Chapter 7.1 Abdominal Myomectomy. Operative Techniques

 Chapter 7 Myomectomy

GENERAL PRINCIPLES

Definition

■ Abdominal myomectomy is performed via a laparotomy incision and is also

referred to open myomectomy. It is the surgical removal of uterine

leiomyomas which leaves the uterus intact. Reproductive-aged patients

continue to have menstrual cycles and are able to theoretically able to

conceive following abdominal myomectomy.

■ Uterine leiomyomas are also called uterine fibroids, myomas, or

fibromyomas. They are benign proliferative, unicellular, wellcircumscribed, pseudoencapsulated, benign growths composed of smooth

muscle and fibrous connective tissue. They are the most common benign

growth of the uterus.

■ The pathogenesis of leiomyomas remains unknown. However, several

pathogenic theories may be associated with uterine fibroids including

genetic predisposition, epigenetic factors, estrogens, progesterone, growth

hormone factors, cytokines, chemokines, and extracellular matrix

components.

Differential Diagnosis

■ Adenomyosis

■ Adenomyoma

■ Leiomyosarcoma

■ Diffuse leiomyomatosis

■ Extrauterine pelvic tumors

■ Ovarian mass

■ Pregnancy

Anatomic Considerations

■ Leiomyomas are unique and symptoms vary among women. The prevalence

of uterine fibroids may approach 60% to 80%; however, the majority of

women are asymptomatic.

■ Asymptomatic women should be reassured and followed clinically.■ Thirty percent of women with fibroids may have significant symptoms.

■ The size of leiomyoma may range from a few millimeters to more than 20

cm.

■ The number of leiomyoma also varies. Most patients have fewer than 10

leiomyomas; however, several case reports of patients with more than 100

leiomyomas removed by abdominal myomectomy have been reported.

■ The weight of each leiomyoma varies. The largest removed by case report

was 65 kg.

■ Uterine fibroids may impact fertility via the following mechanisms:

■ Mechanical blockage of the fallopian tube

■ Abnormal vascularization of the uterus

■ Abnormal endometrial development

■ Chronic intracavitary inflammation

■ Increased uterine contractions

■ Distortion of the endometrial cavity

■ The FIGO classification system characterizes the variable anatomic

locations of fibroids.

■ These benign growths may be located within various regions within the

uterus and cervix including endocervical, intracavitary, submucosal,

intramural, transmural, subserosal exophytic, pedunculated serosal,

parasitic, and may prolapse through the cervix into the vagina.

■ Intramural fibroids are the most common location of fibroids. They

reside in the myometrium. They may be of varying size and number.

Proliferation of fibroids is associated with potential distortion of the

endometrial cavity or the external serosal surface.

■ Submucous leiomyomas are commonly referred to as intracavitary

fibroids. They are variably located within the endometrial cavity.

■ If they grow, they may efface the cervix and be seen in the internal

cervical os.

■ Complete protrusion and prolapse through the cervix may occur such

that the leiomyoma is seen dilating the ectocervix and be present

within the vagina. Vaginal myomectomy is ideal for prolapsing

leiomyomas.

■ Intracavitary fibroids may be associated with intense pelvic cramping,

leukorrhea, foul-smelling vaginal discharge, or aberrant menstrual

bleeding.

■ Intracavitary fibroids can be treated with hysteroscopic resection or

hysteroscopic morcellation.

■ Subserous leiomyomas grow on the outer uterine surface leading to an

irregular surface contour of the uterus.■ They may develop a pedicle of varying width.

■ Fibroids attached to a stalk are mobile and may cause torsion with

acute abdominal or intermittent abdominal pain. Fever may occur if

complete torsion and necrosis of the fibroid occur.

■ Most are asymptomatic and do not cause adverse pregnancy outcomes.

■ Exophytic fibroids may also attach to other peritoneal organs and

develop a collateral blood flow. They are called parasitic fibroids.

■ The more common attachments of parasitic fibroids include bowel,

omentum, and mesentery. Because these lesions are mobile, they may

also be confused with an adnexal mass or abdominal mass of unknown

etiology.

■ If they involve the broad ligament they are called intraligamentary

leiomyomas. This anatomic variant is associated with deviation of the

ureter. Much care must be taken when performing abdominal

myomectomy with intraligamentary leiomyomas to prevent transection

of the ureter.

■ The size, number, and location of fibroids are unique to each patient and

may be associated with a variety of clinical presentations including

menstrual dysfunction, bulk symptoms, pelvic pain, increased abdominal

girth, infertility, or pregnancy-related complications.

■ Menstrual complaints may include heavy menstrual cycles, anemia and pica

as a result of heavy menses, irregular bleeding, postcoital bleeding,

dysmenorrhea, leukorrhea, and passage of large clots, chronic or acute

anemia.

■ Bulk symptoms may include increased abdominal girth, back pain, early

satiety and cosmetic complaints from abdominal distention, constipation,

urinary frequency, urinary urgency, urinary retention, unilateral or

bilateral ureteral obstruction, and varying degrees of hydronephrosis.

■ Pain including dysmenorrhea and dyspareunia.

■ Enlarging uterus may also lead to an inability to visualize the cervix,

making pap test, saline infusion sonography, and endometrial biopsy

difficult.

■ Reproductive-associated symptoms include infertility, recurrent

miscarriage, premature delivery, preterm delivery, and abdominal pain

during pregnancy due to leiomyoma degeneration.

■ Degenerative changes may be seen within the fibroid including:

■ Hyaline degeneration—this represents the most common type of

degeneration and is caused by excessive overgrowth of fibrous elements.

■ Cystic degeneration occurs after hyaline degeneration and results in

myxomatous changes with the development of multiple cystic cavities

within the fibroid.■ Necrosis occurs with impaired blood flow to the fibroid. This is most

often seen in pregnancy. The gross specimen when opened has a dull

reddish color and is due to aseptic degeneration associated with local

hemolysis.

■ Mucoid degeneration is associated with fibroid that are greater than 8

cm. This occurs more often with impaired arterial inflow to the fibroid.

■ Infectious degeneration is more often associated with pedunculated

leiomyomas.

■ Calcific degeneration more commonly seen in postmenopausal women.

■ Sarcomatous degeneration is rare and occurs in up to 1/300 women

undergoing surgery.

■ Women desirous of pregnancy and who have indications for surgery should

have the most minimally invasive uterine-sparing procedure performed by a

skilled gynecologist.

■ Size, number, and location of uterine leiomyoma determine which surgical

procedure may be recommended and surgical skill set required.

