CN211583675U - Prosthesis for shoulder joint - Google Patents

Abstract

The utility model discloses a false body for shoulder joint. The prosthesis for a shoulder joint comprises a constraint structure and a protection structure connected to the constraint structure; the restriction structure has an arc along the coronal plane. The prosthesis accords with the physiological structure of the shoulder joint of the human body, is self-limited in the gap under the shoulder peak, and can reduce the occurrence of adverse events such as foreign body sensation, dislocation, functional failure and the like of a patient. The prosthesis accords with the physiological structure of the shoulder joint of the human body, is self-limited in the gap under the shoulder peak, and can reduce the occurrence of adverse events such as foreign body sensation, dislocation, functional failure and the like of a patient. The shoulder sleeve injury patient is characterized in that the shoulder sleeve injury patient is supported by the protective structure, the shoulder sleeve injury patient is prevented from moving upwards by the shoulder sleeve injury patient, pain caused by impact between tissues is avoided, the force application arm of force of the deltoid muscle is increased, the shoulder joint function of the patient can be improved immediately, the limiting structure is used for being at least partially attached to.

Description

Prosthesis for shoulder joint

Technical Field

The utility model relates to the field of medical equipment, especially relate to a false body for shoulder joint.

Background

The rotator cuff is a muscle-tendon structure connecting the scapula and the humeral head, and is located on the outer layer of the shoulder joint capsule and the inner layer of the deltoid. The rotator cuff is composed of a front rotator cuff (inferior scapular muscle), an upper rotator cuff (superior spinatus) and a rear rotator cuff (inferior spinatus and minor deltoid muscle), and the rotator cuff has certain functions of enabling the upper arm to rotate inwards, outwards and outwards, and has the main functions of stabilizing the position of the humeral head on the glenoid and avoiding pain and the like caused by the humeral head moving upwards to impact the acromion. Therefore, the rotator cuff plays an extremely important role in the maintenance of the stability of the shoulder joint and the movement of the shoulder joint. However, with age, repeated long-term shoulder joint movement, hyperosteogeny under the shoulder or repeated violent movement may cause abrasion and tearing of soft tissues (joint bursa and rotator cuff) under the shoulder, so that the stability and mobility of the humeral head are damaged, the arm of the patient cannot be abducted or lifted during the shoulder joint movement, severe pain is caused by impact between bone or bone and the rotator cuff, the patient cannot sleep at night, and the quality of life and self-care ability are seriously affected.

At present, rotator cuff injury treatment modes mainly comprise surgical treatment, prosthesis implantation and the like. For a less severe rotator cuff injury, better results were obtained with surgical treatment, but for injuries greater than 3cm, the effect of surgical treatment was ambiguous and the recurrence was likely. The prosthesis implantation artificially limits the humeral head to move upwards, avoids pain caused by impact between tissues, further increases the force application arm of the deltoid muscle, and can improve the shoulder joint function of a patient immediately. In the prior art, the prosthesis implantation such as the prosthesis device, the biological pad, etc. may be displaced during the movement of the patient, for example, the displacement of the prosthesis device may cause the pressure distribution to change, the prosthesis is cracked, and the deteriorated contents are released after being exposed to 37 ° for a long time, which may cause further damage to the affected part, and the injection hole has a hard material, which may cause discomfort and foreign body sensation to the patient in a specific action after implantation. The displacement of the biologic pad can cause discomfort, restriction of movement, and even damage to the surrounding soft tissue, further causing injury to the patient. In addition, the prosthetic implants of the prior art have a potential for failure.

SUMMERY OF THE UTILITY MODEL

Based on this, there is a need to provide a prosthesis for shoulder joint that conforms to the physiological structure of human shoulder joint, is self-limited to the subacromial space to solve the implant displacement problem, and reduces the occurrence of adverse events.

A prosthesis for a shoulder joint comprising a constraint structure and a protective structure connected to the constraint structure; the restriction structure has an arc along the coronal plane.

In one embodiment, the constraining structure has a first face and a second face, both of which are curved, the second face for conforming, in whole or in part, to a greater nodule, and the protective structure for supporting an acromion.

In one embodiment, the restriction structure has a curvature along the sagittal plane.

In one embodiment, the radius of curvature of the second face of the confinement structure is 10 to 50 mm.

