US20140296648A1

US20140296648A1 - Surgical access device and wound protector

Info

Publication number: US20140296648A1
Application number: US14/304,346
Authority: US
Inventors: Gennady Kleyman; Gregory Okoniewski
Original assignee: Covidien LP
Current assignee: Covidien LP
Priority date: 2012-03-26
Filing date: 2014-06-13
Publication date: 2014-10-02
Also published as: US8764645B2; EP2644138A2; US20130253276A1; AU2013201369A1; EP2644138A3; CA2808772A1

Abstract

An access device for use in a minimally invasive surgical procedure is disclosed. The access device is configured and adapted to be placed within a body opening to provide access to an underlying body cavity. The access device provides protection to the opening and minimizes contamination and the risk of possible infection.

Description

CROSS REFERENCE TO RELATED APPLICATION

The present application is a continuation of U.S. patent application Ser. No. 13/778,427, filed Feb. 27, 2013 which claims the benefit of and priority to U.S. Provisional Application Ser. No. 61/615,494, filed on Mar. 26, 2012, the entire contents of which are incorporated herein by reference.

BACKGROUND

1. Technical Field
The present disclosure relates to an access device for use in a minimally invasive surgical procedure. In particular, the access device is placed within a tissue tract to provide access to an underlying body cavity while providing protection to the tissue tract.
2. Background of Related Art
During a typical minimally invasive procedure, surgical objects, such as surgical access devices, e.g., trocar and cannula assemblies, or endoscopes, are inserted into the patient's body through an incision or a naturally occurring bodily orifice (e.g., mouth, anus, or vagina) in tissue. To facilitate access to an underlying body cavity, access devices are placed within the within the incision or the naturally occurring bodily orifice. Surgical instruments are placed through the access device.
While it is desirable to minimize the size of an incision or to access internal body structures through a naturally occurring orifice, adequate anatomical exposure is needed to facilitate access to the surgical site. Achieving adequate anatomical exposure can be achieved by separating the walls of the incision or the naturally occurring body orifice. Various retraction devices have been developed to facilitate access to underlying body structures.
As with any surgical procedure, care must be taken to inhibit the possibility of infection that may result if exposed healthy tissue comes in contact with infected or malignant tissue. For example, the spillage of tumor cell clusters may spur the growth of malignant tumors in previously unaffected areas of a patient's body in a process known as tumor seeding. In particular, the sides of a wound a susceptible to infection resulting from contamination. Various wound protection devices have been developed to protect a wound or body orifice during a surgical procedure.
There is a continuing need for new surgical devices that will facilitate access to a surgical site through an incision or naturally occurring bodily orifice while inhibiting contamination of surrounding tissue during the procedure.

SUMMARY

The present disclosure discloses a surgical access device that includes an outer sleeve and one or more inner sleeves that are inwardly disposed of the outer sleeve. The one or more inner sleeves are removable, one at a time, from the surgical access device such that a clean, unused sleeve can be provided without necessitating removal of the surgical access device from the surgical site.
In an embodiment, the surgical access device includes a proximal ring and a distal ring. The outer sleeve is operably coupled to the proximal and distal rings. The proximal and distal rings can function to draw the outer sleeve taut to create a tension in the material of the outer sleeve. This tension may facilitate maintenance of the generally tubular shape of the outer sleeve when the surgical access device is placed within the body opening within the tissue.
The inner sleeves are removably secured to one another and to the outer sleeve. During use, an adhesive layer between the inner sleeves and the outer sleeve can facilitate maintenance of the inner and outer sleeves in a given position relative to one another. A drawstring may be operatively coupled to each of the inner sleeves to facilitate removal of the inner sleeves by proximally translating the drawstring thereby moving the inner sleeve in a corresponding direction.
A method of using the surgical access device is also disclosed. During use, the surgical access device is provided and placed into a body opening. The outer sleeve of the surgical access device facilitates maintaining the body opening in an open state to facilitate access to underlying body structures through the lumen of the surgical access device. As the inner sleeves defining the lumen become contaminated with bodily debris and fluid, the inner sleeves are removed from within the lumen, thereby exposing a previously unexposed inner sleeve and providing the lumen of the surgical access device with a clean surface. Once the desired surgical procedure is completed, the surgical access device is removed from the body opening.
These and other features of the present disclosure will be more fully described with reference to the appended figures.

