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WO2010140036A1 - Méthode de conception d'une prothèse du genou - Google Patents

Méthode de conception d'une prothèse du genou Download PDF

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Publication number
WO2010140036A1
WO2010140036A1 PCT/IB2010/001218 IB2010001218W WO2010140036A1 WO 2010140036 A1 WO2010140036 A1 WO 2010140036A1 IB 2010001218 W IB2010001218 W IB 2010001218W WO 2010140036 A1 WO2010140036 A1 WO 2010140036A1
Authority
WO
WIPO (PCT)
Prior art keywords
knee
prosthesis
designing
features
lateral
Prior art date
Application number
PCT/IB2010/001218
Other languages
English (en)
Inventor
Corneluis Scheffer
David Jacobus Van Den Heever
Pieter Jordaan Erasmus
Edwin Mark Dillon
Original Assignee
Stellenbosch University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Stellenbosch University filed Critical Stellenbosch University
Publication of WO2010140036A1 publication Critical patent/WO2010140036A1/fr
Priority to ZA2011/09251A priority Critical patent/ZA201109251B/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/30—Joints
    • A61F2/3094—Designing or manufacturing processes
    • A61F2/30942—Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/30—Joints
    • A61F2/38—Joints for elbows or knees
    • A61F2/3859—Femoral components
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/30—Joints
    • A61F2/3094—Designing or manufacturing processes
    • A61F2/30942—Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques
    • A61F2002/30948—Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques using computerized tomography, i.e. CT scans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/30—Joints
    • A61F2/3094—Designing or manufacturing processes
    • A61F2/30942—Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques
    • A61F2002/30952—Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques using CAD-CAM techniques or NC-techniques
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/30—Joints
    • A61F2/38—Joints for elbows or knees
    • A61F2002/3895—Joints for elbows or knees unicompartimental

