CROSS REFERENCE TO RELATED APPLICATION
BACKGROUND
Technical Field
[0002] The present disclosure relates to a surgical portal apparatus adapted to permit the introduction of surgical instrumentation into a patient's body in sealing engagement therewith. In particular, the present disclosure is directed to a surgical portal apparatus having an expandable cannula adapted to permit the introduction of a variety of different sized and shaped surgical objects.
Background of Related Art
[0003] In laparoscopic procedures surgery is performed in the interior of the abdomen through a small incision; in endoscopic procedures surgery is performed in any hollow viscus of the body through a narrow tube or cannula inserted through a small entrance incision in the skin. Laparoscopic and endoscopic procedures generally require that any instrumentation inserted into the body be sealed, i.e. provisions must be made to ensure that gases do not enter or exit the body through the incision as, for example, in surgical procedures in which the surgical region is insufflated. Moreover, laparoscopic and endoscopic procedures often require the surgeon to act on organs, tissue, and vessels far removed from the incision, thereby requiring that any instruments used in such procedures be relatively long and narrow.
[0004] For such procedures, the introduction of a tube into certain anatomical cavities such as the abdominal cavity is usually accomplished by use of a trocar assembly made up of a cannula assembly and an obturator assembly. Since the cannula assembly provides a direct passage for surgical instrumentation from outside the patient's body to access internal organs and tissue, it is important that the cannula assembly maintain a relatively fluid-tight interface between the abdominal cavity and the outside atmosphere. The cannula assembly generally includes a cannula attached to a cannula housing containing a seal assembly adapted to maintain a seal across the opening of the cannula housing.
[0005] Since surgical procedures in the abdominal cavity of the body require insufflating gases to raise the cavity wall away from vital organs, the procedure is usually initiated by use of a Verres needle through which a gas such as CO
2 is introduced into the body cavity, thereby creating a pneumoperitoneum. The gas provides a positive pressure which raises the inner body wall away from internal organs, thereby providing the surgeon with a region within which to operate and avoiding unnecessary contact with the organs by the instruments inserted through the cannula assembly. An obturator of the obturator assembly is inserted into the cannula assembly and used to puncture the abdominal wall. Following removal of the obturator assembly from the cannula assembly, laparoscopic or endoscopic surgical instruments may be inserted through the cannula assembly to perform surgery within the abdominal cavity.
[0006] Without the obturator assembly to block the flow of insufflation gas out from the cavity, other structure must be provided to maintain a relatively fluid-tight interface between the abdominal cavity and the outside atmosphere. Generally in the context of insufflatory surgical procedures, there are two sealing requirements for cannula assemblies. The first requirement is to provide a substantially fluid-tight seal when an instrument is not being introduced into or is not already present in the cannula. The second requirement is to provide a substantially fluid-tight seal when an instrument is being introduced into or is already present in the cannula. Additionally, as endoscopic and laparoscopic surgical procedures and techniques have advanced, it has become desirable to accommodate surgical instrumentation of varying outside diameters through a single cannula assembly in a given surgical procedure, thereby minimizing the number of cannulae required and facilitating efficiency in the surgical procedure. It is further desirable to maintain a seal about the instrument for manipulation of the instrument within the cannula assembly.
[0007] Although attempts have been made to provide a seal assembly as part of or for use in conjunction with a cannula assembly which maintains the integrity of the seal between the body cavity and the atmosphere outside the patient's body, seal systems provided to date have failed to address the full range of surgeons' needs.
SUMMARY
[0008] Accordingly, the present disclosure is directed to a surgical portal apparatus including a housing and a portal member extending from the housing. The portal member is dimensioned for insertion within tissue to access an underlying tissue site and defines a longitudinal axis. The portal member includes an outer wall having a longitudinal opening for reception of a surgical object. The outer wall includes first and second peripheral segments extending along the longitudinal axis. The first peripheral segment includes a substantially rigid material and the second peripheral segment includes a substantially elastomeric material. The first peripheral segment and the second peripheral segment cooperate to permit the outer wall to radially expand from a first condition where the outer wall defines a first internal dimension to a second condition where the outer wall defines a second internal dimension greater than the first internal dimension upon insertion of the surgical object.
[0009] The outer wall may include a plurality of first peripheral segments and a plurality of second peripheral segments. The first and second peripheral segments may be arranged in alternating radial relation relative to the longitudinal axis. The first and second peripheral segments each may extend along the longitudinal axis for at least a majority of the length of the portal member. A connector segment may be disposed between the housing and the portal member. The connector segment may comprise an elastomeric material. The connector segment may be adapted for displacement upon movement of the outer wall from the first condition to the second condition. The connector segment may be dimensioned to restrict passage of the portal member within the tissue when displaced and when the outer wall is in the second condition.
