SPECIMEN RETRIEVAL DEVICE

Abstract

A specimen retrieval device includes a tubular body, an inner shaft slidably positioned within a longitudinal bore of the tubular body, and a specimen bag supported on the distal portion of the inner shaft. In embodiments, the tubular body tubular body is formed of a lubricious material. The specimen bag is formed from a pattern and welded by a radiofrequency welder. The specimen bag includes a tail section through which the inner shaft passes, and the tail section may be attached to a handle at a proximal portion of the inner shaft.

Claims

1-13. (canceled)

14. A specimen retrieval device comprising: a tubular body defining a longitudinal bore, the tubular body having a proximal portion, a distal portion, and a hand grip supported on the proximal portion of the tubular body; an inner shaft having a proximal portion, a distal portion, an actuation handle supported on the proximal portion of the inner shaft, and a support member extending from the distal portion of the inner shaft; a specimen bag supported on the support member at the distal portion of the inner shaft, the specimen bag including an open end, a body, and a tail portion having an enclosed longitudinal bore through which the inner shaft passes, the open end defining a mouth having a channel; and a suture within the channel at the mouth of the open end of the specimen bag, wherein the inner shaft is movable in relation to the tubular body from a non-actuated position in which the specimen bag is positioned in a non-deployed state within the longitudinal bore of the tubular body to an actuated position in which the specimen bag is positioned in a deployed state externally of the distal portion of the tubular body.

15. The specimen retrieval device of claim 14, wherein a proximal portion of the tail portion of the specimen bag has a hole, and the actuation handle includes a post which passes through the hole at the proximal portion of the tail portion of the specimen bag.

16. The specimen retrieval device of claim 15, wherein the post is chamfered.

17. The specimen retrieval device of claim 14, wherein the support member includes a pair of resilient fingers which support the specimen bag and open the open end of the specimen bag in the deployed state.

18. The specimen retrieval device of claim 17, wherein the resilient fingers are positioned adjacent the open end of the specimen bag to open the specimen bag when the specimen retrieval device is in the deployed state.

19. The specimen retrieval device of claim 14, wherein the tubular body is formed of a lubricious material.

20. The specimen retrieval device of claim 19, wherein the tubular body includes a polymeric material combined with the lubricious material.

21. The specimen retrieval device of claim 20, wherein the lubricious material includes hydrophilic polymers, siloxanes, polycarbonates, urethanes, parylenes, or combinations thereof.

22. The specimen retrieval device of claim 20, wherein the lubricious material includes a siloxane selected from polydimethylsiloxanes, hexamethyldisiloxanes, polyester-modified methylphenyl polysiloxanes, or combinations thereof.

23. The specimen retrieval device of claim 20, wherein the tubular body is formed of a combination of a siloxane and a polycarbonate.

24. The specimen retrieval device of claim 14, wherein the tail portion of the specimen bag includes a reinforcement tab.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Various embodiments of the presently disclosed specimen retrieval device are described herein below with reference to the drawings, wherein:

[0020] FIG. 1 is a side perspective view of an exemplary embodiment of the presently disclosed specimen retrieval device in a deployed state;

[0021] FIG. 2 is an exploded view of the specimen retrieval device shown in FIG. 1;

[0022] FIG. 3 is a side view of a pattern suitable for forming a specimen bag of the specimen retrieval device of the present disclosure;

[0023] FIG. 4 is a side view of the pattern for forming a specimen bag shown in FIG. 2, showing folding of portions of the pattern to produce features of the specimen bag;

[0024] FIG. 5 is a side view of the pattern for forming a specimen bag shown in FIG. 3, showing folding of additional portions of the pattern to produce additional features of the specimen bag;

[0025] FIG. 6 is a side view of the pattern for forming a specimen bag shown in FIG. 4, showing folding of additional portions of the pattern to produce additional features of the specimen bag;

[0026] FIG. 7 is an enlarged view of the indicated area of detail shown in FIG. 1;

[0027] FIG. 8 is an enlarged perspective view of a proximal portion of the specimen retrieval device shown in FIG. 1 with an actuation handle in an advanced position;

[0028] FIG. 9 is a distal view of the actuation handle of the specimen retrieval device shown in FIG. 8;

[0029] FIG. 10 is a top view of the actuation handle and a hand grip of the specimen retrieval device shown in FIG. 1;

[0030] FIG. 11 is a top view of the specimen retrieval device shown in FIG. 1; and

[0031] FIG. 12 is a top view of the specimen retrieval device shown in FIG. 11, depicting the withdrawal of the specimen bag into the tubular body of the specimen retrieval device.