■ These factors influence surgical approach, specifically whether a vaginal,

hysteroscopic, abdominal, mini-laparotomy, laparoscopic, or robotic

myomectomy is advisable.

■ Individual characteristics of uterine fibroids also influence length of

surgery, surgical risks, intraoperative and postoperative blood loss,

infectious morbidity, complications, and risk of recurrence.

■ Surgical intervention may be indicated in patients with:

■ Failed medical therapy for the treatment of symptomatic disease

■ Intracavitary distortion leading to infertility or recurrent miscarriage

■ Unrelenting abdominal pain due to acute leiomyoma torsion,

degeneration, or vaginal prolapse

■ Failure of medical therapy for intractable or heavy menstrual dysfunction

■ While uncommon, obstruction of ureters, renal insufficiency, marked

hydronephrosis, or acute urinary retention may predispose to

intervention

■ Concern for leiomyosarcoma

Nonoperative Management

Hysterectomy has been the traditional therapy offered to women with uterine

fibroids, increasingly women are interested in less invasive therapy. Women

with minimal fibroid symptomatology are advised to consider “watchful

waiting” or monitoring that can include periodic clinical examination,

imaging, and journaling of their symptoms. The frequency of office visits and

testing should be based on clinical symptoms. Nonoperative management and

alternative to hysterectomy procedures such as uterine fibroid embolization(UFE) and endometrial ablation options are only for women who do not

desire future fertility but request uterine sparing procedures. Medical therapy

including hormonal therapy, levonorgestrel intrauterine device, tranexamic

acid, NSAIDs, and GnRH agonist therapy are well suited for women who wish

to retain their fertility.

However, quality-of-life (QOL) indicators must be considered in women

with uterine fibroids and clinicians inquire about them as they may help to

determine whether nonoperative management, watchful waiting, or surgical

intervention is needed. The patient should be queried about QOL-related

factors including:

■ Fears about her health

■ Impact on her relationships

■ Emotions

■ Sexual functioning

■ Body image

■ Loss of control

■ Hopelessness

A recent survey of 968 reproductive-aged women noted:

■ Patients waited 3.6 years before seeking treatment

■ 41% saw >2 health providers for diagnosis

■ 28% missed work due to leiomyoma symptoms

■ 24% believed that symptoms prevented career potential

■ 79% expressed desire for treatment that does not involve invasive surgery

■ 51% desired uterine preservation

■ 43% wanted fertility preservation if they are less than 40 years of age

Nonextirpative uterine surgery should be considered for all women who

desire pregnancy. Women of the African diaspora have the highest prevalence

and burden of fibroid-related disease.

■ Additionally, they have the greatest progressive symptomatology, younger

age of onset, greater size, and number of fibroids when compared to other

ethnic groups.

■ The etiology and genetic predisposition for this racial difference are

unknown.

■ In certain geographic regions in the United States, the incidence of

leiomyomas among women of the African diaspora is three to four times

that of Caucasian women.

Uterine fibroid embolization (UFE) is a minimally invasive outpatient

procedure performed by an interventional radiologist for the treatment of

symptomatic uterine fibroids in women who do not desire fertility yet desireuterine preservation. Treatment is performed under conscious sedation and

does not require an abdominal incision. Embolization results in ischemic

infarction of the leiomyomata and decreased vascularity. Normal

myometrium is spared.

Within 4 to 6 months the uterine fibroid diminishes in size, the fibroids

undergo hyaline degeneration, and the volume and size of the uterus

decrease. Shrinkage may continue up to 1 year after UFE. Among women

with >90% fibroid infarction, there is more symptom relief and fewer

subsequent treatments than in women with a lower infarction rate.

Magnetic resonance-guided focused ultrasound (MRgFUS) is a noninvasive

outpatient treatment option for symptomatic uterine fibroids. It was approved

by the FDA in 2004 for the treatment of uterine fibroids. Its labeling includes

use for women who desire pregnancy. MRgFUS is an outpatient procedure

that takes 2 to 4 hours and is performed under conscious sedation without an

abdominal incision.

The objective of MRgFUS is to deliver focused high-energy ultrasound

waves into the fibroid causing thermal coagulation of targeted tissue. With

the patient lying prone, the ultrasound waves are focused by lenses or

reflectors and pass through the skin and nontarget tissue and delivers

sonications (heat) to targeted fibroids. It has been compared to the principle

of focusing the sun’s rays with a magnifying glass to burn a hole in a piece of

paper.

Preprocedural magnetic resonance imaging (MRI) is required to determine

suitable candidates for MRgFUS. Fibroids most amenable to MRgFUS

treatment are those that are homogeneous and hyperintense (dark) on T2-

weighted images. They should also enhance because degenerated/infarcted

fibroids have lost their blood supply and will not respond to treatment.

Contraindications to MRgFUS include:

■ Patients with pacemakers

■ Prior UFE

■ Sensitivity to MR contrast agents

■ Severe claustrophobia

■ Patient’s body habitus exceeds the limitations of the MRI scanner

■ Pedunculated fibroids

■ Adenomyosis

■ Abdominal scarring with bowel in the pathway of the ultrasound beam

■ Intrauterine device (it would have to be removed prior to the procedure)

■ Obese patients may have too much subcutaneous fat such that the fibroid

would be out of the range of the ultrasound beam.

■ The ultrasound focus depth is limited to 12 cm for the standard protocols

or to 7 cm if enhanced sonications are performed.■ If the fibroid is out of these ranges due to obesity, then MRgFUS will not

be successful.

■ When compared to UFE there were more women excluded from MRgFUS.

In fact, in one enrollment study, only 14% of women qualified for

participation into. Limitations of the procedure include patients with

multiple abdominal scars. Numerous scars may make it difficult to

determine a safe pathway for treatment in order to avoid bowel, bladder,

or pelvic adhesions. Dominant fibroids greater than 8 to 10 cm may take

too long to sonicate in one setting.

Risks are very low but reports of skin burns to the abdomen, damage to

structures near the fibroid, nerve stimulation causing temporary back or leg

pain, and DVT.

Reported outcomes of MRgFUS include:

■ Pelvic pain and pressure resolve most quickly

■ Decrease pressure on the bladder

■ Improvements in menstrual bleeding may take 4 to 6 months

■ QOL indicators improved (heavy menstrual bleeding, nonbleeding

symptoms of fibroids and QOL impact)

■ Patients with fibroids that have the lowest signal intensity have better

symptom relief and demonstrated a higher technical success.

