JP6803826B2 - Osteojoint parts and osteosynthesis part formation method - Google Patents
Osteojoint parts and osteosynthesis part formation method Download PDFInfo
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Description
本発明は、骨折治療用の位置決め機能付きの骨接合部品に関するものである。 The present invention relates to an osteosynthesis component with a positioning function for fracture treatment.
動物等の骨折治療を行うに当たり、現在ではCTスキャン(コンピュータ断層撮影)のデータを基に、骨折した骨の表面形状を反映した骨接合部品を製作し治療を行う場合がある。また、骨接合部品は骨の形状に沿った形状であるため、手術中に骨接合部品の取り付け方向(身体側と末端側の方向)を間違えることは少ないと考えられている。 In treating fractures of animals and the like, at present, based on CT scan (computed tomography) data, there are cases where osteosynthesis parts that reflect the surface shape of the fractured bone are manufactured and treated. In addition, since the osteosynthesis component has a shape that follows the shape of the bone, it is considered unlikely that the attachment direction of the osteosynthesis component (direction of the body side and the end side) is mistaken during the operation.
しかし、特許文献1に記載の骨接合部品では、関節等の特異的な形状が存在しない部位の骨折治療においては、おおよその取り付け位置を決めることは可能だが、粉砕骨折等の骨と骨の間に隙間が存在する症例の場合は、骨接合部品の取り付け方向を間違えるミスが発生する可能性が大きい。 However, with the osteosynthesis component described in Patent Document 1, in the treatment of fractures in a part such as a joint where a specific shape does not exist, it is possible to roughly determine the attachment position, but between bones such as crushed fractures. In the case where there is a gap in the bone joint, there is a high possibility that a mistake will occur in the mounting direction of the osteosynthesis component.
粉砕骨折のように折れた骨と骨の間に隙間がある症例を整復する場合、従来の施術では医師の知識や経験を基にして整復し、骨接合部品を取り付ける場合が多い。さらに、整復用の骨接合部品の配置に関しても曖昧な部分があり、折れた骨を骨折前と同じ位置に整復し、骨接合部品を配置するのは困難である。特に、粉砕骨折等の骨と骨との間に隙間がある場合は骨接合部品の取り付け方向を間違えるミスが発生する可能性が大きい。 When reducing a case where there is a gap between the broken bones such as a crushed fracture, in the conventional treatment, the reduction is often performed based on the knowledge and experience of a doctor, and an osteosynthesis component is attached. Furthermore, there is an ambiguity regarding the arrangement of the osteosynthesis parts for reduction, and it is difficult to reduce the broken bone to the same position as before the fracture and to arrange the osteosynthesis parts. In particular, when there is a gap between bones such as a crushed fracture, there is a high possibility that a mistake in the attachment direction of the osteosynthesis component will occur.
本発明は、粉砕骨折等の治療であっても、骨を骨折前の位置と思われる予想位置に整復可能な位置決め機能を有する骨接合部品を提供することを目的とする。 An object of the present invention is to provide an osteosynthesis component having a positioning function capable of reducing a bone to a predicted position that is considered to be a position before the fracture even in the treatment of a crushed fracture or the like.
本発明の骨接合部品は、動物の骨の骨折部を固定する骨接合部品において、一端部分が前記骨折部の身体側の折れた第1骨の表面に接触し他端部分が前記骨折部の末端側の折れた第2骨の表面に接触する骨接合部品本体と、前記骨接合部品本体に配置され前記第1骨の破断面に接触する第1部材と、前記骨接合部品本体に配置され前記第2骨の破断面に接触する第2部材とを設けた、ことを特徴とする。 The osteosynthesis part of the present invention is an osteosynthesis part for fixing a fractured portion of an animal bone, one end of which is in contact with the surface of the broken first bone on the body side of the fractured portion and the other end of the fractured portion. An osteosynthesis component body that contacts the surface of the broken second bone on the terminal side, a first member that is arranged on the osteosynthesis component body and contacts the fracture surface of the first bone, and an osteosynthesis component body that is arranged on the osteosynthesis component body. It is characterized in that a second member that comes into contact with the fracture surface of the second bone is provided.
