Kevin Koch1, Matthew Koff2, Thomas Bauer3, and Hollis Potter2
1Radiology, Medical College of Wisconsin, Milwaukee, WI, United States, 2MRI Division, Hospital for Special Surgery, New York, NY, United States, 3Anatomic Pathology and Orthopaedic Surgery, Cleveland Clinic, Cleveland, OH, United States
Synopsis
The
deposition of metal particles near total joint replacements has substantial
impact on patient morbidity. Current
standards of clinical management of patients with symptomatic total hip
replacements are highly leveraged on the presence of wear debris in
periprosthetic tissues. Our group has
recently developed methods to perform off-resonance based identification of
metal particle deposits. Here, we
provide analysis on the source of tissue-based metal particle Larmor frequency
offsets. The results of this analysis provide
new insight on the role of off-resonance observables in the progression of symptomatic
failed total hip replacements.
Introduction
Our
previous work utilized off-resonance mapping techniques to identify and
localize regions of suspected metallic debris in the synovial tissues surrounding
implanted total hip arthroplasty constructs1,2. We validated our analysis
by comparing our in-direct assessment of debris to direct-measures of debris by
examination of histologic samples near the implant in patients who underwent revision
THA surgery. The results only found a weak correlation between the observed MRI
off-resonance pockets and histologic metallosis scores2. The
lack of a strong correlation of these metrics was unexpected. A potential confounding factor is that these
analyses assumed that deposits of conglomerated particles produce the
off-resonance signature that we are observing using MRI methods.
In
the present study, we utilize simulations, to show that our prior assumption is
not well-founded and we formulate an alternative hypothesis on the source of
this off-resonance observed metallosis phenomena in MRI.
Methods
A
Monte Carlo simulation was developed to estimate off-resonance signatures
within an 8mm (2mm side length) cubic voxel for a variety of potential
macroscopic CoCr particle distribution densities with 30um granulation. A magnetic susceptibility of 1000ppm was
utilized for the cobalt-chromium debris, which was then passed through a
forward-dipole model that predicts MR-observable off-resonance fields 4,5.
The simulation was run in Monte-Carlo fashion for 1000 iterations for
particle densities ranging from 0.05 to 0.5% by volume. A final
off-resonance signature for the voxel was estimated by taking the mean of all
off-resonance in regions not occupied by the particles themselves, followed by mean
and standard deviations for all simulation in the Monte Carlo analysis. Results
The
results of one of the Monte-Carlo simulations, assuming a particle density of
15% by volume, is shown in Figure 1. The average voxel off-resonance values for a
range of particle densities results (±SD) is shown in Figure 2. Figure 3 shows 6 cases near
suspected metallosis cases in failed total hip replacements that demonstrate
large pockets of off-resonance in the suspected regions of tissue disease.
These observations utilize methods we have previously presented1,2. Discussion
The
results indicate that large conglomerated cobalt-chromium particles themselves
cannot be the source of the off-resonance signature that is detected. Six sample
cases of patients with a failed THA due to suspected metallosis (Fig. 3)
demonstrate large pockets of off-resonance1,2 in the suspected
regions of affected tissue. The local off-resonance signature in these regions
is 600 Hz to 1.5 kHz and cannot be attributed to the type of conglomerated
particles analyzed in our simulation. As a result, a strong correlation between
large, histologically observed metal particles and MR-based off-resonance
detection should neither be assumed nor expected.
An
alternative for the source of the off-resonance signature seen in the revision
THA patients (Fig. 3) is the presence of locally disassociated soluble cobalt
ions. It is well known that cobalt and chromium disassociate
through corrosion processes, which is the motivating principle for blood serum
ion testing in patients with symptomatic total hip replacements. In patients
with corrosion following hip arthroplasty, a Fenton-like reaction occurs,
resulting in reactive oxygen species, formation of iron deposits and cell
migration, which leads to tissue necrosis and substantial patient morbidity6
Cobalt disassociates into bivalent and trivalent states, which combine to form
cobalt-oxides, cobalt-chloride, and other molecules7. We
hypothesize that disassociated ionic cobalt, in its paramagnetic compound
formulation, could produce the off-resonance distributions we are observing. For
example, cobalt-chloride has a paramagnetic susceptibility (0.16 ppm/mM )8
that is larger than that of gadolinium compounds (0.11
ppm/mM)9. Using
this number, we can approximate that a concentration of cobalt-chloride at
roughly 60mM will yield the 600Hz offsets we are detecting at 1.5T. This
is, of course, neglecting other molecular forms of disassociated cobalt ions,
such as cobalt-oxides, which have similar orders of magnitude in their
paramagnetic magnetic susceptibilities. This simplistic analysis
provides a viable explanation connecting MR-based off-resonance observations in
regions of likely metal deposition.
The
clinical impact of this potential biomarker is significant. If
disassociated cobalt is the source of observed MR off-resonance signatures, it may
provide valuable information on the presence or likelihood of adverse local tissue
reactions near hip arthroplasty prior to discernible damage
noted on MRI evaluation with artifact reduction sequences such as the 3D
multispectral imaging techniques. Future work to elucidate this
connection could include mass spectrometry analysis and histomorphometry on
tissue samples acquired from revisions surgeries to correlate cobalt compound
concentrations, inflammation, and MR-observed off resonance effects. Acknowledgements
This work was supported by NIAMS/NIH (R01-AR064840).
The content is solely the responsibility of the authors and does not necessarily represent
the official views of the National Institutes of Health. The work was also supported by a grant from the Advancing a Healthier Wisconsin Research and Education ProgramReferences
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