This application claims priority from U.S. provisional application Ser. No. 60/867,061, filed Nov. 22, 2006.
FIELD OF THE INVENTIONThe present invention relates generally to vaginal hysterectomies.
BACKGROUND OF THE INVENTIONLess invasive surgical procedures for undertaking hysterectomies have become popular, owing to the faster recovery times, improved cosmesis, and lower risks they afford compared to conventional hysterectomies. Least invasive hysterectomy procedures typically involve one of three primary approaches—vaginal hysterectomy, total laparoscopic hysterectomy (TLH), and laparoscopically assisted vaginal hysterectomy (LAVH) with TLH being the least invasive approach. TLH is less invasive than LAVH because it avoids the trauma normally caused by the expansion induced to the vaginal area to permit access of the surgeon's hands to the cervical area.
Difficulty, however, is encountered when employing vaginal, TLH and LAVH techniques due to inherent limitations on visibility, anatomical identification, and the ability to manipulate organs (especially the uterus). In the case of TLH, these limitations are particularly pronounced because of a higher degree of difficulty in securing the uterine arteries and ligaments associated with this approach.
Other limitations associated with vaginal, TLH and LAVH surgical approaches include limited exploratory ability and surgical control. Vaginal, TLH and LAVH approaches can also result in the unnecessary shortening of the vagina due to the limitations discussed above. These difficulties and limitations have slowed the move by surgeons to use the least invasive surgical approach for hysterectomies.
Accordingly, the present invention critically recognizes that it would be advantageous to provide improved methods and apparatus for less invasive hysterectomies, particularly in visualizing interior body structures.
SUMMARY OF THE INVENTIONIn one implementation, a cannula, possibly containing an obturator, is directed into the vagina, through the cervix and into the uterus. Then the distal wall (also referred to as “fundus”) of the uterus is transversed using a penetrating element at the distal portion of the cannula. The cannula is secured to the wall of the uterus with a gas seal or pair of gas sealing devices and the obturator, if provided, is removed to facilitate the introduction of an endoscope into the cannula and into the abdominal cavity. The abdominal cavity is then insufflated with gas. A luer side valve may be used to insufflate via the cannula. Or, the abdomen can be insufflated prior to cannula insertion via a veress needle or similar device in the pouch of Douglas or abdomen. The uterus with its attached fallopian tubes, arteries, ligaments and connective tissue is located, with or without ovaries, isolated from these structures and removed using instruments placed through the cannula, the working lumen of the endoscope or delivered transvaginally.
Although the embodiments described may be particularly applicable for removal of the uterus, the systems, methods and devices described may also be useful for other operations performed through natural body orifices and the embodiments detailed may have other potential applications for pancreatic, liver and gall bladder, appendix and gastro-intestinal systems as well.
In an aspect, an assembly for transuterine visualization of a transvaginal hysterectomy includes an elongated transuterine cannula configured for advancement through the vagina and uterus to a distal wall of the uterus. A sealing device engaged with the transuterine cannula can engage the cannula with the distal wall. Further, a penetrating element is associated with the transuterine cannula to fenestrate the distal wall to form an opening therein. An endoscope can be advanced through the cannula and the opening in the distal uterine wall into the peritoneal space to provide visualization of anatomical structure in the peritoneal space. A disinfectant can be introduced into the uterus prior to fenestration.
The penetrating element may be established by a distal tip of the transuterine cannula. Or, the penetrating element can be established by a cutting device advanceable through the transuterine cannula.
The transuterine cannula can be secured to the distal wall of the uterus using a gas seal. In some embodiments the transuterine cannula is secured to the distal wall of the uterus using a pair of gas sealing devices. The gas sealing devices can be inflatable balloons.
In non-limiting implementations a veress cannula may be slidably engageable with a lumen of the endoscope to fenestrate the distal uterine wall. A dissecting device may be provided for cutting the anatomical structure in the peritoneal space for which the endoscope provides visualization. In some embodiments one or more of the transuterine cannula and endoscope can articulate while in a patient.
