The present invention relates generally to a medical device for implantation in a femoral bone.
The hip joint is a synovial joint, joining the pelvis to the proximal portion of the femoral bone. Synovial joints are the most common types of joints in mammals, and are typical of nearly all limb joints. The contacting surfaces of said the pelvic, the acetabulum, and the contacting surface of the femoral bone, the caput femur, are smooth and rounded, and covered by articular cartilage. A synovial membrane, encapsulates the joint, forming a hip joint cavity, which contains synovial fluid. Outside the synovial membrane is a fibrous capsule and ligaments, forming an articular capsule.
There are both natural and pathological processes leading to deteriorated joint function. With age and wear, the articular cartilage becomes less effective as a shock absorber and a lubricated surface. Different degenerative joint diseases, such as arthritis, osteoartrithis, or osteoarthrosis, accelerate the deterioration.
Hip joint Osteoarthritis is a syndrome in which low-grade inflammation results in pain in the hip joints, caused by abnormal wearing of the Cartilage that acts as a cushion inside if the hip joint. This abnormal wearing of the cartilage also results in a decrease of the joints lubricating fluid called Synovial fluid. Hip joint Osteoarthritis is estimated to affect 80% of all people over 65 years of age, in more or less serious forms.
The present treatment for hip osteoarthritis comprises NSAID drugs, local injections of Hyaluronic acid or Glucocorticoid to help lubricating the hip joint, and replacing parts of the hip joint with a prosthesis through hip joint surgery.
The replacing of parts of the hip joint is one of the most common surgeries to date performed at hundreds of thousands of patients in the world every year. The most common method comprises placing a metal prosthesis in Femur and a plastic bowl in Acetabulum. This operation is done through an incision in the hip and upper thigh and through Fascia Iata and the lateral muscles of the thigh. To get access to the joint, the supporting Capsule attached to Femur and Ilium needs to be penetrated, making it difficult to get a fully functional joint after the surgery. Femur is then cut at the neck with a bone saw and the prosthesis is placed in femur either with bone cement or without. Acetabulum is slightly enlarged using an Acetabular reamer, and the plastic bowl is positioned using screws or bone cement.
The complications after hip joint surgery includes dislocation of the hip joint and loosening of the prosthesis from its fixation in the femoral bone. The loosening and/or dislocation of the prosthesis could be induced by an abnormal strain being placed on the hip joint from e.g. the patient falling or making a rapid movement of the hip, or by a bodily macrophage reaction.
A medical device for fixation in a femoral bone of a patient is provided, the medical device comprises: a connecting portion adapted to be connected to a prosthetic hip joint contacting portion, an expanding portion, and a bone contacting surface on the expanding portion. The expanding portion could be adapted to be at least partially inserted into the femoral bone of a patient and to expand within the femoral bone, such that the bone contacting surface is placed in contact with the inside of the femoral bone for fixating the medical device to the femoral bone. By the fixation using an expanding portion a sturdy fixation is achieved without the need to go into or penetrate bone, or the need for fixation using bone cement.
According to one embodiment the medical device comprises a bent portion placed between the connecting portion and an end portion of the medical device, e.g. for adjusting to the anatomy of the femoral bone.
According to one embodiment, the connecting portion could comprise a fixating portion adapted to fixate a prosthetic contacting portion. The fixating portion could comprise a threaded portion, which could enable the screw-fixation of a prosthetic hip joint contacting portion to the connecting portion.
According to one embodiment, the medical device has a centrally placed longitudinal axis reaching from the connecting portion to an end portion, and the expanding portion comprises a plurality of expansion members adapted to expand radially away from the longitudinal axis. By the plurality of expansion members the force from the expansion members is evenly distributed throughout the surface of the inside of the femoral bone.
The medical device could according to any of the embodiments herein have a centrally placed longitudinal axis reaching from the connecting portion to an end portion, and the medical device could comprise a plurality of expanding portions distributed axially along the longitudinal axis of the medical device.
According to one embodiment the medical device could comprise a plurality of expanding portions distributed axially along the longitudinal axis of the medical device and being adapted to radially expand independently of each other to allow different expansion of the different expanding portions.
According to another embodiment the medical device could comprise expanding portions placed between the bent portion and the end portion, or between the bent portion and the connecting portion.
According to yet another embodiment the medical device comprises a first and a second expanding portion, the first expanding portion is placed between the bent portion and the connecting portion, and the second expanding portion is placed between the bent portion and the end portion.
According to yet another embodiment the medical device comprises a plurality of expanding portions distributed axially along a longitudinal axis of the medical device, the plurality of expanding portions are placed between the bent portion and the end portion or between the bent portion and the connecting portion.
