Patient specific instruments for use in, for instance, knee arthroplasty procedures such as total or partial knee replacements.
Knee arthritis and trauma in various forms can cause loss of joint cartilage, including for example, osteoarthritis, excessive wear or sudden trauma, rheumatoid arthritis, or infectious arthritis. When joint cartilage is worn away, the bone beneath the cartilage is left exposed, and bone-on-bone contact can be very painful and damaging. Other types of problems can occur when the bone itself becomes diseased. Conventional solutions for these types of joint problems may be total or partial knee replacements.
In some knee arthroplasty procedures, for example, in preparing a femur to receive a femoral implant, a series of resections are made to the distal end of the femur. In “distal cut first” techniques, the first cut is a distal planar resection. Conventionally, after the distal resection has been made, a “four-in-one” cutting guide is positioned on the distal end of the femur relative to the planar distal resection. The four-in-one cutting guide typically includes four slots for guiding a cutting instrument to create a series of cuts on the distal femur. In some instances, the four-in-one cutting guide is placed on the distal femoral resection, making posterior bone cuts to the medial and lateral condyles, making posterior chamfer bone cuts to the medial and lateral condyles, making an anterior bone cut to the distal femur, and making an anterior chamfer bone cut.
It is important that the four-in-one cutting guide be positioned correctly on the distal end of the femur with respect to the distal cut since the position and orientation of the four-in-one guide (and the cuts made using it) will control the position and orientation of the femoral implant in at least some degrees of freedom. In some instances, properly positioning and orienting these resections to achieve optimal positions and orientations for the femoral implant can be difficult and time consuming. For example, some traditional four-in-one cutting guides have a planar surface that mates directly against the distal femur cut, and thus, in at least some instances, constitutes a planar joint that can be translated in at least two degrees of freedom and rotated in at least one degree of freedom (e.g., translated in medial/lateral and anterior/posterior directions and rotated in internal/external manners). The rotational and translational alignment of the guide may be set by drilling two pin holes into the distal femur. The four-in-one guide has two integrated pins that are then positioned inside the two drilled holes and the guide is then impacted against the distal cut. As force is applied to the center of the four-in-one cutting guide to secure the guide to the bone, a moment can be created that rotates the four-in-one cutting guide so that the position of the guide when it is secured to the bone is different from the intended position of the guide. Other factors can also cause improper position and/or orientation of the cutting guide on the distal cut. If the cutting guide is not properly positioned and oriented on the bone, the four cuts will be inaccurate and the femoral implant will not be implanted correctly, which may result in improper kinematics, biomechanics, or other undesirable performance.
Instrumentation, systems and methods, including patient-matched instrumentation, systems and methods, for facilitating orthopaedic procedures including knee arthroplasty procedures are disclosed herein. Certain implementations constitute alignment guides for aligning instrumentation on a distal femur. Portions of the guide may have surfaces that are generally a negative of the patient's anatomy, or are designed and adapted to substantially conform to a portion of the patient's anatomy, such as portions of the distal femur. Such surfaces can be formed using data obtained from the specific patient by conventional imaging devices or other techniques, such as x-ray, CT scans, MRI scans, or ultrasound, and using computer aided-design and manufacturing techniques.
In some implementations, the alignment guide includes one or more patient-matched surfaces for contacting un-altered anatomy of a patient as well as one or more planar surfaces (which may or may not also be customized to the specific patient) for contacting altered anatomy (e.g., a planar resection of the distal femur) of the patient.
In one general aspect, a femoral cutting guide includes guide slots for guiding the movement of cutting tools relative to a distal portion of a femur, a surface feature adapted to at least partially conform to a resected surface of the distal portion of the femur, and either a posterior-facing surface adapted to conform to an anterior, unaltered surface of the distal portion of the femur or an anterior-facing surface adapted to conform to a posterior, unaltered surface of the distal portion of the femur.
