1. Technical Field
The present disclosure relates generally to a surgical device for use in a minimally invasive surgical procedure. More particularly, the present disclosure relates to instrumentation for use in a minimally invasive surgical procedure that facilitate both the placement and use of the instruments within the surgical site.
2. Background of Related Art
A minimally invasive surgical procedure is one in which a surgeon enters a patient's body through one or more small openings in the patient's skin or a naturally occurring opening (e.g., mouth, anus, or vagina). As compared with traditional open surgeries, minimally invasive surgical procedures have several advantages and disadvantages. Minimally invasive surgeries include arthroscopic, endoscopic, laparoscopic, and thoracic surgeries. Advantages of minimally invasive surgical procedures over traditional open surgeries include reduced trauma and recovery time for patients.
However, some disadvantages include a lack of direct visualization of the surgical site and reduced dexterity of instruments, as compared to traditional open surgeries. In particular, the simultaneous manipulation of the viewing instrument and surgical instruments that are inserted into the opening may be complicated. One complication arises from the difficulty in visualizing surgical instruments on a monitor that is operably coupled to the viewing instrument.
One surgical technique used to increase the ability of the surgeon to visualize and access critical anatomy is triangulation. Triangulation is a principle in which the surgical instrument and the viewing instrument are held so that their tips form the apex of an imaginary triangle. In particular, the viewing instruments may be in the middle of the surgical field, and the surgical instruments may be angled with respect to the viewing instrument as to form an imaginary triangle.
In minimally invasive surgical procedures through a single opening, straight and rigid surgical instruments are inserted through a single incision. To control the instruments, a surgeon often crosses his hands. The lack of triangulation makes visualization and access of critical anatomy potentially difficult. Furthermore, it is desirable to coordinate the positions of end effectors of the surgical instruments.
Consequently, a continuing need exists for improved minimally invasive surgical devices.
Disclosed herein is a surgical system for use during a minimally invasive surgical procedure. In particular, a minimally invasive surgical triangulation system is disclosed. The minimally invasive surgical triangulation system includes a seal anchor member that is transitionable between a first condition and a second condition.
The seal anchor member includes a leading portion, a trailing portion, and an intermediate section positioned between the leading and trailing portions. At least two ports extend longitudinally through the intermediate section. Each port defines a longitudinal axis through which a surgical instrument is placed.
The surgical instrument includes a shaft that is rotatable about the longitudinal axis of the port. By rotating the shaft of the surgical instrument within the port, the orientation of the surgical instrument is transitioned between first and second orientations. When the surgical instruments have the first orientation, the triangulation system is in a first condition. Conversely, the triangulation system is in the second condition when the surgical instruments are in the second orientation.
Moreover, the minimally invasive surgical triangulation system defines a width that corresponds to the orientation of the shaft of the surgical instrument within the port. In an embodiment, the shaft of the surgical instrument defines a contour that is generally S-shaped. Depending on the orientation of the shafts of the surgical instruments within the ports, the shafts of the surgical instruments collectively define either a bulb shape or a coiled, helical shape. When the shafts define a bulb shape, the greatest distance between any two points along the surface of the shafts is greater than when the shafts define a coiled or helical shape. Consequently, the width of the triangulation system is greater in the second condition in which the shafts define a bulb shape than when the triangulation system is in the first condition and the shafts define a coiled or helical shape.
Placement of the triangulation system within a body opening defined within tissue is facilitated when the triangulation system is in the first condition as compared to when it is in the second condition. Once placed inside the body opening, the surgical instruments are triangulated with respect to one another by rotating the shafts of the surgical instrument and transitioning the shafts to define the bulb shape. Once the desired surgical procedure is performed, the triangulation system is transitioned back to the first condition to facilitate removal of the triangulation system from the body opening.
Methods of using the triangulation system are also disclosed including providing the triangulation system, placing the triangulation system while in the first condition having the reduced profile or width into a body opening to access an underlying body cavity. Once within the triangulation system is placed within body opening, the surgical instruments are triangulated with respect to one another by actuating the surgical instruments, thereby transitioning the triangulation system to the second condition. Once the triangulation system is the second condition, a desired surgical procedure is performed. Upon completion of the desired surgical procedure, the triangulation system is transitioned back to the first condition to facilitate the removal of the triangulation system from the surgical site.
