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Uterine Fibroid Embolization 337
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the existing fibroid, presenceof extrauterine blood supply,growth of new fibroids, or etiologies other than myomas.
Resolution of dysmenorrhea and bulk-related symptoms has been reported to be in the 80% to 90% range. The potential rea­sons for lack of complete response in these patients are discussed below.
In a recent study of 2112 eligible patients, a change in symp­tom severity and health-related quality of life among patients treated with UFE was reported.[10] At 12 months, symptom improvement was observed in 94.53% of patients, with the mean symptom score improving from 58.61 to 19.23 (P 0.001). The mean health-related quality-of-life score improved from 46.95 to
86.68 (P 0.001). Hysterectomy was required in only 2.9% of patients in the first 12 months.
Reduction in the volume of the fibroids depends on the tumors’ initial size, vascularity, and presence or absence of pre­vious spontaneous infarcts. It averages around 50% to 60% decrease in volume and is continuous over time, with the max­imum rate of shrinkage occurring in the first 6 to 12 months post embolization.[8] The degree of reduction in the volume of leiomyomas after UFE is unpredictable and cannot be guaran­teed in any one patient. For this reason, we recommend surgery to women who seek cosmetic relief from fibroids. Despite the emphasis of many physicians and patients on the size of fibroids, there appears to be no correlation between reduction in fibroid volume and degree of relief from symptoms after UFE.
Studies addressing the long-term efficacy of UFE have con­firmed the durability of this procedure in patients with symp­tomatic fibroids. Spies et al. [11] followed 200 consecutive patients who had undergone UFE. Of the 182 patients with com­plete follow-up data, 73% remained symptom-free at 5 years.
Although UFE results in a decrease in fibroidsizeandstopsthe pathologic preferential flow away from the muscle of the uterus, its role in the treatment of fibroid-related infertility has not been comprehensively studied to date. For this reason, UFE is not rec­ommended for treatment of infertility until more data become available.
the point anastomosis. Fibroid devascularization is hence unaf­fected. Disruption of flow at any point proximal to these anas­tomoses, which may occur with uterine artery ligation, will not cause fibroid infarction and lasting symptom relief in women with this type of anastomosis.
In type II anastomosis, direct parasitization of the flow from the ovarian arteries to the fibroids occurs. Although connections to the intramural uterine artery may exist, flow to the fibroid is anatomically independent of uterine artery. This occurs in approximately 8% of women and may be an important cause of procedural failure after UFE.[12]
Conversely, in type III anastomosis, the ovarian supply is mainly from the uterine artery through the tubal arteries. Inde­pendent ovarian arteries are not seen. At angiography, the observed flow is therefore toward the ovary. This pattern of flow has been observed in approximately 6% of arteries. This pattern of flow will not change the efficacy of fibroid devascularization but may be a cause of ovarian failure.
UFE VERSUS SURGERY
Several studies have compared UFE with surgery, either abdomi­nal myomectomyor hysterectomy. Inthe first suchstudy, the out­comes of two uterine-sparing procedures (UFE and abdominal myomectomy) were retrospectively compared in 111 patients.[9] Efficacy,complication, and recovery periods were the main study outcome measures of this analysis. Results are summarized in Tables 12.2.1 and 12.2.2.
Statistical analysis of these results revealed that UFE is signif­icantly better than myomectomy in relieving menorrhagia, with both procedures being equallyeffective in controlling pelvicpain. There was a trend toward better improvement in symptoms of mass effect, such as urinary frequency and constipation, after myomectomy.
Comparison of other outcome measures, such as postproce­dural pain, recovery period, and complications, all favored UFE
CAUSES OF UFE FAILURE
Clinical failure of UFE occurs in a relatively small number of patients. There are several causes for failure, including coexis­tence of other pelvic pathologies not responding to UFE, unre­alistic patient expectations, and inadequate embolization lead­ing to suboptimal fibroid infarction, which may be the result of extrauterine arterial flow to the fibroids. Ovarian arteries are the most important source of such collateral flow.