According to one embodiment, the expanding portion comprises a deformable expanding portion, wherein the expanding portion expands by the deformable expanding portion deforming, such that the bone contacting surface is placed in contact with the inside of the femoral bone for fixating the medical device to the femoral bone, wherein the deformable expanding portion allows a larger contact with the bone contacting surface.
According to one embodiment, the medical device further comprises an operating device adapted to operate the expanding portion. The operation device could comprising a flexible member in communication with the connecting portion and the end portion, the flexible member adapted to be pulled in the direction of the connecting portion for exerting an axial force on a part of the operating device causing, at least partially, radial expansion of the expanding portion. In other embodiments, the operation device could comprise an elastic operation device adapted to exert an elastic force on the expanding portion. The elastic operation device could for example be a spring.
According to one embodiment, the medical device further comprises an adjustment device for adjusting the tension of the elastic operation device and thus the force exerted by the expansion members. The operating device could further comprise a conical member adapted to contact a corresponding surface of the expanding portion for expanding the expanding portion. In one embodiment, the operating device could comprise a rotatable threaded portion adapted to engage a corresponding threaded portion of the medical device for expanding the expanding portion. The operating device could according to one embodiment comprise a rotatable threaded portion adapted to engage a corresponding threaded portion of the conical member for operating the conical member and thereby the corresponding surface of the expanding portion for expanding the expanding portion.
The bone contacting surface according to any of the embodiments herein could comprise at least one tapered member adapted to at least partially enter the bone of the inside of the collum femur, or the bone contacting surface could comprise a porous micro or nano structure adapted to promote the in-growth of bone in the medical device.
The medical device according to any of the embodiments, could further comprise a stabilizing member, which could be a stabilizing member adapted to be placed in contact with a cut surface of the femoral bone and/or an outer surface of the femoral bone. The stabilizing member could according to one embodiment be operable for exerting a force on the femoral bone for further fixating the medical device to the femoral bone.
The femoral bone comprises a longitudinal axis extending along the femoral bone, and the stabilizing member could according to one embodiment be adapted to extend on the outside of the femoral bone along a stabilizing portion of the longitudinal axis, and the expanding portion could be adapted to extend on the inside of the femoral bone, along at least a portion of the stabilizing portion of the longitudinal axis, such that a portion of the femoral bone is clamped between the expanding portion on the inside of the femoral bone and the stabilizing member on the outside of the femoral bone.
According to one embodiment, the medical device further comprises a prosthetic hip joint contacting portion which could be adapted to be detachably fixated to a fixating portion of the connecting portion. The fixating portion of the prosthetic hip joint contacting portion could comprise a threaded portion corresponding to a threaded portion of the fixating portion of the connecting portion, such that the prosthetic hip joint contacting portion can be screwed on to the connecting portion.
In any of the embodiments herein, the prosthetic contacting portion could comprise a spherical convex contacting portion or a spherical concave contacting portion, and the prosthetic contacting portion could comprises the stabilizing described in relation to any of the embodiments herein.
According to yet another embodiment, the prosthetic contacting portion could be rotatable in relation to the connecting portion, and the prosthetic contacting portion could be mechanically connected to an operating device operating the expanding portion, such that the expanding portion can be expanded by rotating the prosthetic contacting portion. The medical device could further comprise a locking member adapted to lock the prosthetic contacting portion in relation to the connecting portion.
According to one embodiment, the medical device further comprises a locking member adapted to lock the prosthetic contacting portion in relation to the connecting portion.
According to one embodiment, the prosthetic contacting portion comprises an artificial caput femur surface.
A method for mounting anyone of the embodiments herein for fixation of the medical device in a femoral bone of a patient is further provided. The method comprising: cutting the skin, dissecting a hip region of a patient, surgically affecting and open the femoral bone, inserting the expanding portion of the medical device at least partially into the femoral bone, and expanding within the femoral bone the expanding portion such that the bone contacting surface is placed in contact with the inside of the femoral bone for fixating the medical device direct or indirect to the femoral cortical bone.
According to one embodiment, the medical device comprises a plurality of expanding portions distributed axially along a longitudinal axis of the medical device and the method further comprises the steps of; expanding said plurality of expanding portions towards the femoral cortical bone.
According to one embodiment, the medical device further comprises an operating device adapted to operate the expanding portion, and the method further comprises the steps of: operating manually or by a motor the expanding portion to fixate the device towards the femoral cortical bone.
According to one embodiment, the expanding portions is suspended and adjustable to adjust the tension towards the femoral cortical bone, and the method comprises the steps of; adjusting the expanding portion of the device.