Tranexamic acid is an oral, nonhormonal, antifibrinolytic medical therapy

used only during menstruation in women with symptomatic fibroids–related

ovulatory heavy menstrual bleeding. Women with heavy menstrual periods

reportedly have high fibrinolytic activity due to increased endometrial levels

of plasmin and plasminogen activators. Tranexamic acid works by reversibly

blocking lysine binding sites on plasminogen, thus preventing plasmin from

interacting with lysine residues on the fibrin polymer, causing subsequent

fibrin degradation.

Tranexamic acid has been available for more than 40 years in clinical

practice and often is prescribed as an over-the-counter therapy in many

countries. In the United States, it requires a prescription. The recommended

dose is: tranexamic acid 650 mg, take two tablets by mouth every 8 hours, to

commence with the onset of menstrual bleeding for a maximum of 5 days. Its

onset of action is rapid but requires every 8 hours dosing due to short halflife. Eliminated through the kidneys, it has a half-life of 2 to 3 hours.

Tranexamic acid reduces menstrual blood loss (MBL) by 26% to 60%.

Numerous studies demonstrate that it is an effective treatment of heavy

ovulatory menstrual bleeding in women with uterine fibroids; has low sideeffect profile, favorable safety profile, and is well tolerated by patients.

Thromboembolic events have not been reported with oral treatmentregimens for the treatment of heavy menstrual bleeding. When compared to

placebo, NSAIDs, or oral cyclical luteal phase progesterone, tranexamic acid

significantly improved QOL. Levonorgestrel-releasing intrauterine system

reduced mean blood loss more than tranexamic acid in clinical trials.

Tranexamic acid should not be prescribed to women with prior history of

embolic disease, active thromboembolism, intrinsic risk for thrombosis, or

currently using hormonal therapy.

Gonadotropin-releasing (GnRH) analogs (Lupron [TAP Pharmaceutical

Products, Inc. Lake Forest, IL] may be considered for short-term use in

women with symptomatic uterine fibroids and as adjunct to surgical therapy.

GnRH agonists decrease uterine size and myoma volume by decreasing levels

of estrogen and progesterone to menopausal values. They induce myoma

degeneration, cause hyaline degeneration, decrease in the size of leiomyoma

cells, reduce extracellular matrix, and decrease blood flow to the uterus.

When used for short duration (<6 months), most women become temporally

amenorrheic, have improvement in hemoglobin, and notice a decrease in

uterine size by 40% to 60%.

GnRH analogs are often beneficial to women 50 years old or older. GnRH

therapy given for 6 months will stop menstruation with improvement in bulk

symptoms and cessation of menstruation. After 6 months of therapy, GnRH is

stopped and the patient monitored for transition into natural menopause. If

symptoms recur and patient has not entered menopause, then another 6

months of GnRH therapy instituted. Quite often these patients will enter

natural menopause and not require surgical intervention and avoid surgery if

menopause occurs shortly after completion of therapy.

Ulipristal is not currently available in this country; however, clinical trials

are underway. Promising research in Europe has demonstrated the benefits of

Ulipristal. Ulipristal is a synthetic steroid derived from 19-norprogesterone. It

is a selective progesterone receptor modulator that binds to progesterone

receptors. It exerts antiproliferative, pro-apoptotic, and antifibrotic action on

leiomyoma cells. The binding and antagonist potency with glucocorticoid

receptors is reduced compared to mifepristone.

■ Recent randomized controlled trials comparing Ulipristal to placebo and

Lupron have shown a statistically significant improvement in leiomyoma

size, QOL indicators, and decrease in fibroid and uterine volume.

■ After 13 weeks, Ulipristal controlled uterine bleeding in 91% of 96

women who received Ulipristal 5 mg/d and uterine volume decreased

21%.

■ Compared to 92% of 98 women who took 10 mg/d and uterine volume

decreased 12%.

■ Compared to 19% of 48 women who took placebo and had improvementof uterine bleeding with a 3% increase in uterine volume.

Levonorgestrel Intrauterine System

Increasingly, women with uterine fibroids, that do not distort the endometrial

cavity and with a uterine size of less than 12 to 14 gestation weeks, with

heavy bleeding have been rigorously evaluated. Improvement in primary

outcome of patient-reported scores has noted improvements in domains

(practical difficulties, social life, family life, work and daily routine,

psychological well-being, and physical health). Dysmenorrhea improved in

women using levonorgestrel intrauterine system. Menstrual blood flow

decreased and 20% to 40% of women experience amenorrhea. More women

using levonorgestrel intrauterine systems continued with therapy compared to

routine medical therapy. Low rates of surgical intervention were noted.

IMAGING AND OTHER DIAGNOSTICS

■ Several imaging modalities exist to detect uterine fibroids including

transvaginal ultrasound (TVUS), saline infusion sonography (SIS), and MRI

with gadolinium contrast. Less commonly is CAT scan employed.

■ Most patients have an initial TVUS which can differentiate a pelvic mass

from a pregnancy, adnexal mass, or uterine fibroids. However, results may

be inconclusive in some patients. Transvaginal ultrasound alone may miss

one-sixth intracavitary lesions in reproductive-aged women. This author

believes that saline infusion sonography should be performed when the

patient has complaints of heavy menstrual bleeding, intermenstrual

spotting, leukorrhea, or recurrent pregnancy loss, as it is more sensitive in

detecting intracavitary pathology.

■ Fortunately, the cost differential between TVUS and MRI is decreasing, thus

making MRI more accessible to more patients and physicians who care for

women with fibroids.

■ MRI with gadolinium contrast is the preferred imaging modality for

abdominal myomectomy. It is more definitive in determining the size,

number, and location of uterine fibroids, as well as how far from the

serosal edge the myoma is located. Additionally, the lateral and posterior

aspects of the pelvis can be better differentiated with MRI than with TVUS.

■ When intracavitary fibroids are larger than 3 to 4 cm, it may be difficult

to distend the uterine cavity with SIS. In these situations, MRI of the

pelvis is advised.

■ MRI can differentiate an adnexal mass from exophytic fibroids and is

possible with MRI of the pelvis.

■ Cervical fibroids can be better delineated with MRI.

■ MRI of the pelvis can differentiate cellular degenerative changesincluding calcification, necrosis, and possible sarcomatous changes.

PREOPERATIVE PLANNING

■ The patient should have a CBC with platelets, type, and screen available,

and a negative pregnancy test on the day of surgery.

■ If the blood loss is expected to be greater than 500 mL, consider using cell

saver intraoperatively, consider perioperative autologous blood donation,

and correct anemia.

■ Short-term use of preoperative GnRH therapy considered in women who

have symptomatic anemia and fail hormonal therapy or is contraindicated.

