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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">ETM</journal-id>
<journal-title-group>
<journal-title>Experimental and Therapeutic Medicine</journal-title>
</journal-title-group>
<issn pub-type="ppub">1792-0981</issn>
<issn pub-type="epub">1792-1015</issn>
<publisher>
<publisher-name>D.A. Spandidos</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3892/etm.2017.5607</article-id>
<article-id pub-id-type="publisher-id">ETM-0-0-5607</article-id>
<article-categories>
<subj-group>
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Biomechanical analysis of brachial plexus injury: Availability of three-dimensional finite element model of the brachial plexus</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>Mihara</surname><given-names>Atsushi</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Kanchiku</surname><given-names>Tsukasa</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Nishida</surname><given-names>Norihiro</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref>
<xref rid="c1-etm-0-0-5607" ref-type="corresp"/></contrib>
<contrib contrib-type="author"><name><surname>Tagawa</surname><given-names>Haruki</given-names></name>
<xref rid="af2-etm-0-0-5607" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author"><name><surname>Ohgi</surname><given-names>Junji</given-names></name>
<xref rid="af2-etm-0-0-5607" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author"><name><surname>Suzuki</surname><given-names>Hidenori</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Imajo</surname><given-names>Yasuaki</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Funaba</surname><given-names>Masahiro</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Nakashima</surname><given-names>Daisuke</given-names></name>
<xref rid="af1-etm-0-0-5607" ref-type="aff">1</xref></contrib>
<contrib contrib-type="author"><name><surname>Chen</surname><given-names>Xian</given-names></name>
<xref rid="af2-etm-0-0-5607" ref-type="aff">2</xref></contrib>
<contrib contrib-type="author"><name><surname>Taguchi</surname><given-names>Toshihiko</given-names></name>
<xref rid="af2-etm-0-0-5607" ref-type="aff">2</xref></contrib>
</contrib-group>
<aff id="af1-etm-0-0-5607"><label>1</label>Department of Orthopedic Surgery, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi 755-8505, Japan</aff>
<aff id="af2-etm-0-0-5607"><label>2</label>Department of Mechanical Engineering, Yamaguchi University, Ube, Yamaguchi 755-8505, Japan</aff>
<author-notes>
<corresp id="c1-etm-0-0-5607"><italic>Correspondence to</italic>: Dr Norihiro Nishida, Department of Orthopedic Surgery, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505, Japan, E-mail: <email>nishida3@yamaguchi-u.ac.jp</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>02</month>
<year>2018</year></pub-date>
<pub-date pub-type="epub">
<day>11</day>
<month>12</month>
<year>2017</year></pub-date>
<volume>15</volume>
<issue>2</issue>
<fpage>1989</fpage>
<lpage>1993</lpage>
<history>
<date date-type="received"><day>20</day><month>07</month><year>2017</year></date>
<date date-type="accepted"><day>02</day><month>10</month><year>2017</year></date>
</history>
<permissions>
<copyright-statement>Copyright: &#x00A9; Mihara et al.</copyright-statement>
<copyright-year>2018</copyright-year>
<license license-type="open-access">
<license-p>This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by-nc-nd/4.0/">Creative Commons Attribution-NonCommercial-NoDerivs License</ext-link>, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.</license-p></license>
</permissions>
<abstract>
<p>Adult brachial plexus injuries frequently lead to significant and permanent physical disabilities. Investigating the mechanism of the injury using biomechanical approaches may lead to further knowledge with regard to preventing brachial plexus injuries. However, there are no reports of biomechanical studies of brachial plexus injuries till date. Therefore, the present study used a complex three-dimensional finite element model (3D-FEM) of the brachial plexus to analyze the mechanism of brachial plexus injury and to assess the validity of the model. A complex 3D-FEM of the spinal column, dura mater, spinal nerve root, brachial plexus, rib bone and cartilage, clavicle, scapula, and humerus were conducted. Stress was applied to the model based on the mechanisms of clinically reported brachial plexus injuries: Retroflexion of the cervical, lateroflexion of the cervical, rotation of the cervical, and abduction of the