In non-limiting embodiments a vacuum shroud can surround a distal end of the endoscope and can communicate with a source of vacuum to attract the distal wall of the uterus proximally toward the endoscope to facilitate fenestration of the distal wall. A vaginal guide may be provided that is closely received in a vagina of a patient. The guide may be formed with at least one hole slidably supporting the transuterine cannula.
In some embodiments an obturator is disposable in the transuterine cannula to facilitate advancing the transuterine cannula to the distal wall of the uterus. The obturator can have a frusto-conical distal segment terminating in a rounded distal tip, and at least the distal tip bears a bipolar electrode array for fenestrating the distal wall of the uterus.
In some embodiments the transuterine cannula is formed with a distal neck and a shoulder proximal to the neck and adjoined thereto. The shoulder is wider than the neck for abutting an inner surface of the distal wall of the uterus with the neck disposed in the opening thereof.
In some embodiments a uterine stabilizing balloon surrounds a portion of the transuterine cannula and has an inflatable configuration, wherein the stabilization balloon substantially fills the uterus to facilitate manipulation of the uterus, and a deflated configuration, wherein the stabilization balloon is configured to facilitate advancing the transuterine cannula into the uterus.
The cannula and balloon structure may be able to flex within any part of the vagina, cervix, or uterus, allowing for extra uterine manipulation for better antero or retro flexion of the uterus to assist with visualizing structures of the abdomen.
A non-limiting transuterine cannula may define an outer surface and may include at least one working channel external to the outer surface. A vaginal positioning guide that is closely receivable in a vagina can be provided if desired. The guide receives the transuterine cannula therethrough. The vaginal positioning guide can bear at least one tissue dissector for fenestrating the vagina. The vaginal positioning guide can include a balloon that is inflatable to substantially fill the vagina to anchor the guide in the vagina when the transuterine cannula extends therethrough into the uterus.
In another aspect, a transuterine cannula has a cannula body having a length sufficient to advance the transuterine cannula through the vagina of a patient to the distal wall of the uterus of the patient with at least a proximal segment of the transuterine cannula remaining outside the patient's body. At least one sealing member is engaged with a distal segment of the transuterine cannula to hold the transuterine cannula against the distal wall of the uterus.
The details of the present invention, both as to its structure and operation, can best he understood in reference to the accompanying drawings, in which like reference numerals refer to like parts, and in which:
BRIEF DESCRIPTION OF THE DRAWINGSFIG. 1 is an anterior cross sectional view of the uterus;
FIG. 2 is a view of the uterus ofFIG. 1 with an embodiment of the invention placed into the uterus, with the interior lumens of one non-limiting transuterine cannula shown in phantom;
FIG. 3 is a diagrammatic view of the transuterine cannula placed through the wall of the uterus;
FIG. 4 is a perspective view showing the viewing endoscope emerging through the transuterine cannula past the distal wall of the uterus and into the peritoneal space, and also showing a dissecting device advanced through the vaginal wall to anatomical structure to be transected;
FIG. 5 is a perspective view of a veress cannula being advanced into the working channel of the endoscope prior to engaging the endoscope with the transuterine cannula ofFIG. 4;
FIG. 6 is a cut-away view showing the transuterine cannula ofFIG. 4 advanced through the distal wall of the uterus and the endoscope bent for retrograde visualization, with the sealing balloons omitted for clarity;
FIG. 7 is a cut-away view illustrating the use of the transuterine cannula with the transvaginal dissecting device shown inFIG. 4;
FIG. 8 is a side view of a transuterine cannula with endoscope and instrument in the peritoneal space, illustrating that all three components can be articulated during use;
FIG. 9 shows an alternate endoscope that may be used with the present transuterine cannula to attract the distal wall of the uterus inward prior to fenestrating the distal wall;
FIG. 10 is a perspective view of a vaginal guide through which the present transuterine cannula may be advanced;