[0010] The first peripheral segments may be substantially equidistally radially spaced and the second peripheral segments may be substantially equidistally radially spaced. At least three or four first peripheral segments and at least three or four second peripheral segments may be provided.
[0011] Each first peripheral segment may include a rib extending radially inwardly towards the longitudinal axis. The ribs may be positioned to contact the surgical object to facilitate expansion of the outer wall from the first condition to the second condition. The ribs of adjacent first peripheral segments may define pathways for passage of insufflation gas through the portal member. The ribs of adjacent first peripheral segments may be dimensioned to substantially align the surgical object with the longitudinal axis. The housing may include an insufflation inlet port in communication with the pathways.
[0012] A zero closure valve may be included to close the longitudinal opening in the absence of the surgical object. An object seal may be included to intersect the longitudinal axis and is adapted to establish a substantial seal about the surgical object.
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] The above and other aspects, features, and advantages of the present disclosure will become more apparent in light of the following detailed description when taken in conjunction with the accompanying drawings in which:
[0014] FIG. 1 is a side elevational view of a surgical portal apparatus in a first condition in accordance with the present disclosure;
[0015] FIG. 2 is an axial cross sectional view of the surgical portal apparatus of
FIG. 1;
[0016] FIG. 3 is a side cross sectional view of the housing of the surgical portal apparatus of
FIGS. 1 and
2; and
[0017] FIG. 4 is a side elevational view of the surgical portal apparatus of
FIGS. 1-3 in a second condition.
DETAILED DESCRIPTION OF EMBODIMENTS
[0018] The surgical portal apparatus of the present disclosure provides a substantial seal between a body cavity of a patient and the outside atmosphere before, during and after insertion and manipulation of a surgical instrument through the seal thereof.
[0019] The surgical portal apparatus of the present disclosure contemplates the introduction and manipulation of various types of instrumentation adapted for insertion through a trocar and/or cannula assembly while maintaining a substantially fluid-tight interface about the instrument to preserve the atmospheric integrity of a surgical procedure from leakage. Examples of instrumentation include, but are not limited to, clip appliers, graspers, dissectors, retractors, staplers, laser probes, photographic devices, endoscopes and laparoscopes, tubes, and the like. Furthermore, these surgical instruments can be designed with a variety of tip configurations and a variety of diameters. Such instruments will collectively be referred to as "instruments" or "instrumentation" or "surgical objects."
[0020] 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 description, and as is traditional when referring to relative positioning on an object, the term "proximal" refers to the end of the apparatus that is closer to the user and the term "distal" refers to the end of the apparatus that is farther from the user. In the following description, well-known functions or constructions are not described in detail to avoid obscuring the present disclosure in unnecessary detail.
[0021] Referring now to the drawings, in which like reference numerals identify identical or substantially similar parts throughout the several views,
FIGS. 1-3 and
FIG. 4 illustrate a surgical portal apparatus
100. In accordance with the present disclosure, the surgical portal apparatus
100 includes a housing
110, an object seal
120, and a portal member
130. The portal member
130 extends from the housing
110 and is dimensioned for insertion within tissue to access an underlying tissue site. The portal member
130 defines a longitudinal axis
112 (FIG. 1). The portal member
130 and the housing
110 have a longitudinal opening
114 (FIGS. 1 and
3) for reception of a surgical object "I." As shown in
FIG. 3, an object seal
120 is disposed in mechanical cooperation with the housing
110 and defines a passage for reception of a surgical object "I"
(FIG. 4) in substantial sealed relation therewith. More specifically, the object seal
120 intersects the longitudinal axis
112 and is adapted to establish a substantial seal about the surgical object "I." A zero closure valve
122 (FIG. 3), (e.g., a duckbill valve) can also be disposed in mechanical cooperation with the housing
110. The zero closure valve
122 is adapted to close the longitudinal opening
114 in the absence of the surgical object "I."
[0022] As shown in
FIGS. 1 and
4, portal apparatus
100 includes connector segment
111 which connects the housing
110 with portal member
130. Connector segment
111 is generally annular in configuration and, in one embodiment, is fabricated from an elastomeric material. Connector segment
111 may be secured to housing
110 and portal member
130 through conventional means. Connector segment
111 is adapted to transition from a first generally parallel and concentric arrangement with respect to the longitudinal axis
112 (FIG. 2) to a second angulated or tapered arrangement with respect to the longitudinal axis
(FIG. 4) during transition of the apparatus
100 as discussed hereinbelow in greater detail.
