Koray Ertan1, Peter B Roemer2, and Brian Rutt1
1Radiology, Stanford University, Stanford, CA, United States, 2Roemer Consulting, Lutz, FL, United States
Synopsis
Keywords: Gradients, Gradients, PNS, Peripheral Nerve Stimulation, Safety, Bioeffects, Magnetic Fields
Peripheral Nerve Stimulation
(PNS) remains as a limiting factor for gradient coils despite the recent
advances. PNS thresholds varies significantly across population group. In this
study, E-fields are simulated on simplified body model population with randomized
realistic body dimensions and different patient landmark positions. It is shown
that multivariate linear model with body dimensions and z-offset location as
the independent variables can accurately predict the maximum E-field on the
surface which can also be used to predict PNS thresholds. This simple
multivariate model may pave the way to estimate subject specific PNS thresholds
using simple anatomical measurements.
Introduction
Peripheral nerve
stimulation (PNS) has become a significant limiting factor for high performance
gradient coils, including latest generation head gradients.
E-field calculation
using simplified body models is an accepted method for predicting PNS
thresholds of both head and body gradient coils1. Our previously introduced
E-field calculation method was shown to predict population-mean experimental
PNS measurements2. We integrated this method into our gradient
design code, demonstrating the ability to design PNS-optimal gradient coils2,3.
Population-average
PNS thresholds (either measured or calculated) are generally used on scanners to
set safety limits. There may be significant advantages in being able to predict
PNS thresholds rapidly and accurately for individual subjects, but this has not
been achieved to date; for example, prior studies have not found significant
correlations between PNS thresholds and anatomical measurements4.
Our
computationally-efficient method of calculating E-fields on simplified body
models with realistic head, neck and shoulder geometries allows us study
E-field variations over large populations of body models, using realistic body
dimensions drawn from established anthropomorphic databases5. The
aim of the present work was to construct and test linear models for predicting maximum
body surface E-field, Emax, which is known to correlate well with
PNS thresholds1,2. We trained and tested our models using populations
of body models that spanned the full range of body dimensions and position
offsets.Methods
We analyzed two
existing head gradient coils, one symmetric (H4) and one asymmetric (ESP)2,
which have significantly different field characteristics. B-field profiles were
simulated in Sim4Life (ZMT MedTech AG, Zurich). E-fields were calculated on
standardized body models with simplified geometry and uniform interior
electrical properties; these included head, neck, shoulder, and torso regions
as shown in Figure 11. We used our fast E-field calculation method to
calculate E-fields and to extract maximum surface E-field per unit slew rate, Emax,
over large populations of body models in which body dimensions were selected
randomly from published adult male and female statistical distributions5.
Nine relevant head/neck/shoulder dimensions were varied, initially in an
independent fashion, to study the sensitivity of Emax to change in
each parameter. Later, sets of 100 male and 100 female body models with random
selection of all nine dimensions were generated for each coil and each axis. E-fields
were calculated on the surface and Emax extracted. Additional random
populations were placed at three different z-offsets (z=-2,0,2 cm) to study the
effect of subject Z-location. For each gradient coil and axis, multivariate
linear models were fit using body dimensions and z-offsets as the independent
variables and Emax as the dependent variable. Populations were split
in half for model training and testing.Results
Figure 2 shows
that E-field distributions vary significantly between small (2.5%ile), medium
(50%ile) and large (97.5%ile) body models, with larger models typically showing
higher values of Emax. The sensitivities of Emax to
independent changes in each of the nine-dimension parameters (defined as the
slope of Emax vs dimension) are shown in Figure 3. Results show both
positive and negative sensitivities that vary significantly in strength and
with dimension parameter for different gradient coils and axes. Emax
varies highly linearly with each dimension (R2>0.95) except for ESP-XZ which
exhibits some non-linearities. With this evidence of linearity, we then fit multivariate
linear models using randomly selected training samples consisting of 50 male
and 50 female models. We found that for all coils and axes, R2 values for the
multivariate fits exceeded 0.99. Additionally, the multivariate models were tested
using independent randomly selected test samples, in all cases demonstrating
highly accurate prediction of Emax (normalized RMSE<1% for all cases).
Detailed results and analyses of multivariate linear models are shown in Figure
4. When subject Z-location (z-offset) was included in the training and test
data, normalized RMSE slightly increased but remained less than 3.5% (Figure 5). Discussion and Conclusion
Our results show
that Emax is accurately predicted using multivariate linear models that
only require knowledge of a few key body dimensions. Our prior work has shown
that population PNS thresholds are accurately predicted (to within 20%) from
population-averaged Emax and that this methodology adheres to IEC
standards1. We believe, therefore, that the present work
demonstrates a practical pathway toward accurate subject-specific PNS threshold
prediction using simple multivariate modeling.
We found that Emax
varies by nearly 100% across the adult body model populations, and this
variation corresponds well with the variation of PNS thresholds between
subjects observed in experimental PNS studies2,6,7. We hypothesize,
therefore, that by estimating Emax for an individual, we will be able
to predict that individual’s PNS thresholds with reasonable accuracy. This
would allow the customization of PNS limits on the scanner to the individual
subject, for the first time. The present work also shows that Emax
can be calculated either by fast E-field calculation method if a body model is
constructed to match the individual anatomy, or via simple linear models that
require knowledge of only a few key dimensions. Future work will test this
hypothesis, as well as extending the methodology to explore more complex body
models8 and a wider range of gradient coils.Acknowledgements
We acknowledge research support from the
National Institutes of Health (NIH R01 EB025131 and NIH U01 EB025144). We
acknowledge ZMT Zurich MedTech AG for their Sim4Science support.References
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