Specimen capture stapler

Abstract

A surgical stapling device includes an end effector and a handle assembly operably coupled to the end effector. The end effector includes an anvil assembly and a cartridge assembly. The surgical stapling device also includes a specimen bag adhered to both the anvil assembly and the elongated support channel of the cartridge assembly. The specimen bag includes a drawstring within a drawstring housing. Once the surgical stapling device is inserted into a patient's body and the anvil assembly and the cartridge assembly are open, a tissue specimen is placed into the specimen bag. The anvil assembly and the cartridge assembly are then closed on the tissue specimen and the surgical stapling device is fired. The specimen bag then separates from the surgical stapling device and both the surgical stapling device and the specimen bag are removed from the patient.

Description

TECHNICAL FIELD

The present disclosure relates generally to surgical apparatuses for use in minimally invasive surgical procedures, such as endoscopic and/or laparoscopic procedures, and more particularly, the present disclosure relates to a surgical apparatus including a specimen retrieval device for collecting body tissue(s) and/or body fluid(s) during these procedures.

BACKGROUND

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 to pass through incisions and penetrate the abdominal wall, thereby permitting endoscopic surgery to be 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 a 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, graspers, cutters, applicators, and the like, which are designed to fit through additional cannulas.

When removing certain tissues from the body cavity, for example tumor tissue, it is important that the tumor tissue does not come into contact with healthy or uninvolved tissue. If tumor tissue or tissue parts have to be removed, they may be introduced into an “extraction bag,” also referred to herein as a “specimen bag,” at the site where the tumor or diseased tissue has been detached from the surrounding tissue, after which the specimen bag is withdrawn from the body, thereby minimizing contact of the diseased tissue with healthy tissue.

Improved devices, including specimen bags for use in minimally invasive surgical procedures, remain desirable.

SUMMARY

The present disclosure provides surgical stapling devices and methods for using the devices. In embodiments, a surgical stapling device of the present disclosure includes an end effector including an anvil assembly and a cartridge assembly pivotally coupled to one another, the anvil assembly and the cartridge assembly being relatively movable such that the end effector is movable between an open position and a clamped position. The surgical stapling device of the present disclosure also includes a specimen bag including a body and a mouth defining an open end, the mouth attached to the anvil assembly and the cartridge assembly such that movement of the end effector to the open position moves the mouth of the specimen bag to an open position.

In some embodiments, the mouth of the specimen bag includes a drawstring housing having a drawstring therein.

Methods of the present disclosure include, in embodiments, advancing a surgical stapling device including an anvil assembly and a cartridge assembly into a body cavity adjacent tissue to be removed from a patient's body and placing the tissue to be removed from the patient's body into a specimen bag having a mouth attached to the anvil assembly and the cartridge assembly. The anvil assembly and the cartridge assembly are closed on the tissue and the surgical stapling device is fired to separate a tissue specimen from the tissue.

In some embodiments, the method of the present disclosure further includes grasping the tissue specimen to pull the tissue specimen deeper into the specimen bag.

In other embodiments, grasping the tissue specimen to pull the tissue specimen deeper into the specimen bag occurs after firing the surgical stapling device.

In embodiments, the method of the present disclosure further includes closing the mouth of the specimen bag after firing the surgical stapling device.

Closing the mouth of the specimen bag occurs, in embodiments, by proximally pulling a drawstring encompassing the mouth of the specimen bag.

In some embodiments, proximally pulling the drawstring encompassing the mouth of the specimen bag further includes detaching the mouth of the specimen bag from the anvil assembly and the cartridge assembly.

In other embodiments, proximally pulling the drawstring encompassing the mouth of the specimen bag further includes detaching the specimen bag from an adapter assembly of the surgical stapling device.

In yet other embodiments, proximally pulling the drawstring encompassing the mouth of the specimen bag includes removing the specimen bag from the patient's body.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the present disclosure are described herein with reference to the accompanying drawings, wherein:

FIG. 1 is a perspective view of a surgical stapling device including a handle housing, an adapter assembly, an end effector, and a specimen bag attached thereto in accordance with an embodiment of the present disclosure;

FIG. 2 is a perspective view, of the end effector and the specimen bag, including a drawstring and drawstring housing, of the surgical stapling device shown in FIG. 1;

FIG. 3 is a cross-sectional view taken along section line 3-3 of FIG. 1;

FIG. 4 is an enlarged view of the indicated area of detail shown in FIG. 3;

FIG. 5 is a top view of the distal portion of the surgical stapling device shown in FIG. 1 during a surgical procedure as the specimen bag is being deployed;

FIG. 6 is a top view of showing the specimen bag of the present disclosure after firing of the surgical stapling device shown in FIG. 5;

FIG. 7 is a top view showing the detachment of the specimen bag from the surgical stapling device shown in FIG. 6; and

FIG. 8 is a side view showing removal of the drawstring and the drawstring housing from a patient's body after detachment of the specimen bag from the surgical stapling device shown in FIG. 7.

DETAILED DESCRIPTION OF EMBODIMENTS

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.

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.

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.