FIGS. 11 and 12 are side views of the distal ends of obturators that can be advanced through the transuterine cannula and used to fenestrate the distal wall of the uterus;
FIGS. 13 and 14 are side views of another alternate transuterine cannula with a shoulder stop, with portions shown in phantom;
FIG. 15 is a side view of yet another alternate transuterine cannula with uterine stability balloon and uterine manipulation handle;
FIGS. 16 and 17 are side views of alternate transuterine cannulae with exterior lumina;
FIGS. 18-20 are perspective, side, and schematic views, respectively, of a vaginal positioning guide with transvaginal tissue dissectors, with any one of the transuterine cannulae shown in the preceding figures being advanceable through a central channel of the vaginal positioning guide into the uterus; and
FIG. 21 is a schematic side view of the distal portion of an endoscope with perforated shunt veress cannula.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTFor perspective,FIG. 1 shows diagram of the female reproductive system including thevagina10,cervix12,uterus14,fallopian tubes16aand16b,andovaries18aand18b.The distal portion of thevaginal walls20 terminate at the cervix12 which serves as the entrance to theuterus14 and theuterine cavity21. Thiscavity21 has a distaluterine wall22 which forms at least the distal portion of theuterus14. Theuterus14 is joined at its distal end by thefallopian tubes16aand16b.These tubes are conduits between theovaries18aand18bat each side of the uterus and the uterine cavity.
As perhaps best shown inFIG. 3, the ovaries are .suspended and secured to the lowerabdominal cavity24 with various ligaments such as theuterosacral ligament30, the broad ligament generally designated32, theovarian ligament34, and thesuspensory ligament36. In addition, blood vessels that supply blood to the reproductive organs are located at various places around the uterus. Typically, most if not all of the ligaments and blood vessels associated with the uterus must be transected to execute a hysterectomy.
An embodiment of the invention is shown inFIG. 2 and comprises atransuterine cannula40 sized for introduction through thevagina10,cervix12 anduterus14 and through thewall22 of the uterus. Thetransuterine cannula40 may be made of axially rigid plastic or metal that is biocompatible and that may be coated with an anti-bacterial agent.
Anobturator41 may be placed through acentral lumen42 of thetransuterine cannula40 to stiffen thetransuterine cannula40 and provide column strength to advance the transuterine cannula assembly into position. Theobturator41 is removable and can be withdrawn from thetransuterine cannula40 after the transuterine cannula is in position. Thecentral lumen42 of the transuterine cannula is large enough to accommodate a flexible endoscope orlaparoscope46 into thecentral lumen42 once theobturator41 is withdrawn. Transuterine cannulas with central lumens of various sizes can be utilized but preferably thetransuterine cannula40 is large enough to accommodate anendoscope46 with an outside diameter of between five millimeters (5 mm) and sixteen millimeters (16 mm) and more preferably between 8 mm and 14 mm. Most preferably thecentral lumen42 should be large enough to accommodate anendoscope46 with an outside diameter of up to 12 mm.
Furthermore, the internal diameter of thecentral lumen42 preferably is sized similar to the outside diameter of theendoscope46 so that when theendoscope46 is placed through the central lumen, the walls of thecentral lumen42 effectively seal around theendoscope46 and inhibit fluids from passing along the outside surface of the endoscope and out thecentral lumen42.
Alternatively or in addition, as best shown inFIG. 3seals43aand43bcan be positioned at the points where theendoscope46 exits the proximal and distal portions of thetransuterine cannula40 to respectively seal around the proximal and distal portions of the endoscope and prevent leakage.
Referring back toFIG. 2, in some implementations thedistal end47 of thetransuterine cannula40 may be formed with or may include a penetratingelement48. In the non-limiting embodiment shown, the penetratingelement48 may be a sharpened blade that is angled with respect to the longitudinal axis of thetransuterine cannula40 and that cuts a hole through theuterine wall22 as the transuterine cannula is rotated and advanced distally against the wall. In other implementations the penetratingelement48 may include a diathermy element that can cauterize and/or cut through uterine tissue. The penetratingelement48 may use other cutting mechanisms including mechanical, chemical, thermo electrical or optical.