BRIEF DESCRIPTION OF THE DRAWINGS

By way of description only, embodiments of the present disclosure will be described with reference to the accompanying drawings, in which:

FIG. 1 is a cross-sectional view of a surgical access device in accordance with the present disclosure positioned within a tissue tract and shown in a first condition;

FIG. 2 is a cross-sectional view of the surgical access device of FIG. 1 shown in a second condition;

FIG. 3 is a top view of an embodiment of a surgical access device in accordance with the present disclosure;

FIG. 4A is a perspective view of an embodiment of a surgical access device in accordance with the present disclosure and shown in a first condition;

FIG. 4B is a partially cutaway view of the surgical access device of FIG. 4A;

FIG. 5A is a perspective view of the surgical access device of FIG. 4A shown relative to tissue and in an intermediate condition;

FIG. 5B is the surgical access device as shown in FIG. 5A in a second condition;

is a front view of a surgical access device in accordance with the present disclosure;

FIG. 6A is a front view of an introducer device; and

FIG. 6B is a front view of the introducer device of FIG. 6A shown placed within the surgical access device of FIG. 1.

DETAILED DESCRIPTION

Particular embodiments of the present disclosure will be described herein with reference to the accompanying drawings. In the figures and in the description that follows, in which like reference numerals identify similar or identical elements, the term “proximal” will refer to the end of the apparatus that is closest to the operator during use, while the term “distal” will refer to the end that is farthest from the operator during use.
A first embodiment of a surgical access device will now be described with reference to FIGS. 1 and 2. The surgical access device 10 is configured and adapted to be placed within a body opening “O”, e.g., a naturally occurring bodily orifice (e.g., mouth, anus, or vagina) or an incision or wound within a patient's skin “S”. The surgical access device 10 is configured and adapted to provide access to underlying body cavity “C” while providing protection to the surfaces of the body opening “O”.
The surgical access device 10 includes a trailing or proximal portion 5 and a leading or distal portion 3. The proximal portion 5 of the surgical access device 10 includes a proximal ring 2. The distal portion 3 of the surgical device 10 includes a distal ring 4. An intermediate section 7 is positioned between the proximal portion 5 and the distal portion 3. As shown in FIGS. 1 and 2, the intermediate section 7 includes an outer sleeve 8 and one or more inner sleeves 6. The intermediate section 7 defines a lumen 11 longitudinally extending along longitudinal axis “X”.
The outer sleeve 8 is fixed to the proximal ring 2 and the distal ring 4. The outer sleeve 8 may be formed from a length of flexible material that is drawn taut by spacing the proximal ring 2 apart from the distal ring 4 along longitudinal axis “X”. In embodiments, the outer sleeve 8 may be formed from a rigid, semi-rigid, or compressible material to facilitate anchoring of the seal anchor member 10 within the body opening “O”.
Disposed within and removably coupled to the outer sleeve 8 are one or more inner sleeves 6. The one or more sleeves 6 are positioned between and are removably coupled to the proximal and distal rings 2, 4. The one or more sleeves 6 may each be removably coupled to the proximal ring 2 at fixation point 16 and to the distal ring 4 at fixation point 14. The one or more inner sleeves 6 may be formed from a flexible material that is drawn taut by the proximal and distal ring 2, 4. Each inner sleeve 6 may be removably coupled to fixation points 14, 16 by an adhesive. When drawn taut, the one or more inner sleeves 6 are tensioned and will resist deformation, thereby maintaining a generally cylindrical shape.
In an embodiment, as shown in FIG. 3, the inner sleeves 6 and the outer sleeve 8 may form a single structure. Micro-perforations 6 a between each inner sleeve 6 and the outer sleeve 8 facilitate separation of individual inner sleeves 6 from each other and the outer sleeve 8 upon the application of a force F upon an inner sleeve 6.
As shown in FIGS. 1 and 2, a drawstring 12 may be secured to a distal end of each inner sleeve 6. Upon application of force F to the inner sleeve 6 (FIG. 2) in the proximal direction, the inner sleeve 6 separates from the fixation point 14. Continued application of force F to the inner sleeve 6 results in separation of the inner sleeve 6 from fixation point 16 and the removal of the inner sleeve 6 from the lumen 11.
Another embodiment of a surgical access device will now be described with reference to FIGS. 4A and 4B. A surgical access device 20 includes a series of tubular structures 21, 22, 23 that are frictionally engaged with one another. The tubular structures 21, 22, 23 may be formed from a rigid or semi-rigid material to resist the biasing force of the body opening O to maintain the tubular shape of the tubular structures 21, 22, 23. Although shown as including three tubular structures 21, 22, 23, the surgical access device 20 may include a greater or lesser number of such tubular structures. The outermost tubular structure 21 forms an intermediate section 28 that interacts with the walls of the body opening O. An hour-glass configuration of the intermediate section 28 may facilitate securement of the surgical access device 20 within the body opening O. The proximal and distal ends 27, 29 of the surgical access device 20 may be flanged to facilitate securing of the surgical access device 20 within the body opening O.
As shown best in FIG. 4B, the surfaces 21 a, 22 a, 23 a of the tubular structures 22, 23 may include an adhesive layer to inhibit movement of the tubular structures with respect to one another. A drawstring 13 may be coupled to the tubular structures 21, 22, 23 to facilitate removal of each tubular structure 22, 23 from the surgical access device 20. When one of the tubular structures 21, 22, 23 (i.e., the structure having an exposed surface) becomes contaminated, the tubular structure can be removed while maintaining the surgical access device 20 within the body opening O. As shown in FIGS. 5A and 5B, a surgeon H may proximally translate tubular structure 23 in the direction indicated by arrows A, thereby leaving behind the remaining unused tubular structures 21, 22.
An introducer device 50 may be used to facilitate placement of the surgical access device 10. As shown in FIG. 6A, the introducer device 50 includes a tapered distal end 56, and elongated tubular structure 54, and a flanged proximal end 52. As shown in FIG. 6B, the introducer device is configured and adapted to be placed within the lumen 11 of the surgical access device 10, and the proximal end 52 of the introducer device 50 is configured and adapted to engage the proximal end 5 of the surgical access device 10 such that distal translation of the introducer device 50 pushes the surgical access device into the body opening O of tissue T. In addition, the tapered distal end 56 of the introducer device 50 facilitates placement of the introducer device 50 into the lumen 11 of the surgical access device. Furthermore, the tapered distal end 56 of the introducer device 50 may facilitate the creation or enlargement of the body opening O within the skin S of tissue T.
A method of using the surgical access devices described herein will now be discussed with respect to surgical access device 10. First, introducer 50 may be placed within lumen 11 of the surgical access device 10. The surgical access device 10 is then placed into the body opening O of tissue T by inserting the introducer 50 along with the surgical access device 10 into the body opening O. The tapered distal end 56 facilitates insertion of the surgical access device 10 and helps stretch the body opening O to accommodate reception of the surgical access device 10. The surgical access device 10 is then anchored within the body opening O. The shape, e.g., an hour-glass configuration, of the surgical access device 10 facilitates the anchoring of the surgical access device 10 within the body opening O.
Once the surgical access device 10 is placed within the body opening O, the desired surgical procedure is performed. During the course of the surgery, it may be advantageous to remove inner sleeves 6 as they become contaminated to facilitate maintaining a clean working environment. Removal of the inner sleeves 6 is accomplished by translating each inner sleeve 6 proximally out from the lumen 11. Applying force F in a proximal direction to the drawstring 12 results in separation of the inner sleeve 6 from the surgical access device, and the exposure of the surface of the next remaining inner sleeve 6 or the inner surface of the outer sleeve 8. Once the desired surgical procedure is completed, the surgical access device 10 is removed from the body opening O.
It will be understood by those skilled in the art that various modifications and changes in form and detail may be made to the present disclosure without departing from the scope and spirit of the same. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular embodiments. While several embodiments of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto. Rather, the disclosure is intended to be read as broadly in scope as the art will allow.

