MODELLING DIAPHRAGM KINEMATICS FOR 3D SIMULATION LIVER ACCESS Bello F, Villard P-F and MD Reyes Dept. of Biosurgery and Surgical Technology Imperial College London 10th Floor QEQM, St Mary's Hospital Praed Street, London W2 1NY, UK i. PROJECT AIM Understanding the behaviour of the diaphragm muscle in order to develop a model that simulates with accuracy its movement and the role that it plays on liver displacement. ii. METHODS Research on previous work about diaphragm physiology was focused on its anatomical, histological and mechanical components. The data obtained was analysed and compared to determine viability and validity for its use. Based primarily on the work presented in [2-4] we obtained the main physiological components involved in displacement of the diaphragm and studied how each one of them determines the excursion and the vectors towards which the diaphragm will move. Once all the data was obtained and analysed, we organized it in order to apply it to the previously generated model shown in Fig 1.1.1 by the non-rigid registration technique. Non-rigid registration is a process for determining the correspondence of features between images collected at different times or using different imaging modalities. The correspondences can be used to change the appearance, by rotating, translating, stretching etc., of one image so it more closely resembles another so the pair can be directly compared, combined or analyzed as is further explained in [8]. Fig. 1.1.1 Results of displacement obtained by non-rigid registration of a set of 2 CT Scans in 2 different stages of the breathing cycle. Fig. 1.1.2 Model of a Diaphragm obtained by non-rigid registration of the same CT scans in figure 1.1.1 Before discussing how the vectors and displacement measures of the diaphragm were defined, we will make a brief review of respiratory kinematics focusing in the anatomy of the diaphragm and the role it plays in lung volume capacities and intraabdominal content distribution. RESPIRATORY KINEMATICS The diaphragm is the primary muscle of respiration. It is a narrow, dome-shaped sheet of muscle that, in mechanics, would be called a membrane because of its properties of flexure after an external load is applied. When this membrane contracts, as it happens in the inhaling process, it pushes downward and spreads out, increasing the vertical dimension of the chest cavity and driving up abdominal pressure. This increase in pressure drives the abdominal contents (i.e. the liver) down and out, which, as a consequence, increases the transverse diameter of the chest cavity. Contraction, when used referring to the muscular system, implies the generation of tension by muscle fibers commanded by motor neurons. The product of muscle thickness and stress paralleling the fiber bundles gives the tension in the diaphragm and the contraction, as a product of this tension, would follow the trajectory from its fiber’s origin to its insertions. The muscular fibers may be grouped according to their origins and insertions into three parts; sternal, costal, and vertebral. The sternal part arises by two fleshy slips from the back of the xiphoid process; the costal part from the inner surfaces of the cartilages and adjacent portions of the lower six ribs on each side; and the vertebral part from the aponeurosic arches, named the arcuate ligaments (lumbocostal arches), and from the lumbar vertebrae by two pillars or crura (Fig.1.2) [6]. Fig. 1.2 In this figure, in an axial view from below the muscle fibers inserting into a Central Tendon can be observed. The crura attached to the lumbar vertebrae. The diaphragm muscle attaches in the chest wall (CW) and the fibers radiate inwards inserting into a Central Tendon (CT). The zone of apposition is that part of the diaphragm that is apposed an inner aspect of the rib cage. The pericardium is attached to the CT on its upper surface; the circumferential part is muscular. During inspiration, the lowest ribs are fixed; and from these and the crura the muscular fibers contract and draw downwards and forwards the central tendon with the attached pericardium. In this movement the, curvature of the diaphragm is scarcely altered, the dome moving downwards nearly parallel to its original position and pushing before it the abdominal viscera. The descent of the abdominal viscera is permitted by the extensibility of the abdominal wall, but the limit of this is soon reached. The central tendon, applied to the abdominal viscera, then becomes a fixed point for the action of the Diaphragm, the effect of which is to elevate the lower ribs and through them to push forwards the body of the sternum and the upper ribs. The right cupola of the diaphragm, lying on the liver, has a greater resistance to overcome than the left, which lies over the stomach, but to compensate for this, the right crus and the fibers of the right side generally are stronger than those on the left. During quiet expiration, the diaphragm passively relaxes and returns to its equilibrium position moving around a centimeter or two up and down, average of 1.5 and 1.7 standing and supine respectively [7]. During exercise, it can move more than 10 cm Once the anatomy