Laparoscopic sacrocolpopexy with mesh fixation: a randomized trial comparing synthetic cyanoacrylate glue to sutures - Scorecard - MDSpire

Laparoscopic sacrocolpopexy with mesh fixation: a randomized trial comparing synthetic cyanoacrylate glue to sutures

  • By

  • Gery Lamblin

  • Graziella Moufawad

  • Cécile Becque

  • Chloé Miguet

  • Stéphanie Moret

  • Sophie Warembourg

  • Erdogan Nohuz

  • Charles-André Philip

  • October 7, 2025

  • 0 min

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Clinical Scorecard: A Randomized Trial of Laparoscopic Sacrocolpopexy with Mesh: Comparing Synthetic Cyanoacrylate Adhesive to Suturing Techniques

At a Glance

CategoryDetail
ConditionPelvic organ prolapse (POP), specifically apical or anterior POP (POP-Q stage III/IV)
Key MechanismsMesh fixation during laparoscopic sacrocolpopexy using either synthetic cyanoacrylate glue (Ifabond™) or conventional suturing
Target PopulationWomen ≥ 18 years old with symptomatic apical or anterior POP requiring surgical correction
Care SettingGynecological surgery department, laparoscopic surgical setting

Key Highlights

  • Laparoscopic sacrocolpopexy is the gold standard for apical compartment POP with >90% success rates but requires advanced surgical skills.
  • Synthetic cyanoacrylate glue (Ifabond™) for mesh fixation reduces operative time and surgical complexity compared to suturing.
  • The randomized controlled trial showed synthetic glue is safe, effective, and time-saving with comparable anatomical and functional outcomes.

Guideline-Based Recommendations

Diagnosis

  • Include women with symptomatic apical or anterior POP at POP-Q stage III/IV for surgical intervention.
  • Exclude patients with asymptomatic prolapse, POP-Q stages I/II, pregnancy, significant comorbidities, or mesh/glue allergies.

Management

  • Perform laparoscopic sacrocolpopexy using polypropylene mesh fixed either by synthetic cyanoacrylate glue or non-absorbable sutures.
  • Use Ifabond™ glue applied dropwise at multiple fixation points on anterior and posterior vaginal walls for mesh fixation.
  • Fix mesh to sacrum with sutures in both groups and close peritoneum to retroperitonealize the mesh.

Monitoring & Follow-up

  • Schedule follow-up visits at 1, 12, and 24 months postoperatively to assess operative outcomes, complications, pain, quality of life, sexual function, and urinary incontinence.

Risks

  • Consider potential allergic reactions to mesh or glue.
  • Monitor for intraoperative complications and early postoperative pain.
  • Be aware of the inflammatory response associated with cyanoacrylate glue degradation products.

Patient & Prescribing Data

Women undergoing laparoscopic sacrocolpopexy for symptomatic apical or anterior POP (POP-Q stage III/IV).

Synthetic cyanoacrylate glue (Ifabond™) is a safe and effective alternative to suturing for mesh fixation, reducing operative time without compromising anatomical or functional outcomes.

Clinical Best Practices

  • Ensure surgeon proficiency with laparoscopic sacrocolpopexy and familiarity with glue application techniques.
  • Use standardized mesh fixation points and consistent glue volumes (1.5 mL per procedure) for reproducible results.
  • Maintain strict patient selection criteria to optimize surgical outcomes and minimize risks.
  • Perform mesh fixation to sacrum with sutures regardless of anterior/posterior mesh fixation method.
  • Close peritoneum to retroperitonealize mesh and reduce adhesion risks.

References

Original Source(s)

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