The majority of vascular communications between theuterus and ovary aretoosmall to be visualized atangiography and do not affect the outcome of UFE.However, threemain types ofovarian­to-uterine artery anastomosis that are of prognostic significance have been described at angiography.[12]
The most common anastomosis is type I, which occurs in approximately 28% of women with symptomatic fibroids. The ovarian artery connects to the intramural uterine artery via the tubal segment, with flows toward the uterus. Type I anastomo­sis is a substantial source of collateral flow to the uterus and fibroids. In this type, ovarian artery supply is not a likely source of UFE failure because the embolization typically occurs distal to
Table 12.2.1: Percent Response after Abdominal Myomec­tomy (AM) and UFE
Menor- Pain Mass Effect rhagia, % Number,% Number,%
Response Category AM UFE AM UFE AM UFE
6 (resolved) 27 60 38.5 29.5 65 19
5 (significantly improved)
4 (moderately improved)
3 (no change) 9 2 4 3 0 5
2 (moderately worse) 4.5 0 4 0 0 0
1 (significantly worse) 0 0 0 0 0 0
% Improvement 86.5 98 92 97 100 95
Adapted from Razavi MK, et al. [9].
36 32 15.5 44 26 57
23 6 38 23.5 9 19
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Table 12.2.2: Comparison of Other Outcome Measures
AM, mean (range)
Inpatient hospital days 2.9 (2–7) 0 ≤ 0.05
Days on pain medications 8.7 (2–47) 5.1 (1–21) ≤ 0.05
Days to normal activity 36 (7–120) 8 (1–49) ≤ 0.05
Secondary interventions,% 10 8 NS
Estimated blood loss, mL 376
(50–2000)
Complications,% 25 10 0.5
NS, not significant. Adapted from Razavi MK, et al. [9]
UFE, mean (range) P value
Minimal
(Table 12.2.2). The need for secondary interventions during the study period was similar in both groups.
The complications included nonautologous blood transfu­sion (n =3), wound infection (n = 2), adhesion (n = 2), read­mission for ileus (n = 1), and chronic pelvic pain (n =2) among the myomectomy patients. Complications in the fibroid embolization group included endometritis requiring readmis­sion for intravenous antibiotics (n = 1), readmission for pelvic pain (n = 1), and menopause (n = 4). All those who experi­enced menopause after fibroid embolization were older than 46 years.
In a prospective randomized study of 63 women with intra­mural fibroids larger than 4 cm who desired future fertility, Mara et al. [13] compared UFE to myomectomy. Similar to the study by Razavi et al. [9], UFE was associated with fewer hospital days, procedure time, blood loss, and disability period. Complication rate and follicle-stimulating hormone (FSH) levels were similar at 6 months, although the UFE group reported a lower rate of symptom relief.
UFE has also been compared with hysterectomy. Pinto et al. [14] conducted a prospectiveanalysis of hysterectomyversusUFE in 60 patients. UFE was associated with fewer complications and a shorter hospital stay.Spies etal. [15],in a prospectivemulticen­ter trial of UFE versus hysterectomy, reported similar results. In this study, pain relief was more common among those with hys­terectomy, with both groups experiencing marked improvement in other symptoms and quality-of life-scores, with no difference between them. Complications were more frequent in the hys­terectomy group (50% vs. 27.5%).
In a cost-effectiveness analysis, Beinfeld et al. [16] developed a decision model to compare the costs and effectiveness of UFE and hysterectomy. They concluded that UFE is less expensive and more effective than hysterectomy. In their model, however, when the quality-of-life adjustmentwas eliminated, the twoprocedures were equally effective.
UFE AND PREGNANCY
The issue of pregnancy after UFE has been addressed in only a small number of studies. Kim et al. [17] reviewed their experi-
ence in 94 patients and concluded that UFE with PVA particles does not seem to affect fertility among women who do not use contraception.
Based on their study of 671 women who underwent UFE, Carpenter et al. [18] observed no increased obstetric-associated risk, with the exception of the number of patients who under­went cesarean section. In a similar large multicenter clinical reg­istry of 555 patients with a mean age of 43 years, the enrolled women were followed prospectively.[19] Thirty-one percent of the patients were younger than 40 years. Although it is unclear as to what fraction of women who were trying to get pregnant actually did, 24 pregnancies were reported in women who were an average age of 34 years. There were four spontaneous abor­tions and four preterm deliveries. Abnormal placentation was seen in three women. The authors concluded “women are able to achieve pregnancies after uterine artery embolization, and most resulted in term deliveries and appropriately grown newborns.” Close monitoring of placental status, however,wasrecommended in this study.
In comparison with myomectomy, McLucas et al. [20] and Goldberg et al. [21] reached opposite conclusions. The McLucas group observed no difference in pregnancy outcome between those who underwent UFE versus those who had myomectomy, whereas the Goldberg group reported a higher incidence of complications in UFE patients. It should be noted that both these studies suffer from major methodologic flaws, and their results should be interpreted with caution.