Please note that any embodiment or part of embodiment as well as any method or part of method could be combined in any way. All examples herein should be seen as part of the general description and therefore possible to combine in any way in general terms.
The invention is now described, by way of example, with reference to the accompanying drawings, in which:
b shows the collum femur in section,
a shows the step of removing a proximal part of the caput femur,
b shows the cross section A-A of the collum femur,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
c shows the medical device according to a one embodiment, in a first state,
d shows the medical device according to a one embodiment, in a second state,
e shows the medical device according to a one embodiment, in a first state,
f shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
c shows the medical device according to a one embodiment, in a first state,
d shows the medical device according to a one embodiment, in a second state,
e shows the medical device according to a one embodiment, in a first state,
f shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, when placed in a femoral bone,
b shows the medical device according to a one embodiment, when placed in a femoral bone,
c shows the medical device according to a one embodiment, when placed in a femoral bone,
d shows the medical device according to a one embodiment, when placed in a femoral bone,
a shows the medical device according to a one embodiment, when placed in a femoral bone,
b shows the medical device according to a one embodiment, when placed in a femoral bone,
c shows the medical device according to a one embodiment, when placed in a femoral bone,
d shows the medical device according to a one embodiment, when placed in a femoral bone,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, when placed in a femoral bone,
b shows a portion of the medical device and the femoral bone, in section,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
a shows the medical device according to a one embodiment, in a first state,
b shows the medical device according to a one embodiment, in a second state,
The hip joint is a synovial ball and socket joint which permits a large motion range for allowing a plurality of different movements of the lower limb. From a neutral position the following movements of the hip joint are normally possible: Lateral or external rotation, 30° with the hip extended, 50° with the hip flexed, medial or internal rotation 40°, extension or retroversion 20°, flexion or anteversion 140°, abduction 50° with hip extended, 80° with hip flexed, adduction 30° with hip extended, 20° with hip flexed.
The anatomy of the hip joint and its surroundings is further disclosed in: Marieb et al., Human Anatomy, 2003, Benjamin Cummings, San Francisco, pages 195-202 and in Moore et al., Clinically oriented anatomy, 1999, Lippincott, Williams & Wilkins, Baltimore, pages 501-653, both hereby incorporated by reference.
A severe but yet common complication following hip joint surgery is the loosening of the prosthesis from its fixation in the femoral bone. The loosening could be induced by an abnormal strain being placed on the hip joint from e.g. the patient falling or making a rapid movement of the hip. Most hip joint prosthesis are made from a material harder than the bone to which the prosthesis is fixated, which adds to the tension created between the fixations and the bone of the patient. Bone cement could further be used to fixate prosthesis, which could create a bodily macrophage reaction excavating the bone cement and thus causing loosening of the prosthesis. Other fixations, such as fixations using orthopedic screws penetrating the bone could also create a bodily reaction rejecting the foreign matter of the medical device. Eliminating the use of bone cement and orthopedic screws, and at the same time creating a stabile fixation would be very advantageous, furthermore, creating a fixation that has the ability to move slightly in the fixation in response to exposure to force e.g. from the patient falling would be even more advantageous.
In the following a detailed description of preferred embodiments of the present invention will be given. In the drawing figures, like reference numerals designate identical or corresponding elements throughout the several figures. It will be appreciated that these figures are for illustration only and are not in any way restricting the scope of the invention. Thus, any references to direction, such as “up” or “down”, are only referring to the directions shown in the figures. Also, any dimensions etc. shown in the figures are for illustration purposes.
The functional position of an implantable medical device or prosthesis is the position in which the hip joint can perform functional hip movements.
Elastic deformation is when a material deforms under stress (e.g. external forces), but returns to its original shape when the stress is removed. A more elastic material is to be understood as a material having a lower modulus of elasticity. The elastic modulus of an object is defined as the slope of its stress-strain curve in the elastic deformation region. The elastic modulus is calculated as stress/strain, where stress is the force causing the deformation, divided by the area to which the force is applied; and strain is the ratio of the change caused by the stress.
Elasticity is to be understood as a materials ability to deform in an elastic way.