Turning now to FIG. 1, a surgical stapling device 10 in accordance with an embodiment of the present disclosure is in the form of a handheld surgical instrument. The surgical stapling device 10 includes a handle assembly 100, an adapter assembly 200, and an end effector 300. The handle assembly 100 is configured for selective connection with the adapter assembly 200 and, in turn, the adapter assembly 200 is configured for selective connection with the end effector 300.

The surgical stapling device 10 may be a manual surgical stapling device or a powered surgical stapling device. A powered device includes one or more motors and an internal or external power source, whereas the manual device has a movable handle and a mechanism for driving the functions of the apparatus. Examples of such stapling devices include those disclosed in U.S. Pat. Nos. 5,865,361; 5,782,396; 8,672,206; and International WO 04/032,760, the entire disclosures of each of which are incorporated by reference herein.

The handle assembly 100, the adapter assembly 200, and the end effector 300 will only further be described to the extent necessary to disclose aspects of the present disclosure. For a detailed description of the structure and function of exemplary handles, adapter assemblies, and end effectors, reference may be made to commonly owned U.S. Patent Appl. Pub. No. 2016/0310134, the entire disclosure of which is incorporated by reference herein.

With reference now to FIG. 1, the handle assembly 100 includes a housing shell 112, including a proximal half-section 112a and a distal half-section 112b. The housing shell 112 includes a plurality of actuators 116 (e.g., finger-actuated control buttons, knobs, toggles, slides, interfaces, and the like) for activating various functions of the surgical device 10 (FIG. 1). As noted above, the handle 112 may include a power source (not shown) configured to power and control various operations of the surgical device 10 or the handle 112. Alternatively, it is also envisioned that the handle 112 may be manually powered.

Referring now to FIGS. 1-2, the end effector 300 is in the form of a single use loading unit. It should be understood, however, that other types of end effectors may also be used with the surgical device 10 of the present disclosure including, for example, end-to-end anastomosis loading units, multi-use loading units, transverse loading units, and curved loading units.

The end effector 300 includes a proximal body portion 310 and a tool assembly 320. The proximal body portion 310 of the end effector 300 is releasably attachable to the distal cap 206 of the adapter assembly 200 (FIG. 1) and the tool assembly 320 is pivotally attached to the proximal body portion 310 of the end effector 300. The tool assembly 320 of the end effector 300 includes an anvil assembly 330 and a cartridge assembly 340 pivotally coupled to one another such that the tool assembly 320 is movable between an open or unclamped position and a closed or clamped position.

As shown in FIG. 3, the anvil assembly 330 includes an anvil plate 332 and a cover plate 334 secured over the anvil plate 332 such that the cover plate 334 defines an outer surface 334a of the anvil assembly 330.

The cartridge assembly 340 includes a staple cartridge 342 and a cartridge carrier 344.

As depicted in FIGS. 1 and 2, the surgical stapling device 10 of the present disclosure also includes a specimen bag 400 adhered to both the anvil assembly 330 and the cartridge assembly 340 of the end effector 300. The specimen bag 400 includes a body 460 having a generally tubular or elongated configuration that is defined by an openable and closable portion (or mouth) 440 and a closed portion 470 (FIG. 1). The mouth 440 defines an opening 450 that opens when the anvil assembly 330 and the cartridge assembly 340 are in an open position. The specimen bag 400 includes a drawstring 410 within a drawstring housing 420. In embodiments the proximal portion of the drawstring 410 may possess a ring. 430 to facilitate grasping of the drawstring 410 (FIGS. 1 and 2). The drawstring housing 420 is adhered along the length of the adapter assembly 200. The specimen bag 400 may be compressed so that it fits between the anvil assembly 330 and the cartridge assembly 340 and can pass through a cannula, trocar, or similar device (not shown). The drawstring housing 420 will be long enough that it sticks outside of the trocar (not shown).

In other embodiments (not shown) the specimen bag 400 of the present disclosure may be attached to the anvil assembly 330, the cartridge assembly 340 of the end effector 300, or both, using loops that slide over the anvil assembly 330, the cartridge assembly 340 of the end effector 300, or both, to secure the specimen bag thereto. This would allow the specimen bag to be sold as a separate product for use with existing surgical stapling devices.

The body 460 of the specimen bag 400 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 400 may be opaque or clear. In some embodiments, the body 460 of the specimen bag 400 is formed of a nylon material, or combinations of nylon materials.

As shown in greater detail in FIGS. 3 and 4, in embodiments the specimen bag 400 is adhered to both the anvil assembly 330 and the cartridge assembly 340. As shown in FIG. 4, the drawstring housing 420, possessing the drawstring 410 therein, is attached to the anvil 330 and the cartridge assembly 340 using any suitable means, including biocompatible adhesives. Although not depicted, the drawstring 420 is similarly attached to the cartridge assembly.

In use, as shown in FIG. 5, in embodiments a trocar 500 may be introduced through an incision “I” for access to a patient's body cavity “BC”. The end effector 300 is inserted through the trocar 500 so that the anvil assembly 330 and the cartridge assembly 340 are positioned within the body cavity “BC”. A tissue specimen “TS” is placed into the specimen bag 400 which will begin to unfold. The anvil assembly 330 and the cartridge assembly 340 are then closed on the tissue specimen “TS” and the surgical stapling device 10 is fired (not shown).

