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JP4611053B2 - Intra-subject introduction device - Google Patents
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JP4611053B2 - Intra-subject introduction device - Google Patents

Intra-subject introduction device Download PDF

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JP4611053B2
JP4611053B2 JP2005038161A JP2005038161A JP4611053B2 JP 4611053 B2 JP4611053 B2 JP 4611053B2 JP 2005038161 A JP2005038161 A JP 2005038161A JP 2005038161 A JP2005038161 A JP 2005038161A JP 4611053 B2 JP4611053 B2 JP 4611053B2
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capsule
subject
thread
position adjusting
length
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JP2006223382A (en
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利正 赤木
秀樹 下中
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Olympus Medical Systems Corp
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Description

本発明は、所定の機能を実行する機能実行手段を内蔵し、口腔を経由して被検体内に導入されるカプセルと、紐状に形成され、カプセルに対して接続すると共にカプセルが被検体内に導入された際に一部が被検体外に位置し、かかる一部を少なくとも牽引することによってカプセルの位置調整を行う位置調整部材とを備えた被検体内導入装置に関するものである。   The present invention incorporates a function execution means for executing a predetermined function, and is formed in a string shape with a capsule introduced into the subject via the oral cavity, connected to the capsule, and the capsule is in the subject. The present invention relates to an in-subject introduction apparatus provided with a position adjusting member that is partly located outside the subject when introduced into the subject and adjusts the position of the capsule by at least pulling the part.

近年、内視鏡の分野においては、飲込み型のカプセル型内視鏡が提案されている。このカプセル型内視鏡には、撮像機能と無線通信機能とが設けられている。カプセル型内視鏡は、観察(検査)のために被検体の口から飲込まれた後、自然排出されるまでの間、体腔内、例えば胃、小腸などの臓器の内部をその蠕動運動に従って移動し、移動に伴い、例えば0.5秒間隔で被検体内画像の撮像を行う機能を有する。   In recent years, in the field of endoscopes, swallowable capsule endoscopes have been proposed. This capsule endoscope is provided with an imaging function and a wireless communication function. The capsule endoscope is swallowed from the mouth of the subject for observation (examination) until it is spontaneously discharged until it is spontaneously discharged. It has a function of moving and taking images of the in-subject image at intervals of 0.5 seconds, for example.

体腔内を移動する間、カプセル型内視鏡によって体内で撮像された画像データは、順次無線通信により外部に送信され、外部に設けられたメモリに蓄積される。無線通信機能とメモリ機能とを備えた受信機を携帯することにより、被検体は、カプセル型内視鏡を飲み込んだ後、排出されるまでの間に渡って、自由に行動できる。カプセル型内視鏡が排出された後、医師もしくは看護士においては、メモリに蓄積された画像データに基づいて臓器の画像をディスプレイに表示させて診断を行うことができる(例えば、特許文献1参照。)。   While moving inside the body cavity, image data captured inside the body by the capsule endoscope is sequentially transmitted to the outside by wireless communication and stored in a memory provided outside. By carrying a receiver having a wireless communication function and a memory function, the subject can freely act after swallowing the capsule endoscope and before being discharged. After the capsule endoscope is ejected, the doctor or nurse can make a diagnosis by displaying an organ image on the display based on the image data stored in the memory (see, for example, Patent Document 1). .)

ところで、カプセル型内視鏡の外装部分に牽引用の紐状部材を付したものが提案されている。図12は、かかる紐状部材を付したカプセル型内視鏡の構造を示す模式図である。具体的には、図12に示すカプセル型内視鏡は、撮像機構等を内蔵したカプセル101と、一端がカプセル101に対して固定された紐状部材102と、紐状部材102の他端と接続された把持部103とによって構成される。   By the way, the thing which attached the string-like member for a pull to the exterior part of a capsule type endoscope is proposed. FIG. 12 is a schematic diagram showing the structure of a capsule endoscope provided with such a string-like member. Specifically, the capsule endoscope shown in FIG. 12 includes a capsule 101 incorporating an imaging mechanism, a string-like member 102 having one end fixed to the capsule 101, and the other end of the string-like member 102. It is comprised by the connected holding part 103. FIG.

紐状部材102は、被検体内に導入されたカプセル101を外部から牽引するためのものである。具体的には、例えば食道部分における被検体内画像を撮像する場合には、一般的なカプセル型内視鏡は食道において高速に移動するために充分な撮像動作を行うことが困難であるという問題が存在する。従って、図12に示すようにカプセル101に対して紐状部材102の一端を接続すると共に他端に接続された把持部103を医師等が牽引することによって、カプセル101の被検体内における位置または移動速度を調整することが可能である。かかる構成を採用することによって、食道等のような領域であってもカプセル型内視鏡の移動速度を低下させて多数の被検体内画像を撮像することや、既に通過した領域に関して再度被検体内画像を撮像することなどが可能となる。   The string-like member 102 is for pulling the capsule 101 introduced into the subject from the outside. Specifically, for example, when capturing an in-subject image in the esophagus, it is difficult to perform a sufficient imaging operation because a general capsule endoscope moves at high speed in the esophagus. Exists. Therefore, as shown in FIG. 12, the position of the capsule 101 in the subject or the position of the capsule 101 can be obtained by connecting one end of the string-like member 102 to the capsule 101 and pulling the grip portion 103 connected to the other end. It is possible to adjust the moving speed. By adopting such a configuration, even in an area such as the esophagus, the moving speed of the capsule endoscope can be reduced to capture a large number of in-subject images, and the subject can be re-examined with respect to the already passed area. An internal image can be taken.

特開2003−19111号公報Japanese Patent Laid-Open No. 2003-19111

しかしながら、上述した従来のカプセル型内視鏡は、紐状部材102を備えたことにより、飲み込み時またはカプセル101の位置調整を行う際に患者(被検体)の負担が大きいという課題を有する。以下、かかる課題について詳細に説明する。   However, the above-described conventional capsule endoscope has the problem that the burden on the patient (subject) is heavy when swallowed or when the position of the capsule 101 is adjusted because the string-like member 102 is provided. Hereinafter, this problem will be described in detail.

導入する際の被検体の負担を軽減する観点からは、紐状部材102は細い糸状に形成されていることが好ましい。すなわち、従来のカプセル型内視鏡100は口腔を経由して被検体内に導入される構成を有することから、口腔を通過する際に被検体に与える異物感を軽減し、飲みやすくする観点からは紐状部材102を糸状に形成することが必要となる。   From the viewpoint of reducing the burden on the subject at the time of introduction, the string-like member 102 is preferably formed in a thin thread shape. That is, since the conventional capsule endoscope 100 is configured to be introduced into the subject via the oral cavity, from the viewpoint of reducing the feeling of foreign matter given to the subject when passing through the oral cavity and making it easier to drink. It is necessary to form the string-like member 102 in a thread shape.

これに対して、位置調整を行う場合には紐状部材102が糸状に形成されることは好ましくない。すなわち、紐状部材102を用いてカプセル101の位置調整を行う場合には、紐状部材102のうち被検体外に位置する端部(カプセル101と接続する側と反対側の端部)を使用者が牽引すること等によって位置調整が行われることとなり、紐状部材102には張力が生じることとなる。そして、人体の消化器官の構造に鑑みれば明らかなように、カプセル型内視鏡が導入される口腔から食道に至る経路は途中でほぼ直角に湾曲した構造を有することから、カプセル101を食道、胃等まで導入させた場合には、かかる湾曲構造近傍にて紐状部材102と被検体の体内組織(例えば喉頭蓋)とが接触することとなる。所定の張力を生じた紐状部材102が湾曲構造近傍の体内組織と接触した場合には、体内組織に対して紐状部材102から押圧力が印加されることとなり、かかる押圧力の印加に伴い被検体は強い違和感を覚えることとなり、カプセル型内視鏡の使用に伴う被検体の負担が増大することとなる。   On the other hand, when position adjustment is performed, it is not preferable that the string-like member 102 is formed in a thread shape. That is, when the position of the capsule 101 is adjusted using the string-like member 102, the end portion of the string-like member 102 located outside the subject (the end opposite to the side connected to the capsule 101) is used. The position adjustment is performed by the person pulling or the like, and the string-like member 102 is tensioned. And, as is clear in view of the structure of the digestive organs of the human body, since the path from the oral cavity where the capsule endoscope is introduced to the esophagus has a structure that is curved at a substantially right angle, the capsule 101 is esophagus, When it is introduced to the stomach or the like, the string-like member 102 comes into contact with the body tissue of the subject (for example, the epiglottis) in the vicinity of the curved structure. When the string-like member 102 having a predetermined tension comes into contact with the body tissue in the vicinity of the curved structure, a pressing force is applied from the string-like member 102 to the body tissue. The subject will feel a strong sense of incongruity, and the burden on the subject associated with the use of the capsule endoscope will increase.

特に、カプセル型内視鏡を用いた検査終了後にカプセル101を口腔を経由して被検体外に取り出す際には、かかる被検体の負担はより顕著なものとなる。上述したように紐状部材102はカプセル101と一端が接続されるとともに被検体外にて他端を牽引等することによって位置調整を行うものであり、カプセル101の取り出しもかかる位置調整の一態様として同様の操作によって行われることとなる。従って、被検体は、カプセル101が再び被検体外に取り出されるまでの所定時間に渡って喉頭蓋等の体内組織において押圧力を受け続けることとなり、強い違和感を長時間に渡って我慢する必要が生じる。   In particular, when the capsule 101 is taken out of the subject through the oral cavity after the examination using the capsule endoscope, the burden on the subject becomes more conspicuous. As described above, one end of the string-like member 102 is connected to the capsule 101 and the position is adjusted by pulling the other end outside the subject. It will be performed by the same operation. Therefore, the subject continues to receive a pressing force in the body tissue such as the epiglottis for a predetermined time until the capsule 101 is taken out of the subject again, and it is necessary to endure a strong sense of incongruity for a long time. .

また、カプセル101が喉頭蓋等に接触する状況では、紐状部材102とカプセル101の外径の差が大きい。従って、従来のカプセル型内視鏡100を用いた場合には、喉頭蓋を円滑に通過することが困難であり、紐状部材102の外表面とカプセル101の外表面との間の不連続性に起因して、被検体が強い違和感を受けるという課題も有する。   Further, in a situation where the capsule 101 is in contact with the epiglottis or the like, the difference in outer diameter between the string-like member 102 and the capsule 101 is large. Therefore, when the conventional capsule endoscope 100 is used, it is difficult to smoothly pass the epiglottis, and the discontinuity between the outer surface of the string-like member 102 and the outer surface of the capsule 101 is caused. As a result, there is also a problem that the subject receives a strong sense of incongruity.

本発明は、上記に鑑みてなされたものであって、撮像機構等の所定の機能実行手段を内蔵したカプセルに対して紐状部材等の位置調整部材が備えられたカプセル型内視鏡等の被検体内導入装置において、被検体に対するカプセルの導入および導入後の位置調整の際に被検体に及ぼす負担を軽減した被検体内導入装置を実現することを目的とする。   The present invention has been made in view of the above, and is a capsule endoscope or the like in which a position adjustment member such as a string-like member is provided with respect to a capsule incorporating a predetermined function execution unit such as an imaging mechanism. It is an object of the present invention to provide an intra-subject introduction device that reduces the burden on the subject when introducing a capsule into the subject and adjusting the position after introduction.

また、本発明は、カプセルの外径とカプセルを牽引等する紐状部材の外径との間の差に起因した強い違和感を軽減した被検体内導入装置を実現することを目的とする。   Another object of the present invention is to realize an in-subject introduction apparatus that reduces a strong sense of incongruity caused by a difference between an outer diameter of a capsule and an outer diameter of a string-like member that pulls the capsule.