In one embodiment, the thickness of the restriction structure gradually increases from the end away from the protection structure to the end connected with the protection structure.

In one embodiment, the edge of the restriction structure is curved.

In one embodiment, the maximum width of the confinement structure is greater than the maximum width of the protection structure.

In one embodiment, the thickness H1 of the protective structure is 4-14 mm.

In one embodiment, the restriction structure has a linear length H2 along the sagittal plane of H1+15 mm.

In one embodiment, the protection structure comprises an arc segment, and a connection line between two end points of the arc segment and the maximum width of the limiting structure forms an isosceles trapezoid.

In one embodiment, the curvature of the arc line segment is less than or equal to 0.21mm^-1。

In one embodiment, the angle of the lower base angle of the isosceles trapezoid ranges from 45 to 90 degrees.

In one embodiment, the limiting structure has a first accommodating cavity, the protecting structure has a second accommodating cavity communicated with the first accommodating cavity, and the first accommodating cavity and the second accommodating cavity are both used for filling with filler.

In one embodiment, an injection hole is formed in the limiting structure and/or the protecting structure, the injection hole is communicated with the first accommodating cavity and the second accommodating cavity, and a one-way valve is arranged in the injection hole.

The utility model is used for the false body of the shoulder joint accords with the physiological structure of the shoulder joint of the human body, is self-limited in the lower clearance of the shoulder peak, and can reduce the occurrence of adverse events such as foreign body sensation, dislocation, functional failure of patients and the like. The shoulder sleeve injury patient is characterized in that the shoulder sleeve injury patient is supported by the protective structure, the shoulder sleeve injury patient is prevented from moving upwards by the shoulder sleeve injury patient, pain caused by impact between tissues is avoided, the force application arm of force of the deltoid muscle is increased, the shoulder joint function of the patient can be improved immediately, the limiting structure is used for being at least partially attached to.

The utility model discloses a first face and second face of limit structure for shoulder joint's false body are the curved surface, so that limit structure and human humerus head or the whole or partial laminating of major tubercle can let the biggest limiting displacement of limit structure performance so, in the at utmost, avoid the false body to shift.

The utility model discloses a limit structure's for shoulder joint's false body edge is the arc, and this arc structure can suit with shoulder joint, raglan top physiology shape, can not be to patient's activity restriction, can not harm soft tissue on every side.

The utility model discloses a restriction structure for shoulder joint's false body has first holding chamber, and protection architecture has the second holding chamber that communicates with each other with first holding chamber, injects the filler in restriction structure and protection architecture, and protection architecture can laminate the rotator cuff, avoids rotator cuff and acromion or other organizational structure striking in the shoulder joint activity process, and can keep humerus head and acromion distance, maintains shoulder joint activity power arm length, reduces muscle load; the limiting structure can be tightly occluded with the humeral head of the shoulder joint of the human body, so that the limiting capacity is improved. The limit structure and the protection structure can be filled with filling liquid and colloid to achieve the purpose of fitting with the physiological structure of the joint, the shoulder joint function of a patient with rotator cuff injury can be well improved, the special appearance of the prosthesis adapts to the special physiological structure of the shoulder joint of a human body, the purposes of better supporting and reducing impact are achieved, and a better treatment effect is obtained.

The utility model discloses a false body for shoulder joint causes possible foreign body to the patient after for reducing the false body implantation to feel, when first holding chamber with when all filling the filler in the second holding intracavity, the thickness of limit structure is by keeping away from protection architecture's one end to the one end crescent who is connected with protection architecture, also the design of limit structure is the outside thinner, and the head end is bodiness gradually near, and limit structure is to the influence of humerus head during so reducible activity.

Drawings

FIG. 1 is a schematic view of various anatomical surfaces of a human body;

fig. 2 is a schematic side cross-sectional view of a prosthesis for a shoulder joint according to an embodiment of the present invention;

FIG. 3 is a schematic top view of the prosthesis for a shoulder joint shown in FIG. 1;

FIG. 4 is a schematic rear view of the prosthesis for a shoulder joint shown in FIG. 1;

FIG. 5 is a schematic front view of the prosthesis for a shoulder joint shown in FIG. 1;

FIG. 6 is a side schematic view of the prosthesis for a shoulder joint shown in FIG. 1;

