Diagnostic and Operative Hysteroscopy: Polypectomy, Myomectomy, and Endometrial Ablation

Published on 11/04/2015 by admin

Filed under Surgery

Last modified 22/04/2025

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 0 (0 votes)

This article have been viewed 6606 times

Chapter 42 Diagnostic and Operative Hysteroscopy: Polypectomy, Myomectomy, and Endometrial Ablation

INTRODUCTION

Hysteroscopy is an accurate surgical approach for evaluating the uterine cavity and treating a multitude of abnormalities. At its essence, it involves the transcervical placement of a lens and light system into the uterine cavity while using gas or liquid for distension of the cavity. Modern hysteroscopy is performed almost exclusively with the addition of a camera and video monitoring system. Operative hysteroscopy is performed using an electrosurgical resectoscope or a sleeve with an operating channel to accommodate instruments for grasping, biopsying, or cutting with scissors or laser.

Today, in addition to being an excellent diagnostic technique, hysteroscopy has proven to be an effective and minimally invasive treatment for abnormal uterine bleeding, infertility, and early pregnancy loss. Some of the most common uterine pathologic conditions treated by hysteroscopy are polyps and myomas. Even in patients without intrauterine pathology, endometrial ablation, first performed hysteroscopically, has decreased the need for hysterectomy in patients with abnormal uterine bleeding unresponsive to medical therapy.

This chapter describes the standard methods for diagnostic and operative hysteroscopy and then offers details of the hysteroscopic treatment of polyps and fibroids, both submucous and pedunculated intracavitary lesions. The chapter also describes techniques for endometrial ablation, including traditional hysteroscopic ablation and several innovative methods.

HISTORY

Hysteroscopy, first described in the late 1800s, did not find widespread clinical use for more than 100 years. In 1869, Pantaleoni performed the first diagnostic and therapeutic hysteroscopy when he used a modified cystoscope to look into the uterine cavity and cauterize a hemorrhagic growth.1 Early hysteroscopists used a tube to mechanically distend the uterus for visualization. Near the beginning of the 20th century, Dr. Isidor C. Rubin, a New York gynecologist best remembered for Rubin’s test, first used carbon dioxide (CO2) to distend the uterus for hysteroscopy. Around the same time, Professor C. J. Gauss, a German surgeon and descendant of the famous mathematician, first performed hysteroscopy using fluid distension media.2 However, hysteroscopy did not find widespread acceptance for another half-century.3

In the 1970s interest in hysteroscopy renewed, in parallel with the rapid advancement of diagnostic and operative laparoscopy. Probably the most important advances came in the form of improved methods for distending the uterine cavity, including use of viscous and low-density liquid solutions. Around the same time insufflation machines were designed for CO2 and fluid media that utilized high pressure and low flow, rather than the low pressure and high flow used for laparoscopy.46 Carbon dioxide was often used for diagnostic hysteroscopy, and fluid media became the standard for operative hysteroscopy. It was found that isotonic fluid was ideal for most operative procedures, whereas nonconductive hypotonic media was required for electrosurgical procedures.

The use of hysteroscopy became widespread in the 1980s with the development of better optics and lighting and the use of video cameras. Operative techniques for various intrauterine pathologic conditions continued to be developed. Most notably among these may be removal of submucous myomas using an enhanced urologic resectoscope,7 removal of uterine septum,8 and endometrial ablation using laser,9 resectoscopic loop,10 or rollerball.11 Today, hysteroscopy has become a standard diagnostic and therapeutic technique performed by most gynecologists.

INDICATIONS

BASIC HYSTEROSCOPIC EQUIPMENT AND TECHNIQUES

Distension Media

The uterine cavity is a virtual space, which must be distended with either gas or fluid media to visualize the endometrium and intrauterine pathology in three dimensions. In the past, contact hysteroscopy was performed without distension media for diagnostic evaluation of the endometrium based on color, architectural pattern, and contour. Today, diagnostic and operative hysteroscopy are most commonly performed with fluid distension media.

Dextran 70

One of the first fluid distension media used was high-viscosity dextran 70. A 32% solution of dextran 70 in 10% dextrose in water is a nonelectrolytic, nonconductive fluid with syrup-like consistency that can be used for both diagnostic and operative hysteroscopy. Because of its high viscosity, dextran 70 results in minimal leakage through the cervix and tubes. Because it is immiscible with blood, it allows for excellent visibility during surgical procedures. A syringe with manual pressure is most often used during hysteroscopy to slowly infuse dextran 70.

Dextran 70 is rarely used today as hysteroscopic distension media because of several associated problems.13 From an operational perspective, dextran 70 solutions cause instruments such as graspers and scissors to become permanently inoperable if the solution is allowed to dry on the instruments. This problem can usually be avoided by immediate cleaning shortly after finishing the procedure.

Fluid overload is one of the most common serious problems that can result from intravascular intravasation of dextran 70. Each 100mL of dextran 70 absorbed results in an increase in the intravascular volume of 800mL. For this reason, it is recommended to use no more than 500mL of the solution during an individual procedure.

Another risk of intravascular intravasation of dextran 70 is disseminated intravascular coagulopathy. The mechanism of this uncommon complication is suspected to be toxic effects of dextran 70 on pulmonary capillaries.

Finally, allergic reactions to dextran 70 have also been reported. The risk of anaphylaxis while using dextran 70 for hysteroscopy has been estimated to be as high as 1 per 1500 cases.14

Low-Viscosity Fluid

Low-viscosity fluids are the most common distension media used today because they are suitable for both diagnostic and operative hysteroscopy, are relatively inexpensive, and are relatively low risk. Isotonic electrolyte-containing fluids can be used for all operative procedures except those requiring traditional electrosurgery, although technologic advances have allowed its use even with these procedures. Hypotonic nonelectrolyte media is used for most electrosurgery (i.e., resectoscope) procedures.

