US20080045939A1 - Gynecological ablation system with insufflation assisted imaging - Google Patents

Abstract

A method for treating pelvic tumors, such as uterine leiomyomata, includes inserting an ablation apparatus into a pelvic region and positioning the ablation apparatus either proximate or into a pelvic tumor. The method further includes using a laparoscope and an imaging device, such as an ultrasound machine, to confirm the location of the pelvic tumor and placement of the ablation apparatus. Various ablation apparatuses may be used, including those with multiple needles or deployable arms that are inserted into the pelvic tumor and those without arms. The method further includes delivering electromagnetic energy or other energy through the ablation apparatus to the pelvic tumor to ablate the tumor. A surgical system for ablating pelvic tumors is also provided.

Description

FIELD OF THE INVENTION
• The present invention relates to a procedure and system for treating gynecological disorders. More particularly, the present invention relates to the treatment of pelvic tumors.
BACKGROUND OF THE INVENTION
• Benign and malignant tumors can occur in the pelvis. For example, uterine leiomyomata, are muscle cell tumors that occur in 77% of women in the reproductive years. Although uterine leiomyomata rarely (0.1%) progress to cancer, these tumors can cause excessive menstrual bleeding, irregular bleeding, pregnancy loss, infertility, frequency, and pelvic pressure or pain with sexual activity, menses, or daily activities. Women with uterine leiomyomata frequently incur surgical procedures (e.g., hysterectomy, dilatation and curettage, myomectomy, and hysteroscopy), medical and hormonal therapies, office visits, and a variety of radiologic procedures (e.g., ultrasounds, CAT scans, and MRIs), in an effort to treat these tumors. Uterine leiomyomata account for approximately 200,000 hysterectomies per year in the United States alone, at a direct cost of well over $2 billion. Hysterectomies carry a morbidity rate of 1%, with 2,000 deaths per year and 240,000 complications per year in North America.
• Uterine leiomyomata are most often multiple, and may be subserosal (i.e., bulging externally from the uterus), intramural (i.e., growing entirely within the wall of the uterus), submucosal (i.e., hidden within the uterine cavity), or pedunculated (i.e., growing outward with a stalk-like base). Because patients may have multiple uterine leiomyomata at different locations, conservative surgeries may involve both an abdominal and a vaginal (hysteroscopic) approach, thereby necessitating two procedures.
• Investigators have utilized a laser or bipolar cautery to perform myolysis or destruction of these tumors, although neither of these methods is performed in significant numbers today. These methods necessarily destroy normal overlying tissue in order to treat the underlying tumor. As a result the integrity of the uterus is compromised, and harmful scar tissue (e.g., adhesions) may occur. Thus, there is a need for an improved method of treating benign and malignant pelvic tumors that does not damage the overlying tissue. Such an improved method could be used on women who wish to later conceive and subsequently deliver. There is also a need for a single method capable of treating all sizes of subserosal, intramural, submucuosal, and pedunculated tumors in all locations. A single method, which would relieve most or all symptoms of abdominal or pelvic pain/pressure, abnormal uterine bleeding, urinary frequency, infertility, and miscarriage, is also needed. In addition it would be desirable for the method to be less invasive, cheaper, and safer than conventional methods of treating pelvic tumors, and also to allow for uterine preservation.
SUMMARY OF THE INVENTION
• The present invention, also referred to as “the Halt procedure,” is an innovative, outpatient procedure that utilizes electromagnetic energy to effectively ablate pelvic tumors. The invention employs an ablation device that uses radio-frequency (RF) energy to treat pelvic tumors, while sparing the surrounding normal tissue. Although the ablation device utilized in the present invention has FDA approval for ablation of soft tissue tumors, no known reports exist in the medical literature of the ablation device's application to uterine leiomyomata or other pelvic tumors. In addition, current results indicate that, compared to other conservative therapies, the present method is very effective. Thus far, the present invention has provided relief from all of the types of symptoms caused by pelvic tumors, such as uterine leiomyomata. Furthermore, the present invention is versatile, safe, and well-accepted by patients. Advantages of the present invention include a quick recovery time, typically no more than a week, and significant cost savings. More importantly, the present invention provides a practical and efficient way to achieve uterine conservation on an out-patient basis.
