Patrick Korf1, Wolfgang Thaiss2, Ambros J. Beer2, Meinrad Beer3, Dominik Nickel1, and Thomas Vahle1
1Siemens Healthcare GmbH, Erlangen, Germany, 2Department of Nuclear Medicine, University Hospital Ulm, Ulm, Germany, 3Department of Diagnostic and Interventional Radiology, University Hospital Ulm, Ulm, Germany
Synopsis
In
whole-body PET/MR exams, MR-based attenuation correction is usually performed with
a Dixon protocol of an MR VIBE sequence acquired in breath-hold followed by a
segmentation into different tissue classes. As an extension we present a
free-breathing approach for attenuation correction that can be used for
patients that have problems or are even unable to perform the required
breath-holds. The presented approach relies on a self-gated, compressed sensing
accelerated gradient-echo sequence with Cartesian k-space sampling. We
demonstrate the generation of free-breathing attenuation maps in 2 human volunteers
and 10 patients.
Introduction
Whole-body
PET/MR exams require the acquisition of an attenuation map for each single bed
position to obtain quantitative PET images. Currently available MR-based
attenuation correction (MRAC) methods usually rely on breath-hold acquisitions
for bed positions that might be affected by respiratory motion. This approach
leads to good results with cooperative patients. In cases where the patient
cannot perform the breath-hold, resulting attenuation maps can suffer from
artifacts. In patients unable to follow breath-hold commands, such as pediatric
patients, this often leads to the need of anesthesia with the associated, known
risks. In this work, we present a free-breathing approach for attenuation
correction (FB-MRAC) based on a self-gated, compressed sensing accelerated
gradient-echo sequence with Cartesian k-space sampling. FB-MRAC can be used in
the critical bed positions, e.g. thorax and abdomen, which are heavily impacted
by respiratory motion. The remaining bed positions can be acquired with the
default MRAC and be composed resulting in whole-body free-breathing attenuation
maps. In this study, we demonstrate the combination of free-breathing and
breath-hold acquisitions of attenuation maps for whole-body PET/MR exams using human
volunteers and patient data.Methods
All
data were acquired on a 3T Biograph mMR (Siemens Healthcare, Erlangen, Germany)
using the spine coil and body matrix coils. The breath-hold acquisitions were
performed using a 2-point 3D VIBE Dixon prototype sequence with an acquisition
time of 13s per volume. For the free‐breathing acquisitions, the same prototype
sequence was used with an incoherent, variable‐density Cartesian k‐space
sampling, integrated acquisition of a navigation signal, and a compressed‐sensing
(CS) reconstruction with a total acquisition time of 113 seconds [1]. The navigation
signal was used to sort the raw data into 4 motion states followed by the CS
reconstruction. Only the end-expiration motion state was used to generate the
attenuation map. The data were acquired for 2 healthy volunteers using three
bed positions each and 10 patients with single bed positions only. All volunteers
and patients provided written informed consent before the measurements. For the
volunteer data, the first two bed positions were acquired with breath-hold and
free-breathing respectively. The third bed position was acquired using the
breath-hold setup but without a breath-hold command assuming that there is no
severe respiratory motion. After the acquisition of the final bed position, the
attenuation maps were generated using the bone segmentation [2] and the missing
arms were added [3]. Detailed acquisition parameters were as follows: TR 3.96
msec; TE 1.23 / 2.46 msec; flip angle 10°; field‐of‐view 500 × 406.3 x 264 mm3;
voxel size 1.3 × 1.3 × 3 mm3. The protocol with transversal acquisition
and high in-plane resolution yielded Dixon images for clinical reading.Results
Figure 1
shows the comparison of whole-body attenuation maps of a healthy volunteer acquired
in breath-hold and free-breathing respectively. The bone and lung segmentation
worked successfully for both scan setups. In case of the free-breathing acquisition,
the liver dome is closer to desired end-expiration state compared to the
breath-hold acquisition. For both setups no artifacts are visible in the last bed
position where motion was ignored. Figure 2 shows an example comparison of the
Dixon water images acquired with breath-hold (left column) and during free
breathing (right column) in three anatomical orientations. The transversal images
show slightly different cross-sections of the liver due to the different
respiratory positions. The images appear to have a similar sharpness. In case
of the breath-hold acquisition the image impression of the liver is blurred in
both coronal and sagittal reformats, especially towards the liver dome. In contrast to that the reformats appear
sharper when using the free-breathing protocol.Discussion
For both
patient and volunteer data the presented approach can provide free-breathing
high-resolution Dixon images which can be used to generate PET attenuation
maps. The advantage of this method can be seen in the patient example, where
the patient cannot hold the breath for the entire duration of the required
breath-hold leading to blurred images. As a drawback the new method requires
longer reconstruction times due to the demanding CS reconstruction. It may require
further evaluation whether there are cases where this method could fail or
hamper the clinical evaluation. A future direction of improvement would be to
investigate if acquisition time can be further reduced. The new approach could
also be combined with PET motion correction techniques as e.g. discussed in
[4].Conclusion
We
demonstrated a method for free-breathing acquisition of high-resolution Dixon data
suitable for the generation of attenuation maps for simultaneous PET/MR in approximately
two minutes. This approach can be helpful in situations where breath-hold
acquisitions are not possible and definitely lead to higher patient comfort if
breath-holds can be avoided.Acknowledgements
No acknowledgement found.References
[1] Weiss et al.,
J. Magn. Reson. Imaging 2018;47:459–467
[2] Paulus et al.,
J Nucl Med 2015; 56:1061–1066
[3] Blumhagen et
al., Medical Physics 41(2):022303
[4] Kolbitsch et al., Phys Med Biol. 2018 Jun
27;63(13)