The subject invention is directed to surgical access devices, and more particularly, to multi-port access devices for minimally invasive surgical procedures.
Laparoscopic or “minimally invasive” surgical techniques are becoming commonplace in the performance of procedures such as cholecystectomies, appendectomies, hernia repair and nephrectomies. Benefits of such procedures include reduced trauma to the patient, reduced opportunity for infection, and decreased recovery time. Such procedures commonly involve filling or “insufflating” the abdominal (peritoneal) cavity with a pressurized fluid, such as carbon dioxide, to create what is referred to as a pneumoperitoneum.
The insufflation can be carried out by a surgical access device equipped to deliver insufflation fluid, or by a separate insufflation device, such as an insufflation (veress) needle. CONMED Corporation of Utica, N.Y., USA has developed unique surgical access devices that permit ready access to an insufflated surgical cavity without the need for conventional mechanical seals, and it has developed related gas delivery systems for providing sufficient pressure and flow rates to such access devices, as described in whole or in part in U.S. Pat. Nos. 7,854,724 and 8,795,223, the disclosures of which are both herein incorporated by reference in their entireties.
During typical laparoscopic procedures, a surgeon makes three to four small incisions, usually no larger than about twelve millimeters each. Typically the surgical access device is inserted into an incision using a separate inserter or obturator placed therein. Following insertion, the inserter is removed, and the trocar allows access for instruments to be inserted into the abdominal cavity.
A variety of larger access devices are also known in the art for accessing a surgical site through a single relatively large incision to perform minimally invasive procedures, rather than through multiple small incisions. Examples of such devices are disclosed in U.S. Patent Application Publication No. 2013/0012782, the disclosure of which is herein incorporated by reference in its entirety.
Trans-anal minimally invasive surgery (TAMIS) is a specialized minimally invasive approach to removing benign polyps and some cancerous tumors within the rectum and lower sigmoid colon. The benefit of TAMIS is that it is considered an organ-sparing procedure, and is performed entirely through the body's natural opening, requiring no skin incisions to gain access to a polyp or tumor. This scar-free recovery provides a quick return to normal bowel function. Unlike traditional surgery where a major portion of the large intestine is removed, with TAMIS the surgeon will precisely remove the diseased tissue, leaving the rest of the natural bowel lumen intact to function normally. Traditional surgery often requires a large incision and a hospital stay ranging from a few days to more than a week. A TAMIS procedure may only require an overnight stay in the hospital or can be performed as an outpatient procedure, often permitting patients an immediate return to an active lifestyle. TATMe (Trans-anal Total Mesorectal Excision) is a more significant trans-anal procedure.
It would be beneficial to provide a single incision access device having multiple ports with a variety of different port sizes to give a surgeon more options for instrument introduction during a laparoscopic surgical procedure. It would also be beneficial to provide an access device having multiple ports with a variety of different port sizes that enables ready access to natural orifices for performing trans-anal minimally invasive surgical procedures or the like.
An access device for surgical procedures includes an end cap having a rigid body with a flexible support sealingly mounted to the rigid body with at least one separate access port for accommodating introduction of individual surgical instruments into a body of a patient. The at least one access port is sealingly attached to the flexible support and extend in a proximal direction therefrom. The flexible support is of a material more flexible than those of the rigid body and the at least one access port to provide for relative angular movement of the at least one access port to provide flexibility for positioning surgical instruments introduced through the at least one access port.
The flexible support can include a flexible foam material including at least one of a rubber material, a rubber-like material, a VersaFlex material available from VersaFlex Incorporated of Kansas City, Kans., and/or a foam material made from a gel or gel-like material. The foam material can be a closed-cell foam for providing sealing to prevent gas flow therethrough. It is also contemplated that an open-cell foam with an air tight coating can be used. The access ports can be mounted to a distal surface of the flexible support and extend proximally through respective bores in the flexible support to extend proximally from the flexible support. Each access port can include an axially opposed pair of gripping rims with a portion of the flexible support gripped between the gripping rims. The flexible support can have a respective receptacle groove defined therein for receiving each of the gripping rims.
