Obstetrics and Gynecology International

Obstetrics and Gynecology International / 2012 / Article

Clinical Study | Open Access

Volume 2012 |Article ID 376251 | https://doi.org/10.1155/2012/376251

Sara Armitage, Elvis I. Seman, Marc J. N. C. Keirse, "Use of Surgisis for Treatment of Anterior and Posterior Vaginal Prolapse", Obstetrics and Gynecology International, vol. 2012, Article ID 376251, 5 pages, 2012. https://doi.org/10.1155/2012/376251

Use of Surgisis for Treatment of Anterior and Posterior Vaginal Prolapse

Academic Editor: Papa Petros
Received19 Aug 2011
Accepted24 Nov 2011
Published15 Jan 2012


Aim. To evaluate the anatomical success and complication rate of Surgisis in the repair of anterior and posterior vaginal wall prolapse. Methods. A retrospective review of 65 consecutive Surgisis prolapse repairs, involving the anterior and/or posterior compartment, performed between 2003 and 2009, including their objective and subjective success rates using the pelvic organ prolapse quantification (POPQ) system. Results. The subjective success rate (no symptoms and no bulge beyond the hymen) was 92%, and the overall objective success rate (no subsequent prolapse in any compartment) was 66% (43 of 65). The overall reoperation rate for de novo and recurrent prolapse was 7.7% with 3 women undergoing repeat surgery at the same site (anterior compartment). No long-term complications occurred. Conclusions. Surgisis has a definite role in the surgical treatment of prolapse. It may decrease recurrences seen with native tissue repair and long-term complications of synthetic mesh. Its use in posterior compartment repair in particular is promising.

1. Introduction

The satisfactory surgical treatment of vaginal prolapse continues to elude gynaecologists, as evidenced by reports of failure rates ranging from 30% to 70% and a reoperation rate of 30% [13]. Permanent prostheses and mesh kits have been introduced in an attempt to improve these figures, but their use has been tempered by complications and long-term sequelae related to the techniques and materials used [4, 5].

Jia et al. [5] reviewed rates of objective failure and reoperation for failures and mesh excision of absorbable, biological, and nonabsorbable mesh in 3,000 women. For the anterior compartment, the objective failure rates for no mesh, absorbable mesh, biological grafts, and permanent mesh were, respectively, 29%, 23%, 18%, and 9%. However, synthetic mesh was associated with a reoperation rate of 6.6%. Biological grafts had a reoperation rate of 3%, and surgery for mesh excision occurred in another 2.6%. For the posterior compartment, there were insufficient data to determine success rates. In comparison to native tissue repair, there was a trend toward lower failure rates with absorbable and nonabsorbable synthetic meshes but higher failure rates with biological grafts. However, there is much heterogeneity in biological grafts, and most studies evaluated by Jia et al. [5] used a porcine dermal graft.

Surgisis (Cook Surgical, Bloomington, IN) is a biological graft extracted from porcine small intestinal submucosa. In comparison to porcine dermal grafts, Surgisis has a higher collagen content, is acellular, and not cross-linked. In vivo, these characteristics result in graft resorption and replacement by host connective tissue. This may reduce long-term complications, but concerns have been raised about the durability of the resultant repair [6]. To date, very few studies have been published on the use of Surgisis for vaginal prolapse repair [710]. The aim of this study was to determine the success and complication rates of Surgisis in the treatment of anterior and posterior vaginal prolapse over a six-year period.

2. Surgical Procedures and Methods

From 2003 to 2009, 65 women with pelvic organ prolapse have been treated with Surgisis xenograft by four surgeons at the Flinders Urogynaecology Unit. Women treated with Surgisis were those considered at high risk of recurrence from traditional colporrhaphy or who had a recurrence after previous surgery. The treatments involved the anterior, apical, or posterior compartment, singularly or in combination, with the surgical technique adapted accordingly. Concomitant procedures, such as hysterectomy and urethral sling, were performed as clinically indicated.