is understood, we’ll discuss lung volumes and their influence on diaphragm displacement in order to understand how certain measures were assigned and calculated. Lung Volumes The total air content in the lung can be classified as volumes and these can be further divided into capacities as can be observed in Fig. 1.3. The basic lung volumes are Tidal Volume (TV), which is the gas inspired or expired with each breath in quiet breathing. The Inspiratory Reserve Volume (IRV) is the additional air that can be inspired from the end of a normal Inspiration. The Expiratory Reserve Volume (ERV) is the additional air that can be expired from the end of a normal expiration and the Residual Volume (RV) is the air remaining after maximal expiration. Lung can be deducted from these. For example, Total Lung Capacity (TLC) is the sum of RV + IRV + ERV + RV. Vital capacity (VC) is the sum of inspiratory reserve volume plus tidal volume plus expiratory reserve volume (VC= IRV+TV +ERV), the Functional Residual Capacity (FRC) is the air remaining in the lung at the end of a normal expiration FRC= RV + ERV. And finally, Inspiratory Capacity (IC) is the maximum volume of air that can be inspired from an expiratory position (TV + IRV), this capacity is of less clinical significance than the others but, for the aim of this project, it is important to understand how the excursion at some points of the breathing cycle was claculated. Fig. 1.3 Illustration of lung volumes and capacities [9]. MECHANICAL IMPLICATIONS FOR THE DETERMINATION OF VECTORS AND DISPLACEMENT OF THE MODEL DIAPHRAGM In [4] the shape at different lung volumes of a diaphragm was obtained after a 3D reconstruction of MRI obtained images. They studied 4 healthy subjects at 4 different volumes (VLS) in the supine position. This approach allowed the assessment of the diaphragm excursion in its different planes also offered the possibility of quantitative estimations of changes in the total diaphragm surface, area of apposition and area of the diaphragm dome. The interslice gap was of 0.8 mm, flip angle of 90o, and the thickness of the slices 8.0 mm. The procedure was carried out at the following VLS and capacities in the following sequence: RV, FRC, FRC plus one half of inspiratory capacity and TLC. The data observed in fig. 2.1 describes the excursion of the diaphragm at the different VLS and Capacities [4]. The measurements observed are comparable on the ones in other sources, therefore we can confidently base on [4] the displacement applied to our model. In Fig. 2.1 we can observe the average diaphragm silhouettes at the 4 different lung volumes mentioned above. A. left midsagittal plane, B: midcoronal plane and C. right midsagittal plane. The solid circles show the costophrenic angles. Fig 2.1 Diaphragm silhouettes at the 4 different lung volume. A. left midsagittal plane, B: midcoronal plane and C. right midsagittal plane. In A and C we can observe that the posterior zone doesn’t show a significant displacement, while the anterior apposition zone moves forward and upward along the costophrenic angles in function of the contraction of the fibers of the diaphragm muscle, meaning that the ribacage will also move in function of that contraction at the end on the inhalation and going to the former state at the end of the exhalation. We can observe as well that the right diaphragmatic dome has a relative lesser displacement compared with the left dome, but this can be due to the surrounding anatomy, primarily the liver . Meaning the right dome is normally higher than the left one, and the displacement required to achieve the same height is less. The lateral displacement of the diaphragm, as shown in C is of much lesser extent compared with the front and upward excursion, but not of less significance for modelling the diaphragm kinematics. Finally, as stated in the discussion of diaphragm anatomy, the displacement upward and downward of the diaphragm happens in a parallel manner at the central tendon and leaflets areas that are extensions of the central tendon to each side of the diaphragm (see fig. 1.2). This information is of great importance for the assignment of vectors and displacements on the model, as well as the function of each component The action of the diaphragm is complex and the details of its shape and displacement depend on its attachments and surrounding structures. iii. DISCUSSION For the development of the model of the diaphragm and its motion three main aspects have been taken into account: anatomy, excursion displacement and its vectors. The anatomy, described previously, is of interest to infer the physiological components that will help to determine the motion of the diaphragm, for example, when we know where and how the muscle bundles origin and insert, we can assign the muscle stretching extension and, if that is the case, leave the apposition zone motionless. The knowledge that the vertebral part of the diaphragm originates from the arcuate ligaments and crura, both aponeurosic tissue, lead us to the inference that it is a fixed point, as well as the central tendon, but with the difference that the former will not show displacement, while the latter