Definitions

  • This invention relates to a method of designing and manufacturing a knee prosthesis.
  • the knee is the largest, most complicated and incongruent joint in the human body.
  • the articulating surfaces of the knees have complex, asymmetrical shapes and these influence the complex kinematics.
  • the knee is susceptible to injury and chronic diseases, of which osteoarthritis (OA) is most common. This can lead to the loss of function of the knee which can severely impact on the quality of life of the patient.
  • OA osteoarthritis
  • HTO high tibial osteotomy
  • UMR unicompartmental knee replacement
  • TKR total knee replacement
  • a joint substitute or prosthesis In order to function like a natural joint, a joint substitute or prosthesis needs to possess good mechanical strength and stiffness, have a customized geometric size and be made of biocompatible material.
  • a further consideration is the difference between UKR and TKR. It is suggested that UKR restores normal knee kinematics better than TKR because of retaining the cruciate ligaments. It is however still very difficult to perfect natural knee kinematics. This is due to the fact that most UKR prostheses designs are available in standard sizes only and the surface geometry in sagittal view is either of a specific single or multi-radius design which is predetermined by the manufacturer.
  • a method of designing a knee prosthesis which includes imaging a knee; comparing a number of features of the imaged knee to corresponding features of a plurality of reference knees; selecting the features which most closely correspond to those of the imaged knee; and modelling the prosthesis to have an external geometry at least similar to the knee associated with the or each selected feature.
  • the imaging to be three- dimensional; for prosthesis to include an external, articulating surface; for the features to include the anterior length on the medial (APM) and lateral (APL) sides, the medio-lateral length (ML) and the distance between the most anterior points on the medial and lateral condyles (DAC); for the articulating surface of each reference knee to be represented as a mathematical function; and for the articulating surface of the prosthesis to be modelled using the mathematical function associated with each selected feature.
  • Still further features of the invention provide for the use of a pattern recognition algorithm, such as the self organising map (SOM), to compare the features of the imaged knee to the corresponding features of the reference knees and to interpolate an external geometry for the prosthesis from those associated with the selected features.
  • a pattern recognition algorithm such as the self organising map (SOM)
  • the invention also provides a knee prosthesis manufactured in accordance with a design substantially as defined above.
  • the invention further provides a method for providing a prosthesis for a knee which includes obtaining information relating to the knee in a healthy condition, storing the information, and at a later time fabricating the prosthesis based on the stored information.
  • Figure 1 is a computer tomography (CT) image of a knee
  • Figures 2 to 5 are a sagittal and axial view respectively of a medial condyle
  • Figures 6 and 7 are plots comparing a designed surface to an actual surface
  • Figure 8 is a computer-aided design (CAD) model of a prosthesis
  • Figure 9 shows two perspective views of the model in Figure 8 fitted to a knee condyle reconstructed from a CT image.
  • Figure 10 is a perspective view of model prosthesis having a custom bone-prosthesis interface.
  • a method of designing a knee prosthesis in this embodiment a unicompartmental knee replacement (UKR) prosthesis, includes computer tomography (CT) imaging of the knee.
  • CT computer tomography
  • This provides a detailed three dimensional image of the knee and shows diseased or damaged areas together with healthy areas, as shown in Figure 1.
  • a number of features of the knee are then measured from the image and compared to corresponding features of a plurality of healthy reference knees which are stored in a database. These features are also obtained from CT images of healthy knees of people drawn from as wide a population sample as possible. It is envisaged that the database will be continually expanded and that it may be categorised according to gender, population group and the like.
  • the reference features which most closely correspond to those of the image are selected and the geometry of the knees associated with these features used to model the prosthesis on.
  • a number of reference measurements are used. These are measurements relating to features of the knee which are generally not affected by diseases, such as osteoarthritis.
  • the articulating surface of one or both of the femoral condyles becomes damaged.
  • the meniscus and tibial plateau are often also damaged but it is a prosthesis for the condyles that is the focus of this description.
  • the features used may however include any suitable features which are determined not to have been extensively damaged.
  • the most common features include the anterior length on the medial (APM) and lateral (APL) sides, the medio-lateral length (ML) and the distance between the most anterior points on the medial and lateral condyles (DAC).
  • the most efficient method of making the comparison is by way of a computer implemented system.
  • the system uses self organising maps (SOM) as the search mechanism, but several other pattern recognition algorithms can achieve the same outcome.
  • SOM self organising maps
  • the reference measurements can either be taken and input directly in to the system or reference points can be plotted on the electronic image using suitable segmentation software, such as Mimics (Materialise, Leuven, Belgium), and the system then used to calculate measurements and compare these to corresponding points on the reference knees.
  • the corresponding articulating surfaces of the associated condyle or condyles are used as the basis for designing the prosthesis. This is achieved by including in the database a definition of the articulating surfaces of each condyle as mathematical functions, for instance polynomials or splines, and then using the mathematical functions to define the outer, articulating surface of the prosthesis. In this embodiment polynomials are used.
  • the coefficients of the polynomials are stored in the database as the descriptors of the geometries of the relevant portions of the healthy knees.
  • the coefficients were determined using Matlab version 7.0.1 (The Math Works Inc), but any mathematical manipulation software can be used for this purpose.
  • Matlab version 7.0.1 The Math Works Inc
  • Any mathematical manipulation software can be used for this purpose.
  • three dimensional computer models of the healthy knees generated by Mimics or other suitable segmentation software
  • numerous points were plotted along the articulating surfaces of the condyles in both sagittal view, as shown in Figure 6, and the axial view as shown in Figure 7.
  • the coordinates of the points are then imported into Matlab.