For anterior repair, a midline vaginal incision is made from the bladder neck to the anterior fornix, followed by dissection from the pubocervical fascia at the bladder neck to the white line laterally and ischial spines superiorly. A protruding bulge, if present, is reduced with a purse string suture or midline plication. Next, a patient-tailored trapezoid-shaped graft is cut from a 10 × 7 cm sheet of four-layer Surgisis, partially rehydrated, and sutured to the boundaries of the anterior compartment to achieve a snug fit. The graft is first attached at the apex. With intact apical support, the graft is attached to the cervix or the vault scar. When apical support is deficient, it is sutured to the sacrospinous ligaments vaginally or to the uterosacral ligaments laparoscopically. The distal part of the graft is laterally attached to the white line at the level of the bladder neck and then transversally sutured to the bladder neck.

For the posterior compartment, repair starts with an inverted T incision beginning at the hymen and ending below the posterior fornix. The dissection is carried apically to the ischial spines, laterally to the pelvic side wall, and distally to the perineal body fascia. The apical arms of the graft are attached first. Then, the distal portion is trimmed and attached snugly to the perineal body fascia. Tacking sutures are placed to close the gap between the pelvic side wall and the lower half of the graft.

With combined anterior and posterior prolapse, a 20 × 7 cm four-layer Surgisis graft is cut and folded to create apical arms with anterior and posterior trapezoid extensions. The graft is attached superiorly with a nonabsorbable suture; elsewhere, a delayed absorbable suture is used. Redundant vaginal skin is trimmed and the wound closed with locking absorbable suture.

Cystoscopy is performed after anterior repair and a suprapubic catheter inserted under vision. Rectal examination is conducted after posterior repair to ensure absence of suture material in the rectum and exclude compression of the rectum.

Postoperatively, women are reviewed at six weeks, six months, annually up to three years, and then biannually. At each review, they are questioned about prolapse symptoms and bowel, bladder, and sexual function. POPQ assessments [11] are made at each visit. Objective success is defined as POPQ Stage 0 or 1 in all compartments and objective failure as Stage 2 or more in any compartment. Subjective success is defined as having no more than an asymptomatic bulge not protruding beyond the hymen and subjective failure as a recurrence of symptoms with no objective prolapse. Complications were classified and coded according to the International Urogynecological Association (IUGA) and International Continence Society (ICS) joint terminology and classification of the complications related to the use of prostheses and grafts [12].

The study was approved by the Flinders Ethical Committee as an audit activity.

3. Results

Table 1 summarizes the preoperative characteristics of our cohort. Of 65 women treated with Surgisis, 39 (60%) underwent an anterior and posterior repair. Sixteen (25%) had a posterior repair only and 10 (15%) an anterior repair only. Forty-four procedures (68%) involved attachment of Surgisis to either the sacrospinous or uterosacral ligaments. Other concomitant procedures included hysterectomy (37%), continence surgery (15%), hysteropexy (10%), and native tissue repair of another compartment (7.7%). Twenty-three of the total of 103 concomitant procedures were laparoscopically assisted, and none involved open abdominal surgery.


Age in years (median, range)66 (40–84)
Weight in kg (median, range)75 (48–110)
Parity (median, range)2 (0–4)
Previous treatments
 Prolapse surgery2741.5
Prolapse stage (POPQ) [11]
Presenting symptoms
 Vaginal lump5381.5
 Bladder symptoms3756.9
  Recurrent infection23.1
 Bowel symptoms2640.0
  Evacuation difficulty2233.8
  Faecal/flatal incontinence46.2
  Back pain23.1
  Dragging discomfort11.5

The average duration of the combined procedures was 102 minutes with a median of 150 minutes (range: 50–240). Median estimated blood loss was 300 mL (range: 20–1.550 mL). Median duration of hospitalisation was 4 days (range: 2–43), and mean followup was 75 weeks.