• In accordance with one embodiment of the present invention, a method of treating a pelvic tumor includes inserting an ablation device into a pelvic region and positioning the ablation device proximate the pelvic tumor, using a laparoscope and an imaging device to confirm placement of the ablation apparatus. Various ablation devices may be used. For example, the ablation device may include no arms, a plurality of deployable arms, or separate needles that are inserted into the pelvic tumor. The method further includes delivering energy through the ablation device to the pelvic tumor to ablate the tumor. The method uses RF energy, however, other forms of energy, such as microwave, light (e.g., laser), or acoustic (e.g., ultrasound) energy may also be used to ablate the pelvic tumors.
• In accordance with another embodiment of the present invention, a method of treating pelvic tumors includes providing a patient on an operating table, and at least one monitor for a laparoscope and an imaging device, with the at least one monitor located across the operating table from a surgeon and proximate the patient's waist. The at least one monitor may be mounted on a tower located proximate the patient's waist. An energy source and the imaging device are provided adjacent to the at least one monitor, with the energy source and imaging device being located proximate the patient's knees. The method further includes inserting an ablation device into a pelvic region of the patient and positioning the device proximate a pelvic tumor. The location and placement of the ablation device with respect to the pelvic tumor is confirmed using the laparoscope and the imaging device. The method also includes delivering energy to the pelvic tumor to ablate the tumor. The tumor may be maintained at a temperature in the range of approximately 65° C. and 100° C. for at least 7 minutes to ablate the tumor.
• In accordance with still another embodiment of the present invention, a surgical system for treating pelvic tumors in a patient lying on an operating table includes an ablation device, an energy source, a laparoscope, and an imaging device. The energy source is coupled to the ablation device and provides energy to the device to ablate a pelvic tumor. The laparoscope and the imaging device are connected to at least one monitor. The at least one monitor is located the operating table from a surgeon and proximate the patient's waist, while the energy source and imaging device are located alongside the at least one monitor and proximate the patient's knees.
• The present invention procedure may be performed by laparoscopy (i.e., open abdominal incision), percutaneously, or hysteroscopically. The Halt procedure has most often utilized conventional laparoscopy with the additional placement of (1) a supra-pubic port or sleeve (10 mm) at the top of the uterus for an intra-abdominal ultrasound probe and (2) an ablation device, also usually in the lower abdominal region. The Halt procedure has also been performed by a trans-abdominal technique, utilizing conventional trans-abdominal ultrasound and placement of the ablation device trans-abdominally with laparoscopic confirmation, as well as by a trans-cervical technique.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective diagram of a surgical system for ablating pelvic tumors, in accordance with the present invention.
• FIG. 2 is a top plan view of the surgical system ofFIG. 1, illustrating an arrangement of certain equipment with respect to a patient lying on an operating table.
• FIG. 3 is a flowchart illustrating a closed laparotomy method of ablating pelvic tumors in accordance with the present invention.
DETAILED DESCRIPTION OF THE INVENTION
• Referring first toFIG. 1, asurgical system10 for ablating pelvic tumors includes alaparoscope12, avideo monitor14 associated withlaparoscope12, animaging device16, avideo monitor18 associated withimaging device16, anenergy source20 and anablation device22. Laparoscope12, which is inserted into a patient P, is electrically connected tovideo monitor14, which displays an image fromlaparoscope12. As will be explained in greater detail below,laparoscope12 enables a surgeon to view the insertion and placement ofablation device22 into a pelvic region of the patient.
• Imaging device16 is electrically connected tovideo monitor18 and provides images of the patient's pelvic region. These images, which are displayed onvideo monitor18, enable the surgeon to determine the presence and location of any pelvic tumors.Imaging device16 shown inFIG. 1 is an ultrasound machine, and includes anintra-abdominal ultrasound probe24. Instead ofintra-abdominal ultrasound probe24, a transducer (not shown) may be coupled to the ultrasound machine for trans-abdominal ultrasound imaging. In addition, other imaging devices, such as an MRI machine or a CT device, may also be used instead of an ultrasound machine.
• Ablation device22 is a sterile, electrosurgical device that may include a plurality ofretractable arms26.FIG. 1 showsarms26 ofablation device22 deployed in apelvic tumor28. Examples of the ablation device include the Model 30 Electrosurgical Device and the RITA® StarBurst™ XL, both available from RITA Medical Systems, Inc. Eacharm26 ofablation device22 is a retractable curved electrode for delivering energy and has a thermocouple (not shown) located at the distal end. AlthoughFIG. 1 showsablation device22 as including deployable arms, an ablation device without any arms may also be used. Alternatively, the ablation device may include two or more needles that may be inserted into the tumor.