上述した課題を解決し、目的を達成するために、本発明にかかる被検体内導入装置は、所定の機能を実行する機能実行手段を内蔵し、口腔を経由して被検体内に導入されるカプセルと、前記カプセルに対して接続すると共に前記カプセルを被検体内に導入した際に一部が被検体外に残存し、該一部が少なくとも牽引されることによって前記カプセルの位置調整を行う位置調整部材とを備えた被検体内導入装置であって、前記位置調整部材は、前記カプセルを被検体内に導入する際における被検体の体内組織との接触面積よりも、前記カプセルの位置調整を行う際における被検体の体内組織との間の接触面積が大きくなるよう形成されたことを特徴とする。 In order to solve the above-described problems and achieve the object, the in-subject introduction device according to the present invention incorporates function execution means for executing a predetermined function and is introduced into the subject via the oral cavity. A position where the capsule is connected to the capsule and part of the capsule remains outside the subject when the capsule is introduced into the subject, and the capsule is adjusted by at least pulling the part. An in-subject introduction apparatus comprising an adjustment member, wherein the position adjustment member adjusts the position of the capsule more than the contact area of the subject with the body tissue when the capsule is introduced into the subject. It is characterized in that it is formed so as to increase the contact area between the body tissue of the subject when performing.

この発明によれば、位置調整部材は、カプセルを被検体に導入する際よりもカプセルの位置調整を行う際において被検体の体内組織との接触面積が大きくなるよう形成されたため、位置調整の際に位置調整部材が被検体に与える違和感を低減または解消することができる。 According to the present invention, the position adjustment member is formed so that the contact area of the subject with the body tissue is larger when the position of the capsule is adjusted than when the capsule is introduced into the subject. At this time, the uncomfortable feeling that the position adjusting member gives to the subject can be reduced or eliminated.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記位置調整部材は、一部が前記カプセルに対して固定され、前記カプセルを被検体内に導入する際に被検体内部にて当該位置調整部材の外表面を形成する糸状部材と、前記糸状部材よりも大きな外径を有すると共に前記糸状部材を挿通する管路が形成され、前記カプセルが被検体内に導入された後に、前記管路に前記糸状部材を挿通した状態を維持しつつ被検体内に導入され、位置調整を行う際に被検体内部にて当該位置調整部材の外表面を形成するチューブ部材とを備えたことを特徴とする。 In the in-subject introduction apparatus according to the present invention , in the above invention, the position adjusting member is partially fixed to the capsule, and is introduced into the subject when the capsule is introduced into the subject. A thread-like member that forms the outer surface of the position-adjusting member, and a conduit that has a larger outer diameter than the thread-like member and passes through the thread-like member, and after the capsule is introduced into the subject, A tube member that is introduced into the subject while maintaining the state where the thread-like member is inserted through the duct, and forms an outer surface of the position adjusting member inside the subject when the position is adjusted. It is characterized by.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記カプセルと前記位置調整部材との接続部分近傍に、前記カプセルの外表面と前記位置調整部材の外表面との間の不連続性を緩和する錐状部材をさらに備えたことを特徴とする。 In addition, in the above- described invention , the in-subject introduction device according to the present invention may be configured so that a gap between the outer surface of the capsule and the outer surface of the position adjusting member is not present in the vicinity of the connection portion between the capsule and the position adjusting member. It further comprises a conical member that relaxes continuity.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記錐状部材は、前記位置調整部材側の端部にて前記位置調整部材の外径とほぼ等しい外径を有し、前記カプセルに近接するに従って外径が連続的に増加すると共に前記カプセル側の端部にて前記カプセルの当該錐状部材との接触部分における外径とほぼ等しい外径を有するよう形成されたことを特徴とする。 Further, in the subject introduction apparatus according to the present invention , in the above invention, the cone-shaped member has an outer diameter substantially equal to an outer diameter of the position adjusting member at an end portion on the position adjusting member side, The outer diameter increases continuously as it approaches the capsule, and is formed to have an outer diameter substantially equal to the outer diameter at the contact portion of the capsule with the cone-shaped member at the end of the capsule. Features.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記錐状部材は、前記位置調整部材と接続する部分に形成され、前記チューブ部材に形成された管路に所定長に渡って挿入可能な形状を有すると共に前記管路に挿入された際に当該錐状部材と前記チューブ部材との間の接続部分を補強する接続補強部を備えたことを特徴とする。 In the in-subject introduction device according to the present invention , in the above invention, the cone-shaped member is formed in a portion connected to the position adjusting member, and extends over a predetermined length in a conduit formed in the tube member. And a connection reinforcing portion that reinforces a connection portion between the conical member and the tube member when inserted into the conduit.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記カプセルから離隔した側における前記チューブ部材の端部からの押圧力に基づき、被検体内において前記糸状部材が前記位置調整部材の外表面に露出しているか否かを検出する検出手段をさらに備えたことを特徴とする。 In addition, the in-subject introduction device according to the present invention is the above-described invention, wherein the thread-like member is located within the subject based on the pressing force from the end of the tube member on the side separated from the capsule. It is further characterized by further comprising a detecting means for detecting whether or not the outer surface is exposed.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記検出手段は、前記カプセルから離隔した側における前記チューブ部材の端部からの押圧力に応じて長さが変化する弾性部材を備え、前記押圧力の印加方向における前記弾性部材の長さに基づき検出動作を行うことを特徴とする。 Further, the in-subject introduction device according to the present invention is the elastic member according to the above invention, wherein the detection means changes in length according to the pressing force from the end of the tube member on the side away from the capsule. And a detection operation is performed based on the length of the elastic member in the direction in which the pressing force is applied.

また、本発明にかかる被検体内導入装置は、上記の発明において、前記検出手段によって前記糸状部材が露出していないことが示された場合に、かかる状態を維持するよう前記カプセルから離隔した側における前記チューブ部材の端部と前記カプセルとの間における前記糸状部材の長さを固定する固定手段をさらに備えたことを特徴とする。 Further, the in-subject introduction device according to the present invention is the side separated from the capsule so as to maintain this state when the detection means indicates that the filamentous member is not exposed in the above invention. And a fixing means for fixing the length of the thread-like member between the end of the tube member and the capsule.

本発明にかかる被検体内導入装置は、位置調整部材がカプセルを被検体に導入する際よりもカプセルの位置調整を行う際において被検体の体内組織との接触面積が大きくなるよう形成されたため、位置調整の際に位置調整部材が被検体に与える違和感を低減または解消することができるという効果を奏する。   The in-subject introduction apparatus according to the present invention is formed so that the contact area with the body tissue of the subject is larger when the position adjustment member performs the position adjustment of the capsule than when the position adjustment member introduces the capsule into the subject. There is an effect that it is possible to reduce or eliminate the uncomfortable feeling that the position adjusting member gives to the subject during the position adjustment.

以下、この発明を実施するための最良の形態(以下では、単に「実施の形態」と称する)である被検体内導入装置について説明する。なお、図面は模式的なものであり、各部分の厚みと幅との関係、それぞれの部分の厚みの比率などは現実のものとは異なることに留意すべきであり、図面の相互間においても互いの寸法の関係や比率が異なる部分が含まれていることはもちろんである。   Hereinafter, an in-subject introduction apparatus which is the best mode for carrying out the present invention (hereinafter simply referred to as “embodiment”) will be described. Note that the drawings are schematic, and it should be noted that the relationship between the thickness and width of each part, the ratio of the thickness of each part, and the like are different from the actual ones. Of course, the part from which the relationship and ratio of a mutual dimension differ is contained.

(実施の形態1)
まず、実施の形態1にかかる被検体内導入装置について説明する。図1は、本実施の形態1にかかる被検体内導入装置の全体構造を示す模式図である。図1に示すように、本実施の形態1にかかる被検体内導入装置は、所定の機能を実行する機能実行部を内蔵したカプセル1と、紐状の構造を有し、カプセル1と接続され、カプセル1を被検体内に導入した際に一部が被検体外に位置するよう所定長だけ延伸した位置調整部材2と、カプセル1と位置調整部材2とが接続する部分に配置された錐状部材3と、位置調整を行う際に被検体内において糸状部材8(後述)が露出したか否かの検出を行う検出部材4と、使用の際に医師等が被検体内導入装置を把持する際に用いる把持部5とを備える。
(Embodiment 1)
First, the in-subject introduction device according to the first embodiment will be described. FIG. 1 is a schematic diagram illustrating the overall structure of the in-subject introduction device according to the first embodiment. As shown in FIG. 1, the in-subject introduction device according to the first embodiment has a capsule 1 including a function execution unit that executes a predetermined function, a string-like structure, and is connected to the capsule 1. When the capsule 1 is introduced into the subject, the position adjusting member 2 extended by a predetermined length so that a part of the capsule 1 is located outside the subject, and the cone disposed at the portion where the capsule 1 and the position adjusting member 2 are connected. And the detection member 4 for detecting whether or not the filamentous member 8 (described later) is exposed in the subject when the position adjustment is performed, and the doctor or the like grasps the in-subject introduction device during use. And a grip portion 5 used when performing the above.

カプセル1は、所定の形状を有する筐体中に機能実行手段を内蔵した構造を有する。具体的には、プラスチック等の材料によって形成された外装ケース内に機能実行部7が配置され、機能実行部7は、例えば所定の対物光学系およびCCD等の撮像素子を備えることによって被検体内部の画像を撮像する機能等を有する。なお、機能実行部7によって実行される機能としては撮像機能に限定して解釈する必要はない。   The capsule 1 has a structure in which a function execution unit is built in a casing having a predetermined shape. Specifically, the function execution unit 7 is arranged in an outer case formed of a material such as plastic, and the function execution unit 7 includes, for example, a predetermined objective optical system and an imaging element such as a CCD, so that the inside of the subject is And the like. The function executed by the function execution unit 7 need not be interpreted as being limited to the imaging function.

位置調整部材2は、被検体内部におけるカプセル1の位置を調整するためのものであり、被検体内部の体内組織(例えば喉頭蓋)との接触面積が、カプセル1を被検体内に導入する際よりも位置調整を行う際に大きくなるよう形成された構造を有する。なお、カプセル1の位置調整とは、主に機能実行部7による所定機能の実行を行う際に被検体内におけるカプセル1の位置調整を行うことを意味するが、本実施の形態1では、カプセル1を被検体外部に取り出す動作についてもカプセル1の位置を調整することに他ならないことから、かかる取り出し動作に関しても「位置調整」に含まれるものとして以下の説明を行う。   The position adjusting member 2 is for adjusting the position of the capsule 1 inside the subject, and the contact area with the body tissue (for example, epiglottis) inside the subject is more than when the capsule 1 is introduced into the subject. Has a structure formed so as to increase when the position adjustment is performed. The position adjustment of the capsule 1 mainly means that the position of the capsule 1 is adjusted in the subject when the function execution unit 7 executes a predetermined function. Since the operation of taking 1 out of the subject is nothing but the adjustment of the position of the capsule 1, the following description will be given on the assumption that the take-out operation is also included in the “position adjustment”.

本実施の形態1では、位置調整部材2の具体的な構造として、一部がカプセル1に対して固定されると共にカプセル1が被検体に導入される際に少なくとも被検体へ導入される部分に関して位置調整部材2の外表面を形成する糸状部材8と、糸状部材8を挿通する管路を備えると共に糸状部材8よりも大きな外径を有し、カプセル1の位置調整を行う際に被検体内に位置する部分に関して位置調整部材2の外表面を形成するチューブ部材9とを備える。   In the first embodiment, as a specific structure of the position adjusting member 2, at least a part that is fixed to the capsule 1 and is introduced into the subject when the capsule 1 is introduced into the subject. A thread-like member 8 that forms the outer surface of the position-adjusting member 2 and a pipe line through which the thread-like member 8 is inserted and have an outer diameter larger than that of the thread-like member 8, and when adjusting the position of the capsule 1, The tube member 9 which forms the outer surface of the position adjusting member 2 with respect to the part located in this is provided.

