UNIBODY ENDOSKELETAL TRANSTIBIAL PROSTHETIC DEVICES AND DIGITAL FABRICATION WORKFLOW

Abstract

A unibody transtibial prosthetic device includes a socket personalized for a specific patient’s residual limb. A pylon extends from the socket, the pylon being a unitary polymer structure of interconnected elongated supports having open spaces therebetween. The device also includes a foot-ankle complex, the foot-ankle complex being a unitary polymer extending from the pylon, the foot and ankle unitary structure being shaped to provide multi-axial dynamic flex to enable dorsiflexion, plantar flexion, inversion and eversion motion for smooth symmetric gait performance and energy capture and return. The socket, pylon and foot-ankle complex are portions of a unibody.

Claims

1. A unibody transtibial prosthetic device, comprising: a socket configured to attach to a residual limb; a pylon extending from the socket, the pylon being a unitary polymer structure of interconnected elongated supports having open spaces therebetween; and a foot-ankle complex, the foot-ankle complex being a unitary polymer extending from the pylon, the foot and ankle unitary structure being shaped to provide multi-axial dynamic flex.

2. The unibody transtibial prosthetic device of claim 1, wherein the socket, pylon and foot-ankle complex are a unitary single piece.

3. The unibody transtibial prosthetic device of claim 1, wherein the unitary single piece comprises a single polymer.

4. The unibody transtibial prosthetic device of claim 1, wherein the unitary single piece comprises multiple materials with different stiffnesses.

5. The unibody transtibial prosthetic device of claim 1, wherein the pylon is shaped and dimensioned to be within extended external boundaries of the residual limb.

6. The unibody transtibial prosthetic device of claim 1, wherein the interconnected elongated supports define a central open cavity and curve around the open cavity.

7. The unibody transtibial prosthetic device of claim 6, wherein the interconnected elongated supports and open spaces therebetween model a mirrored boundary of a contralateral transtibial leg portion of a patient.

8. The unibody transtibial prosthetic device of claim 6, wherein the central open cavity has a decreasing diameter from the socket to the foot-ankle complex.

9. The unibody transtibial prosthetic device of claim 1, wherein the interconnected elongated supports and open spaces define an endoskeleton shape complementary model of a contralateral transtibial leg portion of a patient.

10. The unibody transtibial prosthetic device of claim 1, wherein the pylon is formed of thermoplastic.

11. The unibody transtibial prosthetic device of claim 1, wherein the foot-ankle complex comprises a split ankle structure.

12. The unibody transtibial prosthetic device of claim 11, wherein the split ankle structure comprises an s-shaped posterior portion and s-shaped anterior portion separated from each other by a gap extending from terminal portion of the s-shaped anterior portion to a sole portion.

13. The unibody transtibial prosthetic device of claim 12, wherein the s-shaped posterior portion is solid and thicker than the s-shaped anterior portion.

14. The unibody transtibial prosthetic device of claim 13, wherein an upper portion of the s-shaped posterior portion is unitary with lowest portion of the pylon.

15. The unibody transtibial prosthetic device of claim 13, wherein the s-shaped anterior portion comprises one or more pass-through openings.

16. The unibody transtibial prosthetic device of claim 11, wherein the sole portion comprises a split toe and a split heel.

17. The unibody transtibial prosthetic device of claim 1, wherein the foot-ankle complex comprises a central strip of stiffer material surrounded by more flexible material.

18. The unibody transtibial prosthetic device of claim 1, wherein an outer surface of the entire transtibial prosthetic device is flexible material and includes a core of stiffer material.

19. A patient specific workflow method for producing a unibody transtibial prosthetic device, the workflow comprising: acquiring patient data via imaging and/or scanning; constructing a 3D model from the patient data; translating the 3D model to 3D printable design of a unibody transtibial prosthesis; 3D printing the unibody transtibial prosthesis.

20. The method of claim 19, wherein the acquiring patient data comprises imaging a contralateral limb and residual limb..