COMPLICATIONS OF UFE
Serious complications after UFE are rare. In a large prospective multicenter study of 3160 patients enrolled in 72 sites, major in­hospital complications occurred in 0.66% of patients.[22] The 30-day complication rate was 4.8%, with no reported deaths. The most common complication was inadequate pain con­trol requiring a hospital visit by 2.4% of patients. One per­cent required additional surgical procedures within the first 30 days, with 0.1% undergoing hysterectomy. Multivariate analysis showed modest increased odds for an adverse event for African Americans, smokers, and those with prior leiomyoma pro­cedures.[22]
Endometritis has been reported to occur in 1% to 4% of patients after UFE. The most common risk factors for infection are the presence of large submucosal fibroids or preexistence of an undetected or incompletely treated pelvis infection. In these patients, aggressive therapy with antibiotics is warranted to pre­vent further progression, which may lead to sepsis and/or hys­terectomy.
A long-term complication of UFE is ovarian failure and early menopause. The risk of ovarian failure is age dependent and highest in women over the age of 45. Review of the literature reveals that less than 1% of women under the age of 40 develop menopause after UFE. This risk increases to 15% for those older than 45 years.[12,23]
Other, less common complications occurring in less than 1% of patients include vessel injury, deep vein thrombosis, and pul­monary embolism.
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POSTPROCEDURAL CARE AND FOLLOW-UP
As mentioned above, the most common reason for postpro­cedural physician visits after UFE is inadequate pain control. Because of the less invasive nature of UFE, occasionally the treat­ing physicians have a tendency to underprescribe pain medica­tions. According to the published studies, women will experience pelvic discomfort for an average of 3 to 4 days after the procedure and may require oral analgesics. Thedegree of pain is highly vari­able, with no reliable preprocedural indicator. Rarely, pain may last longer, but persistent pelvic discomfort for a period longer than 3 weeks or recurrence of pain after an initial abatement requires evaluation.
Postembolization syndrome is a constellation of symptoms including nausea, low-grade fever, and malaise and is common after UFE. This syndromemay last for 4 to 7 days post procedure, and the treatment is supportive, including the use of antiemetic and anti-inflammatory medications.
A self-limiting vaginal spotting with a brownish discharge is also a common finding and may occur for several weeks after embolization. In fewer than10% of women,the discharge may be associated with passing of tissue and clot,which have been shown histologically to be fibroid fragments. Transcervical expulsion of leiomyomas may occur in 1% to 2% of patients and is asso­ciated with pain and bleeding. These are typically submucosal fibroids, which detach into the uterine cavity about 4 to 12 weeks after embolization. Incomplete passage is associated with a high risk of infection andmay require hospitalization and intravenous antibiotics. Delayed passage of leiomyomas for up to a year after UFE has also been reported.[24]
After the initial postprocedural follow-up, patients are seen in follow-up approximately 3 months later. Follow-up MRI is obtained 6 to 12 months later.
Temporary amenorrhea occurs in approximately 5% to 8% of women during the first 3 months following the procedure. Menses resumes in the majority of these women, with no perma­nent sequela. No specific therapy is prescribed in these patients. If amenorrhea persists, a serum FSH may be obtained to evaluate for menopause.
SUMMARY
UFE is auterine-sparing alternative to hysterectomythathas been shown to be an effective therapy for women with fibroids. By permanently eliminating the blood flow to the fibroids, UFE alle­viates symptoms and reduces fibroid volume and uterine size. Advantages include the elimination of surgical risks, treatment of the entire fibroid burden with one therapy, preservation of fertility, and reduction of hospitalization and recovery times. Although the role of UFE in the treatment algorithm for leiomy­omas remains controversial, it should be offered to women who do not desire surgery or those who have failed medical or less invasive surgical therapies before hysterectomy is advised.
REFERENCES
1. Brown BJ, Heaston DK, Poulson AM, Gabert HA, Mineau DE, Miller FJ Jr. Uncontrollable postpartum bleeding: a new approach
to hemostasis through angiographic arterial embolization. Obstet Gynecol. 1979;54(3):361–365.
2. Vedantham S, Goodwin SC, McLucas B, Mohr G. Uterine artery embolization: an underused method of controlling pelvic hemor­rhage. Am J Obstet Gynecol. 1997;176(4):938–948.