糸状部材8は、細い木綿糸等によって糸状に形成された部材であって、一端がカプセル1に対して固定され、他端が被検体外部に位置する把持部5によって固定された構造を有する。図2は、本実施の形態1にかかる被検体内導入装置のうち、カプセル1近傍部分の構造を示す模式図である。図2に示すように、カプセル1の外表面上には所定の凹部を備えた収容部1aが形成され、糸状部材8の一端は収容部1aに挿入された状態で接着剤等を用いて固定されている。   The thread-like member 8 is a member formed in a thread shape by a thin cotton thread or the like, and has a structure in which one end is fixed to the capsule 1 and the other end is fixed by the grasping portion 5 located outside the subject. FIG. 2 is a schematic diagram showing the structure of the vicinity of the capsule 1 in the intra-subject introduction device according to the first embodiment. As shown in FIG. 2, an accommodating portion 1 a having a predetermined recess is formed on the outer surface of the capsule 1, and one end of the thread-like member 8 is fixed with an adhesive or the like while being inserted into the accommodating portion 1 a. Has been.

チューブ部材9は、可撓性の材料によって形成され、糸状部材8の外径よりも大きい外径を有すると共に、糸状部材8を挿通する管路が形成された構造を有する。チューブ部材9は、糸状部材8が管路に挿通された状態で配置されており、かかる状態を維持しつつ糸状部材8に対して自由に移動可能な構造を有する。詳しくは後述するように、チューブ部材9は、カプセル1を被検体内に導入する際には被検体外部に位置した状態を維持し、カプセル1の導入後に糸状部材8を管路に挿通した状態を維持しつつ被検体内に導入され、カプセル1の位置調整の際に被検体内にて位置調整部材2の外表面を形成する機能を有する。なお、かかるチューブ部材9を形成する材料としては、上述の条件を満たすことが可能なものであれば任意の材料を用いることとして良いが、本実施の形態1では、フッ素樹脂によってチューブ部材9を形成することとしている。   The tube member 9 is made of a flexible material, has an outer diameter larger than the outer diameter of the thread-like member 8, and has a structure in which a pipe line through which the thread-like member 8 is inserted is formed. The tube member 9 is arranged in a state where the thread-like member 8 is inserted into the pipe line, and has a structure that can freely move with respect to the thread-like member 8 while maintaining this state. As will be described in detail later, the tube member 9 maintains a state of being located outside the subject when the capsule 1 is introduced into the subject, and the thread-like member 8 is inserted through the conduit after the capsule 1 is introduced. In this case, the outer surface of the position adjusting member 2 is formed in the subject when the capsule 1 is adjusted. As a material for forming the tube member 9, any material may be used as long as the above-described conditions can be satisfied. However, in the first embodiment, the tube member 9 is made of fluororesin. Trying to form.

錐状部材3は、カプセル1と位置調整部材2との接続部分における、カプセル1の外表面と位置調整部材2の外表面との間の不連続性を緩和するためのものである。具体的には、例えば錐状部材3は、位置調整部材2と接続する側の端部の外径が位置調整部材2の外径とほぼ等しい外径を有し、カプセル1と接続する側の端部の外径が、カプセル1における錐状部材3端部と接触する部分の外径とほぼ等しい外径を有し、両端部の間において外径が連続的に変化するよう構成されている。なお、本実施の形態1において「錐状」とは、底面の外周(本実施の形態1の場合、カプセル1の外周部分)と頂点(本実施の形態1の場合、位置調整部材2上の一点)とを結んだ直線の集合によって形成された場合のみならず、底面の外周と頂点との間を結ぶ曲線の集合、例えばsinカーブの集合によって形成された構造も含むこととする。また、好ましくは、錐状部材3は、カプセル1と接触する部分近傍においてはカプセル1の外表面の接線と一致する外表面を有し、位置調整部材2と接触する部分近傍においては位置調整部材2の外表面の接線と一致する外表面を有する構造を有する。さらに、錐状部材3は、錐状形状の頂角の値が30°以下となるよう形成されることが好ましい。かかる頂角の値となるよう形成することによって、カプセル1の外表面と位置調整部材2の外表面との間がより緩やかに変化することとなり、被検体に与える違和感をより効果的に緩和または解消することが可能となるためである。   The conical member 3 is intended to alleviate the discontinuity between the outer surface of the capsule 1 and the outer surface of the position adjusting member 2 at the connection portion between the capsule 1 and the position adjusting member 2. Specifically, for example, the cone-shaped member 3 has an outer diameter of an end portion on the side connected to the position adjusting member 2 and an outer diameter substantially equal to the outer diameter of the position adjusting member 2, and is on the side connected to the capsule 1. The outer diameter of the end portion has an outer diameter substantially equal to the outer diameter of the portion of the capsule 1 that contacts the end portion of the conical member 3, and the outer diameter is configured to continuously change between both end portions. . In the first embodiment, the “conical shape” means the outer periphery of the bottom surface (in the case of the first embodiment, the outer peripheral portion of the capsule 1) and the apex (in the case of the first embodiment, on the position adjusting member 2). It includes not only the case of being formed by a set of straight lines connecting one point), but also a structure formed by a set of curves connecting the outer periphery and the apex of the bottom surface, for example, a set of sin curves. Preferably, the conical member 3 has an outer surface that coincides with the tangent to the outer surface of the capsule 1 in the vicinity of the portion that contacts the capsule 1, and the position adjusting member in the vicinity of the portion that contacts the position adjusting member 2. 2 having a structure having an outer surface coinciding with a tangent to the outer surface. Further, the conical member 3 is preferably formed so that the value of the apex angle of the conical shape is 30 ° or less. By forming the apex angle so as to have a value, the space between the outer surface of the capsule 1 and the outer surface of the position adjusting member 2 changes more gently, and the discomfort given to the subject is more effectively reduced or reduced. This is because it can be eliminated.

図2に示すように、錐状部材3は、複数の小片12a〜12nによって形成されると共に個々の部材の外周部分によって形成される包絡面(図2において破線にて示される面)によって外表面が規定され、かかる外表面が錐状となるよう形成される。具体的には、錐状部材3は、小片12a〜12nのそれぞれが、形成された貫通口に糸状部材8を挿通した状態で順次積層された構造を有する。小片12a〜12nは、それぞれ糸状部材8を挿通する貫通口が形成されたスペーサ10a〜10nとスペーサ10a〜10nから貫通口の貫通方向とほぼ垂直な方向に突出した突起部11a〜11nとを備える。   As shown in FIG. 2, the conical member 3 is formed by a plurality of small pieces 12 a to 12 n and an outer surface by an envelope surface (a surface indicated by a broken line in FIG. 2) formed by the outer peripheral portion of each member. Is defined such that the outer surface is conical. Specifically, the cone-shaped member 3 has a structure in which each of the small pieces 12a to 12n is sequentially stacked in a state where the thread-shaped member 8 is inserted through the formed through-hole. Each of the small pieces 12a to 12n includes spacers 10a to 10n each having a through hole through which the thread-like member 8 is inserted, and protrusions 11a to 11n protruding from the spacers 10a to 10n in a direction substantially perpendicular to the through direction of the through hole. .

突起部11a〜11nは、それぞれ位置調整部材2側が凸となる皿状の形状を有し、かかる皿形状の外周によって錐状部材3の外径が規定される。そして、かかる突起部11a〜11nは、突起部11aの外径が最も大きく、突起部11b、11c、・・と徐々に小さくなるよう形成されている。このため、小片12a〜12nを順次積層した錐状部材3を備えたことによって、本実施の形態1にかかる被検体内導入装置は、カプセル1と位置調整部材2との接続部分において突起部11a〜11nのそれぞれの外周が連続的に変化し、接続部分における外表面の不連続性を緩和することを可能とする。   Each of the protrusions 11a to 11n has a dish shape in which the position adjustment member 2 side is convex, and the outer diameter of the cone-shaped member 3 is defined by the outer periphery of the dish shape. And these protrusion parts 11a-11n are formed so that the outer diameter of the protrusion part 11a is the largest, and the protrusion parts 11b, 11c,. For this reason, by providing the cone-shaped member 3 in which the small pieces 12a to 12n are sequentially stacked, the in-subject introduction device according to the first embodiment has the protrusion 11a at the connection portion between the capsule 1 and the position adjustment member 2. The outer peripheries of ˜11n change continuously, making it possible to alleviate the discontinuity of the outer surface at the connection portion.

また、小片12a〜12nは、互いに固定されること無くそれぞれが別個独立に動作可能な状態で積層されるものとする。かかる構成を用いることにより、錐状部材3全体としては可撓性を有することとなり、糸状部材8の動きにあわせて小片12a〜12nの位置が滑らかに変化し、糸状部材8が湾曲等した場合であっても位置調整部材2とカプセル1との間の接続部分の外表面の連続性を維持することが可能である   Moreover, the small pieces 12a-12n shall be laminated | stacked in the state which can each operate | move independently, without being fixed mutually. By using such a configuration, the cone-shaped member 3 as a whole has flexibility, and the position of the small pieces 12a to 12n smoothly changes in accordance with the movement of the thread-like member 8, and the thread-like member 8 is curved or the like. Even so, it is possible to maintain the continuity of the outer surface of the connecting portion between the position adjusting member 2 and the capsule 1.

さらに、位置調整部材2と接する小片12nにおいて、スペーサ10nは、チューブ部材に形成された管路に対して所定長に渡って挿入可能な突起を備える。かかる突起は、特許請求の範囲における接続補強部の一例として機能するものであって、具体的な構造としては、スペーサ10a等と比較してスペーサ10nを貫通口が形成される方向に所定長だけ延伸させることによって実現される。このような突起がチューブ部材9の管路に所定長だけ挿入されることによって、位置調整部材2と錐状部材3との境界部分における物理的な強度を補強することが可能である。また、チューブ部材9の先端面は、内周の稜線に径Ra、外周の稜線に径Rbの丸みを生ずるよう形成される。内周の稜線が径Raの丸みを有することによりスペーサ10nとの接続が円滑になされ、外周の稜線が径Rbの丸みを有することにより、被検体内にてカプセル1の位置調整を行う際に被検体内部に対して円滑な接触を実現することが可能である。   Further, in the small piece 12n that is in contact with the position adjusting member 2, the spacer 10n includes a protrusion that can be inserted over a predetermined length with respect to a conduit formed in the tube member. Such a protrusion functions as an example of a connection reinforcing portion in the claims. As a specific structure, the spacer 10n has a predetermined length in the direction in which the through hole is formed as compared with the spacer 10a or the like. Realized by stretching. By inserting such a protrusion into the conduit of the tube member 9 for a predetermined length, it is possible to reinforce the physical strength at the boundary portion between the position adjusting member 2 and the cone-shaped member 3. Further, the distal end surface of the tube member 9 is formed so as to have a radius Ra on the inner ridge line and a radius Rb on the outer ridge line. When the inner peripheral ridge line has a radius Ra, the connection with the spacer 10n is smoothly performed, and the outer peripheral ridge line has a radius Rb, thereby adjusting the position of the capsule 1 in the subject. Smooth contact with the inside of the subject can be realized.

