The disclosure relates generally to surgical apparatuses for use in minimally invasive surgical procedures such as endoscopic and/or laparoscopic procedures. More particularly, the disclosure relates to a surgical apparatus including a specimen retrieval device for collecting body tissue(s) and/or body fluid(s) during these procedures.
Minimally invasive surgery, such as endoscopic surgery, reduces the invasiveness of surgical procedures. Endoscopic surgery involves surgery through body walls, for example, viewing and/or operating on the ovaries, uterus, gall bladder, bowels, kidneys, appendix, etc. There are many common endoscopic surgical procedures, including arthroscopy, laparoscopy, gastroentroscopy and laryngobronchoscopy, just to name a few. In these procedures, trocars are utilized for creating incisions through which the endoscopic surgery is performed. Trocar tubes or cannula devices are extended into and left in place in the abdominal wall to provide access for endoscopic surgical tools. A camera or endoscope is inserted through a trocar tube to permit the visual inspection and magnification of the body cavity. The surgeon can then perform diagnostic and/or therapeutic procedures at the surgical site with the aid of specialized instrumentation, such as forceps, cutters, applicators, and the like, which are designed to fit through additional cannulas.
When removing tumor or diseased tissue from a body cavity, it is important that the tumor or diseased tissue does not come into contact with healthy or uninvolved tissue. If tissue parts have to be removed, they may be introduced into a “specimen retrieval bag” or “specimen bag” at the site where the tumor or diseased tissue has been detached from the surrounding tissue. The specimen bag is then withdrawn from the body, thereby minimizing contact of the diseased tissue with healthy tissue.
The disclosure is directed to specimen retrieval devices for use in minimally invasive surgery. In aspects, a specimen retrieval device includes a tubular body defining a longitudinal bore, the tubular body having a proximal portion, a distal portion, and a cut-out portion. The specimen retrieval device also includes a rigid inner shaft having a proximal portion, a distal portion, and a handle supported on the proximal portion of the rigid inner shaft. A drive rod having a proximal portion, a distal portion, and a handle supported on the proximal portion of the drive rod is also provided. A linked arm is connected to a distal portion of the inner rigid shaft and a distal portion of the drive rod, the linked arm including a plurality of linkages that are pivotably coupled to each other, and a specimen bag is supported on the distal portion of the inner rigid shaft and the linked arm, the specimen bag including a body and an opening. The inner rigid shaft is movable in relation to the tubular body from a non-actuated position in which the linked arm and the specimen bag are positioned in a non-deployed state within the longitudinal bore of the tubular body to an actuated position in which the linked arm and the specimen bag are moved to a position externally of the distal portion of the tubular body with the specimen bag in a non-deployed state. The drive rod is movable in relation to the tubular body from a non-actuated position in which the linked arm is positioned in its non-deployed state to an actuated position in which the linked arm is moved to its deployed state to move the specimen bag to its deployed state to form the opening of the specimen bag externally of the distal portion of the tubular body.
In aspects of the disclosure, the linked arm is connected to the distal portion of the inner rigid shaft by a joint, and the linked arm is connected to the distal portion of the drive rod by a joint.
In some aspects, the linked arm is formed of a plurality of linkages joined by a plurality of joints.
In aspects of the disclosure, a portion of the linked arm passes through the cut-out portion at the distal portion of the tubular body when the drive rod is moved in relation to the tubular body from the non-actuated position to the actuated position to form the opening of the specimen bag externally of the distal portion of the tubular body.
In some aspects, moving the drive rod in relation to the tubular body from a non-actuated position in which the linked arm is positioned in a non-deployed state to an actuated position forms a semi-circular opening of the specimen bag.
In other aspects, the inner rigid shaft supports teeth and the drive rod supports a ratchet mechanism which engages with the teeth on the inner rigid shaft to maintain the opening of the specimen bag. The ratchet mechanism may include a distal portion which engages the teeth on the inner rigid shaft, and a torsion spring which urges the distal portion of the ratchet mechanism into engagement with the teeth on the inner rigid shaft.
The specimen bag may be formed of a material selected from nylon, urethane, ripstop nylon, latex, or combinations thereof.
A kit of the present disclosure includes a component for introducing a specimen retrieval device into a patient and a specimen retrieval device of the present disclosure.
Aspects of the disclosed specimen retrieval device are described herein with reference to the drawings wherein:
The disclosure provides a specimen retrieval device for use in minimally invasive surgical procedures. As used herein with reference to the disclosure, minimally invasive surgical procedures encompass laparoscopic procedures and endoscopic procedures, and refer to procedures utilizing trocar tubes, cannula devices, or similar devices having relatively narrow operating portions capable of insertion through a small incision in the skin.