3. Ravina JH, Herbreteau D, Ciraru-Vigneron N, et al. Arterial embolisation to treat myomata. Lancet. 1995;346:671–672.
4. Spies JB, Ascher SA, Roth AR, Kim J, Levy EB,Gomez-JorgeJ. Uter­ine artery embolization for uterine leiomyomata. Obstet Gynecol. 2001;98:29–34.
5. Goodwin SC, McLucas B, LeeM, et al.Uterineartery embolization for the treatment of uterine leiomyomata: midterm results. J Vasc Interv Radiol. 1999;10:1159–1165.
6. Worthington-KirschRL, Popky GL,Hutchins FLJr.Uterine arterial embolization for the management of leiomyomas: quality-of-life assessment and clinical response. Radiology. 1998;208:625–629.
7. Hutchins FL Jr, Worthington-Kirsch R. Embolotherapy for myoma-induced menorrhagia. Obstet Gynecol Clin North Am. 2000;27:397–405.
8. Spies JB, Roth AR, JhaRC, et al. Leiomyomata treated with uterine artery embolization: factors associated with successful symptom and imaging outcome. Radiology. 2002;222:45–52.
9. Razavi MK, Hwang G, Jahed A, Modanloo S, Chen B. Abdomi­nal myomectomy versus uterine fibroid embolization in the treat­ment of symptomatic uterine leiomyomas. AJR Am J Roentgenol. 2003;180(6):1571–1575.
10. Spies JB, Myers ER, Worthington-Kirsch R, Mulgund J, Goodwin S, Mauro M; the FIBROID Registry Investigators. The FIBROID Registry: symptom and quality-of-life status 1 year after therapy. Obstet Gynecol. 2005;106(6):1309–1318.
11. Spies JB, Bruno J, Czeyda-Pommersheim F, Magee ST, Ascher SA, Jha RC. Long-term outcome of uterine artery embolization of leiomyomata. Obstet Gynecol. 2005;106(5):933–939.
12. Razavi MK, Wolanske K, Hwang G, Sze D, Kee S, Dake M. Angio­graphic classification of ovarian to uterine artery anastomoses: incidence and significance in UFE. Radiology. 2002;294:707–712.
13. Mara M, Fucikova Z, Maskova J, Kuzel D, Haakova L. Uterine fibroid embolization versus myomectomy in women wishing to preserve fertility: preliminary results of a randomized controlled trial. Eur J Obstet Gynecol Reprod Biol. 2006;126(2):226–233.
14. Pinto I, Chimeno P, Romo A, et al. Uterine fibroids: uterine artery embolization versus abdominal hysterectomy for treatment – a prospective, randomized, and controlled clinical trial. Radiology. 2003;226(2):425–431.
15. Spies JB, CooperJM, Worthington-Kirsch R, Lipman JC, MillsBB, Benenati JF. Outcome of uterine embolization and hysterectomy for leiomyomas:resultsofamulticenterstudy.Am J Obstet Gynecol. 2004;191(1):22–31.
16. Beinfeld MT,BoschJL,IsaacsonKB,GazelleGS.Cost-effectiveness of uterine artery embolization and hysterectomy for uterine fibroids. Radiology. 2004;230(1):207–213.
17. Kim MD, Kim NK, Kim HJ, Lee MH. Pregnancy following uterine artery embolization with polyvinyl alcohol particles for patients with uterine fibroid or adenomyosis. Cardiovasc Intervent Radiol. 2005;28(5):611–615.
18. Carpenter TT, Walker WJ. Pregnancy following uterine artery embolisation for symptomatic fibroids: a series of 26 completed pregnancies. Br J Obstet Gynaecol. 2005;112(3):321–325.
19. Pron G, Mocarski E, Bennett J, Vilos G, Common A, Vander­burgh L; Ontario UFE Collaborative Group. Pregnancy after uter­ine artery embolization for leiomyomata: the Ontario multicenter trial. Obstet Gynecol. 2005;105(1):67–76.
20. McLucas B, Goodwin S, Adler L, Rappaport A, Reed R, Perrella R. Pregnancy following uterine fibroid embolization. Int J Gynaecol Obstet. 2001;74(1):1–7.
340 Mahmood K. Razavi
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21. Goldberg J, Pereira L, Berghella V, et al. Pregnancy outcomes after treatment for fibromyomata:uterineartery embolization versusla­paroscopic myomectomy. Am J Obstet Gynecol. 2004;191(1): 18–21.
22. Worthington-Kirsch R, Spies JB, Myers ER, et al.; FIBROID Inves­tigators. The Fibroid Registry for outcomes data (FIBROID) for uterine embolization: short-term outcomes. Obstet Gynecol. 2005;106(1):52–59.