本発明の骨接合部品形成方法は、動物の骨の中間部分が骨折した骨折部を固定する骨接合部品を作成するに際し、前記骨折部の身体側の折れた第1骨と前記骨折部の末端側の折れた第2骨、および前記骨折部のない正常骨の形状を測定し、前記第1骨と前記第2骨を、前記測定によって得られた正常骨の形状データに基づいて骨折前の位置と思われる予想位置にデータ上で配置し、データ上で前記予想位置に配置された前記第1骨の表面と前記第2骨の表面の間に骨接合部品本体を接触させた形状データに基づいて、前記骨接合部品本体を貫通して前記第1骨の破断面に接触する位置と方向に第1部材を挿通するための第1貫通孔と、前記骨接合部品本体を貫通して前記第2骨の破断面に接触する位置と方向に第2部材を挿通するための第2貫通孔を形成し、一端が前記骨接合部品本体の裏面側に突出し、他端が前記骨接合部品本体の表面側に突出するように前記第1,第2部材を、前記骨接合部品本体の前記第1,第2貫通孔に挿通する、ことを特徴とする。 In the method for forming an osteosynthesis part of the present invention, when creating an osteosynthesis part for fixing a fractured portion in which an intermediate portion of an animal bone is fractured, the first bone broken on the body side of the fractured portion and the end of the fractured portion The shapes of the second bone with a broken side and the normal bone without the fractured part were measured, and the first bone and the second bone were obtained before the fracture based on the shape data of the normal bone obtained by the measurement. The shape data is arranged on the data at the predicted position that seems to be the position, and the osteosynthesis component body is brought into contact between the surface of the first bone and the surface of the second bone placed at the predicted position on the data. Based on this, the first through hole for inserting the first member in the position and direction of penetrating the osteosynthesis component body and contacting the fracture surface of the first bone, and penetrating the osteosynthesis component body, said. A second through hole for inserting the second member is formed at a position and direction in contact with the fracture surface of the second bone, one end protrudes to the back surface side of the osteosynthesis component body, and the other end is the osteosynthesis component body. The first and second members are inserted into the first and second through holes of the osteosynthesis component main body so as to project toward the surface side of the bone joint.
この構成によれば、骨接合部品を装着する際、獣医師の個人差による整復状態の違いを極力無くし、骨折前の正常な状態に極めて近い治療が可能となり、治癒後の患者(動物等)の日常における活動が再現される。また位置決め機能により誤装着が低減され再手術の抑制につながる。 According to this configuration, when attaching the osteosynthesis part, the difference in the reduction state due to individual differences of the veterinarian is eliminated as much as possible, and the treatment very close to the normal state before the fracture becomes possible, and the patient (animal, etc.) after healing becomes possible. Activities in daily life are reproduced. In addition, the positioning function reduces erroneous mounting and leads to suppression of reoperation.
以下に、本発明の骨接合部品を実施の形態に基づいて説明する。 Hereinafter, the osteosynthesis component of the present invention will be described based on the embodiment.
(実施の形態1)
図1(a)(b)は本発明の骨接合部品を使用した骨折治療部位を示している。
(Embodiment 1)
1 (a) and 1 (b) show a fracture treatment site using the osteosynthesis component of the present invention.
この骨接合部品100は、プレート状の骨接合部品本体101と、骨接合部品本体101に配置された第1部材としての身体側の位置決めピン104と、骨接合部品本体101に配置された第2部材としての末端側の位置決めピン105を有している。 The osteosynthesis component 100 includes a plate-shaped osteosynthesis component main body 101, a positioning pin 104 on the body side as a first member arranged in the osteosynthesis component main body 101, and a second osteosynthesis component main body 101. It has a positioning pin 105 on the terminal side as a member.
この骨接合部品100の構造を、図4に示した骨折治療における概略フローチャートと、従来の骨接合部品による図5に示した骨折治療のフローチャートを比較して説明する。 The structure of the osteosynthesis component 100 will be described by comparing the schematic flowchart of the fracture treatment shown in FIG. 4 with the flow chart of the fracture treatment shown in FIG. 5 using the conventional osteosynthesis component.
まず、従来の骨折治療の場合には、図5のステップS1において、骨折部のCTスキャンデータを取得する。 First, in the case of conventional fracture treatment, CT scan data of the fractured portion is acquired in step S1 of FIG.
ステップS2では、ステップS1によって得られたCTスキャンデータに基づいて3Dデータ上で骨折部を復元する。 In step S2, the fractured portion is restored on the 3D data based on the CT scan data obtained in step S1.
ステップS3では、3Dデータ上で復元した骨折部の骨形状に合わせて骨接合部品を作成する。 In step S3, an osteosynthesis part is created according to the bone shape of the fractured portion restored on the 3D data.
ステップS4では、患部を切開して骨折部を整復する。 In step S4, the affected area is incised and the fractured area is reduced.
ステップS5では、骨接合部品を骨折部に固定し、最後にステップS6で縫合して施術が完了する。 In step S5, the osteosynthesis part is fixed to the fractured portion, and finally sutured in step S6 to complete the procedure.
しかし、粉砕骨折の症例の場合、身体側の折れた骨と末端側の折れた骨の間に隙間があることが多い。このように隙間がある骨折症例の場合、骨折前の骨の状態を把握できず、ステップS3で作成した従来の骨接合部品を使用しても折れた骨を骨折前の位置に配置して整復することが困難である。 However, in the case of crushed fractures, there is often a gap between the broken bone on the body side and the broken bone on the terminal side. In the case of a fracture with a gap like this, the state of the bone before the fracture cannot be grasped, and even if the conventional osteosynthesis part created in step S3 is used, the broken bone is placed at the position before the fracture and reduced. It is difficult to do.
