1. Introduction
The lifetime risk for undergoing a single operation for prolapse (or incontinence) is 11%, with the National Center for Health Statistics reporting 400,000 procedures for these conditions performed annually.[1] Swift et al. described the epidemiologic distribution of pelvic organ prolapse (POP) in a sample of 1004 women presenting for an annual gynecologic exam, evaluated with a validated staging system (Pelvic Organ Prolapse Quantification System or POP-Q).[2,3] Despite a relatively young mean age of 42.7 years, clinically significant (Stage II or greater) vaginal wall descensus was identified in 37% of subjects. In a larger study as part of the Women’s Health Initiative, those between the ages of 50 and 79 were screened for POP through a non-validated system.[4] Of 16,616 subjects with no previous hysterectomy, 41.1% had some form of prolapse, while 38% of 10,727 hysterectomized women exhibited POP. The true incidence of POP is likely higher, as many women may not report their condition due to embarrassment, or they may feel that such changes are a normal part of aging.
2. Anatomy of the pelvic floor
The pelvic floor is comprised of layers of connective tissue and muscle that provide support to the pelvic viscera. The urethra, vagina and rectum are attached to the pelvic sidewalls by the endopelvic fascia, which in turn is supported by the pelvic floor musculature (PFM).[5] The PFM consists of the levator ani (pubococcygeus and iliococcygeus) and coccygeus muscles, providing tonic support to the endoplvic fascia and viscera through a preponderance of type I (slow twitch) fibers.[6] Thus, a robust PFM is essential in maintaining the position of the viscera within the pelvis.
3. Etiology of pelvic organ prolapse
Pelvic organ prolpase represents an attenuation or disruption of the connective tissue comprising the pubocervical endopelvic “fascia” anteriorly or rectovaginal endopelvic “fascia” posteriorly, manifesting as anterior or posterior vaginal wall prolapse, respectively. Additionally, a weak or torn cardinal - uterosacral ligament complex may lead to vaginal apex (cuff post hysterectomy or cervix) descent. Predominant risk factors for POP include age and parity, with partial denervation of the PFM proven to be the result of parturition, senescence, or some combination.[7,8] As the PFM becomes weak, support to the endopelvic fascia and viscera is lost, placing the connective tissue at risk for attenuation and/or discrete breaks with resultant POP. When encountered in a younger subject, POP may reasonably be the sequela of acute obstetric trauma, or the result of a genetic alteration in the proportion of fascial collagen subtypes.[9]
4. Considerations prior to surgical correction of pelvic organ prolapse
The goal of POP repair is to restore pelvic anatomy, and facilitate normal visceral and sexual function. To this end, the surgeon must consider, first and foremost, the integrity of the vaginal apex. The Surgery for Pelvic Organ Prolapse Committee of the 3rd International Consultation on Incontinence noted, “…the apex is the keystone of pelvic organ support”. [10] Additionally, they concluded that anterior and posterior repairs are doomed to fail unless the apex is adequately supported. While multiple approaches exist to address vaginal apical prolapse, choosing the optimal repair is critical to a successful outcome.
In the following text, we will discuss several methods for the repair of apical descensus, examine the surgical evolution from vaginal and abdominal surgery to laparoscopic and robotic approaches, and describe our technique of robot assisted laparoscopic sacrocolpopexy and sacrocervicopexy.
5. Transvaginal surgery for apical prolapse
6. Transvaginal mesh repairs
The introduction of a variety of mesh products has been implemented for the repair of stress urinary incontinence as well as POP. Although a thorough review of this modality is beyond the scope of this chapter, a brief account of contemporary outcomes will be discussed. Several synthetic graft materials have been used historically including expanded PTFE and polyester, with polypropylene being the dominant synthetic used in contemporary kits due its macroporous nature, allowing for tissue in-growth and minimal inflammatory response.[19,20] Commercial kits, designed to allow for minimally invasive mesh insertion, include Elevate (American Medical Systems, Minnetonka, MN, USA) and Gynecare Prolift System (Ethicon Women’s Health and Urology, Somerville, NJ, USA), along with several other products and approaches for mesh support of the vaginal apex. In a review of clinical trials and observational studies addressing apical prolapse repair, Diwadkar and colleagues included 3,425 patients from 24 studies employing vaginal mesh kits, reporting a low rate of reoperation for recurrent POP (1.3 % at 17 months), with an overall complication rate (14.5 %) similar to traditional vaginal (15.3 %) and abdominal (17.1%) approaches.[21] However, the majority of complications associated with mesh kits required surgical intervention under general anesthesia (8.5 %), due in part to mesh erosion (vaginal exposure of synthetic material). In a retrospective review comparing outcomes following Prolift mesh repair, uterosacral ligament suspension and abdominal sacrocolpopexy, no difference in operative success (% with Stage 0 or I at follow-up) was observed between the three groups; however, mean change in apical support was significantly better after abdominal sacrocolpopexy compared to transvaginal mesh repair and uterosacral ligament suspension.[22]
7. Abdominal surgery for apical prolapse
Given the durability of ASC, such an approach is considered by many to represent the “gold standard” in the treatment of apical prolapse. In considering the attendant risks of open abdominal procedures and the availability of burgeoning technology, practitioners have made the logical progression to a less invasive approach using minimally invasive instrumentation in the performance of sacrocolpopexy.