upper limb. The present study analyzed the distribution and strength of strain applied to the brachial plexus during each motion. When the cervical was retroflexed or lateroflexed, the strain was focused on the C5 nerve root and the upper trunk of the brachial plexus. When the upper limb was abducted, strain was focused on the C7 and C8 nerve roots and the lower trunk of the brachial plexus. The results of brachial plexus injury mechanism corresponded with clinical findings that demonstrated the validity of this model. The results of the present study hypothesized that the model has a future potential for analyzing pathological conditions of brachial plexus injuries and other injuries or diseases, including that of spine and spinal nerve root.</p>
</abstract>
<kwd-group>
<kwd>brachial plexus injury</kwd>
<kwd>finite element model</kwd>
<kwd>mechanical property</kwd>
<kwd>spine</kwd>
<kwd>spinal cord</kwd>
<kwd>spinal nerve root</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec sec-type="intro">
<title>Introduction</title>
<p>Adult brachial plexus injuries frequently lead to significant physical disabilities. It could be caused by various mechanisms including falls, powerful sports activities, and motor vehicle trauma. Different mechanisms of injury lead to different injury patterns with different levels of plexus damage (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>). Since severe injuries often lead to permanent disabilities, prevention of the injury is significant. Investigating the mechanism of the injury by biomechanical approaches should provide aid with regard to preventing injuries.</p>
<p>However, there are no reports of a complex three-dimensional finite element model (3D-FEM) of the spine, dura mater, root, and the brachial plexus all in one model till date. The first objective of this study is to construct a complex 3D-FEM of the spine, dura mater, root, and the brachial plexus. In this study, to assess the validity of the model, we analyzed the patterns of clinically reported brachial plexus injuries by applying stress to the model and verified weather the results of the analysis and clinically reported results correspond. Secondly, we inspected the proposed model&#x0027;s availability in studying the prevention of brachial plexus injury.</p>
</sec>
<sec sec-type="materials|methods">
<title>Materials and methods</title>
<sec>
<title/>
<sec>
<title>Model</title>
<p>Using Simpleware ScanIP (Synopsys, Mountain View, CA, USA), a three-dimensional finite element model including the dura mater, vertebrae and intervertebral disk from C2 through Th2, first and second rib bones and costicartilage, right scapula, right clavicle and right humerus was constructed from CT and MRI images of a male human body, supplied by the Visible Human Project (U.S. National Library of Medicine, Bethesda, MD, USA). We constructed the rib bones and costicartilage as the thoracic cage because we believe that the thoracic cage participates in the motion properties of the spine. The reason being that the motion property of the spine and the first rib bone differed between models with or without the thoracic cage and thus it is rational to consider that the model possessing the thoracic cage is considerably likely to reproduce the actual motion of a real human body. We constructed the scapula, clavicle, and humerus to analyze the motion of the upper limb. Since there were no images of the brachial plexus, we extended the right spinal nerve roots of C5 to Th1 in proportion to its anatomical form and constructed a model from the root to the trunk as the right brachial plexus. Injuries of the brachial plexus occur predominantly at levels of root to the trunk (<xref rid="b2-etm-0-0-5607" ref-type="bibr">2</xref>), thus we constructed this level precisely. We extended the trunks of the plexus further to the upper third of the right humerus as a peripheral nerve and fixed the nerves to a rigid plate imitating a muscle. The dura mater was immobilized completely at C2 level. All components of the model were symmetrically meshed with 20-node elements. The total number of isoperimetric 20-node elements was 82,011 and the total number of nodes was 285,694 (<xref rid="f1-etm-0-0-5607" ref-type="fig">Fig. 1</xref>).</p>
<p>We configured the boundary condition using Jvision (JSOL, Tokyo, Japan). The material constant of each component was derived as follows (<xref rid="tI-etm-0-0-5607" ref-type="table">Table I</xref>) according to previous published studies (<xref rid="b3-etm-0-0-5607" ref-type="bibr">3</xref>&#x2013;<xref rid="b6-etm-0-0-5607" ref-type="bibr">6</xref>). Since the brachial plexus is a continuous component from the spinal nerve root, the mechanical property of the spinal nerve root was used for the modeling of brachial plexus.</p>