これに対して実施の形態の骨接合部品100の場合には、折れた骨を骨折前と思われる予想位置に整復可能な位置決め機能を有しているため、身体側の折れた骨102と末端側の折れた骨103の間に隙間111がある骨折症例であっても、骨接合部品100を使用することによって良好に整復できる。 On the other hand, in the case of the osteosynthesis component 100 of the embodiment, since the broken bone has a positioning function that can reduce the broken bone to the expected position considered to be before the fracture, the broken bone 102 on the body side and the end Even in the case of a fracture in which there is a gap 111 between the broken bones 103 on the side, it can be satisfactorily reduced by using the osteosynthesis component 100.
この骨接合部品100は、骨接合部品本体101の一端部分の裏面が、図1(a)(b)に示すように第1骨としての身体側の折れた骨102の表面に接触し、骨接合部品本体101の他端部分の裏面が、第2骨としての末端側の折れた骨103の表面に接触している。なお、図1(a)では骨接合部品本体101に配置された位置決めピン104,105を図示していない。 In the osteosynthesis component 100, the back surface of one end portion of the osteosynthesis component body 101 comes into contact with the surface of the broken bone 102 on the body side as the first bone as shown in FIGS. 1A and 1B, and the bone is formed. The back surface of the other end of the joint component main body 101 is in contact with the surface of the broken bone 103 on the terminal side as the second bone. Note that FIG. 1A does not show the positioning pins 104 and 105 arranged on the osteosynthesis component main body 101.
位置決めピン104,105は、図1(b)に示すように骨接合部品本体101に形成された第1,第2貫通孔106,107に挿通して位置決めされている。位置決めピン104と第1貫通孔106の嵌め合い、および位置決めピン105と第2貫通孔107の嵌め合いは、何れも手動で動かせる中間嵌めにしておく。 As shown in FIG. 1B, the positioning pins 104 and 105 are positioned by being inserted through the first and second through holes 106 and 107 formed in the osteosynthesis component main body 101. The fitting of the positioning pin 104 and the first through hole 106 and the fitting of the positioning pin 105 and the second through hole 107 are all intermediate fittings that can be moved manually.
骨接合部品本体101の裏面に突出した位置決めピン104,105のうちの位置決めピン104は、身体側の折れた骨102の破断面120に接触し、位置決めピン105は、末端側の折れた骨103の破断面121に接触している。位置決めピン104,105の個数は何れも2つである。位置決めピン104,104の中心間の距離L1は、位置決めピン105,105の中心間の距離L2とは異なっている。 Of the positioning pins 104 and 105 protruding from the back surface of the osteosynthesis component main body 101, the positioning pin 104 contacts the fracture surface 120 of the broken bone 102 on the body side, and the positioning pin 105 is the broken bone 103 on the terminal side. It is in contact with the fracture surface 121 of. The number of positioning pins 104 and 105 is two. The distance L1 between the centers of the positioning pins 104 and 104 is different from the distance L2 between the centers of the positioning pins 105 and 105.
骨接合部品本体101の一端部分には、骨接合部品本体101をスクリュー(図示せず)により骨102に固定できるように、複数のスクリュー孔108aが形成されている。骨接合部品本体101の他端部分には、骨接合部品本体101をスクリュー(図示せず)により骨103に固定できるように、複数のスクリュー孔108bが形成されている。 A plurality of screw holes 108a are formed at one end of the osteosynthesis component main body 101 so that the osteosynthesis component main body 101 can be fixed to the bone 102 by a screw (not shown). At the other end of the osteosynthesis component main body 101, a plurality of screw holes 108b are formed so that the osteosynthesis component main body 101 can be fixed to the bone 103 by a screw (not shown).
骨接合部品100を、図2と図4に基づいて更に詳しく説明する。 The osteosynthesis component 100 will be described in more detail with reference to FIGS. 2 and 4.
粉砕骨折の場合には骨折前の骨の位置,形状などが不明であるため、図4のステップS1では、骨102,103をCTスキャン(コンピュータ断層撮影)で測定すると同時に、前足や後ろ足等の左右対称の部位の骨の場合、患部と左右対称となる骨折していない正常骨もCTスキャンで測定する。図2(a)は正常骨をCTスキャンして測定した3Dデータ(3次元データ)から作成した3Dモデル(3次元モデル)201を示す。図2(b)は骨102をCTスキャンして測定した3Dデータから作成した3Dモデル202と、骨103をCTスキャンして測定した3Dデータから作成した3Dモデル203を示す。 In the case of a crushed fracture, the position and shape of the bone before the fracture are unknown. Therefore, in step S1 of FIG. 4, the bones 102 and 103 are measured by CT scan (computed tomography), and at the same time, the forefoot, hindfoot, etc. In the case of a bilaterally symmetric bone, a normal bone that is not fractured and is bilaterally symmetric with the affected part is also measured by CT scan. FIG. 2A shows a 3D model (3D model) 201 created from 3D data (3D data) measured by CT scanning normal bone. FIG. 2B shows a 3D model 202 created from 3D data measured by CT scanning the bone 102 and a 3D model 203 created from the 3D data measured by CT scanning the bone 103.