23. Chrisman HB, Sakter MB, Ryu RK, et al. The impact of uterine fibroid embolization on resumption of menses and ovarian func­tion. J Vasc Interv Radiol. 2000;11:699–703.
24. Spies JB, Spector A, Roth AR, Baker CM, Mauro L, Murphy­Skrynarz K. Complications after uterine artery emboliza­tion for leiomyomas. Obstet Gynecol. 2002;100(5 pt 1):873–
880.
13 HYSTERECTOMY
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Section 13.1. Laparoscopy and Hysterectomy
Farr Nezhat and Jyoti Yadav
The number of hysterectomies, a frequently practiced major sur­gical procedure, varies between different regions and cultures of the world. It reflects differencesin health caresystems, education, and psychosocial attitudes. The highest rates of hysterectomy are found in the United States and Australia (36% and 40%, respec­tively) and the lowest in Italy (15.5%) and France (8.5%).[1–3]
INDICATIONS
Most hysterectomies are performed for leiomyomas,uterine pro­lapse, endometriosis, and gynecologic cancer.[4] The number of hysterectomies for endometriosis doubled between 1965 and 1984, exceeding the increase observed for any other indication and probably reflecting an increased recognition of endometrio­sis. Other indicationsareabnormal uterine bleeding, pelvicinfec­tion and its sequelae,ovarian tumors,and complications of preg­nancy. These indications account for 15% to 21% of all hysterec­tomies.
About 75% of all hysterectomies are done abdominally and 25% vaginally.[4,5] The vaginal approach is primarily used for uterine prolapse. Abdominal hysterectomy is usually done for women with significant pelvic disease, such as endometriosis or pelvic adhesions, which can make a vaginal removal more difficult (Table 13.1.1).[6] Compared to those having a vaginal hysterectomy, women having an abdominal operation have more febrile morbidity, receivemore blood transfusions [5,7],andhave a longerpostoperativehospitalization and convalescence. If more women had a vaginal ratherthanan abdominal approach for their hysterectomy, therapeutic, economic, and social benefits would result.[8]
The route selected depends on the clinical assessment of the pelvic disorder, which is based on the medical history, pelvic examination, ultrasound studies, review of prior operative notes, and the surgeon’s experience in vaginal surgery.[8]
The role of the laparoscope in assisting vaginal hysterec­tomy has been described by Semm since 1984.[9,10] Laparo­scopic hysterectomy using bipolar electrocautery and the endo­scopic stapler was first described in 1989 [11] and 1990 [12], respectively. Kovac and coworkers [13] performed diagnostic laparoscopy in 46 patients scheduled for abdominal hysterec­tomy who, on the basis of clinical indicators, were thought to have a serious pelvic abnormality that contraindicated vaginal hysterectomy. Based on the laparoscopic findings, 42 of the 46 women (91%) were candidates for vaginal hysterectomy, which was done under the same anesthesia. Because clinical assessment of pelvic disease may not be accurate, laparoscopy can reveal whether a vaginal approach is appropriate. For these women,
diagnostic or operative laparoscopy provided the benefits of both vaginal and abdominal approaches without their disadvan­tages (Table 13.1.2). A comparison of the results of abdominal hysterectomy versus laparoscopic hysterectomy in 20 cases was reported by Nezhat et al. in 1992.[14] That report established the validity oflaparoscopicallyassistedvaginal hysterectomy(LAVH) and suggested that it could replace most abdominal hysterec­tomies for benign lesions. The indications for laparoscopically assisted hysterectomy in this series were similar to those listed for abdominal rather than vaginal hysterectomy. All hysterec­tomies were completed successfully endoscopically without sig­nificant complications. Patients had reduced morbidity, blood loss, postoperative discomfort, hospitalization, and recovery time.
A review of the literature reveals many definitions of a laparoscopically assisted hysterectomy. A suggested classification follows:
1. Total laparoscopic hysterectomy (TLH). The hysterectomy is
done laparoscopically; the vaginal cuff may be closed laparo-
scopically or vaginally.
2. Subtotal laparoscopic hysterectomy (SLH). A supracervical
hysterectomy is done laparoscopically.
3. LAVH. The hysterectomy starts laparoscopically, but most
steps, especially the uterosacral and cardinal ligaments, are
done vaginally.