8. Laparoscopic sacrocolpopexy (LSC)
The concept and surgical technique of LSC is similar to that of its open counterpart. With the introduction of laparoscopy to vaginal reconstruction, many studies have been published evaluating the efficacy and safety of LSC as compared to ASC. Overall, LSC appears to be durable, with a low rate of recurrence (0-4%),[28-30] exhibiting favorable quality of life outcomes[28] and high patient satisfaction (96%).[30] Complications are overall infrequent, and include erosions (0-9%), dysparunia (1%), spondylitis (<1%), partial small bowel obstruction (0-4%) and a low conversion to open rate of 2.2%.[28-31] Reported operative times have ranged from 97 min to 219 minutes depending on surgeon experience.[29-30] In two retrospective comparative trials, LSC was associated with lower EBL, shorter hospital stay and increased time in the operating room (OR) as compared to ASC.[27,29] From this data, we may conclude LSC to be non-inferior to it’s open counterpart with a low incidence of adverse events.
9. Robot assisted laparoscopic sacral colpopexy and cervicopexy (RALSC)
The da Vinci surgical system (Intuitive Surgical, Sunnyvale, CA, USA) has augmented traditional laparoscopy adding three-dimensional vision, wristed instrumentation with seven degrees of freedom (versus 3 degrees with laparoscopy) and improved surgical ergonomics. Specific to sacrocolpopexy, the addition of the 4th arm adds facilitation of sigmoid colon reflection.
Robot assist laparoscopic sacrocolpopexy (RALSC) has been found to have similar outcomes to its pure laparoscopic predecessor. Efficacy appears durable with one non-comparative study of 30 patients reporting 6% recurrence at 24 months,[32] and surgical failure in two additional studies ranging from 0 - 4.7% at shorter follow up.[33,34] Such data are comparable to the 7% rate of recurrence reported in a large series of open sacralcolpopexy by Snyder and Krantz.[24] Daneshgardi and colleagues evaluated preoperative and postoperative POP-Q values in patients undergoing RALSC, reporting not only an overall improvement in global POP-Q scores, but statistically significant improvement of anterior, posterior and apical POP-Q scores separately.
Mesh erosion rates are comparable to an open incidence of 7% reported by Kohli and colleagues.[37] Length of hospital stay in 4 series ranges from 1 - 2.4 days[32,33,35,38] with operative times ranging 186 – 328 minutes.[32,34-36,38] One series reported a 25% decrease in procedure time after the initial 10 cases, suggesting a steep, but short learning curve.[36] Complications of RALSC are comparable to LSC. Ureteral injury, enterotomy and cystotomy are infrequent (0 - 1.2%) as is post op small bowel obstruction (4.7%).[32,34,36] While no randomized-controlled trials comparing RALSC to LSC have been published to our knowledge, a retrospective comparison of RALSC with ASC by Geller et al.found the former to be associated with slightly better postoperative POP-Q “C” (apex) improvement, less EBL and shorter hospital stay. While RALSC was observed to have longer operative times, there was no significant difference with respect to intraoperative or postoperative complications between the two groups.[38]
10. Description of RALSC
The patient is given appropriate antibiotic prophylaxis in the preoperative area and sequential pneumatic compression devices are applied for deep venous thrombosis prophylaxis. After intubation, the patient is placed in low - lithotomy position and straps are placed across the shoulders and chest in a criss - cross pattern to secure the patient on the table. The arms are padded and tucked. See Figure 1 for operating room configuration.
After prepping and draping of the abdomen, perineum and vagina, a foley catheter is placed. A Veress needle may be inserted through the umbilicus (or just cephalad) to facilitate insufflation of the abdomen, or the initial trocar may be introduced under direct vision employing a clear blunt–tipped device with lens inside prior to introduction of gas. In patients suspected of having significant midline abdominal adhesions, one may enter the abdomen with a 5 mm laparoscope loaded into a 5 mm clear blunt-tipped trocar at Palmer’s point (3 cm below the left costal margin in the mid-clavicular line) to visualize subsequent midline trocar placement.[39]
The initial 12 mm camera port is inserted no less than 15 cm and no greater than 22 cm from the pubic symphysis in the midline. Prior to placement of lateral trocars, the patient is placed in a steep Trendelenburg tilt. With full insufflation (not to exceed 15 mm Hg), measurements are made on the anterior abdomen to ensure appropriate placement of subsequent trocars, and avoid collision of the robotic arms (Fig. 2). Two lateral 8 mm ports are then placed 10 cm inferolateral to the camera port in the direction of the ipsilateral anterior superior iliac spine (ports 1 and 2). A 3rd 8 mm port is placed 8 – 10 cm superolateral to port 2 (port 3) and a 12 mm assistant port is placed 8 cm lateral to port 1. The robot is docked and ports secured (Fig. 3).