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] FIG. 1A is a perspective view of a preferred embodiment unibody transtibial prosthetic device;

[0017] FIG. 1B is a flowchart of a preferred workflow for providing a custom fit unibody transtibial prosthetic device of FIG. 1A to a patient via imaging and 3D printing;

[0018] FIG. 2 shows a process for generation of a patient fit socket portion;

[0019] FIGS. 3A-3C illustrate respectively a 3D Scan of a tibial region of a contralateral healthy leg, topology optimization of pylon region and a smooth version of the optimized pylon;;

[0020] FIGS. 4A-4C illustrate respective forefoot, heel and u-axis loading conditions;

[0021] FIGS. 5A & 5B illustrate a process for the design of a unibody transtibial prosthetic device based upon a patient’s contralateral healthy limb;

[0022] FIG. 6 illustrates a preferred multi-material foot/ankle complex of the invention;

[0023] FIG. 7 illustrates a preferred multi-material unibody transtibial prosthetic device of the invention with a modified socket.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0024] A preferred embodiment is a unibody transtibial prosthetic device. The preferred device provides an endoskeletal unibody design, bioinspired aspects, and foot design that provides a smooth, symmetrical gait and energy recapture using a purely passive structure and without sliding connections. Another preferred embodiment is a patient-specific design workflow. The workflow includes a series of digital scanning, design, and fabrication steps that enable lower cost, higher precision, better comfort, and a more robust prosthesis to be provided compared to conventional molding, sculpting, and assembly processes. A preferred embodiment is a 3D printed prosthetic limb with a custom fit socket fabricated from a digital model of the residual limb.

[0025] Preferred embodiments of the invention will now be discussed with respect to drawings and experiments. Broader aspects of the invention will be understood by artisans in view of the general knowledge in the art and the description of the experiments that follows.

[0026] FIG. 1A shows a preferred embodiment unibody transtibial prosthetic device 100. The prosthetic device 100 includes a socket 102 configured to attach to a residual limb. A pylon 104 extends from the socket 102. The pylon 104 is a unitary bioinspired truss structure of interconnected elongated supports 106 having open spaces 108 therebetween. It is preferably made from thermoplastic material. A foot-ankle complex 110 is a unitary polymer extending from the pylon 104. The foot-ankle unitary structure 110 is shaped to provide multi-axial dynamic flex to enable dorsiflexion, plantar flexion, inversion and eversion movement for smooth symmetric gait performance.

[0027] It is preferred that the socket 102, pylon 104 and foot-ankle 110 structures are a unitary single piece. Single and multiple materials with different properties in different regions can be used to print a unitary single piece with tailored stiffnesses in different regions. Through the combination of 3D scanning and topology optimization, the pylon 104 can be shaped and dimensioned to be within extended external boundaries of the residual limb and can be very lightweight with the total amount of polymer material in the pylon 104 being minimized to achieve a given targeted K-level of use. Further, the truss structure formed by interconnected supports and nodes and blended with the ankle-foot complex provides a dynamic, multiaxial response during the gait cycle with energy capture and release achieved through the entire shin-ankle-foot. The optimization process for the pylon 104 includes the example discussed below with respect to FIGS. 3A-3C.

[0028] The entire prosthesis can be very lightweight but still be for a K-level 2 through K-level 4. As seen in FIGS. 1, the interconnected elongated supports 106 have connection node portions (“nodes”) 112 and define a central open cavity and curve around the open cavity. That is, the interconnected elongated supports 106 gently curve or arc into the nodes 112 and a cavity exists between the interconnected elongated supports 106 along a central longitudinal axis of the pylon 104. The central open cavity has a decreasing diameter from the socket 104 to the foot-ankle complex 110 in a manner resembling the decreasing size of a human transtibial leg portion. An outer imaginary boundary of the interconnected elongated supports and nodes 112 follows the mirrored shape of the contralateral transtibial leg portion of a patient. With imaging and 3D printing methods of making discussed below, the mirrored model is based upon the 3D scan data from the contralateral transtibial leg portion of a patient, if available. If not available, then another embodiment is a pylon structure that uses starting geometry of a transtibial leg portion from a database. The database model can be selected based on weight, activity level and aesthetics, among other things, and will be scaled to appropriately fit the specific patient. Generally, the interconnected elongated supports 106 and open spaces 108 can define a bioinspired truss structure with an outer boundary that follows the mirrored model of the sound contralateral leg of the patient.