Yet again, thetransuterine cannula40 can have a blunt distal end that establishes a tissue separating design that spreads the tissue fibers rather than cutting them. Alternatively a retractor can be used to pull against the superior uterine wall as the transuterine cannula is introduced to prevent perforation of the bowel or some other structure when the transuterine cannula is inserted through the uterus wall. Further details of such structures are discussed below.
Although not a requirement, the introduction of the transuterine cannula into the patient and subsequent manipulation of reproductive tissues may also be visualized by using fluoroscopy, echo, or other imaging modality.
In some implementations, in addition to or in lieu of theseals43a,43b,to secure thetransuterine cannula40 to the distal wall of the uterus the transuterine cannula can have at least one inflatable balloon and preferably twoballoons50 and51 positioned about the outer surface of the hollow shaft of the transuterine cannula. The balloons are spaced apart by a distance approximately equivalent to the thickness of a uterine wall but this distance can be altered by a sliding mechanism of the balloons which modulates the relative separation between the balloons.
In any case, aninflation lumen54 in the transuterine cannula communicates with the inner portions of theballoons50,51 and the proximal end of the transuterine cannula. Theinflation lumen54 can be used to inflate the balloons with fluid once the transuterine cannula is in position so that they inflate against the outer55 and inner56 surfaces, respectively, of theuterine wall22. When so inflated theballoons50,51 seal around thetransuterine cannula40 so that fluids and more particularly insufflation gas in theabdominal cavity24 does not leak into theuterine cavity21 around the transuterine cannula. Alternatively, artificial septums, pads or cloth, sponges or other means may be utilized also to seal the transuterine cannula at the uterine wall.
If desired, thetransuterine cannula40 can also include aninsufflation lumen60 that can be used to insufflate theabdominal cavity24 with gas. Theinsufflation lumen60 is a conduit that communicates with theabdominal cavity24 at thedistal end47 of the transuterine cannula and terminates at the proximal end of the transuterine cannula so that when the endoscope is placed into the abdominal cavity through the transuterine cannula, gas such as carbon dioxide can be introduced at the proximal end of the insufflation lumen to inflate theabdominal cavity24. In some embodiments this entails introducing the gas into the cannula and out of a port in the cannula into thelumen60, which may be defined by an annular space between the endoscope and cannula. The gas inflates theabdominal space24 and creates sufficient room so that the endoscope can visualize the anatomy and so that instruments introduced into theabdominal cavity24 can be freely manipulated to accomplish the hysterectomy.
Still further, thetransuterine cannula40 can be loaded with a deployable purse string suture system that could be pulled tight to help to gain a better seal between the uterus and the transuterine cannula or to close the uterine incision if the uterus is not to be removed.
Additionally, a cuttingdevice70 may be introduced through another separate lumen in thetransuterine cannula40 into the abdominal cavity. The cuttingdevice70 may be a mechanical cutter, a diathermy cutter, a mono polar, bipolar electrocautery cutter, a laser, or a blade that is used to cut and/or cauterize the ligaments, connective tissue and blood vessels surrounding and attached to the uterus. The cuttingdevice70 cuts through this attached tissue so that the uterus may be isolated and removed. Alternatively the cutting device may be introduced through a working channel in the endoscope or through the wall of thevagina20 as discussed further below. Alternatively the cutting device can be introduced through the abdominal wall. Alternatively, a grasper or tissue manipulator can be placed through the central lumen of the endoscope to grasp or manipulate tissue.
The cutting device may alternatively cut and/or ligate so that tissue may be resected and blood vessels can be tied off and occluded at the same time. Therefore the cutting device may also be a ligation device employing ties, sutures, staples, use coagulation diathermy, laser, ultrasound or any energy modality that could induce hemostasis or clips to ligate.