ステップS2では、3Dモデル202,203に対して、折れた骨を骨折前の骨の位置に配置するための基準となる身体側基準点204bと末端側基準点205bを設定する。基準点は、例えば折れた骨と正常骨に同様に存在する関節部など特徴的な部位で、3Dモデル202の身体側基準点204bに対応する3Dモデル201の基準点を図2(a)の204aとする。3Dモデル203の末端側基準点205bに対応する3Dモデル201の基準点を図2(a)の205bとする。そして、3Dデータ202,203を次のようにして骨折前の位置と思われ予想位置に配置する。 In step S2, the body-side reference point 204b and the terminal-side reference point 205b, which are the reference points for arranging the broken bone at the position of the bone before the fracture, are set for the 3D models 202 and 203. The reference point is a characteristic part such as a joint portion that is similarly present in a broken bone and a normal bone, and the reference point of the 3D model 201 corresponding to the body side reference point 204b of the 3D model 202 is shown in FIG. 2A. It is set to 204a. The reference point of the 3D model 201 corresponding to the terminal reference point 205b of the 3D model 203 is set to 205b in FIG. 2A. Then, the 3D data 202 and 203 are arranged at the expected positions, which are considered to be the positions before the fracture, as follows.
これは図2(c)に示すように、骨の長手方向を軸に180°反転表示した正常骨の3Dデータ206の基準点204aに、身体側基準点204bを基準にして身体側の折れた骨の3Dデータ202を重ね合わせる。重ね合わせることで傾き方向の位置合わせも可能である。同様に末端側基準点205bを基準にして末端側の折れた骨の3Dデータ203を3Dデータ206の基準点205aに重ね合わせることにより、骨折前の正常な状態に極めて近い状態になるように折れた骨を3Dデータ上で配置する。 As shown in FIG. 2 (c), the body side was broken at the reference point 204a of the 3D data 206 of the normal bone, which was inverted 180 ° with respect to the longitudinal direction of the bone, with reference to the body side reference point 204b. The 3D data 202 of the bone is superimposed. It is also possible to align in the tilt direction by overlapping. Similarly, by superimposing the 3D data 203 of the broken bone on the terminal side with the reference point 205a of the 3D data 206 with reference to the reference point 205b on the terminal side, the bone is broken so as to be in a state extremely close to the normal state before the fracture. Place the bones on the 3D data.
ステップS3では、3Dデータ202,203,206などに基づいて、折れた骨102,103に適合する骨接合部品100を製作する。ここでは骨折部111の表面形状と破断面120,121の形状に適合するように、骨接合部品本体101の形状,位置決めピン104,105の長さ,骨接合部品本体101における位置決めピン104,105の挿入位置と角度などを決定して機械加工により骨接合部品100を製作する。位置決めピン104,105の挿入位置と角度に応じて第1,第2貫通孔106,107の骨接合部品本体101における位置と角度が決まる。 In step S3, the osteosynthesis component 100 that fits the broken bones 102 and 103 is manufactured based on the 3D data 202, 203, 206 and the like. Here, the shape of the osteosynthesis component main body 101, the lengths of the positioning pins 104 and 105, and the positioning pins 104 and 105 of the osteosynthesis component main body 101 so as to match the surface shape of the fractured portion 111 and the shapes of the fracture surfaces 120 and 121. The osteosynthesis component 100 is manufactured by machining after determining the insertion position and the angle of the bone joint. The positions and angles of the first and second through holes 106 and 107 in the osteosynthesis component main body 101 are determined according to the insertion positions and angles of the positioning pins 104 and 105.
ステップS4では、患部を切開して露出した骨折部に、骨102の破断面120に位置決めピン104が図1(b)のように接触し、骨103の破断面121に位置決めピン105が接触するように骨接合部品100を装着することによって、患部に隙間111があっても骨102,103を骨折前と思われる予想位置に位置決めして整復できる。 In step S4, the positioning pin 104 comes into contact with the fracture surface 120 of the bone 102 as shown in FIG. 1B, and the positioning pin 105 contacts the fracture surface 121 of the bone 103 with the fractured portion exposed by incising the affected portion. By mounting the osteosynthesis component 100 in this way, even if there is a gap 111 in the affected area, the bones 102 and 103 can be positioned and reduced at the expected position before the fracture.
ステップS5では、スクリュー孔108a,108bから骨102,103にスクリューをねじ込んで、骨接合部品本体101を骨102,103に連結固定した後に、位置決めピン104,105を図1(a)のように骨接合部品本体101から引き抜く。最後にステップS6で患部を縫合して施術が完了する。 In step S5, a screw is screwed into the bones 102 and 103 from the screw holes 108a and 108b to connect and fix the osteosynthesis component main body 101 to the bones 102 and 103, and then the positioning pins 104 and 105 are attached as shown in FIG. 1A. Pull out from the osteosynthesis component body 101. Finally, in step S6, the affected area is sutured to complete the procedure.
