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CN111297521A - Surface shoulder joint prosthesis - Google Patents

Surface shoulder joint prosthesis Download PDF

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Publication number
CN111297521A
CN111297521A CN202010158151.5A CN202010158151A CN111297521A CN 111297521 A CN111297521 A CN 111297521A CN 202010158151 A CN202010158151 A CN 202010158151A CN 111297521 A CN111297521 A CN 111297521A
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CN
China
Prior art keywords
section
prosthesis
shoulder joint
humeral head
connecting rod
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Pending
Application number
CN202010158151.5A
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Chinese (zh)
Inventor
解凤宝
史春宝
郭静
朱更博
侯宇从
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Chunlizhengda Medical Instruments Co Ltd
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Beijing Chunlizhengda Medical Instruments Co Ltd
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Priority to CN202010158151.5A priority Critical patent/CN111297521A/en
Publication of CN111297521A publication Critical patent/CN111297521A/en
Pending legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4014Humeral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic humeral shafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/3094Designing or manufacturing processes
    • A61F2/30942Designing or manufacturing processes for designing or making customized prostheses, e.g. using templates, CT or NMR scans, finite-element analysis or CAD-CAM techniques
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4081Glenoid components, e.g. cups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30772Apertures or holes, e.g. of circular cross section
    • A61F2002/30784Plurality of holes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/3094Designing or manufacturing processes
    • A61F2002/30985Designing or manufacturing processes using three dimensional printing [3DP]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4081Glenoid components, e.g. cups
    • A61F2002/4085Glenoid components, e.g. cups having a convex shape, e.g. hemispherical heads

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Transplantation (AREA)
  • Biomedical Technology (AREA)
  • Veterinary Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Geometry (AREA)
  • Prostheses (AREA)

Abstract

The invention belongs to the field of medical instruments and discloses a surface shoulder joint prosthesis which comprises a humerus head prosthesis matched with the shape of a humerus head of a human body, a connecting rod formed on the inner surface of the humerus head prosthesis and a broach detachably connected with the connecting rod, wherein an external thread section is formed on the connecting rod, an internal thread section matched with the external thread section and a first hollow section communicated with the tail end of the internal thread section are formed on the broach, and the external thread section of the connecting rod rotates to enter the first hollow section through the internal thread section and is accommodated and fixed in the first hollow section. The surface shoulder joint prosthesis can be firmly fixed with humerus bone of a human body, has good stability and wide applicability.

Description

一种表面肩关节假体A superficial shoulder joint prosthesis

技术领域technical field

本发明属于医疗器械技术领域,具体涉及一种表面肩关节假体。The invention belongs to the technical field of medical devices, and in particular relates to a surface shoulder joint prosthesis.

背景技术Background technique

传统的人工肩关节置换术包括肱骨头置换术和人工全肩关节置换术两大类,均需要去除整个肱骨头并安装假体,而表面肩关节置换术只是磨去肱骨头的一部分,在肱骨头的剩余部分套设与肱骨头外形适配的表面肩关节假体。Traditional artificial shoulder arthroplasty includes humeral head arthroplasty and artificial total shoulder arthroplasty, both of which need to remove the entire humeral head and install a prosthesis, while superficial shoulder arthroplasty only removes a part of the humeral head. The remaining part of the head is sheathed with a surface shoulder joint prosthesis adapted to the shape of the humeral head.

现有的表面肩关节假体的结构包括与肱骨表面形状适配的肱骨头假体和形成在肱骨头假体内表面的髓针,在使用时,首先去除肱骨头外层的骨质,在肱骨头上开一个用于安装髓针的孔,将表面肩关节假体的髓针对准肱骨头上的孔,对假体施加外力使得肱骨头假体的内表面与人体肱骨头外表面贴合接触,完成安装。为确保固定效果,也可以在肱骨头上开的孔内设置骨水泥,方便与人体肱骨骨质固定。The structure of the existing surface shoulder joint prosthesis includes a humeral head prosthesis adapted to the shape of the surface of the humerus and a medulla needle formed on the inner surface of the humeral head prosthesis. A hole is opened on the humeral head for installing the medullar needle, and the medullar needle of the surface shoulder joint prosthesis is aligned with the hole on the humeral head, and an external force is applied to the prosthesis to make the inner surface of the humeral head prosthesis fit with the outer surface of the human humeral head. touch to complete the installation. In order to ensure the fixation effect, bone cement can also be arranged in the hole opened on the humeral head to facilitate the fixation with the human humerus bone.

现有的表面肩关节假体虽然能够满足患者需求,但是在实际使用中发现髓针与人体肱骨为锥度压配配合,假体在植入人体并长时间使用时具有锥度压配失效的风险,一旦锥度压配失效,会导致假体在人体内游离并可能会出现切割神经的情况。同时肱骨头假体与髓针一体成型,容易出现肱骨头假体或者髓针的大小尺寸不合适同一患者的现象。Although the existing superficial shoulder joint prosthesis can meet the needs of patients, in actual use, it is found that the medulla needle and the human humerus are taper press fit, and the prosthesis has the risk of taper press fit failure when implanted into the human body and used for a long time. Once the taper press-fit fails, the prosthesis will become free in the body and may cut the nerve. At the same time, the humeral head prosthesis and the pulp needle are integrally formed, and it is easy to cause the phenomenon that the size of the humeral head prosthesis or the pulp needle is not suitable for the same patient.