[0029] The preferred material for the pylon 104 and for the entire prosthesis 100 is a 3D printable thermoplastic. With regard to the pylon 104, the thermoplastic material permits alignment adjustments in the heat zone 128 during a patient fitting, if necessary. In addition, the fit of the socket can be modified via thermoforming any specified region where pressure needs to be increased or decreased. However, a preferred embodiment is a prosthesis that is aligned properly during the design phase and does not require any modifications post-fabrication, and present methods provide a better chance of a patient specific prosthetic that can be used without any post-fabrication methods. While the leg can very closely model a missing leg of a patient, it will be the rare case where some adjustment is not needed. Advantageously, due to the endoskeletal design, by heating the pylon to a pliable temperature, adjustments can be made during a final fitting of a patient.

[0030] The foot-ankle complex 110 includes an s-shaped posterior portion 114 and s-shaped anterior portion 116 separated from each other by a gap 118 extending from a terminal portion 120 of the s-shaped anterior portion 116 to a sole portion 122. This defines a split ankle portion that gives a dynamic response with energy recapture. The gap is preferably small in its upper portion and widens to a teardrop profile shape in its lower portion 118.sub.L. An upper portion 124 of the posterior s-shaped portion 114 can be unitary with a lowest portion of the pylon 104, essentially forming a base of the pylon 104 with the pylon 104 and foot-ankle complex 110 forming a unitary single piece structure with each other and also with the socket 102. To handle more force through the pylon 104 and foot-ankle complex 110, the s-shaped posterior portion 114 can be solid and substantially thicker than the s-shaped anterior portion 116, which itself can include one or more pass-through openings 126. The sole portion 122 may include a split toe 130 and a split heel 132. The split toe and heel are useful for uneven terrain, where exaggerated inversion and eversion is beneficial. Overall, the unitary foot and pylon portions have no mechanical linkages, joints or sliding mechanisms, such as ball-socket connections or multi-link pinned connections, which will result in long-term durability.

[0031] The prosthesis can meet all requirements for government run health systems or insurance carriers. As an example, the United States Medicare program uses “L Codes, such as the following examples.

[0032] L5301 - below knee, molded socket, shin, SACH foot, endoskeletal system (base code). The present prosthesis 100 meets this and L5637 - addition to lower extremity, below knee, total contact socket has total contact surface against residual limb.

[0033] L5645 - addition to lower extremity, below knee, flexible inner socket, external frame inner socket pockets that add flexibility and increase comfort, prominent bone projection can be met with tailored soft areas in the socket.

[0034] L5647 - addition to lower extremity, below knee suction socket. The socket can include a one-way expulsion valve with a suspension sleeve to create a suction fit.

[0035] L5671 - addition to lower extremity, below knee / above knee suspension locking mechanism (shuttle, lanyard or equal), excludes socket insert pin lock. Generally, the socket can be fabricated to work with any conventional attachment scheme, including suspensions.

[0036] L5940 - addition, endoskeletal system, below knee, ultra-light material (titanium, carbon fiber or equal). The present pylon and foot/ankle structure can be very lightweight. The open endoskeleton style components minimize material used, and can also use very light weight. In addition, the use of a single unitary one piece design can eliminate metals used in conventional pylons and attachments between components.

[0037] L5910 - addition, endoskeletal system, below knee, alignable system. As described below, preferred embodiment prosthesis can be adjusted via a thermoforming alignment process.

[0038] L5981 - all lower extremity prostheses, flex-walk system or equal dynamic response integrated pylon foot. The present preferred unitary prosthesis meets this code.

