The invention relates to a method and a device for preventing dislocation of hip arthroplasty implants. The invention prevents dislocation by providing a restraining force on the femoral part of the implant under all movements of the leg. The invention further provides a method for mounting the device on a hip arthroplasty implant.
In most western countries, the typical number of total hip joint arthroplasty every year lies between 0.5-1 ‰ of the population. World-wide an estimated number of 1 million people have a total hip joint arthroplasty every year (2003), with numbers increasing. Although total hip joint arthroplasty is a very successful orthopaedic surgical procedure, it suffers from a serious drawback, namely dislocation of the hip joint. Dislocation typically occurs after a wrong movement of the leg by the patient, whereby the femoral head is drawn out of the cup. The causes are many, e.g. wrong or imprecise placement of the arthroplasty components, looseness in the surrounding tissue, of failure on the patients side to follow the restrictions in movements following from the surgery.
Dislocation after a total hip joint arthroplasty is a common adverse effect for patients having hip arthroplasty implants. Surveys report that 3-5% of the patients experience a dislocation at some point. However, numbers as high as 15% has been reported. A dislocation can occur at any time in the lifetime of the arthroplasty, with an increased risk within the first month after the operation. It is not only a nuisance for the patient, It is also a substantial economical burden to hospitals and insurance companies.
A number of measures have been taken to avoid dislocation, including modification of the components to try and make the arthroplasty more stable. However, any use of locking mechanisms between the femoral ball and the acetabular socket has been fraught with problems. Such constrained sockets fail early because of high stresses arising from impingement between the socket and femoral neck. This may cause the socket to pull out from the bone attachment In the pelvis, or dislodge the ring lock holding the devices together.
A number of flexible constraining devices have been suggested.
U.S. Pat. No. 5,755,907 describes an implantable module for use with a prosthetic joint that utilises a bellows and bearing with a rotating seal for encapsulating the articulating members of the implant. The bellows and the bearing primarily serve the purpose of containing a lubricant to decrease the wear to the articulating parts. The implant module further serves the purpose of keeping the articulating bearing surfaces in proper alignment by providing a spring force from the metallic bellows. The bearing with the rotating seal connects the bellows and femoral neck of the implant. The rotating seal ensures free rotation of the femor in relation to the bellows.
U.S. Pat. No. 6,228,122 discloses a semiconstrained net device to be attached to an acetabular cup and having a net ring around the femoral neck of the implant. The net device serves the purpose of preventing dislocation between the acetabular cup and the replacement femur. The net is fixed at specific positions of the acetabular cup to provide tension only at specific positions of the hip joint. In alternatively embodiments, the net is attached directly to a point on the femoral bone In one end and in the bone adjacent to the acetabular cup in the other end. This however, does not seem practically possible due to the difficulties that occur while placing the bore holes correct in the acetabular rim and hereby getting the correct tension of the semiconstraining device.
The net described in U.S. Pat. No. 6,228,122 is tightened to the cup of the adjacent bone by drawing a string of the net through a hole in the cup or bone. It is described that the tension of the net can be either pre-set or tensioned intraoperatively, presumably by knots on the string. It is a disadvantage of the pre-set tension that the tension of the device can not be precisely adapted to the anatomy of the patient. It is a disadvantage that the intraoperative tensioning can not be performed in a reproducible manner.
In the creative intellectual process leading to the present invention, the inventors have applied their detailed expertise within the field of hip arthroplasty combined with a dynamical and mechanical approach. This has given a thorough understanding of the dynamical aspects of hip dislocation in arthroplasty implants.
It is a problem of the existing devises that they only serve as a stop for preventing the femoral head from popping out of the cup. They do not oppose movement to positions where such popping is likely to occur, and as the forces in play in these positions are extremely large, it is the experience of the Inventors that they either allow dislocation or cannot endure the strain and break.
Dislocation may occur at specific positions of the joint and during special combinations of movements of the leg. Hence, in order for an anti-dislocation device to function properly, It should prevent the joint in reaching positions where dislocations are likely to occur by restraining movements typically leading to those positions. Alternatively the device should provide a further extra securing of the femoral head in the cup at the positions where dislocations are likely to occur. Both these demands may be met by a device which
The device according to present invention provides these functions whilst representing a substitution of the anatomic and physiologic fibrous capsule. In order not to reduce the freedom of movement of the patient's leg, the restraining and securing forces should preferably increase with the amplitude of the movement.