Aspects of the disclosure may be modified for use with various methods for retrieving tissue specimens during minimally invasive surgical procedures, sometimes referred to herein as minimally invasive procedures. Examples of minimally invasive procedures include, for example, cholecystectomies, appendectomies, nephrectomies, colectomies, splenectomies, and the like.
As used herein, the term distal refers to that portion of a specimen retrieval device which is farthest from the user, while the term proximal refers to that portion of the specimen retrieval device of the disclosure which is closest to the user.
Aspects of the disclosure will now be described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. In the following description, well-known functions or constructions are not described in detail to avoid obscuring the disclosure in unnecessary detail.
The specimen retrieval device 10 includes a rigid inner shaft 20 having a distal portion 24, a proximal portion 26, and a handle 28 at the proximal portion 26.
The specimen retrieval device 10 also includes a linked arm 30 having a distal portion 34 and a proximal portion 36. The linked arm 30 is formed of linkages 40, 42 and 44 (
Joints 41, 43, 45 and 47 may have various hinge configurations, including hinge joints (living or multi-component hinges), pivot joints, torsion spring joints, or other suitable joints. Joints 41, 43, 45 and 47 permit the linked arm 30 to deploy and open an opening or mouth 72 of the specimen bag 70 within a patient's body.
As depicted in
A specimen bag 70 (see,
The outer shaft 12, the rigid inner shaft 20, the linked arm 30, and/or the drive rod 60 of the disclosure are made of biocompatible materials within the purview of those skilled in the art, in aspects, polymeric materials. For example, thermoplastic polyurethanes sold under the name PELLETHANE®, offer flexibility and a wide range of hardness. The outer shaft 12 and/or rigid inner shaft 20, for example, may be fabricated from PELLETHANE® 2363-80A, PELLETHANE® 2363-90A, PELLETHANE® 2363-55D, any combination thereof, or any alternatives within the purview of those skilled in the art.
The specimen bag 70 may be made from any suitable biocompatible material (e.g., nylon, urethane, ripstop nylon or latex) capable of forming a flexible collapsible member, or membrane. In aspects, the material from which the specimen bag is made is resilient, antistatic, pyrogen-free, non-toxic, and sterilizable. In aspects, materials used to form the outer shaft 12, the rigid inner shaft 20, the linked arm 30 and/or the drive rod 60 described above may be used to form the specimen bag 70. In other aspects, the specimen bag 70 is formed of materials that are different from those used to form the outer shaft 12, the rigid inner shaft 20, the linked arm 30 and/or the drive rod 60. The specimen bag 70 may be opaque, translucent, or clear.
As depicted in
When the specimen bag 70 is first introduced into a patient's body, the linkages 40, 42 and 44 of the linked arm 30 are disposed in a first, generally linear, orientation relative to one another, which permits their passage through the inner bore 19 of the outer shaft 12 of the specimen retrieval device 10.
As noted above, the linked arm 30 is used to form the opening 72 of the specimen bag 70.
While the linked arm 30 is depicted in
The mechanism by which the drive rod 60 is capable of deploying the linked arm 30 so that the linkages 40, 42 and 44 rotate about joints 41, 43, 45 and 47 to form the opening 72 of the specimen bag 70 is also depicted in
As depicted in
Once the specimen retrieval device of the disclosure has been removed from the patient's body, any tissue specimen may be removed from the specimen bag for further examination and the specimen bag may be discarded.
The specimen bags of the disclosure may be useful for the removal of large tissue specimens from a body cavity. The linked arm of the specimen retrieval device of the present disclosure permits the construction of larger specimen bags, having larger mouths/openings, which permit the introduction of larger tissue specimens therein.
Kits of the disclosure may include both the specimen retrieval device described above, as well as trocars, catheters, graspers, vacuum sources (tubes), combinations thereof, and the like.
While several aspects of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular aspects. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto. Additionally, it is envisioned that the elements and features illustrated or described in connection with one exemplary aspect may be combined with the elements and features of another without departing from the scope of the disclosure, and that such modifications and variations are also intended to be included within the scope of the disclosure. Accordingly, the disclosure is not to be limited by what has been particularly shown and described, except as indicated by the appended claims.
This application claims the benefit of and priority to U.S. Provisional Patent Application No. 62/883,166 filed Aug. 6, 2019, the entire disclosure of which is incorporated by reference herein.
Number | Date | Country | |
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62883166 | Aug 2019 | US |