针对现有技术的表面肩关节假体存在的缺陷,本领域的技术人员希望提出一种与人体肱骨头骨质固定牢固,稳定性良好同时适用性广泛的表面肩关节假体。In view of the defects of the prior art superficial shoulder joint prosthesis, those skilled in the art hope to propose a superficial shoulder joint prosthesis that is firmly fixed to the human humeral head bone, has good stability and has wide applicability.

发明内容SUMMARY OF THE INVENTION

本发明的目的在于提供一种与人体肱骨头骨质固定牢固,稳定性良好同时适用性广泛的表面肩关节假体。The purpose of the present invention is to provide a surface shoulder joint prosthesis which is firmly fixed to the bone of the human humeral head, has good stability and has wide applicability.

根据本发明的表面肩关节假体包括与人体肱骨头形状适配的肱骨头假体、形成在肱骨头假体内表面的连接杆以及与连接杆可拆卸连接的髓针,其中,连接杆上形成有外螺纹段,髓针上形成有与外螺纹段配合的内螺纹段和与内螺纹段的末端相连通的第一空心段,连接杆的外螺纹段经内螺纹段旋转至进入第一空心段,并被容纳固定在第一空心段内。The superficial shoulder joint prosthesis according to the present invention includes a humeral head prosthesis adapted to the shape of the human humeral head, a connecting rod formed on the inner surface of the humeral head prosthesis, and a medulla needle detachably connected with the connecting rod, wherein the connecting rod is on the An external thread segment is formed, an internal thread segment matched with the external thread segment and a first hollow segment communicated with the end of the internal thread segment are formed on the medulla needle, and the external thread segment of the connecting rod is rotated through the internal thread segment to enter the first hollow segment. The hollow section is accommodated and fixed in the first hollow section.

进一步地,髓针上还形成有与内螺纹段的首端相连通的第二空心段,连接杆上还形成有位于外螺纹段与肱骨头假体内表面之间的锥配段,其中,连接杆的外螺纹段经第二空心段穿过内螺纹段进入第一空心段后,锥配段压配在第二空心段内。Further, the medulla needle is also formed with a second hollow segment that communicates with the head end of the internal thread segment, and a taper fitting segment between the external thread segment and the inner surface of the humeral head prosthesis is also formed on the connecting rod, wherein, After the external thread segment of the connecting rod passes through the internal thread segment through the second hollow segment and enters the first hollow segment, the taper fitting segment is press-fitted in the second hollow segment.

进一步地,锥配段的外周壁和/或第二空心段的内周壁构造为粗糙面。Furthermore, the outer peripheral wall of the conical segment and/or the inner peripheral wall of the second hollow segment is configured as a rough surface.

进一步地,外螺纹段形成在连接杆的自由端,外螺纹段的轴向长度小于等于第一空心段的轴向长度。Further, the external thread segment is formed at the free end of the connecting rod, and the axial length of the external thread segment is less than or equal to the axial length of the first hollow segment.

进一步地,锥配段具有自靠近肱骨头假体内表面的第一端朝向远离肱骨头假体内表面的第二端逐渐减小的外径尺寸。Further, the taper fitting segment has an outer diameter dimension that gradually decreases from a first end close to the inner surface of the humeral head prosthesis toward a second end away from the inner surface of the humeral head prosthesis.

进一步地,连接杆上还形成有位于外螺纹段与锥配段之间的过渡段,过渡段的外径尺寸小于外螺纹段的外径尺寸,且过渡段的外径尺寸小于第二端的外径尺寸。Further, the connecting rod is also formed with a transition section between the outer thread section and the taper section, the outer diameter of the transition section is smaller than the outer diameter of the outer thread section, and the outer diameter of the transition section is smaller than the outer diameter of the second end. diameter size.

进一步地,髓针的外表面上还形成有周向分布的多条纵向筋。Further, a plurality of longitudinal ribs distributed circumferentially are formed on the outer surface of the pith needle.

进一步地,髓针的外表面的上部形成有HA+TI涂层,髓针的外表面的中下部形成有多孔立体结构层。Further, an HA+TI coating is formed on the upper part of the outer surface of the pulp needle, and a porous three-dimensional structure layer is formed on the middle and lower part of the outer surface of the pulp needle.

进一步地,肱骨头假体的内表面形成有HA+TI涂层。Further, the inner surface of the humeral head prosthesis is formed with HA+TI coating.

进一步地,肱骨头假体的内表面还形成有多个防旋凸起。Further, a plurality of anti-rotation protrusions are formed on the inner surface of the humeral head prosthesis.

优选地,多个防旋凸起设置成锥形并均匀分布,防旋凸起的轴线与肱骨头假体的直径方向形成夹角。Preferably, the plurality of anti-rotation protrusions are arranged in a conical shape and are evenly distributed, and the axis of the anti-rotation protrusions forms an included angle with the diameter direction of the humeral head prosthesis.