[0039] For a patient-specific fitting and fabrication method, a preferred method is illustrated in FIG. 1B. Patient image acquisition 150 can include photos, scan data or both, with the purpose of creating a digital twin of the patient. Photos can even be taken from a smart phone, which was demonstrated experimentally in the successful fabrication of a patient-specific prosthesis. A 3D model is next created 152 from the images and/or scan data. A preferred modelling is conducted from the photo data using structure from motion (SfM) techniques or with a structured light software (SL). For SfM, see C. Bregler, A. Hertzmann, and H. Biermann, “Recovering non-rigid 3d shape from image streams,” Proceedings IEEE Conference on Computer Vision and Pattern Recognition. CVPR 2000 (Cat. No.PR00662); F. Dellaert, S. Seitz, C. Thorpe, and S. Thrun, “Structure from motion without correspondence,” Proceedings IEEE Conference on Computer Vision and Pattern Recognition. CVPR 2000 (Cat. No.PR00662). For SL, J. Geng, “Structured-light 3d surface imaging: a tutorial,” Advances in Optics and Photonics, vol. 3, no. 2, p. 128, 2011; S. Dunn, R. Keizer, and J. Yu, “Measuring the area and volume of the human body with structured light,” IEEE Transactions on Systems, Man, and Cybernetics, vol. 19, no. 6, p. 1350-1364, 1989. In a preferred embodiment, a smartphone with a facial recognition camera, such as the Apple iPhone XR TrueDepth Camera, is used to scan the patient using an app such as COMB. This enables a low-cost, highly mobile solution to produce a digital twin of the entire patient in STL format. In another embodiment, the facial recognition camera is used to capture only the regions of interest, such as amputated limb and foot and calf sections of their contralateral limb. In another embodiment a structured light scanner is used to scan either the entire patient or specific regions of interest necessary to design the unibody prosthetic limb. In another embodiment, a series of photographs are taken using any digital camera, such as the rear facing camera on any smartphone and reconstructed using the photogrammetry technique to create a point-cloud digital twin of the patient.

[0040] G-code for printing (print model) is generated 154 from the 3D model. This is accomplished via slicing software. Example settings used in experiments included a nozzle size 1.4 mm, layer height 0.7 mm, print speed 2000 mm per minute, nozzle temperature (varies by material between 240-280° C.), bed temperature (varies by material between 90-140° C.), chamber temperature (varies by material between 70-90° C.), infill 100% density. These settings are used in the slicing software, regardless of which software is used. These settings control how the printer behaves during manufacturing. Artisans will recognize adjustments based upon materials being printed. The prosthetic is then printed via 3D printing 156, which can be printing remotely and shipping to a fit practitioner/patient or sending print data for printing near the fit practitioner/patient. This allows a patient to be imaged where they reside and also receive a prosthesis at that location. Testing and adjustment 158 includes the patient testing the prosthetic for fit and performance. A fitting practitioner can make minor adjustments to alignment and socket fit through thermoforming. In a preferred embodiment, a heat gun is used to raise the temperature of the heat zone 128 until it is pliable (above the material’s glass transition temperature and below the material’s melting temperature, checked using a handheld laser temperature gauge). In another embodiment, radiative heating is used to raise the temperature of the heat zone 128 until it is pliable. Other methods such as using a torch/flame may lead to difficulty controlling heat distribution but are still possible methods for heating the heat zone 128. Alignment should be controlled using an alignment jig that would clamp the ankle in place and allow for controlled rotation and translation in the sagittal, frontal, and transverse planes. Rotation should be controlled to less than one degree and translation precision to one millimeter. The socket is heated locally to adjust fit in a specific area where pressure may need to be relieved or increased against the patient’s amputated limb. Adjustments to fit within the socket are achieved manually using a sturdy wooden bar with a rounded end that is pressed into the region of interest to increase or relieve pressure on the patient’s amputated limb. As a note, thermoforming is a common practice in traditional prosthetic clinics as many check sockets, socket liners, etc. are thermoplastics. However, traditional prosthetic sockets often employ composite materials so fit cannot be adjusted. This gives us an advantage because we can easily modify our socket if a patient experiences discomfort either during initial fitting or during a follow up appointment during the device lifetime. The general design of the foot can be standard, i.e. have the S shaped posterior and anterior sections, the split design starting narrow and going to a teardrop shape. However, the actual dimensions of the foot are customized for every patient based on their weight, activity level, use-case, etc.

