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A 3-D Biomechanical Skeleton Parametric Fitting Model from opto-electronic Body Landmarks Measurement for Spinal Deformities Evaluation and Posture Analysis Moreno D’Amico 1,2,3 , Gabriele D’Amico 3 and Piero Roncoletta 3 1 Centro Studi e Valutazione Patologie Vertebrali - Istituto di Riabilitazione S.Stefano Via Aprutina 194, 62016 Porto Potenza Picena -MC, Italy 2 CUMS Le Naiadi - Univ. D'Annunzio 66100 Chieti, Italy 3 Bioengineering & Biomedicine Company, Via Salara 7, 66020 S. Giovanni Teatino -CH, Italy Introduction Spine and posture problems are topics of great interest in both biomechanical research and clinical fields. The development of eidology, i.e. of image-processing based diagnostic technologies like digital X-Ray, CAT Scan, MRI, has determined a real improvement in obtaining an ever increasing anatomical delineation of the involved structures in the evaluation of spine related pathologies. Unluckily, except for dynamic X-Ray, no one of these techniques is able to provide information about the functional state of the rachis and the related patient posture. In this case, optoelectronic measurement approach can be very useful to complete the necessary functional information, but its use in clinical environment requires the following three specific necessities to be satisfied: 1) To develop a detailed skeleton model with particular focus on 3D spine morphology, but at the same time keeping as low as possible the number of body landmarks to be used; 2) To extract as many as possible parameters of clinical significance strictly related to anatomical and anthropometrical subject's characteristics; 3) To represent them in an intuitive and clinical compliant fashion maintaining a biomechanical strictness but hiding the burden of complex mathematical approach. With these three goals in mind, our group started a project to transfer into a complete fully 3D reliable and detailed representation different segmental biomechanical models presented in literature. As result, a complete 3D parametric biomechanical human skeleton model has been developed. It has been conceived in a parametric form in order to be scaled according to each subject characteristics by fitting the 3D anthropometric sizes to opto-electronic measurements. Particular care and studies have been devoted to arrange the 3D human skeleton model parameterisation. The accuracy and precision of this model relies both on anatomical findings (cadaver dissections, in vivo and X-ray measurements, parametric regression equations [4,5,6]) reported in literature and on the approach and signal processing procedures we largely described [1,2]. Given the extraordinary growth of both hardware and software tools, this highly sophisticated computing demanding task can be approached even on relatively low cost powerful PC workstations. This model is currently used as clinical tool for diagnostic and therapeutic purposes in different clinical centres. Several hundreds of patients have been already analysed and followed up with this methodology that proved to be useful for various posture and spine related pathologies (in particular scoliosis, low-back pain etc.). Methods A non-ionising approach based on 3D opto-electronic measurements of body landmarks labelled by passive markers has been chosen to build the 3D parametric biomechanical skeleton model. The developed model can work at different stages of complexity. That is, depending on different analysis purposes and necessities, the parametric scaling can be detailed with several accurate anthropometric measurements and the dimensions of each skeleton component are estimated and fitted to match the subject’s skeleton. To this aim various protocols involving different body labelling have been established for different analyses. To analyse human posture and spinal related pathologies, a 27 markers protocol has been set and tested extensively in clinical environment [1,2,3]. The following anatomical repere points are identified: zygomatic bones, mentum, acromions, sterno- clavicular joints, xyphoid, ASIS, PSIS, knee joints, heels and spinous processes from C7 down to S3 every second vertebra. A special focus has been devoted to identify and model the spine, given the 11 spinous

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Page 1: A 3-D Biomechanical Skeleton Parametric Fitting Model from ...isbweb.org/images/conf/2001/Longabstracts/PDF/0200_0299/0205.pdf · [1,2,3]. The following anatomical repere points are

A 3-D Biomechanical Skeleton Parametric Fitting Model fromopto-electronic Body Landmarks Measurement for Spinal Deformities Evaluation

and Posture AnalysisMoreno D’Amico1,2,3, Gabriele D’Amico3 and Piero Roncoletta3

1Centro Studi e Valutazione Patologie Vertebrali - Istituto di Riabilitazione S.StefanoVia Aprutina 194, 62016 Porto Potenza Picena -MC, Italy2CUMS Le Naiadi - Univ. D'Annunzio 66100 Chieti, Italy

3Bioengineering & Biomedicine Company, Via Salara 7, 66020 S. Giovanni Teatino -CH, Italy