与现有技术相比,本发明的表面肩关节假体具有以下优点:Compared with the prior art, the superficial shoulder joint prosthesis of the present invention has the following advantages:

1)本发明的表面肩关节假体的肱骨头假体与髓针可拆卸设置,使得针对不同患者的肱骨头的尺寸可以选择最适合患者的肱骨头假体和髓针的规格,具有广泛的适用性。同时本发明的表面肩关节假体通过外螺纹段穿过内螺纹段与第一空心段的配合实现肱骨头假体与髓针的固定连接,即表面肩关节假体在安装完成后,外螺纹段与内螺纹段并不保持螺纹配合,而是位于第一空心段内,这样的设置可防止表面肩关节假体在运动过程中,外螺纹段因与内螺纹段保持螺纹配合而发生配合松动的情况的发生,从而有效避免了肱骨头假体与髓针的松脱,与使得本发明的表面肩关节假体具有更好的固定效果。1) The humeral head prosthesis and the medulla needle of the surface shoulder joint prosthesis of the present invention can be detachably arranged, so that the most suitable specifications of the humeral head prosthesis and the medullar needle can be selected according to the size of the humeral head of different patients, and it has a wide range of specifications. applicability. At the same time, the surface shoulder joint prosthesis of the present invention realizes the fixed connection between the humeral head prosthesis and the medulla needle through the cooperation of the external thread segment through the internal thread segment and the first hollow segment, that is, after the surface shoulder joint prosthesis is installed, the external thread The segment and the internal thread segment do not maintain the thread fit, but are located in the first hollow segment. This arrangement can prevent the surface shoulder joint prosthesis from loosening due to the thread fit between the external thread segment and the internal thread segment during the movement of the superficial shoulder joint prosthesis. Therefore, the loosening of the humeral head prosthesis and the pulp needle is effectively avoided, and the surface shoulder joint prosthesis of the present invention has a better fixation effect.

2)通过在髓针上形成有与内螺纹段的首端相连通的第二空心段,连接杆上形成有位于外螺纹段与肱骨头假体内表面之间的锥配段使得肱骨头假体与髓针除了外螺纹段与第一空心段配合固定的方式之外还具有锥配段与第二空心段的圧配固定方式,进一步地避免了肱骨头假体与髓针之间的松脱,从而使得本发明的表面肩关节假体具有更好的固定效果。2) By forming a second hollow section on the medulla needle that communicates with the head end of the inner thread section, and forming a taper section between the outer thread section and the inner surface of the humeral head prosthesis on the connecting rod, the humeral head prosthesis is formed. In addition to the way of cooperating and fixing the external thread section and the first hollow section, the body and the pulp needle also have the mode of cooperating and fixing the taper section and the second hollow section, which further avoids the loosening between the humeral head prosthesis and the pulp needle. Therefore, the surface shoulder joint prosthesis of the present invention has a better fixation effect.

3)通过在髓针的外表面的上部形成有HA+TI涂层,髓针的外表面的中下部形成有多孔立体结构层使得髓针的外表面为粗糙结构从而人体骨质在髓针的外表面易于融入、易于生长。3) The HA+TI coating is formed on the upper part of the outer surface of the pulp needle, and the middle and lower part of the outer surface of the pulp needle is formed with a porous three-dimensional structure layer, so that the outer surface of the pulp needle has a rough structure, so that human bone is in the pulp needle. The outer surface blends easily and grows easily.

4)通过在肱骨头假体的内表面形成有多个锥形并均匀分布的防旋凸起,并将防旋凸起构造成将防旋凸起的轴线与肱骨头假体的直径方向形成夹角使得肱骨头假体与人体肱骨头连接后,防旋凸起可插入人体肱骨头表面,防止肱骨头假体相对人体肱骨头旋转。4) By forming a plurality of conical and evenly distributed anti-rotation protrusions on the inner surface of the humeral head prosthesis, and configuring the anti-rotation protrusions to form the axis of the anti-rotation protrusions with the diameter direction of the humeral head prosthesis The included angle makes the humeral head prosthesis connected with the human humeral head, and the anti-rotation protrusion can be inserted into the surface of the human humeral head to prevent the humeral head prosthesis from rotating relative to the human humeral head.

附图说明Description of drawings

图1为根据本发明的表面肩关节假体的剖面图;1 is a cross-sectional view of a superficial shoulder joint prosthesis according to the present invention;

图2为图1所示的肱骨头假体的第一实施例的结构示意图;Fig. 2 is the structural representation of the first embodiment of the humeral head prosthesis shown in Fig. 1;

图3为图2所示的肱骨头假体的剖面图;Fig. 3 is the sectional view of the humeral head prosthesis shown in Fig. 2;

图4为图1所示的髓针的第一实施例的结构示意图;FIG. 4 is a schematic structural diagram of the first embodiment of the medulla needle shown in FIG. 1;

图5为根据本发明的髓针的第二实施例的结构示意图;5 is a schematic structural diagram of a second embodiment of the medulla needle according to the present invention;

图6为根据本发明的肱骨头假体的第二实施例的结构示意图。6 is a schematic structural diagram of a second embodiment of the humeral head prosthesis according to the present invention.

具体实施方式Detailed ways

为了更好的了解本发明的目的、结构及功能,下面结合附图,对本发明的表面肩关节假体做进一步详细的描述。In order to better understand the purpose, structure and function of the present invention, the superficial shoulder joint prosthesis of the present invention will be described in further detail below with reference to the accompanying drawings.