Major surgical complications occurred in 4 women (6.2%). Three had an estimated blood loss >1.000 mL or required transfusion (IUGA/ICS classification [12]: 7A.T1). One woman suffered a small bowel injury not recognised at the time of laparoscopy (5C.T1.S5). Other complications included 13 (20.0%) vaginal/pelvic infections treated with oral antibiotics (1C.T2.S1/S2), 11 (16.9%) urinary tract infections, 12 women (18.5%) required a suprapubic catheter for more than 7 days (4B.T2), and 7 (10.8%) reported either persistent or de novo dyspareunia (1B.T4.S2). There were no cases of graft exposure, erosion, rejection, or seroma formation.

The objective success rate (POPQ Stage 0 or 1 in all compartments) was 66% (43 of 65). Of 22 objective failures, 16 had an asymptomatic bulge above the hymen giving a subjective success rate of 92%. Three women (4.6%) had repeat surgery; two are planning further surgery; one remained symptomatic but declined further surgery.

Table 2 shows the success rate per compartment repaired, and Table 3 shows the sites affected by recurrence or subsequent prolapse. Of 10 women in the anterior only group, four developed further prolapse: one recurrence of cystocoele and three de novo rectocoeles. One cystocoele and one rectocoele are asymptomatic (Aa = −1, Ap = −1), and two women with rectocoele (Ap = 0) underwent fascial repair. Among 16 women in the posterior only group, four had a subsequent prolapse. Three, all remaining asymptomatic, developed a de novo cystocoele (Aa = −1, Ba = −1, Aa = +1). The affected site was not recorded for the other.

Compartment repairedNo. of patientsObjective cure*Subjective cure*Failure

Anterior10 (15.4%)682
Posterior16 (24.6%)12151
Both39 (60.0%)25363
Total65 (100%)43596

*Objective cure is defined as POPQ stage <2 at the last followup. Subjective cure refers to women with no symptoms, no bulge beyond the hymen, and happy with the result.

Site of subsequent prolapse Compartment repaired
Anterior ( )Posterior ( )Anterior and posterior ( )

Not specified11

*Two women had a subsequent prolapse in two compartments (vault and anterior wall).

Fourteen of 39 women treated with both anterior and posterior Surgisis experienced further prolapse (Table 3). Nine involved the anterior compartment, two the vault and anterior wall, one the vault only, one the posterior compartment only, and, in one, the site was not documented. Three of the anterior compartment recurrences were symptomatic and underwent surgery with permanent polypropylene mesh.

Overall, the anterior recurrence rate was 12 of 49 (24.5%) and the same site reoperation rate (planned and performed) was 3 of 49 (6.1%). After anterior repair two women developed a rectocoele that required repair. The posterior recurrence rate was one in 55 (1.8%) with no reoperations required.

Table 4 displays the timing and site of subsequent prolapse regardless of the site repaired. There was a failure rate of 29% (16% objective and 13% subjective) in women followed up to a year. This rate did not change significantly for those followed up to five years, but absolute numbers are small. Symptomatic recurrences did not appear to increase over time.

Duration of followupNo. of patientsObjective cure*Subjective cure*Failure

Up to 1 year6543596
Up to 3 years3320312
Up to 5 years107100
More than 5 years3230

*Objective cure is defined as POPQ stage <2 at the last followup. Subjective cure refers to women with no symptoms, no bulge beyond the hymen, and happy with the result.

4. Discussion

The quest for the ultimate prolapse repair continues unabated despite the availability of various prosthetic and graft materials. Although it is generally accepted that they result in lower short-term recurrence rates, especially in the anterior compartment, there are also substantial drawbacks. These include significant prosthesis- and graft-related complications, difficulty treating subsequent failures, and no demonstrated benefit on quality of life and sexual function [5, 1315]. The ideal graft material would allow correction of vaginal anatomy whilst maintaining pelvic organ function. It would be biocompatible, inert, sterile, resistant to physical modification, of mechanical stress and shrinkage, readily available, inexpensive, with minimal risks of infection and rejection [16].