Isotonic electrolyte-containing fluids are the most common distension media used for diagnostic hysteroscopy and operative procedures using mechanical instruments, laser, and more recently available bipolar energy. Two commonly used types are 0.9% sodium chloride and lactated Ringer’s solution.

Hypotonic nonelectrolyte-containing fluids are required when the unipolar resectoscope is used, and several types are available. The most common fluids used are 5% mannitol, 3% sorbitol, and 1.5% glycine. The theoretical advantage of 5% mannitol is that it is rapidly broken down by the liver into glycogen and is excreted through the kidney, with a half-life of 100 minutes.15

The advantage of low viscosity fluids over carbon dioxide and hyskon 70 is the ability to easily flush blood, mucus, bubbles, and tissue fragments out of the visual field and uterus. However, proponents of hyskon 70 point out that the miscibility of blood in low viscosity fluids can result in decreased visibility.

The major risk of all low-viscosity fluid media is potentially fatal fluid overload from intravascular absorption. Hypotonic nonelectrolyte media has the additional deadly risk of acute hyponatremia. Both fluids therefore require close monitoring of fluid used and fluid recovered at frequent intervals throughout the hysteroscopic case. Some institutions use a fluid management system (e.g., Dolphin II, CIRCON, British Columbia, Canada) for this purpose.

When a fluid deficit of 1,000mL of nonelectrolyte solution is identified, blood should be drawn to determine electrolyte levels, the procedure should be terminated, and consideration should be given to administering diuretics, with close monitoring of electrolytes. Injection of 3 to 4mL of dilute vasopressin (10 units in 50mL saline solution) into the cervix decreases both intraoperative bleeding and intravasation for at least 20 to 30 minutes.16

DIAGNOSTIC HYSTEROSCOPY

For the majority of the 20th century, the only method available for directly visualizing intrauterine pathology short of hysterectomy was the blind procedure of D&C. In the 1970s, dramatic improvements in optical systems, light sources, and distension media allowed the widespread use of hysteroscopy for accurate diagnosis (and often treatment) of intrauterine pathology.

In the 1980s, the development of hysteroscopes with smaller diameters (<4mm) allowed the use of the hysteroscope for diagnosis without the need for either cervical dilation or anaesthesia. As a result, office hysteroscopy has become a common procedure, which has been documented to have the advantages of patient acceptability, diagnostic accuracy, and cost- effectiveness.17 Hysteroscopy is particularly useful for identifying focal lesions, which are often missed with endometrial sampling.18

HYSTEROSCOPIC POLYPECTOMY

Endometrial polyps are benign growths found within the uterine cavity. They are often asymptomatic and can perhaps remain undetected for decades. In women without symptoms, polyps are often found coincidentally when pelvic ultrasonography is performed for unrelated problems such as pain or during the investigation for infertility.

Polyps are often symptomatic. However, in women with abnormal uterine bleeding, investigation may lead to their detection. Symptoms most often related to uterine polyps include abnormal bleeding, postcoital staining, chronic vaginal discharge, or dysmenorrhea. Polyp-related bleeding is often characterized by increased clotting, intermenstrual or premenstrual spotting, or heavier menstrual flow. There is good evidence that polyps can decrease fertility and that their removal will improve the chances of pregnancy.21

In addition to women with abnormal bleeding and infertility, other women at increased risk for endometrial polyps include women on tamoxifen therapy and women with endocervical polyps, a quarter of whom will also have endometrial polyps.

It is obvious that symptomatic endometrial polyps should be removed. However, it is also important to remove asymptomatic polyps, particularly in postmenopausal women.22 Although the vast majority are benign, endometrial cancer and hyperplasia will be found in approximately 2% of endometrial polyps and are associated with coexisting malignancies elsewhere in the endometrium. In one study of more than 1400 polyps, endometrial cancer was found in 27 polyps (1.8%).22 All but one of these women were postmenopausal, and 26% were asymptomatic.

HYSTEROSCOPIC MYOMECTOMY

Leiomyomas are the primary indication for more than 40% of the 650,000 hysterectomies performed annually in the United States.23 Submucosal myomas likely account for 10% to 20% of all myomas. Many of these can be removed by operative hysteroscopy. In addition to preserving fertility in many cases, a hysteroscopic approach is associated with a shorter recovery period, lower complication rate, and lower cost than hysterectomy.

For a successful surgical outcome, it is important to identify preoperatively the size, number, location, and depth of intramural extension of uterine myoma. Myoma size, number, and location are determinants of complete resectability, the number of surgical procedures necessary for complete resection, the duration of surgery, and the potential complications from fluid overload.24

Numerous studies have demonstrated that preoperative saline infusion sonohysterography gives more information than hysteroscopy in respect of myomas. Chapter 30 reviews the topic of ultrasonography and sonohysterography in detail.

Hysteroscopic Classification of Myomas

A classification system is important to most accurately determine the appropriate method for performing myomectomy and counseling the patient on risk and prognosis. The European Society of Hysteroscopy classification system is based on myoma location and the amount of myoma protruding or encroaching on the endometrial cavity.25 In this system, Type 0 myomas are pedunculated, with the myoma lying completely within the endometrial cavity (Fig. 42-1). Type I myomas are described as sessile, with less than 50% intramural extension (Fig. 42-2). Finally, Type II myomas are submucosal in location, with more than 50% intramural extension. These include transmural myomas, which extend from the submucosal to the serosal edge. When viewed hysteroscopically, Type II myomas appear as a “bulge” into the endometrial cavity. Multiple myomas such as those in Figure 42-3 are not placed within this classification. They should not accessed by hysteroscopy.