FIG. 7 is a schematic view of the prosthesis for a shoulder joint shown in FIG. 1 in cooperation with a human body;

FIG. 8 is a side schematic view of another embodiment of a prosthesis for a shoulder joint; wherein L1 is the length of the prosthesis for the shoulder joint along the coronal plane, L2 is the length of the protective structure in the prosthesis for the shoulder joint along the coronal plane, H1 is the height of the protective structure in the prosthesis for the shoulder joint along the sagittal plane, and H2 is the height of the prosthesis for the shoulder joint along the sagittal plane;

FIG. 9 is a schematic top view of another embodiment of a prosthesis for a shoulder joint; wherein L3 is the width of the protective structure in the prosthesis for the shoulder joint along the horizontal plane and L4 is the width of the restraining structure in the prosthesis for the shoulder joint along the horizontal plane;

FIG. 10 is a schematic top view of another embodiment of a prosthesis for a shoulder joint;

fig. 11 is a schematic top view of another embodiment of a prosthesis for a shoulder joint.

Description of the reference numerals

10: a prosthesis for a shoulder joint; 100: a confinement structure; 110: a first accommodating cavity; 200: a protective structure; 210: a second accommodating cavity; 300: an injection hole; 400: an injection pipe; 500: a one-way valve; 600: and (4) filling materials.

Detailed Description

In order to facilitate understanding of the present invention, the present invention will be described more fully hereinafter with reference to the accompanying drawings. The preferred embodiments of the present invention are shown in the drawings. The invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used in the description of the invention herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items.

Referring to fig. 1, fig. 1 is a schematic diagram defining various anatomical surfaces of a human body. Wherein, sagittal plane 101: the finger is a longitudinal section which divides a human body or a joint into a left part and a right part from the front-back direction, wherein a sagittal plane passing through the middle of the human body is a middle sagittal plane which divides the human body into two parts which are equal to each other on the left and the right; coronal plane 102: the longitudinal section is a longitudinal section which divides a human body or a joint into a front part and a rear part from the left direction and the right direction, and the longitudinal section is vertical to a sagittal plane; horizontal plane 103: also called transverse plane, is a plane parallel to the ground plane and dividing the body or joint into upper and lower parts, which are perpendicular to the coronal and sagittal planes.

Referring to fig. 2, one embodiment of the present invention provides a prosthesis 10 for a shoulder joint including a constraint structure 100 and a protective structure 200 coupled to the constraint structure 100. The limiting structure 100 has a curvature along the coronal plane or the limiting structure 100 and the protective structure 200 have an angle along the coronal plane. Preferably, the restriction structure 100 has a curvature in both the coronal and sagittal planes, with the radius of curvature of the inner surface of the restriction structure 100 being 10 to 50 mm. Specifically, the confinement structure 100 has a first face and a second face, both of which are curved surfaces, e.g., the second face is an inner surface (a surface facing downward as shown in fig. 2). Referring to fig. 7, the second face is adapted to fully or partially conform to the humeral head and/or greater tuberosity and extends from the humeral head to at least partially cover the greater tuberosity. The utility model discloses the people discovers, compares with only covering the humerus head, and restriction structure 100's second face part or whole cover the major tubercle can avoid taking place when the arm carries out activities such as abduction internal rotation the false body aversion breaks away from, can be in with the torn wound protection of rotator cuff tendon simultaneously false body restriction structure is inboard, has further avoided tearing the wound and has strikeed the violent pain of patient with the skeleton striking. This allows the limiting structure 100 to exert an optimal limiting effect, avoiding, to the maximum, the displacement of the prosthesis for the shoulder joint. Preferably, the restriction structure 100 can be in the form of a half-bowl-shaped structure, the restriction structure 100 of the half-bowl-shaped structure being capable of conforming to the humeral head and functioning to maintain the position of the entire prosthesis for the shoulder joint. It is understood that in other embodiments, the structure and shape of the confinement structure 100 is not limited to the above, and the structure and shape of the confinement structure 100 may also be a half-tub, half-bowl, or the like.

Referring to fig. 7, the protective structure 20 is adapted to be supported in the space between the humeral head and the acromion of the human shoulder joint to support the acromion.

Further, referring to fig. 4 and 5, the edge of the restriction structure 100 is arc-shaped, and the edge of the restriction structure 100 is smooth, and the arc-shaped structure can adapt to the physiological shape of the top of the shoulder joint and the rotator cuff, so as to reduce the injury of the outer edge of the restriction structure 100 to the muscle tissue when the shoulder joint moves.

