AI Article Synopsis

  • Laparoscopic uterosacral ligament suspension (LUSLS) is a surgical method designed to treat apical pelvic organ prolapse (POP) by tightening the uterosacral ligaments.
  • A systematic review of 13 studies involving 933 patients indicated a high anatomic success rate of 90%, with even higher rates when combined with hysterectomy.
  • The procedure shows a low complication rate of 1% and a subjective cure rate of 90.5%, but the authors call for more long-term and randomized studies to validate these results.

Article Abstract

Background: Laparoscopic uterosacral ligament suspension (LUSLS) is a technique to correct apical pelvic organ prolapse (POP) by shortening the uterosacral ligaments with sutures.

Objective: A systematic review with meta-analysis of the effectiveness and safety of LUSLS as treatment for apical POP.

Search Strategy: PubMed and Cochrane search using 'pelvic organ prolapse', 'laparoscopy' and 'uterosacral', including synonyms.

Selection Criteria: All articles in English presenting outcome of an original series of women with LUSLS as treatment of apical POP. Case reports were excluded.

Data Collection And Analysis: Study enrollment was performed by two reviewers. Our primary outcome measures were objective and subjective effectiveness of the procedure. Secondary outcome measures regarded complications and recurrence. Bias was assessed with the Newcastle Ottawa Scale.

Main Results: Of 138 hits, 13 studies were included with 933 LUSLS patients. The average follow-up was 22 months. All were nonrandomised cohort studies. The pooled anatomic success rate is 90% for all LUSLS procedures (95% confidence interval [CI] 83.3-95.5). LUSLS with hysterectomy resulted in an anatomic success rate of 96.6% (95% CI 87.5-100) and LUSLS with uterus preservation 83.4% (95% CI 67.7-94.6). The pooled subjective cure rate was 90.5% (95% CI 81.9-96.5). The rate of major complications was 1%.

Conclusions: Laparoscopic uterosacral ligament suspension (with or without uterus preservation) seems to be an effective and safe treatment for women with apical POP, but long-term prospective trials and randomised controlled trials are necessary to confirm these findings.

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Source
http://dx.doi.org/10.1111/1471-0528.17565DOI Listing

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