</sec>
<sec>
<title>Analyzing conditions</title>
<p>We used the LS-DYNA (JSOL) for analyzing. We set four analyzing conditions: Retroflexion of the cervical (case 1), left lateroflexion of the cervical (case 2), left rotation of the cervical (case 3) and abduction of the right upper limb (case 4). These conditions were selected based on mechanisms of brachial plexus injury reported clinically (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>,<xref rid="b7-etm-0-0-5607" ref-type="bibr">7</xref>).</p>
<p>In cases 1&#x2013;3, the rigid plate, second thoracic vertebrae and lower end of the dura mater were configured at complete constraint. Forced angular displacement was applied to the top of the second cervical vertebrae. The degree of angle applied in each case was defined based on the maximum range of motion of the neck in a human body; 33&#x00B0; in case 1, 23.5&#x00B0; in case 2, 25.5&#x00B0; in case 3 (<xref rid="b8-etm-0-0-5607" ref-type="bibr">8</xref>). In the motion of the cervical, the thoracic vertebra do not move because they are immobilized by the thoracic cage. Thus, the rotation center of the forced angular displacement was defined to the center of the bottom of the seventh cervical vertebrae in the three cases.</p>
<p>In case 4, the spinal column, rib bones, clavicle, scapula, and lower end of the dura mater were configured at complete constraint. Forced angular displacement of 30&#x00B0; of abduction was applied to the humerus. We configured the angle to be 30&#x00B0; because over 30&#x00B0; of abduction, the scapula starts upward rotation, and in this model the scapula is at complete constraint (<xref rid="b9-etm-0-0-5607" ref-type="bibr">9</xref>). The rotation center was defined to the center of the glenohumeral joint (<xref rid="f2-etm-0-0-5607" ref-type="fig">Fig. 2</xref>).</p>
<p>The velocity (<italic>V</italic>) of the force applied in each case was configured as 10 km/hr, because motor vehicle accidents, a major factor of brachial plexus injury, occur primarily at velocities lower than 10 km/hr in this country. Using the distance from the point of force applied to the rotation center (<italic>r</italic>), the angular velocity (<italic>w</italic>) was calculated by the following numerical formula: <italic>V=wr</italic></p>
<p>Measurement of distribution and size of strain applied to the brachial plexus in each case mentioned above was conducted. There is no knowledge with regard to the threshold value of strain applied to the brachial plexus when symptoms of injuries appear. However, Singh <italic>et al</italic> have reported that the breaking strain of the dorsal root is 30.8&#x00B1;8.4&#x0025; (<xref rid="b10-etm-0-0-5607" ref-type="bibr">10</xref>). Galbraith <italic>et al</italic> have reported via a tension test of an axon of a giant squid that axonal injury of the white matter occurs from strain level of approximately 28&#x0025; (<xref rid="b11-etm-0-0-5607" ref-type="bibr">11</xref>). Thus in this study we assumed the breaking strain of the brachial plexus at 30&#x0025;.</p>
</sec>
</sec>
</sec>
<sec sec-type="results">
<title>Results</title>
<p><xref rid="f3-etm-0-0-5607" ref-type="fig">Figs. 3</xref>&#x2013;<xref rid="f6-etm-0-0-5607" ref-type="fig">6</xref> illustrates the distribution and size of strain applied to the brachial plexus in each case. In case 1, the strain was focused on the root of C5. Contact of the root and the roof of the intervertebral foramen were observed that led to an increase of strain in one spot. The maximum level of strain was 21&#x0025; (<xref rid="f3-etm-0-0-5607" ref-type="fig">Fig. 3</xref>). In case 2, the strain was focused on the root of C5 and the upper trunk of the plexus. Lateroflexion of the cervical led to a stretch of the upper trunk of the brachial plexus, applying stress diffusely throughout the upper trunk. The maximum level of strain was 15&#x0025; (<xref rid="f4-etm-0-0-5607" ref-type="fig">Fig. 4</xref>). In case 3, no focus of strain was observed and the stress was applied diffusely throughout the brachial plexus (<xref rid="f5-etm-0-0-5607" ref-type="fig">Fig. 5</xref>). In case 4, strain was focused on the lower trunk of the brachial plexus and the roots of C7 and C8. Abduction of the upper limb led to a stretch of the middle and lower trunk, with strain strongly focused in the middle and lower trunk region. The maximum level of strain was 16&#x0025; (<xref rid="f6-etm-0-0-5607" ref-type="fig">Fig. 6</xref>).</p>