Biological grafts from other species (xenografts) have been used to repair hernias and pelvic organ prolapse for many years [17]. They are thought to reduce complications of erosion, fistula formation, and infection seen with permanent prosthetic material [6]. Several xenografts are currently used in vaginal reconstruction [17]. They differ in species of origin (bovine or porcine), site of harvest (pericardium, dermis, intestinal submucosa), sterilisation process, and cross-linking during manufacture.

Surgisis is an acellular, three-dimensional lattice of collagen, and extracellular matrix, not cross-linked, derived from the submucosa of porcine small intestine. Being acellular, Surgisis minimises risks of viral or prion transmission, inflammatory responses, rejection, and exposure [7, 16]. The absence of chemical cross-linking facilitates colonisation by host cells and avoids encapsulation and poor fixation at the graft-host interface, which could weaken the repair [6]. The matrix encourages host angiogenesis, connective tissue and epithelial differentiation and ingrowth, eventually replacing the graft with constructive connective tissue remodelling instead of scar tissue [18]. Graft resorption is believed to reduce long-term complications, such as graft exposure and dyspareunia. Concern remains, however, about the durability of the repair after remodelling [6].

Apart from congress abstracts, there are very few studies on the use of Surgisis in pelvic floor repair. These include one randomised controlled trial of women undergoing anterior compartment repair [8] and three retrospective comparative studies [7, 9, 10]. The randomised trial with 56 patients compared Surgisis with traditional anterior colporrhaphy [8]. The anatomical cure (POPQ Stage 0 or 1) at 12 months was 86.2% with Surgisis and 59.3% with conventional colporrhaphy [8]. Improvement in quality of life was similar in both groups. More intraoperative complications, mainly “excessive” blood loss without transfusion, occurred in the Surgisis group. There were no graft infections or exposures. In women treated for recurrent cystocoele, anterior colporrhaphy had a much higher failure rate than Surgisis (57.1% versus 14.3%). This supports the contention that women with recurrent prolapse are likely to have intrinsically weak support tissue or poor healing, benefiting most from augmented repair.

Chaliha et al. [7] reported on 28 women undergoing either colporrhaphy or Surgisis augmentation for anterior prolapse and found an improvement in objective measurements and quality of life at six months, but no difference at two years. However, lack of randomisation and small numbers limit interpretation of these data. A comparative study by Mouritsen et al. [9], with a median followup of three years, found better results with Surgisis than with anterior or posterior colporrhaphy, but the difference was not statistically significant. Reid and Luo [10] compared 108 bridging graft vaginal paravaginal repairs (89 using Surgisis) with 59 native tissue cystocoele repairs [10]. With bridging grafts, cystocoele persistence was reduced from 10.2% to 4.6% and late recurrences from 22.6% to 4.9% [10].

A randomised trial reported by Paraiso et al. [19] is often considered relevant to the use of porcine implants in rectocoele repair [14]. It compared three different techniques, one of which included a porcine-derived graft (Fortagen). There was a significant improvement in quality of life and sexual function in all groups, but the Fortagen group had the highest anatomical failure rate. However, Fortagen is cross-linked and more prone to encapsulation and poor fixation at the graft-host interface than Surgisis.

The current study presents 65 women followed for a variable time up to six years. Compared with other studies mentioned, our failure rate is slightly higher for the anterior compartment, but lower for the posterior compartment. Our results, relating predominantly to women with previous surgery or considered at increased risk of recurrence, support the use of Surgisis. Most subjective failures also occurred in the unrepaired compartment. The anterior only group had four “failures,” two of which were symptomatic rectocoeles that underwent repair. Of the four “failures” in the posterior only group, three were anterior and they remain asymptomatic. The development of de novo prolapse after repair could be due to a delayed manifestation of generally weak support tissue, undertreatment (prolapse in one compartment missed or masked by prolapse in another), or alteration in the vaginal axis, predisposing to later prolapse. More often than not, pelvic floor dysfunction is not confined to a single support structure [20]. Subclinical poor support in a particular compartment may thus become more manifest after correction of visible prolapse in another [20].