图1示出了根据发明的表面肩关节假体100的结构,包括与人体肱骨头形状适配的肱骨头假体1、形成在肱骨头假体1内表面的连接杆11以及与连接杆11可拆卸连接的髓针2,其中,连接杆11上形成有外螺纹段111,髓针2上形成有与外螺纹段111配合的内螺纹段23和与内螺纹段23的末端相连通的第一空心段21,连接杆11的外螺纹段111经内螺纹段23旋转至进入第一空心段21,并被容纳固定在第一空心段21内。1 shows the structure of a surface shoulder joint prosthesis 100 according to the invention, including a humeral head prosthesis 1 adapted to the shape of a human humeral head, a connecting rod 11 formed on the inner surface of the humeral head prosthesis 1, and a connecting rod 11 formed on the inner surface of the humeral head prosthesis 1 Removably connected medulla needle 2, wherein an external thread segment 111 is formed on the connecting rod 11, and an internal thread segment 23 that cooperates with the external thread segment 111 and a first thread segment that communicates with the end of the internal thread segment 23 are formed on the medulla needle 2. A hollow section 21 , the external thread section 111 of the connecting rod 11 is rotated through the internal thread section 23 to enter the first hollow section 21 , and is accommodated and fixed in the first hollow section 21 .

本发明的表面肩关节假体100在使用时,预先去除人体肱骨头的表面的骨质,并在人体肱骨头的表面开一个用于插入髓针2的孔,在安装本发明实施例一的表面肩关节假体100时,首先根据患者的肱骨头大小选择相应规格的肱骨头假体1和髓针2,将连接杆11对准髓针2,将连接杆11的外螺纹段11经髓针2的内螺纹段23旋入第一空心段21内,并被固定在第一空心段21内,从而使得肱骨头假体1与髓针2连接在一起。然后将髓针2对准预先在人体肱骨头表面上开出的孔,并对肱骨头假体1施加外力,髓针2逐渐深入至孔内,直至肱骨头假体1的内侧面与人体肱骨头的表面贴合,此时表面肩关节假体100与人体肱骨头固定良好。When the superficial shoulder joint prosthesis 100 of the present invention is used, the bone on the surface of the humeral head of the human body is removed in advance, and a hole for inserting the medulla needle 2 is opened on the surface of the humeral head of the human body. When the surface shoulder joint prosthesis 100 is used, first select the humeral head prosthesis 1 and the medulla needle 2 of the corresponding specifications according to the size of the patient's humeral head, align the connecting rod 11 with the medulla needle 2, and insert the external thread section 11 of the connecting rod 11 through the medulla. The internal thread section 23 of the needle 2 is screwed into the first hollow section 21 and fixed in the first hollow section 21 , so that the humeral head prosthesis 1 and the medulla needle 2 are connected together. Then, align the medulla needle 2 with the hole pre-drilled on the surface of the human humeral head, and apply external force to the humeral head prosthesis 1. The medullar needle 2 gradually penetrates into the hole until the inner surface of the humeral head prosthesis 1 is in contact with the human humerus. The surface of the head is fitted, and the surface shoulder joint prosthesis 100 is well fixed to the human humeral head at this time.

需要说明的是,现有的表面肩关节假体一般是一体形成的,即髓针与肱骨头假体是不可拆卸的,这种表面肩关节假体虽然具有不同规格,但是任意一种规格的表面肩关节假体的肱骨头假体和髓针的尺寸是固定不可变的,在实际应用中,同一规格的表面肩关节假体的肱骨头假体和髓针二者中只有一者能够适配患者,使得正常安装表面肩关节假体后,表面肩关节假体容易出现松动的现象,影响后期恢复和表面肩关节假体的使用寿命。本申请通过使肱骨头假体1与髓针2可拆卸设置,使得针对不同患者的肱骨头的尺寸可以选择最适合患者的肱骨头假体1和髓针2的规格,具有广泛的适用性。同时本发明的表面肩关节假体100通过外螺纹段111穿过内螺纹段23与第一空心段21的配合实现肱骨头假体1与髓针2的固定连接,即表面肩关节假体1在安装完成后,外螺纹段111与内螺纹段23并不保持螺纹配合,而是位于第一空心段21内,这样的设置可防止表面肩关节假体100在运动过程中,外螺纹段111因与内螺纹段23保持螺纹配合而发生配合松动的情况的发生,从而有效避免了肱骨头假体1与髓针2的松脱,与使得本发明的表面肩关节假体100具有更好的固定效果。It should be noted that the existing surface shoulder joint prosthesis is generally formed in one piece, that is, the medulla needle and the humeral head prosthesis are not detachable. Although this surface shoulder joint prosthesis has different specifications, the The dimensions of the humeral head prosthesis and the pulp needle of the superficial shoulder joint prosthesis are fixed and invariable. In practical applications, only one of the humeral head prosthesis and the pulp needle of the same specification of the superficial shoulder joint prosthesis can fit. With patients, the superficial shoulder joint prosthesis is prone to loosening after the normal installation of the superficial shoulder joint prosthesis, which affects the later recovery and the service life of the superficial shoulder joint prosthesis. By detaching the humeral head prosthesis 1 and the pulp needle 2, the present application can select the most suitable specifications of the humeral head prosthesis 1 and the pulp needle 2 according to the size of the humeral head of different patients, which has wide applicability. At the same time, the surface shoulder joint prosthesis 100 of the present invention realizes the fixed connection between the humeral head prosthesis 1 and the medulla needle 2 through the cooperation of the external thread segment 111 through the internal thread segment 23 and the first hollow segment 21, that is, the surface shoulder joint prosthesis 1 After the installation is completed, the external thread segment 111 and the internal thread segment 23 do not maintain a thread fit, but are located in the first hollow segment 21. Such a setting can prevent the external thread segment 111 from being damaged during the movement of the superficial shoulder joint prosthesis 100. The loose fit occurs due to the thread fit with the internal thread segment 23, thereby effectively avoiding the loosening of the humeral head prosthesis 1 and the medulla needle 2, and making the surface shoulder prosthesis 100 of the present invention better. Fixed effect.