■ Short-term use of GnRH therapy effectively stops menstrual cycles and

improves anemia. Surgery can be scheduled once anemia has resolved.

■ Short-term use of GnRH therapy considered in patients with anemia and

who refuse blood products. Surgery is scheduled once anemia resolves.

■ Moderate anemia can be improved with oral, IV iron therapy, iron rich

foods, and supplementation with Vitamin C.

■ A consult with blood management is helpful in patients who do not

tolerate oral iron therapy.

■ Iron stores can be repleted promptly with IV iron.

■ Preoperative informed consent is critical. When possible the patient’s

partner or family member should be available for the consultation, with

patient permission. Several components of informed consent must be

discussed and documented:

■ Risk of conversion to hysterectomy:

■ Risk of intraoperative conversion to hysterectomy when diffuse

leiomyomatosis is encountered.

■ Massive intraoperative or postoperative blood loss.

■ Inability to reconstruct the myometrial cavity.

■ Risk of conversion to hysterectomy if a large cervical leiomyoma is

encountered. Removal of broad lower uterine segment fibroids may

detach the cervix or amputate the cervix from the body of the uterus.

■ Intraoperative frozen section reveals leiomyosarcoma.

■ Need for intraoperative or post-operative blood or blood product

transfusion.

■ Risk of postoperative infection and prolonged hospitalization.

■ Risk of ureter injury when a leiomyoma involves the broad ligament or

cervical leiomyoma with distortion of the anatomic pathway of the ureter.

■ Informed consent should also document risk of recurrence, subsequent

infertility, need for C/section, uterine dehiscence/uterine rupture in

pregnancy, postoperative adhesion formation, bowel obstruction, and moredifficult abdominal surgery in the future as a result of postoperative

adhesions.

■ Additional preoperative planning essentials:

■ If the fibroid distorts and abuts or enters the endometrial cavity, removal

must be judicious. Care taken to avoid removal of endometrium

immediately adjacent to the fibroid. Removal of the endometrium may

lead to hypomenorrhea, secondary amenorrhea, and intrauterine

synechiae and infertility.

■ Placement of an intrauterine Foley catheter filled with methylene blue

dye or intrauterine manipulator helps to identify entrance into the

endometrial cavity.

■ If the endometrium is entered, it must be closed separately from the

myometrium.

■ Consider postoperative hysteroscopy to evaluate the endometrium and

exclude intrauterine adhesions.

■ It is imperative to determine if there are intracavitary fibroids present

prior to abdominal myomectomy, especially in women with large

intramural or subserosal fibroids.

■ If the endometrium is ill-defined, nonvisualized, or incompletely seen

with preoperative imaging, diagnostic office hysteroscopy

preoperatively should be performed to exclude intracavitary

leiomyoma.

■ If office hysteroscopy is not available, then intraoperative diagnostic

hysteroscopy should be performed prior to performing the abdominal

myomectomy (same day of surgery).

■ Detection of tubal patency with preoperative hysterosalpingogram (HSG)

is of equivocal use. There have been cases of tubal obstruction noted

perioperatively but resolved when HSG was performed after abdominal

myomectomy.

■ It is the opinion of this author that preoperative HSG is not useful and

would not change recommendation for abdominal myomectomy.

■ Assisted reproductive technology may be indicated for tubal occlusion.

■ Endometrial biopsy should be performed prior to abdominal myomectomy:

■ To exclude leiomyosarcoma

■ There is an increased risk of endometrial hyperplasia in women with

uterine fibroids.

■ Higher concentration of estrone and estradiol sulfatase activity has

been observed in the endometrium overlying a leiomyoma.

■ Cystic, simple, and complex endometrial hyperplasia has been reported

in women with uterine fibroids.

■ While office endometrial biopsy is helpful, remember that the sensitivity ofdetecting endometrial pathology is less in women with increased

endometrial circumference, uterine size, or uterine sounding length. This is

especially true in women with a uterine sounding length of greater than 12

cm.

SURGICAL MANAGEMENT

■ Abdominal myomectomy is indicated in women with symptomatic uterine

fibroids. Generally intramural and subserosal fibroids that cannot be treated

with the laparoscopic or robotic approach are selected for open

myomectomy.

■ Some patients with submucosal and intramural fibroids that protrude into

the endometrial cavity are treated with abdominal myomectomy.

■ Patients with an intracavitary leiomyoma that cannot be removed with a

one-staged hysteroscopic procedure (usually size >5 cm) may be treated

with an abdominal myomectomy approach.

■ Surgical management of uterine fibroids is dictated by fibroid size, number,

direction of growth, location, patient’s desire for definitive treatment and

invasiveness of treatment, and surgeon’s clinical expertise.

■ Recent concerns have been raised about the potential of

leiomyosarcomatous changes within uterine fibroids.

■ There is no set of testing that has high sensitivity in detecting sarcoma

preoperatively, except for preoperative endometrial biopsy that

demonstrates malignancy. However, MRI of the pelvis with and without

contrast, LDH isoenzymes, and gross pathology can increase the suspicion

of malignant degeneration.

■ Leiomyoma sarcomatous changes are defined by mitotic index (>10

mitotic figures per 10 high-power fields, presence of nuclear

hyperchromatism, nuclear pleomorphism, giant cells, and other bizarre

cell form changes).

■ There are no national consensus guidelines for recommending abdominal

myomectomy. However, the following clinical scenarios provide a practical

clinical guide to recommend abdominal myomectomy to women:

■ Symptomatic patients with bulk symptoms, abnormal bleeding, and

cosmetic concerns from increased uterine size.

■ Patients who do not meet inclusion criteria for minimally invasive

options including laparoscopic or robotic myomectomy approach.

■ Patients who do not have access to physicians who perform minimally

invasive myomectomy.

■ More than five uterine fibroids with variable individual size

■ Potential difficulty in reconstruction of the uterus with a laparoscopic or

robotic approach in patients desirous of pregnancy■ Large fibroids in the broad ligament that distorts the ureter

■ MRI pelvic imaging that is highly suggestive of hyaline degeneration

with extensive liquefaction or gelatinous material that would be difficult

to extract with minimally invasive techniques.

■ Extensively calcified leiomyoma that coexist more frequently with

pedunculated subserous leiomyoma. Extensive degeneration of intramural

fibroids may create a “womb stone” more often predisposed to older

women and women from the African diaspora.



Figure 7.1.1. Satinsky clamp on ovarian vessels.

■ Abdominal myomectomy is contraindicated:

■ with coexisting endometrial cancer, cervical cancer, or known

leiomyosarcoma.