Further, referring to fig. 2 and 3, the maximum width of the restriction structure 100 is greater than the maximum width of the protection structure 200, and preferably, as shown in fig. 8, the width L4 at the transition between the restriction structure 100 and the protection structure 200 is greater than the width L3 of the protection structure 200, so as to improve the fit of the restriction structure 100 to the humeral head and greater tuberosity of the shoulder joint of the human body and to cooperate with the subacromial inferior capsular fold inflection to restrict the displacement of the protection structure 200 and the prosthesis for the shoulder joint as a whole. Preferably, the constraining structure 100 and/or the protective structure 200 are capable of deformation, which may be a restorative deformation upon compression, an expansive deformation upon filling with a filler, or other forms of deformation. The limiting structure 100 and/or the protecting structure 200 can be deformed to fit the gap between the humerus head of the shoulder joint of the human body and the shoulder peak of the shoulder joint of the human body, so as to adapt to the special physiological structure of the shoulder joint of the human body, achieve the purposes of better supporting and reducing impact, and obtain better treatment effect. In the filling process, the restriction structure 100 and/or the protection structure 200 can adapt to the physiological structure of the shoulder joint by deformation such as self-expansion after compression or expansion after filling, can be attached to the humeral head of a human body, and can limit the medial and lateral displacement of the prosthesis for the shoulder joint on the shoulder joint by matching with the physiological structure of reverse folding of the shoulder joint bursal crease, and can be limited in the gap under the shoulder peak to avoid dislocation.

In another embodiment, shown in FIG. 8, H1 is the height along the sagittal plane of protective structure 200 in prosthesis 10 for a shoulder joint, i.e., the thickness of protective structure 200, which is preferably 4-14 mm. According to the elastic mechanics principle of the compression of the closed cavity, P is sigma h/r, wherein P is the maximum pressure intensity bearable by the cavity, sigma is the hoop stress intensity of the material of the shell of the cavity, h is the wall thickness of the shell of the cavity, and r is the radius of the minimum position of the cavity. In the position of the gap under the shoulder peak where the shoulder joint prosthesis is implanted, the maximum pressure of mutual extrusion between the shoulder peak and the humeral head is about 88KPa (i.e. P is 88KPa), the height H1 of the shoulder joint prosthesis protection structure is 4-14mm (i.e. the minimum radius r of the cavity of the protection structure is 2-7 mm), and the value range of σ · H is 176-616 KPa · mm, which means the selection of the material of the shoulder joint prosthesis and the specific design of the wall thickness, for example, when the wall thickness H of the shoulder joint prosthesis is 0.1mm, the material with the prosthesis material strength σ ranging from 1760-6160 KPa can be selected at least, and in fact, non-degradable and degradable medical materials such as polyamide, polyester, polyethylene, polylactic acid, polycaprolactone and the like can meet the requirement. Therefore, H1 is preferably 4-14mm, which can realize the function of the shoulder joint prosthesis that the protective structure can support the humeral head and the acromion under the condition of common medical materials and conventional manufacturing precision.

H2 is the height of prosthesis 10 for the shoulder joint along the sagittal plane, which is preferably 9-34 mm. More preferably, the constraint structure 100 has a linear length H2 along the sagittal plane of H1+15mm, which allows the constraint structure 100 to cover the greater tuberosity of the humeral head while avoiding interference with movement of the rotator cuff muscle group due to the oversized constraint structure 100.

Referring to fig. 8, L1 is the length of the prosthesis 10 along the coronal plane for a shoulder joint, which is preferably 30-70 mm. L2 is the length of the protective structure 200 along the coronal plane in a prosthesis 10 for a shoulder joint, which is preferably 10-40 mm. Referring to fig. 9, L3 is the width of the protective structure 200 in the prosthesis 10 for a shoulder joint along a horizontal plane, which is preferably 15-60 mm. L4 is the width of the limiting structure 100 in the prosthesis 10 for a shoulder joint along the horizontal plane, which is preferably 20-70 mm. The above arrangement enables the protective structure 200 to separate the shoulder from the humeral head, and the restriction structure 100 covers the humeral head and greater tuberosity to prevent dislocation.

