This disclosure generally relates to surgical stapling devices and, more particularly, to circular stapling devices for performing anastomosis procedures.
Circular stapling devices for performing surgical procedures such as anastomoses are well known. In an anastomosis procedure, ends of two organ sections are joined with the circular stapling device. Typically, a circular stapling device includes a handle assembly, an elongated shaft or adapter assembly, a reload assembly including a staple cartridge, and an anvil assembly that is mountable to the adapter assembly and is movable in relation to the reload assembly between open and clamped positions. In use, opposed tissue end margins of the organ sections are clamped between an anvil head of the anvil assembly and the staple cartridge and the device is fired to drive an annular array of staples from the staple cartridge through the tissue end margins of the organ sections for deformation against the anvil head. An annular knife positioned within the reload assembly is advanced to core or remove organ tissue interior of the staples to clear an internal tubular passage of the organ sections.
Complications during anastomoses procedures may result in a need for further operation and/or permanent ostomy. One complication is anastomotic leakage. The risk of anastomotic leakage is multi-factorial and may be affected by patient comorbidities, chemotherapy, the presence of microbiome pathogens, and stapling technique. One cause of anastomotic leakage may be due to bilateral dog ear formation. Bilateral dog ear formation results when the tissue end margins are not drawn fully into the reload assembly prior to firing of the circular stapling device. Thus, when the circular stapling device is fired to join the end margins of the organ sections, ends of one or both end margins of the organ sections are stapled in a position that resembles dog ears (
A continuing need exists for a circular stapling device that can form an anastomosis without forming dog ears.
This disclosure is directed to a circular stapling device that includes a reload assembly having a housing and a staple cartridge that define channels through the reload assembly. The channels receive grasping members that are movable within the channels between retracted and extended positions. The grasping members each have a distal portion that includes a tissue engaging member. The grasping members are movable from their extended positions back towards their retracted positions during an anastomosis procedure to pull tissue into the housing of the reload assembly.
One aspect of the disclosure is directed to a circular stapling device including an adapter assembly, a reload assembly, a grasping member, and an anvil assembly. The adapter assembly has a proximal portion and a distal portion and includes an anvil retainer. The reload assembly is supported on the distal portion of the adapter assembly and includes a staple cartridge and a housing that defines a cavity. The housing has a proximal portion and a distal portion. The staple cartridge is supported on the distal portion of the housing and has an annular configuration. The housing and the staple cartridge define at least one channel that extends from the proximal portion of the housing through the staple cartridge. The anvil retainer extends through the cavity defined by the housing. The grasping member is movable within the at least one channel between a retracted position and an extended position and includes a body having a proximal portion and a distal portion. The distal portion of the body of the grasping member includes a tissue engaging portion that extends from the at least one channel to a position distal of the staple cartridge when the grasping member is in the extended position. The anvil assembly is releasably coupled to the anvil retainer and is movable in relation to the staple cartridge between open and clamped positions.
Other aspects of the disclosure are directed to a reload assembly that includes a staple cartridge, a housing, and a grasping member. The staple cartridge has an annular configuration. The housing defines a cavity and has a proximal portion and a distal portion. The staple cartridge is supported on the distal portion of the housing. The housing and the staple cartridge define at least one channel that extends from the proximal portion of the housing through the staple cartridge. The grasping member is movable within the at least one channel between retracted and extended positions and includes a body having a proximal portion and a distal portion. The distal portion of the body of the grasping member includes a tissue engaging portion that extends from the at least one channel to a position distal of the staple cartridge when the grasping member is in the extended position.
Other aspects of this disclosure are directed to a reload including a staple cartridge, a housing, and first and second grasping members. The staple cartridge has an annular configuration and includes an inner periphery. The housing defines a cavity and has a proximal portion and a distal portion. The staple cartridge is supported on the distal portion of the housing. The housing and the staple cartridge define first and second diametrically disposed channels that extend from the proximal portion of the housing through the inner periphery of the staple cartridge. The first and second grasping members are movable within the first and second channels from retracted positions to extended positions. The first and second grasping members each include a body having a proximal portion and a distal portion. The distal portions of the bodies of the first and second grasping members include tissue engaging portions that extend from the first and second channels to positions distal of the staple cartridge when the first and second grasping members are in their extended positions.
In aspects of the disclosure, the at least one channel includes a first channel and a second channel, and the grasping member includes a first grasping member and a second grasping member.
In some aspects of the disclosure, the first grasping member is received within the first channel and the second grasping member is received within the second channel.
In certain aspects of the disclosure, the first and second channels are diametrically opposed to each other.
In aspects of the disclosure, the staple cartridge has an inner periphery and the first and second channels extend through the inner periphery of the staple cartridge.
In some aspects of the disclosure, the tissue engaging portion of each of the first and second grasping members includes a hook portion.
In certain aspects of the disclosure, the tissue engaging portion of each of the first and second grasping members includes first and second jaws that are movable in relation to each other between open and closed positions.
In aspects of the disclosure, the first jaw is pivotably coupled to the second jaw.
In some aspects of the disclosure, the proximal portion of each of the first and second grasping members includes a grip portion.
In certain aspects of the disclosure, the grip portion includes a loop.
In aspects of the disclosure, the body of the grasping member is formed of a resilient material.