Stiffness is to be understood as the resistance of an elastic body to deformation by an applied force.
a shows the proximal part of the caput femur 5 being removed e.g. by means of a bone saw. A surface of a section 601 is thus created perpendicularly to a length axis of the collum 6 and caput 5 femur.
b shows a section A-A of the collum femur 6, as shown in
a shows a medical device for fixation in the femoral bone of a patient. The medical device comprises a connecting portion 653 connected to a prosthetic contacting portion 45, in the embodiment shown being a convex prosthetic contacting portion 45. The medical device further comprising an expanding portion 654, and a bone contacting surface 655 on the expanding portion 654. The expanding portion 654 is adapted to be at least partially inserted into the femoral bone of a patient and to expand within the femoral bone such that the bone contacting surface 655 is placed in contact with the inside of the femoral bone for fixating the medical device to the femoral bone. The medical device has a centrally placed longitudinal axis 656 reaching from the connecting portion 653 to an end portion 657, and wherein the expanding portion 654 comprises a plurality of expansion members 658a-d, adapted to expand radially away from the longitudinal axis 656.
The medical device further comprises an operating device 659 adapted to operate the expanding portion 564, according to the embodiment shown in
The bone contacting surfaces 655, according to the embodiments shown in
b shows the medical device according to the embodiment shown in
c shows the medical device according to an embodiment comprising most elements described with reference to
d shows the medical device according to the embodiment shown in
e shows the medical device according to an embodiment comprising most elements described with reference to
f shows the medical device according to the embodiment shown in
a shows a medical device according to an embodiment in which the expanding portion 654 is identical to the expanding portion of the medical devices disclosed with reference to
In another embodiment (not shown), the medical device comprises two expanding portions, one placed between the end portion 657 and the bent portion 670, and the other one placed between the connecting portion 45 and the bent portion 670.
b shows the medical device according to the embodiment shown in
c shows an embodiment of the medical device similar to the embodiments shown in
d shows the medical device according to the embodiment shown in
e and 4f shows an embodiment of the medical device similar to the embodiments shown in
a shows the medical device described with reference to
b shows the medical device described with reference to
c shows the medical device when placed and expanded in the femoral bone. The medical device shown in
d shows the medical device shown in
a shows the medical device described with reference to
b shows the medical device described with reference to
c shows the medical device described with reference to
d shows the medical device shown in
a and 7b shows the medical device in an embodiment similar to the embodiment disclosed with reference to
b shows the medical device when the elastic operation device 680 has been released such that the expanding portion has been expanded pressing the bone contacting surfaces against the inside of the femoral bone 7.
a and 8b shows an embodiment of the medical device comprising the elements described with references to
b shows the medical device when the elastic operation device 680 has been released such that the expanding portion has been expanded pressing the bone contacting surfaces against the inside of the femoral bone 7, the adjustment device can now be used to adjust the tension of the elastic operation device 680.
a and 9b shows the medical device according to an embodiment in which the expanding portion 654 comprises a deformable expanding portion 654, wherein the expanding portion expands by the deformable expanding portion 654 deforming, such that the bone contacting surface 655 is placed in contact with the inside of the femoral bone for fixating the medical device to the femoral bone. The deformable expanding portion 654 deforms at deformation points 684 by the threaded member 661 pulling the end portion 657 towards the connecting portion 653 thus expanding the expanding portion 654 pushing the bone contacting surfaces 655 radially such that they are placed in contact with the inside of the bone of the femoral bone.
b shows the medical device when the deformable expanding portion 654 has expanded pressing the bone contacting surfaces 655 against the inside of the femoral bone 7.
a shows the medical device according to an embodiment in which the spherical concave contacting portion 110 is identical to the spherical concave contacting portion 110 described with reference to
b shows an embodiment similar to toe embodiment disclosed with reference to
The spherical concave contacting portion as shown in
a and 12b shows the medical device according to an embodiment in which the medical device comprises an operable stabilizing member 668, operable for exerting a force on the femoral bone for further fixating the medical device to the femoral bone. The operable stabilizing member 668 comprises a clamping portion 693 operable by means of an operation screw 692 for clamping a portion of the femoral bone between the clamping portion 693 and the connecting portion 654 of the medical device. The difference between the embodiments of
a shows the medical device according to an embodiment in which the medical device has a centrally placed longitudinal axis 656 reaching from the connecting portion 653 to an end portion 657, wherein the medical device comprises a plurality of expanding portions 654a-d, distributed axially along the longitudinal axis 656 of the medical device. The plurality of expanding portions 654a-d distributed axially along the longitudinal axis 656 of the medical device is adapted to radially expand independently of each other, to allow different expansion of the different expanding portions 654a-d. The different expansion could allow the expanding portions 654a-d to adapt to the uneven surfaces of the anatomy of the inside of the femoral bone. Since the different expanding portions expand independently of each other, one expanding portion 654a will expand until the bone contacting surface 655 of that particular expanding portion is placed in contact with the bone of the inside of the femoral bone, after which the other expanding portions 654b-d will continue to expand until their respective bone contacting surface is placed in contact with the inside of the femoral bone. Each expanding portion comprises four expansion members 658a-d each having a sloped surface 660 corresponding to a sloped surface 696 of the conical members 659, such that the conical members presses the expansion members radially from the longitudinal axis 656 when the conical members 659 are moved in the direction of the connecting portion 653.
b shows the medical device when the expanding portions 654a-d has been expanded for pressing the bone contacting surfaces 655 against the inside of the femoral bone 7.
a shows an embodiment of the medical device similar to the embodiment disclosed with reference to
16
b shows the medical device when the expanding portions 654a-d has been expanded for pressing the bone contacting surfaces 655 against the inside of the femoral bone 7.