根据本发明的表面肩关节假体100,髓针2上还可形成有与内螺纹段23的首端相连通的第二空心段22,连接杆11上还可形成有位于外螺纹段111与肱骨头假体1内表面之间的锥配段112,其中,连接杆11的外螺纹段111经第二空心段22穿过内螺纹段23进入第一空心段21后,锥配段112可压配在第二空心段22内。此时,将肱骨头假体1与髓针2连接起来的过程将是:将肱骨头假体1的连接杆11对准髓针2,连接杆11的外螺纹段111依次进入第二空心段22、内螺纹段23以及第一空心段21,并被固定在第一空心段21内,在这个过程中,锥配段112逐渐进入第二空心段22中,并压配在第二空心段22内。通过该设置使得肱骨头假体1与髓针2除了外螺纹段111与第一空心段21配合固定的方式之外还具有锥配段与第二空心段22的压配固定方式,进一步地避免了肱骨头假体1与髓针2之间的松脱,从而使得本发明的表面肩关节假体100具有更好的固定效果。According to the superficial shoulder joint prosthesis 100 of the present invention, the needle 2 may further be formed with a second hollow section 22 that communicates with the head end of the inner thread section 23, and the connecting rod 11 may be further formed with a second hollow section 22 located between the outer thread section 111 and the end of the inner thread section 23. The taper fitting section 112 between the inner surfaces of the humeral head prosthesis 1, wherein, after the external thread section 111 of the connecting rod 11 passes through the internal thread section 23 through the second hollow section 22 and enters the first hollow section 21, the taper fitting section 112 can be Press fit within the second hollow section 22 . At this time, the process of connecting the humeral head prosthesis 1 and the medulla needle 2 will be: align the connecting rod 11 of the humeral head prosthesis 1 with the medulla needle 2, and the external thread section 111 of the connecting rod 11 will enter the second hollow section in turn 22. The internal thread section 23 and the first hollow section 21 are fixed in the first hollow section 21. During this process, the taper fitting section 112 gradually enters the second hollow section 22 and is press-fitted in the second hollow section within 22. Through this arrangement, the humeral head prosthesis 1 and the medulla needle 2 have a press-fit fixing method of the taper-fitting section and the second hollow section 22 in addition to the fitting and fixing method of the external thread section 111 and the first hollow section 21, which further avoids The loosening between the humeral head prosthesis 1 and the pulp needle 2 is eliminated, so that the surface shoulder joint prosthesis 100 of the present invention has a better fixation effect.

根据本发明的表面肩关节假体100,锥配段112的外周壁和/或第二空心段22的内周壁可构造为粗糙面。由于锥配段112是与第二空心段22压配配合的,通过该设置使得锥配段112与第二空心段22压配后锥配段112不易从第二空心段22中脱出。在另一个实施例中,锥配段112的外周壁和/或第二空心段22的内周壁也可以是光滑面,从而能够实现更准确的配合。According to the surface shoulder joint prosthesis 100 of the present invention, the outer peripheral wall of the tapered fitting segment 112 and/or the inner peripheral wall of the second hollow segment 22 may be configured as a rough surface. Because the taper-fitting section 112 is press-fitted with the second hollow section 22 , this arrangement makes it difficult for the taper-fitting section 112 to escape from the second hollow section 22 after the taper-fitting section 112 is press-fitted with the second hollow section 22 . In another embodiment, the outer peripheral wall of the conical fitting section 112 and/or the inner peripheral wall of the second hollow section 22 may also be smooth, so that more accurate fitting can be achieved.

在如图2所示的实施中,外螺纹段111可形成在连接杆11的自由端,外螺纹段111的轴向长度可小于等于第一空心段21的轴向长度。需要说明的是,本实施例中外螺纹段111要与第一空心段21配合并使得外螺纹段111固定在第一空心段21内,因此,外螺纹111的轴向长度小于等于第一空心段21的轴向长度既要保证外螺纹段111可以旋进第一空心段21内,又要保证第一空心段21与外螺纹段111的配合满足肱骨头假体1与髓针2稳定的连接要求。In the implementation shown in FIG. 2 , the external thread segment 111 may be formed at the free end of the connecting rod 11 , and the axial length of the external thread segment 111 may be less than or equal to the axial length of the first hollow segment 21 . It should be noted that in this embodiment, the external thread segment 111 is to be matched with the first hollow segment 21 so that the external thread segment 111 is fixed in the first hollow segment 21. Therefore, the axial length of the external thread 111 is less than or equal to the first hollow segment. The axial length of 21 should not only ensure that the external thread segment 111 can be screwed into the first hollow segment 21, but also ensure that the cooperation between the first hollow segment 21 and the external thread segment 111 satisfies the stable connection between the humeral head prosthesis 1 and the medulla needle 2. Require.

