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@ARTICLE{Sawall:296163,
author = {S. Sawall$^*$ and E. Baader$^*$ and P. Trapp$^*$ and M.
Kachelriess$^*$},
title = {{CT} material decomposition with contrast agents: {S}ingle
or multiple spectral photon-counting {CT} scans? {A}
simulation study.},
journal = {Medical physics},
volume = {52},
number = {4},
issn = {0094-2405},
address = {College Park, Md.},
publisher = {AAPM},
reportid = {DKFZ-2025-00090},
pages = {2167-2190},
year = {2025},
note = {#EA:E025#LA:E025# / 2025 Apr;52(4):2167-2190},
abstract = {With the widespread introduction of dual energy computed
tomography (DECT), applications utilizing the spectral
information to perform material decomposition became
available. Among these, a popular application is to
decompose contrast-enhanced CT images into virtual
non-contrast (VNC) or virtual non-iodine images and into
iodine maps. In 2021, photon-counting CT (PCCT) was
introduced, which is another spectral CT modality. It allows
for scans with more than two different detected spectra.
With these systems, it becomes possible to distinguish more
than two materials. It is frequently proposed to administer
more than one contrast agent, perform a single PCCT scan,
and then calculate the VNC images and the contrast agent
maps. This may not be optimal because the patient is
injected with a material, only to have it computationally
extracted again immediately afterwards by spectral CT. It
may be better to do an unenhanced scan followed by one or
more contrast-enhanced scans. The main argument for the
spectral material decomposition is patient motion, which
poses a significant challenge for approaches involving two
or more temporally separated scans. In this work, we assume
that we can correct for patient motion and thus are free to
scan the patient more than once. Our goal is then to
quantify the penalty for performing a single
contrast-enhanced scan rather than a clever series of
unenhanced and enhanced scans. In particular, we consider
the impact on patient dose and image quality.We simulate CT
scans of three differently sized phantoms containing various
contrast agents. We do this for a variety of tube voltage
settings, a variety of patient-specific prefilter (PSP)
thicknesses and a variety of threshold settings of the
photon-counting detector with up to four energy bins. The
reconstructed bin images give the expectation values of soft
tissue and of the contrast agents. Error propagation of
projection noise into the images yields the image noise.
Dose is quantified using the total CT dose index (CTDI)
value of the scans. When combining multiple scans, we
further consider all possible tube current (or dose) ratios
between the scans. Material decomposition is done
image-based in a statistical optimal way. Error propagation
into the material-specific images yields the signal-to-noise
ratio at unit dose (SNRD). The winning scan strategy is the
one with the highest total SNRD, which is related to the
SNRD of the material that has the lowest signal-to-noise
ratio (SNR) among the materials to decompose into. We
consider scan strategies with up to three scans and up to
three materials (water W, contrast agent X and contrast
agent Y).In all cases, those scan strategies yield the best
performance that combine differently enhanced scans, for
example, W+WX, W+WXY, WX+WXY, W+WX+WY, with W denoting an
unenhanced scan and WX, WY and WXY denoting X-, Y-, and
X-Y-enhanced scans, respectively. The dose efficiency of
scans with a single enhancement scheme, such as WX or WXY,
is far lower. The dose penalty to pay for these single
enhancement strategies is about two or greater. Our findings
also apply to scans with a single energy bin and thus also
to CT systems with conventional, energy-integrating
detectors, that is, conventional DECT. Dual source CT (DSCT)
scans are preferable over single source CT scans, also
because one can use a PSP on the high Kilovolt spectrum to
better separate the detected spectra. For the strategies and
tasks considered here, it does not make sense to
simultaneously scan with two different types of contrast
agents. Iodine outperforms other high Z elements in nearly
all cases.Given the significant dose penalty when performing
only one contrast-enhanced scan rather than a series of
unenhanced and enhanced scans, one should consider avoiding
the single-scan strategies. This requires to invest in the
development of accurate registration algorithms that can
compensate for patient and contrast agent motion between
separate scans.},
keywords = {material decomposition (Other) / multiple contrast agents
(Other) / virtual noniodine (Other) / virtual non‐contrast
(Other)},
cin = {E025},
ddc = {610},
cid = {I:(DE-He78)E025-20160331},
pnm = {315 - Bildgebung und Radioonkologie (POF4-315)},
pid = {G:(DE-HGF)POF4-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39791354},
doi = {DOI:10.1002/mp.17604},
url = {https://inrepo02.dkfz.de/record/296163},
}