Thetransuterine cannula40 described is a relatively rigid device that when positioned as described, facilitates the introduction of the endoscope into the abdominal cavity. Thetransuterine cannula40 also facilitates the movement of the uterus and cervix so that these organs can be manipulated to provide the endoscope with a better view of target structures and places the structures around the uterus on a stretch to gain better visualization and simplified cutting and coagulation. The transuterine cannula with its balloons also provides an effective method of sealing around the transuterine cannula body as it exits the uterine wall.
In operation for the removal of the uterus, atransuterine cannula40 having anobturator41 inside is placed into the vagina and moved through the cervix and placed against the distal wall of the uterus. As discussed above the uterine wall can be transected and an endoscope advanced through thetransuterine cannula40 and uterine wall for visualization, it being understood that the endoscope is electrically connected to a monitor in the operating room.
To transect the uterine wall thetransuterine cannula40 is manipulated through the uterine wall using a penetrating element positioned at the distal end of the transuterine cannula. The manipulation through the uterine wall may include rotating the transuterine cannula, pushing on the transuterine cannula from the proximal end or alternatively turning on and off the penetrating element. Once the transuterine cannula is positioned across the uterine wall, which can be verified endoscopically or by utilizing marking elements on the body of the transuterine cannula, the obturator is removed and the above-described endoscope or laparoscope or multiple endoscopes (are) is then inserted into the transuterine cannula and advanced to at least the distal portion of the transuterine cannula.
Then sealingelements43a,43b,only one of which may be used and which are positioned about the distal portion of the transuterine cannula, are used to secure thetransuterine cannula40 on the wall of the uterus. Or, as described aboveballoons50,51 are inflated against the proximal and distal surfaces of the uterine wall to sandwich the distal wall of the uterus between the balloons and seal off the inner cavity of the uterus from the abdominal cavity around the transuterine cannula outer wall. Gas is then introduced into the abdominal cavity through an insufflation lumen in the transuterine cannula and the abdominal cavity is inflated to create space so that the uterine structures and anatomy can be directly visualized. Various instruments can be introduced into the abdominal space to ligate, such as endoscopic clip appliers, to coagulate and/or cut various connecting ligaments, fallopian tubes, blood vessels and connective tissue attached to the uterus, or to grasp and manipulate tissue. The uterus is thus isolated from surrounding tissue so that the uterus can be removed. Also, the transuterine cannula system may be deployed through other areas such as the pouch of Douglas, the cul-de-sac, the perineum, colonic/rectal structures.
At this point the uterus can be separated from the vagina and removed through the vagina according to vaginal hysterectomy methods. The removal of the uterus may be assisted by the use of various accessories or instruments that can be introduced through the transuterine cannula, a working lumen of the endoscope or trans-vaginally such as a morcelator system, umbrellas, nets, bags, blades, or hydro- or cryo-dissection devices.
Also, other energy modalities can be used to destroy tissue, such as ultrasound (CUSAR), laser, etc., or tissue ablation modalities may be used, such as chemical morcellation. Alternatively, the transuterine cannula can be removed from the patient and a morcelator system can be introduced through the cervix to remove the uterus. In this case, the morcelator can be placed directly at the cervix and used to pull the uterus down into the morcelator as the uterus is removed.
Now referring toFIG. 4 and ensuing figures for additional details, atransuterine cannula100 is shown advanced through theuterus14 with the distal end of thecannula100 shown positioned through the distal wall of the uterus and in the peritoneal space. Thetransuterine cannula100 may be identical in configuration and operation to thetransuterine cannula40 discussed above, and/or it may embody the following exceptions. Adistal anchoring balloon102 may surround the distal segment of thetransuterine cannula100 as shown and may be inflated once inside the peritoneal space to hold thetransuterine cannula100 in place. Also, an enlargedproximal balloon104, referred to herein as a “stabilizing” balloon, may surround thetransuterine cannula100 and can be inflated when inside the uterus as shown to substantially fill the uterus. Theproximal balloon104 has an inflatable configuration, wherein the balloon substantially fills the uterus to facilitate manipulation of the uterus, and a deflated configuration, wherein the balloon is configured to facilitate advancing thetransuterine cannula100 into the uterus. It is to be understood that a third, smaller sealing balloon similar to theproximal balloon50 shown inFIG. 2 may be disposed between thestabilization balloon104 and the inside surface of the distal wall of the uterus if desired, or thestabilization balloon104 may be used in lieu of theproximal balloon50.