The above-described differently sized prostheses 10 for shoulder joints are suitable for humeral heads of different diameter sizes. For example, for a humeral head diameter of 5cm, it is preferred that H1 be 10-12mm, H2 be 25-27mm, L1 be 55-65mm, L2 be 25-35mm, L3 be 30-50mm, L4 be 55-60mm, and the radius of curvature of the inner surface of the constraining structure 100 be 25-30 mm.

Referring to fig. 8, the thickness of the restriction structure 100 gradually increases from an end away from the protection structure 200 to an end connected to the protection structure 200.

Fig. 10 is a top view of another embodiment of the shoulder joint prosthesis. As shown in fig. 10, the line connecting the maximum widths of the confinement structure 100 constitutes points D and C, and the guard structure 200 includes an arc segment whose ends constitute points a and B. The A, B, C, D points form an isosceles trapezoid, the structure can improve the transmission of a horizontal force value between the AB side and the CD side of the protection structure, when the arm abducts and is lifted, the humerus head rotates towards the inner side of the shoulder glenoid fossa to form a horizontal acting force from the CD to the AB direction on the protection structure, so that the horizontal extrusion between the protection structures is caused, and through the design of the profile of the large-angle trapezoid, the loss of the transmission of the force between the two side edges is reduced, so that the deformation wrinkle caused by the internal strain of the protection structure in the dynamic process of the arm abduction can be reduced. More preferably, the curvature of the arc segment AB is preferably less than or equal to 0.21mm^-1The curvature of the arc line of the CD section is preferably less than or equal to 0.15mm^-1。

The point A and the point D can be connected by one or more straight line segments, or connected by one or more arc segments, or connected by the straight line segments and the arc segments. As shown in FIG. 11, the points A and B include arc segments AB and AB therebetweenBC, wherein the curvature of the arc line of the AB section and the EF section is preferably less than or equal to 0.3mm^-1The curvature of the arc line of the BC section and the DE section is preferably less than or equal to 0.15mm^-1。

100 has a first receiving chamber 110, the protection structure 200 has a second receiving chamber 210 communicating with the first receiving chamber 110, and the first receiving chamber 110 and the second receiving chamber 210 are both filled with a filler 600. In the filling process, after the limiting structure 100 and the protecting structure 200 are filled with the filler 600, the protecting structure 200 can be attached to the rotator cuff, so that the rotator cuff is prevented from colliding with the acromion or other tissue structures in the shoulder joint movement process, the distance between the humeral head and the acromion can be kept, the shoulder joint movement arm length is maintained, and the muscle load is reduced; the limiting structure 100 can be tightly engaged with the humeral head of the shoulder joint of the human body, thereby improving the limiting capability.

Preferably, the restriction structure 100 and the protection structure 200 may be balloons, may be sponge-like elements, or may be non-inflatable structures.

When the limiting structure 100 has the first receiving cavity 110 and the protecting structure 200 has the second receiving cavity 210, the maximum thickness of the limiting structure 100 gradually increases from the end far away from the protecting structure 200 to the end connected to the protecting structure 200. The minimum thickness of the confinement structure 100 is the thickness before filling with the filler or the thickness after compressing the confinement structure 100; the maximum thickness of the confinement structure 100 is the thickness after filling with a filler or the thickness in the self-recovered state after compressing the confinement structure 100. The minimum thickness of the protective structure 200 is the thickness before filling with the filler or the thickness after compressing the protective structure 200; the maximum thickness of the protective structure 200 is the thickness after filling with a filler or the thickness in the self-recovered state after compressing the protective structure 200.

Referring to fig. 2, when the first receiving cavity 110 and the second receiving cavity 210 are filled with the filler 600, the thickness of the limiting structure 100 gradually increases from the end far away from the protecting structure 200 to the end connected to the protecting structure 200. In order to reduce the possible foreign body sensation to the patient after the prosthesis 10 for the shoulder joint is implanted, when the first receiving cavity 110 and the second receiving cavity 210 are both filled with the filler 600, the thickness of the restriction structure 100 gradually increases from the end away from the protection structure 200 to the end connected with the protection structure 200, i.e. the restriction structure 100 is designed to be thinner at the outer side and gradually increases toward the proximal end, so as to reduce the influence of the restriction structure 100 on the humeral head during movement.

