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@ARTICLE{Schneider:142128,
author = {T. M. Schneider and A. Nagel$^*$ and M. Zorn and A.
Wetscherek$^*$ and M. Bendszus and M. Ladd$^*$ and S.
Straub$^*$},
title = {{Q}uantitative susceptibility mapping and 23 {N}a
imaging-based in vitro characterization of blood clotting
kinetics.},
journal = {NMR in biomedicine},
volume = {31},
number = {6},
issn = {0952-3480},
address = {New York, NY},
publisher = {Wiley},
reportid = {DKFZ-2018-02358},
pages = {e3926},
year = {2018},
abstract = {Blood clotting is a fundamental biochemical process in
post-hemorrhagic hemostasis. Although the varying appearance
of coagulating blood in T1 - and T2 -weighted images is
widely used to qualitatively determine bleeding age, the
technique permits only a rough discrimination of coagulation
stages, and it remains difficult to distinguish acute and
chronic hemorrhagic stages because of low T1 - and T2
-weighted signal intensities in both instances. To
investigate new biomedical parameters for magnetic resonance
imaging-based characterization of blood clotting kinetics,
sodium imaging and quantitative susceptibility mapping (QSM)
were compared with conventional T1 - and T2 -weighted
imaging, as well as with biochemical hemolysis parameters.
For this purpose, a blood-filled spherical agar phantom was
investigated daily for 14 days, as well as after 24 days
at 7 T after initial preparation with fresh blood. T1 - and
T2 -weighted sequences, a three-dimensional (3D) gradient
echo sequence and a density-adapted 3D radial projection
reconstruction pulse sequence for 23 Na imaging were
applied. For hemolysis estimations, free hemoglobin and free
potassium concentrations were measured photometrically and
with the direct ion-selective electrode method,
respectively, in separate heparinized whole-blood samples
along the same timeline. Initial mean susceptibility was low
(0.154 ± 0.020 ppm) and increased steadily during the
course of coagulation to reach up to 0.570 ± 0.165 ppm.
The highest total sodium (NaT) values (1.02 ± 0.06
arbitrary units) in the clot were observed initially,
dropped to 0.69 ± 0.13 arbitrary units after one day and
increased again to initial values. Compartmentalized sodium
(NaS) showed a similar signal evolution, and the NaS/NaT
ratio steadily increased over clot evolution. QSM depicts
clot evolution in vitro as a process associated with
hemoglobin accumulation and transformation, and enables the
differentiation of the acute and chronic coagulation stages.
Sodium imaging visualizes clotting independent of
susceptibility and seems to correspond to clot integrity. A
combination of QSM and sodium imaging may enhance the
characterization of hemorrhage.},
cin = {E020},
ddc = {610},
cid = {I:(DE-He78)E020-20160331},
pnm = {315 - Imaging and radiooncology (POF3-315)},
pid = {G:(DE-HGF)POF3-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:29694688},
doi = {10.1002/nbm.3926},
url = {https://inrepo02.dkfz.de/record/142128},
}