One Year Outcome After Robotic Assisted Laparoscopic Sacral Colpopexy, a Case Series Review

Atlantic Health System75 enrolled

Overview

Robotic approach to sacral colpopexy is a relatively new procedure. The literature is scarce in regard to its long-term outcomes. This advanced procedure is offered at MMH through the Urogynecology division. The Investigators setup to review the one year outcome of patients who underwent this procedure using a polypropylene mesh. These outcomes will include anatomical and quality of life measures.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Pelvic Organ Prolapse Urinary Incontinence

Eligibility

Sex: FEMALEMin age: 21 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Any Robotic assisted laparoscopic sacral colpopexy with polypropylene mesh during the study period Exclusion Criteria: * Other graft material than polypropylene. * Enrollment in a different study.

Locations (1)

Atlantic Health Urogynecology

Morristown, New Jersey, United States

Outcomes

Primary Outcomes

1. Objective anatomic outcomes We will use the pelvic organ prolapse quantification system (POP-Q). Objective surgical failure will be defined as any prolapse at or beyond the introitus

Time frame: one year

Secondary Outcomes

2. Prolapse Specific Quality of Life Patients will complete a prolapse specific quality of life instrument prior to and one year after surgery. (PFIQ-7)

Time frame: one year

3. Pelvic organ prolapse related symptoms (PFDI-20)

Time frame: one year

4. Graft-related complications Rates of graft erosion into adjacent organs such as bowel, bladder or vagina - during the study period will be reported.

Time frame: one year

Data from ClinicalTrials.gov

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