DETAILED DESCRIPTION OF EMBODIMENTS

[0032] The present disclosure provides a specimen retrieval device for use in minimally invasive surgical procedures. As used herein with reference to the present disclosure, minimally invasive surgical procedures encompass laparoscopic procedures, arthroscopic procedures, and endoscopic procedures, and refer to procedures utilizing scopes or similar devices having relatively narrow operating portions capable of insertion through a small incision in the skin.

[0033] The aspects of the present 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.

[0034] The presently disclosed specimen retrieval device 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 this description, the term “proximal” is used generally to refer to that portion of the device that is closer to a clinician, while the term “distal” is used generally to refer to that portion of the device that is farther from the clinician. The term “clinician” is used generally to refer to medical personnel including doctors, surgeons, nurses, and support personnel.

[0035] Referring to FIGS. 1-12, and initially with reference to FIGS. 1 and 2, the specimen retrieval device 10 of the present disclosure includes a tubular body 12 having a proximal portion 16 and a distal portion 18, and defining a longitudinal bore 14 that extends between the proximal portion 16 and the distal portion 18. The proximal portion of the tubular body 12 supports a hand grip 15. The specimen retrieval device 10 also includes an inner shaft assembly 20 (FIG. 6) including an inner shaft 22 slidably positioned within the longitudinal bore 14 of the tubular body 12, an actuation handle 25 secured to a proximal portion 24 of the inner shaft 22, and a specimen bag 40 (FIG. 1) supported on a distal portion 26 of the inner shaft 22.

[0036] The hand grip 15 on the tubular body 12 may be formed as a unitary component or, as depicted in FIG. 6, as two separate half components 15a, 15b, that are coupled to one another about the tubular body 12 by one or more suitable coupling methods (e.g., one or more suitable adhesives). In the latter instance, an indent/detent configuration (not shown) may be utilized to facilitate coupling the two separate half components 15a, 15b to one another.

[0037] The actuation handle 25 on the inner shaft 22 may likewise be formed as a unitary component or, in embodiments, as depicted in FIG. 6, as two separate half components 25a, 25b that are coupled to one another by one or more suitable coupling methods (e.g., one or more suitable adhesives).

[0038] The specimen bag 40 includes a body 44 having a generally tubular or elongated configuration that is defined by an openable and closable portion (or mouth) 42 and a closed portion 46 (FIG. 1). The closable portion 42 defines an opening 45. In some embodiments, the specimen bag 40 includes a tail 48 (FIG. 2) having a neck region 47. Alternatively, other specimen bag configurations are envisioned.

[0039] The body 44 of the specimen bag 40 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 embodiments, the material from which the specimen bag is made is resilient, antistatic, pyrogen-free, non-toxic, and sterilizable. The specimen bag 40 may be opaque or clear. In some embodiments, the body 44 of the specimen bag 40 is formed of a nylon material, or combinations of nylon materials. As described in greater detail below, in some embodiments portions of the specimen bag 40 are made of two different nylons that are secured together to form areas of the specimen bag 40 having high strength. In some embodiments, the first nylon material is a 30 denier (“30 D”) polyurethane coated rip-stop nylon; and the second nylon material is a 1000 denier (“1000 D”) polyurethane coated nylon.

[0040] Turning to FIGS. 3-6, methods for forming the specimen bag of the present disclosure will be described. In embodiments, the specimen bag 40 (FIG. 1) is made using a radio-frequency (“RF”) welding process that does not require additional reinforcement at the seams (e.g., sutures, interface materials, etc.). As depicted in FIGS. 3-6, the fabric used to form the specimen bag 40 of the present disclosure is cut to form a pattern 50, with holes 57 along a periphery of the pattern 50. Any means within the purview of those skilled in the art may be used to cut the fabric to form the pattern 50. The holes 57 assist in placement of the pattern 50 on an RF welder (not shown) used to form the specimen bag 40.

[0041] Once the pattern 50 has been cut from the fabric, the pattern 50 is placed onto the radiofrequency (RF) welder and located using the holes 57 running along the periphery of the pattern 50 (not shown).

[0042] After forming the pattern 50 used to form the specimen bag 40, the pattern 50 has various portions that may be folded to form the specimen bag 40, including flaps 51, 52, 53, 54, 55, and 56 (FIG. 3).

