Gianluigi Tiberi1,2, Mauro Costagli1,2, Laura Biagi2, Alessio De Ciantis3, Nunzia Fontana4, Riccardo Stara5,6, Mark R Symms7, Mirco Cosottini8, Renzo Guerrini3, and Michela Tosetti1,2
1Imago7, Pisa, Italy, 2IRCCS Stella Maris Foundation, Pisa, Italy, 3Meyer Children’s Hospital, Firenze, Italy, 4Dipartimento di Ingegneria dell'Informazione, Pisa, Italy, 5National Institute of Nuclear Physics (INFN), Pisa, Italy, 6Stanford University, Stanford, CA, United States, 7General Electric ASL Scientist (EMEA), Pisa, Italy, 8Department of Translational Research and New Surgical and Medical Technologies, Pisa, Italy
Synopsis
In
this study we propose a procedure which allows the prediction of global and
local subject-specific SAR exposure for commonly used 7.0T sequences.
Prerequisites for such prediction are: sequences’ SAR exposure simulated on the
generic anatomic models; subject-specific measured B1+ maps.
Validation has been provided through phantom experiment. We observed that:
SILENT and FLAIR can be safely used in all subjects, both adults and children;
FLAIR is more SAR demanding than SILENT; predicted SAR exposure does not show a significant
variation with subject weight.Target audience.
RF engineers and clinicians interested in safety aspects at UHF, in particular in the application on
pediatric population
Purpose.
Subject-specific SAR
measurements are not available in current MR systems; simulations must be
performed for RF fields and SAR analysis. We combine SAR simulations performed
on generic anatomic models with subject-specific measured B
1+ maps, predicting local and global head SAR.
Methods.
Electromagnetic simulations. We used the Finite Integration
Technique (FIT) in the CST MW Suite. We simulated a 1H 298 MHz quadrature
birdcage head coil (Nova Medical, Wilmington, MA, USA), loaded by a human head model
derived from the 2×2×2 mm3 voxel-size anatomic model Ella (adult, 59
kg), Virtual population, ITIS foundation (Fig. 1). The maximum local (10g) and
global SAR [W/kg] for the two following MR sequences were calculated: 1) Axial
“Zero” Time-of-Echo (ZTE) sequence1 (“SILENT”), 384 FA=4° hard
pulses of 12 usec length, 5 inversion and saturation pulses per TR (TR=525
msec); 2) Sagittal FLAIR2, 240 FA=120° hard pulses of length 336
usec per TR (TR=8 sec). The ratio rSAR
between maximum local and global SAR was computed. Next, we simulated various model positions (rotating
the head at 15°,30°,45° from the original position on z-axis, moving the head
of ±1cm along the 3 axes) recording SAR and rSAR worse case.
Finally, we repeated the procedure with a human head derived from the anatomic
model Billie (child, 35 kg), Virtual population, ITIS foundation. To allow
comparison with phantom experiments, simulations were run with the coil loaded
with a cylindrical phantom (Table I).
Measurements. For 19 adults and 27 children:
we collected age, weight. We acquired |B1,map+| with a Bloch-Siegert3
centred on slices corresponding to those used in simulations: parameters
TR=33 ms, TE=15 ms, RBW=15.6 kHz, thk=3.5mm, matrix-size 64x64, square FOV 22
cm, 2 nex (total acquisition time: 9 s). Measurements were acquired on a
GE MR950 7T human system (GE HealthCare, Milwaukee,WI, USA) using the coil equipped
with a 32-rx array. For each slice where |B1,map+| was
measured, a coefficient C, proportional to avg(|B1,map+|) /B1,nominal+ was calculated and used to scale the SAR simulated on the anatomic models;
selection between Ella or Billie was performed on subject-weight basis.
Phantom experiment. The cylindrical phantom
(Table I) was created as in 4. ΔT generated by SILENT (duration: 462 s) was
measured with a fiberoptic temperature probe (Neoptix Canada LP, Quebec,
Canada, resolution: 0.1 °C) placed at the location of anticipated maximum local
SAR. Before the measurement, the phantom was equilibrated to room temperature;
thermal insulation was achieved as in5. By applying heat equation,
temperature-based measured SAR can be determined5. The temperature sensor
has length of 2 cm; since the mass of 2 cm3 of agar solution is 10
g, we can assume that temperature-based measured SAR is 10g SAR. We acquired |B1+| in the axial slice crossing
the center using the Bloch-Siegert sequence; the coefficient C was calculated
and used to scale the simulated SAR for SILENT.
Results.
The ΔT generated in
the phantom by SILENT measured by fiberoptic temperature probe was 0.3 °C; the
temperature-based measured SAR was 2.74 W/Kg. The predicted phantom maximum
local SAR (10 g) for SILENT sequence was 3.1 W/Kg. Table I summarizes minimum,
maximum, average and standard deviation of the age, weight, predicted global
SAR. Predicted maximum local SAR (Fig 2) is calculated by multiplying the global
SAR by rSAR (3.4 in Ella, 3.2 in Billie).
Discussions and Conclusions.
There is a good agreement between temperature-based measured SAR and the predicted one. SILENT and FLAIR can be safely used in all subjects, both adults
and children; limits on maximum local (10 W/kg) and global (3.2 W/kg) SAR are
met. FLAIR is more SAR demanding than SILENT. Predicted SAR exposure does not
show a significant variation with subject weight. The trend towards higher SAR
exposure as subject weight increases was first shown at 1.5T in6,
where global SAR measurements were reported and a theoretical explanation was
provided. However, the theoretical explanation was derived under the
assumptions of a homogenous cylindrical/spherical load with an externally
homogeneous magnetic field and that the maximum peak power occurs at the
surface of the load; these assumptions are not valid when using a 7T birdcage
coil loaded with heads. At 7T the fields generated by the coil inside the heads
are inhomogeneous, and this leads to inhomogeneous |B1+| and
to hot spots which can occur also far from the surface7. During a
sequence, the system set the power to obtain the desired |B1+|;
it follows that the corresponding SAR can violate the linear increase with subject
weight7.
Acknowledgements
No acknowledgement found.References
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