will displace upwards and downwads (Z-axis) in function of the fiber bundles surrounding it; but, being the one that carries the heart in a much lesser extent than the right and left leaflets. As inferred from Fig. 2.1, the average excursion of the diaphragm on the Z-axis is of 17 mm on a supine position, which has been validated by other sources [2,4,10]. For the other axes however, X-axis corresponding to lateral and Y-axis for front and back, the displacements, even when parallel to the origin, are not comparable to the displacement of the dome. We applied the measures obtained in [4] to designate the displacement, combined with the information obtained at the anatomy review and applied to the vectors and lines of tensions described in [3] and Fig 3.1, 3.2 and 3.3. Fig. 3.1 We can observe the directions of lines of tension from centers of hemidiaphragm domes to zone of apposition. The lines of tension do not proyect, except in narrow isthmus, between spine and xiphoid process. Therefore, tension in one hemidiaphragm is not well transmitted to the other side maintaining its relative independent, but coordinated movement. The blank area, corresponds to the fixed point, the Central Tendon. Fig. 3.2 Diagram of the interaction between tension in medial crural fibers in sagittal plane and tension in transverse direction over domes. Tension across the saddle in medial crura (open arrows), like tension in a laundry line, can make the saddle act as an anchor for fibers pulling laterally and upward over domes (solid arrows) Fig 3.3. Vector of tension exerted by the diaphragm on the lower margin of the ribcage. Shaded area, zone of apposition (fixed area) with dashed line at its upper boundary. As mentioned previously, we obtained excursion and displacement vectors to apply to the model generated using Non-rigid registration (Fig 3.4). From this model we had the nodes or coordinates which will be then be assigned with displacements in function of X, Y and Z vectors. Fig 3.4 Diaphragm model generated by non-rigid registration expressed in “displacement nodes” The nodes of this model can be presented in tabular format as shown on Table 3.1. With this database we created a model that can be manipulated and generated a full grind in order to determine anatomical landmarks with more accuracy Fig 3.5. Table 3.1 Model display on an data source worksheet The anatomical landmarks and the coordinates of Fig 3.5 were then matched in order to create a new data source to which Displacement Vectors and Excursion in function of X, Y and Z (Table 3.2) could be assigned. Fig 3.5 Matching the model created based on our data source worksheet and the anatomical Pattern. Final results determined 16 zones or anatomical landmarks for Displacement and Excursion assignment (see fig 3.6): 1. 2. 3. 4. 5. 6. 7. 8. Anterior Apposition Zone Left Apposition Zone Right Apposition Zone Crura Central Tendon Left Crus Right Crus Left Tendon 9. 10. 11. 12. 13. 14. 15. 16. Right Tendon Anterior Left Muscle Anterior Right Muscle Anterior Central Muscle Posterior Central Muscle Posterior Right Muscle Posterior Left Muscle Posterior Apposition Zone A brief analysis of the anatomy and histology took place for each Landmark and the displacements were calculated. The results are illustrated on fig 3.6. Fig 3.6 Diaphragm Divided in zones for the assignment of Displacement Vectors and excursions as a function of anatomical, histological and phsysiological components. Anterior Apposition Zone: Even when considered as a fixed point, due to the lack of intrinsic motion and inability to full stretching being formed of aponeurosic tissue, it moves upfront as a consequence of the muscle fiber bundles attached to it, generating a pulling force along with the ribcage to the front. Left Crus and Right Crus: Sharing the same properties as the Anterior Apposition zone, but presenting a slight displacement to the Left and Right correspondingly following the extension of the ribs attached. Crura: Being also aponeurosic and completely attached to the spine it becomes a fixed point on every direction. Central Tendon: Being the insertion for the fibers radiating inwards from the CW and attached to the pericardium on its upper surface, it becomes a Fixed point mainly in the X and Y directions; showing displacement only in Z axis in function of the muscle stretching around it. Left and Right Tendons of Leaflets: Share the same histological properties as the Central Tendon. They have an excursion in X, Y and Z axis as a result of the muscle fiber applying a pulling force on them in the direction of the muscle insertions on the CW. Muscles (Anterior, Posterior; Left and Right): Tissue specialized in stretching in every direction as a product of the energy applied to the fibers. The direction assigned for the model mainly corresponds to their given names. Posterior Apposition Zone: Being a continuum of the Crura, spreading to the left and righ following the ribs, it shares the same histological properties and becomes a fixed point, differentiating from the Anterior apposition zone by the fact that these ribs are not affected by the pulling force of the diaphragm and show no real intrinsic