検出部材4は、特許請求の範囲における検出手段の一例として機能するものであって、カプセル1の位置調整を行う際に、被検体内において糸状部材8が表面上に露出されているか否かの判定を行うためのものである。具体的には、例えば図1に示したように検出部材4は、内部を糸状部材8が挿通した状態で把持部5とチューブ部材9との間に配置された弾性部材(例えば、バネ部材)によって構成されている。検出部材4は、カプセル1から離隔した側におけるチューブ部材9の端部と接することによってチューブ部材9からの押圧力を受けることが可能な構成を有する。本実施の形態1では、かかる押圧力に応じた検出部材4の長さ変化に基づき、糸状部材8が被検体内にて位置調整部材2の表面に露出しているか否かを検出することとしている。なお、検出部材4の具体的な動作原理等については後に詳細に説明する。   The detection member 4 functions as an example of detection means in the claims. When the position of the capsule 1 is adjusted, whether or not the filamentary member 8 is exposed on the surface in the subject is determined. This is for making a determination. Specifically, for example, as shown in FIG. 1, the detection member 4 is an elastic member (for example, a spring member) disposed between the grip portion 5 and the tube member 9 with the thread-like member 8 inserted therethrough. It is constituted by. The detection member 4 has a configuration capable of receiving a pressing force from the tube member 9 by contacting the end portion of the tube member 9 on the side separated from the capsule 1. In the first embodiment, based on the change in the length of the detection member 4 according to the pressing force, it is detected whether or not the thread-like member 8 is exposed on the surface of the position adjustment member 2 in the subject. Yes. The specific operation principle of the detection member 4 will be described in detail later.

把持部5は、カプセル1の位置調整の際に使用者が把持する部材として機能する。具体的には、本実施の形態1ではカプセル1の位置調整は、直接的には位置調整部材2を医師等の使用者が牽引することによって行われることとなるが、かかる牽引動作を効率よく行うために、本実施の形態1にかかる被検体内導入装置は、使用者が握りやすい形状の把持部5を備えることとしている。   The grip portion 5 functions as a member that the user grips when adjusting the position of the capsule 1. Specifically, in the first embodiment, the position adjustment of the capsule 1 is performed directly by the user such as a doctor pulling the position adjustment member 2. In order to do this, the in-subject introduction apparatus according to the first embodiment is provided with a grip portion 5 having a shape that is easy for a user to grip.

また、把持部5は、カプセル1と、カプセル1と離隔した側におけるチューブ部材9の端部との間における糸状部材8の長さを固定する機能を有する。具体的には、把持部5にはスリット状の固定部5a、5bが形成されており、固定部5a、5bに糸状部材8を引っ掛けることによって糸状部材8を固定することが可能である。かかる固定部5a、5bによって固定する糸状部材8の部分は任意に変更可能であり、かつ把持部5は検出部材4を介してカプセル1と離隔した側におけるチューブ部材9の端部と接続した構造を有することから、使用者が糸状部材8の任意の部分を固定部5a、5bによって固定することによって、把持部5は、カプセル1と離隔した側におけるチューブ部材9の端部(以下、「把持部側端部」と称する)とカプセル1との間における糸状部材8の長さを固定することが可能である。把持部5がかかる機能を有することによって、後述するように本実施の形態1にかかる被検体内導入装置は、カプセル1を被検体内に導入する際には糸状部材8の長さを充分に確保することによってチューブ部材9が被検体内に導入されることを防止し、カプセル1の位置調整の際には糸状部材8が被検体内にて表面に露出することを防止することを可能としている。   In addition, the grip 5 has a function of fixing the length of the thread-like member 8 between the capsule 1 and the end of the tube member 9 on the side away from the capsule 1. Specifically, slit-shaped fixing portions 5a and 5b are formed in the grip portion 5, and the thread-like member 8 can be fixed by hooking the thread-like member 8 on the fixing portions 5a and 5b. The portion of the thread-like member 8 fixed by the fixing portions 5a and 5b can be arbitrarily changed, and the grip portion 5 is connected to the end portion of the tube member 9 on the side separated from the capsule 1 via the detection member 4. Therefore, when the user fixes an arbitrary portion of the thread-like member 8 with the fixing portions 5a and 5b, the gripping portion 5 is connected to the end portion of the tube member 9 on the side separated from the capsule 1 (hereinafter referred to as “grip”). It is possible to fix the length of the thread-like member 8 between the capsule 1 and the part-side end ”. Since the grasping unit 5 has such a function, as described later, the in-subject introduction device according to the first embodiment sufficiently increases the length of the thread-like member 8 when the capsule 1 is introduced into the subject. By securing, it is possible to prevent the tube member 9 from being introduced into the subject and to prevent the filamentary member 8 from being exposed to the surface within the subject when the position of the capsule 1 is adjusted. Yes.

次に、本実施の形態1にかかる被検体内導入装置の使用態様について説明する。以下では、使用態様として被検体に対するカプセル1の導入、カプセル1の導入後に行われるチューブ部材9の導入、チューブ部材9の導入後に行われる糸状部材8の長さ調整および被検体内におけるカプセル1の位置調整について順次説明する。   Next, a usage mode of the intra-subject introduction device according to the first embodiment will be described. In the following, as usage modes, introduction of the capsule 1 into the subject, introduction of the tube member 9 performed after the introduction of the capsule 1, adjustment of the length of the filamentary member 8 performed after the introduction of the tube member 9, and the capsule 1 in the subject are performed. Position adjustment will be described sequentially.

まず、カプセル1の導入について説明する。図3は、口腔を経由して被検体13内にカプセル1が導入される様子を示す模式図である。図3に示すように、本実施の形態1にかかる被検体内導入装置では、位置調整部材2を構成するチューブ部材9を被検体13の外部に保持しつつカプセル1を被検体13内に導入することとしている。具体的には、カプセル1を導入する際には、あらかじめ把持部5に備わる固定部5a、5bによって固定する糸状部材8の部分を調整することによってチューブ部材9の把持部側端部とカプセル1との間における糸状部材8の長さをチューブ部材9の長さよりも充分大きな値とすることによって、カプセル1近傍にて糸状部材8が露出した部分を確保し、カプセル1の導入に伴って位置調整部材2のうち糸状部材8が露出した部分のみを被検体13内に導入する。   First, introduction of the capsule 1 will be described. FIG. 3 is a schematic diagram showing how the capsule 1 is introduced into the subject 13 via the oral cavity. As shown in FIG. 3, in the in-subject introduction apparatus according to the first embodiment, the capsule 1 is introduced into the subject 13 while holding the tube member 9 constituting the position adjusting member 2 outside the subject 13. To do. Specifically, when the capsule 1 is introduced, the gripping portion side end of the tube member 9 and the capsule 1 are adjusted in advance by adjusting the portion of the thread-like member 8 fixed by the fixing portions 5a and 5b provided in the gripping portion 5. By setting the length of the thread-like member 8 between them to a value sufficiently larger than the length of the tube member 9, a portion where the thread-like member 8 is exposed in the vicinity of the capsule 1 is secured, and the position along with the introduction of the capsule 1 is secured. Only the portion of the adjustment member 2 where the filamentous member 8 is exposed is introduced into the subject 13.

次に、被検体13に対するチューブ部材9の導入について説明する。図4は、チューブ部材9を被検体13に導入する様子を示す模式図である。チューブ部材9を導入する時点において、カプセル1は既に被検体13内に導入されており、糸状部材8は、カプセル1と接続された構造を有するため、糸状部材8の一部は既に被検体13内に導入された状態となっている。   Next, introduction of the tube member 9 to the subject 13 will be described. FIG. 4 is a schematic diagram showing how the tube member 9 is introduced into the subject 13. Since the capsule 1 has already been introduced into the subject 13 when the tube member 9 is introduced, and the thread-like member 8 has a structure connected to the capsule 1, a part of the thread-like member 8 has already been placed in the subject 13. It is in a state of being introduced in.

このため、本実施の形態1では一部が被検体13内に導入された糸状部材8をガイドとして利用することによってチューブ部材9をスムーズに被検体13内に導入することとしている。具体的には、本実施の形態1では、カプセル1を被検体13内に導入した後に、糸状部材8の一部を管路に挿通した状態を維持しつつチューブ部材9を糸状部材8に沿ってカプセル1に接近する方向に移動させる。既に糸状部材8の一部は被検体13内に導入されていることから、糸状部材8に沿ってチューブ部材9を移動させることによってチューブ部材9は円滑に被検体13内に導入されることとなる。   For this reason, in the first embodiment, the tube member 9 is smoothly introduced into the subject 13 by using the filamentary member 8 partially introduced into the subject 13 as a guide. Specifically, in the first embodiment, after the capsule 1 is introduced into the subject 13, the tube member 9 is moved along the threaded member 8 while maintaining a state where a part of the threaded member 8 is inserted into the duct. And move in a direction approaching the capsule 1. Since a part of the filamentous member 8 has already been introduced into the subject 13, the tube member 9 can be smoothly introduced into the subject 13 by moving the tube member 9 along the filamentous member 8. Become.

次に、糸状部材8の長さ調整について説明する。かかる調整は、以後に行われるカプセル1の位置調整の際に被検体13の内部にて糸状部材8が露出することがないようカプセル1とチューブ部材9の把持部側端部との間における糸状部材8の長さを調整するためのものである。   Next, the length adjustment of the thread-like member 8 will be described. Such adjustment is performed in a thread form between the capsule 1 and the end of the tube member 9 on the gripping part side so that the thread member 8 is not exposed inside the subject 13 when the position of the capsule 1 is adjusted thereafter. This is for adjusting the length of the member 8.

図5は、糸状部材8の長さ調整の様子を示す模式図である。カプセル1の被検体13への導入およびチューブ部材9の被検体13への導入が完了した後には、まず、把持部5に備わる固定部5a、5bから糸状部材8を取り外すことによって、糸状部材8に対して把持部5が自由に移動可能な状態にする。そして、かかる状態を維持しつつ把持部5をカプセル1に近接する方向に移動することによって、糸状部材8のうちカプセル1とチューブ部材9の把持部側端部との間に位置する部分の長さを減少させ、かかる部分の糸状部材8の長さと糸状部材8を挿通しているチューブ部材9の長さとを一致させる。   FIG. 5 is a schematic diagram showing how the length of the thread-like member 8 is adjusted. After the introduction of the capsule 1 into the subject 13 and the introduction of the tube member 9 into the subject 13 are completed, first, the thread-like member 8 is removed by removing the thread-like member 8 from the fixing parts 5a and 5b provided in the grasping part 5. In contrast, the gripper 5 is set in a freely movable state. And the length of the part located between the capsule 1 and the grip part side end part of the tube member 9 among the thread-like members 8 by moving the grip part 5 in the direction approaching the capsule 1 while maintaining this state. The length of the thread-like member 8 in this portion is made to coincide with the length of the tube member 9 through which the thread-like member 8 is inserted.

糸状部材8のうちカプセル1とチューブ部材9の把持部側端部との間に位置する部分の長さがチューブ部材9の長さと一致することによって、糸状部材8のかかる部分は、すべてチューブ部材9に覆われることとなり、被検体13内において、位置調整部材2の表面に糸状部材8が露出することが防止されることとなる。しかしながら、カプセル1が被検体13内に導入された状態では、糸状部材8の所定部分の長さとチューブ部材9の長さとの比較を視覚的に行うことは不可能である。従って、本実施の形態1では、検出部材4を用いて長さの比較を行い、両者の長さが一致した際には被検体13内において糸状部材8が位置調整部材2の表面に露出していないものと判断して位置調整動作に移行することとしている。   When the length of the portion located between the capsule 1 and the grip portion side end of the tube member 9 in the thread-like member 8 matches the length of the tube member 9, all the portions of the thread-like member 8 are covered with the tube member. 9 so that the thread-like member 8 is prevented from being exposed on the surface of the position adjusting member 2 in the subject 13. However, in a state where the capsule 1 is introduced into the subject 13, it is impossible to visually compare the length of the predetermined portion of the thread-like member 8 with the length of the tube member 9. Therefore, in the first embodiment, the lengths are compared using the detection member 4, and when both the lengths coincide with each other, the filamentary member 8 is exposed on the surface of the position adjustment member 2 in the subject 13. Therefore, it is determined that the operation has not been performed, and the process proceeds to the position adjustment operation.