■ with fibroids that enlarge and become symptomatic in menopause.

■ Controlling intraoperative blood loss is essential during abdominal

myomectomy. The uterine anatomy and access to the uterine arteries may

dictate choice of technique.

■ Average blood loss for abdominal myomectomy varies between 200 and

800 mL. The risk of blood transfusion is 2% to 28%. Options to decrease

intraoperative bleeding include:

■ Perioperative and intraoperative administration of intravenous

tranexamic acid

■ Intramyometrial injection of a dilute solution of vasopressin

■ Temporary occlusion of the infundibular pelvic ligament blood vessels

with Satinsky clamps (Figs. 7.1.1 and 7.1.2)

■ Tourniquets placed around the uterine arteries when feasible (Figs. 7.1.3

and 7.1.4)

■ Preoperative use of GnRH agonist for women with anemia. Some authorsbelieve that routine use should be avoided as it may distort the cleavage

planes and make enucleation of fibroids more difficult.

■ Perioperative uterine artery embolization



Figure 7.1.2. Satinsky clamps occlude infundibular ligaments.



Figure 7.1.3. Red rubber catheter. Tourniquet around the lower segment.

Positioning

■ The patient should be placed in the dorsal lithotomy position with the legs

appropriately positioned and padded in Allen stirrups.

■ Foam padding should be placed next to the patients’ knees.

■ PAS stocking should be placed prior to the induction of anesthesia.

■ The arms should be placed horizontally on arm boards.

Approach

■ There are no universal guidelines or high-quality data for the use ofprophylactic antibiotics for abdominal myomectomy. Despite the lack of

guidelines, this author utilizes preoperative and additional dosing if surgical

case is greater than 4 hours of blood loss >1.5 L in order to avoid pelvic

infection. This is important for women who desire pregnancy as pelvic

infection may compromise future pregnancy.

■ The team huddle is performed with the patient, nursing, entire surgical

team, and anesthesia to discuss the proposed surgery.

■ This team huddle should outline anticipated length of surgery,

anticipated blood loss, need for antibiotic prophylaxis, and answer

patient-centered concerns.



Figure 7.1.4. Red rubber catheter. Close-up of tourniquet.

■ Confirm that all needed instrumentation is available.

■ If cell saver will be used, then the blood bank team is also included in the

discussion.

■ After induction of anesthesia and legs appropriately placed, an abdominal

bimanual and rectal examination performed.

■ Uterine mobility should be accessed and will aid in the determination of the

abdominal incision.

■ This author advocate’s placement of an intrauterine Foley catheter (10- to

30-cc balloon) filled with a dilute solution of methylene blue dye. If the

endometrial cavity is entered, the blue color of the Foley can be seen and

palpated confirming entrance into the endometrium.

■ Alternatively, a uterine manipulator be placed and methylene blue dye

can be administered through the cannula to determine if the endometrial

cavity has been entered.

■ Occasionally it is difficult to determine the boundaries of the endometrial

cavity once extensive myomectomy has been performed.■ The ability to palpate the intrauterine Foley catheter confirms that the

endometrium has not been entered.

■ Or if the Foley catheter is seen, it can be deflated slightly to close the

endometrial cavity, taking care not to incorporate the Foley catheter

into the suture. As long as the Foley catheter fluid contact remains

intact, the surgeon can be confident that the endometrium is not

compromised.

■ It is important that the endometrial cavity not be incorporated into the

myometrial closure; otherwise, menstrual aberrations including

secondary amenorrhea, hematometria, or secondary infertility may occur.

■ Exploration of the upper and lower abdominal cavity performed to

determine the mobility of the uterus exclude parasitic fibroids, presence

of adhesions, endometriosis, adnexal masses, or unanticipated pathology.

■ When possible the uterus is exteriorized from the peritoneal cavity and

an assessment of the number of fibroids and locations of the fibroids

ascertained.

■ Self-retaining retractors are not routinely used as exteriorization of the

uterus provides ample anatomic exposure.

■ The use of uterine artery tourniquets, placement of Satinsky clamps, or

the use of myometrial vasopressin injection is individualized.

■ Minimal use of peritoneal packing decreases the risk of postoperative

adhesions.

■ Traumatic instruments such as Kocher clamps and forceps with teeth on

the serosa should be avoided. Rather, smooth pick-ups utilized on the

serosa to minimize serosal trauma.

■ Meticulous hemostasis should be evident at the end of surgery.

■ Adhesion barriers should be considered at the conclusion of the surgery

to decrease risk of postoperative adhesions.Procedures and Techniques (Video 7.1)

Perform time out and place mechanical PAS stocking for

thromboprophylaxis

Administer IV tranexamic acid for cases with anticipated blood loss of >500

mL

■ Tranexamic acid 10 mg/kg/dose, in NaCl 0.9% in 100 mL (Cyklokapron)

■ Loading dose given intravenously 15 minutes prior to incision in the operating

room. Maximum infusion rate of 100 mg/min.

■ Intraoperative maintenance dose, tranexamic acid 1,000 mg in NaCl 0.9% 100

mL (Cyklokapron), 1 mg/kg/hr, with maximum total dose 1 g. Use

intraoperatively only and stop infusion at the end of surgery.

■ Tranexamic cannot be used in patients with prior embolic phenomena or who

currently are receiving anticoagulation.

■ Misoprostol (400 mcg) intravaginally or rectally 1 hour prior to surgery.

Administer antibiotics at the induction of anesthesia

Place patient in Allen stirrups

Perform examination under anesthesia

Surgical prep

■ The patient’s mons pubis hair should be clipped in the operating room prior to

the abdominal prep.

■ A wide surgical prep including the abdomen, mons pubis, vulva, vagina, cervix,

mid-thigh, and buttock. The extent of the prep will be dependent upon whether a

low-transverse abdominal incision, vertical incision, or incision that extends above

the umbilicus is utilized.

Sterile draping and additional considerations

■ Sterile drapes placed to cover the abdomen and perineum.

Foley bladder catheter placement

■ Insert a continuous indwelling bladder Foley catheter for continuous

measurement of urine output.

Diagnostic hysteroscopy (if applicable)

■ Ideally the endometrium should be evaluated prior to abdominal myomectomy.However, if preoperative evaluation demonstrated an ill-defined endometrium,

poorly visualized endometrium, or inconclusive imaging of the endometrium, then

diagnostic hysteroscopy should be performed in the OR if it was not performed

in the office.

■ Diagnostic hysteroscopy excludes coexisting intracavitary fibroids or polyps

and should be removed during surgery.

■ Occasionally uterine enlargement and cervical distortion prevent office

hysteroscopic evaluation of the endometrium.