Thus far, Surgisis shows most promise in the treatment of recurrent rectocoele. At Flinders urogynaecology, fascial repair remains the primary approach for posterior prolapse. Surgisis is used for recurrences, and permanent mesh is used when both these procedures failed. For anterior prolapse, the approach is dictated by the integrity of the levator muscle [21], vaginal rugation, and vaginal sacculation. With clinically intact levators and no sacculation, anterior colporrhaphy is the primary approach. With avulsed levators, intact rugae, and no sacculation, laparoscopic paravaginal repair is preferred. The remaining cases of cystocoele are at high risk of recurrence with native tissue repair and require graft or prosthetic augmentation. In these circumstances, Surgisis is used for the primary repair and permanent mesh for recurrences.

In general, the frequency of recurrence after prolapse repair increases with time [22]. There were no indications to that effect in our study. This suggests that Surgisis, when effective, achieves a durable result, perhaps because the new connective tissue is stronger than the original or because the graft offers critical support while the new connective tissue gains in strength. However, 75% of the operations were performed between 2007 and 2009, resulting in only 10 with a followup of more than three years. This emphasises the well-recognized need for long-term followup after prolapse surgery, difficult to achieve as it may be, particularly when people remain asymptomatic.

Conflict of Interests

None of the authors has any conflict of interests, financial or otherwise, in respect of the data or opinions expressed in this paper.

Ethical Approval

This study was approved by the Flinders Ethical Committee as an audit activity not requiring further ethical assessment.


