewer averages to be collected with equivalent SNR and image quality to 1.5T (see
Figure 1 and Likert scores), resulting in faster imaging and less fetal motion artifact.
Unique features of the fetal circulation, including blood flow in the umbilical
vein and ductus venosus, shunting through the foramen ovale from the right to
left atrium, and flow through the ductus arteriosus are visualized with 4D flow
(Figure 3 and 4). These features are difficult to observe with other methods and
the blood flow measurements were in agreement with prior reports (assuming a fetal
weight of 1.5-2kg) [4, 5]. Diagnostic quality images were obtained in the patients,
and, in the case of the CDH patient (Figure 5), the imaging of dynamic motion provided
unique insight regarding potential causes of the underdeveloped left ventricle. Conclusion
The ability to use ‘off-the-shelf’
product sequences without the need for offline reconstruction is promising for DUS-based
fetal cardiac gating to be adapted in clinical workflows, with the caveat that
training is critical to avoid gating-signal dropout and fetal motion artifacts.
Continued development of fast and motion-robust acquisitions will enhance our
ability to reliably capture fetal cardiac motion and blood flow. Acknowledgements
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