• Ablation device22 is coupled toenergy source20, which supplies energy to each of thearms26 ofablation device22.Energy source20 may be an RF generator, such as the Model 500 Generator or the RITA® Model 1500 RF Generator, both available from RITA Medical Systems, Inc. The supply of RE energy fromenergy source20 toablation device22 and to adispersive electrode30 is controlled by an operator control, such as by afoot pedal32. The application of RF energy causes an increase in tumor temperature. At sufficiently high temperatures, cell death occurs, thereby destroying the tumor.
• Energy source20 may further include a mono-polar or bipolar energy source, which allows theablation device22 to utilize traditional mono-polar or bipolar cautery to treat very small, superficial tumors and to ablate the track formed during insertion ofablation device22. Cauterizing the ablation device track reduces or prevents bleeding upon withdrawal ofablation device22 from the patient.
• As better illustrated inFIG. 2, in accordance with the present invention, the equipment ofsurgical system10 is set up about the patient in a non-traditional arrangementFIG. 2 illustrates the patient P lying in a dorsal position on an operating table34. Atower36, which supportsvideo monitor14 forlaparoscope12 and imaging device monitor18, is located proximate the patient's waist, rather than at the foot of operating table34. Since the surgeon S is located on the other side of operating table34 across fromtower36, the surgeon S has a direct view of themonitors14 and18. Video monitors14 and18 need not be provided ontower36; they may be suspended from the ceiling and located on the other side of operating table34 across from the surgeon S. During longer surgical procedures, the placement of video monitors14 and18 directly across from the surgeon is more comfortable for the surgeon, as the surgeon need not turn his/her head toward the foot of operating table34 to viewmonitors14 and18.
• AlthoughFIGS. 1 and 2 show separate video monitors14 and18 forlaparoscope12 andimaging device16, respectively, a single monitor capable of simultaneously displaying multiple images from the laparoscope and the imaging device, such as a picture-in-picture monitor, may also be used. The single monitor would be located across the table from the surgeon S and may be mounted on tower similar totower36, suspended from the ceiling, or otherwise located across the patient from the surgeon for easy viewing by the surgeon.
• Tower36 may include additional equipment (not shown), such as an insufflation machine, a printer, and a light source.Tower36 may be provided with wheels so that it may be easily moved about the operating room. Anadditional monitor37 forlaparoscope12 may also be provided across from a surgical assistant A, who is seated across the table from the surgeon S, at approximately the patient's chest level. Thus,additional monitor37 would be located adjacent the surgeon S.Additional monitor37 may mounted on a movable tower (not shown), suspended from the ceiling, or otherwise appropriately located.
• Imaging device16 andenergy source20, which are not located ontower36, are positioned along operating table34, across from the surgeon S, and toward the foot of operating table34. For example,imaging device16 andenergy source20 may be located proximate the patient's knees.
• A method of treating pelvic tumors, in accordance with one embodiment of the present invention, will now be described, with reference to the flow chart illustrated inFIG. 3. Thismethod50 employs a laparoscopic technique for ablating pelvic tumors. First, atstep52, the patient is prepared for laparoscopy by placing and properly adheringdispersive electrode30 to the lower back of the patient. Atstep54, the patient is then placed under general anesthesia, and the surgeon performs an examination of the pelvic region. A manipulator38 (FIG. 1), such as a tenaculum, is placed on the patient's cervix, and a 14 french foley catheter is inserted into the patient's bladder for emptying the bladder during the surgical procedure.
• Atstep56, the patient is placed in a dorsal position with her arms at her sides, rather than extended out as an airplane, and a blanket and a surgical drape are placed over the patient. This position provides the surgeon and surgical assistant with more room to move about. The dorsal position is also a safer position for the patient than a frog-leg or lithotomy position, as the dorsal position reduces the instance of nerve injuries and provides better circulation. In addition, the dorsal position does not require the use of custom drapes and stirrups. The surgical drape contains pouches for at least one laparoscopic cord. Serial compression devices (not shown) are placed on the patient's legs to improve circulation during the surgical procedure and reduce the possibility of thromboembolism. In addition, the patient may be placed in a bear hugger system (not shown) to maintain the patient's body temperature while under general anesthesia.