Implementations may optionally include one or more of the following features. For example, the guide slots may include an anterior slot for guiding an anterior resection of the distal portion of the femur and a posterior slot for guiding posterior resections on one of a medial or lateral condyle of the distal portion of the femur. The guide slots may further include an anterior chamfer slot for guiding an anterior chamfer resection of the distal portion of the femur and a posterior chamfer slot for guiding a posterior chamfer resection of the distal portion of the femur. The guide slots may include at least two posterior slots for guiding posterior resections of the medial and lateral condyle of the distal portion of the femur. The surface feature may include a substantially planar face adapted to, at least partially, conform to the resected surface of the distal portion of the femur. The cutting guide includes a posterior-facing surface adapted to conform to an anterior, unaltered surface of the distal portion of the femur and an anterior-facing surface adapted to conform to a posterior, unaltered surface of the distal portion of the femur. The anterior, unaltered surface of the distal portion of the femur includes anterior sulcus and patello-femoral groove portions of the distal portion of the femur. The posterior, unaltered surface of the distal portion of the femur includes a posterior sulcus portion of the distal portion of the femur. The anterior and posterior facing surfaces extend generally superiorly from the surface feature, and the surface feature extends between the anterior and posterior facing surfaces. The posterior-facing surface and the anterior-facing surface are established in pre-surgical planning based on imaging data of the distal portion of the femur. The cutting guide may further include one or more apertures configured to guide the placement of provisional fixation pins for coupling the guide to the distal portion of the femur.
In another general aspect, a patient-specific femoral cutting guide includes an anterior portion, a posterior portion, and a substantially planar surface feature. The anterior portion including one or more surfaces adapted to substantially conform to an unaltered, anterior portion of a distal portion of a femur and at least one guide slot for guiding the movement of a cutting tool relative to the unaltered, anterior portion of the distal portion of the femur. The posterior portion including one or more surfaces adapted to substantially conform to an unaltered, posterior portion of the distal portion of the femur and at least one guide slot for guiding the movement of a cutting tool relative to the unaltered, posterior portion of the distal portion of the femur. The substantially planar surface feature extending between the anterior portion and the posterior portion and adapted to at least partially conform to a resected surface of the distal portion of the femur.
Implementations can optionally include one or more of the following features. For example, the relative position of the anterior portion relative to the posterior portion is adjustable. The relative position of the anterior portion relative to the posterior portion is adjustable in a manner that is substantially parallel to the resected surface of the distal portion of the femur when the cutting guide is positioned on the distal portion of the femur.
In another general aspect, a method of resectioning a distal femur includes positioning a surface feature of a cutting guide against a first resected surface of the distal femur, positioning a posterior-facing surface of the cutting guide against an anterior, unaltered surface of the distal femur, positioning an anterior-facing surface of the cutting guide against a posterior, unaltered surface of the distal femur, and using the cutting guide to guide one or more cutting tools relative to the distal femur to form one or more resections of the distal femur.
Implementations can optionally include one or more of the following features. For example, using the cutting guide to form one or more resections of the distal femur includes using an anterior slot for guiding an anterior resection of the distal femur, using posterior slots for guiding posterior resections on the medial and lateral condyles of the distal femur, using anterior chamfer slots for guiding anterior chamfer resections of the distal femur, and using posterior chamfer slots for guiding posterior chamfer resections. The method may include using one or more fixation pins to secure the cutting guide in a particular location relative to the distal femur. Positioning the surface feature of the cutting guide against the first resected surface of the distal femur establishes a superior-inferior positioning of the cutting guide and varus-valgus orientation and angulation when viewed in a sagittal plane of the guide. Positioning the posterior-facing surface of the cutting guide against the anterior, unaltered surface of the distal femur and positioning the anterior-facing surface of the cutting guide against the posterior, unaltered surface of the distal femur establishes the anterior-posterior and medial-lateral positioning of the guide relative to the distal femur and the internal and external rotation of the guide relative to the distal femur. The surface feature includes a substantially planar face adapted to at least partially conform to the first resected surface of the distal femur.
In some implementations, a distal femoral resection may be performed using conventional or non-conventional techniques and apparatus. For example, as shown in
In the particular implementation shown, after the distal resection 18 has been made, a four-in-one cutting guide may be positioned on the distal femoral resection 18 to guide additional resections of the distal femur 10, such as one or more of a posterior resection, an anterior resection, and anterior and posterior chamfer resections. Such resections may prepare the distal femur to receive a femoral implant such as the implant 40 shown in
In the particular implementation shown, the cutting guide 20 is configured to interact with both un-altered and altered anatomy on the distal femur 10 to determine the position and orientation of the cutting guide 20 with respect to the distal femur 10.