[0041] The FIG. 1B method permits very convenient service and business models. For example, a patient can receive a functional prosthetic without ever physically meeting with a traditional specialist. In areas where no skilled prosthetists are available, a non-specialized practitioner should be able to make minor adjustments to the printed limb via the thermoforming process. It is always preferred to have a licensed prosthetist do the fitting and walking test, but in many parts of the world this isn’t feasible and a prosthesis of the invention provides a workable alternative in such situations.

[0042] In preferred fitting and fabrication methods of the invention, imaging of a patient can be conducted remotely, and the data can be sent to the designer and 3D printing facility. Image data of a contralateral limb and portions of a residual limb are used with a preferred method implemented in software to create an optimized patient-specific printed prosthesis in accordance with FIG. 1A. Additional preferred features of the method of FIG. 1B will be understood by artisans with reference to the following discussion of experiments that show imaging, printing, fitting and testing of prototype prostheses of the invention.

[0043] 3D printing can be generally considered an additive fabrication process. Other additive processes can be used. Additive processes should be able to deposit thermoformable materials and preferably allow more than one material in a single deposition, e.g., material extrusion, powder bed fusion and material jetting techniques. Material extrusion is the preferred method. Fused filament fabrication (FFF) is a preferred material extrusion technique.

[0044] The prosthesis can be made from various materials, while a thermoplastic is preferred for adjustment. Typical polymers used for 3D printing are; ABS, PLA, PC, PETG, Nylon, PEI and PEEK. Generally, any material that can be deposited and solidified can be used to form a prosthesis by the present methods. Preferred materials include thermoplastic pellets, filaments, and resins, and may contain additives such as foaming agents, fibers, and particles. Relevant processing temperatures range from 200-500° C. The material must adhere to a previous layer with a sufficient bond strength and should be reformable through the application of heat. The selected material preferably exhibits high elongation and excellent interlayer bonding. High elongation means an ultimate elongation of greater than 150%. Excellent interlayer bonding means high interlayer bonding leading to a tensile strength perpendicular to layers no less than 60% of the tensile strength of the material.

[0045] The 3D printing 156 can advantageously be multi-material printing to produce a unitary single-piece device. Use of multiple materials allows tailoring stiffness locally in the single print, which can improve gait performance, comfort, strength. For example, sensitive contact areas of the socket (see FIG. 7, area 1204) can be made softer than other regions to improve comfort. Another example includes a core-shell pattern where a 1-5 mm shell of the outer surface of the entire unibody (or any of the three portions) is flexible material and the core material is stiffer. Materials such as thermoplastic elastomers, thermoplastic urethans, unfilled nylons and polypropylene, among others, would act as the flexible material, where materials such as chopped carbon or glass fiber filled nylons or polypropylenes, polycarbonate, PEEK, and PEI, among others, could act as the stiff material.

Experimental Data

[0046] Experiments demonstrated cost-effective 3D modeling of a patient’s damaged limb through the use of smartphones and photogrammetry techniques. Some testing used separate components as a precursor to unitary single-piece transtibial prosthesis.

Patient Specific Workflow

[0047] A preferred workflow starts with a scan of amputee via the Comb scanner app (Comb O&P, Chardon, OH) which uses the facial-recognition camera in smartphones to generate 3D models of the patient. Scan data is supplemented by a patient measurement form and used to design a personalized prosthetic limb that follows the external shape of their mirrored contralateral limb. The digital design process for every device is done under the supervision of a certified prosthetist (CPO). The socket is created using scan data and patient measurements with prosthetic design software Neo (Rodin4D, Italy). The pylon with its present bioinspired truss structure is created using topology optimization software nTopology (nTopology, New York, NY) controlled to implement a pylon of the invention having a unitary bioinspired truss structure of interconnected elongated supports. The multi-axial dynamic foot-ankle complex is created in Fusion360 (Autodesk, San Rafael, CA) controlled to implement a foot-ankle complex of the invention that provides multi-axial dynamic flex. Finally, alignment and blending of the socket, pylon, and foot-ankle complex into the present unitary single-piece transtibial prosthesis is done in Meshmixer (Autodesk, San Rafael, CA). The finished model is sliced into G-code the 3D printer can interpret using Simplify3D (Simplify3D, Cincinnati, OH). The Fused filament fabrication (FFF) manufacturing process uses engineering grade thermoplastics to produce a strong and durable endoskeletal prosthetic device. The UniLeg is shipped to a prosthetist or physician who helps the amputee put on their personalized limb and confirms a smooth, symmetric gait. If any modifications are desired, thermoforming can be used to adjust fit and alignment.