このように、骨接合部品100を使用することによって、隙間111がある骨折症例の場合であっても、患部に適合するように骨接合部品本体101に配置した位置決めピン104,105の作用によって、折れた骨を骨折前の位置に極めて正確に位置決めして整復できる。さらに、骨接合部品100の位置決め機能が三次元的に配置可能なため、傾きや廻旋方向も含めた整復が可能で、医師の個人差による整復状態の違いを極力無くして正常状態に極めて近い復元治療ができ、治癒後の患者の日常における活動が再現される。 In this way, by using the osteosynthesis component 100, even in the case of a fracture with a gap 111, the action of the positioning pins 104 and 105 arranged on the osteosynthesis component main body 101 so as to fit the affected part causes The broken bone can be very accurately positioned and reduced to the position before the fracture. Furthermore, since the positioning function of the osteosynthesis component 100 can be arranged three-dimensionally, reduction including tilt and rotation direction is possible, and restoration that is extremely close to the normal state by eliminating the difference in the reduction state due to individual differences of doctors as much as possible. It can be treated and the daily activities of the patient after healing are reproduced.
なお、位置決めピン104は、骨102の破断面120の位置とその傾きなどに適合するように少なくとも2本以上配置する。同様に位置決めピン105は、骨103の破断面121の位置とその傾きなどに適合するように少なくとも2本以上配置する。 At least two positioning pins 104 are arranged so as to match the position of the fracture surface 120 of the bone 102 and its inclination. Similarly, at least two positioning pins 105 are arranged so as to match the position of the fracture surface 121 of the bone 103 and its inclination.
(実施の形態2)
図3(a)(b)は本発明の実施の形態2を示す。
(Embodiment 2)
3A and 3B show the second embodiment of the present invention.
なお、実施の形態1と同様の作用をなすものには同じ符号を付けて説明する。 It should be noted that those having the same function as that of the first embodiment will be described with the same reference numerals.
実施の形態1では位置決めピン104,105の骨接合部品本体101の表面からの突き出し量が同じであったが、実施の形態2では、位置決めピン104の骨接合部品本体101の表面からの突き出し量L11と、位置決めピン105の骨接合部品本体101の表面からの突き出し量L22とが異なっている。 In the first embodiment, the amount of protrusion of the positioning pins 104 and 105 from the surface of the osteosynthesis component main body 101 was the same, but in the second embodiment, the amount of protrusion of the positioning pin 104 from the surface of the osteosynthesis component main body 101. L11 and the amount of protrusion L22 of the positioning pin 105 from the surface of the osteosynthesis component main body 101 are different.
位置決めピン104,105の少なくとも1つ、ここでは位置決めピン104,105のそれぞれにストッパー122が係合している。位置決めピン104,105におけるストッパー122の位置によって突き出し量L11,L22が調節可能に構成されている。 A stopper 122 is engaged with at least one of the positioning pins 104 and 105, here each of the positioning pins 104 and 105. The protrusion amounts L11 and L22 are configured to be adjustable depending on the position of the stopper 122 on the positioning pins 104 and 105.
図3に示す骨接合部品100の位置決め機能を図4に基づいて説明する。 The positioning function of the osteosynthesis component 100 shown in FIG. 3 will be described with reference to FIG.
図4のステップS1,S2を実行し、折れた骨102,103を、3Dデータ上で骨折前と思われる予想位置に配置する。 Steps S1 and S2 of FIG. 4 are executed, and the broken bones 102 and 103 are placed at the predicted positions that are considered to be before the fracture on the 3D data.
ステップS3では、骨接合部品本体101の形状,位置決めピン104,105の長さ,骨接合部品本体101における位置決めピン104,105の挿入位置と角度などを決定して、骨接合部品本体101を機械加工して骨接合部品100を製作する。位置決めピン104は、骨102の破断面120の位置とその傾きなどに適合するように少なくとも2本以上配置する。同様に位置決めピン105は、骨103の破断面121の位置とその傾きなどに適合するように少なくとも2本以上配置する。 In step S3, the shape of the osteosynthesis component main body 101, the lengths of the positioning pins 104 and 105, the insertion positions and angles of the positioning pins 104 and 105 in the osteosynthesis component main body 101, and the like are determined, and the osteosynthesis component main body 101 is machined. The bone joint part 100 is manufactured by processing. At least two positioning pins 104 are arranged so as to match the position of the fracture surface 120 of the bone 102 and its inclination. Similarly, at least two positioning pins 105 are arranged so as to match the position of the fracture surface 121 of the bone 103 and its inclination.
位置決めピン104,105の配置のためには、位置決めピン104を挿通する第1貫通孔106と、位置決めピン105を挿通する第2貫通孔107を、骨接合部品本体101に形成する。具体的には、折れた骨102,103の破断面120,121の形状もCTスキャンで測定したデータにより3Dデータに反映されているため、位置決めピン104の骨接合部品本体101の裏面に突出した部分が破断面120に接触するように、3Dデータの形状に基づいて第1貫通孔106を骨接合部品本体101に形成する。位置決めピン105の骨接合部品本体101の裏面に突出した部分が破断面121に接触するように、3Dデータの形状に基づいて第2貫通孔107を骨接合部品本体101に形成する。 For the arrangement of the positioning pins 104 and 105, a first through hole 106 through which the positioning pin 104 is inserted and a second through hole 107 through which the positioning pin 105 is inserted are formed in the osteosynthesis component main body 101. Specifically, since the shapes of the fractured surfaces 120 and 121 of the broken bones 102 and 103 are also reflected in the 3D data by the data measured by the CT scan, they protrude from the back surface of the osteosynthesis component main body 101 of the positioning pin 104. The first through hole 106 is formed in the osteosynthesis component main body 101 based on the shape of the 3D data so that the portion contacts the fracture surface 120. A second through hole 107 is formed in the osteosynthesis component body 101 based on the shape of the 3D data so that the portion of the positioning pin 105 protruding from the back surface of the osteosynthesis component body 101 comes into contact with the fracture surface 121.