There can be a plurality of access ports, e.g., three, extending proximally from the end cap, evenly spaced circumferentially about the end cap. Each access port can extend from a respective planar facet of the flexible support. Each access port can extend normal from the respective facet of the flexible support. The respective facets can meet at facet junctures, wherein the facet junctures meet each other at an apex of the flexible support. Each facet can be angled at an angle α from a circumferential plane of the end cap. The angle α can be larger than 0° and less than or equal to 60°. All three access ports can be of a uniform size with one another.
The rigid body can define a complete circumferential ring wherein the flexible support is mounted within and spans the circumferential ring forming a complete circumferential seal between the rigid body and the flexible support. The flexible support can be adhered to an inward facing surface of the circumferential ring. The circumferential ring can include a proximal ring portion and a distal ring portion, wherein the flexible support is squeezed between the proximal and distal ring portions. The flexible support can define a respective ring groove for receiving the proximal and distal ring portions.
A bottom body can be included in the access device, having a distally extending tubular body with an access channel defined therethrough for accommodating surgical instruments from the access ports into the rectal cavity or natural orifice of a patient. The bottom body can include an gas inlet in fluid communication with the access channel. The one or more access ports can be configured to form a mechanical seal for insufflation gas for when instruments are inserted through the access ports and when no instruments are inserted through the access ports. The tubular body can be configured for introduction through a natural orifice of a body lumen or through a single incision formed in the wall of the abdominal cavity of a patient. The tubular body can be configured for trans-anal introduction. The end cap can be configured for complete 360° axial rotation relative to the bottom body. The tubular body can be mounted to a main ring portion of the bottom body, and wherein the tubular body is of a less rigid material than that of the main ring portion. The rigid body can include at least one flexible tab configured to engage and disengage the bottom body to selectively permit or prevent relative axial rotation of the multiport end cap and bottom body. Each of the access ports can include a respective seal configured to seal against gas flow when no surgical instrument is introduced therethrough, and to seal around surgical instruments introduced therethrough.
These and other features of the systems and methods of the subject disclosure will become more readily apparent to those skilled in the art from the following detailed description of the preferred embodiments taken in conjunction with the drawings.
So that those skilled in the art to which the subject disclosure appertains will readily understand how to make and use the devices and methods of the subject disclosure without undue experimentation, preferred embodiments thereof will be described in detail herein below with reference to certain figures, wherein:
Reference will now be made to the drawings wherein like reference numerals identify similar structural features or aspects of the subject disclosure. For purposes of explanation and illustration, and not limitation, a partial view of an exemplary embodiment of an access device in accordance with the disclosure is shown in
The access device 10 for surgical procedures includes a multiport end cap 20 and a bottom body 30. The end cap includes a plurality of separate access ports 40 for accommodating introduction of individual surgical instruments into a body of a patient. The access ports 40 extend in a proximal direction, i.e., upwards as oriented in
The bottom body 30 includes an insufflation gas inlet 14 in fluid communication with the access channel 9 through tubular body 8. The insufflation gas inlet 14 shown in
With reference now to
The bottom body 30 includes a plurality of circumferentially spaced apart teeth 18 on the outside of the proximal rim 3. The end cap 20 includes an opposed pair of flexible tabs 16, shown in
With reference now to
With reference now to
Each access port 40 extends from a respective planar facet 25 of the end cap 40. Each access port 40 extends normal from the respective facet 25 of the end cap 20. The respective facets 25 meet at facet junctures 27, wherein the facet junctures meet each other at an apex 29 of the end cap 20. As shown in
With reference now to
Referring now to
With reference now to
Each access port 40 can include a compression ring 68 engaged to the distal end 51 of the access port 40. An inner edge 69 of the flexible supports 64 and 65 compressed between the respective access port 40 and the compression ring 68 to form a sealing engagement between the access ports 40 and the flexible supports 64 and 65. Each paired access port 40 and compression ring 68 include an axially opposed pair of respective gripping rims 71 and 73 with a portion of the respective flexible support 64 and 65 gripped between the gripping rims 71 and 73. Each flexible support has a respective receptacle groove 75 defined therein for engaging each of the gripping rims 71 and 73. Each of the access ports 40 includes a respective seal, much like seal assembly 50 described above, configured to seal against gas flow when no surgical instrument is introduced therethrough, and to seal around surgical instruments introduced therethrough.