FIG. 4 shows that anendoscope106 can be advanced through thetransuterine cannula100 to provide visualization of the peritoneal cavity as shown. Preferably, the endoscope is articulable, meaning it can be bent by means of, e.g., a manipulation wire embedded in the endoscope near its distal end and extending through the endoscope to a manipulator handle as more fully described below. In this way, the endoscope can be bent in a desired direction to visualize, e.g., the Fallopian tube as shown inFIG. 4. Theendoscope106 may define one or more working channels, and an instrument such as but not limited to aligation band108 may be advanced through the working channel to, e.g., ligate a Fallopian tube as shown inFIG. 4.
A dissectingdevice110, which may be a bipolar transection device, may be advanced through the working channel of theendoscope106 or, as shown inFIG. 4, through a vaginal wall to an anatomical structure (e.g., the Fallopian tube) to be cut in the peritoneal space. In this latter approach (i.e., through the vaginal wall) thedissecting device110 may be advanced through the vaginal positioning guide shown inFIGS. 18-20 and discussed at greater length below. In any case, it will readily be appreciated that theendoscope106 extending through thetransuterine cannula100 provides visualization to a surgeon operating thedissecting device110.
FIG. 5 illustrates one non-limiting structure that can be used in lieu of the angled blade-likedistal end47 of thetransuterine cannula40 shown inFIG. 2 to fenestrate the distal wall of the uterus to position thetransuterine cannula100 as shown inFIG. 4. Averess cannula112 can be advanced into a workingchannel114 of theendoscope106 through a shunt lumen as shown, and then theendoscope106 advanced through thetransuterine cannula100 to the inside surface of the distal wall of the uterus. Theveress cannula112 is then advanced out of theendoscope106 and manipulated to fenestrate the uterus, with the distal segment of thetransuterine cannula100 then being advanced through the fenestration to permit manipulation of theendoscope106 into the position shown inFIG. 4. The abdomen may be insufflated with, e.g., carbon dioxide by porting gas through theveress cannula112, or the working channel of the endoscope, or indeed through thetransuterine cannula100.
FIGS. 6 and 7 illustrate additional details of thetransuterine cannula100 andendoscope106. Theendoscope106 may be provided with aproximal handle116 that rotatably bears a manipulatingwheel118. Thewheel118 may be attached to the above-discussed wire, so that a surgeon can turn thewheel118 to bend the distal segment of theendoscope106 as shown inFIG. 6. Also, thetransuterine cannula100 may be formed with aproximal hub120 that can likewise be manipulated by a surgeon, it being understood that thehub120 andwheel118 are outside the patient when the assembly is positioned as shown inFIGS. 4,6, and7. The surgeon can manipulate theproximal hub120 to move thetransuterine cannula100, and owing to the cooperation between thestabilization balloon104 and the uterus, the surgeon can move the uterus somewhat.
FIG. 7 shows schematically that the dissectingdevice110 can be manipulated under visualization provided by theendoscope106 to cut anatomical structure in the peritoneal space. In the case shown, the broad ligament is being cut by the dissectingdevice110. The dissection maybe inspected by means of theendoscope106 to ensure acceptable hemostasis. From below, the uterine arteries can then be transected and the uterus subsequently retrieved through the vagina in accordance with vaginal hysterectomy principles.