This system was originally designed to classify myomas exclusively on hysteroscopic appearance. However, this approach has significant limitations. During hysteroscopy, myomas can be compressed and recede into the myometrium as a result of the pressure of the distension media, thereby preventing full visualization of the myoma. For this reason, preoperative evaluation with ultrasonography is required to accurately determine how many myomas are present and how deeply the myomas penetrate the myometrium.

An ultrasonographic classification system has been developed for intramural myomas that corresponds in part to the hysteroscopic classification and in part to the hysterosalpingography data26 (Table 42-1).

Table 42-1 Hysteroscopic and Sonohysterographic Classification System for Myomas Encroaching Upon the Endometrial Cavity

Hysteroscopic Type25 Sonohysterographic Class26 Description
Type 0 Class 1 Pedunculated myomas, where 100% of the myoma lies within the endometrial cavity with no intramural extension
Type I Class 2 Sessile myomas, with <50% intramural extension
Type II Class 3 Submucous myomas, with >50% intramural extension

Surgical Approach According to Stage

The degree of surgical difficulty and thus the risk to the patient is related to the depth of penetration and size of the myomas. Pedunculated hysteroscopic Type 0 or sonohysterographic Class 1 myomas up to 3cm in dimeter can usually be easily removed hysteroscopically. Larger hysteroscopic Type 0 myomas (>3cm) and hysteroscopic Type I (Class 2 on sonohysterography) myomas can be approached hysteroscopically. However, the risk of fluid intravasation increases as a result of increased surgical time and the opening of myometrial venous channels during resection. Operative hysteroscopy is made more difficult by limited space within the uterus and poor visibility due to an inability to further distend the uterine media and the large amount of myoma “chips” that accumulate within the endometrial cavity. Often, incomplete removal of larger myomas requires two or more separate operative procedures. Only the most experienced hysteroscopist would attempt a hysteroscopic resection of an intracavitary myoma 5cm or larger. Myomas that are large and multiple (see Fig. 42-3) should not be excised by hysteroscopy.

Hysteroscopic resection of hysteroscopic Type II (or sonohysterography Class 3) myomas should only be approached by the most skilled hysteroscopist and are more commonly approached abdominally by laparoscopy or laparotomy. Hysteroscopic removal of Type II myomas is associated with a greater risk of fluid intravasation and uterine perforation and commonly requires two or more procedures for complete removal. Hysteroscopic resection of Type II myomas results in extensive damage to the endometrium, resulting in an increased risk of Asherman’s syndrome as well as decreased fertility and hypomenorrhea. In an attempt to minimize intrauterine adhesions, patients are often treated postoperatively with estrogen and progestin, intrauterine stents, or “second look” hysteroscopy. However, the efficacy of these approaches has not been studied. Because of this risk, hysteroscopic removal of Type II myomas generally should not be used in women who desire future fertility.

Preoperative Medications

Cervical Preparation

Use of a laminaria or misoprostol is recommended to facilitate dilation. Additionally cervical softening agents decrease the risk of cervical tears, decrease the risk of uterine perforation, and decrease the use of unnecessary force to achieve cervical dilation. The most common complications associated with operative hysteroscopic surgery is cervical laceration (Table 42-2).

Table 42-2 Risk of Complications Associated with Endometrial Ablation and Resection13,14

Complication Rate
Intraoperative
Cervical lacerations 4%
Uterine perforation 1.4%
Bowel/bladder/vessel injury Rare
Fluid overload Rare
Postoperative
Infection 0.4%
Hematometra 1–2%
Delayed
Bleeding requiring further surgery 10%
Subsequent endometrial cancer Rare

Laminaria can be inserted into the cervix 12 to 24 hours before surgery. This will facilitate cervical dilation, but requires an extra office visit and cannot be used in women with shellfish or iodine allergy.

Misoprostol can be administered vaginally or orally to soften the cervix, although this indication is not approved by the Food and Drug Administration (FDA). Vaginal misoprostol (200 to 400μg) given 8 to 12 hours before surgery reduces the need for cervical dilation, decreases cervical complications, and reduces operative time in comparison with controls.27 Alternatively, oral misoprostol (400μg) can be given 12 and 24 hours before surgery to soften the cervix and make dilation easier.28 Side effects associated with misoprostol include lower abdominal pain and small amounts of vaginal bleeding.

Technique of Hysteroscopic Myomectomy

Techniques for removing pedunculated and submucosal myomas include avulsion, scissors, wire-loop resection with bipolar or monopolar equipment, vaporization, morcellation, and laser vaporization. In many cases, a combination of several techniques is required to facilitate complete removal. Initial techniques utilized large intrauterine graspers such as Corson graspers that avulsed myomas; however, without utilizing a hysteroscope, complete removal cannot be accurately determined.

In 1978, Neuwirth first reported the use of the monopolar urologic resectoscope for resection of submucosal myomas.29 Hysteroscopic wire-loop resection still remains the most popular method of removing myomas, but newer techniques are emerging.

The development of the continuous flow resectoscope permitted distension of the uterine cavity with fluid and removal of blood and debris. Further improvements in optics, video recording, bipolar technology, and uterine distension systems provided additional safety features for operative hysteroscopic procedures.