</sec>
<sec sec-type="discussion">
<title>Discussion</title>
<p>Injuries of the brachial plexus frequently lead to significant physical disabilities, psychological distress, and socioeconomic hardship. Excluding brachial plexus injuries in infants during delivery, adult brachial plexus injuries predominantly occur in young men or boys with an average age of 20 to 30 years (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>,<xref rid="b2-etm-0-0-5607" ref-type="bibr">2</xref>,<xref rid="b12-etm-0-0-5607" ref-type="bibr">12</xref>&#x2013;<xref rid="b14-etm-0-0-5607" ref-type="bibr">14</xref>). Injuries could be caused by various mechanisms, including penetrating injuries, falls, powerful sports activity, and motor vehicle accidents. In closed injury, pathological types of injury include avulsion of the nerve at root level or rupture or significant stretch at various levels of the brachial plexus (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>,<xref rid="b7-etm-0-0-5607" ref-type="bibr">7</xref>).</p>
<p>Doi <italic>et al</italic> have reported successful outcomes with double free muscle transfer against complete avulsion of the brachial plexus (<xref rid="b14-etm-0-0-5607" ref-type="bibr">14</xref>). Bertelli <italic>et al</italic> have reported satisfactory results in abduction of the shoulder with spinal accessory nerve transfer to the suprascapular nerve in patients with complete brachial plexus injury (<xref rid="b15-etm-0-0-5607" ref-type="bibr">15</xref>). However, even though several surgical treatment options exist, perfect recovery after complete brachial plexus injury is impossible and physical difficulty is inevitable even after surgery (<xref rid="b14-etm-0-0-5607" ref-type="bibr">14</xref>&#x2013;<xref rid="b16-etm-0-0-5607" ref-type="bibr">16</xref>). Therefore, prevention of the injury becomes important. Analyzing the mechanism of injury could provide further knowledge for preventing the injury.</p>
<p>Considerable number of brachial plexus injuries are caused by closed trauma (77&#x2013;91&#x0025;) (<xref rid="b12-etm-0-0-5607" ref-type="bibr">12</xref>,<xref rid="b17-etm-0-0-5607" ref-type="bibr">17</xref>). Nerve injury in these cases is from traction and compression, with traction accounting for 95&#x0025; of closed injuries (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>). Following traction, any combination of avulsion, rupture, or significant stretch might occur throughout the brachial plexus. However, certain patterns of injuries seem to be substantially prevalent. The supraclavicular region is affected considerably frequently (70&#x2013;91&#x0025;) than the retroclavicular or infraclavicular regions (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>,<xref rid="b2-etm-0-0-5607" ref-type="bibr">2</xref>). The roots and trunks are considerably commonly injured compared to the divisions, cords, or branches. Clinically, traction to the brachial plexus occurs when the head and neck are violently moved away from the ipsilateral shoulder or when the upper limb is abducted violently over the head with significant force. The former results in injury to the upper elements of the brachial plexus (C5, C6 roots or upper trunk), and the latter results in injury to the lower elements (C8, T1 roots or lower trunk) (<xref rid="b1-etm-0-0-5607" ref-type="bibr">1</xref>,<xref rid="b7-etm-0-0-5607" ref-type="bibr">7</xref>,<xref rid="b13-etm-0-0-5607" ref-type="bibr">13</xref>). Similar results were reported in cadaver experiments (<xref rid="b7-etm-0-0-5607" ref-type="bibr">7</xref>). It is assumed that panplexal injuries occur when the force of injury is significantly high. Bertelli <italic>et al</italic> reported the frequency of panplexal injury, upper brachial plexus injury, and lower brachial plexus injury within supraclavicular injuries were 50, 47, and 3&#x0025; respectively (<xref rid="b2-etm-0-0-5607" ref-type="bibr">2</xref>).</p>