  • the geometry in sagittal view is divided into two parts with the most posterior point as the common reference point.
  • the coordinates are normalized with the reference point (most posterior point) at coordinate 0,0.
  • the most lateral point of the articulating surface of the condyle is used as reference point 0,0.
  • a polynomial function is then fitted through the points, by first fitting a spline through the points to obtain a smoother set of points for the polynomial function as it minimizes the input error caused when the points are not plotted correctly.
  • the coefficients of a polynomial f(x) of degree n that fit the data f(x(i)) to y(i)) in a least squares sense are then determined.
  • the result f is a vector of length n+1 containing the polynomial coefficients in descending powers.
  • the degree of the polynomials used was determined by examining the behaviour of different polynomials.
  • a 4th order polynomial was selected to describe the condyles in axial view as well as the distal portion of the sagittal view.
  • a 3rd order polynomial was selected to describe the posterior portion of the condyle in sagittal view. This is possible as the posterior portion is shorter than the distal portion and thus requires less points for the polynomial fit
  • the polynomial coefficients for the distal part of the medial condyle may take the following form:
  • the articulating surfaces of the healthy femurs obtained through the CT imaging and cadaveric specimens are analysed in this way to build up the database and the coefficients of each part of each knee as well as the corresponding reference measurements are then used as input to the pattern recognition algorithm, for instance the SOM.
  • the SOM is known in the art and is a type of neural network that is trained using unsupervised learning. Its operation is apparent to those skilled in the art and need not be described in detail here.
  • the SOM attempts to implement the orderly mapping of high-dimensional data onto a regular low-dimensional grid in order to identify hidden relationships between the high-dimensional data.
  • the SOM produces a 2-dimensional representation of the input space, called a map.
  • the SOM is used to produce a map consisting of the coefficients of the polynomials and other reference measurements. These reference measurements are the only measurements taken on the unhealthy knee and are the input to the SOM.
  • the SOM is trained with the data in the database which consists of the polynomial coefficients and the reference measurements. The SOM then attempts to find relationships between the parameters. After training, when the SOM is presented with the input of the reference measurement as described above, it first compares the measurements to find the closest reference measurements and then uses the relationships it has determined to estimate the original articulating surfaces of the unhealthy knee. These it presents as polynomial coefficients and are subsequently used to design the prosthesis as described in more detail below.
  • FIG. 1 a cadaveric specimen was chosen as the unhealthy knee even though it is in fact a healthy knee.
  • the reference measurements were determined using Mimics.
  • the SOM algorithm was used to estimate what the original knee surfaces would look like given these reference measurements as the input.
  • Figures 2 to 5 illustrate the results compared to the actual knee surfaces where Figure 2 is a plot of the lateral condyle in sagittal view, Figure 3 is a plot of the medial condyle in sagittal view, Figure 4 is a plot of the lateral condyle in axial view and Figure 5 is a plot of the lateral condyle in axial view. From these it will be noted that reasonably accurate surfaces compared to the original knee surfaces were produced.
  • the output of the SOM algorithm is a set of coordinates relating to each polynomial. These coordinates are stored as points in a spreadsheet and are used to design the articulating surfaces of the prosthesis. The number of points representing each polynomial can be chosen keeping in mind that more points will give more detail and less points will result in a smoother surface.
  • the points are, in this embodiment, imported into Inventor Professional 2008 (Autodesk), a CAD package used to make solid model designs.
  • the SOM output is a set of coordinates describing the articulating surfaces of the femoral condyle in the sagittal plane and the axial plane. It is however necessary to consider the patient's condyle curvatures in the anterior/posterior plane. This curvature plays an important role in the knee kinematics as the contact areas/points of articulation between the femoral condyles and the tibial surface also follow a curved path. Being individual to each knee, this curvature is, however, generally not taken into account in conventional prostheses and can sometimes lead to the femoral component not fitting on the condyle.
  • Condyle curvature is included in the design of the prosthesis when the reference measurements are made in Mimics by plotting four points on each femoral condyle.
  • the first point is placed in the middle of the most posterior part of the condyle.
  • the second point is placed in the middle of the most proximal part of articulation and a third point is placed in the middle of the most distal point of articulation.
  • the latter point can generally be found on the lateral condyle where a distinct bump is present.
  • a fourth point is placed in the middle about halfway between points one and three. Points one and four will also define the length of the final component to ensure that the length is also specific to the patient.
  • a 2nd order polynomial (a parabola) is used to describe the curvature of the lateral condyle and a 3rd order polynomial is used to describe the curvature of the medial condyle. This is because the curvature tends to be pronounced on the medial side.
  • the same methods are used to derive the polynomials as is the case with the sagittal and axial surfaces.
  • the final output from the Matlab algorithm is a spreadsheet containing two sets of coordinates for each condyle.
  • the first set describes the axial view in two dimensions.
  • the second set describes the sagittal view and coronal view using three dimensions.
  • Table 1 gives an example of the output for the medial condyle.
  • the number of coordinate points can be selected by the operator as can the direction of the curvature based on whether it is for a right knee or a left knee.
  • the output is imported into Inventor and the axial plane coordinates are imported when in 2D sketch mode while the sagittal- coronal plane coordinates are imported when in 3D sketch mode.
  • a spline is fitted through the points. This is first done for the axial view and the resulting spline represents the articulating surface of the femoral condyle in the axial plane.
  • a thickness is then added to the surface. This is accomplished by offsetting the articulating surface spline to the inside. A thickness of 5 mm is typically used.
  • a spline is fitted through the sagittal- coronal plane points. This is done in the 3D sketch mode.
  • the axial plane sketch is positioned to be at the most posterior point of the sagittal- coronal spline, with its midpoint lying on the spline.