[0043] Once positioned on the RF welder, the flaps 51, 52, 53 and 54 are folded over along lines “B” and “C” (FIG. 3) and welded to the fabric (FIG. 4), to form a channel 43 at the mouth 42 of the specimen bag 40 (FIG. 1). The channel 43 may include a suture therein (not shown), which may be used to close the mouth 42 of the specimen bag 40. The flap 55 may then be folded along line “C” (FIGS. 3 and 4) at the proximal portion 59 of the pattern 50 to form a tail section 49 of the specimen bag 40 (FIG. 4).

[0044] As shown in FIG. 2, a reinforcement tab 58 may be placed at the proximal portion 59 of the pattern 50 and flap 55 is folded along line “C” so that the reinforcement tab 58 is sandwiched between the fabric as the flap 50 is folded over and attached to the body 61 of the pattern 50. In embodiments, the reinforcement tab 58 is formed of 1000 D nylon sandwiched between the 30 D fabric used to form the pattern 50. The reinforcement tab 58: adds strength to the 30 D material and also acts as a retention feature to prevent the specimen bag 40 from cinching during initial retraction; aids in placement of the specimen bag 40 on the inner shaft 22 and removal of the specimen bag 40 from the body and/or the inner shaft 22 of the specimen retrieval device 10; prevents the tail 48 from ripping without the need for additional suture reinforcement during retraction; and acts as an indicator of the overall device orientation (with respect to location of mouth 42 of the specimen bag 40) for ease of insertion of a tissue specimen into the specimen bag 40 (not shown).

[0045] Once folded, flaps 51, 52, 53, 54 and 55 are secured by RF welding. The flap 56 is then folded along line “D” and welded with the RF welder to form the body 44 of the specimen bag 40 (FIG. 5).

[0046] The pattern 50 includes a through-hole 60 on flap 55 that allows the RF welder to secure multiple layers of fabric together (not shown), including welding the flap 56 to the pattern 50 through the through-hole 60 on flap 55 at the neck region 47 of the tail 48. This reinforces the neck region 47, which will experience loads during specimen removal.

[0047] The radio-frequency (RF) welding process does not necessitate additional reinforcement via suturing and/or interface materials to bolster the bag seams (found in commercially available products). This combination of the RF welding process and the selection of materials used to form the specimen bag 40 creates a strong, leak proof bag for specimen containment and removal.

[0048] As shown in FIG. 6, the specimen bag 40 has a body 44 and a tail 48 that the inner shaft 22 passes through.

[0049] As depicted in FIGS. 7-10, in embodiments, the actuation handle 25 at the proximal portion 24 of the inner shaft 22 has a post 27 for attaching specimen bag 40 to the actuation handle 25 (instead of carabiner types of attachments that are used by other commercially available devices), by placing the post 27 on actuation handle 25 through a hole 62 at a proximal portion 49 of the tail 48 of the specimen bag 40 (FIG. 7). The use of the post and hole configuration for attaching the tail 48 of the specimen bag 40 to the actuation handle 25 allows for easy and simple removal of the specimen bag 40 from the actuation handle 25. In addition, the design permits a more ergonomic shape for the actuation handle 25, enhancing the deployment and retraction of the specimen bag 40 from the actuation handle 25.

[0050] In embodiments, as depicted in FIGS. 7-10, the post 27 is chamfered, which allows the hole 62 at the tail 48 of the specimen bag 40 to flex over and stay secured to the post 27 until it is ready to be removed.

[0051] Referring to FIG. 6, the distal portion 26 of the inner shaft 22 is coupled to a support member 28 that is configured to support the mouth 42 of the specimen bag 40. In embodiments, the support member 28 includes a pair of resilient fingers 30, 32 that extend distally from the distal portion 26 of the inner shaft 22. In embodiments, the resilient fingers 30, 32 can be integrally formed with the distal portion 26 of the inner shaft 22 such as by molding. Alternatively, a retention pin (not shown) may be used to attach the resilient fingers 30, 32 to the distal portion 26 of the inner shaft 22. The resilient fingers 30, 32 are movable from a spaced non-deformed state (not shown) to a deformed state (FIG. 1) to facilitate placement of the specimen bag 40 into the tubular body 12.

[0052] The resilient fingers 30, 32 return to the non-deformed state when the specimen bag 40 is deployed from the tubular body 12 to open the opening 42 of the specimen bag 40, as described below.

[0053] In an assembled configuration, the hand grip 15 and the actuation handle 25 can be manipulated to facilitate manipulation of the specimen retrieval device 10 and the sliding of the inner shaft 22 within the tubular body 12. More specifically, the hand grip 15 can be grasped by the clinician with one hand and the actuation handle 25 can be grasped by the clinician with the other hand to move the inner shaft 22 within the tubular body 12.