For instance, the cutting guide 20 includes a planar surface feature 32 that mates against and/or substantially conforms to the resected surface 18 of the femur 10. Positioning the planar surface feature 32 of the guide 20 against the resected surface 18 establishes the position and orientation of the guide 20 with respect to the femur 10 in certain degrees of freedom. For example, in this particular implementation, the mating of the planar surface feature 32 with the resected surface 18 establishes the superior-inferior positioning of the guide 20, as well as varus-valgus orientation and angulation when viewed in a sagittal plane of the guide 20.
The cutting guide 20 also includes two surfaces 30 and 31 that are adapted to at least substantially conform to the unique, un-altered geometry of the particular patient's anatomy (although in other implementations other numbers of such surfaces could be included). For instance, as shown in
In the particular implementation shown, the anterior and posterior facing surfaces 30, 31 extend generally superiorly from the planar surface feature 32, which extends between those surfaces 30, 31. Additionally, as shown, unlike planar surface feature 32, the anterior and posterior-facing surfaces 30, 31 are, at least in this particular implementation, non-planar and undulate to correspond to the undulating anatomy they are designed to interact with and conform to.
In other implementations, cutting guides do not necessarily need to include both anterior-facing patient-matched surface 31 and posterior-facing patient-matched surface 30, and may include only one of such surfaces. In other implementations, cutting guides may include more than these two surfaces that are also configured to conform to the patient's un-altered anatomy.
In some implementations, instead of integrated pins, as were included in some conventional four-in-one cutting guides, the patient-matched cutting guide 20 includes at least two apertures 34 for receiving fixation pins to secure the guide to the distal femur 10. The patient-matched surfaces 30, 31 position the cutting guide 20 relative to the resected surface 18 in only one way against the anatomy before the guide is secured. Instead of using two integrated pins, the apertures 34 should be aligned with the holes that were drilled in the distal femur using cutting guide 12. The apertures 34 can provide a check that the cutting guide 20 is properly aligned and that all five cuts will be in alignment per the surgical plan. If the apertures 34 are not aligned with the holes created by the distal cutting block, it could indicate that the distal cutting block or the 4-in-1 cutting guide 20 was not secured in the proper location. Other holes can also be used to secure the cutting guide 20 to the bone. As compared with conventional cutting guides using integrated pins, the cutting guide 20 is properly positioned both before and after it is secured. As described above, with conventional four-in-one cutting guides, a force directed toward the center of the cutting guide 20 to secure the guide 20 to the bone 10 often created a moment that rotated the cutting guide 20 during impaction so that the final position of the guide 20 was different than planned position of the guide 20, which caused inaccurate cuts.
Also disclosed is a method of creating a patient-matched cutting guide. Imaging data taken by any known means such as x-ray, CT scans, MRI scans, ultrasound, etc. is used to obtain patient-specific data about the femur to be resected and other anatomy of potential relevance, such as imaging data of the femoral head and ankle to allow determination of a mechanical axis of the leg. In one implementation, the patient-specific data is used to build a model of the patient's anatomy. Then, the model is used to plan the distal resection. In some implementations, a patient-matched guide is built to guide the distal resection. Next, using the patient-specific data, as well as data about the planned distal resection (including orientation and position of that resection), cutting guide 20 or 120 may be created to conform to the un-altered anatomy of the patient, as well as the altered (resected) anatomy so that the planar face of the cutting guide fits properly on the resected surface after the distal resection has been made. In particular, the imaging data is used to create patient-matched surfaces 30 and/or 31 that will mate against the uncut bone to help guide the remaining resections and to create planar surface 32 that will mate against the distal resection. For example, in some implementations, cutting guide 12 (shown in
According to another non-limiting method, a patient may contact a health care provider regarding joint pain, such as knee pain. The health care provider may then refer the patient to an imaging facility. A technician images the joint, such as by MRI, CT, X-ray, or ultrasound. In one implementation, the technician transmits the image data to a cutting block manufacturer and/or to the health care provider. The cutting block manufacturer manufactures the distal resection block and the four-in-one block using the image data. In some implementations, the cutting block manufacturer or its representative are located at a surgical site facility. For instance, the distal resection block and/or the four-in-one cutting block may be manufactured at or near the site facility where the joint replacement takes place. The health care provider and the cutting block manufacturer may communicate regarding the requirements of at least one of the cutting blocks. Communication may take place via a representative or agent, a telephone network, a computer network, or by any other suitable mode. In one implementation, the patient then visits a surgical site facility for joint replacement, and the health care provider confirms the cutting blocks are matched to the patient. The health care provider places the distal cutting block on the patient. The health care provider makes a distal cut. The health care provider places the patient matched four-in-one cutting block on the patient and makes additional cuts. The health care provider implants a joint prosthesis, such as a knee prosthesis.