■ In the OR, a small rigid or flexible diagnostic hysteroscope can be used to

evaluate the endometrium. Attach sterile IV tubing to the hysteroscope and

manually infuse saline via 60-mL syringes for uterine distension.

■ If an intracavitary fibroid is identified, this author recommends its removal at

the time of the abdominal myomectomy by opening the endometrial cavity,

rather than performing hysteroscopic myomectomy with the abdominal

myomectomy. The endometrium is reapproximated by repairing the

myometrium at the interface of the uterine cavity and endometrial cavity with a

running or interrupted suture of 3-0 polydioxanone (PDSTM) avoiding

placement of suture in the endometrial cavity.

■ If an endometrial polyp is detected, then the endometrial cavity can be opened

and polyp removed concomitantly at the time of myomectomy, and cavity

closed (as previously discussed).

■ This step can be avoided if office or outpatient endometrial evaluation is negative

for intracavitary pathology. Otherwise proceed to the placement of the intrauterine

Foley catheter as described below.

Intrauterine Foley catheter placement

■ Place a heavy-weighted speculum or open-sided speculum in the vagina to

visualize the cervix.

■ Grasp the cervix with a single-toothed tenaculum, dilate the cervix with Hegar

dilators of size 4 to 6, enough to accommodate a 12- to 16-French intrauterine

Foley catheter.

■ Use a Foley with a balloon that can expand to 10 to 30 mL. If the uterine cavity

is greater than 12 cm, it is helpful to employ a Foley catheter guidewire to

atraumatically guide and place the Foley in the uterine cavity until the fundus is

reached.

■ Mix one ampule of methylene blue diluted with 50 cc of saline. After the

intrauterine Foley catheter is placed, distend the balloon with the methylene

blue solution until resistance is met.

■ With extensive myometrial dissection and multiple myometrial defects,

sometimes it is difficult to discern if the endometrium is entered. Placement of

a distended intrauterine Foley balloon helps identify endometrial landmarks.The author recommends this technique because it confirms entrance into the

endometrial cavity if it occurs.

■ The distended balloon can be palpated during the myomectomy alerting the

surgeon when in close proximity to the endometrium. If the surgeon is not

sure of landmarks, the balloon can be further distended or deflated providing

a tactile guide to determine the proximity of the endometrium.

■ If the pigmented blue tinged balloon is seen, it confirms that the endometrial

cavity has been entered during the procedure.

■ Additionally, if suture is inadvertently placed during myometrial closure in the

endometrial cavity, the punctured balloon will rupture and dissipate the darkly

pigmented methylene blue in the surgical site, providing visual feedback that

the endometrial cavity has been breached and corrective measures taken to

ensure that the endometrial cavity is not obliterated during myometrial

closure.

■ At the conclusion of the procedure, gently retract or pull the intrauterine

Foley. If it is still intact, it will not slip out of the cervix and confirms that the

endometrial cavity has not been entered or compromised.

■ If the intrauterine Foley ruptures, consider diagnostic hysteroscopy after

myometrial closure to exclude suture within the endometrium.

Surgical incision

■ Depending upon the size of the uterine fibroid, the mobility of the uterus, or prior

abdominal surgical incisions, a Pfannenstiel incision, Maylard incision, or vertical

abdominal incision is made. This author prefers the Maylard incision when the

uterine size is greater than 15-week gestational weeks and limited uterine mobility

noted under anesthesia. This muscle splitting incision provides excellent lateral

visualization.

■ If the patient has had a prior vertical incision, then that incision may be used.

■ Traditional entrance and safeguards are taken to enter the peritoneal cavity.

Exploration of the abdominal cavity

■ Once the peritoneal cavity has been entered, the surgeon should determine, if

the uterus is mobile, the presence of adhesive peritoneal disease, determine if

there are adnexal masses, endometriosis, or unanticipated surgical findings.

■ If the uterus is mobile, it should be elevated out of the peritoneal cavity.

■ Advise the anesthesiologist that the uterus is being elevated out of the uterine

cavity, especially if it is over 20 weeks gestational size, because changes in the

hemodynamic state can occasionally occur when pressure is taken off of the

great vessels.

■ If uterine mobility limits extirpation of the uterus, then leave the uterus in the

pelvis and extracts as many fibroids until uterine mobility permits exteriorization ofthe uterus and removal of remaining fibroids.

Evaluate and palpate location of all fibroids

■ Choose an incision in which most fibroids can be removed with a single incision.

Sometimes this is not practical as multiple incisions may be needed for safe

removal.

■ A transverse or vertical serosal incision can be utilized.

■ Avoid incisions that will extend into the tubes, cornua, and uterine arteries.

■ Palpate the myometrium throughout the procedure as additional smaller fibroids

may be encountered after enucleation of larger myomas.

■ Anterior incisions are associated with less risk of postoperative adhesions.

However, if a fibroid is posterior it is recommended to make an incision

posteriorly rather than tunnel through anteriorly.

Slowly inject a dilute solution of vasopressin

■ Confirm with the anesthesiologist that vital signs are normal prior to proceeding

with the slow injection of a dilute solution of vasopressin into the leiomyomas

(Tech Fig. 7.1.1).

■ Vasopressin constricts smooth muscle in vascular capillaries, arterioles, and

venules which helps decrease blood loss.

■ A dilute solution of vasopressin ([20 units = 1 ampule] mixed in 200 mL saline)

is slowly injected into multiple uterine sites including the uterine serosa,

intramyometrial or stalk of pedunculated leiomyomas until blanching occurs.

■ A 10-mL control-top syringe and 20- to 22-gauge needle is recommended for

injection.

■ For every 10 mL injected with this ratio, one unit of vasopressin is

administered.

■ Inform the anesthesiologist of the total amount used.

■ Vasopressin can be slowly injected into the planned serosal uterine incision

and myometrium until blanching occurs. Multiple injection sites are made

circumferentially in the myometrium. Always aspirate before injecting additional

vasopressin. Wait 3 to 5 minutes for vasoconstriction before making the

uterine incision.

■ This author injects one fibroid at a time.

■ Record the time of the injection. The half-life of vasopressin is 10 to 30

minutes and the duration of action is 2 to 8 hours. Vasopressin may be

injected intermittently during surgery.

■ Avoid vasopressin in patients with coronary artery, vascular or renal disease

as hypotension, bradycardia, arrhythmias, and death have been reported.



Tech Figure 7.1.1. Slowly inject dilute vasopressin solution.