<p>Based on this prior knowledge, we conducted stress analysis using 3D-FEM of the brachial plexus. We conducted four patterns of stress based on the patterns of mechanisms of injury described clinically. Nishida <italic>et al</italic> have reported a 3D-FEM of the spinal cord to conduct stress analysis of various clinical conditions, such as ossification of the posterior longitudinal ligament (OPLL) and cervical spondylotic myelopathy (CSM) (<xref rid="b18-etm-0-0-5607" ref-type="bibr">18</xref>,<xref rid="b19-etm-0-0-5607" ref-type="bibr">19</xref>). Imajo <italic>et al</italic> have constructed 3D-FEM of the spinal column in different studies (<xref rid="b3-etm-0-0-5607" ref-type="bibr">3</xref>). However, there are no reports of a complex 3D-FEM of the spine, dura mater, root, and the brachial plexus all in one model till date. The overall objective of this study was to develop a complex 3D-FEM of the spine, dura mater, root, brachial plexus, and other components that stimulate the clinical situation appropriately.</p>
<p>In previous studies of 3D-FEM of the spinal cord by Nishida <italic>et al</italic> and Kato <italic>et al</italic>, the mechanical property of a bovine spinal cord was used in the model since it was impossible to obtain fresh human spinal cord (<xref rid="b18-etm-0-0-5607" ref-type="bibr">18</xref>&#x2013;<xref rid="b20-etm-0-0-5607" ref-type="bibr">20</xref>). Li and Dai noted that it was reasonable to employ the mechanical properties of bovine spinal cord because the brain and spinal cord of cattle and humans demonstrate similar injury changes (<xref rid="b21-etm-0-0-5607" ref-type="bibr">21</xref>). In this study, for the spinal nerve root, we used the mechanical property of a porcine nerve root because it was impossible to obtain fresh human spinal nerve root and there were no previous reports that obtained mechanical property of a bovine spinal nerve root. We believe this is reasonable because Olmarker <italic>et al</italic> reported that human and porcine spinal nerve roots demonstrated significant resemblance in both neural and vascular anatomy (<xref rid="b22-etm-0-0-5607" ref-type="bibr">22</xref>).</p>
<p>In our analysis results, retroflexion and lateroflexion of the cervical, simulating a clinical situation of moving the head and neck away from the shoulder, resulted in the focus of strain in the upper trunk and the roots of C5 and C6. From these results, traction of upper region of the brachial plexus is suggested that corresponds to the clinical findings as reported. Abduction of the upper limb resulted in focus of strain in the lower trunk and the roots of C7 and C8. These results, suggesting traction of lower region, also corresponds to clinical findings. Rotation of the cervical resulted in no focus of strain. We believe this result is appropriate because rotation of the neck applies less force of traction to the nerves compared to the other three situations. Overall, we believe that the validity of this model was demonstrated. From our results, discussing approaches of protection from strong force leading to retroflexion or lateroflexion of the neck, or abduction of the upper limb might be acceptable strategies of preventing brachial plexus injuries.</p>
<p>There are certain limitations in this study. Firstly, since there is no knowledge of threshold value of strain when symptoms of brachial plexus injury appear, a quantitative evaluation using the model was impossible. Thus, this is a qualitative study. Subsequently, we could not evaluate upper limb abduction further than 30&#x00B0;. To express further abduction, we require reproducing the upward rotation of the scapula and the motion of other components of the shoulder which is a future task of this model. Reproducing other tissues around the brachial plexus and the cervical spine, such as muscles and vessels might render the model considerably precise and substantially accurate results might be expected. Finally, the lack of assessment of blood flow of the nerves is a major limitation, because loss of blood flow could be a cause of neurological disorder. Significant further tests might include examination of a considerably complicated combination of motion of the cervical and the upper limb and applying further stress to examine the type of motion that leads to panplexal brachial plexus injury with the smallest amount of stress.</p>
<p>Although certain limitations are mentioned above, overall in this study, we were able to illustrate the pathology of brachial plexus injuries with this complex 3D-FEM. The results of the analysis supported the conventional clinical reports. We believe that this model has a potential of being used in various analysis in the future, including studies to prevent brachial plexus injuries.</p>
<p>We constructed a complex 3D-FEM of the spine, dura mater, spinal nerve root, and the brachial plexus all in one model. Retroflexion and lateroflexion of the cervical resulted in upper region brachial plexus injury and abduction of the upper limb resulted in lower region brachial plexus injury.</p>