One non-limiting example of a method of planning for and executing an orthopaedic procedure is shown in
A wide variety of systems may be utilized in performing the procedure shown in
In some implementations, including the implementation shown in
In some implementations, the processor 2600 may include a microprocessor, an application-specific integrated circuit (ASIC), a state machine, or other suitable processor. The processor 2600 may include one processor or any number of processors, and may access code stored in the memory 2800. The memory 2800 may be any non-transitory computer-readable medium capable of tangibly embodying code. The memory 2800 may include electronic, magnetic, or optical devices capable of providing processor 2600 with executable code. Examples of the memory 2800 include random access memory (RAM), read-only memory (ROM), a floppy disk, compact disc, digital video device, magnetic disk, an ASIC, a configured processor, or other storage device.
In some implementations, including the implementation shown in
In the implementations illustrated by
Image processing 1200 is the next step in the implementation of
In various implementations, segmentation may be accomplished by manual, automated, or semi-automated processes. For instance, in some implementations, a technician or other user may (with the assistance of computer assisted design hardware and/or software or other functionality) manually trace the boundary of the anatomy and other structures of interest in each image slice. Alternatively, in some implementations, algorithms or other automated or semi-automated processes could be used to automatically identify the boundaries of interest. In some implementations, only key points on the anatomy or other structures of interest need be segmented. Image processing 1200 such as described above may be used to make a three dimensional model of the patient's anatomy and other features of interest.
The 3D model or other construct representing the patient's anatomy may be used for pre-surgical planning 1400 of the knee arthroplasty procedure. In some implementations, pre-surgical planning 1400 can include one or more of identifying a desired position and orientation of the distal resection and/or the patient-matched surfaces 30 and 31. In various implementations, the planning may be carried out using manual, semi-automated or automated functionality.
The patient-matched guide 20 or 120 may include one or more surfaces that are specifically designed to mimic the patient's particular anatomy (or portions thereof) as determined, for instance, by the 3D model of the anatomy. For instance, in some implementations, the patient-matched surface or surfaces can be a negative mold of the patient's anatomy such that it uniquely conforms to the patient's anatomy in one particular position and orientation. In other words, the patient-matched surface or surfaces may facilitate achieving a desired position and/or orientation of the patient-matched guide 20 or 120 with respect to the patient's particular anatomy because the patient-matched surface will allow the patient-matched guide 20 or 120 to fully seat on the patient's particular anatomy only when the patient-matched guide 20 or 120 is in the desired position and/or orientation.
In some implementations, the geometries and other aspects of the patient-matched surface may be determined in the planning stage by applying a blank of the patient-matched guide 20 or 120 (e.g. a wire-frame or similar digital representation of a blank of the patient-matched instrument) to the 3-D model of the patient's anatomy such that the patient-matched guide 20 or 120 is in the desired position and orientation with respect to the patient's anatomy, and then removing from or adding to portions of the blank to create the patient-matched surface conforming to the surface of the patient's anatomy. In some implementations, earlier processes performed during the planning stage will determine, at least partially or wholly, the position and/or orientation of the blank relative to the 3-D model of the patient's anatomy. For instance, the planned resection position and orientation, in combination with the 3D model, could be used to define the particular shape and other attributes of the patient matched guide.
Once designed, the patient-matched guide 20 or 120 may be manufactured 1600 using any number of known technologies, including, but not limited to, selective laser sintering, 3D printing, stereo-lithography, or other rapid production or custom manufacturing technologies. In some implementations, the rapid production equipment can be remote from the systems involved in the planning and/or designing of the patient-matched instruments, and data or other information sufficient to manufacture the patient-matched instrument(s) can be exported from the planning/design systems to the manufacturing systems in any desirable format.
One of ordinary skill in the art will recognize that additions, deletions, substitutions or other modifications may be made to the non-limiting implementations described above without departing from the scope or spirit of the present invention.
This application claims priority to and the full benefit of U.S. Provisional Application Ser. No. 61/491,917 filed Jun. 1, 2011, and titled “Patient Specific Instrument,” the entire contents of which are incorporated herein by reference.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2012/040373 | 6/1/2012 | WO | 00 | 9/23/2014 |
Number | Date | Country | |
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61491917 | Jun 2011 | US |