Claims

1-7. (canceled)

8. A surgical access device, comprising:

a first tubular member; and

a second tubular member disposed within the first tubular member, the first and second tubular members configured to resist a biasing force of a body opening when the surgical access device is placed within a body opening, wherein the first tubular member is removably coupled to the second tubular member, such that the first tubular member is removable from the second tubular member when the second tubular member is disposed within a body opening.

9. The surgical access device according to claim 8, wherein the second tubular member has an hour-glass configuration.

10. The surgical access device according to claim 8, wherein the first and second tubular members include an adhesive layer to inhibit relative movement therebetween.

11. The surgical access device according to claim 8, further comprising a drawstring attached to the first tubular member, wherein application of a force to the drawstring facilitates removal of the first tubular member from the second tubular member.

12. The surgical access device according to claim 8, wherein the first and second tubular members frictionally engage each other.

13. The surgical access device according to claim 8, wherein the first and second tubular members are formed of a semi-rigid material.

14. The surgical access device according to claim 8, wherein the second tubular member is configured to resist the biasing force of a body opening in the absence of the first tubular member.

15. A surgical access device, comprising:

a proximal ring;

a distal ring; and

an intermediate portion disposed between the proximal and distal rings, the intermediate portion including:

an outer sleeve is securely fixed to the proximal and distal rings; and

an inner sleeve disposed within the outer sleeve, the inner sleeve removably coupled to the proximal and distal rings, such that the inner sleeve is removable from the outer sleeve when the outer sleeve is disposed within a body opening.

16. The surgical access device according to claim 15, wherein the inner sleeve is removably coupled to the proximal and distal rings by an adhesive.

17. The surgical access device according to claim 15, wherein the inner sleeve is configured to resist deformation.

18. The surgical access device according to claim 15, wherein the inner sleeve has a generally cylindrical shape.

19. The surgical access device according to claim 15, wherein the inner and outer sleeves are formed as a single structure.

20. The surgical access device according to claim 15, wherein the inner and outer sleeves define micro-perforations to facilitate separation therebetween.