Meeting paper
SGS paper
Complications requiring reoperation following vaginal mesh kit procedures for prolapse

Presented at the 34th Annual Scientific Meeting of the Society of Gynecologic Surgeons, Savannah, GA, April 14-16, 2008.
https://doi.org/10.1016/j.ajog.2008.07.049Get rights and content

Objective

The objective of the study was to the characterize the symptoms and management of vaginal mesh-related complications requiring operative intervention.

Study Design

This was a case series of patients undergoing excision of vaginal graft material. Only women who had vaginal mesh placement for the correction of pelvic organ prolapse (POP) were included. We describe the symptoms, complications, and management of women treated surgically for vaginal mesh-related complications.

Results

Thirteen referred women underwent surgery for vaginal mesh-related complications. All meshes were Apogee and/or Perigee. Ten had symptomatic mesh exposures, 1 had an exposure with pelvic abscess, and 2 had pain syndromes without mesh exposure. Patients also had rectovaginal fistula, vesicovaginal fistula, recurrent POP, and persistent discharge. Five women had prior surgery for this problem. All patients underwent transvaginal mesh excision and other indicated procedures at our institution, and 6 women required a second surgery at our institution, with a median of 2 surgeries per patient.

Conclusion

Vaginal mesh placement for POP can be associated with pain, exposure, and fistula formation, requiring multiple operative interventions.

Section snippets

Materials and Methods

Surgical billing records of all reconstructive pelvic surgeons (4 urogynecologists, 1 urologist) at the University of Michigan were queried for the excision of any vaginal graft material from 1997 to 2007. The following International Classification of Diseases, 9th revision, codes were used in the search: 57295, revision (including removal) of prosthetic vaginal graft, vaginal approach; 57415, removal of impacted vaginal foreign body (separate procedure) under anesthesia; and 57287, removal or

Results

We identified 13 women who had undergone a removal, excision, or transection of a vaginal mesh that had been placed to treat pelvic organ prolapse. Although we queried billing records from the past 10 years, all cases in this series were performed between August 2005 and November 2007. All 13 women were referred from outside institutions at which their original vaginal mesh surgery had been performed.

All meshes were from the Apogee and/or Perigee system (American Medical Systems, Minnetonka,

Comment

We present a series of 13 women treated at our institution with complications following vaginal mesh surgery for prolapse. All 13 women's prostheses were from the Apogee and/or Perigee repair system. We were unable to determine whether meshes from this system have a higher exposure rate than the other available systems or whether the fact that we saw only Apogee and Perigee complications simply reflects the practice patterns in our referral area.

We found that the majority of these patients had

References (11)

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    Citation Excerpt :

    Mesh fixation has been mentioned as a crucial parameter in the development of mesh-related chronic vaginal pain. Resection of the fixation points has been shown to result in reduction of the tension and pain resolution in 90 % of patients [19,21]. We anticipated the anchorless technique would reduce post-operative complications as well, as the solid frame keeps the mesh stretched so that bunching, crimping, mesh contraction and excessive tensioning of mesh arms are avoided.

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Cite this article as: Margulies RU, Lewicky-Gaupp C, Fenner DE, et al. Complications requiring reoperation following vaginal mesh kit procedures for prolapse. Am J Obstet Gynecol 2008;199:678.e1-678.e4.

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