A laparoscopic approach allows the treatment of intra­abdominal and pelvic disease and the dissection or removal of adnexa. Patients who have suspected pelvic endometriosis undergo a diagnostic laparoscopy to inspect the pelvis. Significant pelvic diseaseis treated endoscopically,and if necessary, adnexec­tomy is performed. The hysterectomy is completed vaginally.[13] Usually, a combined laparoscopic and vaginal approach is used to dissect and remove uterine attachments.[15–19] The extent of laparoscopic and vaginal dissection depends on the gynecol­ogist’s preference and experience with laparoscopic and vaginal operations. A more experienced endoscopist can do the entire hysterectomy laparoscopically.[20] However, TLH may be time consuming, especially if the uterus is more than 16 to 18 weeks’ gestational size. Laparoscopic hysterectomy is useful if the vagina is small and narrow and significant infiltrative pelvic endometrio­sis is present, which would make a vaginal operation difficult. Almost all abdominal hysterectomies for endometriosis can be converted to LAVH.[21] Patients who have the indications for traditional vaginal hysterectomy should not undergo LAVH, vagi­nally assisted laparoscopic hysterectomy, or laparoscopic hys­terectomy.[22]
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Table 13.1.1: Indications for Hysterectomy
Abdominal Vaginal
Hysterectomy,% Hysterectomy,%
Leiomyomas 38 1
Uterine prolapse 1 76
Endometriosis 3 0
Abnormal bleeding 13 9
Adenomyosis 9 8
Pelv ic pain/adhesions
Ovarian tumors 10 0
Uterine neoplasia 15 3
Source: Dicker et al.[5]
PREOPERATIVE EVALUATION
50
Routine preoperative tests include a complete blood count with differential, serum electrolytes, bleeding time, and urinal­ysis. More comprehensive blood studies, thrombin time, partial thrombin time, electrocardiography (ECG), chest radiography, and endometrial biopsy are done as indicated. Amechanical and, at times, anantibioticbowelpreparationisadvised.Consultations with a urologist, colorectal surgeon, and oncologist are sought as necessary. Appropriate informed consent is obtained from the patient after a thorough explanation of the planned operation, its potential risks and benefits, the possibility of laparotomy, and therapeutic alternatives. After an overnight fast, the patient is admitted to the ambulatory surgical unit the morning of her operation.
TECHNIQUE
Laparoscopically Assisted Vaginal Hysterectomy
The patient’s initial position is the same as that for standard laparoscopy. The 10-mm trocar is inserted transumbilically for placement of the operativelaparoscope,andtwo to four accessory trocars are positioned suprapubically.Forthevaginal portion, the patient’s legs arereadjusted to allowvaginal access (Allen Univer­sal stirrups, Allen Medical Systems). With an adjustment under the drapes, the legs are flexed and abducted without redraping. Some gynecologists prefer to place the patient’slegs in candy-cane stirrups for the vaginal portion. Various types of uterine manip­ulators can be placed inside the uterus of facilitate manipulation intraoperatively.
Every operative laparoscopy begins with exploration of the abdominal and pelvic cavity to assess the extent of disease. Anatomic landmarks, anomalies, distortions, and alterations are identified. The locations of the bladder, ureters, colon, rectum, and major blood vessels are noted. The omentumandsmallbowel are evaluated for disease and checked for Veress needle or trocar injury.
After the diagnostic portion, the operator uses the CO
2
laser or othercutting instrument and hydrodissection to resect, ablate, or coagulate implants of endometriosis. An electrocoagulator,
Table 13.1.2: Advantages and Disadvantages of Abdominal, Vaginal,and LaparoscopicallyAssisted VaginalHysterectomy (LAVH)
Abdominal Vaginal LAVH
Exposure Excellent Limited Excellent
Associated pelvic disease
Incision Abdominal Vaginal Abdominal/vaginal
Hospitalization, days
Cost Average Average More expensive
Morbidity, % 30 10 10
Surgical expertise
Oophorectomy Easy ≤25% Easy
Easily treated
3 2–3 1–2
Average gynecologist
Reduced access
Average gynecologist
Easily treated
Experienced endoscopist
clips, staplers, or Endoloops (Ethicon) are used to coagulate or ligate large vessels. Monopolar electrodes, fiber lasers, or the har­monic scalpel maybeused for smallerbleeders.[23] Other instru­ments include bipolar forceps (middle port), suction–irrigator probe (left), and grasping forceps (right).
The bowel is freedfrom the pelvicorgans to expose thepelvis. Ovaries and tubes are dissected from the cul-de-sac or pelvic side wall, and endometriosis or other abnormalities are treated.