Introduction

Spine and posture problems are topics of great interest in both biomechanical research and clinical fields. Thedevelopment of eidology, i.e. of image-processing based diagnostic technologies like digital X-Ray, CAT Scan,MRI, has determined a real improvement in obtaining an ever increasing anatomical delineation of the involvedstructures in the evaluation of spine related pathologies. Unluckily, except for dynamic X-Ray, no one of thesetechniques is able to provide information about the functional state of the rachis and the related patient posture. Inthis case, optoelectronic measurement approach can be very useful to complete the necessary functionalinformation, but its use in clinical environment requires the following three specific necessities to be satisfied: 1) Todevelop a detailed skeleton model with particular focus on 3D spine morphology, but at the same time keeping aslow as possible the number of body landmarks to be used; 2) To extract as many as possible parameters ofclinical significance strictly related to anatomical and anthropometrical subject's characteristics; 3) To representthem in an intuitive and clinical compliant fashion maintaining a biomechanical strictness but hiding the burden ofcomplex mathematical approach. With these three goals in mind, our group started a project to transfer into acomplete fully 3D reliable and detailed representation different segmental biomechanical models presented inliterature. As result, a complete 3D parametric biomechanical human skeleton model has been developed. It hasbeen conceived in a parametric form in order to be scaled according to each subject characteristics by fitting the3D anthropometric sizes to opto-electronic measurements. Particular care and studies have been devoted toarrange the 3D human skeleton model parameterisation. The accuracy and precision of this model relies both onanatomical findings (cadaver dissections, in vivo and X-ray measurements, parametric regression equations[4,5,6]) reported in literature and on the approach and signal processing procedures we largely described [1,2].Given the extraordinary growth of both hardware and software tools, this highly sophisticated computingdemanding task can be approached even on relatively low cost powerful PC workstations. This model iscurrently used as clinical tool for diagnostic and therapeutic purposes in different clinical centres. Severalhundreds of patients have been already analysed and followed up with this methodology that proved to be usefulfor various posture and spine related pathologies (in particular scoliosis, low-back pain etc.).

Methods

A non-ionising approach based on 3D opto-electronic measurements of body landmarks labelled by passivemarkers has been chosen to build the 3D parametric biomechanical skeleton model. The developed model canwork at different stages of complexity. That is, depending on different analysis purposes and necessities, theparametric scaling can be detailed with several accurate anthropometric measurements and the dimensions ofeach skeleton component are estimated and fitted to match the subject’s skeleton. To this aim various protocolsinvolving different body labelling have been established for different analyses. To analyse human posture andspinal related pathologies, a 27 markers protocol has been set and tested extensively in clinical environment[1,2,3]. The following anatomical repere points are identified: zygomatic bones, mentum, acromions, sterno-clavicular joints, xyphoid, ASIS, PSIS, knee joints, heels and spinous processes from C7 down to S3 everysecond vertebra. A special focus has been devoted to identify and model the spine, given the 11 spinous

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processes and 2 PSIS markers 3D measurements, with a correct degree of accuracy and reliability. Indirectmeasurements such as joint centres positions are derived from external markers (for instance, hip joints centresare derived from ASIS and PSIS positions and related pelvis dimension, model and regression function [5,6]).Our experimental recordings are based on the AUSCAN opto-electronic system); anyway this methodology is avery general one and it can be indifferently applied to any stereo-photogrammetric recording system.

Figs.: 1a) Instrumentation and Acquisition set-up; 1b) Passive markers positioning.

In such a way 3D posture taking into account head, trunk, pelvis and legs postural disposition (upper limbs andribs are not considered), as well as 3D spine shape at each metameric level can be represented. Also pelvisorientation and scaling and eventual helicoidal deformation can be evaluated from ASIS and PSIS positions. Thestandard trial session is aimed to completely define subject posture both in orthostatic and in simple dynamicconditions. Each static postural attitude is considered correctly recorded when at least 5, one second lasting,acquisitions are performed. Given the 100Hz opto-electronic device data acquisition rate, this means that aminimum of 500 measurements are averaged per each static postural attitude [1,2,3]. Before averaging, anamount of pre-processing is needed on the acquired 3D raw data in order to comply clinical analysisrequirements. Namely, the frontal plane of the subject is chosen, in each frame, as the plane containing the PSISand parallel to the vertical axis, while his sagittal plane is the one orthogonal to this latter and parallel to thevertical axis. For all the following computations (averaging, clinical parameters extraction both in static anddynamic conditions, etc.) the measurements are re-aligned in the so defined subject's local co-ordinate system.Our studies as well as our clinical experience led us to identify a set of static attitudes (such as indifferentorthostasis with and/or without an under-foot wedge, self-corrected manoeuvres, ante-retroversion static posturalexercises, sitting posture), that can provide a complete documentation of subject postural, balancing andmorphological characteristics.