In addition, the capsule wall of the protection structure 200 can be specifically optimized for different use requirements, such as more exercise requirements, and can be moderately thickened for increasing the service life.

Further, when the first receiving cavity 110 and the second receiving cavity 210 are filled with the filler 600, the thickness of the end of the restriction structure 100 connected to the protection structure 200 is the same as the thickness of the protection structure 200, so as to reduce discomfort of the humeral head during shoulder joint movement.

One of the surfaces of the protective structure 200 is curved so that it substantially conforms to the rotator cuff. Specifically, the protection structure 200 is an arc structure bent downwards on the plane of the transverse axis, the arc structure is adapted to the physiological shape of the top ends of the shoulder joint and the rotator cuff, after the filler 600 is injected, the protection structure 200 can be attached to the rotator cuff, the rotator cuff is prevented from colliding with the acromion or other tissue structures during the movement of the shoulder joint, the distance between the humeral head and the acromion can be kept, the length of the shoulder joint movement arm is maintained, and the muscle load is reduced.

Further, referring to fig. 3 and 5, the limiting structure 100 and/or the protecting structure 200 is provided with an injection hole 300, the injection hole 300 is communicated with the first accommodating cavity 110 and the second accommodating cavity 210, and a one-way valve 500 is provided in the injection hole 300, and the one-way valve 500 can prevent the filler 600 injected through the injection hole 300 from reversely flowing out.

Further, referring to fig. 2 and 6, the prosthesis 10 for shoulder joint further includes an injection tube 400 disposed in the first receiving chamber 110 and/or the second receiving chamber 210 and communicated with the injection hole 300, wherein an outward nozzle of the injection tube 400 is flush with an outer surface of the limiting structure 100 or the protecting structure 200, and a check valve 500 is disposed in the injection tube 400.

Further, as shown in fig. 6, the diameter of the end of the injection pipe 400 communicating with the injection hole 300 is smaller than the inward end thereof.

Preferably, the injection tube 400 has flexibility, which effectively solves the problems of the conventional art that the patient may feel uncomfortable and foreign body sensation during a specific action after implantation.

Further, as shown in fig. 6, the limiting structure 100 and the protection structure 200 are connected to form an integrated structure, and the design of the integrated structure of the limiting structure 100 and the protection structure 200 facilitates mold opening and processing, and has low manufacturing cost.

Further, the restriction structure 100, the protection structure 200 and the injection tube 400 are all made of non-degradable materials. The utility model discloses a restriction structure 100 and protective structure 200 for shoulder joint's false body 10 are made by non-degradable material, have solved the implant in the conventional art and have the problem of degradation inefficacy in the short term, have avoided being used for shoulder joint's false body 10 to break, make it can effectively work for a long time under 37 temperatures, effectively prevent the further damage that the rotten filler internal release led to the fact the affected part.

Further, the limiting structure 100 may be made of materials including, but not limited to, one or more of silicone, polyurethane, rubber, polyamide, polyester, and polyolefin. The protective structure 200 may be made of materials including, but not limited to, one or more of silicone, polyurethane, rubber, polyamide, polyester, and polyolefin. The injection tube 400 is made of a material including, but not limited to, one or more of silicone, polyurethane, rubber, polyamide, polyester, and polyolefin.

Further, referring to fig. 2, the prosthesis 10 for a shoulder joint further includes a filler 600, and the filler 600 is filled in the first receiving cavity 110 and the second receiving cavity 210. Preferably, the filler 600 includes a liquid and/or gel. For example, the filler 600 is water, silica gel, or the like.

In a preferred embodiment, the method of using the prosthesis 10 for a shoulder joint of the present invention comprises the steps of:

firstly, establish the incision on patient's shoulder joint skin, carry out conventional arthroscope and explore, assess patient's rotator cuff condition, when confirming that serious rotator cuff damage and conventional repair mode are not suitable for the treatment, adopt the utility model discloses a prosthesis 10 for shoulder joint intervenes the treatment.

The conventional cleaning of the shoulder joint of the patient is carried out, the space of the subacromial gap and the wide visual field are ensured, the size of the subacromial gap and the width of the greater tuberosity of the humerus head to the edge of the upper joint capsule are measured by utilizing a measurer, and the prosthesis 10 for the shoulder joint and the injection volume of the filler 600 with proper sizes are adaptively selected according to the measurement result of the measurer.