この第1,第2貫通孔106,107に位置決めピン104,105を着脱可能に挿入して骨接合部品本体101に配置すれば、位置決め機能が三次元的に配置可能になり、傾きや廻旋方向も含めた整復が可能になる。この位置決め機能は実施の形態1も同じである。 If the positioning pins 104 and 105 are detachably inserted into the first and second through holes 106 and 107 and arranged in the osteosynthesis component main body 101, the positioning function can be arranged three-dimensionally, and the inclination and rotation directions can be arranged. It is possible to reduce the area including the above. This positioning function is the same as in the first embodiment.
更に具体的には、第1,第2貫通孔106,107の直径は、骨接合部品本体101の短手の長さの15%未満の大きさであって、少なくとも2個以上の貫通孔である。第1,第2貫通孔106,107の直径は、骨接合部品本体101の短手方向の距離が例えば10mmの場合では1.5mm未満となる。位置決めピン104と第1貫通孔106の嵌め合い、位置決めピン105と第2貫通孔107の嵌め合いは、骨接合部品本体101を骨102,103に固定後に位置決めピン104,105を取り外せるように両方とも隙間嵌めにしておく。更に、骨接合部品本体101における位置決めピン104,105の位置決めのために、位置決めピン104,105には骨102,103の断面形状と位置決めピン104,105の接触長さを決定するストッパー122を、骨接合部品本体101の表面側に装着する。 More specifically, the diameters of the first and second through holes 106 and 107 are less than 15% of the short length of the osteosynthesis component main body 101, and at least two or more through holes. is there. The diameters of the first and second through holes 106 and 107 are less than 1.5 mm when the distance in the lateral direction of the osteosynthesis component main body 101 is, for example, 10 mm. The fitting of the positioning pin 104 and the first through hole 106 and the fitting of the positioning pin 105 and the second through hole 107 are both so that the positioning pins 104 and 105 can be removed after fixing the osteosynthesis component main body 101 to the bones 102 and 103. Both are fitted in the gap. Further, in order to position the positioning pins 104 and 105 in the osteosynthesis component main body 101, the positioning pins 104 and 105 are provided with stoppers 122 that determine the cross-sectional shape of the bones 102 and 103 and the contact length of the positioning pins 104 and 105. It is attached to the surface side of the osteosynthesis component main body 101.
ステップS4では、患部を切開して露出した骨折部に、骨102の破断面120に位置決めピン104が図1(b)のように接触し、骨103の破断面121に位置決めピン105が接触するように骨接合部品100を装着することによって、患部に隙間111があっても骨102,103を骨折前と思われる予想位置に位置決めして整復できる。 In step S4, the positioning pin 104 comes into contact with the fracture surface 120 of the bone 102 as shown in FIG. 1B, and the positioning pin 105 contacts the fracture surface 121 of the bone 103 with the fractured portion exposed by incising the affected portion. By mounting the osteosynthesis component 100 in this way, even if there is a gap 111 in the affected area, the bones 102 and 103 can be positioned and reduced at the expected position before the fracture.
この骨接合部品100では、骨接合部品本体101への位置決めピン104,105の配置の違いにより、骨102,103に骨接合部品本体101を装着する際の身体側と末端側を判定し誤装着を防止する機能を設けている。 In the osteosynthesis component 100, due to the difference in the arrangement of the positioning pins 104 and 105 on the osteosynthesis component main body 101, the body side and the terminal side when the osteosynthesis component main body 101 is attached to the bones 102 and 103 are determined and erroneously attached. Is provided with a function to prevent.
つまり、ここでは骨102に接触する身体側の位置決めピン104が挿入される第1貫通孔106の中心間距離L1は、末端側の位置決めピン105が挿入される第2貫通孔107の中心間距離L2に比べ幅広になるように配置する。それにより医師は目視確認だけでなく、位置決めピン104,105に触れることで骨接合部品本体101の正しい装着方向の確認が容易になり、骨接合部品100の誤装着を防止できる。 That is, here, the center-to-center distance L1 of the first through hole 106 into which the body-side positioning pin 104 in contact with the bone 102 is inserted is the center-to-center distance of the second through-hole 107 into which the terminal-side positioning pin 105 is inserted. Arrange so that it is wider than L2. As a result, the doctor can easily confirm not only the visual confirmation but also the correct mounting direction of the osteosynthesis component main body 101 by touching the positioning pins 104 and 105, and can prevent the osteosynthesis component 100 from being erroneously mounted.