The sigmoid is reflected with the fourth arm employing a non-fenestrated grasper in the open position, facilitatating visualization of the sacrum. If the sigmoid shows significant redundancy, additional retraction may be provided by the introduction of a 0 – polypropylene suture on a straight needle passed percutaneously through the left lower abdomen to tether the sigmoid. Several passes are made through the appendices epiploicae and the needle re-passed to exit the abdomen at a point 1 cm lateral to its site of entry. The sigmoid is placed on gentle traction to complete exposure. The peritoneum over the promontory is then incised, with dissection carried out distally to the pelvis in between the right ureter and rectosigmoid. The pre-sacral fat is cleared and the anterior longitudinal ligament exposed (Fig. 4). This area should be well inspected for presacral vessels, the inadvertent injury to which may lead to troublesome bleeding. Should this occur we prefer the use of bipolar cautery or Ligasure® (Covidien, Norwalk, CT, USA) to control hemorrhage.
Using an EEA placed transvaginally, the apex is identified and peritoneum over the cuff incised, allowing for dissection of the vesicovaginal and rectovaginal spaces (Fig. 5). A polypropylene Y- shaped mesh is then passed through the assistant port. The mesh is tailored to ensure coverage of the anterior vaginal wall to a point just above the trigone, and the posterior wall to the level of the perineal body. The anterior limb is secured to the anterior vagina with 6 interrupted sutures of expanded PTFE or braided polyester suture (Fig. 6). Similarly, the posterior limb of the mesh is sutured to the posterior vagina, employing 8 sutures of the same (Fig. 7). Care is taken not to pass the stitch through full thickness vagina.
Next, the single arm of the Y- mesh is brought to the sacral promontory. Excess mesh is trimmed to the appropriate length (Fig. 8). Once the appropriate tension is set the, the mesh may be held with fixed tension with the fourth arm and sutured to the promontory with 2 to 4 interrupted sutures of expanded PTFE or braided polyester (Fig. 9).
Finally, the peritoneum is closed over the mesh to avoid bowel adhesions, potential erosion or small bowel obstruction (Fig. 10). This is accomplished with a running absorbable suture with a Lapra-Ty® (Ethicon Endo-Surgery, Albuquerque, NM, USA) fixed to the end (we prefer 2-0 piloglecaprone 25 stitch due to its relatively short persistence and ability to slide). The abdomen is inspected for bleeding or any unrecognized visceral injury. The vagina is inspected to confirm the apex is well supported.
The camera and robotic ports are subsequently decoupled from robotic arms and all ports removed under direct endoscopic visualization. We close both 12 mm ports with an interrupted suture of 0 polyglactin suture using the Carter-Thomason CloseSure System (Inlet Medical, Eden Prarie, MN, USA). Patients are evaluated for ureteral patency postoperatively with cystoscopy following the intravenous administration of indigo carmine. An anti-incontinence procedure may also be performed at this time if stress urinary incontinence has been diagnosed preoperatively on urodynamic testing with prolapse reduction.
11. Innovations in robotic surgical techniques for apex suspension
Traditional docking of the robot patient cart often restricts access to the patient’s perineum, a potential problem in those patients requiring concomitant vaginal and intracorporeal approaches. In this situation, side docking should be considered. Proper docking requires the patient cart to be aligned with the ipsilateral anterior superior iliac spine and midline camera port. Additionally, this technique may require lateral displacement of the 3rd robotic port, with the 4th port placed in the horizontal plane slightly above the camera site, bisecting the camera and 3rd ports (Fig. 11). We have recently adopted this technique for cases requiring simultaneous perineal and intraabdominal access, including robotic assisted laparoscopic creation of an ileal neovagina, finding overall good range of motion and relative ease of set up.
12. Conclusion
While level 1 evidence favors outcomes of abdominal sacrocolpopexy over sacrospinous ligament repairs, this comes with the attendant morbidity of a traditional open abdominal procedure. Robot assisted laparoscopic sacrocolpopexy offers the ability to support the apex in a fashion similar to the open approach with equal efficacy. This technique offers the advantages of a minimally invasive option using a modality the traditional open surgeon can adopt with a demonstrated steep but short learning curve.
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