Additional methods for hemostasis: tourniquets and clamps

■ Factors that increase blood loss include size, number, and location of

leiomyomas. Tourniquets may be used to decrease bleeding in patients who will

have multiple leiomyomas removed.

■ Dissect the bladder peritoneum.

■ Identify a free space in the broad ligament by palpating the broad ligament

above the internal os. Identify the ureter and uterine artery. Make a 1-cm

incision with an electrosurgical instrument into this free space.

■ Pass a Penrose or red rubber catheter drain in this space and secure tightly

posteriorly and secure with a Kelly clamp.

■ Tourniquets are removed at the completion of the myomectomy.

■ The infundibular ligament with the ovarian artery and vein can be temporarily

compressed with Satinsky clamps. They are removed after completion of the

myomectomy.

Removal of myomas

■ The easiest fibroids to treat are those that are pedunculated. The base of the

pedunculated area should be injected with a dilute solution of vasopressin. The

incision is made into the serosa over the leiomyoma until the pseudocapsule is

reached. Using a towel clamp or single tooth tenaculum, the myoma can be

bluntly dissected away from the stalk. Avoid transection of the fibroid from its

stalk as brisk bleeding might occur and require many sutures for hemostasis.

■ A monopolar instrument set on 30 to 40 W cutting current is used to make a

vertical or horizontal serosal incision. The incision is extended until the

pseudocapsule is reached (Tech Figs. 7.1.2 and 7.1.3). The length of the incisionshould incorporate the majority of the area involved with the fibroid.

■ Grasp the myoma with towel clamps and apply traction to fibroid. Separate the

pseudocapsule from the myoma bluntly with an open 4 × 4 sponge or back of

an empty knife handle (Tech Figs. 7.1.4 to 7.1.6). When the surgeon is in the

appropriate plane the myoma literally peels away from the pseudocapsule and

myometrium.



Tech Figure 7.1.2. Manual compression of fibroid facilitates incision with monopolar

device.



Tech Figure 7.1.3. Incision of pseudocapsule.



Tech Figure 7.1.4. Apply towel clamp to myoma to facilitate myoma enucleation. Grasp

with towel clamp.



Tech Figure 7.1.5. Apply towel clamp to myoma to facilitate myoma enucleation.

Dissection of myoma.



Tech Figure 7.1.6. Dissection with 4 × 4 sponge to develop surgical plane.

■ Avoiding use of fingers to bluntly shell out the fibroids as more bleeding is

encountered because the blood vessels are torn in the periphery and base of

the leiomyoma.

■ Push the surrounding tissue planes away from the fibroid. The towel clamps or

Lahey clamps should be advanced as the fibroid begins to separate from the

myometrium.

■ The surgeon can squeeze the leiomyoma. This will help it bulge out further

from the myometrial bed.

■ With a large fibroid greater than 6 to 8 cm, a myoma cork screw may be used

to apply traction to the myoma helping to enucleate the fibroid. Visible

pseudocapsule that envelops the myoma may be cut in order to extricate the

myoma.

■ Small-surface blood vessels are coagulated with Bovie tip cautery. Hemostasis

should be prioritized throughout the surgical procedure.

■ If the leiomyoma protrudes into the endometrial cavity, identify the

endometrium and separate it from the fibroid. The goal is to not have any

endometrium removed with the leiomyoma.

■ If the endometrial cavity is entered, it must be closed separately from the

myometrium (Tech Fig. 7.1.7). Then the myometrium is reapproximated over the

endometrium, avoiding closure of the endometrial cavity (Tech Figs. 7.1.8 and

7.1.9).

■ Carefully palpate the myometrium after the dominant fibroid is removed in order

to detect other lesions. The decision to close the defects immediately or after

total enucleation of fibroids will depend upon the amount of bleeding that is

encountered.



Tech Figure 7.1.7. Endometrium is opened and identified with a white probe.



Tech Figure 7.1.8. Closure of the endometrial cavity taking care to avoid suture

placement within the cavity. Reapproximate only endometrial edges.



Tech Figure 7.1.9. Final closure of endometrial cavity.

Closure of the myometrial defects

If there are small residual areas of dead space, apply AristaTM (Bard), Floseal

(Baxter International Inc., Hayward, CA), or Surgiflo (Ethicon, San Angelo, TX).

They are thrombin-infused gelatin products and can be placed in the myometrial

bed and dead spaces for additional hemostasis (Tech Fig. 7.1.10).

■ Deeper intramural fibroids should be closed when possible with a three-layer

closure, with zero-delayed reabsorbable suture beginning at the base and

obliterating the space with a continuous-running suture or interrupted figure of

eight sutures (Tech Figs. 7.1.11 and 7.1.12). During suturing, the assistant should

squeeze the uterine walls together to help the surgeon close the myometrium

effectively. Continue this deep-layer closure approximating the myometrium until

the serosal edge is reached.



Tech Figure 7.1.10. Hemostatic agent is applied. In this case, Arista was used between

the myometrial layers.

■ The edges of the serosa are closed with an imbricating continuous, “baseball”

stitch on the serosa. Synthetic absorbable 3-0 sutures are used including

Vicryl, PDS, or Maxon suture, which are associated with delayed absorption

and limited inflammatory response (Tech Fig. 7.1.13).

■ Attempt to bury all surgical knots to a decrease adhesion formation.

■ Place adhesion barriers such as InterceedTM (oxidized cellulose) over the

suture lines, after irrigating the peritoneal cavity and ensuring hemostasis, if

conditions ideal.



Tech Figure 7.1.11. First layer closure of the myometrium with delayed absorbable

suture.



Tech Figure 7.1.12. Final multilayered closure of myometrium.



Tech Figure 7.1.13. Serosal closure.

■ Send all leiomyomas for histological evaluation. Tabulate the number, size, and

aggregate weight of all fibroids.

■ The myometrium should be closed meticulously in a layered fashion. Surgeons

must avoid placement of just a few two or three large through-and-through

closures if the patient is interested in future pregnancy. A limited follow-up of

patients who had abdominal myomectomy with meticulous closure and

subsequent pregnancy observed that the majority of scars were symmetric and

with uniform thickness compared with surrounding myometrium.

■ Maintain awareness of the location of the fallopian tubes and avoid ligation of the

fallopian tubes during myometrial closure.■ Copiously lavage the peritoneal cavity with saline or Ringer lactate solution after

completion of the surgery.

■ Once hemostasis is confirmed, application of an adhesion barrier is advised.

Two current adhesion barriers are currently available for abdominal myomectomy.

Seprafilm, a bioresorbable membrane (Genzyme Corporation, Cambridge, MA),

and Interceed (oxidized regenerated cellulose) have been associated with

decreased postoperative adhesion formation.