These and other features of the current disclosure will be explained in greater detail in the following detailed description of the various embodiments.
Various embodiments of the present disclosure are described hereinbelow with reference to the drawings, wherein:
Particular embodiments of the present disclosure will be described herein with reference to the accompanying drawings. As shown in the drawings and as described throughout the following descriptions, and as is traditional when referring to relative positioning on an object, the term “proximal” will refer to the end of the apparatus that is closest to the clinician during use, and the term “distal” will refer to the end that is farthest from the clinician during use.
With reference to
The trailing end 12 of the seal anchor member 10 defines a first diameter D1, and the leading end 14 of the seal anchor member 10 defines a second diameter D2. The intermediate portion between the trailing and leading ends 12, 14 defines a radial dimension R. The radial dimension R may be less than the first and second diameters D1, D2 of the trailing and leading ends 12, 14, respectively, and may vary along length L of the seal anchor member 10 to define a substantially hour-glass configuration.
The seal anchor member 10 is insertable within tissue tract I defined within body opening I of tissue T. The hour-glass configuration of the intermediate section 16 of the seal anchor member 10 may facilitate anchoring of the seal anchor member 10 within the body opening I. Furthermore, the seal anchor member 10 is configured and adapted to establish a sealing relation with the tissue T. An example of such a seal anchor member 10 is illustrated in U.S. Pat. Pub. 2009/0093752, the entire contents of which are hereby incorporated by reference.
A triangulation system 100 will now be described with respect to
The triangulation system 100 is configured and adapted to transition between a first condition as shown in
The triangulation system 100 may be placed within the body opening I with the surgical instruments 20 placed within the ports 18a-c such that the triangulation system 100 is in the first condition. Alternatively, the surgical instruments 20 may be inserted into the ports 18a-c subsequent to the placement of the seal anchor member 10 into the body opening I. In particular, once the seal anchor member 10 is placed within the body opening I, the surgical instruments 20 may be placed within the ports 18a-c such that the triangulation system 100 is in the first condition. Removal of the triangulation system 100 may be accomplished by removing the entire triangulation system 100 with the surgical instruments 20 placed within the ports 18a-c such that the triangulation system 100 is in the first condition. Alternatively, the surgical instruments 20 may be removed from the ports 18a-c prior to the removal of the seal anchor member 10.
In the first condition, the shafts 24 of the surgical instruments 20 collectively form a generally helical or coiled configuration with each of the shafts 24 in a first orientation with respect to the longitudinal axis S of the ports 18a-c in which the shafts 24 are positioned. As shown best in
As shown in
Transition of the triangulation system 100 to the second condition, as shown in
As shown in
A method of using the triangulation system 100 will now be described. The triangulation system 100 is provided and is placed in the body opening I of tissue T to access the body cavity C. It is advantageous that the profile or width of the triangulation system 100 be as small as possible such that the triangulation system 100 can be placed within a relatively small body opening I without necessitating increasing the size of the body opening I. To this end, the triangulation system 100 is inserted into the body opening I while in the first condition in which the shafts 24 of the surgical instruments 20 collectively define a generally coiled or helical configuration (
Once placed, shafts 24 of the surgical instrument 20 are placed in the body cavity C, the surgical instrument 20 can be actuated to cause triangulation of the end effectors 40 with respect to one another and the viewing portion 35 of viewing instrument 30. By actuating the surgical instruments 20, the shafts 24 of the surgical instruments 20 are rotated along bi-directional arrow Y as shown in
Although the illustrative embodiments of the present disclosure have been described herein with reference to the accompanying drawings, the above description, disclosure, and figures should not be construed as limiting, but merely as exemplifications of particular embodiments. It is to be understood, therefore, that the disclosure is not limited to those precise embodiments, and that various other changes and modifications may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure.
The present application claims the benefit of and priority to U.S. Provisional Application Ser. No. 61/480,073, filed on Apr. 28, 2011, the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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61480073 | Apr 2011 | US |