finite element model for patient-speci c functional

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Finite element model for patient-specific functional simulations of cochlear implants Mario Ceresa 1 , Hans Martin Kjer 2 , Sergio Vera 1 , Noem´ ı Carranza 1 , Frederic Perez 1 , Livia Barazzetti 3 , Pavel Mistrik 4 , Anandhan Dhanasingh 4 , Marco Caversaccio 5 , Martin Stauber 6 , Mauricio Reyes 3 , Rasmus Paulsen 2 and Miguel Angel Gonz´ alez-Ballester 1 1 Alma IT Systems, Barcelona Spain 2 Technical University of Denmark, Lyngby, Denmark 3 University of Bern, Bern, Switzerland 4 Med-El, Innsbruck, Austria 5 Bern University Hospital, Bern, Switzerland 6 Scanco Medical AG, Br¨ uttisellen, Switzerland Abstract. We present an innovative image analyisis pipeline to perform patient-specific biomechanical and functional simulations of the inner hu- man ear. A high-resolution, cadaveric, mCT volumetric image portraying the detailed geometry of the cochlea is converted into a mesh in order to build a Finite Element Method (FEM). The constitutive model for the FEM is based on a Navier-Stokes formulation for compressible Newto- nian fluid, coupled with an elastic solid model. The simulation includes fluid-structure interactions. Further to this, the FEM mesh is deformed to a patient-specific low-resolution Cone Beam CT (CBCT) dataset to propagate functional information to the specific anatomy of the patient. Illustrative results of how the FE-model responds to various acoustic stimuli are shown by analyzing the tonotopic mapping of the cochlear membrane vibration. 1 Introduction Hearing impairment or loss is among the most common reasons for disability. Worldwide, 27% of men and 24% of women above the age of 45 suffer from hearing loss of 26dB or more [1]. A cochlear implant (CI) is a surgically placed device that converts sounds to electrical signals, bypassing the hair cells and directly stimulating the auditory nerve fibers. Extreme care has to be taken when inserting the CI’s electrode array into the cochlea to obtain the best possible improvement in hearing while not damaging residual hearing capabilities [2]. The HEAR-EU project aims at reducing the inter-patient variability in the outcomes of surgical hearing restoration by improving CI designs and surgical protocols. In this context, we propose that the availability of an accurate func- tional model of the cochlea can improve implant design, insertion planning and selection of the best treatment strategy for each patient.

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Page 1: Finite element model for patient-speci c functional

Finite element model for patient-specificfunctional simulations of cochlear implants

Mario Ceresa1, Hans Martin Kjer2, Sergio Vera1,Noemı Carranza1, Frederic Perez1, Livia Barazzetti3, Pavel Mistrik4,

Anandhan Dhanasingh4, Marco Caversaccio5, Martin Stauber6,Mauricio Reyes3, Rasmus Paulsen2 and Miguel Angel Gonzalez-Ballester1

1 Alma IT Systems, Barcelona Spain2 Technical University of Denmark, Lyngby, Denmark

3 University of Bern, Bern, Switzerland4 Med-El, Innsbruck, Austria

5 Bern University Hospital, Bern, Switzerland6 Scanco Medical AG, Bruttisellen, Switzerland

Abstract. We present an innovative image analyisis pipeline to performpatient-specific biomechanical and functional simulations of the inner hu-man ear. A high-resolution, cadaveric, μCT volumetric image portrayingthe detailed geometry of the cochlea is converted into a mesh in order tobuild a Finite Element Method (FEM). The constitutive model for theFEM is based on a Navier-Stokes formulation for compressible Newto-nian fluid, coupled with an elastic solid model. The simulation includesfluid-structure interactions. Further to this, the FEM mesh is deformedto a patient-specific low-resolution Cone Beam CT (CBCT) dataset topropagate functional information to the specific anatomy of the patient.Illustrative results of how the FE-model responds to various acousticstimuli are shown by analyzing the tonotopic mapping of the cochlearmembrane vibration.

1 Introduction

Hearing impairment or loss is among the most common reasons for disability.Worldwide, 27% of men and 24% of women above the age of 45 suffer fromhearing loss of 26dB or more [1]. A cochlear implant (CI) is a surgically placeddevice that converts sounds to electrical signals, bypassing the hair cells anddirectly stimulating the auditory nerve fibers. Extreme care has to be taken wheninserting the CI’s electrode array into the cochlea to obtain the best possibleimprovement in hearing while not damaging residual hearing capabilities [2].

The HEAR-EU project aims at reducing the inter-patient variability in theoutcomes of surgical hearing restoration by improving CI designs and surgicalprotocols. In this context, we propose that the availability of an accurate func-tional model of the cochlea can improve implant design, insertion planning andselection of the best treatment strategy for each patient.