Results and Discussion

From the 3D reconstruction all the 2D clinical parameters claimed for the correct description and biomechanicalcharacterisation of spinal pathology, related to those usually calculated on the radiographic image, are derived(i.e. Cobb and Kypho-Lordotic angles). Moreover, a set of significant biomechanical variables describing thethree-dimensional nature of body posture are obtained, such as frontal and sagittal spinal offsets of each markedmetamere with respect to the vertical axis passing by S3, frontal and sagittal global offsets of each labelledlandmark with respect to the vertical axis passing through the middle point between heels, pelvis frontal andsagittal inclinations, horizontal rotations among shoulders, pelvis and heels, and several more. This step iscompletely automatic and goes through the determination of the limit vertebrae limiting the various curves present,allowing in this way angles computing for both the frontal and sagittal planes (as defined before). In Scoliosisanalysis, an automatic classification according to Moe is provided. Comparisons taking into account spinemorphology have been performed between X-Ray films and opto-electronic processed outcomes to assess theclinical significance of the developed algorithms [7]. For the graphical representation as well as clinical parametervisualisation and enlightening, an MS-Windows software package based on 3D graphic modelling has been

PRINTER

DOUBLE MONITOR PICTURE

HOST COMPUTER&

GRAPH SCREEN

OPTO-ELECTRONICDEVICE

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developed. Figures 2 and 3 represent an example of clinical outcome also compared to X-Ray film evaluation.The easy clinical approach of this procedure suggests its use in routinely clinical evaluation for the study ofPosture. Several hundreds of patients have been already analysed and followed up in different centres with thismethodology that proved to be useful for various posture and spine related pathologies. The developed 3Dhuman skeleton model and software package can be used as stable, accurate, reliable and fast tools for thequantitative identification of human body biomechanical characteristics, for the understanding of spine and posturerelated pathologies as well as a guideline to formulate a diagnosis and a therapy plan.

Fig. 2) 3D skeleton representation (frontal and sagittal view) compared to x-ray film.

Fig. 3) 3D skeleton representation (gait, lateral bendings, top view).

References[1] M. D’Amico et al., 3D Spine Morphology Identification by Mean of Parametric Curve Modelling and Self-Adapted Digital

Filtering, Proceedings of the 8th Int. IMEKO Conf. on Measurement in Clinical Medicine, Dubrovnik, 16-19 September 1998,8/26-8/31, 1998.

[2] M. D’Amico et al., Algorithm for Estimation, Classification and Graphical Representation of Clinical Parameters in theMeasurement of Scoliosis and Spinal Deformities by Means of Non-Ionising Device, in Three Dimensional Analysis ofSpinal Deformity (Eds. M. D’Amico et al.) Proc. Of the 2nd Int. Sym. On 3D Scoliotic Deformities Pescara Sep. 94, 33-38,IOS Press 1995.

[3] M D’Amico et al., The Measurement od the Functional State of Posture and Spine in Low Back Pain Through the 3D Non-Ionising Technique. Kinesiology, 29 (2), 5-16, 1997.

[4] A White. III and M. Panjabi, Clinical Biomechanics of the Spine, Philadelphia, J.B. Lippincott Co., 2nd Ed. 1990, 721[5] P. De Leva, Joint Center Longitudinal Positions Computed from a Selected Subset of Chandler’s data, J. Biomec. 29 (9),

1231-1233, 1996.[6] G. Seidel et al., Hip Joint Center Location from Palpable Bony Landmarks - A Cadaver Study, J. Biom., 28 (8), 995-998, 1995.[7] M. D’Amico and Vallasciani M., Non-Ionising Opto-Electronic Measurement and X-Ray Imaging Two Complementary

Techniques for Spinal Deformities Evaluation and Monitoring: Results of one Year Clinical Activity in Research into SpinalDeformities 1 (Eds J. Sevastik, K. Diab), Proc. of 1st Congress of International Research Society of Spinal Deformities,Stockholm June 1996, 151-154, IOS Press, 1997.