FIG. 8 illustrates that one or more of atransuterine cannula130, anendoscope132 extending through thetransuterine cannula130, andsurgical instrument134 extending through theendoscope132 can be articulated, i.e., bent when positioned in a patient as desired to provide visualization of a target location. By way of illustration, anarticulation wire136 can extend through a channel of theendoscope132 from amanipulator wheel138 outside the patient's body to adistal location140 on theendoscope132, where thewire136 is fastened. Thewheel138 can be manipulated to pull thewire136 to bend theendoscope132 as shown, and then released to allow the material bias of theendoscope132 to straighten the endoscope. It is to be understood that similar articulation structure can be provided for thetransuterine cannula130 andsurgical instrument134. Distal and proximal balloon anchors142,144 that are substantially identical in configuration and operation to theballoons50,51 shown inFIG. 2 can also be provided on thetransuterine cannula130 to engage thetransuterine cannula130 with theuterus14.
In non-limiting implementations, thetransuterine cannula130 has two degrees of freedom, namely, rotation and bending. In contrast, theendoscope132 can have three degrees of freedom, namely, rotation, translation in the proximal and distal dimension through thetransuterine cannula130, and bending. Likewise, thesurgical instrument134 can have three degrees of freedom, namely, rotation, translation in the proximal and distal dimension through theendoscope132, and bending. In non-limiting implementations thesurgical instrument134 may be, e.g., a scissor, grasper, dissector, electrocautery probe, tissue welder, clip applicator, or ligature applicator.
FIG. 9 shows that anendoscope150 can be engaged at its distal end with avacuum shroud152 that is radially continuous, so that theshroud152 can be advanced against the distal wall of the uterus as shown and a vacuum induced in the shroud through a lumen of theendoscope150 to draw the distal wall toward afenestration instrument154, which can be advanced through and distally beyond the working channel of theendoscope150 as shown to fenestrate the inwardly-drawn distal wall. To this end, the interior of thevacuum shroud152 communicates with asource156 of vacuum through the lumen of the endoscope. Thefenestration instrument154 may be, e.g., a bipolar transection device.
With this structure, a vacuum can be drawn in theshroud152 to urge the distal wall of the uterus against thefenestration instrument154 to fenestrate the distal wall while reducing the risk that tissue beyond the distal wall in the peritoneal space might unintentionally be damaged.
FIG. 10 shows a preferably single-piece plasticvaginal guide160 that is shaped and sized for being closely received in a vagina of a patient. Theguide160 is formed with acentral hole162 sized to closely receive a transuterine cannula therethrough in slidable support, andadditional holes164 may be formed in the guide for slidably receiving, e.g., the dissectingdevice110 shown inFIG. 7.Adhesive bands166 can be attached to theguide160 as shown and with the patient's skin to hold the guide in place at the vaginal opening. Theguide160 can be made of a soft elastomer, and it stabilizes the vaginal orifice during hysterectomy while providing access portals and preventing injury that might otherwise occur due to repeated insertion and manipulation of instruments as described above. Theguide160 also provides a resting point and fulcrum for, e.g., the transuterine cannula described herein.
FIGS. 11 and 12 show that anobturator170 of the present invention may be advanced past the distal opening of atransuterine cannula172 with sealingballoons174 to fenestrate the distal wall of the uterus. Specifically, theobturator170 may have a frusto-conical distal segment terminating in a rounded distal tip as shown, and the entire frusto-conical distal segment (FIG. 11) or only the rounded distal tip (FIG. 12) may bear anelectrode array176. Thearray176 can be energized via an energization wire extending through thetransuterine cannula172 for fenestrating the distal wall of the uterus and at the same time cauterizing the cut tissue.
FIGS. 13 and 14 show analternate transuterine cannula180 formed with adistal neck182 and ashoulder184 proximal to theneck182 and adjoined thereto. Theshoulder184 has a larger diameter D1 than the diameter D2 of theneck182. Thus, theshoulder184 is wider than theneck182 for abutting theinner surface186 of thedistal wall188 of the uterus with theneck182 disposed in theopening190 of the wall made by one of the above-described fenestration devices. With this structure, the diameter of theopening190 is reduced while the portion of thetransuterine cannula180 residing in the uterus is relatively large to aid in manipulating the uterus. Also, theshoulder184 self-limits the depth of penetration of thetransuterine cannula180 into the peritoneal space.