As with end cap 20 described above, end cap 60 includes three access ports 40 extending proximally from the end cap 60. One of the access ports 40 connects to the rigid body of end cap 60 through the flexible support 65, wherein the flexible support 65 has a single bellow 66. The remaining two access ports 40 connect to the rigid body of end cap 60 through the flexible support 64, wherein the flexible support 64 has two bellows 66, i.e., a double bellow, as shown in
With reference again to
Referring now to
With reference now to
A bottom body 230 is included in the access device 200, having a distally extending tubular body 202 with an access channel defined therethrough for accommodating surgical instruments from the access ports 40 into the body of a patient as in embodiments described above. The bottom body 230 includes a connection port 203 for connecting a tube set with one or more lumens in fluid communication with the access channel much as described above with respect to access device 10. The access ports 40 are configured to form mechanical seals for insufflation gas for when instruments are inserted through the access ports 40, and when there are no instruments inserted though the access ports 40. The tubular body 202 is mounted to a main ring portion 207 of the bottom body 230, and wherein the tubular body 202 is of a less rigid material than that of the main ring portion 207. The tubular body 202 is configured for introduction through a natural orifice of a body lumen or through a single incision formed in the wall of the abdominal cavity of a patient, for trans-anal introduction, or any other suitable mode of introduction.
As in embodiments described above, the end cap 220 is configured for complete 360° axial rotation relative to the bottom body 230 about longitudinal axis A. The rigid body includes at least one flexible tab 216 configured to engage and disengage the bottom body 230 to selectively permit or prevent relative axial rotation of the multiport end cap 220 and bottom body 230 as described above with respect to access device 10. Each of the access ports 40 includes a respective seal assembly as described with respect to embodiments above.
The access ports 40 are sealingly attached to the flexible support 206 and extend in a proximal direction therefrom, i.e. upwards as oriented in
With reference now to
As with embodiments described above, there are three access ports 40 extending proximally from the end cap 220, evenly spaced circumferentially about the end cap 220, and uniform in size with one another, however it is also contemplated that in an end cap can have ports of sizes that differ from one another as shown schematically in
With reference now to
Each access port 40 includes an axially opposed pair of gripping rims 321, including a proximally extending gripping rim 321 defined on a compression ring 323 joined to the distal end of each access port 40. A portion of the flexible support 306 is gripped between the respective gripping rims 321 of each access port 40. The flexible support 306 has a respective receptacle groove 325 defined therein for receiving each of the gripping rims 321.
With reference now to
A seal guard 412 is seated in an unfixed manner between the cap 404 and the main seal 406 within the access channel 401. The seal guard 412 is of a material that is more rigid that those of the main seal 406 and the duck bill seal 408 to provide protection for the main seal 406 and the duck bill seal 408 when instruments are inserted through access channel 401, and to prevent inversion of the main seal 406 and/or the duck bill seal 408, e.g., when surgical instruments are withdrawn from access channel 401.
With continued reference to
As shown in
The methods and systems of the present disclosure, as described above and shown in the drawings, provide for single incision/natural orifice surgical access with superior properties including minimally invasive, multiple port access with flexibility for relative movement of the access ports. While the apparatus and methods of the subject disclosure have been shown and described with reference to preferred embodiments, those skilled in the art will readily appreciate that changes and/or modifications may be made thereto without departing from the scope of the subject disclosure.