  • the sweep function uses a closed profile, in this case the axial plane sketch, and sweeps it along a chosen path. In this case the path is the sagittal- coronal plane spline which lies in three dimensional space.
  • the sharp edges are rounded using the fillet option.
  • a small cylinder is placed in the inside of the part, on the most posterior point. This helps in aligning the part for the bone-prosthesis interface as described below.
  • Figure 8 shows the solid part created in Inventor.
  • the bone-prosthesis interface is the surface of the prosthesis directly in contact with the patient's femoral condyle.
  • a patient specific bone-prosthesis interface is used.
  • the Inventor model is imported into 3matic version 4.3 (Materialise, Leuven, Belgium) together with the Mimics model of the patient's femur.
  • the femoral component is then moved into the desired implant position using the N points registration function.
  • This function allows a number of points on the one object which should lie flush with the corresponding number on the second object to be defined.
  • the first point is chosen as the most posterior point on the femur. This is a point which is easily identifiable.
  • the corresponding point on the component is in the middle of the small cylinder placed there for this purpose. Points 2, 3 and 4 are then placed to help with the positioning.
  • FIG. 9 shows two views of the component in the desired position.
  • the cut function is used to cut the surface of the femur into the component.
  • the femur is the cutting object and the component is the object being cut.
  • Performing this action produces a bone-prosthesis interface surface on the component complementary to the femoral condyle surface produced by the CT scan.
  • the component should fit perfectly on the patient's condyle once all the cartilage is removed, as shown in Figure 10. There is, however, usually some detail lost in the CT scan and reconstruction in Mimics.
  • the final thickness of the part will be the 5 mm of the original Inventor model minus the volume cut away to form the complementary interface surface.
  • the thickness will thus vary throughout the component. If desired, an analysis can be performed in 3matic to check the thickness to ensure that it stays above a certain limit for strength considerations.
  • the designs generally include one or more posts extending from the prosthesis and which locate in complementary sockets formed in the condyle. Variations to the shape of the post and provision of webs between the post and prosthesis are provided by each of the different designs.
  • Cemented fixation relies on fast-curing bone cement and a solid mechanical bond to hold the prostheses in place.
  • the cement is usually pressed into the distal femoral surfaces and on the inner surface of the prosthesis.
  • Cementless fixation relies on bone growing into the special surface topography to hold the prostheses in place.
  • Cemented fixation shows a slight advantage in terms of avoiding component loosening.
  • a custom bone-prosthesis interface should permit a better fit and hence a smaller post or fin for fixing. It is considered that the optimal fixation method is a thin fin as it produces the largest contact area with the lowest volume. This ensures minimal bone removal and a greater contact area for the fixation. However, strength calculations need to be performed to prevent failure under load. While a post with a small diameter can also give a large contact area with low volume, a post in conjunction with a fin provides superior strength but may be the poorest design in terms of volume. Any suitable method can be used to fix the prosthesis in place.
  • a rapid prototyping process is used to manufacture the prosthesis.
  • Preferred materials are a suitable stainless steel, cobalt chrome and titanium. However, any suitable material and process can be used including the use of CNC devices and the like.
  • the apparatus used will preferably be capable of receiving instructions in a digital format directly from the system used to design the prosthesis.
  • the tibial component does not form part of the current invention. It is, however, envisaged that a polyethylene articulating surface with an all polyethylene insert or a metal-backed tibial (MBT) base plate will be used.
  • the tibial base plate as well as the polyethylene insert will be customized to ensure for a better fit, and higher contact area in order to prevent loosening and wear. This can be done using the CT image data.
  • the prosthesis of the invention allows close reproduction of the original knee surface in a very effective manner. This permits near natural articulation of the knee which in turn reduces discomfort and stress loading resulting in bone failure. It will be appreciated, however, that many other methods of designing a knee prosthesis, particularly regarding the type of imaging used, the manner in which the database is searched and the type and of information which is stored in the database. Also any suitable mathematical method of modelling the prosthesis can be used. For example, instead of using polynomials to define the articulating surfaces, one or more planes can be passed through the knee and the coordinates of intersection of the articulating surface with the planes recorded. A spline can then be fitted, possibly using a least squares method, through the coordinates for each plane. The average for the planes is then calculated and the curve which is obtained is then segmented, into say 1 mm sections, and a centre and radius determined for each section. These are plotted and define the articulating surface. Of course many other suitable modelling methods exist.
  • the invention also provides a method of providing a prosthesis for a knee which includes imaging a patient's knee in a healthy condition and storing the image. Imaging by way of, for example, a CT scan allows a detailed 3- dimesional image of the knee to be obtained, which provides sufficient information to permit fabrication of a prosthesis directly from the image.
  • knee damage such as professional sports players and those with a history of osteoarthritis can thus store images of their knees in a healthy condition to be used in the event of injury or damage.
  • any person could "insure” themselves against knee injury or damage in this way.
  • the stored information may be updated periodically to take into account any changes to the knees. This in itself may act as an early diagnostic tool to indicate diseases or disorders.
  • the information store will preferably be accessible from remote locations to enable information to be received and sent irrespective of the location of the patient imaging facility or fabrication facility. Thus the information store will preferably be accessible through a public communications network, such as the Internet, and may require a fee to be paid for the use thereof.
  • the information stored need not be the CT image but could include information derived from the image, such as mathematical functions defining its articulating surfaces as described above. Fabrication of the prosthesis can take place by way rapid prototyping or any other suitable process.