• Atstep58, the equipment is arranged about operating table34. As illustrated inFIG. 2,tower36, which includes video monitors14 and18, an insufflation machine, a printer and a light source, is placed proximate the patient's waist and across from the surgeon S. The surgical assistant A is seated across the table from the surgeon at about the patient's chest level, withtower34 located behind the assistant and further toward the foot of operating table34.Imaging device16 andenergy source20 are situated alongside operating table34 on the same side as the assistant A and toward the foot of operating table34. Theadditional monitor37 is positioned across from the surgical assistant A at about the patient's chest level.
• Atstep60, the patient P is placed in a trendelenburg position. The surgeon then makes an infra-umbilical or sub-umbilical incision. A verres needle is then inserted into the incision and into the peritoneal cavity. The insufflation machine is then used to insufflate the abdomen with carbon dioxide gas until the abdominal pressure is approximately 15 mm Hg.
• Next, atstep62, a 5 mm trocar and sleeve are inserted through the infra-umbilical or sub-umbilical incision. The trocar is then removed andlaparoscope12 is inserted into the sleeve.Laparoscope12 and monitor14 are then used to verify correct placement oflaparoscope12 within the peritoneal cavity and the absence of any trauma. The sleeve is attached to the carbon dioxide gas supply and includes a valve for controlling the abdominal pressure of the peritoneal cavity.
• Steps60 and62 discussed above describe a closed laparoscopy procedure. For those patients, for whom the surgeon feels an open laparoscopy would be advantageous, the surgeon would make an infra- or sub-umbilical incision and use a combination of blunt and sharp dissection through subcutaneous tissue. The surgeon would then retract the instruments for exposure. When the fascia is visualized, it is grasped with one or more clamps, elevated and incised. This provides a view of the peritoneum below, which may be bluntly or sharply incised. An appropriate laparoscopic sleeve is then placed, and the abdomen is insufflated with carbon dioxide gas. The laparoscope is then inserted into the sleeve.
• Atstep64, the surgeon then useslaparoscope12, while palpating a top of the uterine fundus, to determine an optimal location for an intra-abdominal ultrasound probe. The optimal location is generally at the top of the uterus, rather than supra-pubic. An incision is then made at this location and a 10 mm trocar and sleeve are inserted. The trocar is removed andultrasound probe24 is inserted into the sleeve. By way of example, theultrasound probe24 may be an Aloka model no. UST-5526L-7.5 probe for use with an Aloka model no. SSD140U ultrasound machine.Ultrasound probe24 transmits an image of the pelvic region toultrasound machine16. The image is displayed onultrasound video monitor18, which is located ontower36 proximate video monitor14 forlaparoscope12. Thus, the surgeon may simultaneously view the images on video monitors14 and18. As discussed above, a single monitor that simultaneously displays images fromlaparoscope12 andimaging device16 may be used instead ofseparate monitors14 and18.
• Atstep66, the surgeon examines the entire pelvis and abdomen to confirm the presence or absence of any pathologies. The surgeon also useslaparoscope12 andultrasound probe24 to visualize any tumors, such as uterine leiomyomata. In particular, the surgeon takes note of the number of tumors, and the location and size of each, and compares that information with previously acquired data.
• Atstep68, the surgeon determines an order for treating the tumors. This order is determined based on the locations of the various tumors, and whether or not the tumors are accessible from a single midline location or require different locations from which to access the tumors. For example, if two tumors are generally along the same track ofablation device22, the surgeon will first ablate the deeper tumor and, upon retraction ofablation device22, ablate the remaining tumor. In addition, the surgeon may choose to ablate first a portion of the tumor that is furthest away from the vasculature and work toward the vasculature, or vice versa.
• Atstep70, the surgeon testsablation device22 to ensure that it is operating properly.Ablation device22 is connected togenerator20, and proper feedback from the thermocouples, if any, is observed. In particular, the surgeon operatesfoot pedal32, or any other appropriate operator control, to activate the supply of RF energy fromgenerator20 and notes an appropriate rise in temperature and any peaks.
• Atstep72, if the surgeon decides that all of the tumors are approachable via a single midline location, the surgeon makes an incision, approximately 2.5 to 3.0 mm long, and insertsablation device22. Entry ofablation device22 is observed usinglaparoscope12. The surgeon usesultrasound probe24 to visualize the size and location of the tumors with respect toablation device22.