両者の長さが一致した際には、チューブ部材9のカプセル1側端部が錐状部材3と接触することによって、チューブ部材9は、カプセル1から離隔する方向に押圧力を与えられることとなる。チューブ部材9は座屈しがたい所定の強度を有する部材によって構成されることから、錐状部材3からの押圧力はチューブ部材9の把持部側端部まで伝達され、把持部側端部と接触した検出部材4に所定の押圧力が印加されることとなる。上述のように検出部材4はバネ等の弾性部材によって形成されることから押圧力に伴い押圧力印加方向に関する長さが収縮することとなり、かかる長さの変化に応じてチューブ部材9と錐状部材3との接触に起因した押圧力印加の有無、すなわち被検体13内における糸状部材8の露出の有無を検出し、検出結果を長さによって示すこととなる。具体的には、使用者は、検出部材4の長さlがあらかじめ定めた所定長l0以下となった時点で、チューブ部材9のカプセル1側端部が錐状部材3と接触し、被検体13内において糸状部材8が露出した部分が解消したものと判断して、糸状部材8を再び固定部5a、5bを用いて固定する。このような処理を行うことによって、被検体13の内部にて糸状部材8はチューブ部材9によって完全に覆われることとなり、かかる状態で位置調整を行うことによって糸状部材8と被検体13内の体内組織とが直接接触することが回避されることとなる。 When both lengths coincide with each other, an end of the tube member 9 on the capsule 1 side comes into contact with the conical member 3 so that the tube member 9 is given a pressing force in a direction away from the capsule 1. Become. Since the tube member 9 is composed of a member having a predetermined strength that is difficult to buckle, the pressing force from the conical member 3 is transmitted to the grip portion side end portion of the tube member 9 and contacts the grip portion side end portion. A predetermined pressing force is applied to the detected member 4. As described above, since the detection member 4 is formed by an elastic member such as a spring, the length in the pressing force application direction contracts with the pressing force, and the tube member 9 and the cone shape correspond to the change in the length. The presence / absence of a pressing force applied due to contact with the member 3, that is, the presence / absence of the exposure of the filamentary member 8 in the subject 13 is detected, and the detection result is indicated by the length. Specifically, the user, when the length l of the detection member 4 is equal to or less than a predetermined length l 0 a predetermined capsule 1 end of the tube member 9 is in contact with the cone-shaped member 3, the It is determined that the portion where the thread-like member 8 is exposed in the specimen 13 is eliminated, and the thread-like member 8 is fixed again using the fixing portions 5a and 5b. By performing such a process, the thread-like member 8 is completely covered with the tube member 9 inside the subject 13, and by adjusting the position in this state, the thread-like member 8 and the body inside the subject 13 are covered. Direct contact with the tissue will be avoided.

次に、カプセル1の位置調整について説明する。図6は、カプセル1の位置調整として、カプセル1を被検体13外部に取り出す場合を例に説明するための模式図である。上述した糸状部材8の長さ調整を経ることによって、糸状部材8は被検体13内においてチューブ部材9によって完全に覆われることとなる。このため、被検体13内では、図6に示すように被検体内導入装置の外表面はカプセル1、錐状部材3およびチューブ部材9のみによって構成されることとなり、これらの構成要素のみが被検体13の体内組織と接触し得ることとなる。   Next, the position adjustment of the capsule 1 will be described. FIG. 6 is a schematic diagram for explaining the case where the capsule 1 is taken out of the subject 13 as an example of position adjustment of the capsule 1. By passing through the length adjustment of the filamentous member 8 described above, the filamentous member 8 is completely covered by the tube member 9 in the subject 13. Therefore, in the subject 13, as shown in FIG. 6, the outer surface of the in-subject introduction apparatus is composed only of the capsule 1, the conical member 3, and the tube member 9, and only these components are covered. It can come into contact with the body tissue of the specimen 13.

上述した糸状部材8の長さ調整の説明からも明らかなようにチューブ部材9は、糸状部材8の長さ調整を行うことによって一端が錐状部材3と接触した状態となっており、カプセル1に対して一端が固定された糸状部材8と共に、位置調整部材2として一体的に動作することとなる。そして、位置調整部材2を構成する糸状部材8の他端は固定部5a、5bによって把持部5に対して固定されていることから、位置調整部材2は、把持部5を介してカプセル1(および錐状部材3)を牽引すること等が可能となり、かかる作用によってカプセル1の位置調整を行っている。   As is clear from the description of the length adjustment of the thread-like member 8 described above, the tube member 9 is in a state in which one end is in contact with the cone-like member 3 by adjusting the length of the thread-like member 8, and the capsule 1 With the thread-like member 8 having one end fixed thereto, the position adjusting member 2 operates integrally. Since the other end of the thread-like member 8 constituting the position adjusting member 2 is fixed to the gripping part 5 by the fixing parts 5a and 5b, the position adjusting member 2 is connected to the capsule 1 ( Further, the cone-shaped member 3) can be pulled, and the position of the capsule 1 is adjusted by this action.

位置調整の一例として、カプセル1を被検体13の外部に取り出す場合について図6を参照しつつ説明する。カプセル1は機能実行部7による機能実行のため食道またはさらに深部に導入されていることから、位置調整部材2は、図6にも示すように口腔と食道の境界付近で湾曲した状態となり、かかる湾曲部分またはその周辺にて被検体13の体内組織と接触することとなる。そして、位置調整部材2は、上述の糸状部材8の長さ調整によって被検体13内部において糸状部材8がすべてチューブ部材9によって覆われており、チューブ部材9の外径は糸状部材8の外径よりも大きな値を有するよう形成される。従って、位置調整部材2(正確には位置調整部材2を構成するチューブ部材9)と体内組織との接触面積は、糸状部材8が体内組織と接触する場合と比較して大きな値となる。   As an example of position adjustment, a case where the capsule 1 is taken out of the subject 13 will be described with reference to FIG. Since the capsule 1 is introduced into the esophagus or deeper for function execution by the function execution unit 7, the position adjusting member 2 is curved near the boundary between the oral cavity and the esophagus as shown in FIG. In contact with the body tissue of the subject 13 at or around the curved portion. In the position adjusting member 2, the thread member 8 is entirely covered with the tube member 9 inside the subject 13 by adjusting the length of the thread member 8 described above, and the outer diameter of the tube member 9 is the outer diameter of the thread member 8. Is formed to have a larger value. Therefore, the contact area between the position adjusting member 2 (more precisely, the tube member 9 constituting the position adjusting member 2) and the body tissue is a large value compared to the case where the thread-like member 8 contacts the body tissue.

その後、カプセル1が引き出されるに従って被検体13の体内組織と接触する部材は位置調整部材2から錐状部材3に変わる。錐状部材3は、位置調整部材2と接触する部分における外径が位置調整部材2の外径とほぼ等しいことから、接触部材の変化の際における体内組織との接触面積は、位置調整部材2が接触している際とほぼ等しい値となる。その後、体内組織と接触する部材は錐状部材3、カプセル1と変化するが、錐状部材3は錐状に形成されることから、体内組織との接触面積が急激に変化することはない。さらに、錐状部材3はカプセル1との接触部分においてカプセル1の外径とほぼ等しい外径となるよう形成されていることから、体内組織と接触する部材が錐状部材3からカプセル1に変化する際にも接触面積はほぼ同一の値に維持されることとなる。以上のことから、位置調整部材2の端部から錐状部材3およびカプセル1に渡って体内組織と接触する際には、接触面積の値は緩やかに増加することとなり、急激な接触面積の変化が生じることなくカプセル1が被検体13の外部に取り出されることとなる。   Thereafter, as the capsule 1 is pulled out, the member that comes into contact with the body tissue of the subject 13 changes from the position adjustment member 2 to the conical member 3. Since the outer diameter of the cone-shaped member 3 at the portion in contact with the position adjusting member 2 is substantially equal to the outer diameter of the position adjusting member 2, the contact area with the body tissue when the contact member changes is the position adjusting member 2. It is almost the same value as when touching. Thereafter, the members that come into contact with the body tissue are changed to the cone-shaped member 3 and the capsule 1, but since the cone-shaped member 3 is formed in a cone shape, the contact area with the body tissue does not change abruptly. Further, since the conical member 3 is formed to have an outer diameter substantially equal to the outer diameter of the capsule 1 at the contact portion with the capsule 1, the member that contacts the body tissue changes from the conical member 3 to the capsule 1. In this case, the contact area is maintained at substantially the same value. From the above, when contacting the body tissue from the end of the position adjusting member 2 to the conical member 3 and the capsule 1, the value of the contact area gradually increases and a sudden change in the contact area occurs. The capsule 1 is taken out of the subject 13 without the occurrence of.

次に、本実施の形態1にかかる被検体内導入装置の利点について説明する。まず、本実施の形態1にかかる被検体内導入装置は、被検体13に対するカプセル1の導入の際および導入後の位置調整の際に被検体13の負担を軽減できるという利点を有する。   Next, advantages of the in-subject introduction device according to the first embodiment will be described. First, the in-subject introduction apparatus according to the first embodiment has an advantage that the burden on the subject 13 can be reduced when the capsule 1 is introduced into the subject 13 and when the position is adjusted after the introduction.

上述したように、カプセル1を導入する際のみを考慮すれば、位置調整部材は体積が小さくなるよう形成することが好ましい。一般的な被検体内導入装置は口腔を経由して被検体内に導入されるものであり、被検体内導入装置全体としての体積が小さければ小さいほど被検体(患者)が異物感を感じることなく嚥下させることが可能となるためである。そして、位置調整部材は所定長だけ延伸した線状の部材によって形成されることから、体積を低減することは外径を低減することとほぼ同義となり、導入時の負担を軽減する観点からは外径を低減した位置調整部材を使用するのが一般的であった。   As described above, considering only the time when the capsule 1 is introduced, the position adjusting member is preferably formed so as to have a small volume. A general intra-subject introduction device is introduced into the subject via the oral cavity, and the smaller the volume of the whole intra-subject introduction device, the more the subject (patient) feels a foreign body. This is because it is possible to swallow without any problems. Since the position adjusting member is formed by a linear member extended by a predetermined length, reducing the volume is almost synonymous with reducing the outer diameter, and from the viewpoint of reducing the burden at the time of introduction. In general, a position adjusting member having a reduced diameter is used.

しかしながら、かかる構成とした場合には、導入後のカプセルの位置調整の際に不都合が生じることとなる。すなわち、位置調整の際に糸状の位置調整部材が被検体の体内組織と接触した場合には、位置調整部材にかかる張力に起因した圧力が体内組織との接触部分に集中することとなり、被検体は位置調整に伴い強い違和感を覚えることとなる。   However, such a configuration causes inconvenience when adjusting the position of the capsule after introduction. That is, when the thread-like position adjustment member comes into contact with the body tissue of the subject during position adjustment, the pressure due to the tension applied to the position adjustment member concentrates on the contact portion with the body tissue, and the subject Will feel a strong sense of incongruity as the position is adjusted.

これに対して、本実施の形態1にかかる被検体内導入装置では、位置調整部材2は、カプセル1を被検体13に導入する際における体内組織との接触面積よりも、カプセル1の位置調整を行う際における接触面積が大きくなるよう構成されている。このように構成することによって、カプセル1の導入時に被検体に異物感を与えることを回避しつつ、カプセル1の位置調整を行う際に被検体が感じる違和感を軽減することが可能である。すなわち、位置調整の際に生じる違和感は、位置調整部材2に生じる張力に起因した押圧力が原因であり、かかる押圧力の値を低減することによって違和感を低減・解消することが可能である。そのため、本実施の形態1では位置調整部材2に関して位置調整の際に体内組織との接触面積を増加するよう形成することでかかる押圧力を分散して体内組織の単位面積あたりに与える押圧力を低下させることによって、違和感の低減・解消を可能としている。   In contrast, in the in-subject introduction apparatus according to the first embodiment, the position adjustment member 2 adjusts the position of the capsule 1 rather than the contact area with the body tissue when the capsule 1 is introduced into the subject 13. The contact area when performing is increased. With this configuration, it is possible to reduce the sense of incongruity felt by the subject when adjusting the position of the capsule 1 while avoiding giving the subject a foreign object sensation when the capsule 1 is introduced. That is, the uncomfortable feeling that occurs during the position adjustment is caused by the pressing force caused by the tension generated in the position adjusting member 2, and the uncomfortable feeling can be reduced or eliminated by reducing the value of the pressing force. Therefore, in the first embodiment, the position adjusting member 2 is formed so as to increase the contact area with the body tissue at the time of position adjustment, so that the pressing force distributed per unit area of the body tissue is distributed. By reducing it, it is possible to reduce or eliminate a sense of incongruity.