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Transplantation (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Veterinary Medicine (AREA)
  • Vascular Medicine (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Physics & Mathematics (AREA)
  • Geometry (AREA)
  • Manufacturing & Machinery (AREA)
  • Prostheses (AREA)

Abstract

La méthode de conception d'une prothèse du genou ci-décrite comprend l'imagerie d'un genou, de préférence, dans les trois dimensions, et la comparaison d'un certain nombre de caractéristiques du genou imagé avec les caractéristiques correspondantes d'une pluralité de genoux de référence. Les caractéristiques qui sont comparées comprennent la longueur antérieure sur les côtés médiaux (AMP) et latéraux (APL), la longueur médio-latérale (ML) et la distance entre les points les plus antérieurs sur les condyles médiaux et latéraux (DAC). Les caractéristiques des genoux de référence qui correspondent le plus étroitement à celles du genou imagé sont sélectionnées et la prothèse est modélisée de manière à avoir une géométrie externe au moins similaire au genou associé à la ou à chaque caractéristique sélectionnée.
PCT/IB2010/001218 2009-06-05 2010-05-24 Méthode de conception d'une prothèse du genou WO2010140036A1 (fr)

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ZA2011/09251A ZA201109251B (en) 2009-06-05 2011-12-15 A method of designing a knee prosthesis

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ZA200903924 2009-06-05
ZA2009/03924 2009-06-05

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Cited By (18)

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WO2013056036A1 (fr) * 2011-10-14 2013-04-18 Conformis, Inc. Procédés et systèmes pour l'identification, l'évaluation, le modelage et la réparation de disparités anatomiques dans le remplacement d'articulation
CN103584932A (zh) * 2013-10-23 2014-02-19 华南理工大学 用于全膝置换术的膝关节股骨假体的设计方法及制造方法
US8690945B2 (en) 2001-05-25 2014-04-08 Conformis, Inc. Patient selectable knee arthroplasty devices
US8882847B2 (en) 2001-05-25 2014-11-11 Conformis, Inc. Patient selectable knee joint arthroplasty devices
US8906107B2 (en) 2001-05-25 2014-12-09 Conformis, Inc. Patient-adapted and improved orthopedic implants, designs and related tools
US8932363B2 (en) 2002-11-07 2015-01-13 Conformis, Inc. Methods for determining meniscal size and shape and for devising treatment
US9020788B2 (en) 1997-01-08 2015-04-28 Conformis, Inc. Patient-adapted and improved articular implants, designs and related guide tools
US9055953B2 (en) 2001-05-25 2015-06-16 Conformis, Inc. Methods and compositions for articular repair
US9180015B2 (en) 2008-03-05 2015-11-10 Conformis, Inc. Implants for altering wear patterns of articular surfaces
US9308091B2 (en) 2001-05-25 2016-04-12 Conformis, Inc. Devices and methods for treatment of facet and other joints
US9387079B2 (en) 2001-05-25 2016-07-12 Conformis, Inc. Patient-adapted and improved articular implants, designs and related guide tools
US9495483B2 (en) 2001-05-25 2016-11-15 Conformis, Inc. Automated Systems for manufacturing patient-specific orthopedic implants and instrumentation
US9603711B2 (en) 2001-05-25 2017-03-28 Conformis, Inc. Patient-adapted and improved articular implants, designs and related guide tools
JP2017509368A (ja) * 2014-02-07 2017-04-06 エピサーフ アイピー−マネジメント アクチエボラグ 軟骨修復用手術キットを製造するための方法およびノード
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WO2021028038A1 (fr) * 2019-08-14 2021-02-18 Mecuris GmbH Procédé mis en œuvre par ordinateur pour créer une forme fonctionnelle, système de traitement de données et support lisible par ordinateur

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