In this description, a hip arthroplasty implant comprises at least the following components, an acetabular cup to be mounted in the acetabular cavity of a pelvis, a femoral stem to be mounted in the proximal end of a femoral bone and having a femoral neck, and a femoral head to be mounted on the femoral neck and to be situated in a receiving cavity of the acetabular cup. These components will be referred to throughout the text.
In general, any movement of a physical object can be resolved into a translation of the object to obtain its new position followed by a rotation around a properly chosen axis to obtain its new orientation. In a similar fashion, any normal movement of a hip joint can be resolved into two rotations around perpendicular axes; a rotation around a first axis through the centre of the femoral neck followed by a rotation around a second axis through the centre of the femoral head, which axis is perpendicular to the first axis. In the present specification, rotation around the first axis is referred to as axial rotation, whereas rotation around the second axis is referred to as planar rotations (as the femoral neck spans a plane during this). Almost all movements of the leg include combinations of axial and planar rotations. The above description of hip joint movements is by no means the only possible choice, but serves to unambiguously define the scope of the present invention and can be used to describe all possible hip joint movements.
In a first aspect, the invention provides a device for preventing dislocation of a hip arthroplasty implant, the device comprising
It is of importance that the second rim is fastened in fixed relation to the femoral neck and that it is fastened to at least partly circumvent the femoral neck. The fixed fastening means that the femoral neck can not rotate without twisting the collar. Thus, any movement involving axial rotations will twist the tubular collar and thereby also stretch it along its longitudinal axis. Thereby, the tubular collar will execute a force restraining the movement of the femoral neck and a force pulling the femoral head towards the receiving cavity of the cup. These forces arise because the longitudinal stretching generates a force which can be resolved into two perpendicular components. A first component is perpendicular to the neck and represents a force restraining the movement. A second component is parallel to the neck and represents a securing force for holding the femoral head in the cup (please refer to
As the forces work on the femoral neck, and not the head itself, it is important that they work on all sides of the neck at the same time. If not, the total resulting securing force component may be asymmetric resulting in a skew pull of the neck towards the cup. Therefore, it is an important feature that the second rim is fastened so as to at least partly circumvent the femoral neck. Preferably, the tubular collar, the rims and the fastenings means completely encircle the neck etc., however, for the purpose of mounting or assembling the device, it may be advantageous to have small open or incomplete sections.
The tubular collar may be a mesh woven in the form of an open stocking by e.g. cross-linked HMDPE fibres, polyethylene fibres, or fibres of other known biocompatible materials. The fabric of the mesh preferably consists of bioacceptable material. To provide the longitudinal stretching force, the tubular collar is preferably elastic in at least a longitudinal direction. The elasticity should be chosen so that the collar is stretched without tearing by the forces In play when the device is mounted on a grown up human being. Further, the tubular collar may be elastic in a radial direction. The elastic properties of the mesh are related to the weaving technique used in the fabric.
In alternative embodiments, the tubular collar may be formed by a continuous sheet or membrane of known, elastic biocompatible material such as artificial rubbers. The elastic material is preferably enforced to increase it strength and/or elasticity and/or providing a maximum stretching limit for the material. The tubular collar may also incorporate a bellows comprising metal springs. In all embodiments, the tubular collar preferably has the shape of a truncated cone.
The first and second fastening means preferably comprise first and second rings attached to the first and the second rim. The first ring may have one or more protrusions on, or incisions in, a first surface so that it can be assembled with a surface part of the acetabular cup, or with a flange to be fixed on the acetabular cup, having at least one corresponding incision or protrusion. There exist a large number of possible designs for attaching the first rim to the acetabular cup, all of which provide the essential feature of easy fixation using only biocompatible materials.
In a preferred embodiment, the second ring attached to the second rim has a slot for receiving a clamp formed as an open ring to be inserted in said slot. The femoral neck, or a flange to be fixed on the femoral neck, has an outer circumference with a shape corresponding to a shape of the inner circumference of said clamp. By mounting the second ring on the femoral neck (or the flange), the clamp can be inserted in the slot to fix the ring on the femoral neck.
Alternatively, the second ring may have one or more protrusions on or incisions In an internal circumference so that it can be mounted on the femoral neck, or a flange to be fixed on the femoral neck, having at least one corresponding incision or protrusion around its outer circumference.
This will allow for each of the end of the tubular collar to be fixed at several different positions so that the collar can be mounted In a position where it is not twisted.