また、本実施の形態1にかかる被検体内導入装置は、カプセル1の導入の際と位置調整の際とで体内組織との接触面積を変化させる構造を実現するために、位置調整部材2は、糸状部材8とチューブ部材9とを備えた構造を有する。そして、カプセル1を被検体13内に導入する際には糸状部材8によって位置調整部材2の外表面を形成し、カプセル1の位置調整を行う際にはより外径の大きいチューブ部材9によって位置調整部材2の外表面を形成することにより、単純な構造によって位置調整部材2の体内組織に対する接触面積の変化を実現することが可能である。すなわち、糸状部材8は例えば木綿糸によって形成することが可能であり、チューブ部材9に関しても既存のチューブを流用することによって容易に実現することが可能であり、本実施の形態1における機能を実現するために特別の機構を作成する等の必要がないという利点を有する。   In addition, the in-subject introduction apparatus according to the first embodiment is configured so that the position adjustment member 2 has a structure in which the contact area with the body tissue is changed between the introduction of the capsule 1 and the position adjustment. The structure has a thread-like member 8 and a tube member 9. When the capsule 1 is introduced into the subject 13, the outer surface of the position adjusting member 2 is formed by the thread-like member 8, and when the position of the capsule 1 is adjusted, the outer member is positioned by the tube member 9 having a larger outer diameter. By forming the outer surface of the adjustment member 2, it is possible to realize a change in the contact area of the position adjustment member 2 with the body tissue with a simple structure. That is, the thread-like member 8 can be formed of, for example, cotton thread, and the tube member 9 can be easily realized by diverting an existing tube, and the function in the first embodiment is realized. Therefore, there is an advantage that it is not necessary to create a special mechanism.

また、本実施の形態1では、チューブ部材9は、上述のようにカプセル1(および糸状部材8の一部)を被検体13内に導入した後に別途導入することとしている。そして、チューブ部材9は、形成した管路内に糸状部材8を取り込みつつ被検体13内に導入される構造を採用することから、チューブ部材9の導入の際には糸状部材8がガイドとして機能することとなり、チューブ部材9をスムーズに被検体13内に導入することが可能である。このため、チューブ部材9を備えたことによって被検体13が新たに違和感を覚えることが抑制され、かかる観点からも被検体13(患者)の負担を軽減できることとなる。   In the first embodiment, the tube member 9 is separately introduced after the capsule 1 (and a part of the thread-like member 8) is introduced into the subject 13 as described above. Since the tube member 9 adopts a structure in which the thread member 8 is introduced into the subject 13 while taking the thread member 8 into the formed conduit, the thread member 8 functions as a guide when the tube member 9 is introduced. Thus, the tube member 9 can be smoothly introduced into the subject 13. For this reason, the provision of the tube member 9 suppresses the subject 13 from newly feeling uncomfortable, and the burden on the subject 13 (patient) can be reduced from this viewpoint.

また、本実施の形態1にかかる被検体内導入装置は、錐状部材3を備えたことによって、カプセル1の外表面と位置調整部材2の外表面との間の不連続性を緩和または解消し、カプセル1の位置調整の際にカプセル1と位置調整部材2との間の境界およびその周辺が体内組織と接触した場合に被検体13に違和感を与えることを回避している。すなわち、被検体13の体内組織において異物との接触面積が不連続に変化した場合には強い違和感を覚えることとなるが、本実施の形態1では、錐状部材3を配置することによって接触面積の変化が連続的なものとなることから、かかる違和感の発生を低減または解消することが可能である。   In addition, the in-subject introduction apparatus according to the first embodiment is provided with the conical member 3 so as to reduce or eliminate the discontinuity between the outer surface of the capsule 1 and the outer surface of the position adjusting member 2. When the position of the capsule 1 is adjusted, it is avoided that the subject 13 feels uncomfortable when the boundary between the capsule 1 and the position adjusting member 2 and its periphery come into contact with the body tissue. That is, when the contact area with the foreign substance in the body tissue of the subject 13 changes discontinuously, a strong sense of incongruity is felt, but in the first embodiment, the contact area is provided by disposing the conical member 3. Since this change becomes continuous, it is possible to reduce or eliminate the occurrence of such discomfort.

さらに、本実施の形態1にかかる被検体内導入装置では、検出部材4を利用することによって、被検体13内において糸状部材8が位置調整部材2の外表面上に露出しているか否かを使用者が容易に認識することが可能である。このため、本実施の形態1にかかる被検体内導入装置は、カプセル1の位置調整を行う際に糸状部材8が被検体13の体内組織と接触することを防止することが可能であり、被検体13が違和感を覚えることをさらに確実に抑制することが可能であるという利点を有する。   Furthermore, in the in-subject introduction apparatus according to the first embodiment, by using the detection member 4, it is determined whether or not the thread-like member 8 is exposed on the outer surface of the position adjustment member 2 in the subject 13. The user can easily recognize it. For this reason, the in-subject introduction device according to the first embodiment can prevent the thread-like member 8 from coming into contact with the body tissue of the subject 13 when the position of the capsule 1 is adjusted. This has the advantage that the specimen 13 can be more reliably suppressed from feeling uncomfortable.

(実施の形態2)
次に、実施の形態2にかかる被検体内導入装置について説明する。本実施の形態2にかかる被検体内導入装置は、被検体に導入されたカプセルの位置調整の際に、被検体内部において糸状部材が表面上に露出することがないよう糸状部材の長さ調整を行う機構を新たに備える。
(Embodiment 2)
Next, the intra-subject introduction device according to the second embodiment will be described. The in-subject introduction apparatus according to the second embodiment adjusts the length of the thread-like member so that the thread-like member is not exposed on the surface inside the subject when the position of the capsule introduced into the subject is adjusted. A new mechanism is provided.

図7は、本実施の形態2にかかる被検体内導入装置の構成を示す模式図である。なお、図7以下において、実施の形態1と同様の符号・名称を付した構成要素は、以下で特に言及のない限り実施の形態1と同様の構造・機能を有することとする。   FIG. 7 is a schematic diagram illustrating a configuration of the intra-subject introduction device according to the second embodiment. In FIG. 7 and subsequent figures, components having the same reference numerals and names as those of the first embodiment have the same structures and functions as those of the first embodiment unless otherwise specified.

図7に示すように、本実施の形態2にかかる被検体内導入装置は、実施の形態1と同様にカプセル1、位置調整部材2および錐状部材3および検出部材4を備える一方で、実施の形態1における把持部5と異なる構成を有する把持部15を新たに備えた構造を有する。なお、理解を容易にする観点から、図7では把持部15は内部構造を明らかとした状態で図示される。   As shown in FIG. 7, the in-subject introduction apparatus according to the second embodiment includes the capsule 1, the position adjustment member 2, the conical member 3, and the detection member 4 as in the first embodiment. The grip part 15 having a configuration different from that of the grip part 5 in the first embodiment is newly provided. Note that, from the viewpoint of facilitating understanding, in FIG. 7, the gripping portion 15 is illustrated in a state in which the internal structure is clarified.

把持部15は、操作の際に使用者が把持する目的に加え、糸状部材8の長さ調整を行う際の検出部材4の検出動作に対応して糸状部材8の一部を自己に対して固定する機能を有する。具体的には、把持部15は、糸状部材8の長さを調整する長さ調整部17と、検出部材4によって被検体内にて糸状部材8が露出していないことが示された場合に長さ調整部17の動作を停止させ、糸状部材8の長さを固定する固定部18とを所定のケース16に対して配置した構造を有する。   In addition to the purpose of gripping the user during the operation, the gripping part 15 responds to the detection operation of the detection member 4 when adjusting the length of the thread-like member 8, and part of the thread-like member 8 with respect to itself. Has the function of fixing. Specifically, the grip 15 is used when the length adjustment unit 17 that adjusts the length of the thread member 8 and the detection member 4 indicate that the thread member 8 is not exposed in the subject. It has a structure in which the operation of the length adjusting portion 17 is stopped and a fixing portion 18 for fixing the length of the thread-like member 8 is arranged with respect to a predetermined case 16.

長さ調整部17は、ケース16内に配置され、所定軸を中心に回転可能であると共に回転動作に伴い糸状部材8の巻き取り動作および放出動作を行う滑車19と、ケース16の外表面上に配置され、滑車19と一体的に回転するよう形成された回転ノブ20とを備える。長さ調整部17がこのような構成を有することによって、使用者は、回転ノブ20を時計回りまたは反時計回りに回転させることにより滑車19を回転させ、糸状部材8の長さ調整を行うことが可能である。   The length adjusting unit 17 is disposed in the case 16, can rotate about a predetermined axis, and performs a winding operation and a discharging operation of the thread-like member 8 in accordance with the rotation operation, and a pulley 19 on the outer surface of the case 16. And a rotation knob 20 formed to rotate integrally with the pulley 19. When the length adjusting unit 17 has such a configuration, the user rotates the pulley 19 by rotating the rotary knob 20 clockwise or counterclockwise to adjust the length of the thread-like member 8. Is possible.

固定部18は、特許請求の範囲における固定手段の一例として機能するものであって、所定の条件下で回転ノブ20の回転動作を停止することによって糸状部材8の長さを固定する機能を有する。具体的には、固定部18は、所定の条件下で回転ノブと接触し、回転ノブ20の回転動作を停止させるノブ停止部材21と、ノブ停止部材21を固定するための係止部材22およびバネ部材23と、ノブ停止部材21を固定する際に、ノブ停止部材21に形成された突起部21a(後述)を収容するための空隙部分たる突起収容部24と、外周に歯溝25aが形成され、滑車19と一体的に回転可能なラチェットホイール25(図7にて図示省略)とを備える。   The fixing portion 18 functions as an example of a fixing means in the claims, and has a function of fixing the length of the thread-like member 8 by stopping the rotation operation of the rotary knob 20 under a predetermined condition. . Specifically, the fixing portion 18 is in contact with the rotary knob under a predetermined condition and stops the rotation operation of the rotary knob 20, a locking member 22 for fixing the knob stop member 21, and When the spring member 23 and the knob stop member 21 are fixed, a protrusion accommodating portion 24 that is a gap portion for accommodating a protrusion 21a (described later) formed on the knob stop member 21 and a tooth groove 25a are formed on the outer periphery. And a ratchet wheel 25 (not shown in FIG. 7) that can rotate integrally with the pulley 19.