Performing operative hysteroscopic myomectomy requires four essential components:

Uterine Distension

To minimize intravasation of distension media, the lowest intrauterine pressure (i.e., intrauterine distension) should be used that allows a clear view. In many cases, an intrauterine pressure of 70 to 80 mm Hg will be adequate. In some cases, an intrauterine pressure of 100 to 150 mm Hg may be required for a limited period of time to obtain adequate visibility. Higher intrauterine pressures are acceptable as long as the maximum fluid deficits allowable for electrolyte or electrolyte-free solutions are not superseded.

The fluid deficit should be continuously calculated, preferably with an automated system. When electrolyte-free solutions are being used (i.e., glycine, sorbitol, or mannitol), the procedure should be discontinued when a fluid deficit of 1000mL is reached and serum electrolyte levels should be promptly obtained. When electrolyte solutions are used (e.g., saline) the procedure should be discontinued when a fluid deficit of 1500 to 2000mL is reached and a diuretic administered to decrease the risk of pulmonary edema.

Intermittently, the intrauterine pressure should be lowered to 30 mm Hg or the least amount of pressure that is possible. This rapid reduction in intrauterine pressure will aid in enucleation of the myoma, via a decompression mechanism that releases the encapsulated myoma from its myometrial bed. The myoma may appear to increase in size. In fact, more myoma protrudes into the endometrial cavity, allowing a more complete resection without having to resect myometrium.

The high intrauterine pressure created with automated fluid pumps, elevation of fluid bags, and compression of fluid medium with blood pressure cuffs may create an iatrogenic negative hysteroscopic view, in part by pushing the leiomyoma or other subtle lesions. Decreasing the intrauterine pressure frequently and repeatedly allows the full appreciation of the myoma size.

Special Techniques

Fertility Preservation

If the patient desires fertility, overzealous resection of the myometrium must be avoided. Asherman’s syndrome may occur when large portions of overlying endometrial tissue are resected with a sessile myoma. Patients who desire fertility and have multiple intracavitary myomas, especially those with myomas on opposite walls, may require resection on two separate occasions to minimize chances of intrauterine synechiae developing postoperatively.

For women wishing to maintain or preserve fertility who undergo large myoma resection or have resection of “kissing lesions,” many gynecologists will empirically administer high-dose estrogen in an effort to re-epithelize the endometrium and decrease the risk of intrauterine adhesions. A typical regimen is conjugated estrogen 0.625 to 1.25mg twice daily or estradiol 2mg twice daily for 25 days, followed by 12 days of medroxyprogesterone 10mg.

Another approach is to place a postoperative intrauterine stent. Either a pediatric catheter inflated with 15 to 20 cc or a balloon uterine stent specifically designed for this purpose may be inserted for 7 to 10 days to prevent the juxtaposition of the uterine walls.

A final approach is to perform office hysteroscopy within the first 7 to 14 days after extensive myomectomy to evaluate the endometrium for synechiae. If detected early, the adhesions are filmy and easily lysed with the distal tip of the hysteroscope. In some circumstances hysteroscopic visualization every 7 to 10 days may be required until regeneration of the endometrium is confirmed and filmy adhesions treated. When performed too late, dense fibrous adhesions may be encountered, requiring operative hysteroscopic adhesiolysis.

ENDOMETRIAL ABLATION

Endometrial ablation was developed as a minor surgical procedure to treat women with intractable heavy menses unresponsive to medical management who no longer desire fertility. Each year approximately 200,000 women undergo an endometrial ablation. Compared to hysterectomy, endometrial ablation offers the advantages of avoiding the morbidity and prolonged recovery associated with major surgery and allows conservation of the uterus.

In the past decade, methods for endometrial ablation have been developed that do not require hysteroscopy. In patients with relatively normal uteri, these nonhysteroscopic techniques have been found to be just as effective as hysteroscopic techniques, and appear to be safer and less technically demanding. Both traditional hysteroscopic and contemporary nonhysteroscopic methods for endometrial ablation are described here.

Preoperative Evaluation

A thorough preoperative evaluation is imperative because many serious diseases can present as abnormal uterine bleeding. The investigation and management of abnormal uterine bleeding is described in Chapter 21. A brief overview is given here to highlight the importance of a proper evaluation before a surgical procedure.

The evaluation begins with a detailed history, physical examination, and ultrasonographic imaging. Important laboratory tests for evaluation of women with menorrhagia include a pregnancy test, thyrotropin level, and complete blood count with platelet count. Many clinicians recommend a platelet function screen or a von Willebrand ristocetin cofactor. If the platelet function screen is abnormal, testing for von Willebrand’s disease is indicated. A recent study reported 47% of reproductive-age women with menstrual dysfunction were found to have a hemostatic abnormality such as platelet dysfunction, von Willebrand’s disease, or coagulation factor deficiencies.33

Risks

Complications of endometrial ablation are uncommon, and many are even less common with the newer ablative techniques compared to hysteroscopic techniques. The interoperative risks include fluid overload, uterine perforation, cervical lacerations, and bowel injury (see Table 42-2). These complications are more common in women undergoing traditional hysteroscopic ablation and resection techniques.

Postoperative complications include hematometra and infection. Prophylactic antibiotics are often used, but have not been shown to decrease the infection risk.

Delayed complications include continued bleeding heavy enough to require repeat ablation or hysterectomy. A concern in the early years of ablation was that the procedure might decrease the ability to make an early diagnosis of cancer of the endometrium by masking early bleeding. Although endometrial cancer has been reported after ablation, delayed diagnosis has yet to be documented. If a woman who has had an endometrial ablation later requires hormone replacement therapy, progesterone therapy is required because the remaining viable endometrium puts the patient at risk for hyperplasia or malignancy if unopposed estrogen is used.