図3(b)に示すように骨接合部品本体101の表面から外側に突出する身体側の位置決めピン104の突き出し量L11を、末端側の位置決めピン105の突き出し量L22よりも長くすることで、医師が位置決めピン104,105を触れたときの感触の違いにより、骨接合部品100の身体側と末端側の判定が容易になり誤装着を防止できる確率が更に高くなる。 As shown in FIG. 3B, the protrusion amount L11 of the positioning pin 104 on the body side protruding outward from the surface of the osteosynthesis component main body 101 is made longer than the protrusion amount L22 of the positioning pin 105 on the terminal side. Due to the difference in feel when the doctor touches the positioning pins 104 and 105, it becomes easier to determine the body side and the end side of the osteosynthesis component 100, and the probability of preventing erroneous mounting is further increased.
なお、位置決めピン104,105の中心間距離や突き出し量は必ずしも身体側を大きくする必要は無く、骨接合部品100の身体側と末端側が判定できれば良い。 The distance between the centers of the positioning pins 104 and 105 and the amount of protrusion do not necessarily have to be increased on the body side, and it is sufficient that the body side and the terminal side of the osteosynthesis component 100 can be determined.
ステップS5では、スクリュー孔108a,108bから骨102,103にスクリューをねじ込んで、骨接合部品本体101を骨102,103に連結固定した後に、位置決めピン104,105を図1(a)のように骨接合部品本体101からストッパー122とともに引き抜く。最後にステップS6で患部を縫合して施術が完了する。 In step S5, a screw is screwed into the bones 102 and 103 from the screw holes 108a and 108b to connect and fix the osteosynthesis component main body 101 to the bones 102 and 103, and then the positioning pins 104 and 105 are attached as shown in FIG. 1A. It is pulled out from the osteosynthesis component main body 101 together with the stopper 122. Finally, in step S6, the affected area is sutured to complete the procedure.
なお、顎の骨等の左右対称形状の骨の骨折の場合も、過去のCTスキャン等のデータや周囲の骨の状態から骨折前の状態を算出し、上記と同様に骨接合部品にて粉砕骨折等の治療に用いることができる。 In the case of a bilaterally symmetrical bone fracture such as a jaw bone, the state before the fracture is calculated from the data such as past CT scans and the state of the surrounding bone, and crushed with the osteosynthesis part in the same manner as above. It can be used for the treatment of bone fractures and the like.
なお、位置決めピン104,105の全部を第1,第2貫通孔106,107に隙間嵌めして骨接合部品本体101に装着したが、位置決めピンの一部を骨接合部品本体101に隙間嵌めして装着し、位置決めピンの残りを骨接合部品本体101に締まり嵌めして装着し、隙間嵌めして骨接合部品本体101に装着した前記位置決めピンの一部だけにストッパー122を装着することもできる。 All of the positioning pins 104 and 105 were gap-fitted into the first and second through holes 106 and 107 and attached to the osteosynthesis component main body 101, but a part of the positioning pins was gap-fitted into the osteosynthesis component body 101. It is also possible to attach the stopper 122 to only a part of the positioning pin which is attached by tightening the rest of the positioning pin to the osteosynthesis component main body 101 and then fitting the positioning pin to the osteosynthesis component main body 101 by gap fitting. ..
なお、L1≠L2、かつL11≠L22であったが、L1=L2、かつL11≠L22とすることもできる。 Although L1 ≠ L2 and L11 ≠ L22, it is also possible to set L1 = L2 and L11 ≠ L22.
本発明は、医師の個人差による整復状態の違いを極力無くして正常状態に極めて近い復元治療が可能となり、治癒後の患者(動物)の日常における活動が再現され、骨折部を固定する各種外科手術などに関連する医療産業の品質向上に寄与する。 The present invention enables restoration treatment that is extremely close to the normal state by eliminating the difference in the reduction state due to individual differences of doctors as much as possible, reproduces the daily activities of the patient (animal) after healing, and various surgeries for fixing the fractured part. Contribute to improving the quality of the medical industry related to surgery.
100 骨接合部品
101 骨接合部品本体
102 身体側の折れた骨(第1骨)
103 末端側の折れた骨(第2骨)
104 身体側の位置決めピン(第1部材)
105 末端側の位置決めピン(第2部材)
106 身体側の第1貫通孔
107 末端側の第2貫通孔
108a,108b スクリュー孔
111 粉砕骨折で生じる隙間
120 折れた骨の身体側の破断面
121 折れた骨の末端側の破断面
201 正常状態の3Dデータ
202 身体側の折れた骨の3Dデータ
203 末端側の折れた骨の3Dデータ
204a 正常骨の身体側基準点
205a 正常骨の末端側基準点
204b 骨102の身体側基準点
205b 骨103の末端側基準点
206 正常骨の反転した3Dデータ
100 Bone joint part 101 Bone joint part body 102 Broken bone on the body side (first bone)
103 Broken bone on the terminal side (second bone)
104 Body side positioning pin (first member)
105 Terminal side positioning pin (second member)
106 First through hole on the body side 107 Second through hole on the terminal side 108a, 108b Screw hole 111 Gap caused by crushed fracture 120 Fracture surface on the body side of the broken bone 121 Fracture surface on the terminal side of the broken bone 201 Normal state 3D data 202 3D data of broken bone on the body side 203 3D data of broken bone on the terminal side 204a Body side reference point of normal bone 205a Terminal side reference point of normal bone 204b Body side reference point of bone 102 205b Bone 103 End-side reference point 206 Inverted 3D data of normal bone
Claims (6)
一端部分が前記骨折部の身体側の折れた第1骨の表面に接触し他端部分が前記骨折部の末端側の折れた第2骨の表面に接触する骨接合部品本体と、
前記骨接合部品本体に配置され前記第1骨の破断面に接触する第1部材と、
前記骨接合部品本体に配置され前記第2骨の破断面に接触する第2部材とを設けた、
骨接合部品。 In the osteosynthesis part that fixes the fractured part of the animal bone
An osteosynthesis component body in which one end contacts the surface of the broken first bone on the body side of the fractured portion and the other end contacts the surface of the broken second bone on the terminal side of the fractured portion.