This application is a Continuation of U.S. patent application Ser. No. 15/790,582, filed Oct. 23, 2017, the contents of which is incorporated herein by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
4844484 | Antonini et al. | Jul 1989 | A |
4998740 | Tellier | Mar 1991 | A |
6482181 | Racenet et al. | Nov 2002 | B1 |
6551270 | Bimbo | Apr 2003 | B1 |
7244244 | Racenet et al. | Jul 2007 | B2 |
7753901 | Piskun et al. | Jul 2010 | B2 |
7854724 | Stearns et al. | Dec 2010 | B2 |
7892337 | Palmerton et al. | Feb 2011 | B2 |
7930782 | Chen | Apr 2011 | B2 |
8109873 | Albrecht et al. | Feb 2012 | B2 |
8187177 | Kahle et al. | May 2012 | B2 |
8187178 | Bonadio et al. | May 2012 | B2 |
8226553 | Shelton, IV et al. | Jul 2012 | B2 |
8251900 | Ortiz et al. | Aug 2012 | B2 |
8262622 | Gonzales et al. | Sep 2012 | B2 |
8273017 | Moreno | Sep 2012 | B1 |
8328761 | Widenhouse et al. | Dec 2012 | B2 |
8475490 | Hess et al. | Jul 2013 | B2 |
8480683 | Fowler et al. | Jul 2013 | B2 |
8485970 | Widenhouse et al. | Jul 2013 | B2 |
8574153 | Richard | Nov 2013 | B2 |
8602983 | Kleyman | Dec 2013 | B2 |
8763895 | Colman et al. | Jul 2014 | B2 |
8764647 | Kleyman | Jul 2014 | B2 |
8795163 | Widenhouse et al. | Aug 2014 | B2 |
8795223 | Stearns et al. | Aug 2014 | B2 |
8795326 | Richard | Aug 2014 | B2 |
8945002 | Oberlander et al. | Feb 2015 | B2 |
9101354 | Albrecht et al. | Aug 2015 | B2 |
9113951 | Richard et al. | Aug 2015 | B2 |
9131835 | Widenhouse et al. | Sep 2015 | B2 |
9173677 | Marczyk et al. | Nov 2015 | B2 |
9289200 | Dang et al. | Mar 2016 | B2 |
9408597 | Bonadio et al. | Aug 2016 | B2 |
9474518 | Richard | Oct 2016 | B2 |
9597112 | Stearns et al. | Mar 2017 | B2 |
20040167543 | Mazzocchi | Aug 2004 | A1 |
20040167559 | Taylor | Aug 2004 | A1 |
20060041291 | Buzawa | Feb 2006 | A1 |
20060085006 | Ek | Apr 2006 | A1 |
20090036745 | Bonadio et al. | Feb 2009 | A1 |
20090227843 | Smith et al. | Sep 2009 | A1 |
20100081880 | Widenhouse | Apr 2010 | A1 |
20100228092 | Ortiz et al. | Sep 2010 | A1 |
20100228094 | Ortiz | Sep 2010 | A1 |
20110124967 | Morgan | May 2011 | A1 |
20110251465 | Kleyman | Oct 2011 | A1 |
20120130185 | Pribanic | May 2012 | A1 |
20130012782 | Stearns et al. | Jan 2013 | A1 |
20160287817 | Mastri et al. | Oct 2016 | A1 |
20170056064 | Zergiebel et al. | Mar 2017 | A1 |
20190117255 | Kleyman et al. | Apr 2019 | A1 |
20190117257 | Kleyman et al. | Apr 2019 | A1 |
Number | Date | Country |
---|---|---|
2281519 | Feb 2011 | EP |
2010082449 | Apr 2010 | JP |
2017094205 | Jun 2017 | JP |
101022754 | Mar 2011 | KR |
2010082722 | Jul 2010 | WO |
Entry |
---|
PCT International Search Report dated Jan. 18, 2019, issued during the prosecution of corresponding PCT International Patent Application No. PCT/US2018/052361, filed Sep. 24, 2018. |
PCT International Preliminary Examination Report on Patentability and Written Opinion dated Apr. 28, 2020, issued during the prosecution of PCT International Patent Application No. PCT/US2018/052361. |
PCT International Preliminary Examination Report on Patentability and Written Opinion dated Apr. 28, 2020, issued during the prosecution of PCT International Patent Application No. PCT/US2018/052527. |
Extended European Search Report dated Jun. 23, 2021, issued during the prosecution of European Patent Application No. EP 18870627.9. |
Japanese Office Action dated May 11, 2021, issued during the prosecution of Japanese Patent Application No. JP 2020522677. |
Number | Date | Country | |
---|---|---|---|
20190374250 A1 | Dec 2019 | US |
Number | Date | Country | |
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Parent | 15790582 | Oct 2017 | US |
Child | 16545187 | US |