  1. P. K. Sand, S. Koduri, R. W. Lobel et al., “Prospective randomized trial of polyglactin 910 mesh to prevent recurrence of cystoceles and rectoceles,” American Journal of Obstetrics and Gynecology, vol. 184, no. 7, pp. 1357–1364, 2001. View at: Publisher Site | Google Scholar
  2. A. M. Weber, M. D. Walters, M. R. Piedmonte, and L. A. Ballard, “Anterior colporrhaphy: a randomised trial of 3 surgical techniques,” American Journal of Obstetrics & Gynecology, vol. 185, pp. 1299–1306, 2001. View at: Google Scholar
  3. A. L. Olsen, V. J. Smith, J. O. Bergstrom, J. C. Colling, and A. L. Clark, “Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence,” Obstetrics and Gynecology, vol. 89, no. 4, pp. 501–506, 1997. View at: Publisher Site | Google Scholar
  4. B. Jacquetin and M. Cosson, “Complications of vaginal mesh: our experience,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 20, no. 8, pp. 893–896, 2009. View at: Publisher Site | Google Scholar
  5. X. Jia, C. Glazener, G. Mowatt et al., “Efficacy and safety of using mesh or grafts in surgery for anterior and/or posterior vaginal wall prolapse: systematic review and meta-analysis,” An International Journal of Obstetrics and Gynaecology, vol. 115, no. 11, pp. 1350–1361, 2008. View at: Publisher Site | Google Scholar
  6. E. C. Trabuco, C. J. Klingele, and J. B. Gebhart, “Xenograft use in reconstructive pelvic surgery: a review of the literature,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 18, no. 5, pp. 555–563, 2007. View at: Publisher Site | Google Scholar
  7. C. Chaliha, U. Khalid, L. Campagna, G. A. Digesu, B. Ajay, and V. Khullar, “SIS graft for anterior vaginal wall prolapse repair—a case-controlled study,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 17, no. 5, pp. 492–497, 2006. View at: Publisher Site | Google Scholar
  8. P. C. Feldner, R. A. Castro, L. A. Cipolotti, C. A. Delroy, M. G. F. Sartori, and M. J. B. C. Girão, “Anterior vaginal wall prolapse: a randomized controlled trial of SIS graft versus traditional colporrhaphy,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 21, no. 9, pp. 1057–1063, 2010. View at: Publisher Site | Google Scholar
  9. L. Mouritsen, M. Kronschnabl, and G. Lose, “Long-term results of vaginal repairs with and without xenograft reinforcement,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 21, no. 4, pp. 467–473, 2010. View at: Publisher Site | Google Scholar
  10. R. I. Reid and K. Luo, “Site-specific prolapse surgery. II. Vaginal paravaginal repair augmented with either synthetic mesh or remodelling xenograft,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 22, no. 5, pp. 601–609, 2011. View at: Publisher Site | Google Scholar
  11. R. C. Bump, A. Mattiasson, K. Bo et al., “The standardization of terminology of female pelvic organ prolapse and pelvic floor dysfunction,” American Journal of Obstetrics and Gynecology, vol. 175, no. 1, pp. 10–17, 1996. View at: Google Scholar
  12. B. T. Haylen, R. M. Freeman, S. E. Swift et al., “An International Urogynecological Association (IUGA) / International Continence Society (ICS) joint terminology and classification of the complications related directly to the insertion of prostheses (meshes, implants, tapes) & grafts in female pelvic floor surgery,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 22, no. 1, pp. 3–15, 2011. View at: Publisher Site | Google Scholar
  13. R. Foon, P. Toozs-Hobson, and P. M. Latthe, “Adjuvant materials in anterior vaginal wall prolapse surgery: a systematic review of effectiveness and complications,” International Urogynecology Journal and Pelvic Floor Dysfunction, vol. 19, no. 12, pp. 1697–1706, 2008. View at: Publisher Site | Google Scholar
  14. C. Maher, B. Feiner, K. Baessler, E. J. Adams, S. Hagen, and C. M. Glazener, “Surgical management of pelvic organ prolapse in women,” Cochrane Database of Systematic Reviews, vol. 4, Article ID CD004014, 2010. View at: Google Scholar
  15. J. N. Nguyen, “The use of grafts for anterior vaginal prolapse repair: pros and cons,” Current Opinion in Obstetrics and Gynecology, vol. 20, no. 5, pp. 501–505, 2008. View at: Publisher Site | Google Scholar
  16. C. C. G. Chen, B. Ridgeway, and M. F. R. Paraiso, “Biologic grafts and synthetic meshes in pelvic reconstructive surgery,” Clinical Obstetrics and Gynecology, vol. 50, no. 2, pp. 383–411, 2007. View at: Publisher Site | Google Scholar
  17. K. Griffis and D. S. Hale, “Grafts in pelvic reconstructive surgery,” Clinical Obstetrics and Gynecology, vol. 48, no. 3, pp. 713–723, 2005. View at: Publisher Site | Google Scholar
  18. J. Hodde, “Extracellular matrix as a bioactive material for soft tissue reconstruction,” ANZ Journal of Surgery, vol. 76, no. 12, pp. 1096–1100, 2006. View at: Publisher Site | Google Scholar
  19. M. F. R. Paraiso, M. D. Barber, T. W. Muir, and M. D. Walters, “Rectocele repair: a randomised trial of three surgical techniques including graft augmentation,” American Journal of Obstetrics & Gynecology, vol. 195, pp. 1762–1771, 2006. View at: Google Scholar
  20. P. E. P. Petros, The Female Pelvic Floor: Function, Dysfunction and Management According to the Integral Theory, Springer, New York, NY, USA, 3rd edition, 2011.
  21. H. P. Dietz, V. Chantarasorn, and K. L. Shek, “Levator avulsion is a risk factor for cystocele recurrence,” Ultrasound in Obstetrics and Gynecology, vol. 36, no. 1, pp. 76–80, 2010. View at: Publisher Site | Google Scholar
  22. B. L. Shull, C. Bachofen, K. W. Coates, and T. J. Kuehl, “A transvaginal approach to repair of apical and other associated sites of pelvic organ prolapse with uterosacral ligaments,” American Journal of Obstetrics and Gynecology, vol. 183, no. 6, pp. 1365–1374, 2000. View at: Publisher Site | Google Scholar

Copyright © 2012 Sara Armitage et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles