Format

Send to

Choose Destination
See comment in PubMed Commons below
Am J Obstet Gynecol. 2002 Dec;187(6):1473-80; discussion 1481-2.

Long-term success of abdominal sacral colpopexy using synthetic mesh.

Author information

1
Division of Urogynecology and Reconstructive Pelvic Surgery, Department of Obstetrics, Gynecology, and Women's Health, University of Louisville Health Sciences Center, Ky, USA. pculligan@louisville.edu

Abstract

OBJECTIVE:

The aim was to determine the minimum meaningful study period required for prospective trials involving sacral colpopexy.

STUDY DESIGN:

This is a retrospective analysis of 245 patients who underwent sacral colpopexy. Postoperative pelvic organ prolapse quantitation was our objective end point. In an effort to control for selection bias, patients who returned for postoperative examinations were compared with those who did not for clinical and demographic information. A validated prolapse-specific quality of life instrument was used to determine the subjective end points.

RESULTS:

Objective failure (any postoperative POP-Q point > or = stage II) was found in 37 (15.1%) patients. Of these, 26 (70.3%) occurred within 6 months, and 30 (81.1%) occurred within 1 year. Another 5 objective failures were discovered between 1 and 2 years after surgery for a total of 94.6% of failures occurring within 2 years. There were no clinically significant differences between the groups of women with and without objective postoperative follow-up, indicating minimal selection bias.

CONCLUSION:

It is reasonable to construct randomized controlled trials involving sacral colpopexy that only include 1- or 2-year follow-up.

PMID:
12501049
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Support Center