[0023] With continued reference to
FIGS. 1-2, portal member
130 includes outer wall
131. Outer wall
131 includes at least one first peripheral segment
132, and at least one second peripheral segment
134. In one embodiment, at least three, and possibly, four first peripheral segments
132 are provided and, at least three, possibly, four second peripheral segments
134 are provided. In one embodiment, first peripheral segments
132 and second peripheral segments
134 are arranged in alternating radial relation relative to the longitudinal axis
112 and extend along the longitudinal axis
112. Each first peripheral segment portion
132 may be substantially equidistally radially spaced about the longitudinal axis. Similarly, second peripheral segment portions
134, etc. may be substantially equidistally radially spaced about the longitudinal axis
112.
[0024] Each first peripheral segment
132 may be fabricated at least in part from a substantially rigid material and each second peripheral segment
134 may be fabricated at least in part from a substantially elastomeric material. Suitable rigid materials include steel, titanium, aluminum or rigid polymeric materials. Suitable elastomeric materials include natural rubber, polyisoprene or any other suitable elastomeric material. First and second peripheral segments
132, 134 may extend along the longitudinal axis
112 for at least a majority of the length "I" of the portal member
130. Second peripheral segments
134 may be integrally and/or monolithically formed with connector segment
111 for example during a molding process. In addition, it is envisioned that second peripheral segments
134 and connector segment
111 may be molded as a single unit and subsequently connected to housing
110 and first peripheral segments via an over molding process to connect the components.
[0025] First peripheral segments
132, second peripheral segments
134 and, optionally connector segment
111, cooperate to permit the outer wall
131 to radially expand from a first condition where the outer wall
131 defines a first internal dimension to a second condition where the outer wall
131 defines a second internal dimension greater than the first internal dimension upon insertion of the surgical object "I."
[0026] At least one, e.g., or all first peripheral segments
132, or portions thereof, may include at least one radially inwardly (towards the longitudinal axis
112) protruding rib
136. Each rib
136 is positioned to contact the surgical object "I" to facilitate expansion of the outer wall
131 from the first condition to the second condition. A plurality of inwardly protruding ribs
136 are shown disposed about the longitudinal axis
112. Each inwardly protruding rib
136 is configured and dimensioned to contact and guide surgical objects "I" disposed therein down the portal member
130.
[0027] With reference to
FIG. 4, each second peripheral segment
134 is configured and dimensioned to expand to permit outer wall
131 to expand to the second internal dimension. In one embodiment, about
300 percent circumferential strain is required to expand outer wall
131 to the second internal dimension. The degree or level of strain may be altered or modified by varying the ratio of rigid and elastomeric materials constituting the first and second peripheral segments
132, 134, respectively.. Each second peripheral segment
134 may avoid contact with the surgical objects "I" disposed therein. Furthermore, during transition from the first condition to the second condition, connector segment
111 may displace to become angulated or obliquely arranged (e.g., tapered) to the longitudinal axis
112 to accommodate the expansion of second peripheral segments
134. Connector segment
111, in the condition of
FIG. 4, may also function as an anchor to engage the body tissue "t" (in phantom) thereby preventing over insertion of the portal apparatus
100.
[0028] Referring again to
FIGS. 1 and
4, the portal member
130 is configured and dimensioned to be expandable from a first condition
(FIG. 1) having a diameter of about
4.5mm to a second condition
(FIG. 4) having a diameter of about
12.5mm. Other dimensions are also envisioned. The portal member
130 includes an internal dimension "K" defined by the internal surface thereof. The internal dimension
113 is configured and dimensioned to radially expand from the first condition to the second condition. Thus, the portal member
130 can accommodate a plurality of different surgical objects "I" during the reception and manipulation thereof. Furthermore, by virtue of at least protruding ribs
136, the portal member
130 is configured and dimensioned to inhibit surgical objects "I" from angling away from the longitudinal axis
112 during the manipulation of each surgical object "I" disposed within the portal member
130. For example, the protruding ribs
136 assist in maintaining concentricity of the instrument "I" with respect to the longitudinal axis
112.
