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Patient Selectable Joint Arthroplasty Devices and Surgical Tools

a patient-selectable, joint technology, applied in the field of orthopaedic methods, systems and prosthetic devices, can solve the problems of serious physical deformity and debilitation, limited repair ability of cartilage, and uncertain clinical outcomes of biologic replacement materials such as allograft and autograft systems and tissue scaffolds. to achieve the effect of accurately placing the implant into a d

Inactive Publication Date: 2011-09-01
CONFORMIS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This approach minimizes bone loss, enhances joint congruity, and improves the integration of replacement materials with native tissues, reducing the risk of complications and extending the lifespan of joint replacements by achieving a precise anatomical fit, thereby improving functional outcomes.

Problems solved by technology

Adult cartilage has a limited ability of repair; thus, damage to cartilage produced by disease, such as rheumatoid and / or osteoarthritis, or trauma can lead to serious physical deformity and debilitation.
, 1989. However, clinical outcomes with biologic replacement materials such as allograft and autograft systems and tissue scaffolds have been uncertain since most of these materials cannot achieve a morphologic arrangement or structure similar to or identical to that of normal, disease-free human tissue it is intended to
replace. Moreover, the mechanical durability of these biologic replacement materials remains u
Implantation of these prosthetic devices is usually associated with loss of underlying tissue and bone without recovery of the full function allowed by the original cartilage and, with some devices, serious long-term complications associated with the loss of significant amount of tissue and bone can include infection, osteolysis and also loosening of the implant.
Further, joint arthroplasties are highly invasive and require surgical resection of the entire or the majority of the articular surface of one or more bones.
The reaming results in a loss of the patient's bone stock.
2000. Implantation of these prosthetic devices is usually associated with loss of underlying tissue and bone without recovery of the full function allowed by the original cartilage and, with some devices, serious long-term complications associated with the loss of significant amounts of tissue and bone can cause loosening of the im
plant. One such complication is oste
eplaced. Since the patient's bone stock is limited, the number of possible replacement surgeries is also limited for joint arth
As can be appreciated, joint arthroplasties are highly invasive and require surgical resection of the entire, or a majority of the, articular surface of one or more bones involved in the repair.
Reaming results in a loss of the patient's bone stock and over time subsequent osteolysis will frequently lead to loosening of the prosthesis.
Further, the area where the implant and the bone mate degrades over time requiring the prosthesis to eventually be replaced.
Since the patient's bone stock is limited, the number of possible replacement surgeries is also limited for joint arthroplasty.
In short, over the course of 15 to 20 years, and in some cases even shorter time periods, the patient can run out of therapeutic options ultimately resulting in a painful, non-functional joint.
Accordingly, these devices are not designed to substantially conform to the actual shape (contour) of the remaining cartilage in vivo and / or the underlying bone.
Thus, integration of the implant can be extremely difficult due to differences in thickness and curvature between the patient's surrounding cartilage and / or the underlying subchondral bone and the prosthesis.
However, currently available devices do not always provide ideal alignment with the articular surfaces and the resultant joint congruity.
Poor alignment and poor joint congruity can, for example, lead to instability of the joint.
In the knee joint, instability typically manifests as a lateral instability of the joint.

Method used

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  • Patient Selectable Joint Arthroplasty Devices and Surgical Tools
  • Patient Selectable Joint Arthroplasty Devices and Surgical Tools
  • Patient Selectable Joint Arthroplasty Devices and Surgical Tools

Examples

Experimental program
Comparison scheme
Effect test

example 1

Design and Construction of a Three-Dimensional Articular Repair System

Areas of cartilage are imaged as described herein to detect areas of cartilage loss and / or diseased cartilage. The margins and shape of the cartilage and subchondral bone adjacent to the diseased areas are determined. The thickness of the cartilage is determined. The size of the articular repair system is determined based on the above measurements. (FIGS. 12-14). In particular, the repair system is either selected (based on best fit) from a catalogue of existing, pre-made implants with a range of different sizes and curvatures or custom-designed using CAD / CAM technology. The library of existing shapes is typically on the order of about 30 sizes.

The implant is a chromium cobalt implant (see also FIGS. 12-14 and 17-19). The articular surface is polished and the external dimensions slightly greater than the area of diseased cartilage. The shape is adapted to achieve perfect or near perfect joint congruity utilizing s...

example 2

Minimally Invasive, Arthroscopically Assisted Surgical Technique

The articular repair systems are inserted using arthroscopic assistance. The device does not require the 15 to 30 cm incision utilized in unicompartmental and total knee arthroplasties. The procedure is performed under regional anesthesia, typically epidural anesthesia. The surgeon can apply a tourniquet on the upper thigh of the patient to restrict the blood flow to the knee during the procedure. The leg is prepped and draped in sterile technique. A stylette is used to create two small 2 mm ports at the anteromedial and the anterolateral aspect of the joint using classical arthroscopic technique. The arthroscope is inserted via the lateral port. The arthroscopic instruments are inserted via the medial port. The cartilage defect is visualized using the arthroscope. A cartilage defect locator device is placed inside the diseased cartilage. The probe has a U-shape, with the first arm touching the center of the area of dis...

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Abstract

Disclosed herein are methods, compositions and tools for repairing articular surfaces repair materials and for repairing an articular surface. The articular surface repairs are customizable or highly selectable by patient and geared toward providing optimal fit and function. The surgical tools are designed to be customizable or highly selectable by patient to increase the speed, accuracy and simplicity of performing total or partial arthroplasty.

Description

FIELD OF THE INVENTIONThe present invention relates to orthopedic methods, systems and prosthetic devices and more particularly relates to methods, systems and devices for articular resurfacing. The present invention also includes surgical molds designed to achieve optimal cut planes in a joint in preparation for installation of a joint implant.BACKGROUND OF THE INVENTIONThere are various types of cartilage, e.g., hyaline cartilage and fibrocartilage. Hyaline cartilage is found at the articular surfaces of bones, e.g., in the joints, and is responsible for providing the smooth gliding motion characteristic of moveable joints. Articular cartilage is firmly attached to the underlying bones and measures typically less than 5 mm in thickness in human joints, with considerable variation depending on joint and site within the joint. In addition, articular cartilage is aneural, avascular, and alymphatic. In adult humans, this cartilage derives its nutrition by a double diffusion system thr...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61B17/56
CPCA61B5/4504Y10T29/49A61B5/4523A61B5/4528A61B5/4533A61B17/154A61B17/155A61B17/157A61B17/158A61B17/1666A61B17/1675A61B17/1746A61B19/50A61B19/5244A61B2017/568A61B2019/505A61B2019/508A61F2/30756A61F2/30942A61F2/38A61B17/1677A61B17/1682A61B17/1703A61B17/1767A61B17/15A61B17/1739G06F17/50A61B5/4514A61B34/20A61B34/10A61B2034/108A61B2034/105B33Y80/00G06F30/00G06F30/10
Inventor FITZ, WOLFGANGLANG, PHILIPP
Owner CONFORMIS
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