Page 2: Finite element model for patient-speci c functional

The cochlea is a spiral shaped structure, wrapped around a conical bone(modiolus) with a characteristic indentation in its inner side (bony spiral lam-ina) [3]. Attached to the bony spiral lamina is the basilar membrane, that sep-arates the cochlea into two scalae, scala tympani and scala media. The thirdcochlear scala is called scala vestibuli and is separated from scala media by theReissner’s membrane. When a sound wave is propagated through the fluid thatfills the cochlea (perilymph) the complex oscillatory pattern of the basilar mem-brane separates the frequencies of a propagating sound, acting as a mechanicalspectrum analyzer. This is caused by the variation of the mechanical propertiesof the basilar membrane along its length: at the apex it is large and elastic whileat its base it is thin and stiff. Due to this, low frequencies are keener to res-onate on the membrane at the apex of the cochlea, while higher frequencies atthe base. This is known as tonotopic mapping of the frequencies in the cochlea.Mechanical vibrations are translated into electrical stimulation of the auditorynerve in the organ of Corti, a cellular structure located on the top of the basilarmembrane and containing sensory cells, called hair cells [3].

We present in this paper a simulation model of the interaction between fluidand structure in the human cochlea. A finite element model (FEM) is builtfrom μCT data, incorporating bone, fluid and an elastic membrane with variablestiffness. Regarding related work on the simulation of cochlear function, Edomet al. [4] present a computational model for dynamical phenomena in the cochleawith viscous effects and cochlear responses to non-harmonic stimuli. Their workuses a simplified, non-anatomical geometry, and is based on finite volume (FV)simulations [5]. Because of the coupling with elastic structural equations in fluid-structure interaction, a FEM approach such as ours is more natural and thuspreferred over the FV method.

Propagating the FEM model built from μCT data to clinical Cone Beam CT(CBCT) data allows to obtain patient-specific simulations of the mechanics ofthe cochlea, which in turn is of great interest for the optimization of the implant.

The rest of the paper is structured as follows: Section 2 describes image ac-quisition and processing, Section 3 describes the FE model and its use in cochlearfunction simulation. Results are reported in Section 4. Finally, discussion anddirections for future work are provided in Section 5.

2 Imaging and segmentation

A cadaveric sample of the temporal bone region was scanned with a high-resolution Scanco µCT 100 system (Scanco Medical AG, Switzerland). Thedataset has a nominal isotropic resolution of 24.5 µm. The other available data-sets consist of a cone-beam CT (CBCT) scan with a nominal resolution of 150µm. Segmentation and creation of the FE model was performed on the µCTdataset to exploit the superior anatomical details. We use a CBCT scan as apatient-specific dataset because µCT scans cannot be taken on living patientsdue to the high amount of radiation involved and the small sample size allowed,while the CBCTs are appropriate for clinical use in patients. Even in the µCT

Page 3: Finite element model for patient-speci c functional

dataset the resolution was not sufficient to detect Reissner’s membrane and weconsider scala media and scala vestibuli as a single scala.

Fig. 1. a) Segmented transversal slice of the µCT, showing the cochlea (blue) and thespiral lamina (red). b) Surface reconstruction of the cochlea, built from the µCT data.

The µCT dataset was segmented using a semi-automatic level-set method [6]and manual corrections. Fig. 1a shows a transversal slice of the µCT image,where the cochlea is segmented in blue and the spiral lamina in red. The resultingsurface segmentation was regularized with a surface reconstruction technique [7]to obtain a surface more suited for generating a FEM mesh. Fig. 1b shows a 3Dsurface reconstruction based on the µCT data.

3 Finite Element Model

The FEM mesh is built from the segmented µCT dataset. The basilar membranewas only partly visible in the dataset, and severely damaged due to the samplepreparation process. Therefore, an approximating surface was manually fit tothe remaining portions of the bony spiral lamina of the cochlear wall (Fig. 2a).The software ICEM-CFD (ANSYS) was employed to build a tetrahedral meshmodel with two different domains, one for the membrane and another for thecochlear scale (Fig. 2b).

For the fluid domain we use the general formulation for Newtonian fluid [8]:

ρ

(∂u

∂t+ u · ∇u

)= −∇p+∇ ·

(µ(∇u + (∇u)T )

)+∇ (λ∇ · u) + ρg (1)

where u models the velocity of the fluid, µ is the dynamic viscosity coefficient, pis the thermodynamic pressure, λ the volume viscosity, ρ the density and g repre-sents the gravity force. In current model we do not consider the effects of volumeviscosity. Numerical values for the required parameters are ρ = 998.3 Kg/m3 andµ = 1.002e−3 Pa · s.

Page 4: Finite element model for patient-speci c functional

Fig. 2. a) Geometry of the FEM of the cochlea. Different colors represent the boundaryconditions: violet (walls), blue (inlet), pink (outlet), green (lateral wall of the basilarmembrane), red (base of the basal membrane). b) Tetrahedral mesh of the cochlearstructures with visible boundary conditions. Internal structures of the basilar mem-brane are not visible.