• Next, atstep74, the surgeon manipulates the patient's uterus using other techniques to stabilize the uterus.
• Atstep76, after the surgeon has stabilized the uterus and located the tumors, the surgeon guidesablation device22 into the uterus and the into a wall of the uterus. The surgeon may guideablation device22 by changing the position of the uterus relative toablation device22. In addition, the surgeon may rotate the ablation device for better penetration of the uterine wall with less movement of the uterus.Ablation device22 has a plurality of markings (not shown) that enable the surgeon to note the depth of penetration ofdevice22. Confirmation of the location and placement ofablation device22 are provided by bothlaparoscope12 andultrasound probe24.
• Next, atstep78, the surgeon advances the tip ofablation device22 to an appropriate depth for treating a tumor. In doing so, the needle makes only a very small puncture. For example, an ablation device having a needle of 16 gauge may produce a puncture site of approximately 1 mm to 2 mm in diameter. The appropriate depth depends on the size of the tumor. Whenablation device22 has been inserted to the appropriate depth,arms26 ofablation device22 are deployed to the appropriate extent in thetumor28, as illustrated inFIG. 1. A 30° scope is used to ensure that all of thearms26 remain within the confines of the tumor and do not extend outside of the organ.Arms26 may effectively anchorablation device22 intumor28.
• Atstep80, the surgeon then records a baseline starting temperature of the tumor. The temperature of the tumor is obtained by the thermocouples located at the distal ends ofarms26 ofablation device22.
• Atstep82, the surgeon then ablates the tumor by supplying RE energy fromgenerator20 toablation device22.Wile generator20 is activated, it is important to monitor the temperature or impedance of all parts of the ablation device. If the temperature or impedance for any part ofablation device22 is abnormal, it could indicate that that part of the device is external to the organ.
• RF energy is supplied to the tumor to raise the temperature of the tumor, such that it is in the range of between approximately 65° C. and 100° C., for about 14 minutes. Cell death occurs at a temperature of about 65° C. However, since these tumors are heterogeneous and, therefore, can differ in density, vasculature and content, a preferred target temperature range for ablating pelvic tumors is between 85° C. and 100° C. For small tumors the target time may be between approximately 7 minutes and 14 minutes. One of ordinary skill in the art, however, will appreciate that ablation times of less than 7 minutes may also be adequate.
• The temperature of the tumor, as provided by the thermocouples, is monitored and recorded at least at a 7 minutes and a 14 minutes interval. Thus, at least a baseline starting temperature, half-time temperature, and end-of-ablation-period temperature are recorded for each tumor. While RF energy is being delivered to the tumor, the surgeon keeps an eye on themonitors14 and18 to ensure that none of thearms26 ofablation device22 inadvertently extends through the tumor. The uterus can contract as it is heated, causingarms26 ofablation device22 to project from the tumor and contact normal tissue, which may be damaged by the RF energy. When the tumor has been sufficiently ablated,energy source20 is turned off.
• After each ablation, atstep84 the uterus is irrigated with fluid. The fluid prevents the serosa from drying out as a result of the carbon dioxide gas that is pumped into the abdomen.
• If the tumor is larger than the ablation field for the given ablation device, then atstep86, the surgeon may need to repositionablation device22 within another part of the tumor and reapply RE energy, repeatingsteps76 through84. Thus, if the tumors are greater in size than the ablation capacity ofablation device22, multiple applications of energy, of overlapping ablation areas, may be necessary to ablate the bulk of the tumor. For tumors less than 3 cm, however, a single application of the RF energy should be sufficient to ablate the tumor.
• Atstep88, the surgeon then repositionsablation device22 at the next tumor. The surgeon may leaveablation device22 in the same track, if the next tumor is along the same line of approach. The surgeon would retractarms26 and advance or withdrawablation device22 as needed for entry into another tumor. The surgeon would then repeat the ablation sequence ofstep76 throughstep86 described above.
• If the subsequent tumor is in a different location, the surgeon may retractarms26 ofablation device22 and withdrawablation device22, while applying a mono-polar cautery to reduce or prevent bleeding from the ablation device track. Alternatively, rather than completely withdrawablation device22 andre-insert ablation device22 through another incision, repeatingsteps72 through86, the surgeon may withdrawablation device22 until it is only 0.5 cm to 1 cm deep and adjust the uterus until the desired angle of approach is obtained and properly locatingablation device22 withultrasound probe24 or applying traction or pushing inward withuterine manipulator38.