Ureteral Evaluation and Dissection
The direction and location of both ureters are identified from the pelvic brim to the cardinal ligaments, where they are no longer visible. This is undertaken early in the operation, before pelvic side wall peritoneum becomes edematous or opaque and ureteral peristalsis is inhibited due to irritation by the CO
pneu-
2
moperitoneum or hydrodissection. The course of the ureters is marked superiorly with the laser or electrocoagulation so that they can be identified while the broad ligament and adnexa are dissected (Figure 13.1.1). For extensive endometriosis, very wide dissection, as is done during radical hysterectomy, is sometimes necessary.[16,17]To identifytheuretersatthe level of thecardinal ligaments, the peritoneum is opened above or below the ureter and hydrodissection is carried out. A peritoneal incision is made, and the ureter is identified toward its course tothe bladder. Small bleeding vessels are coagulated by laser or electrosurgery. If the uterosacral ligaments are dissected, theureterisretracted laterally and the uterosacral ligaments are dissected at their origin from the cervix. The uterine vessels run superiorly. They are isolated and safely coagulated. When the pelvic anatomy is distorted, it may be saferto do acystoscopyand place catheters in both ureters for better identification.
Upper Broad Ligament and Adnexa
If adnexectomy is indicated, after electrocoagulation and tran­section of the round ligaments 2 to 3 cm from the uterus, the infundibulopelvic ligament is coagulated and cut. If the endoscopic linear stapler is used, the appendage is grasped with
Hydrodissection
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in infundibulo­pelvic ligament
A
laser
CO
2
incising the peritoneum
B
C
Figure 13.1.1. (A) After an opening is made above the ureter in the peritoneum, retroperitoneal hydrodissection is carried out. (B) Using the suction–irrigator probe as a backstop, an opening is made above the ureter with the CO the back of the bladder by using blunt hydrodissection.
Peritoneum retracted to expose ureter
laser. (C) The ureter is dissected from the pelvic brim to
2
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First application of stapling device (ENDOPATH ELC 35) on infundibulopelvic ligament
AB
Figure 13.1.2. (A) The linear stapler is applied across the infundibulopelvic ligament. Ureteral evaluation before transection of the ligament is very important. (B) Second application of the stapler across the infundibulopelvic ligament. The round ligament may be included.
forceps. It is retracted medially and caudally to stretch and out­line the infundibulopelvic ligament,whichis grasped andsecured with the stapler.Auterinemanipulator(HUMI[CooperSurgical] or other uterine manipulator) placed inside the uterus vaginally is helpful in retracting the uterus in the opposite direction, facil­itating the stretch on the infundibulopelvic ligament. The sta­pler is not fired until the contained tissue is identified and the ureteral position is confirmed. Once it is transected, the staple line is examined for placement and hemostasis. After infundibu­lopelvic ligament transection, the adnexa and uterine fundus are retracted in the opposite direction. Tissue of the upper broad ligament, including the round ligament, is grasped, secured, and cut after safemargins have been established(Figure 13.1.2A). The infundibulopelvic ligament and the round ligament occasionally are cut with asingle staple application (Figure 13.1.2B).Any other hemostatic cutting device (LigaSure, Valleylab; Harmonic ACE, Ethicon Endo-Surgery) may be used in a similar fashion on all vascular pedicles.
Development of the Bladder Flap
If the adnexa are preserved, the round ligament is coagulated and cut approximately 3 cm from the uterus (Figure 13.1.3). Using hydrodissection, the anterior leaf of the broad ligament is opened toward the vesicouterine fold and the bladder flap is developed (Figure 13.1.4).The anterior leaf ofthe broad ligament is grasped with forceps, elevated, and dissected from the anterior lower uterine segment with hydrodissection and the CO
2
laser, monopolar scissors, or any harmonic device (Figure 13.1.5). The utero-ovarian ligament, proximal tube, and mesosalpinxareelec­trodesiccated and cut, andtheposterior leaf of thebroadligament is opened (Figure 13.1.6). Similarly, the round ligament, fallop-
ian tube, andutero-ovarian ligament canbe grasped closeto their insertion into the uterus with the endoscopic linear stapler and then secured, stapled, and severed (Figure 13.1.7). The distal end of the stapler or bipolar forceps must be kept free of the bladder and ureter.
Electrodesiccation of the round ligament
Uterus
Ovary
Figure 13.1.3. The round ligament is coagulated and cut 2 to 3 cm lateral to the uterus.