Abdominal closure

■ Once completed, the nurses should perform the final instrument, needle,

sponge, and ancillary equipment counts.

■ The fascia and skin closure is performed per physician preference.

Perform vaginal sweep

■ At the completion of surgery, remove the intrauterine Foley catheter.

■ Perform a “vaginal sweep” to make sure that no foreign bodies are left in the

vagina.PEARLS AND PITFALLS

Confirm that abdominal myomectomy is indicated

Recommending surgery for minimal clinical symptoms or for symptoms that will not be

alleviated with surgery increases the risk of unnecessary operative complications

Exclude intracavitary fibroids even if the patient has multiple intramural and serosal

fibroids

Failure to remove intracavitary fibroids may cause menstrual dysfunction, infertility, or

may leiomyoma prolapse after surgery

Identify ureter if fibroids distort the broad ligament and cervix

Injury or transection of ureter

Meticulous myometrial and serosal closure

Increased intraoperative and postoperative blood loss. Increased risk for

postoperative adhesions

Place intrauterine Foley catheter in order to identify entrance into the endometrium

Inadvertent closure of the endometrial cavity can be associated with secondary

infertility, Asherman syndrome, and intracavitary distortion

POSTOPERATIVE CARE

■ Postoperatively the patient is admitted to the hospital for 1 to 3 days until

standard postoperative milestones are met.

■ Patient is ambulatory

■ Taking fluids

■ Pain is controlled

■ Afebrile and stable vital signs

■ Serial CBC and platelet count until labs are stable. Additional postoperative

labs followed if the patient has other comorbidities including renal, liver

disease, or diabetes.

■ Evaluate this patient for coagulopathy if large blood loss occurs.

■ Early ambulation and early feeding are advisable. Both of these help to

decrease atelectasis pneumonia, postsurgical embolism (DVT or pulmonary

emboli), and decrease postoperative ileus.

■ Utilize postoperative incentive spirometry.

■ Approximately 12% to 67% of women have a nonlocalizing fever 48 hours

after myomectomy. Generally, no focal findings are limited. However,

standard fever works up and clinical examination is recommended.

■ Consider withholding nonsteroidal pain medications if moderate or

significant intraoperative bleeding.■ Follow serial CBC and coagulation panel if large intraoperative blood loss

occurs. Evaluate the patient for disseminated intravascular coagulation if

the patient continues to bleed postoperatively.

■ Use of the patient-controlled analgesia (PCA) is often favored by patients

and nursing staff for management of postoperative pain. Generally, after

the first 24 hours, the PCA pump is discontinued and oral narcotic therapy

and NSAIDs begin.

■ When stable, the indwelling Foley catheter is removed the morning after

surgery.

■ The patient can be discharged home when afebrile, vital signs, and labs are

stable, tolerates liquids, and able to ambulate.

■ Homegoing discharge instructions should be reviewed with the surgeon.

Additionally, homegoing written discharge instructions are given.

■ Special emphasis must communicated with the patient prior to discharge:

■ Patient instructed to call if she has a persistent temperature of greater

than 100 degrees.

■ Nausea, vomiting, leg pain, new onset anxiety, or shortness of breath.

■ Reminder to keep the incision dry. Call if redness, discharge, wound

separation, foul smell, change in color (dusky or black color), or increasing

tenderness occurs.

■ Avoid vaginal intercourse for four weeks.

■ May shower immediately and cover the wound.

■ No heavy lifting of more than 10 pounds.

■ Resume hormonal contraception four weeks after surgery.

■ Arrange for postoperative follow-up four weeks after surgery.

■ Review pathology.

■ Discuss route of delivery based on complexity of the abdominal

myomectomy.

■ Most patients return to work and full activities 4 to 6 weeks after surgery.

■ Wait 3 to 6 months before attempting pregnancy.

OUTCOMES

■ Morbidity and mortality are similar to an abdominal hysterectomy.

However, complications such as vaginal vault prolapse and injury to the

bladder and ureters are lower in patients undergoing abdominal

myomectomy compared to abdominal hysterectomy.

■ Bulk symptoms and heavy menstrual bleeding are greatly improved in 80%

of women undergoing abdominal myomectomy when fibroids are

completely removed.

■ Approximately 36% of women develop postoperative adhesions.■ While generally improved, pelvic pain and dysmenorrhea may not be

completely alleviated if coexisting adenomyosis or endometriosis exists.

■ Prospective, randomized controlled studies are lacking regarding the

impact of abdominal myomectomy on fertility. Fibroids can distort tubal

anatomy and the uterine cavity. Male factors also impact fertility outcomes.

Small series document a 57% conception rate following abdominal

myomectomy.

■ The number of women who wish to conceive after abdominal myomectomy

is unknown, thus making fertility outcomes difficult to calculate.

■ Among women with recurrent pregnancy, loss or prior infertility successful

pregnancies have been associated with abdominal myomectomy.

■ The rate of recurrence of uterine fibroids is variable depending upon the

length of time of follow-up after surgery.

■ Among patients followed for 7 to 10 years after surgery, 21% to 34%

required subsequent surgery for fibroid-related symptoms.

■ Additional factor affecting recurrence of fibroids includes age of initial

surgery, interval pregnancy after myomectomy, age of patient, race, and

the number of fibroids removed.

■ Despite these limitations, uterine sparing surgical options should be

available to women who have this preference even if there are no plans for

childbearing.

COMPLICATIONS

■ Complications from abdominal myomectomy include:

■ Infectious morbidity

■ Respiratory

■ Atelectasis

■ Pneumonia

■ Urinary tract infection

■ Wound infection

■ Microscopic abscesses within the myometrium

■ Endometritis

■ Embolic

■ Deep venous vein thrombosis

■ Pulmonary embolism

■ Intraoperative and postoperative bleeding

■ Acute

■ Delayed

■ Coagulopathy

■ Infertility■ Obstruction of the fallopian tube

■ Iatrogenic closure of the endometrium leading to secondary

amenorrhea

■ Asherman syndrome due to complete or incomplete removal of the

endometrium when performing myomectomy that involves myomas

that abut the endometrium. Endometrium overlying the leiomyoma

may be inadvertently removed.

■ Postoperative bowel adhesions

■ Uterine rupture during pregnancy or partial uterine dehiscence

■ If the patient becomes pregnant following the procedure, she should be

informed to contact her obstetrician promptly if abdominal pain occurs

during pregnancy.

■ Fetal loss

■ Postpartum hemorrhage

■ Hysterectomy

■ Death

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