结合图2、图3,锥配段112可具有自靠近肱骨头假体1内表面C的第一端F朝向远离肱骨头假体1内表面C的第二端G逐渐减小的外径尺寸。通过该设置使得锥配段112在与第二空心段22逐渐圧配时其接触面逐渐增加,增加结构的稳定性,同时患者在日后正常活动肩关节时产生的压应力可以使假体越来越紧,保证表面肩关节假体的稳定性。2 and 3, the taper fitting section 112 may have an outer diameter that gradually decreases from the first end F close to the inner surface C of the humeral head prosthesis 1 toward the second end G away from the inner surface C of the humeral head prosthesis 1 . Through this arrangement, the contact surface of the conical fitting section 112 is gradually increased when it is gradually fitted with the second hollow section 22, thereby increasing the stability of the structure. At the same time, the compressive stress generated when the patient normally moves the shoulder joint in the future can make the prosthesis more and more The tighter it is, the more stable the superficial shoulder prosthesis is.

如图1、图2所示,连接杆11上还可形成有位于外螺纹段111与锥配段112之间的过渡段113,过渡段113的外径尺寸可小于外螺纹段111的外径尺寸,且过渡段113的外径尺寸可小于第二端G的外径尺寸。由于本实施例中作为肱骨头假体1和髓针2之间连接作用的是外螺纹段111和第一空心段21配合、锥配段112和第二空心段22配合,因此通过上述设置使得过渡段113既能够稳定连接外螺纹段111和锥配段112,同时当外螺纹段111旋进髓针2的第一空心段21时,过渡段113不会被第二空心段22和内螺纹段23卡住。As shown in FIG. 1 and FIG. 2 , a transition section 113 between the external thread section 111 and the taper matching section 112 may also be formed on the connecting rod 11 , and the outer diameter of the transition section 113 may be smaller than the outer diameter of the external thread section 111 . size, and the outer diameter of the transition section 113 may be smaller than the outer diameter of the second end G. Since the connection between the humeral head prosthesis 1 and the medulla needle 2 in this embodiment is the cooperation between the external thread segment 111 and the first hollow segment 21, and the cooperation between the taper segment 112 and the second hollow segment 22, the above arrangement makes the The transition section 113 can stably connect the male thread section 111 and the taper section 112, and at the same time, when the male thread section 111 is screwed into the first hollow section 21 of the needle 2, the transition section 113 will not be affected by the second hollow section 22 and the female thread. Segment 23 is stuck.

在如图4所示的髓针2的一个实施例中,髓针2的外表面上可还形成有周向分布的多条纵向筋24。通过该设置可避免髓针2在插入人体肱骨头后发生旋转,防止表面肩关节假体100脱位。In one embodiment of the medulla needle 2 as shown in FIG. 4 , a plurality of longitudinal ribs 24 distributed circumferentially may be further formed on the outer surface of the medulla needle 2 . This arrangement can prevent the medulla needle 2 from rotating after being inserted into the human humeral head, and prevent the dislocation of the superficial shoulder joint prosthesis 100 .

如图4所示,髓针2的外表面的上部A可形成有HA+TI涂层(羟基磷灰石与纯钛混合涂层)25,髓针2的外表面的中下部B可形成有多孔立体结构层26。本发明的髓针2的HA+TI涂层和多孔立体结构层26均形成在髓针2的实体结构的表面上,其中髓针2的上部形成有第二空心段22、内螺纹段23以及第一空心段21,因此髓针2的外表面的上部具有由第二空心段22、内螺纹段23以及第一空心段21组成的孔结构,并不是完全封闭的实体结构,而髓针2的中下部是完全封闭的实体结构,连接杆11与髓针2的连接正是通过非完全封闭的实体结构连接的,因此这一结构又是受力的位置,要求其既有较高的强度。现有技术中常采用在假体表面喷涂TI涂层(纯钛涂层)的方法提高骨融入的性能,然而TI是惰性金属,缺乏骨诱导能力,在与人体生理环境接触时,不能与骨形成化学键合,无法促进新骨生长。本实施例中通过在髓针2的外表面的上部形成HA(羟基磷灰石)+TI涂层25使得髓针2的外表面的上部具有粗糙的外表面,人体骨质能够附着HA+TI涂层25生长,另外由于HA是人体骨骼的主要无机组成成分,具有优异的生物活性和骨传导能力。因此HA+TI涂层一方面具有良好的生物相容性和生物活性,另一方面具有更高的结合强度。这里所说的多孔立体结构层26与人体骨质的多孔结构类似,例如可以是3D打印骨小梁结构,易于人体骨质生长。需要说明的是,由于多孔立体结构层是多孔结构,其强度不高,因此将多孔立体结构层设置在髓针2的外表面的中下部B,即封闭的实体结构部分,确保髓针2具有较高强度。As shown in FIG. 4 , an HA+TI coating (a mixed coating of hydroxyapatite and pure titanium) 25 may be formed on the upper part A of the outer surface of the pulp needle 2 , and the middle and lower part B of the outer surface of the pulp needle 2 may be formed with Porous three-dimensional structure layer 26 . The HA+TI coating and the porous three-dimensional structure layer 26 of the pulp needle 2 of the present invention are both formed on the surface of the solid structure of the pulp needle 2, wherein the upper part of the pulp needle 2 is formed with a second hollow section 22, an internal thread section 23 and The first hollow section 21, so the upper part of the outer surface of the pulp needle 2 has a hole structure composed of the second hollow section 22, the inner thread section 23 and the first hollow section 21, which is not a completely closed solid structure, while the pulp needle 2 The middle and lower part of the device is a completely closed solid structure, and the connection between the connecting rod 11 and the medulla needle 2 is connected by a non-completely closed solid structure, so this structure is a force-bearing position, requiring both high strength. . In the prior art, the method of spraying TI coating (pure titanium coating) on the surface of the prosthesis is often used to improve the performance of bone integration. However, TI is an inert metal and lacks osteoinductive ability. When it is in contact with the human physiological environment, it cannot form with bone. Chemically bonded, cannot promote new bone growth. In this embodiment, the HA (hydroxyapatite)+TI coating 25 is formed on the upper part of the outer surface of the pulp needle 2, so that the upper part of the outer surface of the pulp needle 2 has a rough outer surface, and the human bone can attach HA+TI The coating 25 grows, and since HA is the main inorganic component of human bones, it has excellent biological activity and osteoconductivity. Therefore, the HA+TI coating has good biocompatibility and bioactivity on the one hand, and higher binding strength on the other hand. The porous three-dimensional structure layer 26 mentioned here is similar to the porous structure of human bone, for example, it can be a 3D printed bone trabecular structure, which is easy for human bone to grow. It should be noted that, since the porous three-dimensional structure layer is a porous structure, its strength is not high, so the porous three-dimensional structure layer is arranged on the middle and lower part B of the outer surface of the pulp needle 2, that is, the closed solid structure part, to ensure that the pulp needle 2 has higher strength.