Round ligament
Fallopian tube
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Foley catheter in bladder
Bladder
Cut round ligament
Fallopian tube
Hydrodissection develops the bladder flap.
Figure 13.1.4. While the anterior leaf of the broad ligament is elevated with hydrodissection, the anterior leaf of the broad ligament is opened toward the vesicouterine fold.
Uterus
The uterovesical peritoneum is identified, grasped, and ele­vated with forceps while scissors, laser, or a harmonic device is used to dissect the bladder off the cervix. The bladder pillars are identified, coagulated, and cut. The bladder is dissected from the uterus by pushing downward with the tip of a blunt probe along the vesicocervical plane until the anterior cul-de-sac is exposed completely (Figure 13.1.8).
In patients who have severe anterior cul-de-sac endometriosis or adhesions or a history of previous cesarean deliveries, sharp dissection of the vesicouterine fold often is necessary. Injecting 5 to 10 mL of indigo carmine in the patient’s intravenous line and looking for its presence in the peritoneal cavity isone waytodetect bladder trauma. However, the best method to identify bladder injury is either by cystoscopyorbydistendingthebladder with300
to 400 mL of sterile milk and performing a careful laparoscopic inspection for any leaks.
Uterine Vessels
After the bladder is dissected from the anterior cervix, the uterine vessels are identified, desiccated, and cuttofree the lateral borders of the uterus (Figure 13.1.9). If single clips or linear staplers are used, the vessels are skeletonized to prevent slippage of the clips. As the uterine vessels are grasped and cut, the safety and position of the ureters should be checked. This can be done more easily if they are marked, exposed, or catheterized at the beginning of the procedure.The hysterectomy is completed vaginally orcontinued laparoscopically.
The bladder flap is dissected down to the cervix.
Figure 13.1.5. The bladder is elevatedand further separated fromthe cervix. It ispushed downward using sharp and blunt dissection and hydrodissection.
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Obliterated hypogastric artery
Round ligament
as the width of the linear stapler is 12 mm. Because of the short distance between the cervix and the ureter, the risk of ureteral injury by the stapler increases. Using contralateral retraction of the uterus, the cardinal ligament is dissected to identify tissue planes, vessels, and the ureter. Once the ureter is displaced later­ally,the cardinal ligamenttissue closest tothe cervix is coagulated and transected(Figure 13.1.10). Alternatively,the linear stapler is applied on both theuterinevesselsandthe cardinal ligament (Fig­ure 13.1.11).The harmonic scalpel or LigaSure may be used as an alternative.
Uterus
Coagulation and dissection of the ovarian ligament and mesosalpinx
Figure 13.1.6. The proximal tube, mesosalpinx, and utero-ovarian lig­ament are coagulated and cut.
Cardinal Ligament
At the level of the cardinal ligaments, the ureter and the descend­ing branches of the uterine artery are close to one another and the cervix. Therefore, cardinal ligament dissection must be pre­cise to prevent bleeding and ureteral injury. The linear stapler is used only if the parametrium is dissected with ample margins
Anterior and Posterior Culdotomy
A folded wetgauzeinaspongeforcepsoronthetipofaright-angle Heaney retractor marks the anterior or posterior vaginal fornix. The vaginal wall is tented and transected horizontally (Figures
13.1.12, 13.1.13). Newer uterine manipulators on the market are fitted with cups of varying sizes (KOH Colpotomizer, Cooper Surgical) that fit onto the cervix anddelineate thevaginalfornices, enabling easy transaction of the vaginal cuff. Additionally, they are fitted with a balloon that maintains the pneumoperitoneum once the vagina is opened.
Vaginal Portion of Hysterectomy
The laparoscopic portion temporarily ends before or after the anterior or posterior culdotomy. Dissecting and resecting the uterus are done vaginally using standard techniques. Once the uterus is removed, the vaginal cuff is closed. To ensure sup­port of the vaginal vault, the vaginal angles are attached to the uterosacral and cardinal ligaments with absorbable sutures. The vaginal cuff is closed transverselyor vertically, and any coexisting cystocele or rectocele is repaired. Once the vaginal part is com­pleted andthe cuff is closed, the laparoscopic procedure resumes.
First application of linear stapler on the upper portion of the broad ligament
Right adnexa has been dissected and removed
Application of stapler on the upper portion of the broad ligament
A B
Figure 13.1.7. (A) The linear stapler is applied on the upper portion of the broad ligament while preserving the adnexa. (B) The linear stapler is applied on the upper broad ligament while removing the adnexa.