<p>We were able to illustrate certain pathology of brachial plexus injury, demonstrating the validity of this model. There is a future potential of using this model for analyzing pathological conditions including the spine and spinal nerve roots.</p>
</sec>
</body>
<back>
<ack>
<title>Acknowledgements</title>
<p>The authors express their gratitude to the cooperation provided by the members of the Medical and Mechanical Engineering Laboratory of Yamaguchi University Graduate School, and graduate students from this Mechanical Engineering Laboratory.</p>
</ack>
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</ref-list>
</back>
<floats-group>
<fig id="f1-etm-0-0-5607" position="float">
<label>Figure 1.</label>
<caption><p>The complex 3D FEM. The spine, dura mater, spinal nerve root, brachial plexus, thoracic cage, and the upper limb was constructed. The spinal nerve roots of C5 to Th1 was extended in proportion to its anatomical form as the brachial plexus.</p></caption>
<graphic xlink:href="etm-15-02-1989-g00.tif"/>
</fig>
<fig id="f2-etm-0-0-5607" position="float">
<label>Figure 2.</label>
<caption><p>Analyzing conditions. (A) The spine was retroflexed 33&#x00B0;. (B) The spine was lateroflexed 23.5&#x00B0;. (C) The spine was rotated 25.5&#x00B0;. (D) The humerus was abducted 30&#x00B0;.</p></caption>
<graphic xlink:href="etm-15-02-1989-g01.jpg"/>
</fig>
<fig id="f3-etm-0-0-5607" position="float">
<label>Figure 3.</label>
<caption><p>Results for retroflexion of the spine. Strain focused on the root of C5. The maximum strain rate was 21&#x0025;.</p></caption>
<graphic xlink:href="etm-15-02-1989-g02.jpg"/>
</fig>
<fig id="f4-etm-0-0-5607" position="float">
<label>Figure 4.</label>
<caption><p>Results for lateroflexion of the spine. Strain focused on the root of C5 and the upper trunk of the plexus. The maximum strain rate was 15&#x0025;.</p></caption>
<graphic xlink:href="etm-15-02-1989-g03.jpg"/>
</fig>
<fig id="f5-etm-0-0-5607" position="float">
<label>Figure 5.</label>
<caption><p>Results for rotation of the spine. No focus of strain was observed and the stress was applied diffusely throughout the brachial plexus.</p></caption>
<graphic xlink:href="etm-15-02-1989-g04.jpg"/>
</fig>
<fig id="f6-etm-0-0-5607" position="float">
<label>Figure 6.</label>
<caption><p>Results for abduction of the humerus. Strain focused on the lower trunk of the brachial plexus and the roots of C7 and C8. The maximum strain rate was 16&#x0025;.</p></caption>
<graphic xlink:href="etm-15-02-1989-g05.jpg"/>
</fig>
<table-wrap id="tI-etm-0-0-5607" position="float">
<label>Table I.</label>
<caption><p>The mechanical property of each components of the model.</p></caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="bottom">Author, Year</th>
<th align="center" valign="bottom">Component</th>
<th align="center" valign="bottom">Young&#x0027;s modulus</th>
<th align="center" valign="bottom">Poisson&#x0027;s ratio</th>
<th align="center" valign="bottom">(Refs.)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Imajo <italic>et al</italic> 2009</td>
<td align="left" valign="top">Bone</td>
<td align="center" valign="top">10,000</td>
<td align="center" valign="top">0.3</td>
<td align="center" valign="top">(<xref rid="b3-etm-0-0-5607" ref-type="bibr">3</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Imajo <italic>et al</italic> 2009</td>
<td align="left" valign="top">Intervertebral disk</td>
<td align="center" valign="top">3.4</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">(<xref rid="b3-etm-0-0-5607" ref-type="bibr">3</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Pal 2014</td>
<td align="left" valign="top">Costicartilage</td>
<td align="center" valign="top">10</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">(<xref rid="b4-etm-0-0-5607" ref-type="bibr">4</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Tencer <italic>et al</italic> 1985</td>
<td align="left" valign="top">Dura mater</td>
<td align="center" valign="top">129</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">(<xref rid="b5-etm-0-0-5607" ref-type="bibr">5</xref>)</td>
</tr>
<tr>
<td align="left" valign="top">Nishida <italic>et al</italic> 2015</td>
<td align="left" valign="top">Spinal nerve root, Brachial plexus</td>
<td align="center" valign="top">2</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">(<xref rid="b6-etm-0-0-5607" ref-type="bibr">6</xref>)</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</article>