Continued menstruation after ablation is not considered to be a complication. The reported amenorrhea rate is as high as 40% after hysteroscopic ablation and nonhysteroscopic methods. Endometrial ablation should only be offered to women who are willing to accept eumenorrhea, hypomenorrhea, or cyclic bleeding rather than amenorrhea as a final clinical result.

Endometrial Ablation Techniques

Currently there are eight different methods to perform endometrial ablation. The three first-generation hysteroscopic techniques include electrosurgical endomyometrial resection, electrosurgical rollerball ablation, and laser ablation.

Second-generation techniques, also referred to as global methods, were developed that do not use hysteroscopy to perform the ablation. Hysteroscopy is an integral part of only one of these systems (i.e., Hydro ThermAblator). However, many clinicians perform diagnostic hysteroscopy before using any of the global methods.

First-Generation Hysteroscopic Endometrial Ablation

In the early 1980s, endometrial ablation was established as an alternative to hysterectomy for treatment of menstrual dysfunction in women with intractable menorrhagia. Mimicking the physiologic effect of Asherman’s syndrome, the ultimate goals of endometrial ablation were to create severe endometrial scarification and secondary amenorrhea. Initially, Goldrath and colleagues reported laser endometrial ablation using the Nd:YAG laser fiber through the operating port of a hysteroscope. However, this method waned in popularity due to costs and riks of complications in less experienced hands.9

Endomyometrial resection utilizing a resectoscope was first reported by DeCherney and Polan in 1983.34 This technique utilizes unipolar electrocautery and is performed with hypotonic nonelectrolyte-containing distension media. This technique was the forerunner of hysteroscopic rollerball endometrial ablation, which has become the “gold standard” to which all emerging endometrial ablation technology is compared. This technique, which also uses a resectoscope, was popularized by Vancaillie in 1989.11 Each of these devices destroys the basalis layer of the endometrium and is designed to result in hypomenorrhea or amenorrhea.

Review of the first decade of hysteroscopic ablation revealed relatively good results as well as moderate difficulties. Cumbersome equipment, patient safety, need for highly trained operating room staff, hampered visibility, and both intraoperative and postoperative complications hindered widespread application of hysteroscopic endometrial ablation.

Technique of Hysteroscopic Rollerball Endometrial Ablation

The general concept of hysteroscopic endometrial ablation involves thorough destruction of the basalis layer, cornua, and lower uterine segment. Currently there are three methods available to perform hysteroscopic endometrial ablation: rollerball desiccation, endomyometrial resection and desiccation, and laser endometrial desiccation, although the latter technique is rarely used today. For this reason, only the first two techniques are reviewed here.

Systematic Plan of Ablation

Following a systematic surgical plan ensures optimal clinical outcomes. Excellent visualization of the entire uterine cavity and endocervix is imperative. All intrauterine landmarks are clearly delineated hysteroscopically before initiating the procedure. Once a panoramic view of the endometrium is accomplished, the surgeon should determine if there is any previously unrecognized pathology. If a subtle lesion is discovered, then a directed biopsy with a wire-loop electrode is performed and the specimen labeled and submitted separately.

Once the surgeon visualizes all of the landmarks, the lower uterine segment is cauterized circumferentially to mark the endpoint and lowest level of endometrial ablation therapy. Ablation of the endocervix is avoided to minimize the risk of cervical stenosis. Cervical stenosis can result in cyclic pain, dysmenorrhea and, in severe cases, hematometra.

After the lower uterine segment is identified and coagulated circumferentially, the cornua and fundal region are treated initially. The roller-ball is advanced to the fundus and then directed at the cornua utilizing a “touch technique” to desiccate the cornua. It must be remembered that the thinnest region of the uterus is at the cornua and cesarian section scars. Extra care must be taken to avoid forward pressure, which could cause perforation. The most challenging part is the fundus because the roller-ball cannot truly be rolled against the fundus.

Next the posterior wall, followed by the lateral walls and anterior walls, is treated. Traditional technique utilizes direct tissue contact, such that one half of the roller-ball is buried in the endomyometrial juncture. Always activate the foot pedal when the electrode is moving toward the surgeon. To avoid the risk of perforation, the surgeon should avoid any forward movement of an activated electrode to decrease the risk of burns to the pelvic viscera. Intermittently, the roller-ball may need to be cleaned and debris evacuated to provide optimal visualization.

At the conclusion of the endometrial ablation procedure, the intrauterine pressure is reduced to identify small bleeders, which may be treated with coagulation current.

Technique of Endomyometrial Resection

The technique of endomyometrial resection was pioneered by DeCherney and colleagues.10 The 90-degree wire loop, generally 3 to 4mm deep, is buried into the endometrium, and using 60 to 80 watts of pure cutting current, is advanced under direct view to the lower uterine segment. The endomyometrial junction is shaved off, creating crescent-shaped tissue fragments.

Causes of Endometrial Ablation Failure

The majority of patients who undergo endometrial ablation are satisfied with their clinical outcome; at least 90% will notice symptomatic improvement. However, 5% to 10% of patients may ultimately be required to undergo additional intervention, such as repeat ablation or hysterectomy.

The most frequently associated factors noted with endometrial ablation failures include the following:

Endometrial ablation outcomes can be improved by scheduling the procedure immediately after menses. The early proliferative phase yields better results than operating during the secretory phase. Pharmacologic pretreatment with danazol or GnRH analogues also improves outcomes.

Hysteroscopic endometrial ablation is an outpatient procedure associated with a rapid return to work, minimal complications, and high patient satisfaction. Approximately 20% to 60% of patients undergoing endometrial ablation with roller-ball techniques will achieve amenorrhea, 65% to 70% will become hypomenorrheic, and 5% to 10% will fail. Approximately 10% of patients treated by endometrial ablation will require a subsequent operation.35 Women receiving appropriate preoperative counseling may find this attractive in treating menstrual disorders.