在如图2所示的实施例中,肱骨头假体1的内表面C也可形成有HA+TI涂层。由于肱骨头假体1的内表面C与人体肱骨头接触,因此通过该设置使得肱骨头假体1的内表面C形成粗糙的结构,易于人体骨质生长。In the embodiment shown in FIG. 2 , the inner surface C of the humeral head prosthesis 1 may also be formed with an HA+TI coating. Since the inner surface C of the humeral head prosthesis 1 is in contact with the humeral head of the human body, through this arrangement, the inner surface C of the humeral head prosthesis 1 forms a rough structure, which is easy for human bone to grow.

如图2所示,肱骨头假体1的内表面C还可形成有多个防旋凸起12。通过该设置使得肱骨头假体1与人体肱骨头连接后,防旋凸起12可插入人体肱骨头表面,防止肱骨头假体1相对人体肱骨头旋转。As shown in FIG. 2 , a plurality of anti-rotation protrusions 12 may also be formed on the inner surface C of the humeral head prosthesis 1 . Through this arrangement, after the humeral head prosthesis 1 is connected with the human humeral head, the anti-rotation protrusion 12 can be inserted into the surface of the human humeral head to prevent the humeral head prosthesis 1 from rotating relative to the human humeral head.

在如图3所示的实施例中,多个防旋凸起12可设置成锥形并均匀分布,防旋凸起12的轴线D可与肱骨头假体1的直径E方向形成夹角α。通过该设置使得防旋凸起12的轴线D与肱骨头假体1的直径方向E形成夹角α,因此防旋凸起对人体肱骨头的作用力方向(在防旋凸起12的轴线方向)与发生旋转时的作用力方向(在垂直于直径E的方向)不共线,从而使得防旋凸起12在插入人体肱骨头后不易旋转。In the embodiment shown in FIG. 3 , a plurality of anti-rotation protrusions 12 can be arranged in a conical shape and evenly distributed, and the axis D of the anti-rotation protrusions 12 can form an included angle α with the direction of the diameter E of the humeral head prosthesis 1 . Through this setting, the axis D of the anti-rotation protrusion 12 and the diameter direction E of the humeral head prosthesis 1 form an included angle α, so the direction of the force of the anti-rotation protrusion on the human humeral head (in the direction of the axis of the anti-rotation protrusion 12 ) ) is not collinear with the force direction (in the direction perpendicular to the diameter E) when the rotation occurs, so that the anti-rotation protrusion 12 is not easy to rotate after being inserted into the human humeral head.

需要说明的是,在本发明实施例的表面肩关节假体100中,由于髓针2的外表面的中下部B具有多孔立体机构层26,髓针2的外表面的上部A和肱骨头假体1的内表面C具有HA+TI涂层,可确保人体骨质与表面肩关节假体100融合、生长良好,因此不需用骨水泥固定,还可以避免由于日后肩关节活动时骨水泥脱落或携带人体骨质一同脱落。但是由于现有技术中由于上述实施例一的髓针的成本较高,因此使用骨水泥连接的情况仍然比较常见,对此,在如图5所示的实施例中还示出了一种应用骨水泥连接的髓针2的结构,与如图4所示的实施例的髓针2相比,本实施例的髓针2的区别仅在于外表面未设置HA+TI涂层25和多孔立体结构26。It should be noted that, in the superficial shoulder joint prosthesis 100 of the embodiment of the present invention, since the middle and lower part B of the outer surface of the medulla needle 2 has the porous three-dimensional mechanism layer 26, the upper part A of the outer surface of the medulla needle 2 and the humeral head prosthesis The inner surface C of the body 1 is coated with HA+TI, which can ensure that the human bone is fused with the surface shoulder joint prosthesis 100 and grows well, so it does not need to be fixed with bone cement, and it can also prevent the bone cement from falling off due to future shoulder joint activities. Or fall off with human bones. However, due to the high cost of the medulla needle in the first embodiment in the prior art, it is still relatively common to use bone cement for connection. For this, an application is also shown in the embodiment shown in FIG. 5 . The structure of the medulla needle 2 connected with bone cement, compared with the medulla needle 2 of the embodiment shown in FIG. 4 , the difference between the medulla needle 2 of this embodiment is only that the outer surface is not provided with the HA+TI coating 25 and the porous three-dimensional Structure 26.