FIG. 14 illustrates this latter principle in greater detail. Distal and proximal sealing balloons192,194 that may be substantially identical in configuration and operation to theballoons102,104 shown inFIG. 4 can be provided on thetransuterine cannula180 and inflated on opposite sides of the distal uterine wall. The above-describedobturator170 can then be advanced into the wall to fenestrate it, at which point theneck182 of thetransuterine cannula180 can be pushed through the fenestration with theshoulder184 abutting the inner surface of the distal uterine wall to limit the distance theneck192 can be pushed into the peritoneal space.
FIG. 15 shows atransuterine cannula200 that has aproximal handle202 outside the patient that can be manipulated to move the uterus as desired. In the embodiment shown inFIG. 15, a uterine portion204 of thetransuterine cannula200 may include proximal and distal sealing balloons206 for sealing against opposite sides of the distal uterine wall, and astabilization balloon208 for substantially filling the uterus when inflated. Theballoons206,208 can be inflated by porting inflation fluid through an inflation lumen210 of thetransuterine cannula200, which can be closed off after inflation using aflap valve212 on thehandle202 as shown to hold theballoons206,208 in the inflated configurations. If desired, theinflation lumen212 can be connected to an external source of vacuum and aproximal gasket214 can be provided around the inside periphery of the proximal end of the inflation lumen210 to establish a seal between the source of vacuum and lumen. Anarrow segment216 of thehandle202 may be disposed in the vagina when thetransuterine cannula200 is positioned as intended with the sealingballoons206 inflated on opposite sides of the distal uterine wall.
FIG. 16 shows atransuterine cannula220 with anouter surface222, and twoexternal tubes224 forming lumens extending along theouter surface222 to provide working channels external to thetransuterine cannula220.FIG. 17 shows atransuterine cannula226 with a singleexternal tube228. The transuterine cannulas shown inFIGS. 16 and 17 can have bevelled distal tips as shown for cutting tissue, and are shown in slightly articulated configurations.
FIGS. 18-20 show avaginal positioning guide230 that is closely receivable in a vagina for receiving one of the above-described transuterine cannulae through acentral lumen232 of theguide230. Essentially, thevaginal positioning guide230 includes aballoon234 that is inflatable to substantially fill the vagina to anchor the guide in the vagina when the transuterine cannula extends through thecentral lumen232 and into theuterus14.
As shown, theguide230 may be constructed with one and preferably twolateral lumens236. Thelateral lumens236 can be established by respective tubes that are disposed in theballoon234.Respective tissue dissectors238 can extend through thelateral lumens236 for fenestrating the vagina, so that, e.g., one or more of thedissectors238 can be used as the dissectingdevice110 shown inFIG. 7. Or, thedissectors238 can be removed after fenestrating the vagina and asubstitute dissecting device110 advanced through the lateral lumen and vaginal wall to an anatomical structure to be dissected as described above. If desired, as best shown inFIG. 19 thedistal portion240 of one or bothlateral lumens236 can be angled outwardly from the axis of the respectiveproximal portion242 as shown.
FIG. 21 shows a multiperforated veress shunt cannula250 that is slidably engageable with a lumen of an endoscope252 that is in all essential respects identical in construction and configuration to the endoscopes described previously and that consequently may be engaged with atransuterine cannula254 as set forth above. Theshunt cannula250 is a sharpeneddistal end256 as shown andmultiple holes258. Theshunt cannula250 accordingly may be advanced through the uterine wall as shown and into the abdominal cavity to establish a pathway for fluid (e.g., CO2) communication from the uterine space of a patient to the abdominal cavity of the patient.
While the particular METHODS AND APPARATUS FOR NATURAL ORIFICE VAGINAL HYSTERECTOMY are herein shown and described in detail, it is to be understood that the subject matter which is encompassed by the present invention is limited only by the claims.