Imaging and Modelling

[0048] Pervasively available smartphone imaging technology is useful to create 3D models of the patient. The Comb scanner app (Comb O&P, Chardon, OH) uses the front-facing facial-recognition camera available on many smartphones, e.g. the TrueDepth camera on iPhones (Apple, Cupertino, CA). Imaging can be performed on-site anywhere in the world and the scan data and measurement form are then sent to a fabricator (or a cloud operated by the fabricator). At a minimum, scans are taken of the amputee’s residual limb and contralateral side.

Socket Design

[0049] Scan data from the amputee’s residual limb is used as the starting shape for the socket, in a process illustrated in FIG. 2. Modifications are made with Neo (Rodin4D, Italy) to properly distribute load and prevent pressure spots. The process is as follows: (1) the mesh is cleaned, smoothed, and the volume is reduced by 3% (a1,2); (2) a 2 cm wide by 1 cm deep slot is carved for the patellar tendon bar, which is a primary load-bearing feature, and the medial-lateral area is compressed by 2% (b1,2); (3) socket trim lines are delineated to allow proper knee mobility and the socket walls are thickened to 4 mm (c); (4) an extruded section at the distal end is created to house the shuttle-lock (d). Modification values can change from patient to patient, and this process can benefit from guidance by a CPO.

Pylon Design

[0050] A pylon of the invention is designed to be strong and 3D printable, while reducing material use to reduced cost and manufacturing time. The pylon is expected to withstand a series of compressive and torque loads based on patient weight and activity level and following ISO standard 10328. Topology optimization (TO) software nTopology (nTopology, New York, NY) is used to generate an optimal truss structure consistent to provide the unitary bioinspired truss structure of interconnected elongated supports having open spaces therebetween. The mirrored model of the transtibial section of the amputee’s contralateral limb is used to generate the pylon. In cases where a bilateral amputee doesn’t have a sound limb, a generic transtibial limb can be selected from a database and then reoriented and scaled to fit the patient. Model preparation for TO requires the definition of design space (FIG. 3A), where topology is optimized, and boundary condition regions (top and bottom disks in FIG. 3A), where loads and constraints are placed. Topology optimization is performed with the objective of maximizing stiffness.

[0051] The resultant mesh (FIG. 3B) was exported as an STL file and then imported into mesh modeling software Meshmixer (Autodesk, San Rafael, CA) to be smoothed and scaled to the correct dimensions. The final personalized bio-truss structure of the invention, FIG. 3C, has an outer contour that follows that of the mirrored contralateral limb of the specific amputee. A significant advantage of the endoskeletal truss structure is that it can deform without buckling, which enables adjustment of alignment by thermoforming.

Ankle-Foot Complex

[0052] The foot-ankle complex is designed to provide a multi-axial dynamic response to enable dorsiflexion, plantar flexion, inversion and eversion motion for smooth symmetric gait performance and energy capture and return, which is illustrated in FIGS. 4A-4C. As discussed above, the foot-ankle complex includes s-shaped posterior and s-shaped anterior sections that are separated from each other by a gap. This defines a split ankle that enables plantar flexion during heel-strike, demonstrated in FIG. 4C. As the person transitions to mid-stance, FIG. 4B, the split ankle gap closes, providing stability. Transitioning to terminal stance, the entire foot-ankle complex coils to capture energy, FIG. 4A, which will be released to drive forward into the next gait cycle. The top of the ankle-foot complex is blended into the base of the pylon, which provides a smooth transfer of load from the ground through the dynamic pylon up to the socket. The sole portion may include a split toe and split heel. The split toe and heel are useful for uneven terrain, where exaggerated inversion and eversion is beneficial.