• Small, superficial, subserosal fibroids (e.g., less than 1 cm) may be ablated with a mono-polar cautery atstep90. Bipolar paddles may also be used if the fibroid extends from the wall of the uterus. Similarly, if the tumor is pedunculated, the surgeon may treat or incise the stalk. Mono-polar or bipolar cautery may be applied to subserosal, intramural, and submucuos leiomyomata. In addition, other pelvic pathologies are treated as appropriate.
• After all of the tumors have been ablated, atstep92, the surgeon confirms hemostasis, withdrawsablation device22, and applies a mono-polar cautery withablation device22 to the puncture sites, if necessary. A small amount of irrigation fluid may be left in the pelvis.
• Finally, atstep94, documentation, including videotapes, ultrasound photographs, and photographs from the laparoscope are obtained. The sleeves are opened to allow the escape of the carbon dioxide gas. The patient is then removed from the trendelenburg position, and a local anesthetic agent is injected into the incisions. The surgeon then repairs the fascia of the 10 mm incision using an absorbable suture, S-retractors to facilitate visualization of the fascial edges. Alis™ clamps are used to facilitate grasping for elevating the fascial edges for suturing, re-approximating the subcutaneous tissue with sutures, closing the skin, and placing Steristrip™ bandages. The surgeon then removes thedispersive electrode30 and examines the surrounding skin.
• The patient is transported to a recovery room, where she will remain until she is tolerating liquids, ambulating with assistance, and voiding adequately.
• If the patient's uterus is very large (e.g., 16 weeks or greater), the above-described laparoscopic technique may be less effective. Accordingly, a direct trans-abdominal insertion ofablation device22 is performed with laparoscopic confirmation only (e.g., no intra-abdominal ultrasound confirmation). In this method the patient is prepared in the same manner as that described above atstep52. The surgeon also performs a pelvic examination, positions the patient, arranges the equipment, forms an infra-umbilical incision, insufflates the patient's abdomen, and insertslaparoscope12, as instep54 through to step62 above. Specifically, the surgeon inspects the abdomen and documents the presence or absence of bowel adhesions or other pathologic conditions that would render this method inappropriate.
• Next, the surgeon releases the gas from the patient's abdomen, allowing the abdominal wall to contact an anterior portion of the uterus. A sterile cover drape over a transducer allows for trans-abdominal ultrasound imaging using a non-sterile transducer (not shown). The ultrasound is used to locate and measure the tumors.
• The surgeon then makes an incision forablation device22 and insertsablation device22, using abdominal ultrasonography to guide its insertion.Ablation device22 may be inserted percutaneously, or trans-abdominally, into the tumor in the uterus.
• Ablation device22 is positioned at a tumor andarms26 are deployed in the tumor, just as described above with respect to the laparoscopic method. Prior to applying RF energy to the tumor, the surgeon insufflates the abdomen and performs a laparoscopy to confirm that none of thearms26 ofablation device22 extend beyond the uterine tissue.
• The surgeon then applies RE energy to the tumor, in the same manner as described atstep80 throughstep84 above, including recording the baseline, half-time, and end-of-ablation-period temperatures. The surgeon may use the same approach as described above to ablate multiple pelvic tumors. Upon withdrawal of theablation device22, the surgeon fulgurates the ablation device track with a mono-polar cautery. Thus, remaining steps are the same asstep86 throughstep94 described above.
• The above-described methods enable the surgeon to ablate substantially all of a tumor from a single, ablation device puncture site. In addition, depending on the location of the tumors, multiple tumors may be ablated from a puncture site. The methods further enable the surgeon to treat all sizes of tumors in any area of the pelvic region.
• The foregoing description of the preferred embodiments of the present invention have been provided for illustrative purposes only. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed. Various modifications may be made without departing from the spirit and scope of the inventions as set forth in the appended claims. For example, although the present invention has been described with respect to the treatment of uterine leiomyomata, the present invention may also be used to treat other pelvic tumors, such as those present in the ovaries. The present invention may be performed using a trans-cervical technique or a hysteroscopic technique, in addition to the laparoscopic and trans-abdominal techniques described above. The scope of the invention is defined by the following claims.