In an alternative embodiment, the second fastening means comprises a ring attached to the second rim, which ring can be fixedly mounted around the femoral neck by shrink fitting. Alternatively, the second fastening means comprises a ring attached to the second rim, which ring can be fixedly mounted around the femoral neck by at least one bolt, crew, clamp or clip. There exist a large number of possible designs for attaching the second rim to the femoral neck, all of which provide the essential feature of prevent longitudinal and rotational movement of the second rim along/around the femoral neck.
In a second aspect, the invention provides a method for stabilisation of a hip arthroplasty implant with a device for preventing dislocation of the hip arthroplasty implant, the device for preventing dislocation comprising an elastic tubular collar having a first open end to be mounted in fixed relation to and at least partly encircling the receiving cavity of the acetabular cup, and a second open end to be mounted in fixed relation to and at least partly circumventing the femoral neck, the method preventing dislocation of the hip arthroplasty implant by the steps of
The movements of the joint away from the neutral position may be described by the previously defined axial and planar rotations. Alternatively, the movements may be described by the movements of the leg using the anatomical terms from the following definitions:
The movement of the leg may be described by the following movements:
In the experience of the inventors, dislocation is especially likely to occur under movements that are similar but inverse to those used by surgeons to relocate dislocated joints. These may be described as a combination of flexion and inward rotation and perhaps adduction.
The forces in play under movements of the joint of the hip implant will be described in larger detail elsewhere in the specification.
In a third aspect, the invention provides a method for mounting a device for preventing dislocation on a hip arthoplasty implant,
the device for preventing dislocation comprising
The position of the femoral component during mounting of the device Is Important for the performance. Preferably, the tubular collar should be uniformly tight when the leg is In a neutral position, so as to act upon movements towards positions where dislocations are likely to occur. However, the leg has many natural positions (when the patient is standing, lying, sitting etc.), and an appropriate position should be chosen. When an appropriate neutral position is chosen, attention should be paid to acetabular inclination and anteversion and leg length, among other things.
As described in relation to the first aspect, the first and second fastening means preferably comprise first and second rings attached to the first and the second rim. These rings are to be attached at the acetabular cup and at the femoral neck, respectively. As the femoral head is larger that the circumference of the second ring, the second ring is preferably mounted on the femoral neck before putting on the femoral head. Optionally, only the second ring is mounted, in which case the collar can be fastened to the second ring at a later stage.
The device and methods according to the invention is adapted to be used for hip arthoplasty in humans, but may also be applicable for dogs, horses, or other mammals.
Also shown in
The fastening means 22 and 25 provides the fixation of the collar to the cup and the stem. The collar can in principle be fastened to either the cup or stem prior to the operation. However, typically the collar can cause inconvenience during mounting of the stem and cup in the patient. For this reason, the mounting and final fastening of the collar will preferably be done at the end of the hip arthroplasty operation. During the final fastening, the tubular collar should be at least substantially uniformly tight and straight (little or no twisting) with the leg In a neutral position. It is therefore Important that the fastening means can fix the collar at several positions around the first axis 10.
The ring 30 further has two or more holes 33 for screws or bolts to fix the ring 30 to the part 34.
When the joint of the Implant undergoes planar rotations, one side of the collar is stretched as illustrated in
As described previously, axial rotations as illustrated in
When the movement is a combination of planar and axial rotations, as most normal movements are, the stretching/slacking of
Thus, the twisting of the collar enhances the anti-dislocation effect of the device.
As mentioned previously, the restraining and securing forces provided by the collar may increase with the amplitude of the movement. This will increase the freedom of movement of the leg for small amplitudes while increasing the restraining and securing forces for large amplitudes. The response of the collar depends on its elasticity, which depends on the applied material and the weave of the mesh.
The tubular collar of the device according to the invention may be embodied in many different ways, all providing the essential features. A large number of designs and materials may be applied.
The spring force from a typical metal spring will increase linearly with the distance In most of its dynamical range. This is illustrated by the curve 91 in the graph 90 Of
In a preferred embodiment, the tubular collar response with a force which Increase nonlinearly with an amplitude of a movement of the femoral neck. In another embodiment, the tubular collar response with a force which increase at least substantially linearly with an amplitude of a movement of the femoral neck.
Number | Date | Country | Kind |
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PA 2003 00894 | Jun 2003 | DK | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/DK04/00412 | 6/14/2004 | WO | 2/27/2007 |