To estimate the safety and efficacy of performing modified anterior transvaginal mesh surgery using polypropylene mesh for treatment of advanced urogenital prolapse after hysterectomy (stage III and IV vc Pelvic Organ Prolapse Quantification \[POP-Q\] system staging).
Pelvic reconstructive procedures were primarily performed using the transvaginal four arm polypropylene mesh, which was inserted through: upper arms- anterior part of obturator foramens, lower arms-ischiorectal fossas and sacrospinal ligaments. All patients underwent hysterectomy in the past apart from one which underwent vaginal hysterectomy during the procedure. Perineoplasty was performed additionally, if indicated. Subjective and objective evaluations included Pelvic Organ Prolapse Quantification \[POP-Q\] staging, preoperative and 1-year postoperative questionnaires were performed.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
180
Pelvic reconstructive procedures were performed with the use of 4-arm mesh:upper arms through- anterior part of obturator foramens, lower arms-ischiorectal fossas and sacrospinal ligaments.
patients fulfilled questionnaire before and 1 year after procedure
patients fulfilled questionnaire before and 1 year after procedure
2nd Gynecology Department
Lublin, Poland
Pelvic Organ Prolapse Quantification (POPQ) 1 year after procedure
assessment of POPQ 1 year after mesh operation, Pelvic Organ Prolapse Quantification system (POP-Q) refers to an objective, site-specific system for describing, quantifying, and staging pelvic support in women. It provides a standardized tool for documenting, comparing, and communicating clinical findings with proven interobserver and intraobserver reliability
Time frame: 1 year
Sexual function 1 year after procedure
assessment of sexual function before and 1 year after the procedure with the use of The Female Sexual Function Index questionnaire
Time frame: 1 year
Urinary incontinence 1 year after procedure
assessment of urinary incontinence before and 1 year after the procedure with the use of the Urogenital Distress Inventory (UDI 6) and the Incontinence Impact Questionnaire (IIQ 7) questionnaire
Time frame: 1 year
quality of life 1 year after procedure
assessment of quality of life before and 1 year after the procedure with the use of The Short Form Health Survey (SF 36)
Time frame: 1 year
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Pelvic Organ Prolapse staging before and 1 year after the procedure
Postoperative questionnaire assessing quality of life fulfilled by patients 1 year after procedure
patients fulfilled questionnaire before and 1 year after procedure