A first member arranged on the osteosynthesis component body and in contact with the fracture surface of the first bone,
A second member arranged on the osteosynthesis component main body and in contact with the fracture surface of the second bone is provided.
Osteosynthesis parts.
前記骨接合部品本体を貫通して設け、
前記骨接合部品本体から前記第1骨の破断面とは反対側に突出した前記第1部材の突き出し量が、前記骨接合部品本体から前記第2骨の破断面とは反対側に突出した前記第2部材の突き出し量と異なることを特徴とする、請求項1に記載の骨接合部品。 The first and second members are
Provided by penetrating the main body of the osteosynthesis component
The amount of protrusion of the first member protruding from the osteosynthesis component body to the side opposite to the fracture surface of the first bone protrudes from the osteosynthesis component body to the side opposite to the fracture surface of the second bone. The osteosynthesis component according to claim 1, wherein the amount of protrusion of the second member is different from that of the second member.
前記第2部材の個数は2つであり、
前記骨接合部品本体での前記2つの第1部材の中心間の距離は、前記2つの第2部材の中心間距離と異なることを特徴とする、請求項1または2に記載の骨接合部品。 The number of the first members is two.
The number of the second members is two.
The osteosynthesis component according to claim 1 or 2, wherein the distance between the centers of the two first members in the osteosynthesis component body is different from the distance between the centers of the two second members.
前記骨の破断面に接触する前記第1部材または前記第2部材の長さを前記ストッパーによって調節可能に構成したことを特徴とする、
請求項1〜3の何れかに記載の骨接合部品。 At least one member of the first member and the second member is provided with a stopper that comes into contact with the surface of the osteosynthesis component body.
The length of the first member or the second member in contact with the fracture surface of the bone is adjustable by the stopper.
The osteosynthesis component according to any one of claims 1 to 3.
前記骨折部の身体側の折れた第1骨と前記骨折部の末端側の折れた第2骨、および前記骨折部のない正常骨の形状を測定し、
前記第1骨と前記第2骨を、前記測定によって得られた正常骨の形状データに基づいて骨折前の位置と予想される予想位置にデータ上で配置し、
データ上で前記予想位置に配置された前記第1骨の表面と前記第2骨の表面の間に骨接合部品本体を接触させた形状データに基づいて、前記骨接合部品本体を貫通して前記第1骨の破断面に接触する位置と方向に第1部材を挿通するための第1貫通孔と、前記骨接合部品本体を貫通して前記第2骨の破断面に接触する位置と方向に第2部材を挿通するための第2貫通孔を形成し、
一端が前記骨接合部品本体の裏面側に突出し、他端が前記骨接合部品本体の表面側に突出するように前記第1,第2部材を、前記骨接合部品本体の前記第1,第2貫通孔に挿通する、骨接合部品形成方法。 In creating an osteosynthesis part that secures a fractured part of an animal's bone
The shapes of the broken first bone on the body side of the fractured portion, the broken second bone on the terminal side of the fractured portion, and the normal bone without the fractured portion were measured.
The first bone and the second bone are arranged on the data at the predicted position before the fracture based on the shape data of the normal bone obtained by the measurement.
Based on the shape data in which the osteosynthesis component main body is brought into contact between the surface of the first bone and the surface of the second bone arranged at the predicted position on the data, the osteosynthesis component main body is penetrated and said. In the position and direction of contacting the fracture surface of the first bone, the first through hole for inserting the first member and the position and direction of penetrating the main body of the osteosynthesis component and contacting the fracture surface of the second bone. A second through hole for inserting the second member is formed,
The first and second members are projected so that one end projects toward the back surface side of the osteosynthesis component body and the other end projects toward the front surface side of the osteosynthesis component body, and the first and second members of the osteosynthesis component body. A method of forming an osteosynthesis part that is inserted through a through hole.
請求項5記載の骨接合部品形成方法。 A plurality of the first through holes are formed at intervals in the osteosynthesis component main body, and a plurality of the second through holes are formed at intervals in the osteosynthesis component main body.
The method for forming an osteosynthesis component according to claim 5.
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