The embodiments disclosed with reference to
The stabilizing member disclosed throughout the description and/or the medical device comprising the expanding portion disclosed throughout the description, could be further fixated using an adhesive, such as bone cement, or a mechanical fixation element, such as orthopedic screws.
The medical device according to any of the embodiments could comprise at least one material selected from a group consisting of: polytetrafluoroethylene (PTFE), perfluoroalkoxy (PFA) and fluorinated ethylene propylene (FEP). It is furthermore conceivable that contacting portions, the elastic operation device, or the entire medical device comprises a metal alloy, such as cobalt-chromium-molybdenum or titanium or stainless steel. Further conceivable materials are polyethylene, such as cross-linked polyethylene or gas sterilized polyethylene. The use of ceramic material is also conceivable, in the contacting surfaces or the entire medical device such as zirconium or zirconium dioxide ceramics or alumina ceramics. The part of the medical device in contact with human bone for fixation of the medical device to human bone, such as the bone contacting surface, could comprise a poorhouse structure which could be a porous micro or nano-structure adapted to promote the growth-in of human bone in the medical device for fixating the medical device. The porous structure could be achieved by applying a hydroxy-apatite (HA) coating, or a rough open-pored titanium coating, which could be produced by air plasma spraying, a combination comprising a rough open-pored titanium coating and a HA top layer is also conceivable. The contacting portions could be made of a self lubricated material such as a waxy polymer, such as PTFE, PFA, FEP, PE and UHMWPE, or a powder metallurgy material which could be infused with a lubricant, which preferably is a biocompatible lubricant such as a Hyaluronic acid derivate. It is also conceivable that the material of contacting portions or surfaces of the medical device herein is adapted to be constantly or intermittently lubricated. According to some embodiments the parts or portions of the medical device could comprise a combination of metal materials and/or carbon fibers and/or boron, a combination of metal and plastic materials, a combination of metal and carbon based material, a combination of carbon and plastic based material, a combination of flexible and stiff materials, a combination of elastic and less elastic materials, Corian™ or acrylic polymers.
Please note that any embodiment or part of embodiment as well as any method or part of method could be combined in any way. All examples herein should be seen as part of the general description and therefore possible to combine in any way in general terms.
Number | Date | Country | Kind |
---|---|---|---|
0900957-2 | Jul 2009 | SE | national |
0900958-0 | Jul 2009 | SE | national |
0900959-8 | Jul 2009 | SE | national |
0900960-6 | Jul 2009 | SE | national |
0900962-2 | Jul 2009 | SE | national |
0900963-0 | Jul 2009 | SE | national |
0900965-5 | Jul 2009 | SE | national |
0900966-3 | Jul 2009 | SE | national |
0900968-9 | Jul 2009 | SE | national |
0900969-7 | Jul 2009 | SE | national |
0900970-5 | Jul 2009 | SE | national |
0900972-1 | Jul 2009 | SE | national |
0900973-9 | Jul 2009 | SE | national |
0900974-7 | Jul 2009 | SE | national |
0900976-2 | Jul 2009 | SE | national |
0900978-8 | Jul 2009 | SE | national |
0900981-2 | Jul 2009 | SE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/SE10/50804 | 7/12/2010 | WO | 00 | 1/6/2012 |
Number | Date | Country | |
---|---|---|---|
61229738 | Jul 2009 | US | |
61229739 | Jul 2009 | US | |
61229743 | Jul 2009 | US | |
61229745 | Jul 2009 | US | |
61229746 | Jul 2009 | US | |
61229747 | Jul 2009 | US | |
61229748 | Jul 2009 | US | |
61229751 | Jul 2009 | US | |
61229752 | Jul 2009 | US | |
61229755 | Jul 2009 | US | |
61229761 | Jul 2009 | US | |
61229767 | Jul 2009 | US | |
61229778 | Jul 2009 | US | |
61229786 | Jul 2009 | US | |
61229789 | Jul 2009 | US | |
61229796 | Jul 2009 | US | |
61229735 | Jul 2009 | US |