GLOBAL ENDOMETRIAL ABLATION TECHNIQUES

Since December 1997, the FDA has approved the following five devices for endometrial ablation in the United States:

Table 42-3 lists the different devices and the specific patient characteristics. In theory, all these devices can be used in an office setting.

ThermaChoice UBT System

The ThermaChoice UBT System was the first of the second-generation endometrial ablation technology systems and received FDA approval in 1997. As such, it has the longest clinical data regarding outcomes of any second-generation technology. Initially, the device was made of a latex balloon and lacked an internal impeller; however, an evolution in the technology has occurred.

Currently, the device is packaged individually and consists of a single-use silicone balloon catheter with an internal impeller, umbilical cable, and reusable controller that monitors uterine pressure, temperature, and treatment time continually. A variety of anesthesia has been described with this technology, which includes general anesthesia, local paracervical block with intravenous sedation, and regional anesthesia.

After the cervix is dilated, uterine cavity length is determined and the balloon is inserted and filled with 5% dextrose in water (D5W). The physician observes the controller and continues to distend the balloon until the intrauterine pressure reaches 160 to 180 mm Hg, with a maximum instillation of 35mL. Most uterine cavities typically require 6 to 15mL. After the pressure stabilizes for 30 to 45 seconds, the treatment cycle begins. There is an initial warming cycle when the temperature reaches 87°C (188°F). The physician maintains the intrauterine pressure between 160 and 180 mm Hg by slowly adding more D5W as needed. Higher amenorrhea rates occur when the intrauterine pressure is maintained between 160 and 180 mm Hg during the entire treatment phase. Treatment is completed after 8 minutes, the controller terminates automatically, and the balloon is deflated, removed, and discarded. The physician can monitor temperature, treatment time, and intrauterine pressure continuously.

In the FDA trial, a 3-minute suction curettage was used before performing ablation with the ThermaChoice device. More recently, physicians have scheduled during the early proliferative phase or pretreated with GnRH analogues, oral contraceptive pills, or danacrine.

Recent modifications in the balloon, ThermaChoice III, have increased the performance and safety of the device. Enhancements include silicone material, deeper thermal injury, a distensible catheter that holds 35mL of fluid, and the ability to treat the lower uterine segment and cornua region more effectively. Recent clinical data support a better overall performance with respect to success or amenorrhea using the ThermaChoice III device compared to the ThermaChoice I.

Although not originally evaluated for use with myomas, case series have demonstrated efficacy with their presence.36 These data showed a significant and statistically similar reduction in menstrual blood flow and increase in hemoglobin values with no intraoperative complications.

With the ThermaChoice III device, the physician must constantly be engaged in the treatment cycle. Uterine contractions likely occur due to heating of the uterine cavity and often precipitously increase the intrauterine pressure. The surgeon should quickly respond to the rising pressure by opening the pressure valve, which releases a small amount of fluid to maintain the ideal pressure. The small catheter size requires little cervical dilation, which minimizes the risk of cervical laceration and uterine perforation. However, in the event of uterine perforation, the pressure drops abruptly, terminating treatment.

Safety features incorporated into the device abort the procedure if the pressure reaches 210 mm Hg or if the pressure is less than 45 mm Hg after device activation. If the temperature inside the balloon exceeds 95°C (203°F) for 2 seconds, or falls below 75°C (167°F) for 15 seconds, or is unable to reach 87°C (188°F) within 4 minutes of preheating, the controller automatically terminates the procedure.

HerOption Uterine Cryoblation Therapy System

The second global endometrial ablation technology approved by the FDA in April 2001 was the HerOption Uterine Cryoblation Therapy System. This technology uses a cryoprobe and proprietary compressed gas mixture that freezes the endometrium to below 100°C, thereby destroying the endometrial lining. It creates the largest depth of necrosis (9 to12mm) of the second-generation devices. In the FDA trial, patients were pretreated with a single dose of leuprolide acetate (3.75mg intramuscularly). The unit consists of a console, a cryoprobe, and disposable sheath that fits over the cryoprobe. FDA guidelines require continuous transabdominal ultrasound guidance to monitor progression of the ice ball created during the procedure.

The device requires only 5- to 6-mm dilation for insertion of the probe. After the probe is placed into the uterine cavity, ultrasound images are performed that confirm placement of the device within the uterine cavity. The unit then initiates a 3- to 5-minute prefreezing cycle is activated, which heats the tissue to 37°C. Saline solution is inserted into the device to clear air, and ablation begins. The FDA trial used one 4-minute freeze at the initial cornu treated. A short heat cycle follows each treatment to dislodge the adherent endometrium, followed by one 6-minute freeze at the opposite cornu. Ultrasound monitoring permits individualized monitoring based on progression of the ice ball. The unit terminates treatment automatically when a 10-minute treatment cycle occurs.

New treatment protocols incorporating additional treatment of the lower uterine segment may improve amenorrhea rates. No inherent safety mechanism exists to terminate the procedure automatically if perforation is suspected. Patients feel little pain and the procedure can be performed in the office setting. One of the key limitations is the difficulty in visualization of the uterus by ultrasound in obese patients.

Hydro ThermAblator (HTA) System

Also approved in April 2001, the Hydro ThermAblator is a software-controlled, hysteroscopic thermal-ablation system composed of an operational unit, heated canister, and sterile procedure set. Additionally, the system requires use of USP 0.9% sodium chloride solution and a small, rigid hysteroscope. Hydrostatic pressure maintains the intrauterine pressure between 50 and 55 mm Hg—below the threshold for opening the fallopian tubes—and provides a measure of safety.