Claims (17)

1-26. (canceled)

27. A surgical system for ablating pelvic tumors in a patient, the system comprising:

an ablation device for insertion into a pelvic region of a patient;

an energy source coupled to the ablation device for providing energy to the ablation device;

a laparoscope for insertion into the patient; and

an imaging device for observing a location of the ablation device within the patient,

wherein the laparoscope and the imaging device are connected to at least one monitor, the at least one monitor being located across the operating table from a surgeon and proximate the patient's waist, and wherein the energy source and the imaging device are located adjacent the first and second monitors and proximate the patient's knees.

28. The surgical system ofclaim 27, wherein the imaging device is an ultrasound machine.

29. The surgical system ofclaim 27, wherein the energy source is an RF energy source.

30. (canceled)

31. The surgical system ofclaim 27, wherein the imaging probe images a location of the ablation device within the pelvic region of the patient.

32. The surgical system ofclaim 27, wherein the energy source is selected from the group consisting of a microwave energy source, a light energy source, and an acoustic energy source.

33. The surgical system ofclaim 27, wherein the laparoscope and the intra-abdominal imaging probe are operably coupled to at least one monitor.

34. The surgical system ofclaim 32, further comprising an operator control operably coupled to the energy source said operator control being a foot pedal.

35. The surgical system ofclaim 42, wherein the pelvic tumor is a uterine fibroid.

36. The surgical system ofclaim 35, further comprising a mechanical manipulator configured to engage and manipulate a uterus of the patient to position the uterine fibroid for ablation.

37. The surgical system ofclaim 36, further comprising an insufflation device disposed in a configuration for insufflating the abdomen and creating an air pocket adjacent the uterus hosting the uterine fibroid, said air pocket creating a space extending from the ablation device to the laparoscope.

38. A surgical system as inclaim 27, wherein the pelvic tumor is a uterine fibroid and further comprising a manipulator for manipulating the position of the uterus.

39. The surgical system ofclaim 38, further comprising an insufflation device disposed in a configuration for insufflating the abdomen and creating an air pocket adjacent the uterus hosting the uterine fibroid and extending to said laparoscope to allow imaging of the uterus by said laparoscope.

40. The surgical system ofclaim 27, further comprising an insufflation device disposed in a configuration for insufflating the abdomen and creating an air pocket adjacent the uterus hosting the uterine fibroid, said air pocket defining a space between said ablation device and said laparoscope to allow imaging of said uterus by said laparoscope.

41. The surgical system ofclaim 40, further comprising a manipulating device position to engage the uterus.

42. The surgical system ofclaim 41, wherein said ablation device, laparoscope and ultrasound probe are positioned relative to each other so that when said ablation device is in said tumor, said ultrasound probe is in contact with a surface of the uterus hosting said tumor.

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