In some aspects of the disclosure, the stapling device includes a handle assembly, and the proximal portion of the adapter assembly is coupled to the handle assembly.
Other features of the disclosure will be appreciated from the following description.
Various aspects of a circular stapling device according to aspects of the disclosure are described herein below with reference to the drawings, wherein:
The disclosed circular stapling 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. However, it is to be understood that disclosed aspects of the circular stapling device are merely exemplary of the disclosure and may be embodied in various forms. Well-known functions or constructions are not described in detail to avoid obscuring the disclosure in unnecessary detail. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the disclosure in virtually any appropriately detailed structure.
In this description, the term “proximal” is used generally to refer to that portion of the device that is closer to a clinician during use of the device in its customary fashion, while the term “distal” is used generally to refer to that portion of the device that is farther from the clinician during use of the device in its customary fashion. In addition, directional terms such as front, rear, upper, lower, top, bottom, and similar terms are used to assist in understanding the description and are not intended to limit the disclosure. Further, the term “clinician” is used generally to refer to medical personnel including doctors, nurses, surgeons, and support personnel.
This disclosure is directed to a circular stapling device that includes a reload assembly having a housing, an annular staple cartridge, and grasping members. The housing and the staple cartridge define channels that receive the grasping members. The grasping members are movable through the channels between retracted and extended positions to grasp tissue and draw the tissue into the housing during an anastomosis procedure.
Although the stapling device 10 is illustrated as a powered stapling device, it is envisioned that aspects of this disclosure could be incorporated into a manually powered stapling device. U.S. Pat. No. 10,022,126 (hereinafter “the '126 Patent”) discloses an exemplary manually actuated circular stapling device.
The end effector 16 of the stapling device 10 includes an anvil assembly 30 and a shell or reload assembly 32. The anvil assembly 30 includes an anvil shaft 34 and an anvil head 36. The anvil shaft 34 includes a proximal portion 38 and a distal portion 40 that supports the anvil head 36. In aspects of the disclosure, the anvil head 30 is pivotably coupled to the anvil shaft 34 and is movable from an operative position to a pivoted or tilted position. In the tilted position, the profile of the anvil head 36 is minimized to facilitate passage of the anvil assembly 30 through an organ section. The proximal portion 38 of the anvil shaft 34 is adapted to releasably engage an anvil retainer 42 of the stapling device 10. In aspects of the disclosure, the proximal portion 38 of the anvil shaft 34 includes resilient fingers 44 that define a longitudinal bore that receives the anvil retainer 42 of the stapling device 10 to releasably couple the anvil assembly 30 to the anvil retainer 42. For a detailed description of an anvil shaft and anvil retainer suitable for use with the stapling device 10, see the '126 Patent.
The reload assembly 32 includes an annular knife blade 60 that includes a cutting edge 60a. The knife blade 60 is movable within the cylindrical cavity 50a of the housing 50 and within an annulus of the staple cartridge 52 from a retracted position to an advanced position. In the retracted position of the knife blade 60, the cutting edge 60a of the knife blade 60 is recessed within the housing 50 (
Although not shown, the reload assembly 32 also includes a pusher that is movably supported within the housing 50 from a retracted position to an advanced position to eject the staples (not shown) from the staple cartridge 52. The pusher and the knife blade 60 can be coupled to each other and move in unison between their retracted and advanced positions. Alternately, the pusher can be moved between its retracted and advanced positions independently of the knife blade 60 to eject the staples from the staple cartridge 52, and the knife blade 60 can be subsequently moved between its advanced and retracted positions to cut tissue clamped between the anvil assembly 30 and the staple cartridge 52 of the reload assembly 32.
The anvil retainer 42 extends from the adapter assembly 14 through the cylindrical cavity 50a of the housing 50. In aspects of the disclosure, the anvil retainer 42 includes a distal trocar portion 66 that is received within the anvil shaft 34 of the anvil assembly 30 to releasably couple the anvil assembly 30 to the anvil retainer 42. The anvil retainer 42 is movable between advanced and retracted positions to move the anvil assembly 30 in relation to the staple cartridge 52 between the open and clamped positions.
The housing 50 of the reload assembly 32 defines channels 70 that extend through the housing 50 from a proximal portion of the housing 50 to the distal portion of the housing 50. In aspects of the disclosure, the channels 70 communicate with channels 70a that extend through the staple cartridge 52. The channels 70 and 70a in the housing 50 and the staple cartridge 52 define a continuous channel through the reload assembly 32. In aspects of the disclosure, the channels 70a exit the staple cartridge 52 at diametrically opposed positions on an inner periphery or edge 78 of the staple cartridge 52 (
The distal portion of the elongate body 82 of each of the grasping members 80 includes a tissue engaging portion 86 that is configured to grasp tissue positioned on the staple cartridge 52. In aspects of the disclosure, the tissue engaging portion 86 of each of the grasping members 80 includes a hook portion 86a. Alternately other tissue engaging configurations are envisioned. In aspects of the disclosure, the elongate body 82 is formed from a resilient material such as spring steel.
Persons skilled in the art will understand that the instruments and methods specifically described herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments. 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 disclosure. As well, one skilled in the art will appreciate further features and advantages of the disclosure based on the above-described embodiments. Accordingly, the disclosure is not to be limited by what has been particularly shown and described, except as indicated by the appended claims.