or extrinsic displacement. iv. RESULTS The displacement vectors were assigned and ordered to a complete set of 5 405 nodes as follow (table 4.1). Table 4.1 Table only showing the assigned displacements and vectors to 20 of the 5 405 total nodes. Finally, the vectors displacement were “translated” and applied to the original model on which the real displacement could be later visualized in a more global manner (fig 4.1). Fig 4.1 Graphic showing the movement of the diaphragm with colours corresponding to the amplitud of the displacements A summary of the displacements assigned to each zone can is described in the following tables: Description by Zones ZONE AXIS X MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1 1 -0,004 0,31 0,55 MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 4,5 5 4,77 0,033 0,18 MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 5 6 5,28 0,1 0,32 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1 -1,7 -1,8 0,01 0,11 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,1 2 1,17 0,23 0,48 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,1 3 0,55 0,51 0,71 Y AP ZONE Z AP ZONE LEFT AP ZONE RIGHT POST AP ZONE CENTRAL TENDON MIN DISPLACEMENT 1,7 MAX DISPLACEMENT 2 MIN DISPLACEMENT 0,1 MAX DISPLACEMENT 2 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT 1,89 Y AVERAGE DISPLACEMENT 0,54 Z AVERAGE DISPLACEMENT 0 3 0,51 MIN DISPLACEMENT 0 MAX DISPLACEMENT 0 MIN DISPLACEMENT 0 MAX DISPLACEMENT 0,25 MIN DISPLACEMENT 0 MAX DISPLACEMENT 0,35 X AVERAGE DISPLACEMENT 0 Y AVERAGE DISPLACEMENT 0,16 Z AVERAGE DISPLACEMENT 0,13 VARIABILITY 0,014 STANDARD DEVIATION 0,12 VARIABILITY 0,33 STANDARD DEVIATION 0,57 VARIABILITY STANDARD DEVIATION 0,39 0,63 VARIABILITY 0 STANDARD DEVIATION 0 VARIABILITY 0,01 STANDARD DEVIATION 0,11 VARIABILITY 0,02 STANDARD DEVIATION 0,13 X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 1,25 -0,05 0,33 0,57 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,25 2 1,02 0,44 0,66 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 10 14,5 12,56 2,53 1,59 AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 0 0 AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 0 0 MIN DISPLACEMENT MAX DISPLACEMENT -1,25 X MIN DISPLACEMENT MAX DISPLACEMENT 0 0 Y CRURA MIN DISPLACEMENT MAX DISPLACEMENT 0 0 Z MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 2 0,16 0,14 0,37 LEFT CRUS RIGHT CRUS LEFT TENDON RIGHT TENDON MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1,5 0 -0,59 0,36 0,6 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 0 0 0 0 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 1,5 0,27 0,24 0,49 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 1,5 0,38 0,12 0,35 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 0 0 0 0 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 1,5 1,5 0,49 0,47 0,68 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -2 1,4 -1,7 0,05 0,22 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 2 0,53 0,24 0,49 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 13 15 14,22 0,35 0,59 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 1,4 2 1,78 0,03 0,19 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0 2 0,63 0,2 0,44 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 13,2 16 15,37 0,87 0,93 RIGHT ANTERIOR MUSCLE LEFT ANTERIOR MUSCLE ANTERIOR CENTRAL MUSCLE POSTERIOR CENTRAL MUSCLE X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 1,5 1,19 0,02 0,14 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 2,4 3,5 2,79 0,12 0,34 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 3 15 9,55 15,27 3,91 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1,5 -1,1 -1,35 0,02 0,15 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,1 1 0,63 0,16 0,4 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,75 2 1,54 0,27 0,52 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1 1 -0,03 0,16 0,41 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 2,2 5 4,16 0,72 0,85 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 6 14,5 9,2 7,31 2,7 MIN DISPLACEMENT MAX DISPLACEMENT 1 MIN DISPLACEMENT MAX DISPLACEMENT X AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1,6 1,6 0,21 1,6 1,28 MIN DISPLACEMENT MAX DISPLACEMENT Y AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,25 0,6 0,52 0,02 0,11 MIN DISPLACEMENT MAX DISPLACEMENT Z AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 10 14,5 10,41 0,94 0,97 X RIGHT POSTERIOR MUSCLE MIN DISPLACEMENT MAX DISPLACEMENT 0,7 1,4 AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,97 0,08 0,28 AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,81 0,28 0,53 Y MIN DISPLACEMENT MAX DISPLACEMENT 0,3 1,8 Z MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 5 14 8,2 5,69 2,38 MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION -1,3 -0,2 0,61 0,15 0,39 MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 0,5 1,8 1,01 0,2 0,45 X LEFT POSTERIOR MUSCLE Y Z MIN DISPLACEMENT MAX DISPLACEMENT AVERAGE DISPLACEMENT VARIABILITY STANDARD DEVIATION 4 14 8,03 5,62 2,37 Further research should be done to prove the feasibility of this methodology and standardization of this displacement. 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