[0029] Referring additionally to
FIGS. 1, 3, and
4, the housing
110 further includes an insufflation inlet port
140 disposed thereon. As illustrated in
FIG. 4, also contemplated is a plurality of pathways
142 disposed in fluid communication with the insufflation inlet port
140. The plurality of pathways
142 are circumferentially disposed about the longitudinal axis
112 between adjacent inwardly protruding ribs
136. In other words, the ribs
136 of adjacent first peripheral segments
132 define pathways
142 for passage of insufflation gas through the portal member
130. The pathways
142 are in fluid communication with the insufflation port
140.
[0030] In use, a surgical object "I" is inserted into the housing
110 and passed through the object seal
120 and the zero closure valve
122 and into the internal dimension
113 of the portal member
130. If the surgical object "I" has a dimension that exceeds the diameter of the outer wall
131 in the first condition
(FIG. 1) of the portal member
130, the object contacts the ribs
136 and applied forces causing expansion of the second peripheral segments
134 and transitioning of the connector segment
111 whereby the portal member
130 assumes the second condition
(FIG. 4) in order to accommodate the surgical object "I". The ribs
136 assist in biasing the object "I' towards a generally aligned position with respect to the longitudinal axis
112. Upon withdrawal of the surgical object "I" from the portal member
130, the second peripheral segments
134 and connector segment
111 return, under the normal resiliency of their material of fabrication, to the first condition
(FIG. 1).
[0031] 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. For example, portal apparatus
100 may be adapted for reception of a hand of a surgeon during, e.g., a hand assisted laparoscopic procedure. Therefore, the above description should not be construed as limiting, but merely as exemplifications preferred embodiments. Thus the scope of the embodiments should be determined by the appended claims and their legal equivalents, rather than by the examples given.
1. A surgical portal apparatus, which comprises:
a housing; and
a portal member extending from the housing, the portal member dimensioned for insertion within tissue to access an underlying tissue site and defining a longitudinal axis, the portal member including an outer wall having a longitudinal opening for reception of a surgical object, the outer wall including first and second peripheral segments extending along the longitudinal axis, the first peripheral segment including a substantially rigid material and the second peripheral segment including a substantially elastomeric material, the first peripheral segment and the second peripheral segment cooperating to permit the outer wall to radially expand from a first condition where the outer wall defines a first internal dimension to a second condition where the outer wall defines a second internal dimension greater than the first internal dimension upon insertion of the surgical object.
2. The surgical portal apparatus according to claim 1 wherein the outer wall includes a plurality of first peripheral segments and a plurality of second peripheral segments, the first and second peripheral segments being arranged in alternating radial relation relative to the longitudinal axis.
3. The surgical portal apparatus according to claim 2 wherein the first and second peripheral segments each extend along the longitudinal axis for at least a majority of the length of the portal member.
4. The surgical portal apparatus according to claim 3 including a connector segment disposed between the housing and the portal member, the connector segment comprising an elastomeric material.
5. The surgical portal apparatus according to claim 4 wherein the connector segment is adapted for displacement upon movement of the outer wall from the first condition to the second condition.
6. The surgical portal apparatus according to claim 5 wherein the connector segment is dimensioned to restrict passage of the portal member within the tissue when the outer wall is in the second condition.
7. The surgical portal apparatus according to claim 3 wherein the first peripheral segments are substantially equidistally radially spaced.
8. The surgical portal apparatus according to claim 7 wherein the second peripheral segments are substantially equidistally radially spaced.
9. The surgical portal apparatus according to any preceding claim including at least three first peripheral segments and at least three second peripheral segments.
10. The surgical portal apparatus according to any of claims 1 to 8 including at least four first peripheral segments and at least four second peripheral segments.
11. A surgical portal apparatus according to claim 2 wherein each first peripheral segment includes a rib extending radially inwardly towards the longitudinal axis, the rib positioned to contact the surgical object to facilitate expansion of the outer wall from the first condition to the second condition.
12. The surgical portal apparatus according to claim 11 wherein the ribs of adjacent first peripheral segments define pathways for passage of insufflation gas through the portal member.
13. The surgical portal apparatus according to claim 11 wherein the ribs of adjacent first peripheral segments are dimensioned to substantially align the surgical object with the longitudinal axis.
14. The surgical portal apparatus according to claim 12 wherein the housing includes an insufflation inlet port.
15. The surgical portal apparatus according to claim 2 including a zero closure valve adapted to close the longitudinal opening in the absence of the surgical object.
16. The surgical portal apparatus according to claim 2 including an object seal intersecting the longitudinal axis adapted to establish a substantial seal about the surgical object.