[0054] The tubular body 12 and/or the inner shaft assembly 22 of the present disclosure are made of biocompatible materials within the purview of those skilled in the art, in embodiments, polymeric materials. For example, the tubular body 12 and/or the inner shaft assembly 22 may be made of polycarbonates or thermoplastic polyurethanes sold under the name PELLETHANE®, which offer flexibility and a wide range of hardness. The tubular body 12 and/or the inner shaft assembly 22, for example, may be fabricated from PELLETHANE® 2363-80A, PELLETHANE® 2363-90A, PELLETHANE® 2363-55 D, any combination thereof, or any alternatives within the purview of those skilled in the art.

[0055] In embodiments, the tubular body 12 is made of a polymeric material combined with a lubricious material. Examples of suitable lubricious material include hydrophilic polymers, siloxanes, polycarbonates, urethanes, and/or parylenes, among other lubricious materials within the purview of those skilled in the art. In embodiments, a siloxane may be used as the lubricious material. Suitable siloxanes include, but are not limited to, polydimethylsiloxanes, hexamethyldisiloxanes, polyester-modified methylphenyl polysiloxanes, combinations thereof, and the like. In other embodiments, a combination of a siloxane and a polycarbonate may be used to form the tubular body 12.

[0056] For example, in some embodiments, the tubular body is made of a blend of a polycarbonate with a siloxane, which is extruded into the form of the tubular body. The siloxane improves lubricity for the passage of the inner shaft assembly and the specimen bag through the outer tube to deploy the specimen bag in the patient's body.

[0057] In some embodiments, the tubular body 12 and the inner shaft assembly 22 are formed of the same material. In other embodiments, the tubular body 12 and the inner shaft assembly 22 are formed of different materials.

[0058] In embodiments, the mouth 42 of the specimen bag 40 has a pull string 70 attached thereto (FIG. 11), as well as resilient fingers 30, 32 attached thereto. In other embodiments, the resilient fingers 30, 32 and the pull string 70 may be received in the cuff 43 formed at the mouth 42 of the specimen bag 40.

[0059] In use, the tubular body 12 of the specimen retrieval device 10 can be inserted through an incision (not shown) with the specimen bag 40 furled about the inner shaft 22 and positioned within the tubular body 12 to position the specimen bag 40 in a body cavity adjacent a surgical site. When the tubular body 12 is properly positioned, the clinician can grip the hand grip 15.

[0060] The clinician then pushes the actuation handle 25 on the proximal portion 24 of the inner shaft 22 distally in relation to the hand grip 15 and the tubular body 12 (not shown), so the distal portion 26 of the inner shaft 22, including the specimen bag 40, exits the distal portion 18 of the tubular body 12 (FIG. 1). Once the specimen bag 40 has exited the tubular body 12, the resilient fingers 30, 32 (FIG. 4) return to their non-deformed state, thereby opening the mouth 42 of the specimen bag 40 to ensure the specimen bag 40 is deployed (FIG. 11).

[0061] As depicted in FIG. 12, after a tissue specimen (not shown) has been placed in the specimen bag 40, the pull string 70 is pulled proximally (indicated by arrows “A” in FIG. 12) to pull the pull string 70 proximally, thus cinching the mouth 42 of the specimen bag 40 closing the opening 42, and withdrawing a portion of the specimen bag 40 into the inner shaft 12 (indicated by arrow “B” in FIG. 12). As depicted in FIG. 12, the proximal portion 72 of the pull string 70 may be in the form of a loop 74 that may assist in pulling the pull string 70.

[0062] Kits of the present disclosure may include both the specimen retrieval device described above, as well as trocars, graspers, vacuum sources (tubes), combinations thereof, and the like. In some embodiments, these additional devices, such as graspers and/or vacuum sources, may be used to break up the tissue specimen in the specimen bag prior to removing the specimen retrieval device from the body cavity.

[0063] Once the specimen retrieval device of the present disclosure has been removed from the patient's body, any tissue specimen may be removed from the specimen bag 40 for further examination and the specimen bag 40 may be discarded.

[0064] While several embodiments 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 embodiments. 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 embodiment may be combined with the elements and features of another without departing from the scope of the present disclosure, and that such modifications and variations are also intended to be included within the scope of the present disclosure. Accordingly, the invention is not to be limited by what has been particularly shown and described, except as indicated by the appended claims.