ノブ停止部材21は、検出部材4の長さに応じて移動する構造を有すると共に、検出部材4の長さがあらかじめ定めたl0以下となった際に回転ノブ20の動作を停止させる機能を有する。具体的には、ノブ停止部材21は、ケース16に形成された管路に対して摺動可能な円筒状の形状を有すると共に、回転ノブ20から離隔した側の端部が検出部材4の端部と一体的に動作するよう形成され、回転ノブ20に近接する側の端部に、歯溝25aと嵌合するための剣先21bが形成された構造を有する。かかる構造を有することにより、チューブ部材9からの押圧力に応じて検出部材4の長さが収縮した際には、ノブ停止部材21は回転ノブ20に近接する方向に移動し、先端に形成された剣先21bが歯溝25aに嵌合して回転ノブ20の動作を停止することとなる。また、ノブ停止部材21は、係止部材22が配置された側に、摺動方向に対して所定角だけ傾斜した傾斜面を備えた突起部21aが形成されており、ノブ停止部材21の移動によって突起部21aが突起収容部24内に位置した際にノブ停止部材21は係止部材22によって固定され、上述の嵌合状態が維持されることとなる。 The knob stop member 21 has a structure that moves according to the length of the detection member 4 and also has a function of stopping the operation of the rotary knob 20 when the length of the detection member 4 becomes equal to or less than a predetermined l 0. Have. Specifically, the knob stop member 21 has a cylindrical shape that is slidable with respect to the conduit formed in the case 16, and the end portion on the side separated from the rotary knob 20 is the end of the detection member 4. It has a structure in which a sword tip 21b for fitting with the tooth gap 25a is formed at an end portion on the side close to the rotary knob 20. With this structure, when the length of the detection member 4 contracts according to the pressing force from the tube member 9, the knob stop member 21 moves in the direction close to the rotary knob 20 and is formed at the tip. The sword tip 21b is fitted into the tooth gap 25a and the operation of the rotary knob 20 is stopped. Further, the knob stop member 21 is formed with a protrusion 21 a having an inclined surface inclined by a predetermined angle with respect to the sliding direction on the side where the locking member 22 is disposed. Thus, when the protruding portion 21a is positioned in the protruding portion receiving portion 24, the knob stop member 21 is fixed by the locking member 22, and the above-described fitting state is maintained.

係止部材22およびバネ部材23は、検出部材4が所定の長さまで収縮した際に、ノブ停止部材21を固定するためのものである。具体的には、係止部材22は、ノブ停止部材21の摺動方向と垂直な方向に摺動可能な状態で配置されると共に、ノブ停止部材21に近接する方向にバネ部材23によって付勢された構造を有する。そして、係止部材22の先端には、ノブ停止部材21に形成された突起部21aにおける傾斜面と接触するよう傾斜面が形成されている。   The locking member 22 and the spring member 23 are for fixing the knob stop member 21 when the detection member 4 contracts to a predetermined length. Specifically, the locking member 22 is arranged in a state slidable in a direction perpendicular to the sliding direction of the knob stop member 21 and is biased by the spring member 23 in a direction close to the knob stop member 21. Has a structured. And the inclined surface is formed in the front-end | tip of the latching member 22 so that the inclined surface in the projection part 21a formed in the knob stop member 21 may be contacted.

次に、本実施の形態2にかかる被検体内導入装置の動作のうち、本実施の形態2に特徴的な糸状部材8の固定動作について説明する。図8および図9は、糸状部材8の固定動作を説明するための模式図である。実施の形態1において説明したように、被検体内にチューブ部材9を導入した後に糸状部材8の長さを調整することによって、チューブ部材9のカプセル1側端部が錐状部材3と接触し、錐状部材3から与えられた押圧力は、チューブ部材9内を伝達されて検出部材4の長さを収縮させる。そして、上述したように回転ノブ20から離隔した側におけるノブ停止部材21の端部は検出部材4の端部と一体的に動作するよう形成されていることから、検出部材4が圧縮されることによってノブ停止部材21も滑車19に近接する方向に移動する。   Next, of the operations of the intra-subject introduction device according to the second embodiment, the fixing operation of the thread-like member 8 that is characteristic of the second embodiment will be described. FIG. 8 and FIG. 9 are schematic views for explaining the fixing operation of the thread-like member 8. As described in the first embodiment, by adjusting the length of the thread-like member 8 after the tube member 9 is introduced into the subject, the end portion on the capsule 1 side of the tube member 9 comes into contact with the conical member 3. The pressing force applied from the conical member 3 is transmitted through the tube member 9 and contracts the length of the detection member 4. And since the edge part of the knob stop member 21 in the side spaced apart from the rotation knob 20 is formed so that it may operate | move integrally with the edge part of the detection member 4 as mentioned above, the detection member 4 is compressed. As a result, the knob stop member 21 also moves in the direction approaching the pulley 19.

かかるノブ停止部材21の移動に伴いノブ停止部材21上に形成された突起部21aも移動し、かかる移動にともなって係止部材22は、ノブ停止部材21から離隔する方向(図8における下方向)に移動する。このため、滑車19に近接する方向に移動する際には、係止部材22はノブ停止部材21の移動を妨げることはない。   Along with the movement of the knob stop member 21, the projection 21a formed on the knob stop member 21 also moves, and with this movement, the locking member 22 moves away from the knob stop member 21 (downward direction in FIG. 8). ) For this reason, when moving in the direction close to the pulley 19, the locking member 22 does not hinder the movement of the knob stop member 21.

その後、ノブ停止部材21はさらに滑車19に近接する方向にさらに移動し、検出部材4の長さがl(≦l0)となった際に、図9に示すようにノブ停止部材21の先端に形成された剣先21bが、歯溝25aに嵌合する。上述したように、歯溝25aは、滑車19と一体的に回転するよう形成されたラチェットホイール25上に形成されており、剣先21bが歯溝25aに嵌合することによって、ラチェットホイール25が回転不能な状態となり、ラチェットホイール25と一体的に回転する滑車19も回転不能となる。 Thereafter, the knob stop member 21 further moves in the direction closer to the pulley 19, and when the length of the detection member 4 becomes l (≦ l 0 ), as shown in FIG. The sword tip 21b formed on the tooth is fitted into the tooth gap 25a. As described above, the tooth groove 25a is formed on the ratchet wheel 25 formed so as to rotate integrally with the pulley 19, and the ratchet wheel 25 rotates when the sword tip 21b is fitted into the tooth groove 25a. The pulley 19 that is in an incapable state and rotates integrally with the ratchet wheel 25 is also unable to rotate.

また、検出部材4の長さがlとなった際には、ノブ停止部材21に形成された突起部21aは係止部材22に対して滑車19に近接する側に移動しており、具体的には突起収容部24内に移動している。従って、係止部材22は突起部21aの押圧力から開放され、バネ部材23の弾性力によってノブ停止部材21に近接する方向(図8における上方向)に移動し、突起部21aと係止部材22とは図8に示す位置関係となり、それぞれノブ停止部材21の摺動方向と垂直な面同士が接触し、両者間に働く力はノブ停止部材21の摺動方向となる。このため、係止部材22は突起部21aの作用によってノブ停止部材21と垂直な方向に移動することはなく、突起部21aは突起収容部24の中に閉じこめられることとなり、ノブ停止部材21は、突起部21aが突起収容部24に収容された状態で固定されることとなる。ノブ停止部材21がかかる状態で固定されることによって、回転ノブ20は回転不能な状態に維持されることとなり、糸状部材の長さは以後変化することなく固定される。   Further, when the length of the detection member 4 becomes 1, the protrusion 21a formed on the knob stop member 21 moves to the side closer to the pulley 19 with respect to the locking member 22, Has moved into the protrusion accommodating portion 24. Therefore, the locking member 22 is released from the pressing force of the protrusion 21a, and moves in a direction (upward direction in FIG. 8) close to the knob stop member 21 by the elastic force of the spring member 23, and the protrusion 21a and the locking member 8, the surfaces perpendicular to the sliding direction of the knob stop member 21 are in contact with each other, and the force acting between them is the sliding direction of the knob stop member 21. For this reason, the locking member 22 does not move in the direction perpendicular to the knob stop member 21 by the action of the protrusion 21a, and the protrusion 21a is confined in the protrusion accommodating portion 24. Thus, the protrusion 21a is fixed in a state of being accommodated in the protrusion accommodating portion 24. By fixing the knob stop member 21 in such a state, the rotary knob 20 is maintained in a non-rotatable state, and the length of the thread-like member is fixed without change thereafter.

次に、本実施の形態2にかかる被検体内導入装置の利点について説明する。本実施の形態2にかかる被検体内導入装置は、実施の形態1にて説明した利点に加え、糸状部材8の固定を自動的に行うことが可能である。すなわち、本実施の形態2では、上述したように検出部材4の長さが所定長l0以下となったことに対応してノブ停止部材21が滑車19の回転を停止させ、かつ係止部材22等の作用によってノブ停止部材21は滑車19の回転を停止させる位置にて固定される。従って、使用者は、検出部材4の長さによって示される検出結果に応じて糸状部材8の固定操作を自ら行う必要はなく、糸状部材8の固定を容易に行うことが可能である。 Next, advantages of the in-subject introduction device according to the second embodiment will be described. In addition to the advantages described in the first embodiment, the in-subject introduction apparatus according to the second embodiment can automatically fix the thread-like member 8. That is, in the second embodiment, the length of the detection member 4 knob stop member 21 corresponds to equal to or less than a predetermined length l 0 stops the rotation of the pulley 19 as described above, and the locking member The knob stop member 21 is fixed at a position where the rotation of the pulley 19 is stopped by the action of 22 or the like. Therefore, the user does not need to perform the fixing operation of the thread-like member 8 according to the detection result indicated by the length of the detection member 4, and can easily fix the thread-like member 8.

以上、実施の形態1、2に亘って本発明を説明したが、本発明は上述の実施の形態1、2によって限定して解釈されるべきではなく、当業者であれば様々な実施例、変形例等に想到することが可能である。例えば、錐状部材3の構造として、皿状の突起部11を備えた小片12を積層した構造以外のものを用いることとしても良い。   As described above, the present invention has been described over the first and second embodiments. However, the present invention should not be construed as being limited to the first and second embodiments described above. It is possible to conceive variations and the like. For example, as the structure of the conical member 3, a structure other than the structure in which the small pieces 12 including the dish-shaped protrusions 11 are stacked may be used.

図10は、錐状部材の変形例について示す模式図である。図10に示すように、錐状部材26は錐状の形状を有する部材によって一体的に形成されており、例えばポリウレタンを材料とすることで可撓性を実現することとしている。このように単一の部材によって錐状部材を形成することも有効であり、ポリウレタン等の柔軟な材料を用いて形成することによって、糸状部材8の変形等に容易に追随可能な錐状部材を実現することができる。   FIG. 10 is a schematic diagram showing a modification of the conical member. As shown in FIG. 10, the conical member 26 is integrally formed by a member having a conical shape. For example, flexibility is realized by using polyurethane as a material. In this way, it is also effective to form the conical member by a single member. By forming the conical member using a flexible material such as polyurethane, a conical member that can easily follow deformation of the thread-like member 8 or the like can be obtained. Can be realized.

また、実施の形態2において、糸状部材8の固定動作を行う固定部18に関して、検出部材4の長さ変化に基づき各部材が機械的に作用することによって糸状部材8の固定動作を行うこととした。しかしながら、かかる機械的な作用によるのではなく、例えば電子的な制御機構を用いつつ糸状部材8の固定動作を行うこととしても良い。   Further, in the second embodiment, regarding the fixing portion 18 that performs the fixing operation of the thread-like member 8, the fixing action of the thread-like member 8 is performed by each member acting mechanically based on the change in the length of the detection member 4. did. However, instead of such mechanical action, for example, the fixing operation of the thread-like member 8 may be performed using an electronic control mechanism.