After firing the stapler, as shown in FIG. 6, the tissue specimen “TS” remains within the specimen bag 400, with the tissue remaining in the patient's body “TR” having a staple line “S” at the point of stapling.

Forceps may then be used to grasp the tissue specimen “TS” to pull the tissue specimen “TS” deeper into the specimen bag 400 (not shown).

As shown in FIG. 7, once the tissue specimen “TS” is fully in the specimen bag 400, the drawstring 410 is pulled proximally (not shown) to close the specimen bag 400. While the specimen bag 400 is closing, the drawstring housing 420 detaches from the anvil assembly 330 and the cartridge assembly 340.

The drawstring housing 420 is then pulled to detach it from the adapter assembly 200 (not shown). At this point, the entire specimen bag 400 and drawstring housing 420 are completely detached from the surgical stapling device 10 and the surgical stapling device 10 can be removed from the patient (not shown). As shown in FIG. 8, the drawstring housing 420 with the drawstring 410 therein are then ready for removal through the trocar 300 by proximally pulling the drawstring housing 420 and the drawstring 410 therein (indicated by arrow “A” in FIG. 8). Next, the trocar 500 can be removed from the patient while the doctor ensures the specimen bag 400 remains closed by maintaining tension on the drawstring 410 (not shown), after which the specimen bag 400 can be removed from the patient (not shown).

Once the tissue specimen is removed from the patient, it will most likely be used for histopathological testing to ensure no cancer cells remain next to the cut line.

The devices and methods of the present disclosure provide several advantages over previous specimen retrieval devices.

For example, use of the devices of the present disclosure permits the direct placement of a diseased tissue specimen into a specimen bag to minimize the risk of spreading cancer cells during removal of the diseased tissue specimen from within a body cavity. It also reduces the maneuvering required with conventional devices to get the tissue specimen into the specimen bag, which can lead to the tissue specimen mistakenly coming in contact with healthy tissue.

In addition, the methods and devices of the present disclosure permit carrying out histopathology closer to the staple line, without having to worry about fluids being released from unhealthy tissue. With current practice, the best sample from the resected tissue is that portion closest to the cut line, to determine if any cancer daughter cells are left on the remaining healthy tissue. When the diseased tissue is cut, it is stapled as well. In some cases, the stapling deforms the tissue so that it can no longer be used for histopathology, therefore the pathologist must use the next closest sample of undamaged tissue, which is the width of three staples lines away from the cut line. However, if the resected tissue is not stapled, any contents inside the tissue could be expelled into its containing cavity. This could lead to an infection in the abdominal cavity. Using the devices and methods of the present disclosure, by immediately quarantining the resected tissue in a specimen bag, the risk of abdominal infection is less of a concern if the tissue being removed is not stapled or stapled with only one staple row far enough from the cut line to allow for histopathology.

Finally, less equipment is needed since the specimen bag and the stapling reload are combined.

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.

Claims

1. A surgical stapling device, comprising: an end effector including an anvil assembly and a cartridge assembly pivotally coupled to one another, the anvil assembly and the cartridge assembly being relatively movable such that the end effector is movable between an open position and a clamped position; anda specimen bag including a body and a mouth defining an open end, the mouth attached to the anvil assembly and the cartridge assembly such that movement of the end effector to the open position moves the mouth of the specimen bag to an open position.

2. The surgical stapling device according to claim 1, wherein the mouth of the specimen bag includes a drawstring housing having a drawstring therein.

3. A method, comprising: advancing a surgical stapling device including an anvil assembly and a cartridge assembly into a body cavity adjacent tissue to be removed from a patient's body;placing the tissue to be removed from the patient's body into a specimen bag having a mouth attached to the anvil assembly and the cartridge assembly;closing the anvil assembly and the cartridge assembly on the tissue; andfiring the surgical stapling device to separate a tissue specimen from the tissue.

4. The method of claim 3, further comprising grasping the tissue specimen to pull the tissue specimen deeper into the specimen bag.

5. The method of claim 4, wherein grasping the tissue specimen to pull the tissue specimen deeper into the specimen bag occurs after firing the surgical stapling device.

6. The method of claim 3, further comprising closing the mouth of the specimen bag after firing the surgical stapling device.

7. The method of claim 6, wherein closing the mouth of the specimen bag occurs by proximally pulling a drawstring encompassing the mouth of the specimen bag.

8. The method of claim 7, wherein proximally pulling the drawstring encompassing the mouth of the specimen bag further includes detaching the mouth of the specimen bag from the anvil assembly and the cartridge assembly.

9. The method of claim 8, wherein proximally pulling the drawstring encompassing the mouth of the specimen bag further includes detaching the specimen hag from an adapter assembly of the surgical stapling device.

10. The method of claim 8, wherein proximally pulling the drawstring encompassing the mouth of the specimen bag includes removing the specimen bag from the patient's body.