In the solid domain, we are modeling biological soft tissues with possiblylarge deformation. To this end, we use the finite deformation formulation [9]

ρ0u−∇ · S = ρ0b0

S = FS(C)

F = I +∇uC = FTF

(2)

where ρ0 is the density of the body in the reference position, S is the first Piola-Kirchhoff stress tensor, and b0 = b0(x(p, t), t) is the body force measured perunit mass. The response function S(C) characterizes the second Piola-Kirchhoffstress as a function of the right Cauchy-Green tensor C. Here we use:

S = λTr(E)I + 2µE (3)

where E is the strain tensor:

E =1

2(C − I). (4)

and I the identity matrix. In order to obtain a tonotopic frequency response asper Greenwood’s model [10,11], the basilar membrane is modeled as an elasticsolid with a stiffness s(x) variable along its length:

s(x) = mω2(x), (5)

w(x) = 2πfr(x) = 2πA(102.1−60x − kG) (6)

Page 5: Finite element model for patient-speci c functional

where A and kG are two parameters used to fit the model to experimental data.Here we use values A = 165.4 and kG = 0.85 as suggested in [11]. However, inthis formula x refers to the linear distance from the base, which is not easilyobtained from the geometry of the coiled cochlea. To overcome this problem, weparameterized the surface of the membrane using the arrival time of an Eikonalequation as the distance from the base. The Eikonal equation was solved with afast marching scheme [12].

We implemented the FEM using the Elmer open-source solver [13]. We con-sidered a fluid-solid interaction at low Reynolds’s number because of the smallvelocity of the fluid in the cochlear partition and its low viscosity [4,14]. To applythe pressure stimuli, a transient sinusoidal boundary condition of 1 Pa is appliedbetween the inlet and the outlet. In order to solve the fluid-structure interactionwe use an alternating optimization heuristic where the Navier-Stokes equationsfor the fluid domain are solved first and under the assumption of a constant ge-ometry; then, the surface forces acting on the solids are calculated and utilizedto calculate stress and displacement of the elastic structure. Eventually, the fluiddomain is solved again, this time using the resulting displacement velocities asfixed boundary conditions. This procedure repeats until the solution converges.

4 Results

Figure 3 shows the Eikonal parameterization (left) and the resulting stiffnesscalculated with Eq 6. For this initial comparison, we selected four frequenciesinside the human hearing spectrum (20kHz, 2kHz, 200Hz, 20Hz) and simulatedthe response of our FE-model to that stimulus.

Fig. 3. Models of the basilar membrane: (left) parameterization with the Eikonal equa-tion. Notice how the isothermal surfaces in black are evenly spaced; (right) stiffnessof the membrane as calculated from the Greenwood model in logaritmic scale. Noticehow the membrane is stiffer at the base than in the apex.

A separate simulation was run for each stimulation frequency. In order toset the desidered time resolution, we considered that our highest stimulation

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frequency (20kHz) corresponds to an oscillation period of 50 µs. Thus we chosea time step of 1 μs. In order to increase the robustness of the estimations, weobserve at least 10 periods of each oscillations, for a total simulation time of500 µs or 500 time-steps.

Each simulation took approximately 60 minutes on an HP Z620 workstationwith 10 cores and 16 GB of RAM with OpenMPI [15] enabled. We observe thatthe peaks of oscillations of the basilar membrane are distributed according toGreenwood’s model (Fig. 4). This effect is of great interest for the optimizationof electrode placement in hearing-impaired subjects.

Fig. 4. Agreement of the simulated model (points) with the Greenwood model (con-tinue blue line).

5 Discussion and Future Work

We presented an innovative image analyisis pipeline to perform patient-specificbiomechanical and functional simulations of the human ear. The framework iscapable of deforming the mesh created from high-resolution μCT images to aclinical CBCT scan, thus transferring the results of the simulations to a realpatient anatomy. This enables the direct comparison of peaks location betweendifferent patients and can be of great use for implant optimization.

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Future works include using many μCT images to capture more anatomicaldetails for the FE-model. Work is already in progress to obtain a large amountof high-resolution μCT cadaveric scans. In addition, the constitutive modelsand boundary conditions used in our experiments will be refined as new ex-periments are carried out, in order to ensure full physiological compliance. Onthe methodological side, we are also working on extending this framework tocreate a statistical shape model (SSM) to study the effects of population vari-ability on simulation results and to explore the design parameter space in orderto find optimal values for a design fitting the whole population. This work isa step forward towards a complete personalization of CI surgery where arrayinsertion strategy and expected response could be planned well ahead of thesurgery. Virtual testing of new implants will in the future help surgeons to selectthe best implant accordingly to the anatomy of the patient. Further, being ableto study the whole range of cochlear shapes and frequency distribution of thetarget population will lead to better fitting implants, as well as a considerablecost reduction in the design process. In order to assess the appropriateness ofan implant, further development should be done to define the different scenar-ios of the implant, in terms of positions where it is likely to be placed and thepercentage of residual hearing preserved.

6 Acknowledgments

HEAR-EU is a collaborative project between Alma IT Systems, Med-El, ScancoMedical, the Univ. of Bern, The Univ. Hospital of Bern and the Technical Univ.of Denmark.

The research leading to HEAR-EU results has received funding from the Eu-ropean Union Seventh Frame Programme (FP7/2007-2013) under grant agree-ment n◦ 304857

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