図11は、電子的な制御に基づき固定動作を行う固定部27の機能ブロックを示す模式的なブロック図である。図11に示すように、固定部27は、検出部材4の長さを測定する測定部28と、測定部28の測定結果に基づき被検体内において糸状部材8が位置調整部材2の外表面に露出したか否かを判定する判定部29と、判定結果に基づき長さ調整部17の駆動状態を制御する制御部30と、測定部28の測定結果を表示する表示部31とを備える。このように電子的に制御する構成を採用することによって固定部の機能を実現することが可能である。なお、表示部31を備えることとしたのは、測定部28によって検出部材4の長さが数値データの形式で表されるため、かかる数値データを視覚的に表示することによって使用者の便宜を図るためである。また、制御部30による駆動状態制御に関して、固定部18の場合と同様に長さ調整部17の動作を停止させる機能のみを備えることとしても良いが、一旦動作を停止させた後、再び長さ調整部17が動作可能となるよう制御する、停止解除部としての機能を持たせることも好ましい。また、検出部材4に関してもバネ等の弾性部材以外の構造、例えば圧力センサを用いて形成することとしても良いし、長さ調整部17についても、使用者が操作する回転ノブ20の代わりに、滑車19を回転させるモータ等を備えることとしても良い。   FIG. 11 is a schematic block diagram illustrating functional blocks of the fixing unit 27 that performs a fixing operation based on electronic control. As shown in FIG. 11, the fixing unit 27 includes a measurement unit 28 that measures the length of the detection member 4, and the filamentary member 8 on the outer surface of the position adjustment member 2 in the subject based on the measurement result of the measurement unit 28. The determination part 29 which determines whether it was exposed, the control part 30 which controls the drive state of the length adjustment part 17 based on a determination result, and the display part 31 which displays the measurement result of the measurement part 28 are provided. The function of the fixed portion can be realized by adopting such a configuration that is electronically controlled. The reason why the display unit 31 is provided is that the length of the detection member 4 is expressed in the form of numerical data by the measuring unit 28. Therefore, the numerical data is displayed visually for the convenience of the user. This is for the purpose of illustration. Moreover, regarding the drive state control by the control unit 30, it is possible to provide only the function of stopping the operation of the length adjusting unit 17 as in the case of the fixed unit 18, but once the operation is stopped, the length is again set. It is also preferable to provide a function as a stop release unit that controls the adjustment unit 17 to be operable. Further, the detection member 4 may be formed using a structure other than an elastic member such as a spring, for example, a pressure sensor, and the length adjustment unit 17 is also replaced with the rotary knob 20 operated by the user. A motor or the like that rotates the pulley 19 may be provided.

さらに、位置調整部材に関しても、実施の形態1、2に示したように糸状部材8およびチューブ部材9によって形成する構成に限定されない。例えば、位置調整部材として、体液と反応して膨張する特性の材料を用いて形成することによって、カプセル1を被検体内に導入する際には糸状部材8と同等の外径となる一方で、カプセル1の導入後所定時間が経過することによって外径がチューブ部材9と同等となるよう形状を変化させることとしても良い。   Further, the position adjusting member is not limited to the configuration formed by the thread-like member 8 and the tube member 9 as shown in the first and second embodiments. For example, when the capsule 1 is introduced into the subject by forming the position adjusting member using a material that expands by reacting with a body fluid, the outer diameter is equal to that of the thread-like member 8. The shape may be changed so that the outer diameter becomes equal to that of the tube member 9 when a predetermined time elapses after the capsule 1 is introduced.

実施の形態1にかかる被検体内導入装置の全体構成を示す模式図である。1 is a schematic diagram illustrating an overall configuration of an intra-subject introduction device according to a first embodiment. 被検体内導入装置のうちカプセル近傍部分の構造を詳細に示す模式図である。It is a schematic diagram which shows in detail the structure of a capsule vicinity part among in-subject introduction apparatuses. カプセルを被検体内に導入する際の状態を示す模式図である。It is a schematic diagram which shows the state at the time of introduce | transducing a capsule in a subject. カプセル導入後にチューブ部材を導入する際の状態を示す模式図である。It is a schematic diagram which shows the state at the time of introducing a tube member after capsule introduction. チューブ部材導入後に行われる糸状部材の長さ調整について説明するための模式図である。It is a schematic diagram for demonstrating the length adjustment of the thread-like member performed after a tube member introduction. カプセルの位置調整にについて説明するための模式図である。It is a schematic diagram for demonstrating about the position adjustment of a capsule. 実施の形態2にかかる被検体内導入装置の全体構成を示す模式図である。FIG. 6 is a schematic diagram illustrating an overall configuration of an intra-subject introduction device according to a second embodiment. 糸状部材の固定動作について説明するための模式図である。It is a schematic diagram for demonstrating the fixing operation of a thread-like member. 糸状部材の固定動作について説明するための模式図である。It is a schematic diagram for demonstrating the fixing operation of a thread-like member. 錐状部の変形例を示す模式図である。It is a schematic diagram which shows the modification of a cone-shaped part. 固定部の変形例を示す模式的なブロック図である。It is a typical block diagram which shows the modification of a fixing | fixed part. 従来のカプセル型内視鏡の構成を示す模式図である。It is a schematic diagram which shows the structure of the conventional capsule type | mold endoscope.

符号の説明Explanation of symbols

1 カプセル
1a 収容部
2 位置調整部材
3 錐状部材
4 検出部材
5 把持部
5a、5b 固定部
7 機能実行部
8 糸状部材
9 チューブ部材
10a〜10n スペーサ
11a〜11n 突起部
12a〜12n 小片
13 被検体
15 把持部
16 ケース
17 長さ調整部
18 固定部
19 滑車
20 回転ノブ
21 ノブ停止部材
21a 突起部
22 係止部材
23 バネ部材
24 突起収容部
26 錐状部材
27 固定部
28 測定部
29 判定部
30 制御部
31 表示部
101 カプセル
102 紐状部材
103 把持部
DESCRIPTION OF SYMBOLS 1 Capsule 1a Storage part 2 Position adjustment member 3 Conical member 4 Detection member 5 Gripping part 5a, 5b Fixing part 7 Function execution part 8 Threaded member 9 Tube member 10a-10n Spacer 11a-11n Protrusion part 12a-12n Small piece 13 Subject DESCRIPTION OF SYMBOLS 15 Grip part 16 Case 17 Length adjustment part 18 Fixing part 19 Pulley 20 Rotation knob 21 Knob stop member 21a Protrusion part 22 Locking member 23 Spring member 24 Protrusion accommodating part 26 Conical member 27 Fixing part 28 Measurement part 29 Determination part 30 Control unit 31 Display unit 101 Capsule 102 String member 103 Gripping unit

Claims (7)

所定の機能を実行する機能実行手段を内蔵し、口腔を経由して被検体内に導入されるカプセルと、前記カプセルに対して接続すると共に前記カプセルを被検体内に導入した際に一部が被検体外に残存し、該一部が少なくとも牽引されることによって前記カプセルの位置調整を行う位置調整部材とを備えた被検体内導入装置であって、
前記位置調整部材は
前記カプセルを被検体内に導入する際における被検体の体内組織との接触面積よりも、前記カプセルの位置調整を行う際における被検体の体内組織との間の接触面積が大きくなるよう形成されており、かつ、
一部が前記カプセルに対して固定され、前記カプセルを被検体内に導入する際に被検体内部にて当該位置調整部材の外表面を形成する糸状部材と、
前記糸状部材よりも大きな外径を有すると共に前記糸状部材を挿通する管路が形成され、前記カプセルが被検体内に導入された後に、前記管路に前記糸状部材を挿通した状態を維持しつつ被検体内に導入され、位置調整を行う際に被検体内部にて当該位置調整部材の外表面を形成するチューブ部材と、
を有し、
前記カプセルから離隔した側における前記チューブ部材の端部において前記糸状部材が被検体内で前記位置調整部材の外表面に露出しているか否かを検出する検出手段を備えたことを特徴とする被検体内導入装置。
A function execution means for executing a predetermined function is incorporated, and a capsule is introduced into the subject via the oral cavity, and a part of the capsule is connected to the capsule and introduced into the subject. An in-subject introduction apparatus comprising a position adjustment member that remains outside the subject and adjusts the position of the capsule by being at least partially pulled;
It said position adjusting member,
Than the contact area with the body tissue of the subject at the time of introducing the capsule into the subject, it is formed such that the area of contact between the body tissue of the subject at the time of adjusting the position of the capsule is increased And
A thread-like member that is partially fixed to the capsule and forms the outer surface of the position adjusting member inside the subject when the capsule is introduced into the subject;
A conduit having an outer diameter larger than that of the thread-like member and passing through the thread-like member is formed, and the state where the thread-like member is inserted into the duct after the capsule is introduced into the subject is maintained. A tube member that is introduced into the subject and forms an outer surface of the position adjusting member inside the subject when the position is adjusted;
Have
A detection means for detecting whether or not the filamentary member is exposed on the outer surface of the position adjusting member in the subject at the end of the tube member on the side remote from the capsule. Intrasample introduction device.
前記カプセルと前記位置調整部材との接続部分近傍に、前記カプセルの外表面と前記位置調整部材の外表面との間の不連続性を緩和する錐状部材をさらに備えたことを特徴とする請求項に記載の被検体内導入装置。 The cone-shaped member which relieves discontinuity between the outer surface of the capsule and the outer surface of the position adjusting member is further provided in the vicinity of a connection portion between the capsule and the position adjusting member. Item 2. The intra-subject introduction device according to Item 1 . 前記錐状部材は、前記位置調整部材側の端部にて前記位置調整部材の外径とほぼ等しい外径を有し、前記カプセルに近接するに従って外径が連続的に増加すると共に前記カプセル側の端部にて前記カプセルの当該錐状部材との接触部分における外径とほぼ等しい外径を有するよう形成されたことを特徴とする請求項に記載の被検体内導入装置。 The conical member has an outer diameter substantially equal to the outer diameter of the position adjusting member at the end on the position adjusting member side, and the outer diameter continuously increases as the position approaches the capsule. The in-subject introduction apparatus according to claim 2 , wherein the end portion of the capsule is formed to have an outer diameter substantially equal to an outer diameter at a contact portion of the capsule with the conical member. 前記錐状部材は、前記位置調整部材と接続する部分に形成され、前記チューブ部材に形成された管路に所定長に渡って挿入可能な形状を有すると共に前記管路に挿入された際に当該錐状部材と前記チューブ部材との間の接続部分を補強する接続補強部を備えたことを特徴とする請求項またはに記載の被検体内導入装置。 The conical member is formed in a portion connected to the position adjusting member, has a shape that can be inserted into a pipe formed in the tube member over a predetermined length, and when inserted into the pipe the body-insertable apparatus according to claim 2 or 3, further comprising a connection reinforcing portion to reinforce the connection portion between the Kirijo member and the tube member. 前記検出手段は、前記カプセルから離隔した側における前記チューブ部材の端部からの押圧力に基づき、被検体内において前記糸状部材が前記位置調整部材の外表面に露出しているか否かを検出するとを特徴とする請求項のいずれか一つに記載の被検体内導入装置。 The detection means detects whether or not the thread-like member is exposed on the outer surface of the position adjusting member in the subject based on a pressing force from the end of the tube member on the side away from the capsule. the body-insertable apparatus according to any one of claims 1 to 4, wherein the arc. 前記検出手段は、前記カプセルから離隔した側における前記チューブ部材の端部からの押圧力に応じて長さが変化する弾性部材を備え、前記押圧力の印加方向における前記弾性部材の長さに基づき検出動作を行うことを特徴とする請求項に記載の被検体内導入装置。 The detection means includes an elastic member whose length changes according to the pressing force from the end of the tube member on the side separated from the capsule, and based on the length of the elastic member in the pressing force application direction. 6. The intra-subject introduction apparatus according to claim 5 , wherein a detection operation is performed. 前記検出手段によって前記糸状部材が露出していないことが示された場合に、かかる状態を維持するよう前記カプセルから離隔した側における前記チューブ部材の端部と前記カプセルとの間における前記糸状部材の長さを固定する固定手段をさらに備えたことを特徴とする請求項またはに記載の被検体内導入装置。 When the detection means indicates that the thread-like member is not exposed, the thread-like member between the end of the tube member and the capsule on the side away from the capsule is maintained to maintain this state. The in-subject introduction device according to claim 5 or 6 , further comprising a fixing means for fixing the length.
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