The prosthesis 10 for the shoulder joint, which has not been injected with the filler 600, is placed in the subacromial space using the passage established by the arthroscope, and then the restriction structure 100, the protection structure 200 are flattened under the arthroscope using the arthroscopic instrument and moved to the proper position.

The syringe is connected to the injection tube 400, and the filler 600 is slowly injected into the first receiving cavity 110 and the second receiving cavity 210 of the restriction structure 100 and the protection structure 200 using the syringe. The injector is disconnected from the injection tube 400, the patient's limb is passively moved, and the restriction structure 100 and the protection structure 200 are observed to be in place and displaced within the passive range of motion, such as to close the skin incision.

The utility model discloses a false body 10 for shoulder joint has permanent practical nature, accords with human shoulder joint physiology structure, from being limited to the clearance under the acromion, can reduce adverse events such as patient's foreign body sensation, dislocation, functional failure and take place. The limiting structure 100 and the protecting structure 200 can be filled with fillers 600 such as liquid, colloid and the like, so that the purpose of fitting with the physiological structure of the joint is achieved, the shoulder joint function of a patient with rotator cuff injury can be well improved, the special appearance of the shoulder joint prosthesis adapts to the special physiological structure of the shoulder joint of a human body, the purposes of better supporting and reducing impact are achieved, and a better treatment effect is obtained. Wherein, the protection structure 200 can limit the humerus head of the patient with rotator cuff injury from moving upwards, thereby avoiding pain caused by impact between tissues, further increasing the force application arm of the deltoid muscle and improving the shoulder joint function of the patient immediately. The limiting structure 100 enables the support body to realize position stabilization in the shoulder joint through a self-limiting structure, and reduces adverse events such as foreign body sensation, dislocation, functional failure and the like of a patient.

The technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.

The above-mentioned embodiments only represent some embodiments of the present invention, and the description thereof is specific and detailed, but not to be construed as limiting the scope of the present invention. It should be noted that, for those skilled in the art, without departing from the spirit of the present invention, several variations and modifications can be made, which are within the scope of the present invention. Therefore, the protection scope of the present invention should be subject to the appended claims.

Claims (13)

1. A prosthesis for a shoulder joint, comprising a constraint structure and a protection structure connected to the constraint structure; the restriction structure has an arc along the coronal plane.

2. A prosthesis for a shoulder joint as claimed in claim 1 wherein the constraint structure has a first face and a second face, both of which are curved, the second face being adapted to wholly or partially conform to a greater tuberosity and the protective structure being adapted to support a acromion.

3. A prosthesis for a shoulder joint as claimed in claim 1 wherein the constraint structure has a curvature along the sagittal plane.

4. A prosthesis for a shoulder joint as claimed in claim 2 wherein the radius of curvature of the second face of the restraining structure is 10 to 50 mm.

5. A prosthesis for a shoulder joint as claimed in claim 1, wherein the thickness of the restraining structure increases from an end remote from the protective structure to an end connected to the protective structure.

6. A prosthesis for a shoulder joint as claimed in claim 1, wherein the edges of the restraining structure are arcuate.

7. A prosthesis for a shoulder joint according to claim 1, wherein the maximum width of the restraining structure is greater than the maximum width of the protective structure.

8. A prosthesis for a shoulder joint according to claim 1, characterized in that the thickness H1 of the protective structure is 4-14 mm.

9. A prosthesis for a shoulder joint as claimed in claim 8 wherein the constraint structure has a linear length H2 along the sagittal plane of H1+15 mm.

10. A prosthesis for a shoulder joint according to claim 1, characterized in that the protection structure comprises an arc segment, the two end points of which form an isosceles trapezium with the line of maximum width of the restriction structure.

11. A prosthesis for a shoulder joint according to claim 10, characterized in that the curvature of the arc segment is ≤ 0.21mm^-1。

12. A prosthesis for a shoulder joint according to claim 10, characterized in that the angle of the lower base angle of the isosceles trapezoid is in the range 45-90 °.

13. A prosthesis for a shoulder joint according to any one of claims 1 to 12, wherein the restriction structure has a first receiving chamber and the protection structure has a second receiving chamber communicating with the first receiving chamber, the first and second receiving chambers being adapted to be filled with a filler.

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