此外,仍然需要说明的是,对于不同患者的肱骨头的症状,需要对不同患者的人体肱骨头作不同的处理,由此可使得去除表面骨质的人体肱骨头具有不同的形状。例如,包覆型肱骨头是为了适用对于大结节骨质增生、硬化、肩袖损伤的患者,需要采用如图6所示实施例的包覆型肱骨头假体1以增加关节面的可接触范围,图6中所示的包覆型肱骨头假体的与图2所示的肱骨头假体的区别仅在于内表面形状不同。需要注意的是,针对患者的肱骨头的不同症状,肱骨头假体1的内表面的形状也可作相应改变,在此不再赘述。In addition, it still needs to be explained that for the symptoms of the humeral head of different patients, the human humeral head of different patients needs to be treated differently, so that the human humeral head from which the superficial bone is removed can have different shapes. For example, the covered humeral head is suitable for patients with hyperostosis, sclerosis and rotator cuff injury of the greater tuberosity, and the covered humeral head prosthesis 1 according to the embodiment shown in FIG. Contact range, the wrap-type humeral head prosthesis shown in FIG. 6 differs from the humeral head prosthesis shown in FIG. 2 only in the shape of the inner surface. It should be noted that, according to different symptoms of the patient's humeral head, the shape of the inner surface of the humeral head prosthesis 1 can also be changed accordingly, which will not be repeated here.

最后应说明的是:以上各实施例仅用以说明本发明的技术方案,而非对其限制;尽管参照前述各实施例对本发明进行了详细的说明,本领域的普通技术人员应当理解:其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分或者全部技术特征进行等同替换;而这些修改或者替换,并不使相应技术方案的本质脱离本发明各实施例技术方案的范围,其均应涵盖在本发明的权利要求和说明书的范围当中。尤其是,只要不存在结构冲突,各个实施例中所提到的各项技术特征均可以任意方式组合起来。本发明并不局限于文中公开的特定实施例,而是包括落入权利要求的范围内的所有技术方案。Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention, but not to limit them; although the present invention has been described in detail with reference to the foregoing embodiments, those of ordinary skill in the art should understand that: The technical solutions described in the foregoing embodiments can still be modified, or some or all of the technical features thereof can be equivalently replaced; and these modifications or replacements do not make the essence of the corresponding technical solutions deviate from the technical solutions of the embodiments of the present invention. The scope of the invention should be included in the scope of the claims and description of the present invention. In particular, as long as there is no structural conflict, each technical feature mentioned in each embodiment can be combined in any manner. The present invention is not limited to the specific embodiments disclosed herein, but includes all technical solutions falling within the scope of the claims.

Claims (10)

1. A surface shoulder joint prosthesis is characterized by comprising a humerus head prosthesis matched with the shape of a humerus head of a human body, a connecting rod formed on the inner surface of the humerus head prosthesis, and a broach detachably connected with the connecting rod, wherein an external thread section is formed on the connecting rod, an internal thread section matched with the external thread section and a first hollow section communicated with the tail end of the internal thread section are formed on the broach, and the external thread section of the connecting rod rotates to enter the first hollow section through the internal thread section and is contained and fixed in the first hollow section.
2. The superficial shoulder joint prosthesis of claim 1, wherein the broach further has a second hollow section formed thereon communicating with a head end of the internal thread section, and the connecting rod further has a tapered section formed thereon between the external thread section and the inner surface of the humeral head prosthesis, wherein the tapered section is press-fitted into the second hollow section after the external thread section of the connecting rod passes through the internal thread section via the second hollow section into the first hollow section.
3. The surface shoulder joint prosthesis of claim 2, wherein the outer peripheral wall of the tapered section and/or the inner peripheral wall of the second hollow section is configured as a roughened surface.
4. The surface shoulder joint prosthesis of claim 2, wherein the externally threaded section is formed at a free end of the connecting rod, the externally threaded section having an axial length that is less than or equal to an axial length of the first hollow section.
5. The facial shoulder joint prosthesis of any one of claims 2-4, wherein the tapered section has an outer diameter dimension that gradually decreases from a first end proximal to the inner surface of the humeral head prosthesis toward a second end distal to the inner surface of the humeral head prosthesis.
6. The surface shoulder joint prosthesis of claim 5, wherein the connecting rod further defines a transition section therebetween, the transition section having an outer diameter dimension less than an outer diameter dimension of the outer threaded section and an outer diameter dimension less than an outer diameter dimension of the second end.
7. The surface shoulder joint prosthesis of any one of claims 1-4, wherein the outer surface of the broach is further formed with a plurality of circumferential longitudinal ribs.
8. The surface shoulder joint prosthesis of any one of claims 1-4, wherein an upper portion of the outer surface of the broach is formed with an HA + TI coating, and a middle-lower portion of the outer surface of the broach is formed with a porous three-dimensional structural layer.
9. The superficial shoulder joint prosthesis of any of claims 1-4, wherein the inner surface of the humeral head prosthesis is formed with an HA + TI coating.
10. The facial shoulder joint prosthesis of claim 9, wherein the inner surface of the humeral head prosthesis is further formed with a plurality of anti-rotation protrusions.
CN202010158151.5A 2020-03-09 2020-03-09 Surface shoulder joint prosthesis Pending CN111297521A (en)

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