During the priming phase, room-temperature saline solution circulates within the system for 2 minutes by way of a gravity-flow system. During the active-treatment phase, the heating element is activated. When the saline temperature reaches 80°C, the 10-minute treatment cycle is initiated, which increases the temperature to 90°C continually. After the treatment is completed, a cool-down period begins. After 1 minute, the post-treatment flush phase is completed and the device is withdrawn. This minimizes the risks of cervical, vulvar, and vaginal burns.

Safety features of the HTA, unlike other second-generation devices, include continuous hysteroscopic monitoring before, during, and after therapy. The turbulence of the endometrial debris and heated saline solution may create a compromised hysteroscopic view.

In the FDA trial, cervical ulcerations due to thermal damage were reported in 13% of patients and resolved within 1 month without additional therapy. Patients were treated with a double dose of leuprolide acetate (7.5mg intramuscularly) that was administered 3 weeks before ablation. Severe burns to the vagina or external genitalia have been reported with this device.

NovaSure Endometrial Ablation System

The NovaSure Endometrial Ablation System received FDA approval in September 2001. The NovaSure system consists of the disposable device, radiofrequency (RF) controller, CO2 canister, desiccant, footswitch, and power cord. The device delivers RF energy to treat the endometrial lining of the uterine cavity. The disposable device is inserted transcervically into the uterine cavity. The uterine cavity length (measured during sounding) and width (measured by the device) are key-entered into the RF controller to automatically calculate the power level required for treatment of the uterine cavity of the given size. By pressing the footswitch, the cavity integrity assessment cycle is initiated, and when the cavity integrity assessment test is successfully passed, the ablation cycle is then initiated by the second activation of the footswitch. The RF treatment time averages approximately 90 seconds.

The system monitors the tissue impedance (resistance) to the flow of electrical current continuously and stops the procedure when the impedance of 50 ohms is achieved. Neither concomitant hysteroscopic visualization nor endometrial pretreatment is required. The automatic cavity integrity assessment system is designed to determine whether a defect or uterine perforation is present, and the device position feedback feature allows detection of inadvertent insertion of the device into a false passage.

Advantages of the NovaSure device include the shortest treatment time compared to any other device, and unlike other devices, the FDA pivotal trials were performed at any time during the endometrial cycle and conducted without endometrial pretreatment with leuprolide or D&C. One disadvantage is that if overdilation of the cervix occurs, the CO2 integrity test may fail, and placement of an additional cervical tenaculum to occlude the cervix may be necessary.

Microwave Endometrial Ablation System

The Microsulis Microwave Endometrial Ablation System received FDA approval in September 2003. Microwave energy desiccates the endometrium hemispherically at a fixed high frequency of 9.2 GHz. The entire unit features a touchscreen interface with an embedded microprocessor, microwave generator, and two transmission cables (microwave and data cables).

Treatment consists of destroying the endometrium to a depth of 5 to 6mm, with temperatures during treatment rising to 70°C to 80°C. In the clinical randomized trial, all patients were treated with a GnRH agonist. Strict guidelines must be followed because of the potential for injury.

An integral component of the preoperative office evaluation requires transvaginal ultrasound measurement of the uterine myometrium. The myometrium must be at least 10mm thick to use this device. If GnRH therapy is used after the baseline myometrial measurements, a repeat ultrasound must be performed at least 10 to 14 days before surgery to ensure that use of GnRH did not adversely thin the myometrium to less than 10mm. The myometrial thickness should be recorded as a permanent component of the clinical record in the outpatient chart.

On the day of surgery, after the uterus is sounded and then dilated to 9mm, intraoperative hysteroscopy must be performed. Landmarks, including visualization of the fundus, endometrium, and tubal ostia, must confirm that there is no uterine perforation. A D&C should never be performed with microwave technology, because theoretically, it could thin the myometrium and predispose the patient to thermal injury.

During the initial 5 seconds of applicator placement, the temperature rise gate (TRG) calculates intrauterine temperature increase. If the rise in temperature is normal, the procedure is continued; otherwise, the procedure is aborted spontaneously. An abnormal TRG signals possible false passage or applicator perforation. The applicator is then placed near the fundus and moved from side to side until the temperature reaches 70°C. After fundal warming occurs, treatment of the remaining uterine cavity is undertaken by a series of movements of the applicator from side to side from the cornua to midendometrial body, until the endocervix is reached. A built-in computer link allows the physician to monitor the overall treatment. Total treatment time is usually 2 to 5 minutes.

Advantages of this system include brief treatment times, the highest level of amenorrhea in the intent-to-treat group in comparison with other ablation systems, and the ability to treat uterine cavities with lengths up to 14 cm.

PEARLS

REFERENCES

1 Schenk LM, Coddington CC3rd. Laparoscopy and hysteroscopy. Obstet Gynecol Clin North Am. 1999;26:1-22.

2 Gauss CJ. Hysteroskopie. Arch Gynaekol. 1928;133:18-24.

3 Neuwirth RS. Hysteroscopy and gynecology: Past, present, and future. J Am Assoc Gynecol. 2001;8:193-198.

4 Edstrom K, Fernstrom I. The diagnostic possibilities of a modified hysteroscopic technique. Acta Obstet Gynecol Scand. 1970;79:327-330.

5 Lindemann HJ. Eine neue Untersuchungsmethode fur die Hysteroskopie. Endoscopy. 1971;4:194-197.

6 Quinones R, Alvaredo-Duran A, Aznar-Ramos R. Tubal catheterization: Application of a new technique. Am J Obstet Gynecol. 1972;114:164-169.