Digital Alignment and Integration

[0053] The socket, pylon, and foot-ankle complex are aligned and blended into the single-piece UniLeg in Meshmixer (Autodesk, San Rafael, CA), as illustrated FIGS. 5A and 5B. Alignment is guided using the mirrored model of the contralateral limb. A cylinder is drawn that runs through the middle of the mirrored leg to align the knee and ankle positions, FIG. 5A. The resulting unibody design, FIG. 5B, can be fully printed in one piece. The only commercial component used is a shuttle lock and pin system to secure the residual limb in the socket. If necessary, an on-site prosthetist or physician can make minor adjustments to alignment and socket fit through thermoforming. A heat gun is used to raise the temperature of the pylon until it is pliable, which allows manual rotation and translation in the sagittal, frontal, and transverse planes. Adjustments to fit within the socket are achieved by heating the region of interest to pliability and then using a sturdy wooden bar with a rounded end that is pressed into the region of interest to increase or relieve pressure on the patient’s residual limb.

[0054] Thermoforming is a common practice in traditional prosthetic clinics as many check sockets are thermoplastics. However, traditional prosthetic sockets often employ composite materials so fit cannot be adjusted. The inventive prosthesis provides a great advantage as it can be easily modified via thermoforming if a patient experiences discomfort either during initial fitting or during a follow up appointment during the device lifetime.

Validation With a Patient Fitting

[0055] A patient was fitted with a unibody transtibial prosthetic device of the invention. Alignment was assessed in anterior and lateral planes with the patient standing. For proper TKA alignment, the trochanter (hip), knee, and ankle points must fall along a vertical line when standing. To quantify the benefits of the present unibody transtibial prosthetic device, a comparison of weight, cost, and time of design were made against a patient’s existing prosthetic device. Weight comparison between the devices revealed a 55% weight reduction from the conventional prosthetic, which weighed 4 pounds, to the present device weighing only 1.8 lbs. Lighter weight devices reduce metabolic cost during activity and are often reported to be more comfortable. Time of design and manufacture was compared between the two design methodologies. Total traditional transtibial prosthetic leg time for design and manufacture was estimated at 14 days. This estimate includes measurements (1 Day), mold creation (3 Days), socket creation (6 Days), and assembly and alignment (4 Days). In comparison, the present unibody design and manufacture time is 16 hours, which consists of data acquisition (1 Hour), design time (3 Hours), and printing time (12 Hours).

Modified Designs

[0056] FIG. 6 shows a preferred foot/ankle complex 1102 that is consistent with the general shape, arrangement, and structure of the foot/ankle complex 110 of FIG. 1A. The foot/ankle complex 1102 includes central strip 1104 of stiffer material surrounded by more flexible material 1106. The ratio of the two materials controls energy return, flexibility, and dynamic range. While not shown in FIG. 6, the foot/ankle complex 1102 is unitary with a pylon section and socket section.

[0057] FIG. 7 illustrates a unibody prosthetic 1202 of the invention that includes one or more (interior/patient contact side) pockets 1204 of flexible material of pressure sensitive areas of the patient’s amputated limb. These areas can be identified by the patient or physician during visit to the clinic as scanning occurs.

Experiment Observations

[0058] The demonstrated imaging and 3D printing workflow can be used to provide prosthetic devices to virtually any person cared by a practitioner that has a smart phone for imaging, which can benefit rural communities, where high-tech, medical imaging devices such as CT scanners are not available or cost-prohibitive. The workflow provides custom-fitted prostheses that are comfortable and high-performance.

[0059] While specific embodiments of the present invention have been shown and described, it should be understood that other modifications, substitutions and alternatives are apparent to one of ordinary skill in the art. Such modifications, substitutions and alternatives can be made without departing from the spirit and scope of the invention, which should be determined from the appended claims.

[0060] Various features of the invention are set forth in the appended claims.