7 Neuwirth RS, Amin HK. Excision of submucous fibroids with hysteroscopic control. Am J Obstet Gynecol. 1976;126:95-99.

8 Daly DC, Tohan N, Walters C, Riddick DH. Hysteroscopic resection of the uterine septum in the presence of a septate cervix. Fertil Steril. 1983;39:560-563.

9 Goldrath MH, Fuller TA, Segal S. Laser photovaporization of the endometrium in the treatment of menorrhagia. Am J Obstet Gynecol. 1981;140:14-19.

10 DeCherney AH, Diamond MP, Lavy G, Polan ML. Endometrial ablation for intractable uterine bleeding: Hysteroscopic resection. Obstet Gynecol. 1987;70:668-670.

11 Vancaillie TG. Electrocoagulation of the endometrium with the ball-end resectosope. Obstet Gynecol. 1989;74:425-427.

12 Loffer FD. Complications of hysteroscopy—their cause, prevention, and correction. J Am Assoc Gynecol Laparosc. 1995;3:11-26.

13 Cooper JM, Brady RM. Intraoperative and early postoperative complications of operative hysteroscopy. Obstet Gynecol Clin North Am. 2000;27:347-366.

14 Ahmed N, Falcone T, Tulandi T, Houle G. Anaphylactic reaction because of intrauterine 32% dextran-70 instillation. Fertil Steril. 1991;55:1014-1016.

15 Marlow JL. Media and delivery systems. Obstet Gynecol Clin North Am. 1995;22:409-422.

16 Corson SL, Brooks PG, Serden SP, et al. Effects of vasopressin administration during hysteroscopic surgery. J Reprod Med. 1994;39:419-423.

17 Bradley L, Widrich T. State-of-the-art flexible hysteroscopy for office gynecologic evaluation. J Am Assoc Gynecol Laparosc. 1995;2:263-267.

18 Nagele F, O’Connor H, Davies A, et al. 2500 outpatient diagnostic hysteroscopies. Obstet Gynecol. 1996;88:87-92.

19 Serden SP. Diagnostic hysteroscopy to evaluate the cause of abnormal uterine bleeding. Obstet Gynecol Clin North Am. 2000;27:277-286.

20 Apgar B, Dewitt D. Diagnostic hysteroscopy. Am Family Phys. 1999;46:19S-26S.

21 Perez-Medina T, Bajo-Arenas J, Salazar F, et al. Endometrial polyps and their implication in the pregnancy rates of patients undergoing intrauterine insemination: A prospective, randomized study. Hum Reprod. 2005;20:1632-1635.

22 Martin-Ondarza C, Gil-Moreno A, Torres-Cuesta L, et al. Endometrial cancer in polyps: A clinical study of 27 cases. Eur J Gynaecol Oncol. 2005;26:55-58.

23 Farquhar CM, Steiner CA. Hysterectomy rates in the United States 1990–1997. Obstet Gynecol. 2002;99:229-234.

24 Emanuel MH, Verdel MJ, Wamsteker K. A prospective comparison of transvaginal ultrasonography and diagnostic hysteroscopy in the evaluation of patients with abnormal uterine bleeding: Clinical implications. Am J Obstet Gynecol. 1995;172:547-552.

25 Wamsteker K, de Kruif J. Transcervical hysteroscopic resection of submucous fibroids for abnormal uterine bleeding: Results regarding the degree of intramural extension. Obstet Gynecol. 1993;82:736-740.

26 Bradley LD, Falcone T, Magen AB. Radiographic/imaging techniques for the diagnosis of abnormal uterine bleeding. Obstet Gynecol Clin North Am. 2000;27:245-276.

27 Preutthipan S, Herabutya Y. Vaginal misoprostol for cervical priming before operative hysteroscopy: A randomized controlled trial. Obstet Gynecol. 2000;96:890-894.

28 Thomas JA, Leyland N, Durand N, Windrim RD. The use of oral misoprostol as a cervical ripening agent in operative hysteroscopy: A double-blind, placebo-controlled trial. Am J Obstet Gynecol. 2002;186:876-879.

29 Neuwirth RS. A new technique for and additional experience with hysteroscopic resection of submucous fibroids. Am J Obstet Gynecol. 1978;131:91-94.

30 Phillips DR, Nathanson HG, Milim SJ, et al. The effect of dilute vasopressin solution on blood loss during operative hysteroscopy: A randomized controlled trial. Obstet Gynecol. 1996;88:761-766.

31 Goldenberg M, Zolti M, Bider D, et al. The effect of intracervical vasopressin on the systemic absorption of glycine during hysteroscopic endometrial ablation. Obstet Gynecol. 1996;87:1025-1029.

32 Indman PD. Use of carboprost to facilitate hysteroscopic resection of submucous myomas. J Am Assoc Gynecol Laparosc. 2004;11:68-72.

33 Philipp CS, Faiz A, Dowling N, et al. Age and the prevalence of bleeding disorders in women with menorrhagia. Obstet Gynecol. 2005;105:61-66.

34 DeCherney A, Polan ML. Hysteroscopic mangement of intrauterine lesions and intractable uterine bleeding. Obstet Gynecol. 1983;61:392-397.

35 Stabinsky S, Einstein M, Breen J. Modern treatments of menorrhagia attributable to dysfunctional uterine bleeding. Obstet Gynecol Surv. 1999;54:251-262.

36 Soysal ME, Soysal SK, Vicdan K. Thermal balloon ablation in myoma-induced menorrhagia under local anesthesia. Gynecol Obstet Invest. 2001;51:128-133.